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Record Information

Version

5.0

Status

Detected and Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2022-09-22 18:34:15 UTC

HMDB ID

HMDB0000949

Secondary Accession Numbers

HMDB00949

Metabolite Identification

Common Name

Tetrahydrocortisol

Description

Tetrahydrocortisol belongs to the class of organic compounds known as 21-hydroxysteroids. These are steroids carrying a hydroxyl group at the 21-position of the steroid backbone. Based on a literature review a significant number of articles have been published on Tetrahydrocortisol.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

  Mrv0541 02231218502D          

 26 29  0  0  1  0            999 V2000
    9.3003  -10.2731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3222   -9.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9410  -12.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6697  -11.9729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8430  -11.0467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2028  -11.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5717  -10.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7111  -10.3946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5129  -12.3089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7577   -9.4995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6576   -9.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2417  -11.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8136  -11.8712    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.6990  -11.1485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4277  -10.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0290   -9.8863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8826   -9.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9997  -10.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2710  -11.0976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4571   -9.9372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.2503   -9.7103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.8004  -10.2757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0849  -12.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3297   -9.4487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7399   -8.3679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1076   -8.8977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 19  1  1  1  0  0  0
 20  2  1  1  0  0  0
  3 12  1  0  0  0  0
  3  4  1  0  0  0  0
  4 14  1  0  0  0  0
  5  7  1  0  0  0  0
  5 13  1  0  0  0  0
  6 15  1  0  0  0  0
  6  8  1  0  0  0  0
  7 19  1  0  0  0  0
  8 21  1  0  0  0  0
  9 13  1  0  0  0  0
  9 12  1  0  0  0  0
 10 20  1  0  0  0  0
 10 16  1  0  0  0  0
 11 17  1  0  0  0  0
 11 22  1  0  0  0  0
 12 19  1  0  0  0  0
 13 23  1  6  0  0  0
 14 15  1  0  0  0  0
 14 18  1  0  0  0  0
 15 20  1  0  0  0  0
 16 24  1  1  0  0  0
 16 18  1  0  0  0  0
 21 17  1  0  0  0  0
 17 25  2  0  0  0  0
 18 19  1  0  0  0  0
 20 21  1  0  0  0  0
 21 26  1  6  0  0  0
M  END

HMDB0000949
     RDKit          3D
Tetrahydrocortisol
 60 63  0  0  0  0  0  0  0  0999 V2000
   -2.5867   -1.6106   -0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1816   -0.2289    0.0894 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8048    0.1488    1.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3022   -0.0339    1.2930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9245    0.7595    0.1989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2109    2.0515    0.6594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1802    0.7625   -1.0920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041    0.7297   -0.9863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1259    0.2154   -2.2919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6414    0.2079   -2.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0088   -0.4481   -1.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053    0.0106    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0323   -0.4519    1.3937 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1369   -1.7895    1.6699 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3890    0.0549    1.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1307   -0.4253    0.2353 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3966   -1.8871    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988    0.0630   -1.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3557   -0.3423   -2.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236   -0.0635   -1.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4489    0.3054    0.0058 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2255    1.6880    0.0224 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4977   -0.1045    0.9421 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8015   -1.2763    1.0348 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1901    0.8931    1.7752 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7212    2.1755    1.5429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8884   -2.2353    0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5530   -1.5297   -0.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8954   -2.1338   -0.9688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012    1.1677    1.6576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4641   -0.6102    2.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5129   -1.1057    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7246    0.3506    2.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9360    0.2989   -0.0081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7770    2.2612    1.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4473    1.7315   -1.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5562   -0.0209   -1.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2796    1.7168   -0.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4753    0.9144   -3.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5784   -0.7757   -2.5454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2728    1.2500   -2.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3084   -0.3504   -3.2087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0400   -1.5454   -1.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5814    1.1364    0.1335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5507    0.0872    2.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5299   -2.3543    0.9889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3338    1.1625    1.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8382   -0.3000    2.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6728   -2.2208    1.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2489   -2.1518   -0.4664 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5386   -2.4939   -0.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3826    1.1694   -0.9634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2607    0.2227   -3.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3466   -1.4144   -2.3229 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1670    0.8224   -1.9697 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4201   -0.8929   -1.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2027    2.0867   -0.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1063    0.6718    2.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2894    0.8859    1.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2336    2.7955    2.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
  8  2  1  0
 18 11  1  0
 12  2  1  0
 21 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  1
 14 46  1  0
 15 47  1  0
 15 48  1  0
 17 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 22 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
M  END

  Mrv0541 02231218502D          

 26 29  0  0  1  0            999 V2000
    9.3003  -10.2731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3222   -9.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9410  -12.3597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6697  -11.9729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8430  -11.0467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2028  -11.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5717  -10.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7111  -10.3946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5129  -12.3089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7577   -9.4995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6576   -9.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2417  -11.9220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8136  -11.8712    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.6990  -11.1485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4277  -10.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0290   -9.8863    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.8826   -9.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9997  -10.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2710  -11.0976    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4571   -9.9372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.2503   -9.7103    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.8004  -10.2757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0849  -12.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3297   -9.4487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7399   -8.3679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1076   -8.8977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 19  1  1  1  0  0  0
 20  2  1  1  0  0  0
  3 12  1  0  0  0  0
  3  4  1  0  0  0  0
  4 14  1  0  0  0  0
  5  7  1  0  0  0  0
  5 13  1  0  0  0  0
  6 15  1  0  0  0  0
  6  8  1  0  0  0  0
  7 19  1  0  0  0  0
  8 21  1  0  0  0  0
  9 13  1  0  0  0  0
  9 12  1  0  0  0  0
 10 20  1  0  0  0  0
 10 16  1  0  0  0  0
 11 17  1  0  0  0  0
 11 22  1  0  0  0  0
 12 19  1  0  0  0  0
 13 23  1  6  0  0  0
 14 15  1  0  0  0  0
 14 18  1  0  0  0  0
 15 20  1  0  0  0  0
 16 24  1  1  0  0  0
 16 18  1  0  0  0  0
 21 17  1  0  0  0  0
 17 25  2  0  0  0  0
 18 19  1  0  0  0  0
 20 21  1  0  0  0  0
 21 26  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0000949

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@]12C[C@H](O)C3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@]2(O)C(=O)CO

> <INCHI_IDENTIFIER>
InChI=1S/C21H34O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h12-16,18,22-24,26H,3-11H2,1-2H3/t12?,13-,14?,15?,16+,18?,19+,20+,21+/m1/s1

> <INCHI_KEY>
AODPIQQILQLWGS-OBRSLYEHSA-N

> <FORMULA>
C21H34O5

> <MOLECULAR_WEIGHT>
366.4917

> <EXACT_MASS>
366.240624198

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
40.89070801334035

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-hydroxy-1-[(2S,5R,14R,15S,17S)-5,14,17-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]ethan-1-one

> <ALOGPS_LOGP>
1.38

> <JCHEM_LOGP>
1.1134999679999997

> <ALOGPS_LOGS>
-2.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.866131690656431

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.584777685879395

> <JCHEM_PKA_STRONGEST_BASIC>
-1.356956600538469

> <JCHEM_POLAR_SURFACE_AREA>
97.99

> <JCHEM_REFRACTIVITY>
97.60139999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.66e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-1-[(2S,5R,14R,15S,17S)-5,14,17-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]ethanone

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000949
     RDKit          3D
Tetrahydrocortisol
 60 63  0  0  0  0  0  0  0  0999 V2000
   -2.5867   -1.6106   -0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1816   -0.2289    0.0894 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8048    0.1488    1.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3022   -0.0339    1.2930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9245    0.7595    0.1989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2109    2.0515    0.6594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1802    0.7625   -1.0920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041    0.7297   -0.9863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1259    0.2154   -2.2919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6414    0.2079   -2.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0088   -0.4481   -1.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053    0.0106    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0323   -0.4519    1.3937 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1369   -1.7895    1.6699 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3890    0.0549    1.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1307   -0.4253    0.2353 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3966   -1.8871    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988    0.0630   -1.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3557   -0.3423   -2.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236   -0.0635   -1.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4489    0.3054    0.0058 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2255    1.6880    0.0224 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4977   -0.1045    0.9421 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8015   -1.2763    1.0348 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1901    0.8931    1.7752 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7212    2.1755    1.5429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8884   -2.2353    0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5530   -1.5297   -0.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8954   -2.1338   -0.9688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012    1.1677    1.6576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4641   -0.6102    2.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5129   -1.1057    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7246    0.3506    2.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9360    0.2989   -0.0081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7770    2.2612    1.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4473    1.7315   -1.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5562   -0.0209   -1.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2796    1.7168   -0.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4753    0.9144   -3.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5784   -0.7757   -2.5454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2728    1.2500   -2.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3084   -0.3504   -3.2087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0400   -1.5454   -1.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5814    1.1364    0.1335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5507    0.0872    2.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5299   -2.3543    0.9889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3338    1.1625    1.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8382   -0.3000    2.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6728   -2.2208    1.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2489   -2.1518   -0.4664 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5386   -2.4939   -0.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3826    1.1694   -0.9634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2607    0.2227   -3.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3466   -1.4144   -2.3229 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1670    0.8224   -1.9697 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4201   -0.8929   -1.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2027    2.0867   -0.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1063    0.6718    2.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2894    0.8859    1.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2336    2.7955    2.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
  8  2  1  0
 18 11  1  0
 12  2  1  0
 21 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  1
 14 46  1  0
 15 47  1  0
 15 48  1  0
 17 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 22 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      17.361 -19.176   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.135 -16.988   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.557 -23.071   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.917 -22.349   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.640 -20.621   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.779 -20.616   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.001 -19.898   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      23.727 -19.403   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      15.891 -22.977   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.081 -17.732   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      25.494 -17.664   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.251 -22.254   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.585 -22.160   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      19.971 -20.811   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.332 -20.089   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      18.721 -18.454   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      24.048 -17.137   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.666 -19.993   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.306 -20.716   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.387 -18.549   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      22.867 -18.126   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      25.761 -19.181   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      13.225 -22.882   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      17.415 -17.638   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      23.781 -15.620   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      22.601 -16.609   0.000  0.00  0.00           O+0
CONECT    1   19                                                            
CONECT    2   20                                                            
CONECT    3   12    4                                                       
CONECT    4    3   14                                                       
CONECT    5    7   13                                                       
CONECT    6   15    8                                                       
CONECT    7    5   19                                                       
CONECT    8    6   21                                                       
CONECT    9   13   12                                                       
CONECT   10   20   16                                                       
CONECT   11   17   22                                                       
CONECT   12    3    9   19                                                  
CONECT   13    5    9   23                                                  
CONECT   14    4   15   18                                                  
CONECT   15    6   14   20                                                  
CONECT   16   10   24   18                                                  
CONECT   17   11   21   25                                                  
CONECT   18   14   16   19                                                  
CONECT   19    1    7   12   18                                             
CONECT   20    2   10   15   21                                             
CONECT   21    8   17   20   26                                             
CONECT   22   11                                                            
CONECT   23   13                                                            
CONECT   24   16                                                            
CONECT   25   17                                                            
CONECT   26   21                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

COMPND    HMDB0000949
HETATM    1  C1  UNL     1      -2.587  -1.611  -0.299  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.182  -0.229   0.089  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.805   0.149   1.397  1.00  0.00           C  
HETATM    4  C4  UNL     1      -4.302  -0.034   1.293  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.924   0.760   0.199  1.00  0.00           C  
HETATM    6  O1  UNL     1      -5.211   2.051   0.659  1.00  0.00           O  
HETATM    7  C6  UNL     1      -4.180   0.763  -1.092  1.00  0.00           C  
HETATM    8  C7  UNL     1      -2.704   0.730  -0.986  1.00  0.00           C  
HETATM    9  C8  UNL     1      -2.126   0.215  -2.292  1.00  0.00           C  
HETATM   10  C9  UNL     1      -0.641   0.208  -2.311  1.00  0.00           C  
HETATM   11  C10 UNL     1       0.009  -0.448  -1.120  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.705   0.011   0.148  1.00  0.00           C  
HETATM   13  C12 UNL     1      -0.032  -0.452   1.394  1.00  0.00           C  
HETATM   14  O2  UNL     1      -0.137  -1.790   1.670  1.00  0.00           O  
HETATM   15  C13 UNL     1       1.389   0.055   1.421  1.00  0.00           C  
HETATM   16  C14 UNL     1       2.131  -0.425   0.235  1.00  0.00           C  
HETATM   17  C15 UNL     1       2.397  -1.887   0.194  1.00  0.00           C  
HETATM   18  C16 UNL     1       1.399   0.063  -1.022  1.00  0.00           C  
HETATM   19  C17 UNL     1       2.356  -0.342  -2.076  1.00  0.00           C  
HETATM   20  C18 UNL     1       3.724  -0.063  -1.437  1.00  0.00           C  
HETATM   21  C19 UNL     1       3.449   0.305   0.006  1.00  0.00           C  
HETATM   22  O3  UNL     1       3.226   1.688   0.022  1.00  0.00           O  
HETATM   23  C20 UNL     1       4.498  -0.104   0.942  1.00  0.00           C  
HETATM   24  O4  UNL     1       4.801  -1.276   1.035  1.00  0.00           O  
HETATM   25  C21 UNL     1       5.190   0.893   1.775  1.00  0.00           C  
HETATM   26  O5  UNL     1       4.721   2.175   1.543  1.00  0.00           O  
HETATM   27  H1  UNL     1      -2.888  -2.235   0.592  1.00  0.00           H  
HETATM   28  H2  UNL     1      -3.553  -1.530  -0.881  1.00  0.00           H  
HETATM   29  H3  UNL     1      -1.895  -2.134  -0.969  1.00  0.00           H  
HETATM   30  H4  UNL     1      -2.501   1.168   1.658  1.00  0.00           H  
HETATM   31  H5  UNL     1      -2.464  -0.610   2.160  1.00  0.00           H  
HETATM   32  H6  UNL     1      -4.513  -1.106   1.273  1.00  0.00           H  
HETATM   33  H7  UNL     1      -4.725   0.351   2.266  1.00  0.00           H  
HETATM   34  H8  UNL     1      -5.936   0.299  -0.008  1.00  0.00           H  
HETATM   35  H9  UNL     1      -4.777   2.261   1.511  1.00  0.00           H  
HETATM   36  H10 UNL     1      -4.447   1.731  -1.611  1.00  0.00           H  
HETATM   37  H11 UNL     1      -4.556  -0.021  -1.810  1.00  0.00           H  
HETATM   38  H12 UNL     1      -2.280   1.717  -0.773  1.00  0.00           H  
HETATM   39  H13 UNL     1      -2.475   0.914  -3.080  1.00  0.00           H  
HETATM   40  H14 UNL     1      -2.578  -0.776  -2.545  1.00  0.00           H  
HETATM   41  H15 UNL     1      -0.273   1.250  -2.402  1.00  0.00           H  
HETATM   42  H16 UNL     1      -0.308  -0.350  -3.209  1.00  0.00           H  
HETATM   43  H17 UNL     1       0.040  -1.545  -1.211  1.00  0.00           H  
HETATM   44  H18 UNL     1      -0.581   1.136   0.133  1.00  0.00           H  
HETATM   45  H19 UNL     1      -0.551   0.087   2.242  1.00  0.00           H  
HETATM   46  H20 UNL     1      -0.530  -2.354   0.989  1.00  0.00           H  
HETATM   47  H21 UNL     1       1.334   1.163   1.380  1.00  0.00           H  
HETATM   48  H22 UNL     1       1.838  -0.300   2.370  1.00  0.00           H  
HETATM   49  H23 UNL     1       2.673  -2.221   1.216  1.00  0.00           H  
HETATM   50  H24 UNL     1       3.249  -2.152  -0.466  1.00  0.00           H  
HETATM   51  H25 UNL     1       1.539  -2.494  -0.210  1.00  0.00           H  
HETATM   52  H26 UNL     1       1.383   1.169  -0.963  1.00  0.00           H  
HETATM   53  H27 UNL     1       2.261   0.223  -3.021  1.00  0.00           H  
HETATM   54  H28 UNL     1       2.347  -1.414  -2.323  1.00  0.00           H  
HETATM   55  H29 UNL     1       4.167   0.822  -1.970  1.00  0.00           H  
HETATM   56  H30 UNL     1       4.420  -0.893  -1.560  1.00  0.00           H  
HETATM   57  H31 UNL     1       3.203   2.087  -0.880  1.00  0.00           H  
HETATM   58  H32 UNL     1       5.106   0.672   2.869  1.00  0.00           H  
HETATM   59  H33 UNL     1       6.289   0.886   1.565  1.00  0.00           H  
HETATM   60  H34 UNL     1       5.234   2.796   2.124  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3    8   12
CONECT    3    4   30   31
CONECT    4    5   32   33
CONECT    5    6    7   34
CONECT    6   35
CONECT    7    8   36   37
CONECT    8    9   38
CONECT    9   10   39   40
CONECT   10   11   41   42
CONECT   11   12   18   43
CONECT   12   13   44
CONECT   13   14   15   45
CONECT   14   46
CONECT   15   16   47   48
CONECT   16   17   18   21
CONECT   17   49   50   51
CONECT   18   19   52
CONECT   19   20   53   54
CONECT   20   21   55   56
CONECT   21   22   23
CONECT   22   57
CONECT   23   24   24   25
CONECT   25   26   58   59
CONECT   26   60
END

HMDB0000949
     RDKit          3D
Tetrahydrocortisol
 60 63  0  0  0  0  0  0  0  0999 V2000
   -2.5867   -1.6106   -0.2994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1816   -0.2289    0.0894 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8048    0.1488    1.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3022   -0.0339    1.2930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9245    0.7595    0.1989 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2109    2.0515    0.6594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1802    0.7625   -1.0920 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7041    0.7297   -0.9863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1259    0.2154   -2.2919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6414    0.2079   -2.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0088   -0.4481   -1.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053    0.0106    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0323   -0.4519    1.3937 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1369   -1.7895    1.6699 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3890    0.0549    1.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1307   -0.4253    0.2353 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3966   -1.8871    0.1944 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3988    0.0630   -1.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3557   -0.3423   -2.0765 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7236   -0.0635   -1.4374 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4489    0.3054    0.0058 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2255    1.6880    0.0224 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4977   -0.1045    0.9421 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8015   -1.2763    1.0348 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1901    0.8931    1.7752 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7212    2.1755    1.5429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8884   -2.2353    0.5925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5530   -1.5297   -0.8807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8954   -2.1338   -0.9688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012    1.1677    1.6576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4641   -0.6102    2.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5129   -1.1057    1.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7246    0.3506    2.2656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9360    0.2989   -0.0081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7770    2.2612    1.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4473    1.7315   -1.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5562   -0.0209   -1.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2796    1.7168   -0.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4753    0.9144   -3.0799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5784   -0.7757   -2.5454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2728    1.2500   -2.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3084   -0.3504   -3.2087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0400   -1.5454   -1.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5814    1.1364    0.1335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5507    0.0872    2.2423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5299   -2.3543    0.9889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3338    1.1625    1.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8382   -0.3000    2.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6728   -2.2208    1.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2489   -2.1518   -0.4664 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5386   -2.4939   -0.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3826    1.1694   -0.9634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2607    0.2227   -3.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3466   -1.4144   -2.3229 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1670    0.8224   -1.9697 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4201   -0.8929   -1.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2027    2.0867   -0.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1063    0.6718    2.8686 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2894    0.8859    1.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2336    2.7955    2.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
  8  2  1  0
 18 11  1  0
 12  2  1  0
 21 16  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 12 44  1  0
 13 45  1  1
 14 46  1  0
 15 47  1  0
 15 48  1  0
 17 49  1  0
 17 50  1  0
 17 51  1  0
 18 52  1  0
 19 53  1  0
 19 54  1  0
 20 55  1  0
 20 56  1  0
 22 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-Hydroxy-1-(3,11,17-trihydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl)-ethanone	HMDB
3a,11b,17,21-Tetrahydroxy-5b-pregnan-20-one	HMDB
3b,11b,17,21-Tetrahydroxy-5b-pregnan-20-one	HMDB
3b,11b,17a,21-Tetrahydroxy-5b-pregnan-20-ON	HMDB
5b-Tetrahydrocortisol	HMDB, Generator
Dihydrocortison	HMDB
tetrahydro-Cortisol	HMDB
Urocortisol	HMDB, ChEBI
3alpha,5beta-Tetrahydrocortisol	ChEBI
5beta-Pregnane-3alpha,11beta,17alpha,21-tetrol-20-one	ChEBI
5beta-Tetrahydrocortisol	ChEBI
Tetrahydrohydrocortisone	ChEBI
3a,5b-Tetrahydrocortisol	Generator
3Α,5β-tetrahydrocortisol	Generator
5b-Pregnane-3a,11b,17a,21-tetrol-20-one	Generator
5Β-pregnane-3α,11β,17α,21-tetrol-20-one	Generator
5Β-tetrahydrocortisol	Generator

Chemical Formula

C₂₁H₃₄O₅

Average Molecular Weight

366.4917

Monoisotopic Molecular Weight

366.240624198

IUPAC Name

2-hydroxy-1-[(2S,5R,14R,15S,17S)-5,14,17-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]ethan-1-one

Traditional Name

2-hydroxy-1-[(2S,5R,14R,15S,17S)-5,14,17-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]ethanone

CAS Registry Number

53-02-1

SMILES

C[C@]12C[C@H](O)C3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@]2(O)C(=O)CO

InChI Identifier

InChI=1S/C21H34O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h12-16,18,22-24,26H,3-11H2,1-2H3/t12?,13-,14?,15?,16+,18?,19+,20+,21+/m1/s1

InChI Key

AODPIQQILQLWGS-OBRSLYEHSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 21-hydroxysteroids. These are steroids carrying a hydroxyl group at the 21-position of the steroid backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Hydroxysteroids

Direct Parent

21-hydroxysteroids

Alternative Parents

Substituents

Progestogin-skeleton
21-hydroxysteroid
20-oxosteroid
Pregnane-skeleton
3-hydroxysteroid
Oxosteroid
11-beta-hydroxysteroid
11-hydroxysteroid
3-alpha-hydroxysteroid
17-hydroxysteroid
Tertiary alcohol
Alpha-hydroxy ketone
Cyclic alcohol
Ketone
Secondary alcohol
Polyol
Primary alcohol
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Excreta

Biofluid or Excreta

Urine (PMID: 15560936)

Tissue

Nervous tissue

Hepatic tissue (HMDB: HMDB0000949)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0000949)

Source

Endogenous

Endogenous (HMDB: HMDB0000949)

Animal

Animal (HMDB: HMDB0000949)

Exogenous

Food

Food (HMDB: HMDB0000949)

Animal origin

Poultry

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Exogenous (HMDB: HMDB0000949)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Steroidogenesis (HMDB: HMDB0000949)
Fatty Acid Metabolism (HMDB: HMDB0000949)

Disease pathway

Apparent Mineralocorticoid Excess Syndrome (HMDB: HMDB0000949)
3-beta-Hydroxysteroid Dehydrogenase Deficiency (PathBank: SMP0120650)
Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency (PathBank: SMP0120672)
11-beta-Hydroxylase Deficiency (CYP11B1) (PathBank: SMP0120858)
Corticosterone Methyl Oxidase I Deficiency (CMO I) (PathBank: SMP0120860)
Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH (HMDB: HMDB0000949)
Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH (PathBank: SMP0120470)
21-Hydroxylase Deficiency (CYP21) (PathBank: SMP0120640)
17-alpha-Hydroxylase Deficiency (CYP17) (PathBank: SMP0120849)
Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency (PathBank: SMP0120450)
Corticosterone Methyl Oxidase II Deficiency (CMO II) (PathBank: SMP0120642)

Lipid metabolism pathway (HMDB: HMDB0000949)

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0000949)

Cellular process

Cell signaling (HMDB: HMDB0000949)

Biochemical process

Lipid transport (HMDB: HMDB0000949)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0000949)

Molecular messenger

Hormone (HMDB: HMDB0000949)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0000949)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.47 g/L	ALOGPS
logP	1.38	ALOGPS
logP	1.11	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	12.58	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	97.6 m³·mol⁻¹	ChemAxon
Polarizability	40.89 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	185.401	31661259
DarkChem	[M-H]-	179.781	31661259
AllCCS	[M+H]+	191.663	32859911
AllCCS	[M-H]-	193.265	32859911
DeepCCS	[M-2H]-	226.501	30932474
DeepCCS	[M+Na]+	202.067	30932474
AllCCS	[M+H]+	191.7	32859911
AllCCS	[M+H-H2O]+	189.2	32859911
AllCCS	[M+NH4]+	194.0	32859911
AllCCS	[M+Na]+	194.6	32859911
AllCCS	[M-H]-	193.3	32859911
AllCCS	[M+Na-2H]-	193.9	32859911
AllCCS	[M+HCOO]-	194.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tetrahydrocortisol	C[C@]12C[C@H](O)C3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@]2(O)C(=O)CO	2549.9	Standard polar	33892256
Tetrahydrocortisol	C[C@]12C[C@H](O)C3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@]2(O)C(=O)CO	3037.7	Standard non polar	33892256
Tetrahydrocortisol	C[C@]12C[C@H](O)C3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@]2(O)C(=O)CO	3253.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Tetrahydrocortisol,1TMS,isomer #1	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O)C(=O)CO	3267.2	Semi standard non polar	33892256
Tetrahydrocortisol,1TMS,isomer #2	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O)C(=O)CO	3284.3	Semi standard non polar	33892256
Tetrahydrocortisol,1TMS,isomer #3	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=O)CO	3312.6	Semi standard non polar	33892256
Tetrahydrocortisol,1TMS,isomer #4	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O)C(=O)CO[Si](C)(C)C	3280.7	Semi standard non polar	33892256
Tetrahydrocortisol,1TMS,isomer #5	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O)C(=CO)O[Si](C)(C)C	3220.1	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #1	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O)C(=O)CO	3192.1	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #10	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3240.4	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #2	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=O)CO	3218.5	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #3	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O)C(=O)CO[Si](C)(C)C	3218.4	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #4	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O)C(=CO)O[Si](C)(C)C	3131.8	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #5	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=O)CO	3297.6	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #6	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O)C(=O)CO[Si](C)(C)C	3295.5	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #7	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O)C(=CO)O[Si](C)(C)C	3204.9	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #8	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=O)CO[Si](C)(C)C	3330.3	Semi standard non polar	33892256
Tetrahydrocortisol,2TMS,isomer #9	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO)O[Si](C)(C)C	3244.6	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #1	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=O)CO	3180.1	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #10	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3221.6	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #2	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O)C(=O)CO[Si](C)(C)C	3196.7	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #3	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O)C(=CO)O[Si](C)(C)C	3098.3	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #4	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=O)CO[Si](C)(C)C	3232.2	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #5	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO)O[Si](C)(C)C	3149.5	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #6	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3148.5	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #7	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=O)CO[Si](C)(C)C	3283.7	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #8	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO)O[Si](C)(C)C	3181.2	Semi standard non polar	33892256
Tetrahydrocortisol,3TMS,isomer #9	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3182.5	Semi standard non polar	33892256
Tetrahydrocortisol,4TMS,isomer #1	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=O)CO[Si](C)(C)C	3220.7	Semi standard non polar	33892256
Tetrahydrocortisol,4TMS,isomer #2	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO)O[Si](C)(C)C	3123.4	Semi standard non polar	33892256
Tetrahydrocortisol,4TMS,isomer #3	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3125.1	Semi standard non polar	33892256
Tetrahydrocortisol,4TMS,isomer #4	C[C@]12CC[C@@H](O)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3175.6	Semi standard non polar	33892256
Tetrahydrocortisol,4TMS,isomer #5	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3169.9	Semi standard non polar	33892256
Tetrahydrocortisol,5TMS,isomer #1	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3116.6	Semi standard non polar	33892256
Tetrahydrocortisol,5TMS,isomer #1	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3044.7	Standard non polar	33892256
Tetrahydrocortisol,5TMS,isomer #1	C[C@]12CC[C@@H](O[Si](C)(C)C)CC1CCC1C2[C@@H](O[Si](C)(C)C)C[C@@]2(C)C1CC[C@]2(O[Si](C)(C)C)C(=CO[Si](C)(C)C)O[Si](C)(C)C	3352.9	Standard polar	33892256
Tetrahydrocortisol,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1C[C@@]2(C)C(CC[C@]2(O)C(=O)CO)C2CCC3C[C@H](O)CC[C@]3(C)C21	3518.1	Semi standard non polar	33892256
Tetrahydrocortisol,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1CC[C@@]2(C)C(CCC3C2[C@@H](O)C[C@@]2(C)C3CC[C@]2(O)C(=O)CO)C1	3526.1	Semi standard non polar	33892256
Tetrahydrocortisol,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@]1(C(=O)CO)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3554.8	Semi standard non polar	33892256
Tetrahydrocortisol,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(=O)[C@@]1(O)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3543.7	Semi standard non polar	33892256
Tetrahydrocortisol,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=CO)[C@@]1(O)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3456.6	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H]1C[C@@]2(C)C(CC[C@]2(O[Si](C)(C)C(C)(C)C)C(=O)CO)C2CCC3C[C@H](O)CC[C@]3(C)C21	3694.4	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3721.9	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC(=O)[C@@]1(O)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	3711.3	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1C[C@@]2(C)C(CC[C@]2(O)C(=O)CO)C2CCC3C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]3(C)C21	3661.8	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=CO)[C@@]1(O)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	3581.3	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1CC[C@@]2(C)C(CCC3C2[C@@H](O)C[C@@]2(C)C3CC[C@]2(O[Si](C)(C)C(C)(C)C)C(=O)CO)C1	3758.6	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC(=O)[C@@]1(O)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3776.7	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=CO)[C@@]1(O)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3670.3	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC(=O)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3817.3	Semi standard non polar	33892256
Tetrahydrocortisol,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=CO)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3709.3	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(=O)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	3917.4	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3911.0	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@H]1C[C@@]2(C)C(CC[C@]2(O[Si](C)(C)C(C)(C)C)C(=O)CO)C2CCC3C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]3(C)C21	3847.3	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=CO)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	3811.4	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC(=O)[C@@]1(O)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	3843.0	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	3798.3	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=CO)[C@@]1(O)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	3770.8	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC(=O)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3988.7	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=CO)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3871.1	Semi standard non polar	33892256
Tetrahydrocortisol,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	3883.2	Semi standard non polar	33892256
Tetrahydrocortisol,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC(=O)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	4065.0	Semi standard non polar	33892256
Tetrahydrocortisol,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	4032.6	Semi standard non polar	33892256
Tetrahydrocortisol,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=CO)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	4009.7	Semi standard non polar	33892256
Tetrahydrocortisol,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O[Si](C)(C)C(C)(C)C)C[C@@]21C	3987.8	Semi standard non polar	33892256
Tetrahydrocortisol,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC=C(O[Si](C)(C)C(C)(C)C)[C@@]1(O[Si](C)(C)C(C)(C)C)CCC2C3CCC4C[C@H](O[Si](C)(C)C(C)(C)C)CC[C@]4(C)C3[C@@H](O)C[C@@]21C	4074.4	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (Non-derivatized) - 70eV, Positive	splash10-000j-3539000000-bf3e8ad7a2d21593e681	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (4 TMS) - 70eV, Positive	splash10-0fe3-1311189000-3a0cfdea998a0531cb8b	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_3_2) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_3_3) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_3_4) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_3_5) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tetrahydrocortisol GC-MS (TMS_3_6) - 70eV, Positive	Not Available	2021-11-06	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 10V, Positive-QTOF	splash10-0002-0019000000-5967aef805edb472d5a5	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 20V, Positive-QTOF	splash10-0532-0059000000-6e3db383f9bda6aa194a	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 40V, Positive-QTOF	splash10-01p9-1492000000-2266b6b18ef46f0eec05	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 10V, Negative-QTOF	splash10-014i-0009000000-5471dbe684b873e5784d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 20V, Negative-QTOF	splash10-0ap1-2039000000-d95c86b33b8f11b83354	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 40V, Negative-QTOF	splash10-0a4i-9086000000-0e28c8ffdf44e3e921fe	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 10V, Positive-QTOF	splash10-014i-0009000000-31730eb1a915ec83558e	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 20V, Positive-QTOF	splash10-00kb-1926000000-49f68aeefa3e0ecff93e	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 40V, Positive-QTOF	splash10-00mk-4930000000-ad7e5d12918fff3d0452	2021-09-21	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 10V, Negative-QTOF	splash10-014r-0009000000-599710d9e5fe39c6c2e8	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 20V, Negative-QTOF	splash10-066r-5009000000-934cc72c238c468a325b	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tetrahydrocortisol 40V, Negative-QTOF	splash10-00kf-1079000000-515731aac544f36e01c8	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
Steroidogenesis
Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency		Not Available
Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH		Not Available
Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia due to 17 Alpha-hydroxylase Deficiency		Not Available
17-alpha-hydroxylase deficiency (CYP17)		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Urine	Detected and Quantified	0.19 (0.18-0.24) umol/mmol creatinine	Adult (>18 years old)	Male	Normal	11085621	details
Urine	Detected and Quantified	0.14 (0.086-0.17) umol/mmol creatinine	Adult (>18 years old)	Female	Normal	11085621	details
Urine	Detected and Quantified	0.21 +/- 0.038 umol/mmol creatinine	Adult (>18 years old)	Female	Normal	15560936	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details
Urine	Detected and Quantified	0.20 +/- 0.023 umol/mmol creatinine	Adult (>18 years old)	Female	Eating disorder	15560936	details
Urine	Detected and Quantified	0.62 +/- 0.085 umol/mmol creatinine	Adult (>18 years old)	Female	Eating disorder	15560936	details
Urine	Detected and Quantified	0.00024 +/- 0.00020 umol/mmol creatinine	Adult (>18 years old)	Female	Stress urinary incontinence	12707870	details

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022333

KNApSAcK ID

Not Available

Chemspider ID

5655

KEGG Compound ID

C05472

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Tetrahydrocortisol

METLIN ID

Not Available

PubChem Compound

44725717

PDB ID

Not Available

ChEBI ID

28320

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1836601

References

Synthesis Reference

Gould, David H.; Oliveto, Eugene P. 17a-Hydroxycorticosterone and intermediates. (1957), US 2783254 19570226 CAN 51:62564 AN 1957:62564

Material Safety Data Sheet (MSDS)

Not Available

General References

Shackleton C, Malunowicz E: Apparent pregnene hydroxylation deficiency (APHD): seeking the parentage of an orphan metabolome. Steroids. 2003 Oct;68(9):707-17. [PubMed:14625002 ]
Mune T, White PC: Apparent mineralocorticoid excess: genotype is correlated with biochemical phenotype. Hypertension. 1996 Jun;27(6):1193-9. [PubMed:8641723 ]
Weykamp CW, Penders TJ, Schmidt NA, Borburgh AJ, van de Calseyde JF, Wolthers BJ: Steroid profile for urine: reference values. Clin Chem. 1989 Dec;35(12):2281-4. [PubMed:2591044 ]
Kerstens MN, van der Kleij FG, Boonstra AH, Sluiter WJ, van der Molen JC, Navis G, Dullaart RP: Angiotensin administration stimulates renal 11 beta-hydroxysteroid dehydrogenase activity in healthy men. Kidney Int. 2004 Jun;65(6):2065-70. [PubMed:15149319 ]
Koren W, Grienspuhn A, Kuznetsov SR, Berezin M, Rosenthal T, Postnov YV: Enhanced Na+/H+ exchange in Cushing's syndrome reflects functional hypermineralocorticoidism. J Hypertens. 1998 Aug;16(8):1187-91. [PubMed:9794723 ]
Rosler A, Leiberman E, Rosenmann A, Ben-Uzilio R, Weidenfeld J: Prenatal diagnosis of 11beta-hydroxylase deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1979 Oct;49(4):546-51. [PubMed:314453 ]
Melander O, Frandsen E, Groop L, Hulthen UL: No evidence of a relation between 11beta-hydroxysteroid dehydrogenase type 2 activity and salt sensitivity. Am J Hypertens. 2003 Sep;16(9 Pt 1):729-33. [PubMed:12944030 ]
Quinkler M, Zehnder D, Lepenies J, Petrelli MD, Moore JS, Hughes SV, Cockwell P, Hewison M, Stewart PM: Expression of renal 11beta-hydroxysteroid dehydrogenase type 2 is decreased in patients with impaired renal function. Eur J Endocrinol. 2005 Aug;153(2):291-9. [PubMed:16061836 ]
Rapetti S, Francia G, Iacono C, Martignoni G, Contessi G, Brunelli M, Galvanin F, Serio G: An unusual case of Cushing's syndrome due to ACTH-independent macronodular adrenal hyperplasia. Chir Ital. 2003 Mar-Apr;55(2):235-41. [PubMed:12744099 ]
Panin LE, Tuzikov FV, Gimautdinova OI: Tetrahydrocortisol-apolipoprotein A-I complex specifically interacts with eukaryotic DNA and GCC elements of genes. J Steroid Biochem Mol Biol. 2003 Dec;87(4-5):309-18. [PubMed:14698212 ]

Enzymes

Enzyme Details

1. Aldo-keto reductase family 1 member C4

General function:: Involved in oxidoreductase activity
Specific function:: Catalyzes the transformation of the potent androgen dihydrotestosterone (DHT) into the less active form, 5-alpha-androstan-3-alpha,17-beta-diol (3-alpha-diol). Also has some 20-alpha-hydroxysteroid dehydrogenase activity. The biotransformation of the pesticide chlordecone (kepone) to its corresponding alcohol leads to increased biliary excretion of the pesticide and concomitant reduction of its neurotoxicity since bile is the major excretory route.
Gene Name:: AKR1C4
Uniprot ID:: P17516
Molecular weight:: 37094.57

Reactions

Tetrahydrocortisol + NAD → Dihydrocortisol + NADH + Hydrogen Ion	details
Tetrahydrocortisol + NADP → Dihydrocortisol + NADPH + Hydrogen Ion	details

Showing metabocard for Tetrahydrocortisol (HMDB0000949)

MOL for HMDB0000949 (Tetrahydrocortisol)

3D MOL for HMDB0000949 (Tetrahydrocortisol)

3D SDF for HMDB0000949 (Tetrahydrocortisol)

3D-SDF for HMDB0000949 (Tetrahydrocortisol)

PDB for HMDB0000949 (Tetrahydrocortisol)

3D PDB for HMDB0000949 (Tetrahydrocortisol)

SMILES for HMDB0000949 (Tetrahydrocortisol)

INCHI for HMDB0000949 (Tetrahydrocortisol)

Structure for HMDB0000949 (Tetrahydrocortisol)

3D Structure for HMDB0000949 (Tetrahydrocortisol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

Enzymes

Reactions