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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2013-05-17 00:55:03 UTC
Update Date2022-03-07 03:17:43 UTC
HMDB IDHMDB0060342
Secondary Accession Numbers
  • HMDB60342
Metabolite Identification
Common Name2-(S-Glutathionyl)acetyl chloride
Description2-(S-Glutathionyl)acetyl chloride belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. 2-(S-Glutathionyl)acetyl chloride is a very strong basic compound (based on its pKa). 2-(S-Glutathionyl)acetyl chloride exists in all living organisms, ranging from bacteria to humans. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.
Structure
Data?1563866047
SynonymsNot Available
Chemical FormulaC12H18ClN3O7S
Average Molecular Weight383.805
Monoisotopic Molecular Weight383.055398342
IUPAC Name(2S)-2-amino-4-{[(1R)-1-[(carboxymethyl)-C-hydroxycarbonimidoyl]-2-[(2-chloro-2-oxoethyl)sulfanyl]ethyl]-C-hydroxycarbonimidoyl}butanoic acid
Traditional NameC12H18clN3O7S
CAS Registry NumberNot Available
SMILES
[H][C@](N)(CCC(O)=N[C@@]([H])(CSCC(Cl)=O)C(O)=NCC(O)=O)C(O)=O
InChI Identifier
InChI=1S/C12H18ClN3O7S/c13-8(17)5-24-4-7(11(21)15-3-10(19)20)16-9(18)2-1-6(14)12(22)23/h6-7H,1-5,14H2,(H,15,21)(H,16,18)(H,19,20)(H,22,23)/t6-,7-/m0/s1
InChI KeyQUWRSBQWJGCKIV-BQBZGAKWSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassDihydrofurans
Sub ClassFuranones
Direct ParentButenolides
Alternative Parents
Substituents
  • 2-furanone
  • Dicarboxylic acid or derivatives
  • Enol ester
  • Enoate ester
  • Alpha,beta-unsaturated carboxylic ester
  • Carboxylic acid ester
  • Lactone
  • Carboxylic acid derivative
  • Carboxylic acid
  • Oxacycle
  • Chloroalkene
  • Vinyl chloride
  • Vinyl halide
  • Haloalkene
  • Carbonyl group
  • Organohalogen compound
  • Organochloride
  • Organooxygen compound
  • Organic oxide
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External Descriptors
Ontology
Not AvailableNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.2 g/LALOGPS
logP-2ALOGPS
logP-3.2ChemAxon
logS-3.3ALOGPS
pKa (Strongest Acidic)1.82ChemAxon
pKa (Strongest Basic)9.54ChemAxon
Physiological Charge-3ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area182.87 ŲChemAxon
Rotatable Bond Count12ChemAxon
Refractivity84.9 m³·mol⁻¹ChemAxon
Polarizability35.87 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+177.60630932474
DeepCCS[M-H]-175.24830932474
DeepCCS[M-2H]-208.92930932474
DeepCCS[M+Na]+184.15730932474
AllCCS[M+H]+178.632859911
AllCCS[M+H-H2O]+176.332859911
AllCCS[M+NH4]+180.632859911
AllCCS[M+Na]+181.232859911
AllCCS[M-H]-177.432859911
AllCCS[M+Na-2H]-177.832859911
AllCCS[M+HCOO]-178.432859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
2-(S-Glutathionyl)acetyl chloride[H][C@](N)(CCC(O)=N[C@@]([H])(CSCC(Cl)=O)C(O)=NCC(O)=O)C(O)=O4347.9Standard polar33892256
2-(S-Glutathionyl)acetyl chloride[H][C@](N)(CCC(O)=N[C@@]([H])(CSCC(Cl)=O)C(O)=NCC(O)=O)C(O)=O2704.7Standard non polar33892256
2-(S-Glutathionyl)acetyl chloride[H][C@](N)(CCC(O)=N[C@@]([H])(CSCC(Cl)=O)C(O)=NCC(O)=O)C(O)=O3337.6Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
2-(S-Glutathionyl)acetyl chloride,1TMS,isomer #1C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O3181.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,1TMS,isomer #2C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O3122.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,1TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O3165.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,1TMS,isomer #4C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O3114.0Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,1TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)C(=O)O3241.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)O[Si](C)(C)C3038.7Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #10C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C3106.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #11C[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C3279.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #2C[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C3059.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C3089.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #4C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O3154.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O3031.1Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C3003.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #7C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O3127.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C3031.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O3155.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C2978.2Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #10C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3038.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #11C[Si](C)(C)OC(=NCC(=O)O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3184.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #12C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3071.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #13C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3203.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #14C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C3179.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #2C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C3002.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #3C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3068.1Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C2984.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3096.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #6C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3107.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #7C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O3224.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #8C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C2941.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TMS,isomer #9C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3053.7Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C)O[Si](C)(C)C2925.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3131.2Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #11C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3162.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #2C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3029.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #3C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3044.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #4C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3171.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O3042.7Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #6C[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C3183.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #7C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3206.7Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #8C[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2989.2Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TMS,isomer #9C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3151.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2992.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2850.0Standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3882.6Standard polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3136.0Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2861.1Standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4078.1Standard polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3142.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C2899.1Standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #3C[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4236.0Standard polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3140.7Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C2915.3Standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #4C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C4039.3Standard polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3097.1Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2910.5Standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,5TMS,isomer #5C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4091.3Standard polar33892256
2-(S-Glutathionyl)acetyl chloride,6TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3124.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,6TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C2937.4Standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,6TMS,isomer #1C[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C3685.5Standard polar33892256
2-(S-Glutathionyl)acetyl chloride,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O3354.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O3276.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O3384.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O3324.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)C(=O)O3421.0Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C3440.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C3530.0Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)N([C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C3643.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(CC[C@H](N)C(=O)O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C3456.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C3509.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O3558.2Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O3454.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C3411.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O3504.2Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C3500.1Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O3585.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3616.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3669.5Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=NCC(=O)O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3820.1Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3735.1Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3887.4Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3849.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3653.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3700.6Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C3639.2Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O3708.1Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O3750.2Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O3859.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C3612.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O3709.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSCC(=O)Cl)N=C(CC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3783.0Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4028.2Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4073.0Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3841.9Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3885.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCC(=N[C@@H](CSCC(=O)Cl)C(O)=NCC(=O)O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4063.1Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC(=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O3878.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O)O[Si](C)(C)C(C)(C)C4055.8Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)CN=C(O)[C@H](CSCC(=O)Cl)N=C(CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4087.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)N[C@@H](CCC(O)=N[C@@H](CSCC(=O)Cl)C(=NCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3836.3Semi standard non polar33892256
2-(S-Glutathionyl)acetyl chloride,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)CN=C(O[Si](C)(C)C(C)(C)C)[C@H](CSCC(=O)Cl)N=C(O)CC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4047.4Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 2-(S-Glutathionyl)acetyl chloride GC-MS (Non-derivatized) - 70eV, Positivesplash10-052u-8029000000-324c56f17994090f48eb2017-09-20Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-(S-Glutathionyl)acetyl chloride GC-MS (4 TMS) - 70eV, Positivesplash10-0a4i-4310279000-9c4fc8665e7da781e3142017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-(S-Glutathionyl)acetyl chloride GC-MS (TBDMS_2_3) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-(S-Glutathionyl)acetyl chloride GC-MS (TBDMS_3_2) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-(S-Glutathionyl)acetyl chloride GC-MS (TBDMS_4_7) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-(S-Glutathionyl)acetyl chloride GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 2-(S-Glutathionyl)acetyl chloride GC-MS ("2-(S-Glutathionyl)acetyl chloride,2TBDMS,#3" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 10V, Positive-QTOFsplash10-0g5i-2159000000-39febf94c6c5a174f1142015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 20V, Positive-QTOFsplash10-00di-9782000000-f948d78248213c9398f62015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 40V, Positive-QTOFsplash10-00di-9530000000-8fe6fe1aea8b1b1e7c482015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 10V, Negative-QTOFsplash10-06si-1319000000-6f9b6df89090f7f53b9d2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 20V, Negative-QTOFsplash10-0a4i-3923000000-90175f07c7cd3d67709e2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 40V, Negative-QTOFsplash10-0596-5900000000-1475da48240fd5656f332015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 10V, Positive-QTOFsplash10-001i-0039000000-d760339369cddc0464fa2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 20V, Positive-QTOFsplash10-001s-2933000000-56c257ec3a56dc94ada02021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 40V, Positive-QTOFsplash10-000i-9510000000-72c153ea79ce99841cda2021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 10V, Negative-QTOFsplash10-05fr-0192000000-187c7a023576f60034e02021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 20V, Negative-QTOFsplash10-0ac3-1890000000-9c8da758934152c4b3e12021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 2-(S-Glutathionyl)acetyl chloride 40V, Negative-QTOFsplash10-0006-5900000000-7731c5a92bff6f55f9102021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID10128368
KEGG Compound IDC14865
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound11954073
PDB IDNot Available
ChEBI ID34253
Food Biomarker OntologyNot Available
VMH IDM00565
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Magrane M: UniProt Knowledgebase: a hub of integrated protein data. Database (Oxford). 2011 Mar 29;2011:bar009. doi: 10.1093/database/bar009. Print 2011. [PubMed:21447597 ]

Only showing the first 10 proteins. There are 19 proteins in total.

Enzymes

General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM2
Uniprot ID:
P28161
Molecular weight:
25744.395
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM1
Uniprot ID:
P09488
Molecular weight:
25711.555
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in protein disulfide oxidoreductase activity
Specific function:
Significant glutathione conjugating activity is found only with the model substrate, 1-chloro-2,4-dinitrobenzene (CDNB).
Gene Name:
GSTK1
Uniprot ID:
Q9Y2Q3
Molecular weight:
31565.605
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in glutathione transferase activity
Specific function:
Also functions as a glutathione peroxidase.
Gene Name:
MGST3
Uniprot ID:
O14880
Molecular weight:
16516.185
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. May govern uptake and detoxification of both endogenous compounds and xenobiotics at the testis and brain blood barriers.
Gene Name:
GSTM3
Uniprot ID:
P21266
Molecular weight:
26559.32
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTA1
Uniprot ID:
P08263
Molecular weight:
25630.785
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. Has a wide substrate specificity.
Gene Name:
MGST1
Uniprot ID:
P10620
Molecular weight:
17598.45
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles. Active on 1-chloro-2,4-dinitrobenzene.
Gene Name:
GSTM4
Uniprot ID:
Q03013
Molecular weight:
25561.095
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in glutathione transferase activity
Specific function:
Conjugation of reduced glutathione to a wide number of exogenous and endogenous hydrophobic electrophiles.
Gene Name:
GSTM5
Uniprot ID:
P46439
Molecular weight:
25674.455
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails
General function:
Involved in enzyme activator activity
Specific function:
Can catalyze the production of LTC4 from LTA4 and reduced glutathione. Can catalyze the conjugation of 1-chloro-2,4-dinitrobenzene with reduced glutathione.
Gene Name:
MGST2
Uniprot ID:
Q99735
Molecular weight:
16620.4
Reactions
1,1-Dichloroethylene epoxide + Glutathione → 2-(S-Glutathionyl)acetyl chloride + Hydrochloric aciddetails
2-(S-Glutathionyl)acetyl chloride + Glutathione → 2-(S-Glutathionyl)acetyl glutathione + Hydrochloric aciddetails

Only showing the first 10 proteins. There are 19 proteins in total.