CHEBI:136118 - (4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoic acid
ChEBI ID CHEBI:136118
ChEBI ASCII Name (4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoic acid
Definition A hydroperoxydocosapentaenoic acid that is (4Z,7Z,10Z,13Z,15E)-docosapentaenoic acid carrying a hydroperoxy substituent at position 17S.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information No supplier information found for this compound.
Download Molfile XML SDF
Formula C22H34O4
Net Charge 0
Average Mass 362.504
Monoisotopic Mass 362.24571
InChI InChI=1S/C22H34O4/c1-2-3-15-18-21(26-25)19-16-13-11-9-7-5-4-6-8-10-12-14-17-20-22(23)24/h5-8,11-14,16,19,21,25H,2-4,9-10,15,17-18,20H2,1H3,(H,23,24)/b7-5-,8-6-,13-11-,14-12-,19-16+/t21-/m0/s1
InChIKey ISPMDQHJXOPONJ-RUPKWMQGSA-N
SMILES OC(CC/C=C\C/C=C\C/C=C\C/C=C\C=C\[C@H](CCCCC)OO)=O
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoic acid (CHEBI:136118) has functional parent (4Z,7Z,10Z,13Z,16Z)-docosa-4,7,10,13,16-pentaenoic acid (CHEBI:65136)
(4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoic acid (CHEBI:136118) is a hydroperoxydocosapentaenoic acid (CHEBI:189823)
(4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoic acid (CHEBI:136118) is conjugate acid of (4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoate (CHEBI:133796)
Incoming (4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoate (CHEBI:133796) is conjugate base of (4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosapentaenoic acid (CHEBI:136118)
IUPAC Name
(4Z,7Z,10Z,13Z,15E,17S)-17-hydroperoxydocosa-4,7,10,13,15-pentaenoic acid
Synonyms Sources
(17S)-HPDoPE(n-6) ChEBI
(17S)-HPDPA(n-6) ChEBI
(17S)-hydroperoxy-(4Z,7Z,10Z,13Z,15E)-docosapentaenoic acid ChEBI
Last Modified
18 February 2022