17-HETE

Details

Stereochemistry	RACEMIC
Molecular Formula	C20H32O3
Molecular Weight	320.4663
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	4
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CCCC(O)C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O

InChI

InChIKey=OPPIPPRXLIDJKN-JPURVOHMSA-N

InChI=1S/C20H32O3/c1-2-16-19(21)17-14-12-10-8-6-4-3-5-7-9-11-13-15-18-20(22)23/h3,5-6,8-9,11-12,14,19,21H,2,4,7,10,13,15-18H2,1H3,(H,22,23)/b5-3-,8-6-,11-9-,14-12-

HIDE SMILES / InChI

Molecular Formula	C20H32O3
Molecular Weight	320.4663
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	4
Optical Activity	( + / - )

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
ATPase activity 3 Target ID: GO:0016887 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8897975 \| https://www.ncbi.nlm.nih.gov/pubmed/9186856	Inhibitor 8504

PubMed

Title	Date	PubMed
Subterminal hydroxyeicosatetraenoic acids: Crucial lipid mediators in normal physiology and disease states.	2019-02-01	30543782
Cytochrome P450-derived renal HETEs: storage and release.	1997-06	9186856
Cytochrome P-450-dependent HETEs: profile of biological activity and stimulation by vasoactive peptides.	1996-10	8897975

Substance Class	Chemical Created by `admin` on `Wed Apr 02 21:23:45 GMT 2025` Edited by `admin` on `Wed Apr 02 21:23:45 GMT 2025`
Record UNII	4R7YVU4N5L
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

(±)17-HETE

Preferred Name

English

17-HETE

Common Name

English

5,8,11,14-Eicosatetraenoic acid, 17-hydroxy-, (all-Z)-

Systematic Name

English

(5Z,8Z,11Z,14Z)-17-Hydroxy-5,8,11,14-eicosatetraenoic acid

Systematic Name

English

17-Hydroxy-eicosatetraenoic acid

Common Name

English

5,8,11,14-Eicosatetraenoic acid, 17-hydroxy-, (5Z,8Z,11Z,14Z)-

Systematic Name

English

17-Hydroxy-5Z,8Z,11Z,14Z-eicosatetraenoic acid

Systematic Name

English

Code System Code Type Description

PUBCHEM

6442740

Created by admin on Wed Apr 02 21:23:45 GMT 2025 , Edited by admin on Wed Apr 02 21:23:45 GMT 2025

PRIMARY

FDA UNII

4R7YVU4N5L

Created by admin on Wed Apr 02 21:23:45 GMT 2025 , Edited by admin on Wed Apr 02 21:23:45 GMT 2025

PRIMARY

CAS

128914-47-6

Created by admin on Wed Apr 02 21:23:45 GMT 2025 , Edited by admin on Wed Apr 02 21:23:45 GMT 2025

PRIMARY

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