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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 of 16(RS)-HETE

SMILES

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

InChI

InChIKey=JEKNPVYFNMZRJG-UFINWASNSA-N
InChI=1S/C20H32O3/c1-2-3-16-19(21)17-14-12-10-8-6-4-5-7-9-11-13-15-18-20(22)23/h4-5,8-11,14,17,19,21H,2-3,6-7,12-13,15-16,18H2,1H3,(H,22,23)/b5-4-,10-8-,11-9-,17-14-

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

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Cytochrome P-450-dependent HETEs: profile of biological activity and stimulation by vasoactive peptides.
1996-10
Substance Class Chemical
Created
by admin
on Wed Apr 02 20:52:39 GMT 2025
Edited
by admin
on Wed Apr 02 20:52:39 GMT 2025
Record UNII
SZ82Y6XRG9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
16(RS)-HETE
Common Name English
(±)16-HETE
Preferred Name English
5,8,11,14-Eicosatetraenoic acid, 16-hydroxy-, (5Z,8Z,11Z,14Z)-
Systematic Name English
5,8,11,14-Eicosatetraenoic acid, 16-hydroxy-, (all-Z)-
Systematic Name English
(5Z,8Z,11Z,14Z)-16-Hydroxy-5,8,11,14-eicosatetraenoic acid
Systematic Name English
16-HETE
Common Name English
Code System Code Type Description
CAS
128914-46-5
Created by admin on Wed Apr 02 20:52:39 GMT 2025 , Edited by admin on Wed Apr 02 20:52:39 GMT 2025
PRIMARY
PUBCHEM
6442739
Created by admin on Wed Apr 02 20:52:39 GMT 2025 , Edited by admin on Wed Apr 02 20:52:39 GMT 2025
PRIMARY
FDA UNII
SZ82Y6XRG9
Created by admin on Wed Apr 02 20:52:39 GMT 2025 , Edited by admin on Wed Apr 02 20:52:39 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE