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Details

Stereochemistry ACHIRAL
Molecular Formula C18H30O2
Molecular Weight 278.4296
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 3
Charge 0

SHOW SMILES / InChI
Structure of PINOLENIC ACID

SMILES

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

InChI

InChIKey=HXQHFNIKBKZGRP-URPRIDOGSA-N
InChI=1S/C18H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h6-7,9-10,13-14H,2-5,8,11-12,15-17H2,1H3,(H,19,20)/b7-6-,10-9-,14-13-

HIDE SMILES / InChI

Molecular Formula C18H30O2
Molecular Weight 278.4296
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 3
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:40:29 GMT 2025
Edited
by admin
on Mon Mar 31 22:40:29 GMT 2025
Record UNII
B810C93MD7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PINOLENIC ACID
MI  
Common Name English
5,9,12-OCTADECATRIENOIC ACID, CIS
Preferred Name English
PINOLENIC ACID [MI]
Common Name English
5,9,12-OCTADECATRIENOIC ACID, (5Z,9Z,12Z)-
Systematic Name English
CIS,CIS,CIS-5,9,12-OCTADECATRIENOIC ACID
Systematic Name English
Code System Code Type Description
MERCK INDEX
m8832
Created by admin on Mon Mar 31 22:40:29 GMT 2025 , Edited by admin on Mon Mar 31 22:40:29 GMT 2025
PRIMARY Merck Index
FDA UNII
B810C93MD7
Created by admin on Mon Mar 31 22:40:29 GMT 2025 , Edited by admin on Mon Mar 31 22:40:29 GMT 2025
PRIMARY
WIKIPEDIA
Pinolenic acid
Created by admin on Mon Mar 31 22:40:29 GMT 2025 , Edited by admin on Mon Mar 31 22:40:29 GMT 2025
PRIMARY
PUBCHEM
5312495
Created by admin on Mon Mar 31 22:40:29 GMT 2025 , Edited by admin on Mon Mar 31 22:40:29 GMT 2025
PRIMARY
CAS
16833-54-8
Created by admin on Mon Mar 31 22:40:29 GMT 2025 , Edited by admin on Mon Mar 31 22:40:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID00895852
Created by admin on Mon Mar 31 22:40:29 GMT 2025 , Edited by admin on Mon Mar 31 22:40:29 GMT 2025
PRIMARY
CHEBI
86136
Created by admin on Mon Mar 31 22:40:29 GMT 2025 , Edited by admin on Mon Mar 31 22:40:29 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST
TARGET -> AGONIST