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Details

Stereochemistry ACHIRAL
Molecular Formula C27H44O2
Molecular Weight 400.6371
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 3
Charge 0

SHOW SMILES / InChI
Structure of GEFARNATE

SMILES

CC(C)=CCC\C(C)=C\CC\C(C)=C\CCC(=O)OC\C=C(/C)CCC=C(C)C

InChI

InChIKey=ZPACYDRSPFRDHO-ROBAGEODSA-N
InChI=1S/C27H44O2/c1-22(2)12-8-14-24(5)16-10-17-25(6)18-11-19-27(28)29-21-20-26(7)15-9-13-23(3)4/h12-13,16,18,20H,8-11,14-15,17,19,21H2,1-7H3/b24-16+,25-18+,26-20+

HIDE SMILES / InChI

Molecular Formula C27H44O2
Molecular Weight 400.6371
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 Fri Dec 15 15:25:59 UTC 2023
Edited
by admin
on Fri Dec 15 15:25:59 UTC 2023
Record UNII
1ISE2Y6ULA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GEFARNATE
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
GEFANIL
Brand Name English
DA-688
Code English
GEFARNATE [MART.]
Common Name English
GEFARNATE [JAN]
Common Name English
Gefarnate [WHO-DD]
Common Name English
GEFARNATE [MI]
Common Name English
TRANS-3,7-DIMETHYL-2,6-OCTADIENYL 5,9,13-TRIMETHYL-4,8,12-TETRADECATRIENOATE
Common Name English
DA 688
Code English
gefarnate [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC A02BX07
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
WHO-VATC QA02BX07
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
NCI_THESAURUS C29698
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
WHO-VATC QA02BX77
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
WHO-ATC A02BX77
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C73187
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-121-0
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
EPA CompTox
DTXSID0048636
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
FDA UNII
1ISE2Y6ULA
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
SMS_ID
100000084519
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
MESH
D005778
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
EVMPD
SUB07889MIG
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
ChEMBL
CHEMBL2105085
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
PUBCHEM
5282182
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
INN
1546
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
DRUG BANK
DB12079
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
MERCK INDEX
m5681
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
Gefarnate
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
DRUG CENTRAL
1281
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
CAS
51-77-4
Created by admin on Fri Dec 15 15:25:59 UTC 2023 , Edited by admin on Fri Dec 15 15:25:59 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY