U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C21H26O3
Molecular Weight 326.4293
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 4
Charge 0

SHOW SMILES / InChI
Structure of ACITRETIN

SMILES

COC1=C(C)C(C)=C(\C=C\C(C)=C\C=C\C(C)=C\C(O)=O)C(C)=C1

InChI

InChIKey=IHUNBGSDBOWDMA-AQFIFDHZSA-N
InChI=1S/C21H26O3/c1-14(8-7-9-15(2)12-21(22)23)10-11-19-16(3)13-20(24-6)18(5)17(19)4/h7-13H,1-6H3,(H,22,23)/b9-7+,11-10+,14-8+,15-12+

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
ACITRETIN
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
INN   USAN  
Official Name English
ACITRETINE
Common Name English
ACITRETIN [EP MONOGRAPH]
Common Name English
ACITRETIN [MI]
Common Name English
ACITRETIN [USP-RS]
Common Name English
ACITRETIN [USAN]
Common Name English
ACITRETIN [USP IMPURITY]
Common Name English
NEOTIGASON
Common Name English
ETRETIN
Common Name English
9-(4-METHOXY-2,3,6-TRIMETHYLPHENYL)-3,7-DIMETHYL-2,4,6,8-NONATETRAENOIC ACID
Systematic Name English
acitretin [INN]
Common Name English
ACITRETIN [USP MONOGRAPH]
Common Name English
ACITRETIN [ORANGE BOOK]
Common Name English
RO 10-1670
Code English
ACITRETIN [MART.]
Common Name English
2,4,6,8-NONATETRAENOIC ACID, 9-(4-METHOXY-2,3,6-TRIMETHYLPHENYL)-3,7-DIMETHYL-, (ALL-E)-
Common Name English
RO-10-1670/000
Code English
SORIATANE
Brand Name English
RO 10-1670/000
Code English
ACITRETIN [VANDF]
Common Name English
ACITRETIN [HSDB]
Common Name English
Acitretin [WHO-DD]
Common Name English
(all-E)-9-(4-Methoxy-2,3,6-trimethylphenyl)-3,7-dimethyl-2,4,6,8-nonatetraenoic acid
Common Name English
Classification Tree Code System Code
NDF-RT N0000007700
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
NDF-RT N0000175607
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
NDF-RT N0000007700
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
WHO-ATC D05BB02
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
NDF-RT N0000007700
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
WHO-VATC QD05BB02
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
NDF-RT N0000007700
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
NCI_THESAURUS C804
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
LIVERTOX NBK548784
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
NDF-RT N0000007700
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
Code System Code Type Description
CHEBI
50173
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
RS_ITEM_NUM
1011007
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
PUBCHEM
5284513
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
DRUG BANK
DB00459
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
RXCUI
16818
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY RxNorm
LACTMED
Acitretin
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
USAN
X-94
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
ChEMBL
CHEMBL1131
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
INN
5530
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
MESH
D017255
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
SMS_ID
100000084604
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
MERCK INDEX
m1373
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID6022553
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
DRUG CENTRAL
78
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
WIKIPEDIA
ACITRETIN
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
FDA UNII
LCH760E9T7
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
ECHA (EC/EINECS)
259-474-4
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
HSDB
7187
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
NCI_THESAURUS
C985
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
DAILYMED
LCH760E9T7
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
IUPHAR
7598
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
EVMPD
SUB05240MIG
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
CAS
55079-83-9
Created by admin on Fri Dec 15 15:02:54 UTC 2023 , Edited by admin on Fri Dec 15 15:02:54 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of ACITRETIN
METABOLITE (PARENT)
Structure of ETRETINATE
METABOLITE (PARENT)
Structure of RO-23-4293
METABOLITE (PARENT)
Structure of ISOACITRETIN
METABOLITE (PARENT)
Structure of RO-23-3571
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966