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Details

Stereochemistry ACHIRAL
Molecular Formula C23H31NO2
Molecular Weight 353.4977
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 4
Charge 0

SHOW SMILES / InChI
Structure of MOTRETINIDE

SMILES

CCNC(=O)\C=C(C)\C=C\C=C(C)\C=C\C1=C(C)C(C)=C(OC)C=C1C

InChI

InChIKey=IYIYMCASGKQOCZ-DJRRULDNSA-N
InChI=1S/C23H31NO2/c1-8-24-23(25)14-17(3)11-9-10-16(2)12-13-21-18(4)15-22(26-7)20(6)19(21)5/h9-15H,8H2,1-7H3,(H,24,25)/b11-9+,13-12+,16-10+,17-14+

HIDE SMILES / InChI

Molecular Formula C23H31NO2
Molecular Weight 353.4977
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 4
Optical Activity NONE

MOTRETINIDE is a retinoic acid derivative. It is used as a topical agent in the treatment of mild to moderate acne.

Approval Year

PubMed

PubMed

TitleDatePubMed
Ro 11-1430, a new retinoic acid derivative for the topical treatment of acne.
1981
Motretinide versus benzoyl peroxide in the treatment of acne vulgaris.
1984
Retinoids--which dermatological indications will benefit in the near future?
2001 Sep-Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:16:50 UTC 2023
Edited
by admin
on Fri Dec 15 15:16:50 UTC 2023
Record UNII
W786807KL1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MOTRETINIDE
INN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
RO 11-1430
Code English
all-trans-N-Ethyl-9-(4-methoxy-2,3,6-trimethylphenyl)-3,7-dimethyl-2,4,6,8-nonatetraenamide
Common Name English
MOTRETINIDE [USAN]
Common Name English
MOTRETINIDE [MART.]
Common Name English
Motretinide [WHO-DD]
Common Name English
RO-11-1430
Code English
motretinide [INN]
Common Name English
NSC-351523
Code English
MOTRETINIDE [MI]
Common Name English
TASMADERM
Brand Name English
2,4,6,8-NONATETRAENAMIDE, N-ETHYL-9-(4-METHOXY-2,3,6-TRIMETHYLPHENYL)-3,7-DIMETHYL-, (ALL-E)-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C804
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
WHO-ATC D10AD05
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
WHO-VATC QD10AD05
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C90940
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
CAS
56281-36-8
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
DRUG CENTRAL
1849
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
DRUG BANK
DB13368
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
NSC
351523
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
PUBCHEM
6314185
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
FDA UNII
W786807KL1
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
MERCK INDEX
m7640
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY Merck Index
SMS_ID
100000080394
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
WIKIPEDIA
MOTRETINIDE
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
ChEMBL
CHEMBL519260
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
EVMPD
SUB09077MIG
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
INN
4233
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
ECHA (EC/EINECS)
260-094-6
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
EPA CompTox
DTXSID30878633
Created by admin on Fri Dec 15 15:16:50 UTC 2023 , Edited by admin on Fri Dec 15 15:16:50 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY