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

Details

Stereochemistry ACHIRAL
Molecular Formula C23H30N2O2S
Molecular Weight 398.562
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of LINAROTENE

SMILES

C\C(=N/NC1=CC=C(C=C1)S(C)(=O)=O)C2=CC3=C(C=C2)C(C)(C)CCC3(C)C

InChI

InChIKey=KGRBTTOECAZCNW-LFVJCYFKSA-N
InChI=1S/C23H30N2O2S/c1-16(24-25-18-8-10-19(11-9-18)28(6,26)27)17-7-12-20-21(15-17)23(4,5)14-13-22(20,2)3/h7-12,15,25H,13-14H2,1-6H3/b24-16+

HIDE SMILES / InChI
Linarotene is arotinoid derivative. It is an antikeratolytic agent. Linarotene had been in preclinical phase by Ortho Pharmaceutical (Johnson & Johnson) and BASF Pharma for the treatment of skin disorders. However, this research was discontinued.

Approval Year

Name Type Language
BASF 52404
Preferred Name English
LINAROTENE
INN   USAN  
INN   USAN  
Official Name English
BASF-52404
Code English
LINAROTENE [USAN]
Common Name English
RWJ-24834
Code English
linarotene [INN]
Common Name English
5',6',7',8'-TETRAHYDRO-5',5',8',8'-TETRAMETHYL-2'-ACETONAPHTHONE (E)-(P-(METHYLSULFONYL)PHENYL)HYDRAZONE
Systematic Name English
RWJ 24834
Code English
ETHANONE, 1-(5,6,7,8-TETRAHYDRO-5,5,8,8-TETRAMETHYL-2-NAPHTHALENYL)-, (4-(METHYLSULFONYL)PHENYL)HYDRAZONE, (E)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C26017
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
Code System Code Type Description
SMS_ID
100000082315
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY
FDA UNII
S3WF2KTK27
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY
CAS
127304-28-3
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY
NCI_THESAURUS
C77397
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105568
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY
PUBCHEM
9577741
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY
INN
6836
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY
EVMPD
SUB08516MIG
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY
USAN
CC-79
Created by admin on Mon Mar 31 21:32:32 GMT 2025 , Edited by admin on Mon Mar 31 21:32:32 GMT 2025
PRIMARY