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

Details

Stereochemistry ACHIRAL
Molecular Formula C14H17N5
Molecular Weight 255.3183
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SOTIRIMOD

SMILES

CC(C)CN1C(C)=NC2=C1C3=NC=CC=C3N=C2N

InChI

InChIKey=ZXBCLVSLRUWISJ-UHFFFAOYSA-N
InChI=1S/C14H17N5/c1-8(2)7-19-9(3)17-12-13(19)11-10(18-14(12)15)5-4-6-16-11/h4-6,8H,7H2,1-3H3,(H2,15,18)

HIDE SMILES / InChI

Molecular Formula C14H17N5
Molecular Weight 255.3183
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sotirimod is designed to treat actinic keratosis and other conditions and is a follow-up of Aldara (active substance: imiquimod). Sotirimod and imiquimod are immunomodulatory drugs that activate the body's immune system to combat skin changes such as actinic keratosis. Sotirimod is immunostimulants and Toll-like receptor 7 agonist. Sotirimod was originally developed by 3M Pharmaceuticals, then licensed to Meda in Europe for the treatment of actinic keratosis in 2007. Sotirimod had been in phase III development for the treatment of actinic keratosis. However, there is no recent development report for this study.

Approval Year

Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:04:07 GMT 2023
Edited
by admin
on Fri Dec 15 16:04:07 GMT 2023
Record UNII
X04FQM7J4M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SOTIRIMOD
INN   USAN  
USAN   INN  
Official Name English
R-850
Code English
S-30594
Code English
2-Methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amine
Systematic Name English
sotirimod [INN]
Common Name English
SOTIRIMOD [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C308
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
Code System Code Type Description
PUBCHEM
6450818
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107373
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
CAS
227318-75-4
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
FDA UNII
X04FQM7J4M
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
DRUG BANK
DB05680
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
SMS_ID
300000034448
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
NCI_THESAURUS
C76687
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
USAN
RR-12
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
INN
8718
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID80177269
Created by admin on Fri Dec 15 16:04:07 GMT 2023 , Edited by admin on Fri Dec 15 16:04:07 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY