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
SMILES
CC(C)CN1C(C)=NC2=C(N)N=C3C=CC=NC3=C12
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)
| 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.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:18:03 GMT 2025
by
admin
on
Mon Mar 31 18:18:03 GMT 2025
|
| Record UNII |
X04FQM7J4M
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C308
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
6450818
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
CHEMBL2107373
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
227318-75-4
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
X04FQM7J4M
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
DB05680
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
300000034448
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
C76687
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
RR-12
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
8718
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY | |||
|
DTXSID80177269
Created by
admin on Mon Mar 31 18:18:03 GMT 2025 , Edited by admin on Mon Mar 31 18:18:03 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
TARGET -> AGONIST |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|
