Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H22N4O5S |
| Molecular Weight | 406.456 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(NC2=CC=C(C=C2S(=O)(=O)NC(=O)NC(C)(C)C)[N+]([O-])=O)C=C1
InChI
InChIKey=SILRUCMXYIKULW-UHFFFAOYSA-N
InChI=1S/C18H22N4O5S/c1-12-5-7-13(8-6-12)19-15-10-9-14(22(24)25)11-16(15)28(26,27)21-17(23)20-18(2,3)4/h5-11,19H,1-4H3,(H2,20,21,23)
| Molecular Formula | C18H22N4O5S |
| Molecular Weight | 406.456 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Pharmacological characterization of N-tert-butyl-N'-[2-(4'-methylphenylamino)-5-nitrobenzenesulfonyl]urea (BM-573), a novel thromboxane A2 receptor antagonist and thromboxane synthase inhibitor in a rat model of arterial thrombosis and its effects on bleeding time. | 2004-05 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:38:30 GMT 2025
by
admin
on
Mon Mar 31 23:38:30 GMT 2025
|
| Record UNII |
8E9L957C3G
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID301121600
Created by
admin on Mon Mar 31 23:38:30 GMT 2025 , Edited by admin on Mon Mar 31 23:38:30 GMT 2025
|
PRIMARY | |||
|
8E9L957C3G
Created by
admin on Mon Mar 31 23:38:30 GMT 2025 , Edited by admin on Mon Mar 31 23:38:30 GMT 2025
|
PRIMARY | |||
|
284464-83-1
Created by
admin on Mon Mar 31 23:38:30 GMT 2025 , Edited by admin on Mon Mar 31 23:38:30 GMT 2025
|
PRIMARY | |||
|
5312142
Created by
admin on Mon Mar 31 23:38:30 GMT 2025 , Edited by admin on Mon Mar 31 23:38:30 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |