SB 204741 manufacturers
- SB 204741
-
- $34.00 / 1mg
-
2024-11-19
- CAS:152239-46-8
- Min. Order:
- Purity: 99.83%
- Supply Ability: 10g
- SB 204741
-
- $1.00 / 1KG
-
2024-10-22
- CAS:152239-46-8
- Min. Order: 1KG
- Purity: MIn98%HPLC/LC
- Supply Ability: 100KGS
|
| SB 204741 Basic information |
Product Name: | SB 204741 | Synonyms: | SB 204741;N-(1-METHYL-1H-5-INDOLYL)-N'-(3-METHYL-5-ISOTHIAZOLYL)UREA;N-(1-METHYL-1H-INDOLYL-5-YL)-N''-(3-METHYL-5-ISOTHIAZOLYL)UREA;1-(1-Methyl-1H-indol-5-yl)-3-(3-Methylisothiazol-5-yl)urea;Urea, N-(1-methyl-1H-indol-5-yl)-N'-(3-methyl-5-isothiazolyl)-;1-(1-methyl-5-indolyl)-3-(3-methyl-5-isothiazolyl)urea;3-(3-METHYL-1,2-THIAZOL-5-YL)-1-(1-METHYLINDOL-5-YL)UREA;human,inhibit,SB204741,5-HT Receptor,Inhibitor,remodeling,Serotonin Receptor,selective,SB 204741,isoproterenol-induced,affinity,SB-204741,5-hydroxytryptamine Receptor,myocardial | CAS: | 152239-46-8 | MF: | C14H14N4OS | MW: | 286.35 | EINECS: | | Product Categories: | API | Mol File: | 152239-46-8.mol |  |
| SB 204741 Chemical Properties |
Melting point | >195°C (dec.) | storage temp. | 2-8°C | solubility | DMSO: ~18 mg/mL, soluble | form | solid | color | orange | Stability: | Hygroscopic |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36 | WGK Germany | 3 |
| SB 204741 Usage And Synthesis |
Uses | SB 204741 is a potent, selective SR-2B antagonist. | Definition | ChEBI: 1-(1-methylindol-5-yl)-3-(3-methyl-1,2-thiazol-5-yl)urea is a member of ther class of ureas that is urea in which a hydrogen attached to one of the nitrogens has been replaced by an N-methylindol-5-yl group, while a hydrogen attached to the other nitrogen has been replaced by a 3-methyl-1,2-thiazol-5-yl group. It is a potent and selective antagonist for the 5-hydroxytryptamine 2B (5-HT2B) receptor. It has a role as a receptor modulator and a serotonergic antagonist. It is a member of ureas, a member of indoles and a member of 1,2-thiazoles. | Biological Activity | Potent and selective 5-HT 2B receptor antagonist (pA 2 = 7.95). Displays ≥ 135-fold selectivity over 5-HT 2C (pK i = 5.82), 5-HT 2A (pK i < 5.2), 5-HT 1A , 1D , 1E , 5-HT 3 and 5-HT 4 receptors. | storage | Room temperature |
| SB 204741 Preparation Products And Raw materials |
|