Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 2073102 | BMS-1166 | 1818314-88-3 | 98% Min. |  |
| BMS-1166is a potent PD-1/PD-L1 interaction inhibitor with an IC50 of 1.4 nM, antagoni | ||||
| 2071615 | BAY-1816032 | 1891087-61-8 | 98% Min. |  |
| BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazole | ||||
| 2071553 | BAY-2402234 | 2225819-06-5 | 98% Min. |  |
| BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor | ||||
| 2071550 | BMVC-8C3O | 1301708-12-2 | 98% Min. |  |
| BMVC-8C3O is a DNA G-quadruplexe (G4) ligand which can induce topological conversion | ||||
| 2071532 | BAY-545 | 1699717-32-2 | 98% Min. |  |
| BAY-545 is a potent and selective antagonist of the A2B adenosine receptor. | ||||
| 52004 | Belnacasan | 273404-37-8 | 98% | _273404-37-8.png) |
| Belnacasan is a prodrug ofVRT-043198, a caspase-1 inhibitor that was developed by Ver | ||||
| 2062901 | BMS-1001 | 2113650-03-4 | 98% Min. |  |
| 2062328 | 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine | 1549360-60-2 | 98% Min. |  |
| 202327 | 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine hydrochloride | 1628263-43-3 | 98% Min. |  |
| 2062316 | 4-bromo-2-fluoro-1-propan-2-yloxybenzene | 202865-80-3 | 98% Min. | |
| 2062315 | 1-bromo-4-propan-2-ylsulfonylbenzene | 70399-02-9 | 98% Min. | |
| 2062305 | 5-(2,4-bis(benzyloxy)-5-isopropylphenyl)-N-ethyl-4-iodoisoxazole-3-carboxamide | 741414-22-8 | 98% Min. |  |
| 2062028 | 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)-quinoxaline | 1083325-87-4 | 96% Min. | -quinoxaline_1083325-87-4.png) |
| 2062001 | (3-bromoprop-1-en-2-yl)benzene | 3360-54-1 | 95% | benzene_3360-54-1.png) |
| 2051512 | BW-A 78U | 101155-02-6 | 98% Min. |  |
| BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM. | ||||
| S-204156 | 9-bromo-2-hydroxy-7-methyl-4H-pyrido[1,2-a]pyrimidin-4-one | 663619-90-7 | 98% Min. |  |
| 204505 | BB-Cl-Amidine | 1802637-39-3 | 98% Min. | -1-(1H-benzimidazol-2-yl)-4-[(2-chloro-1-iminoethyl)amino]butyl.jpg) |
| BB-Cl-Amidine is a Novel Therapeutic for Canine and Feline Mammary Cancer via Activat | ||||
| 204301 | BAY-218 | 2162982-11-6 | 98% Min. |  |
| BAY-218, also known as BAY-2335218, is a potent and selective small-molecule AhR inhi | ||||
| 6111902 | Blarcamesine ( AVex-73 ; AE-37 ) | 195615-83-9 | 98.0% | _195615-83-9.png) |
| ANAVEX2-73 (blarcamesine) is a Sigma-1 receptor agonist and muscarinic receptor modul | ||||
| ITI007_3 | (6bR,10aS)-3-methyl-2,3,6b,7,8,9,10,10a-octahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline | 313368-85-3 | 95% Min. |  |
| ITI007_2 | (6bR,10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline-8-carboxylic acid ethyl ester | 313369-16-3 | 96% Min. |  |
| Sun-shine Chemical is a supplier Lumateperone and its intermediate from 100g scale to | ||||
| ITI007_1 | 6-bromo-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride | 1059630-11-3 | 95% Min. |  |
| Sun-shine Chemical is a supplier ofLumateperone, we may provideLumateperone and its i | ||||
| 511191 | 3-bromo-7-nitro-1-tosyl-1H-indole | 2091135-02-1 | 96% Min. |  |
| 193285 | BMS-986104 | 1622180-31-7 | >98% |  |
| BMS-986104 is a potent and selective S1P1 receptor modulator, which demonstrates liga | ||||
| 193263 | BAY-1316957 | 1613264-40-6 | >98% |  |
| BAY-1316957 is a highly potent, selective, orally available human prostaglandin E2 re | ||||
| 193255 | BMS-986158 | 1800340-40-2 | >98% |  |
| BMS-986158 is a potent and selective BET inhibitor. BMS-986158 binds to the acetyl-ly | ||||
| 193207 | BMS-986163 | 1801151-09-6 | >98% |  |
| BMS-986163 a Negative Allosteric Modulator of GluN2B with Potential Utility in Major | ||||
| 193121 | BAY-293 | 2244904-70-7 | >98% |  |
| BAY-293 is a potent SOS1 inhibitors that block RAS activation via disruption of the R | ||||
| 19351 | BMS-816336 | 1009583-20-3 | >98% |  |
| BMS-816336 is an orally active, potent and selective 11β-HSD1 inhibitor. BMS-816336 | ||||
| 19341 | Belvarafenib | 1446113-23-0 | >98% |  |
| Belvarafenib, also known as GDC-5573, HM95573, RG6185, is a selective inhibitor of th | ||||