Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
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. | |
2062001 | (3-bromoprop-1-en-2-yl)benzene | 3360-54-1 | 95% | |
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. | |
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% | |
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 | ||||
192221 | Burixafor HBr | 1191450-19-7 | >98% | |
Burixafor, also known as TG-0054, is an orally bioavailable inhibitor of CXC chemokin | ||||
191284 | BMS-986142 | 1643368-58-4 | >98% | |
BMS-986142 is a potent, selective, reversible BTK inhibitor. | ||||
191282 | Blu667 | 2097132-94-8 | >98% | |
Blu667 is a highly potent and selective RET inhibitor with an IC50 of 0.4 nM for wild | ||||
191257 | BAY1238097 | 1564268-08-1 | >98% | |
BAY1238097 is a potent and selective BET inhibitor. BAY1238097 binds to the acetylate | ||||
191253 | BMS-189453 | 166977-43-1 | >98% | |
BMS-189453, also known as BMS453, is a potent and selective RARβ agonist and a poten | ||||
191213 | BI-671800 | 1093108-50-9 | >98% | |
BI-671800 is a CRTH2 antagonist that treats patients with asthma. BI 671800 is associ |
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