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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
2062901BMS-10012113650-03-498% Min.
20623286-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine1549360-60-298% Min.
2023276-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine hydrochloride1628263-43-398% Min.
20623164-bromo-2-fluoro-1-propan-2-yloxybenzene202865-80-398% Min.
20623151-bromo-4-propan-2-ylsulfonylbenzene70399-02-998% Min.
20623055-(2,4-bis(benzyloxy)-5-isopropylphenyl)-N-ethyl-4-iodoisoxazole-3-carboxamide741414-22-898% Min.
20620287-bromo-2-(1-methyl-1H-pyrazol-4-yl)-quinoxaline1083325-87-496% Min.
2062001(3-bromoprop-1-en-2-yl)benzene3360-54-195%
2051512BW-A 78U101155-02-698% Min.
BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM.
S-2041569-bromo-2-hydroxy-7-methyl-4H-pyrido[1,2-a]pyrimidin-4-one663619-90-798% Min.
204505BB-Cl-Amidine1802637-39-398% Min.
BB-Cl-Amidine is a Novel Therapeutic for Canine and Feline Mammary Cancer via Activat
204301BAY-2182162982-11-698% Min.
BAY-218, also known as BAY-2335218, is a potent and selective small-molecule AhR inhi
6111902Blarcamesine ( AVex-73 ; AE-37 )195615-83-998.0% 
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]quinoxaline313368-85-395% 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 ester313369-16-396% Min.
Sun-shine Chemical is a supplier Lumateperone and its intermediate from 100g scale to
ITI007_16-bromo-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride1059630-11-395% Min.
Sun-shine Chemical is a supplier ofLumateperone, we may provideLumateperone and its i
5111913-bromo-7-nitro-1-tosyl-1H-indole2091135-02-196% Min.
193285BMS-9861041622180-31-7>98%
BMS-986104 is a potent and selective S1P1 receptor modulator, which demonstrates liga
193263BAY-13169571613264-40-6>98%
BAY-1316957 is a highly potent, selective, orally available human prostaglandin E2 re
193255BMS-9861581800340-40-2>98%
BMS-986158 is a potent and selective BET inhibitor. BMS-986158 binds to the acetyl-ly
193207BMS-9861631801151-09-6>98%
BMS-986163 a Negative Allosteric Modulator of GluN2B with Potential Utility in Major
193121BAY-2932244904-70-7>98%
BAY-293 is a potent SOS1 inhibitors that block RAS activation via disruption of the R
19351BMS-816336 1009583-20-3>98%
BMS-816336 is an orally active, potent and selective 11β-HSD1 inhibitor. BMS-816336
19341Belvarafenib1446113-23-0>98%
Belvarafenib, also known as GDC-5573, HM95573, RG6185, is a selective inhibitor of th
192221Burixafor HBr1191450-19-7>98%
Burixafor, also known as TG-0054, is an orally bioavailable inhibitor of CXC chemokin
191284BMS-9861421643368-58-4>98%
BMS-986142 is a potent, selective, reversible BTK inhibitor.
191282Blu6672097132-94-8>98%
Blu667 is a highly potent and selective RET inhibitor with an IC50 of 0.4 nM for wild
191257BAY12380971564268-08-1>98%
BAY1238097 is a potent and selective BET inhibitor. BAY1238097 binds to the acetylate
191253BMS-189453 166977-43-1>98%
BMS-189453, also known as BMS453, is a potent and selective RARβ agonist and a poten
191213BI-6718001093108-50-9>98%
BI-671800 is a CRTH2 antagonist that treats patients with asthma. BI 671800 is associ