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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
20103006Benzyl(2S,5R)-5-amino-2-methylpiperidine-1-carboxylatehydrochloride1207853-23-398% Min.
2091907Benpyrine racemate1333714-43-498% Min.
(Rac)-Benpyrine is a racemate of Benpyrine. (Rac)-Benpyrine is a potent and orally ac
2091906BAY-24169642242464-44-298% Min.
BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist
2091902BI-8949991660117-38-398% Min.
BI-894999 is a potent and selective BET inhibitor potentially useful for the Treatmen
20912061-Bromo-4-(2-butoxyethoxy)benzene39255-24-898% Min.
20912034-(2-Butoxyethoxy)phenylboronic acid279262-28-198% Min.
20912016-bromo-2-ethyl-N,8-dimethylimidazo[1,2-a]pyridin-3-amine1628264-07-298% Min.
208192BCH001384859-58-9≧98.0%
BCH001,a specific PAPD5 inhibitor, restored telomerase activity and telomere length i
2073102BMS-11661818314-88-398% Min.
BMS-1166is a potent PD-1/PD-L1 interaction inhibitor with an IC50 of 1.4 nM, antagoni
2071615BAY-18160321891087-61-898% Min.
BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazole
2071553BAY-24022342225819-06-598% Min.
BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor
2071550BMVC-8C3O1301708-12-298% Min.
BMVC-8C3O is a DNA G-quadruplexe (G4) ligand which can induce topological conversion
2071532BAY-5451699717-32-298% Min.
BAY-545 is a potent and selective antagonist of the A2B adenosine receptor.
52004Belnacasan273404-37-898%
Belnacasan is a prodrug ofVRT-043198, a caspase-1 inhibitor that was developed by Ver
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_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.