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Cas Index 1

• 1303515-32-3 | BI-187004 (Catalog# : 21224)BI-187004, also known as VTP-34072, is an 11β-hydroxysteroid dehydrogenase 1 inhibit
• 1207853-23-3 | Benzyl(2S,5R)-5-amino-2-methylpiperidine-1-carboxylatehydrochloride (Catalog# : 20103006)
• 1333714-43-4 | Benpyrine racemate (Catalog# : 2091907)(Rac)-Benpyrine is a racemate of Benpyrine. (Rac)-Benpyrine is a potent and orally ac
• 1660117-38-3 | BI-894999 (Catalog# : 2091902)BI-894999 is a potent and selective BET inhibitor potentially useful for the Treatmen
• 1628264-07-2 | 6-bromo-2-ethyl-N,8-dimethylimidazo[1,2-a]pyridin-3-amine (Catalog# : 2091201)
• 1818314-88-3 | BMS-1166 (Catalog# : 2073102)BMS-1166is a potent PD-1/PD-L1 interaction inhibitor with an IC50 of 1.4 nM, antagoni
• 1891087-61-8 | BAY-1816032 (Catalog# : 2071615)BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazole
• 1301708-12-2 | BMVC-8C3O (Catalog# : 2071550)BMVC-8C3O is a DNA G-quadruplexe (G4) ligand which can induce topological conversion
• 1699717-32-2 | BAY-545 (Catalog# : 2071532)BAY-545 is a potent and selective antagonist of the A2B adenosine receptor.
• 1549360-60-2 | 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine (Catalog# : 2062328)
• 1628263-43-3 | 6-bromo-2-ethyl-8-methylimidazo[1,2-a]pyridin-3-amine hydrochloride (Catalog# : 202327)
• 1083325-87-4 | 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)-quinoxaline (Catalog# : 2062028)
• 101155-02-6 | BW-A 78U (Catalog# : 2051512)BW-A 78U is a PDE4 inhibitor with an IC50 of 3 μM.
• 1802637-39-3 | BB-Cl-Amidine (Catalog# : 204505)BB-Cl-Amidine is a Novel Therapeutic for Canine and Feline Mammary Cancer via Activat
• 195615-83-9 | Blarcamesine ( AVex-73 ; AE-37 ) (Catalog# : 6111902)ANAVEX2-73 (blarcamesine) is a Sigma-1 receptor agonist and muscarinic receptor modul
• 1059630-11-3 | 6-bromo-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride (Catalog# : ITI007_1)Sun-shine Chemical is a supplier ofLumateperone, we may provideLumateperone and its i
• 1622180-31-7 | BMS-986104 (Catalog# : 193285)BMS-986104 is a potent and selective S1P1 receptor modulator, which demonstrates liga
• 1613264-40-6 | BAY-1316957 (Catalog# : 193263)BAY-1316957 is a highly potent, selective, orally available human prostaglandin E2 re
• 1800340-40-2 | BMS-986158 (Catalog# : 193255)BMS-986158 is a potent and selective BET inhibitor. BMS-986158 binds to the acetyl-ly
• 1801151-09-6 | BMS-986163 (Catalog# : 193207)BMS-986163 a Negative Allosteric Modulator of GluN2B with Potential Utility in Major
• 1009583-20-3 | BMS-816336 (Catalog# : 19351)BMS-816336 is an orally active, potent and selective 11β-HSD1 inhibitor. BMS-816336
• 1446113-23-0 | Belvarafenib (Catalog# : 19341)Belvarafenib, also known as GDC-5573, HM95573, RG6185, is a selective inhibitor of th
• 1191450-19-7 | Burixafor HBr (Catalog# : 192221)Burixafor, also known as TG-0054, is an orally bioavailable inhibitor of CXC chemokin
• 1643368-58-4 | BMS-986142 (Catalog# : 191284)BMS-986142 is a potent, selective, reversible BTK inhibitor.
• 1564268-08-1 | BAY1238097 (Catalog# : 191257)BAY1238097 is a potent and selective BET inhibitor. BAY1238097 binds to the acetylate
• 166977-43-1 | BMS-189453 (Catalog# : 191253)BMS-189453, also known as BMS453, is a potent and selective RARβ agonist and a poten
• 1093108-50-9 | BI-671800 (Catalog# : 191213)BI-671800 is a CRTH2 antagonist that treats patients with asthma. BI 671800 is associ
• 1912445-55-6 | BMS-986195 (Catalog# : 1811264)BMS-986195 is a potent, covalent, irreversible inhibitor of Bruton’s tyrosine kinas
• 1609392-27-9 | BMS-986165 (Catalog# : 1810163)BMS-986165 potently binds to the Tyk2 pseudokinase domain (Ki = 0.02 nM). BMS-986165
• 1611493-60-7 | Bictegravir (Catalog# : 187181)Bictegravir, also known as GS-9883, is a potent, unboosted, once-Daily HIV-1 Integras