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• 1055-55-6 | Bunamidine hydrochloride (Catalog# : 20271)Bunamidine is a anti-parasitic drug, which was approved by FDA for the treatment of t
• 1303515-32-3 | BI-187004 (Catalog# : 21224)BI-187004, also known as VTP-34072, is an 11β-hydroxysteroid dehydrogenase 1 inhibit
• 1207853-23-3 | (2S,5R)-5-氨基-2-甲基哌啶-1-甲酸苄酯盐酸盐 (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-1166是一种有效的PD-1 / PD-L1相互作用抑制剂，IC50为1.4 nM，可拮抗
• 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-A是一种通过激活内质网应激途径治疗犬和猫乳腺癌的新型疗
• 195615-83-9 | Blarcamesine ( AVex-73 ; AE-37 ) (Catalog# : 6111902)ANAVEX2-73 (blacamesine) 是一种 Sigma-1 受体激动剂和毒蕈碱受体调节剂
• 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是一种强效的选择性S1P1受体调节剂，具有配体偏倚信号转
• 1613264-40-6 | BAY-1316957 (Catalog# : 193263)BAY-1316957是一种高效、选择性、口服的人前列腺素E2受体亚型4 (hEP
• 1800340-40-2 | BMS-986158 (Catalog# : 193255)BMS-986158是一种有效的选择性BET抑制剂。BMS-986158与BET蛋白BRD中的乙
• 1801151-09-6 | BMS-986163 (Catalog# : 193207)BMS-986163是GluN2B的负变构调节剂，在重度抑郁症中具有潜在的应用
• 1009583-20-3 | BMS-816336 (Catalog# : 19351)BMS-816336是一种口服活性、有效和选择性的11β-HSD1抑制剂。BMS- 8163
• 1446113-23-0 | Belvarafenib (Catalog# : 19341)Belvarafenib，又名GDC-5573、HM95573、RG6185，是RAF家族激酶的选择性抑制
• 1191450-19-7 | Burixafor HBr (Catalog# : 192221)Burixafor，又名TG-0054，是CXC趋化因子受体4 (CXCR4)的口服生物利用抑
• 1643368-58-4 | BMS-986142 (Catalog# : 191284)BMS-986142是一种高效、选择性、可逆的BTK抑制剂。
• 1564268-08-1 | BAY1238097 (Catalog# : 191257)BAY1238097是一种有效的选择性BET抑制剂。BAY1238097与BET蛋白BRD上乙酰
• 166977-43-1 | BMS-189453 (Catalog# : 191253)BMS-189453也被称为BMS453,是一个强有力的和选择性RARβ受体激动剂和
• 1093108-50-9 | BI-671800 (Catalog# : 191213)BI-671800是一种治疗哮喘患者的CRTH2拮抗剂。BI 671800与症状控制单纯
• 1912445-55-6 | BMS-986195 (Catalog# : 1811264)BMS-986195是一种有效，共价，Bruton’s酪氨酸激酶的不可逆抑制剂(B
• 1609392-27-9 | BMS-986165 (Catalog# : 1810163)BMS-986165是具有选择性、强效、变构抑制剂的酪氨酸激酶2 (Tyk2)。