编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
20103006 | (2S,5R)-5-氨基-2-甲基哌啶-1-甲酸苄酯盐酸盐 | 1207853-23-3 | 98% Min. | ![]() |
2091907 | Benpyrine racemate | 1333714-43-4 | 98% Min. | ![]() |
(Rac)-Benpyrine is a racemate of Benpyrine. (Rac)-Benpyrine is a potent and orally ac | ||||
2091906 | BAY-2416964 | 2242464-44-2 | 98% Min. | ![]() |
BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist | ||||
2091902 | BI-894999 | 1660117-38-3 | 98% Min. | ![]() |
BI-894999 is a potent and selective BET inhibitor potentially useful for the Treatmen | ||||
2091206 | 4-溴-(2-丁氧基乙氧基)苯 | 39255-24-8 | 98% Min. | ![]() |
2091203 | 4-(2-丁氧基乙氧基)苯基硼酸 | 279262-28-1 | 98% Min. | ![]() |
2091201 | 6-BROMO-2-ETHYL-N,8-DIMETHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE | 1628264-07-2 | 98% Min. | ![]() |
208192 | BCH001 | 384859-58-9 | ≧98.0% | ![]() |
BCH001是一种特异性PAPD5抑制剂,可在DC患者诱导的多能干细胞中恢 | ||||
2073102 | BMS-1166 | 1818314-88-3 | 98% Min. | ![]() |
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 | ||||
2071615 | BAY-1816032 | 1891087-61-8 | 98% Min. | ![]() |
BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazole | ||||
2071553 | BAY-2402234 | 2225819-06-5 | 98% Min. | ![]() |
BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor | ||||
2071550 | BMVC-8C3O | 1301708-12-2 | 98% Min. | ![]() |
BMVC-8C3O is a DNA G-quadruplexe (G4) ligand which can induce topological conversion | ||||
2071532 | BAY-545 | 1699717-32-2 | 98% Min. | ![]() |
BAY-545 is a potent and selective antagonist of the A2B adenosine receptor. | ||||
52004 | Belnacasan | 273404-37-8 | 98% | ![]() |
Belnacasan (VX-765) 是 VRT-043198 的口服生物活性前药,VRT-043198 是有效 | ||||
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-溴-2-羟基-7-甲基-4H-吡啶并[1,2-a]嘧啶-4-酮 | 663619-90-7 | 98% Min. | ![]() |
204505 | BB-Cl-Amidine | 1802637-39-3 | 98% Min. | ![]() |
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 | ||||
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 (blacamesine) 是一种 Sigma-1 受体激动剂和毒蕈碱受体调节剂 | ||||
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. | ![]() |