产品目录
| 编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
|---|---|---|---|---|
| 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. | -quinoxaline_1083325-87-4.png) |
| 2062001 | (3-bromoprop-1-en-2-yl)benzene | 3360-54-1 | 95% | benzene_3360-54-1.png) |
| 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. | -1-(1H-benzimidazol-2-yl)-4-[(2-chloro-1-iminoethyl)amino]butyl.jpg) |
| 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% | _195615-83-9.png) |
| ANAVEX2-73 (blacamesine) 是一种 Sigma-1 受体激动剂和毒蕈碱受体调节剂 | ||||
| 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]quinoxaline | 313368-85-3 | 95% 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 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. |  |
| 193285 | BMS-986104 | 1622180-31-7 | >98% |  |
| 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 | ||||
| 193263 | BAY-1316957 | 1613264-40-6 | >98% |  |
| 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 | ||||
| 193255 | BMS-986158 | 1800340-40-2 | >98% |  |
| 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 | ||||
| 193207 | BMS-986163 | 1801151-09-6 | >98% |  |
| 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 | ||||
| 193121 | BAY-293 | 2244904-70-7 | >98% |  |
| BAY-293是一种有效的SOS1抑制剂，通过破坏IC50为21 nM的RAS-SOS1的相互 | ||||
| 19351 | BMS-816336 | 1009583-20-3 | >98% |  |
| BMS-816336是一种口服活性、有效和选择性的11β-HSD1抑制剂。BMS- 8163 | ||||
| 19341 | Belvarafenib | 1446113-23-0 | >98% |  |
| Belvarafenib，又名GDC-5573、HM95573、RG6185，是RAF家族激酶的选择性抑制 | ||||
| 192221 | Burixafor HBr | 1191450-19-7 | >98% |  |
| Burixafor，又名TG-0054，是CXC趋化因子受体4 (CXCR4)的口服生物利用抑 | ||||
| 191284 | BMS-986142 | 1643368-58-4 | >98% |  |
| BMS-986142是一种高效、选择性、可逆的BTK抑制剂。 | ||||
| 191282 | Blu667 | 2097132-94-8 | >98% |  |
| BLU-667是一种有效的选择性 RET 抑制剂， IC50 为0.4 nM，对突变体 RET | ||||
| 191257 | BAY1238097 | 1564268-08-1 | >98% |  |
| BAY1238097是一种有效的选择性BET抑制剂。BAY1238097与BET蛋白BRD上乙酰 | ||||
| 191253 | BMS-189453 | 166977-43-1 | >98% |  |
| 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 | ||||
| 191213 | BI-671800 | 1093108-50-9 | >98% |  |
| 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 | ||||