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Cas号索引 2

• 2770960-52-4 | BIIB-129 (Catalog# : 24025)BIIB129 是一种布鲁顿酪氨酸激酶 (BTK) 的共价、选择性小分子抑制剂
• 2769954-39-2 | BLU-451 (Catalog# : 20668)BLU-451, also known as LNG-451, orally bioavailable, central nervous system (CNS) pen
• 2513289-74-0 | BSJ-04-122 (Catalog# : 20550)
• 2095116-40-6 | brigimadlin (Catalog# : 20533)Brigimadlin is an E3 ubiquitin-protein ligase Mdm2 inhibitor with potential as an ant
• 2607829-38-7 | BDTX-1535 (Catalog# : 20512)BDTX-1535 是一种突变选择性、不可逆的第四代 EGFR 抑制剂。
• 2140301-96-6 | Brepocitinib Tosylate (Catalog# : 232252)Brepocitinib ( PF-06700841 ) is an orally available, selective inhibitor of non-recep
• 2098836-45-2 | BRD4 degrader AT1 (Catalog# : 20496)BRD4 degrader AT1 is an analogue of MZ1. It shows improved selectivity for BRD4 degra
• 2531244-56-9 | BJJF078 (Catalog# : 20492)BJJF078 is a potent inhibitor of recombinant human and mouse Transglutaminase enzyme
• 2760881-74-9 | BRD0639 (Catalog# : 20485)BRD0639 is a potent PRMT5 inhibitor. BRD0639 engages the target in cells, disrupts PR
• 2114324-48-8 | BMS-986251 (Catalog# : 20445)
• 2376257-44-0 | Bexotegrast ( PLN-74809 ) (Catalog# : 171680)Bexotegrast（同义词：PLN-74809）是一种小分子、双重选择性 αVβ1 / α
• 2766481-17-6 | BGB 15025 ; BGB-15025 ; BGB15025 (Catalog# : 171452)BGB-15025 是一种有效的选择性 HPK1 抑制剂，在多种肿瘤模型中作为
• 2477812-42-1 | N-乙基-2-(4-甲酰基苯基)乙酰胺 (Catalog# : 20419)
• 2097334-15-9 | Benzeneacetic acid, 4-[[(2,4-dimethylbenzoyl)oxy]methyl]-, methyl ester (Catalog# : 20391)
• 2230836-55-0 | BI-3406 (Catalog# : 21234)BI-3406 is Potent & Selective SOS1::KRAS Inhibitor (IC50=5 nM), which Opens a New
• 2056261-41-5 | BRD0705 (Catalog# : 202112701)BRD0705 is a potent, paralog selective and orally active GSK3α inhibitor. BRD0705 ca
• 2141955-96-4 | BLU-782 (Catalog# : 20121701)
• 2242464-44-2 | BAY-2416964 (Catalog# : 2091906)BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist
• 279262-28-1 | 4-(2-丁氧基乙氧基)苯基硼酸 (Catalog# : 2091203)
• 2225819-06-5 | BAY-2402234 (Catalog# : 2071553)BAY-2402234 is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor
• 273404-37-8 | Belnacasan (Catalog# : 52004)Belnacasan (VX-765) 是 VRT-043198 的口服生物活性前药，VRT-043198 是有效
• 2113650-03-4 | BMS-1001 (Catalog# : 2062901)
• 202865-80-3 | 4-bromo-2-fluoro-1-propan-2-yloxybenzene (Catalog# : 2062316)
• 2162982-11-6 | BAY-218 (Catalog# : 204301)BAY-218, also known as BAY-2335218, is a potent and selective small-molecule AhR inhi
• 2091135-02-1 | 3-bromo-7-nitro-1-tosyl-1H-indole (Catalog# : 511191)
• 2244904-70-7 | BAY-293 (Catalog# : 193121)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
• 2097132-94-8 | Blu667 (Catalog# : 191282)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
• 2166387-64-8 | BI-3812 (Catalog# : 19124)BI-3812是BCL6 BTB/POZ区域与多个共抑制因子相互作用的有效抑制剂。
• 2080306-23-4 | BAY-299 (Catalog# : 1811262)BAY-299是一种有效且具有选择性的BRD1和TAF1抑制剂（IC50的值分别为
• 298708-79-9 | BAY41-4109消旋体 (Catalog# : 1791117)Bay41-4109消旋体是对Bay41-4109和S-异构体Bay41-4109 R-异构体的混合物。