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Cas号索引 2

• 2507-91-7 | Gloxazone (Catalog# : 20304)Gloxazone is an effective but toxic anaplasmacide.
• 2407529-33-1 | Giredestrant tartrate (Catalog# : 20263)Giredestrant tartrate (GDC-9545 tartrate), a non-steroidal ER ligand, is an orally ac
• 2183470-12-2 | GCN2iB (Catalog# : 2071802)GCN2iB is an ATP-competitive GCN2 inhibitory compound with a better pharmacokinetic p
• 2101626-26-8 | GSK2894631A (Catalog# : 2071528)GSK2894631A is a hematopoietic PGD synthase (HPGDS) inhibitor.
• 2361659-62-1 | GSK8612 (Catalog# : 2071527)GSK8612 is a potent and highly selective TBK1 inhibitor. GSK8612 inhibited recombinan
• 2049868-46-2 | GSK-963 (Catalog# : 193185)GSK-963，也被称为GSK'963或GSK963，是一种有效的和选择性的RIP1激
• 2138814-32-9 | GSK3004774 (Catalog# : 192281)GSK3004774是一种有效的、不可吸收的CaSR激动剂，人、小鼠和大鼠Ca
• 2095432-71-4 | GSK269962盐酸盐 (Catalog# : 192201)GSK269962是一种选择性ROCK抑制剂，对ROCK-I和ROCK- II的IC50值分别为1.6
• 2245255-65-4 | GSK-2807 (Catalog# : 19185)GSK-2807是一种有效且具有选择性的SMYD3的SAM-竞争性抑制剂。
• 2009273-67-8 | GNE-6640 (Catalog# : 1812291)GNE-6640是一种新型选择性USP7抑制剂，可诱导肿瘤细胞死亡。GNE-664
• 2070864-35-4 | GENZ-882706 (Catalog# : 1810176)GENZ-882706是一种有效的集落刺激因子-1受体(CSF-1R)抑制剂。
• 2077980-83-5 | GLL398 (Catalog# : 185313)GLL398是口服选择性雌激素受体下调物。
• 278779-30-9 | GW4064 (Catalog# : 16071018)GW-4064 is a selective agonist of FXR (EC50 = 15 nM).2 It displays no activity at oth
• 263890-70-6 | GR148672X (Catalog# : 032404)Coming soon!
• 22978-25-2 | GW9662 (Catalog# : 52304)GW9662 is a selective PPAR antagonist forPPARwithIC50of 3.3 nM, with at least 100 to
• 2803470-63-3 | HC-7366 (Catalog# : 25076)HC-7366 is a potent and selective activator of the general control nonderepressible 2
• 2247396-91-2 | HC-5404 抑制剂 (Catalog# : 25001)HC-5404 是一种新型、高选择性、有效的PERK抑制剂。
• 2922069-42-7 | HH-0043 (Catalog# : 24077)
• 2094810-82-7 | HFY-4A (Catalog# : 20661)HFY-4A is a HDAC inhibitor. HFY-4A inhibits breast cancer cell proliferation, migrati
• 257943-19-4 | Hynic-TOC (Catalog# : 20658)Hynic-TOC is a ligand for making 99mTc-Hynic-TOC as an imaging agent in the diagnosti
• 2071224-39-8 | HDAC-IN-58 (Catalog# : 20568)HDAC-IN-58 is a HDAC inhibitor.
• 28194-09-4 | 4,5-二碘-1H-1H-1,2,3-三氮唑 (Catalog# : 20521)
• 2569527-64-4 | HM43239 (Catalog# : 20517)HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibit
• 27192-20-7 | 5-溴-6-环丙基嘧啶-4-醇 (Catalog# : 20482)
• 2086183-72-2 | 1H-Indazole-1-acetic acid, 3-acetyl-5-bromo-, 1,1-dimethylethyl ester (Catalog# : 20422)
• 221675-35-0 | 1H-吡咯并[2,3-B]吡啶-2-羧酸乙酯 (Catalog# : 20388)
• 201847-54-3 | H-BETA-ALA-AMC TFA (Catalog# : 2071633)
• 2158197-70-5 | HS-1371 (Catalog# : 192223)HS-1371是一种新型的RIP3-介导坏死性凋亡激酶抑制剂。HS-1371以ATP-竞
• 271-47-6 | 1H-吡唑并[3,4-C]吡啶 (Catalog# : 1781503)1H-吡唑并[3,4-C]吡啶，1H-pyrazolo[3,4-c]pyridine
• 2244136-58-9 | Irafamdastat (Synonyms: BMS-986368) (Catalog# : 25154)Irafamdastat (BMS-986368；以前称为 ABX-1772) 是一种口服、中枢神经渗透