Search By Initial

Cas Index 2

• 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, also known as GSK'963 or GSK963, is a potent and selective inhibitor of
• 2138814-32-9 | GSK3004774 (Catalog# : 192281)GSK3004774 is a potent, nonabsorbable agonist of CaSR, with an pEC50 of 7.3, 6.6 and
• 2095432-71-4 | GSK269962 HCl (Catalog# : 192201)GSK269962 is a selective ROCK inhibitor with IC50 values of 1.6 and 6 nM for ROCK-I a
• 2245255-65-4 | GSK-2807 (Catalog# : 19185)GSK-2807 is a potent and selective, SAM-competitive inhibitor of SMYD3.
• 2009273-67-8 | GNE-6640 (Catalog# : 1812291)GNE-6640 is a novel selective USP7 inhibitor, inducing tumor cell death. GNE-6640 enh
• 2070864-35-4 | GENZ-882706 (Catalog# : 1810176)GENZ-882706 is a potent colony stimulating factor-1 receptor (CSF-1R) Inhibitor.
• 2077980-83-5 | GLL398 (Catalog# : 185313)GLL398 is an Oral Selective Estrogen Receptor Downregulator.
• 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 (Catalog# : 25001)HC-5404 is a novel, highly selective and potent PERK inhibitor.
• 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 | 1H-1,2,3-triazole, 4,5-diiodo- (Catalog# : 20521)
• 2569527-64-4 | HM43239 (Catalog# : 20517)HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibit
• 27192-20-7 | 4(3H)-Pyrimidinone, 5-bromo-6-cyclopropyl- (Catalog# : 20482)
• 2086183-72-2 | 1H-Indazole-1-acetic acid, 3-acetyl-5-bromo-, 1,1-dimethylethyl ester (Catalog# : 20422)
• 221675-35-0 | 1H-Pyrrolo[2,3-b]pyridine-2-carboxylic acid, ethyl ester (Catalog# : 20388)
• 201847-54-3 | H-BETA-ALA-AMC TFA (Catalog# : 2071633)
• 2158197-70-5 | HS-1371 (Catalog# : 192223)HS-1371 is a novel kinase inhibitor of RIP3-mediated necroptosis. HS-1371 directly bi
• 271-47-6 | 1H-pyrazolo[3,4-c]pyridine (Catalog# : 1781503)1H-pyrazolo[3,4-c]pyridine
• 2244136-58-9 | Irafamdastat (Synonyms: BMS-986368) (Catalog# : 25154)Irafamdastat (BMS-986368; formerly known as ABX-1772) is an oral, CNS-penetrant, smal
• 2408840-26-4 | Imlunestrant (Catalog# : 25104)Imlunestrant is a biochemical