Crene Biotechnology,API,pharmaceutical intermediates,small molecules,prostaglandins,chemicals

+ AII PRODUCTS

- Prostaglandins - Custom Synthesis - PARP Inhibitors - PI3K Inhibitors - FAK Inhibitors - AKT Inhibitors - C-Kit Inhibitors - VEGFR Inhibitors - c-Met Inhibitors - CDK Inhibitors - CYP17 Inhibitors - DNA/RNA Inhibitors - mTOR Inhibitors - SRC Inhibitors - Others - Veterinary APIs

Catalog No	CAS NO	Product name
CR2659	444805-28-1	CMX001 Brincidofovir HDP-CDV Brincidofovir, also known as CMX001, HDP-CDV and HDPCDV, is DNA polymerase inhibitor potentially for the treatment of cytomegalovi..
CR2658	62284-79-1	L-p-Bromotetramisole oxalate L-p-Bromotetramisole is a cell-permeable inhibitor of all four human AP isoenzymes (Kis =18 and 56 µM for PLAP and NSAP, resp..
CR2657	1802326-66-4	JNJ-63533054 JNJ 63533054 is a potent and selective GPR139 agonist (EC50 = 16 nM) that is brain and cell penetrant. JNJ 63533054 is selective f..
CR2656	863774-58-7	Dimethylenastron Dimethylenastron is an inhibitor of mitotic motor kinesin Eg5 (IC50 = 200 nM). Dimethylenastron suppresses human pancreatic cancer..
CR2651	832720-36-2	Elagolix sodium salt Elagolix, also known as NBI56418 and ABT-620, is a Gonadotropin-Releasing Hormone (GnRH) Antagonist. Elagolix inhibits gonadatropi..
CR2650	834153-87-6	Elagolix NBI56418 ABT-620 Elagolix, also known as NBI56418 and ABT-620, is a Gonadotropin-Releasing Hormone (GnRH) Antagonist. Elagolix inhibits gonadatropi..
CR2649	142356-33-0	6-(BOC-AMINO)-HEXYL BROMIDE An intermediate used in the synthesis of fluorescent indicators and various inhibitorsProperties Density: 1.189g/cm3Boiling Poin..
CR2648	1446502-11-9	Enasidenib AG-221 Enasidenib, aslo known as AG-221 and CC-90007, is a potent and selective IDH2 inhibitor with potential anticancer activity (IDH2 =..
CR2647	1204669-58-8	Epacadostat Epacadostat, also known as INCB024360 or INCB24360, is an orally available hydroxyamidine and inhibitor of indoleamine 2,3-dioxyge..
CR2646	896720-20-0	VX-11e VX-11e (VTX-11e, Vertex-11e) is a potent, selective, and orally bioavailable ERK2 inhibitor with Ki of <2 nM, over 200-fold sel..

首页上一页当前第110/244页共2436条记录每页10条108 109110111 112 下一页尾页