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Catalog No CAS NO Product name
CR3273
1401242-74-7
ML277
ML277(CID53347902) is a novel, potent and selective K(v)7.1 (KCNQ1) potassium channel activator with EC50 of 270 nM. IC50 value: 2..
CR3272
1351758-81-0
HG-10-102-01
HG-10-102-01 is a potent and selective inhibitor of wild-type LRRK2(IC50=23.3 nM) and the G2019S mutant(IC50=3.2 nM) IC50 Value: 2..
CR3271
1191911-26-8
CZC-25146
CZC-25146 is a potent and selective LRRK2 inhibitor. Leucine-rich repeat kinase-2 (LRRK2) mutations are the most important cause o..
CR3270
1910124-24-1
GSK6853
GSK6853 is a potent (300 pM), soluble, cell active (20 nM), and highly selective inhibitor of the BRPF1 bromodomain, and demonstra..
CR3269
1457983-28-6
G-749
G-749 is a novel FLT3 inhibitor that showed potent and sustained inhibition of the FLT3 wild type and mutants including FLT3-ITD, ..
CR3268
516480-79-8
BML-277
BML-277, also known as Chk2 Inhibitor II, is a Chk2 (checkpoint kinase 2) inhibitor. BML-277 protects T cells from apoptosis by co..
CR3267
837422-57-8
WH-4-023
WH-4-023 is a potent and selective dual Lck/Src inhibitor with IC50 of 2 nM/6 nM for Lck and Src kinase respectively. The lymphocy..
CR3266
1374828-69-9
GNE-0877
GNE-0877 is a highly potent and selective LRRK2 inhibitor. Leucine-rich repeat kinase 2 (LRRK2) has drawn significant interest in ..
CR3264
62717-42-4
SKF-38393 HCl
SKF-38393, aslo known as (+/-)-SKF-38393, is a synthetic compound of the benzazepine chemical class which acts as a selective D1/D..
CR3263
20012-10-6
SKF-38393 HBr
Synonyms: SKF 38393 hydrobromide;(±)-SKF 38393 hydrobromide;SKF 38393;(±)-1-phenyl-2,3,4,5-tetrahydro-(1H)-3-benzazepi..
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Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
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