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Catalog No CAS NO Product name
CS0088
1624117-53-8
XY1
XY1 is a close analog of SGC707 that is completely inactive against PRMT3 at concentrations as high as 100 µM. It is intended..
CS0086
158081-99-3
CP-105696
CP 105696 is a potent and selective leukotriene B4(LTB4) receptor antagonist. In vitro, CP-105696 inhibited LTB4 (0.3 nM) binding ..
CS0084
947914-18-3
ML365
ML365 is a potent and selective K2P3.1 TASK-1 channel blocker. ML365 blocks TASK1 channels in both the thallium influx fluorescent..
CS0083
221244-14-0
1-NM-PP1
1NM-PP1 is a potent Mutant Kinases Inhibitor.A highly potent (IC50=4.3 nM) and uniquely specific tyrosine kinase inhibitor of a ra..
CS0082
1442684-77-6
AM-2394
AM-2394 is a potent and selective Glucokinase agonist (GKA), which catalyzes the phosphorylation of glucose to glucose-6-phosphate..
CS0081
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..
CS0080
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..
CS0079
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..
CS0078
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..
CS0076
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, ..
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