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Catalog No CAS NO Product name
CR3280
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..
CR3279
885325-71-3
MK-8745
MK-8745 is a novel Aurora-A specific inhibitor. MK8745 induced apoptotic cell death in a p53-dependent manner when tested in vitro..
CR3278
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 ..
CR3277
1033735-94-2
GNE-493
GNE-493 is a low molecular weight, potent dual inhibitor of pan-PI3 kinases and mTOR. GNE-493 displays approximately equipotent in..
CR3276
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..
CR3275
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 r..
CR3274
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..
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..
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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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