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CaMK

Chemical Structure Cat. No. Product Name CAS No.
A-3 Hydrochloride Chemical Structure
BCP37347 A-3 Hydrochloride 78957-85-4
A-3 hydrochloride is an inhibitor of PKA, PKC, and casein kinase I and II, and MLCK.
KN92 Chemical Structure
BCP35203 KN92 176708-42-2
KN-92 is an inactive derivative of KN-93.
A 484954 Chemical Structure
BCP28798 A 484954 142557-61-7
A 484954 is a selective inhibitor of eEF2K with IC50 value of 0.28 μM.
NH125 Chemical Structure
BCP29662 NH125 278603-08-0
NH125 is a selective eEF-2 kinase inhibitor with IC50 of 60 nM, >125-fold selectivity over PKC, PKA, and CaMKII, and also a potent histidine kinase inhibitor.
Cefatrizine Chemical Structure
BCP07924 Cefatrizine 51627-14-6
Cefatrizine, also known as BL-S-640 and S-640P, is a eukaryotic elongation factor-2 kinase inhibitor with an anti-proliferative activity toward breast cancer cells.
CaMKII-IN-1 Chemical Structure
BCP19054 CaMKII-IN-1 1208123-85-6
CaMKII-IN-1 is a potent and highly selective CaMKII inhibitor with IC50 of 63 nM; significantly high selectivity against CaMKIV, MLCK, p38a, Akt1, and PKC.
KN62 Chemical Structure
BCP02708 KN62 127191-97-3
KN-62 is selective, cell-permeable inhibitor of CaM kinase II (IC50 = 0.9 μM).
STO-609 acetate Chemical Structure
BCP19299 STO-609 acetate 1173022-21-3
STO-609 is a cell-permeable inhibitor of calcium/calmodulin-dependent kinase kinases (CaMKK) isoforms CaMKKα and CaMKKβ (Ki = 80 and 15 ng/ml, respectively).
STO-609 Chemical Structure
BCP25514 STO-609 52029-86-4
STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively.
KN93 Chemical Structure
BCP02439 KN93 139298-40-1
KN-93 is a selective inhibitor of Ca2+/calmodulin-dependent kinase II (CaMKII), competitively blocking CaM binding to the kinase (Ki = 370 nM).
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