Home   >  
Neuro Signaling Pathway
  >  
CaMK

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

CaMK

Chemical Structure Cat. No. Product Name CAS No.
Calmidazolium chloride Chemical Structure
BCP46455 Calmidazolium chloride 57265-65-3
Calmidazolium chloride is a calmodulin (CaMK) antagonist, antagonizing CaM-dependent phosphodiesterase and calmodulin-induced activation of erythrocyte Ca2+-transporting ATPase with IC50s of 0.15 and 0.35 μM, respectively. Also in anti-cancer research. Calmidazolium binds to CaMK with a Kd of 3 nM.
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.
12下一页共 17 条记录 1 / 2 页 
0086-13720134139