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CaMK

CaMK

货号 产品名 CAS号 信息
CSN19242 STO-609 52029-86-4 STO-609 is a specific inhibitor of the Ca2+/Calmodulin-dependent protein kinase kinase (CaM-KK) that inhibits the activities of recombinant CaM-KKα and CaM-KKβ isoforms, with Ki values of 80 and 15 ng/mL, respectively, and also inhibits their autophosphorylation activities.
CSN20312 SMP-114 215174-50-8 SMP-114 is a CaMKII inhibitor with oral bioavailability and mediates the reduction SR Ca(2+) leak and arrhythmogenic cellular correlates.
CSN16664 NH125 278603-08-0 NH125 is a selective eEF-2 kinase inhibitor with IC50 of 60 nM, also a potent histidine kinase inhibitor.
CSN21344 Methophenazine 388-51-2 Metofenazate is a selective calmodulin inhibitor.
CSN18794 KN-93 Phosphate 1188890-41-6 KN-93 Phosphate, a potent Ca2+/calmodulin-dependent protein kinase II (CaMKII) selective inhibitor with Ki of 370 nM, is the water soluble version of KN-93.
CSN11255 KN-93 139298-40-1 KN-93 is a potent Ca2+/calmodulin-dependent protein kinase II (CaMKII) selective inhibitor with Ki of 370 nM.
CSN16913 KN-92 Phosphate 1135280-28-2 KN-92 phosphate is an inactive derivative of KN-93. KN-93 is a selective inhibitor of Ca2+/calmodulin-dependent kinase II (CaMKII), competitively blocking CaM binding to the kinase (Ki = 370 nM).
CSN19064 KN-92 176708-42-2 KN-92 is an inactive derivative of KN-93. KN-93 is a selective inhibitor of Ca2+/calmodulin-dependent kinase II (CaMKII), competitively blocking CaM binding to the kinase (Ki = 370 nM).
CSN17850 KN-92 HCl 1431698-47-3 KN-92 HCl a selective inhibitor of Ca2+/calmodulin-dependent kinase II (CaMKII), competitively blocking CaM binding to the kinase (Ki = 370 nM).
CSN23191 W-5 HCl 61714-25-8 Calmodulin antagonist
CSN23190 W-13 HCl 88519-57-7 Calmodulin antagonist
CSN23192 W-9 HCl 69762-85-2 Calmodulin antagonist
CSN22737 Calmidazolium Chloride 57265-65-3 Calmidazolium Chloride is a calmodulin antagonist.
CSN10417 Berbamine 478-61-5 Berbamine, a natural product isolated and purified from the roots of Cocculus orbiculatus (L.) DC., has high binding affinity toward the (GGA)8 G-quadruplex, and is a promising agent to suppress liver cancer growth by targeting CAMKII.
CSN10418 Berbamine HCl 6078-17-7 Berbamine 2HCl, a natural product isolated and purified from the roots of Cocculus orbiculatus (L.) DC., has high binding affinity toward the (GGA)8 G-quadruplex, and is a promising agent to suppress liver cancer growth by targeting CAMKII.
CSN20471 Arcyriaflavin A 118458-54-1 Arcyriaflavin A is a potent inhibitor of cdk4/cyclin D1 (IC50 = 59 nM) and CaM kinase II (IC50 = 25 nM) but displays selectivity over several other kinases in vitro (IC50 values for inhibition of PKA and PKC are > 2 and > 100 μM respectively). It can also inhibit human cytomegalovirus (HCMV) replication in vitro (IC50 = 200 nM).
CSN22660 A-7 HCl 79127-24-5 A-7 HCl is a potent calmodulin antagonist.
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