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CaMK
| Cat. No. | Product Name | CAS No. | Information |
|---|---|---|---|
| CSN19242 | STO-609 | 52029-86-4 | STO-609 is a specific inhibitor of the Ca2Calmodulin-dependent protein kinase kinase CaM-KK that inhibits the activities of recombinant CaM-KK and CaM-KK isoforms with Ki values of 80 and 15 ngmL 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 |
| CSN11255 | KN-93 | 139298-40-1 | KN-93 is a potent Ca2calmodulin-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 Ca2calmodulin-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 Ca2calmodulin-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). |
| CSN20998 | DehydropachyMic acid | 77012-31-8 | Dehydropachymic acid is extracted from the root of wolfiporia cocos (Schw.) Ryv. with antiinflammatory activity. |
| 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. |
| CSN22660 | A-7 HCl | 79127-24-5 | A-7 HCl is a potent calmodulin antagonist. |
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