| Cat.No. | Name | Information |
|---|---|---|
| M7336 | STO-609 | STO-609 is a specific selective CaM kinase kinase inhibitor, inhibits the activities of recombinant CaM-KK alpha and CaM-KK beta isoforms, with K(i) values of 80 and 15 ng/ml, respectively. |
| M52414 | CaMKII inhibitory peptide KIIN | CaMKII inhibitory peptide KIIN is a potent inhibitor of CaMKII. |
| M52413 | Autocamtide-3 | Autocamtide-3, a 13-amino-acid peptide containing Thr287, is a selective CaMKII (Ca2+/calmodulin-dependent kinase II) (CaMK) substrate. |
| M42636 | CS587 | CS587 is a specific inhibitor of CaMK1D with neurocytotoxicity at 10 μM. |
| M42635 | Autocamtide-3 acetate | Autocamtide-3 acetate, a 13-amino-acid peptide containing Thr287, is a selective CaMKII (Ca2+/calmodulin-dependent kinase II) (CaMK) substrate. |
| M29547 | Ph-HTBA | Ph-HTBA is a high-affinity, brain-penetrating modulator for CaMKIIα. Ph-HTBA has binding affinity for CaMKIIα with a Kd value of 757 nM. Ph-HTBA can be used for the research of ischemia and neurodegenerative disorders. |
| M28067 | Lavendustin C | Lavendustin C is a potent Ca2+ calmodulin-dependent kinase II (CaMK II) inhibitor with an IC50 of 0.2 µM. Lavendustin C inhibits EGFR-associated tyrosine kinase (IC50=0.012 µM) and pp60c-src(+) kinase (IC50=0.5 µM) . |
| M14557 | CaMKII-IN-1 | 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. |
| M14556 | Autocamtide-2-related inhibitory peptide TFA | Autocamtide-2-related inhibitory peptide (TFA) is a highly specific and potent inhibitor of CaMKII with an IC50 of 40 nM. |
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