KS 501
KS 501 is a potent and selective calmodulin inhibitor. KS 501 inhibits the activation of calmodulin kinase I and II, but has less effect against cyclic adenosine 3’,5’-monophosphate (cyclic AMP)-sensitive kinase. KS 501 inhibits the enzyme through interfering with calmodulin activation rather than through a direct effect on the enzyme. KS 501 can be used for the study of leukemia.
For research use only. We do not sell to patients.
- CAS No.: 120634-86-8
- Formula: C33H48O10
- Molecular Weight:604.73
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
KS 501 (0-100 μM) inhibits calmodulin-sensitive phosphodiesterase activity in a concentration-dependent manner (IC50 = 0.8 μM)[1].
KS 501 (0.25-2 μM) shows a decreasing inhibitory effect on phosphodiesterase activity as the concentration of calmodulin increases[1].
KS 501 (10-40 μM) inhibits calmodulin-dependent synapsin I phosphorylation at 40 μM, while 10 μM has no inhibitory effect on basal activity and instead causes slight stimulation[1].
KS 501 (10-40 μM) inhibits the phosphorylation of synapsin I at site 1 (a substrate of calmodulin kinase I) and sites 2 and 3 (a substrate of calmodulin kinase II)[1].
KS 501 (10-40 μM) only partially inhibits synapsin I phosphorylation of cAMP-sensitive protein kinase (PKA)[1].
KS 501 (0-120 μM) inhibits the proliferation of L1210/S cells (IC50 = 80 μM)[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 120634-86-8
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Molecular Weight 604.73
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Formula C33H48O10
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SMILES
O[C@@H]1[C@H](O)[C@@H](OC2=C(C(CCCCCCC)=CC(O)=C2)C(OC3=CC(CCCCCCC)=CC(O)=C3)=O)O[C@@]1([C@H](O)CO)[H]
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)