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Biological Data
Biological description | Potent calmodulin antagonist. Cell permeable. Napthalenesulfonamide W-7 analog. Inhibits calmodulin activated PDE activity (IC50 = 3 µM). |
Solubility & Handling
Storage instructions | Room temperature |
Solubility overview | Soluble in DMSO (50mM) |
Important | This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use. |
Chemical Data
Chemical name | N-(10-Aminodecyl)-5-chloro-1-naphthalenesulfonamide hydrochloride |
Chemical structure | |
Molecular Formula | C20H29ClN2O2S.HCl |
PubChem identifier | 44119113 |
SMILES | C1=CC2=C(C=CC=C2Cl)C(=C1)S(=O)(=O)NCCCCCCCCCCN.Cl |
InChiKey | XDJCAQBTSCRBHS-UHFFFAOYSA-N |
References for A-7 hydrochloride
References are publications that support the biological activity of the product
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Direct interaction of calmodulin antagonists with Ca2+/calmodulin-dependent cyclic nucleotide phosphodiesterase.
Itoh H et al (1984) J Biochem 96(6) : 1721-6. -
Naphthalenesulfonamides as calmodulin antagonists.
Hidaka H et al (1983) Methods Enzymol 102 : 185-94.
Potent, cell-permeable calmodulin (CaM) antagonist