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| Product | Description | |
|---|---|---|
| w-7 Hydrochloride | W-7 hydrochloride is a selective calmodulin antagonist. W-7 hydrochloride inhibits the Ca2+-calmodulin-dependent phosphodiesterase and myosin light chain kinase with IC50 values of 28 μM and 51 μM, respectively. W-7 hydrochloride induces apoptosis and has antitumor activity. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 61714-27-0. Molecular formula: C16H22Cl2N2O2S. Mole weight: 377.33. Purity: >99 %. Canonical SMILES: O=S(C1=C2C=CC=C(Cl)C2=CC=C1)(NCCCCCCN)=O.[H]Cl. Product ID: ACM61714270. Alfa Chemistry ISO 9001:2015 Certified. |  |
| W-7 hydrochloride | W-7 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 61714-27-0. Pack Sizes: 100mg. US Biological Life Sciences. |  Worldwide |
| W-7 hydrochloride | W-7 hydrochloride is a calmodulin antagonist that inhibits Ca2+-calmodulin-dependent phosphodiesterase (IC50 = 28 μM) and myosin light chain kinase (IC50 = 51 μM). W-7 is used as a vascular relaxing agent. Uses: Vascular relaxing agent. Synonyms: W-7 hydrochloride; W-7 hydrochloride; W-7 hydrochloride; W-7 HCl; W 7 HCl; W7 HCl; N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide hydrochloride. Grades: ≥98% by HPLC. CAS No. 61714-27-0. Molecular formula: C16H21ClN2O2S.HCl. Mole weight: 377.33. |  |
| W-7 hydrochloride | W-7 hydrochloride is a selective calmodulin antagonist. W-7 hydrochloride inhibits the Ca 2+ -calmodulin -dependent phosphodiesterase and myosin light chain kinase with IC 50 values of 28 μM and 51 μM, respectively [1] [2]. W-7 hydrochloride induces apoptosis and has antitumor activity [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 61714-27-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100912. |  |
| Calmodulin Antagonist W-7 (Actomyosin Inhibitor) (N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide hydrochloride) | W7 is a vascular relaxing agent which affects vascular smooth muscle actomyosin. W7, a Protein Kinase Inhibitor, is an inhibitor of actomyosin superprecipitation, produces relaxation of isolated rabbit arterial strips and antagonizes the contraction of the strips induced by various contractile agonists. W7 is also a calmodulin antagonist that binds to calmodulin and inhibits Ca2+/calmodulin-regulated enzyme activities. Group: Biochemicals. Alternative Names: N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide hydrochloride. Grades: Molecular Biology Grade. CAS No. 61714-27-0. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| W-7, Hydrochloride - CAS 61714-27-0 | A cell-permeable and reversible calmodulin antagonist that inhibits myosin light chain kinase (IC?? = 51 μM) and Ca2+-calmodulin-dependent phosphodiesterase (IC?? = 28 μM). Group: Fluorescence/luminescence spectroscopy. |  |
| W-5 hydrochloride | W-5 hydrochloride is a calmodulin antagonist. W-5 hydrochloride inhibits phosphodiesterase activation with an IC 50 value of 240 μM. W-5 hydrochloride can be used as a negative control for W-7 (HY-100912) [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 61714-25-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-100911. | |
| W-9 hydrochloride | W-9 hydrochloride is a calmodulin antagonist that inhibits calmodulin-activated PDE activity with an IC50 of 72 μM. Synonyms: W-9 hydrochloride; W 9 hydrochloride; W9 hydrochloride; N-(6-Aminohexyl)-5-chloro-2-naphthalenesulfonamide hydrochloride; W-7 Isomer hydrochloride. CAS No. 69762-85-2. Molecular formula: C16H21ClN2O2S.HCl. Mole weight: 377.33. | |
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