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Antitumor effect of a calmodulin antagonist on the growth of solid sarcoma-180.

作者信息

Ito H, Hidaka H

出版信息

Cancer Lett. 1983 Jun;19(2):215-20. doi: 10.1016/0304-3835(83)90157-x.

DOI:10.1016/0304-3835(83)90157-x
PMID:6883309
Abstract

A calmodulin antagonist, N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7), proved to have antitumor activity against solid Sarcoma-180. In particular, intraperitoneal injection of W-7 strongly inhibited the growth of solid Sarcoma-180 in mice given a daily dose, 10 mg/kg for 10 consecutive days. A chlorine deficient analogue, N-(6-aminohexyl)-1-naphthalenesulfonamide (W-5), which interacts weakly with calmodulin, had no antitumor activity against solid Sarcoma-180, in a dose similar to that of W-7. Thus, W-7, a calmodulin antagonist may inhibit the growth of solid Sarcoma-180 by modulation of the Ca2+-calmodulin-dependent processes.

摘要

相似文献

1
Antitumor effect of a calmodulin antagonist on the growth of solid sarcoma-180.
Cancer Lett. 1983 Jun;19(2):215-20. doi: 10.1016/0304-3835(83)90157-x.
2
Inhibition of the acrosome reaction of sea urchin spermatozoa by a calmodulin antagonist, N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7).钙调蛋白拮抗剂N-(6-氨基己基)-5-氯-1-萘磺酰胺(W-7)对海胆精子顶体反应的抑制作用
J Exp Zool. 1983 Jun;226(3):471-3. doi: 10.1002/jez.1402260318.
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N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide, a calmodulin antagonist, inhibits cell proliferation.N-(6-氨基己基)-5-氯-1-萘磺酰胺,一种钙调蛋白拮抗剂,可抑制细胞增殖。
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4354-7. doi: 10.1073/pnas.78.7.4354.
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N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide(W-7), a calmodulin antagonist, also inhibits phospholipid-sensitive calcium-dependent protein kinase.N-(6-氨基己基)-5-氯-1-萘磺酰胺(W-7),一种钙调蛋白拮抗剂,也能抑制磷脂敏感性钙依赖性蛋白激酶。
Biochim Biophys Acta. 1983 Jan 4;755(1):144-7. doi: 10.1016/0304-4165(83)90284-2.
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Hydrophobic interaction of the Ca2+-calmodulin complex with calmodulin antagonists. Naphthalenesulfonamide derivatives.Ca2+ -钙调蛋白复合物与钙调蛋白拮抗剂的疏水相互作用。萘磺酰胺衍生物。
Mol Pharmacol. 1982 Sep;22(2):403-7.
6
Two types of calcium-dependent protein phosphorylations modulated by calmodulin antagonists. Naphthalenesulfonamide derivatives.钙调蛋白拮抗剂调节的两种钙依赖性蛋白磷酸化。萘磺酰胺衍生物。
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7
Symmetric covalent linkage of N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7) results in novel derivatives with increased inhibitory activities against calcium/calmodulin complex.N-(6-氨基己基)-5-氯-1-萘磺酰胺(W-7)的对称共价连接产生了对钙/钙调蛋白复合物具有增强抑制活性的新型衍生物。
Drug Des Discov. 1999 Nov;16(3):203-16.
8
Effects of N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide and other calmodulin antagonists (calmodulin interacting agents) on calcium-induced contraction of rabbit aortic strips.N-(6-氨基己基)-5-氯-1-萘磺酰胺及其他钙调蛋白拮抗剂(钙调蛋白相互作用剂)对兔主动脉条钙诱导收缩的影响。
J Pharmacol Exp Ther. 1981 May;217(2):494-9.
9
Calmodulin antagonist W-7 inhibits aggregation of human platelets induced by platelet activating factor.钙调蛋白拮抗剂W-7可抑制血小板活化因子诱导的人血小板聚集。
Proc Soc Exp Biol Med. 1983 Mar;172(3):393-5. doi: 10.3181/00379727-172-3-rc1.
10
Reversible inhibition of keratinocyte thymidine incorporation by the calmodulin antagonist, W-7.钙调蛋白拮抗剂W-7对角质形成细胞胸苷掺入的可逆性抑制作用。
J Dermatol. 1990 Jul;17(7):403-8. doi: 10.1111/j.1346-8138.1990.tb01666.x.

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