Volume 31, Issue 7
Heterocyclic Compounds
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ChemInform Abstract: A Novel Class of Na+ and Ca2+ Channel Dual Blockers with Highly Potent anti-Ischemic Effects.

Hirokazu Annoura

Hirokazu Annoura

Suntory Inst. Bioorg. Res., Shimamoto, Osaka 618, Japan

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Kyoko Nakanishi

Kyoko Nakanishi

Suntory Inst. Bioorg. Res., Shimamoto, Osaka 618, Japan

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Mayumi Uesugi

Mayumi Uesugi

Suntory Inst. Bioorg. Res., Shimamoto, Osaka 618, Japan

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Atsuko Fukunaga

Atsuko Fukunaga

Suntory Inst. Bioorg. Res., Shimamoto, Osaka 618, Japan

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Atsuko Miyajima

Atsuko Miyajima

Suntory Inst. Bioorg. Res., Shimamoto, Osaka 618, Japan

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Yoshiko Tamura-Horikawa

Yoshiko Tamura-Horikawa

Suntory Inst. Bioorg. Res., Shimamoto, Osaka 618, Japan

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Shigeki Tamura

Shigeki Tamura

Suntory Inst. Bioorg. Res., Shimamoto, Osaka 618, Japan

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First published: 10 June 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The synthesis of novel arylpiperidines (IV) and (VI) which exhibit highly potent blocking effects for both neuronal Na+ and Ca++ channels with extremely low affinity for dopamine D2 receptors is reported. Among these compounds the piperidine (VIa) exhibits remarkable neuroprotective activity.

chemical structure image

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