Synthesis and Pharmacological Properties of Silicon-Containing 1,4-Dihydropyridine Derivatives: Calcium Channel Antagonists and α1 Adrenoceptor Antagonists of the Sila-niguldipine Type-Reference-Cited by-同舟云学术

Synthesis and Pharmacological Properties of Silicon-Containing 1,4-Dihydropyridine Derivatives: Calcium Channel Antagonists and α1 Adrenoceptor Antagonists of the Sila-niguldipine Type

Published:2003-12-24 Issue:3 Volume:23 Page:361-366
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Heinrich Tilman¹,Burschka Christian¹,Warneck Julie¹,Tacke Reinhold¹

Affiliation:

1. Institut für Anorganische Chemie, Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany, and Amedis Pharmaceuticals Ltd., 162 Cambridge Science Park, Milton Road, Cambridge CB4 0GP, U.K.

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om0305622

Reference24 articles.

1. Re-examining the Clinical Safety and Roles of Calcium Antagonists in Cardiovascular Medicine

2. The pharmacology of ion channels: with particular reference to voltage-gated Ca2+ channels

3. (+)-Niguldipine binds with very high affinity to Ca2+ channels and to a subtype of α1-adrenoceptors

4. Discovery of .alpha.1a-Adrenergic Receptor Antagonists Based on the L-Type Ca2+ Channel Antagonist Niguldipine

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