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• W1982772055 abstract "Medicinal Research ReviewsVolume 9, Issue 2 p. 123-180 Article Ca2+ channel ligands: Structure-function relationships of the 1,4-dihydropyridines Dr. David J. Triggle, Dr. David J. Triggle School of Pharmacy, State University of New York, Buffalo, New York Dr. David J. Triggle: received the degrees of B.Sc. and Ph.D. in chemistry from the Universities of Southampton and Hull, respectively, in the United Kingdom. His interests, initially in physical-organic chemistry, switched during a postdoctoral fellowship in Ottawa with Bernard Belleau studying the synthesis of muscarine and related compounds. Following further postdoctoral work in London Dr. Triggle returned to North America and since 1962 has been in Buffalo where his work has focused for some 25 years on the relationships between chemical structure and biological activity with particular reference for the past 10 years on drugs affecting Ca2+ regulation. His contributions in the whole area of ion transport systems have been significant and fundamental.Search for more papers by this authorDr. David A. Langs, Dr. David A. Langs Medical Foundation of Buffalo, Buffalo, New York Dr. David Langs: received his Ph.D. in inorganic chemistry from the State University of New York at Buffalo in 1968. After postdoctoral research positions at Georgetown University and the University of Sydney, he joined the Medical Foundation of Buffalo in 1973. His interests have included investigating the structure-activity relationships of steroids, prostaglandins, pep-tide hormones, membrane ionophores, and antibiotics. He has collaborated with Dr. Triggle in his analysis of calcium channel drugs since 1984. Dr. Langs is regarded as one of the world's leaders in the application of diffraction methods to solve crystal structures of ever increasing complexity.Search for more papers by this authorDr. Ronald A. Janis, Dr. Ronald A. Janis Miles Institute For Preclinical Pharmacology, New Haven, Connecticut Dr. Janis: is presently Principal Staff Scientist at the Institute for Preclinical Pharmacology, Miles Inc. His current work is on the development of Ca2+ channel antagonists, and on putative endogenous ligands for Ca2+ channels. Before joining Miles Inc. in 1980, he was Associate Professor in the Department of Physiology of Northwestern University Medical Center where he worked on second messengers and protein phosphorylation. His postdoctoral training was with Dr. E.E. Daniel at the University of Alberta. He completed his doctoral training with Dr. D.J. Triggle in 1972. His undergraduate studies were in medicinal chemistry, Faculty of Pharmaceutical Sciences, at the University of British Columbia.Search for more papers by this author Dr. David J. Triggle, Dr. David J. Triggle School of Pharmacy, State University of New York, Buffalo, New York Dr. David J. Triggle: received the degrees of B.Sc. and Ph.D. in chemistry from the Universities of Southampton and Hull, respectively, in the United Kingdom. His interests, initially in physical-organic chemistry, switched during a postdoctoral fellowship in Ottawa with Bernard Belleau studying the synthesis of muscarine and related compounds. Following further postdoctoral work in London Dr. Triggle returned to North America and since 1962 has been in Buffalo where his work has focused for some 25 years on the relationships between chemical structure and biological activity with particular reference for the past 10 years on drugs affecting Ca2+ regulation. His contributions in the whole area of ion transport systems have been significant and fundamental.Search for more papers by this authorDr. David A. Langs, Dr. David A. Langs Medical Foundation of Buffalo, Buffalo, New York Dr. David Langs: received his Ph.D. in inorganic chemistry from the State University of New York at Buffalo in 1968. After postdoctoral research positions at Georgetown University and the University of Sydney, he joined the Medical Foundation of Buffalo in 1973. His interests have included investigating the structure-activity relationships of steroids, prostaglandins, pep-tide hormones, membrane ionophores, and antibiotics. He has collaborated with Dr. Triggle in his analysis of calcium channel drugs since 1984. Dr. Langs is regarded as one of the world's leaders in the application of diffraction methods to solve crystal structures of ever increasing complexity.Search for more papers by this authorDr. Ronald A. Janis, Dr. Ronald A. Janis Miles Institute For Preclinical Pharmacology, New Haven, Connecticut Dr. Janis: is presently Principal Staff Scientist at the Institute for Preclinical Pharmacology, Miles Inc. His current work is on the development of Ca2+ channel antagonists, and on putative endogenous ligands for Ca2+ channels. Before joining Miles Inc. in 1980, he was Associate Professor in the Department of Physiology of Northwestern University Medical Center where he worked on second messengers and protein phosphorylation. His postdoctoral training was with Dr. E.E. Daniel at the University of Alberta. He completed his doctoral training with Dr. D.J. Triggle in 1972. His undergraduate studies were in medicinal chemistry, Faculty of Pharmaceutical Sciences, at the University of British Columbia.Search for more papers by this author First published: April/June 1989 https://doi.org/10.1002/med.2610090203Citations: 221 AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume9, Issue2April/June 1989Pages 123-180 RelatedInformation" @default.
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• W1982772055 date "1989-04-01" @default.
• W1982772055 modified "2023-10-03" @default.
• W1982772055 title "Ca2+ channel ligands: Structure-function relationships of the 1,4-dihydropyridines" @default.
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