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PMID: 1663840 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Synthesis of diazipine and [3H]diazipine: novel dihydropyridines as photoaffinity probes of calcium channels.

Chemical & pharmaceutical bulletin ·Vol. 39 ·No. 7 ·1991-07-00 ·Pages 1860-2

Taki M, Kuniyasu A, Nakayama H, Kanaoka Y

Abstract

Diazipine and [3H]diazipine were synthesized as new 1,4-dihydropyridine photoaffinity ligands containing a phenyldiazirine group. After simple high performance liquid chromatography separation, both compounds were purified in good overall yields. [3H]Diazipine (21.2 Ci/mmol) was synthesized in two steps from commercially available [3H]ethanolamine. Diazipine competitively inhibited [3H]PN200-110 binding to the calcium channel of cardiac membranes with high affinity.

MeSH Terms
Affinity Labels/chemical synthesis Animals Azirines/chemical synthesis,chemistry,pharmacology Calcium Channels/drug effects Dihydropyridines/chemical synthesis,chemistry,pharmacology In Vitro Techniques Isotope Labeling Myocardium/metabolism Swine
Chemicals
Affinity Labels Azirines Calcium Channels Dihydropyridines diazipine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Taki M
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Kuniyasu A
Nakayama H
Kanaoka Y
Article Info
Journal
Chemical & pharmaceutical bulletin
Abbr.
Chem Pharm Bull (Tokyo)
ISSN
0009-2363
Published
1991-07-00
Pages
1860-2
Language
English
Region
Japan
NLM ID
0377775
Subset
IM
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