Synthesis and L-type calcium channel blocking activity of new chiral oxadiazolothiazinones-Reference-Cited by-同舟云学术

Synthesis and L-type calcium channel blocking activity of new chiral oxadiazolothiazinones

Published:2015-03 Issue: Volume:92 Page:481-489
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Carosati Emanuele^ORCID,Ioan Pierfranco,Barrano Giovanni Battista,Caccamese Salvatore,Cosimelli Barbara,Devlin Frank J.,Severi Elda,Spinelli Domenico,Superchi Stefano,Budriesi Roberta

Funder

University of Bologna

Istituto Nazionale per le Ricerche Cardiovascolari (INRC), Italy

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

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5. Inhibition of MDR1 activity in vitro by a novel class of diltiazem analogues:: towards new candidates;Viale;J. Med. Chem.,2009

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1. Mononuclear Rearrangement of the Z-Phenylhydrazones of Some 3-Acyl-1,2,4-oxadiazoles: Effect of Substituents on the Nucleophilic Character of the >C═N–NH–C6 H5 Chain and on the Charge Density of N-2 of the 1,2,4-Oxadiazole Ring (Electrophilic Counterpart);The Journal of Organic Chemistry;2019-01-29

2. Comparative spectroscopic and electrochemical study of N-1 or N-2-alkylated 4-nitro and 7-nitroindazoles;Arabian Journal of Chemistry;2017-09

3. New Methods for the Synthesis of 3-Amino-6,7-Dihydro-5H-Cyclopenta[c]Pyridine-4-Carbonitriles and Cyclopenta[d]Pyrazolo[3,4-b]Pyridines via a Smiles-type Rearrangement;Journal of Heterocyclic Chemistry;2016-06-28

4. Understanding Oxadiazolothiazinone Biological Properties: Negative Inotropic Activity versus Cytochrome P450-Mediated Metabolism;Journal of Medicinal Chemistry;2016-03-23