New chiral methyloxyiminomethyl (MOIM) β-adrenergic antagonists. (S)- and (R)-N-[3-(alkylamino)-2-hydroxypropylidene](p-chlorophenylmethyloxy)amines as probes for determining enantiomeric specificity in the class of MOIM-type β-adrenergic blocking agents-Reference-Cited by-同舟云学术

New chiral methyloxyiminomethyl (MOIM) β-adrenergic antagonists. (S)- and (R)-N-[3-(alkylamino)-2-hydroxypropylidene](p-chlorophenylmethyloxy)amines as probes for determining enantiomeric specificity in the class of MOIM-type β-adrenergic blocking agents

Published:1996-01 Issue:3 Volume:31 Page:199-206
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Balsamo A,Breschi MC,Chiellini G,Macchia B,Macchia M,Manera C,Saccà P,Scatizzi R

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference30 articles.

1. The proposal of an unified model for the interpretation of the activity of different classes ofβ-adrenergic agents

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3. Molecular orbital studies on the mechanism of drug-receptor interaction. 2. .beta.-Adrenergic drugs. An approach to explain the role of the aromatic moiety

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2. ChemInform Abstract: New Chiral Methyloxyiminomethyl (MOIM) β-Adrenergic Antagonists. ( S)- and (R)-N-(3-(Alkylamino)-2-hydroxypropylidene)(p- chlorophenylmethyloxy)amines as Probes for Determining Enantiomeric Specificity in the Class of MOIM-Type β-Adre;ChemInform;2010-08-05

3. The [(methyloxy)imino]methyl moiety (MOIMM) in the design of a new type of β-adrenergic blocking agent;European Journal of Medicinal Chemistry;1999-04

4. Synthesis and β-Adrenergic Properties of (Z)-N-[3-(Alkylamino)-2-hydroxypropylidene](aryl-methyloxy)amines: Effects of the Configuration Around the Methyloxyiminomethyl (MOIM) Double Bond on the Biopharmacological Properties of MOIM-type β-Blocking Agents;Bioorganic & Medicinal Chemistry;1998-11

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