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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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B MACCHIA

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Journal of Medicinal Chemistry|March 20, 1992

Conformational effects on the activity of drugs. 13. A revision of previously proposed models for the activation of alpha- and beta-adrenergic receptorsB Macchia, A Balsamo, M C Breschi, et al.

Drug Design and Delivery|May 1, 1988

An anomalous effect of N-isopropyl substitution in determining beta-adrenergic activityB Macchia, A Balsamo, A Lapucci, et al.

Journal of Medicinal Chemistry|May 13, 1994

The [(methyloxy)imino]methyl moiety as a bioisoster of aryl. A novel class of completely aliphatic beta-adrenergic receptor antagonistsB Macchia, A Balsamo, M C Breschi, et al.

Journal of Medicinal Chemistry|October 15, 1993

Conformationally restrained analogs of sympathomimetic catecholamines. Synthesis, conformational analysis, and adrenergic activity of isochroman derivativesB Macchia, A Balsamo, M C Breschi, et al.

Journal of Medicinal Chemistry|April 1, 1987

Role of the (acyloxy)methyl moiety in eliciting the adrenergic beta-blocking activity of 3-(acyloxy)propanolaminesB Macchia, A Balsamo, A Lapucci, et al.

European Journal of Medicinal Chemistry|March 25, 2000

Synthesis, inhibitory activity towards human leukocyte elastase and molecular modelling studies of 1-carbamoyl-4-methyleneaminoxyazetidinonesB Macchia, D Gentili, M Macchia, et al.

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Search research articles

Showing results (21-30 of 26) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 26 results.

Journal of Medicinal Chemistry|March 20, 1992

Conformational effects on the activity of drugs. 13. A revision of previously proposed models for the activation of alpha- and beta-adrenergic receptorsB Macchia, A Balsamo, M C Breschi, et al.

Drug Design and Delivery|May 1, 1988

An anomalous effect of N-isopropyl substitution in determining beta-adrenergic activityB Macchia, A Balsamo, A Lapucci, et al.

Journal of Medicinal Chemistry|May 13, 1994

The [(methyloxy)imino]methyl moiety as a bioisoster of aryl. A novel class of completely aliphatic beta-adrenergic receptor antagonistsB Macchia, A Balsamo, M C Breschi, et al.

Journal of Medicinal Chemistry|October 15, 1993

Conformationally restrained analogs of sympathomimetic catecholamines. Synthesis, conformational analysis, and adrenergic activity of isochroman derivativesB Macchia, A Balsamo, M C Breschi, et al.

Journal of Medicinal Chemistry|April 1, 1987

Role of the (acyloxy)methyl moiety in eliciting the adrenergic beta-blocking activity of 3-(acyloxy)propanolaminesB Macchia, A Balsamo, A Lapucci, et al.

European Journal of Medicinal Chemistry|March 25, 2000

Synthesis, inhibitory activity towards human leukocyte elastase and molecular modelling studies of 1-carbamoyl-4-methyleneaminoxyazetidinonesB Macchia, D Gentili, M Macchia, et al.

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