Výsledky vyhledávání - "J.-F. Mayaux"

Akademický článek

An Allosteric Ribozyme Regulated by Doxycyline This work was supported by Aventis Gencell and by a grant from the Volkswagen Foundation (Priority program "conformational control") to M.F. We thank M. Blind, G. Mayer, D. Proske, and G. Sengle (Universität Bonn) for helpful discussions as well as J. Crouzet, J. F. Mayaux, and M. Finer (Aventis Gencell) for support.

Autor: Piganeau N; Kekulé-Institut für Organische Chemie und Biochemie Gerhard Domagk-Strasse 1, 53121 Bonn (Germany)., Jenne A, Thuillier V, Famulok M

Publikováno v: Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2001 Oct 01; Vol. 40 (19), pp. 3503.

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Betulinic Acid Derivatives: A New Class of Human Immunodeficiency Virus Type 1 Specific Inhibitors with a New Mode of Action

Autor: A. Bousseau, Y. Lelievre, Y. Ribeill, N Dereu, J.-C. Gueguen, Y. Henin, J.-B. Le Pecq, M. Evers, F. Soler, E. De Clercq, D. Reisdorf, I. Morize, J F Mayaux, Rudi Pauwels, C Poujade, C. James

Publikováno v: Journal of Medicinal Chemistry. 39:1056-1068

A series of omega-undecanoic amides of lup-20(29)-en-28-oic acid derivatives were synthesized and evaluated for activity in CEM 4 and MT-4 cell cultures against human immunodeficiency virus type 1 (HIV-1) strain IIIB/LAI. The potent HIV inhibitors wh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::050517349681e5f63e2cc58c8e4b47e9
https://doi.org/10.1021/jm950670t

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ChemInform Abstract: Betulinic Acid Derivatives: A New Class of Human Immunodeficiency Virus Type 1 Specific Inhibitors with a New Mode of Action

Autor: A. Bousseau, Y. Lelievre, Y. Henin, M. Evers, J.-B. Le Pecq, C Poujade, C. James, E. De Clercq, J F Mayaux, Rudi Pauwels, I. Morize, D. Reisdorf, Y. Ribeill, F. Soler, N Dereu, J.-C. Gueguen

Publikováno v: ChemInform. 27

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e32f14723289347d57c559eccdb13ab0
https://doi.org/10.1002/chin.199627201

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ChemInform Abstract: Betulinic Acid Derivatives: A New Class of Specific Inhibitors of Human Immunodeficiency Virus Type 1 Entry

Autor: C Poujade, J F Mayaux, T Huet, A. Bousseau, Rudi Pauwels, J.‐C. Carry, N Dereu, F. Soler, Y. Henin, J.-B. Le Pecq, M. Evers, E. De Clercq

Publikováno v: ChemInform. 27

A novel series of omega-aminoalkanoic acid derivatives of betulinic acid were synthesized and evaluated for their activity against human immunodeficiency virus (HIV). The anti-HIV-1 activity of several members of this new series was found to be in th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::089bbef12d62be11947b0e631916d3fd
https://doi.org/10.1002/chin.199627202

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HIV-1 Aspartic Proteinase: High-Level Production and Automated Fluorometric Screening Assay of Inhibitors

Autor: B. Cambou, Yves Lelièvre, C. Giuliacci, Terence Cartwright, G. Jung, A. Dugué, Fabienne Parker, J. Boiziau, J.-F. Mayaux, Ph.-H. Hirel, D. Outerovitch, C. Peltiers, R. Boulay

Publikováno v: Antiviral Chemistry and Chemotherapy. 1:9-15

The 99-amino-acid HIV-1 aspartic proteinase was expressed to high levels in Escherichia coli using a T7 expression system. About 50% of the insoluble material after sonication of the bacteria was composed of aggregated proteinase. Subsequent renatura

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::67967e6bee1ddfce1fafeade4687ff30
https://doi.org/10.1177/095632029000100103

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Betulinic acid derivatives: a new class of specific inhibitors of human immunodeficiency virus type 1 entry

Autor: Rudi Pauwels, A. Bousseau, Y. Henin, J.-B. Le Pecq, M. Evers, C Poujade, E. De Clercq, F. Soler, T Huet, J F Mayaux, J.‐C. Carry, N Dereu

Publikováno v: Journal of medicinal chemistry. 39(5)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ebf1fd91b6d74939fa8447fe095f402
https://pubmed.ncbi.nlm.nih.gov/8676342

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Septide: an agonist for the NK1 receptor acting at a site distinct from substance P

Autor: L, Pradier, J, Ménager, J, Le Guern, M D, Bock, E, Heuillet, V, Fardin, C, Garret, A, Doble, J F, Mayaux

Publikováno v: Molecular pharmacology. 45(2)

The hexapeptide [pGlu6,Pro9]substance P (SP)6-11, septide, has been shown to be an agonist as potent as SP in eliciting smooth muscle contraction in several in vitro preparations, while being a poor competitor of labeled SP binding. These results, as

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f50f05a170ec8a8fba9378712f49978b
https://pubmed.ncbi.nlm.nih.gov/7509440

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