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Results: 1-9 |
Results: 9
NOVEL CONFORMATIONALLY EXTENDED NAPHTHALENE-BASED INHIBITORS OF FARNESYLTRANSFERASE
Authors: BURNS CJ GUITTON JD BAUDOIN B LELIEVRE Y DUCHESNE M PARKER F FROMAGE N COMMERCON A
Citation: Cj. Burns et al., NOVEL CONFORMATIONALLY EXTENDED NAPHTHALENE-BASED INHIBITORS OF FARNESYLTRANSFERASE, Journal of medicinal chemistry, 40(12), 1997, pp. 1763-1767
BETULINIC ACID-DERIVATIVES - A NEW CLASS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 SPECIFIC INHIBITORS WITH A NEW MODE OF ACTION
Authors: EVERS M POUJADE C SOLER F RIBEILL Y JAMES C LELIEVRE Y GUEGUEN JC REISDORF D MORIZE I PAUWELS R DECLERCQ E HENIN Y BOUSSEAU A MAYAUX JF LEPECQ JB DEREU N
Citation: M. Evers et al., BETULINIC ACID-DERIVATIVES - A NEW CLASS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 SPECIFIC INHIBITORS WITH A NEW MODE OF ACTION, Journal of medicinal chemistry, 39(5), 1996, pp. 1056-1068
LOCAL CONSTRAINED SHIFTY PSEUDOPEPTIDES INHIBITORS OF RAS-FARNESYL TRANSFERASE
Authors: BYK G DUCHESNE M PARKER F LELIEVRE Y GUITTON JD CLERC FF BECQUART J TOCQUE B SCHERMAN D
Citation: G. Byk et al., LOCAL CONSTRAINED SHIFTY PSEUDOPEPTIDES INHIBITORS OF RAS-FARNESYL TRANSFERASE, Bioorganic & medicinal chemistry letters, 5(22), 1995, pp. 2677-2682
CONSTRAINED ANALOGS OF KCVFM WITH IMPROVED INHIBITORY PROPERTIES AGAINST FARNESYL TRANSFERASE
Authors: CLERC FF GUITTON JD FROMAGE N LELIEVRE Y DUCHESNE M TOCQUE B JAMESSURCOUF E COMMERCON A BECQUART J
Citation: Ff. Clerc et al., CONSTRAINED ANALOGS OF KCVFM WITH IMPROVED INHIBITORY PROPERTIES AGAINST FARNESYL TRANSFERASE, Bioorganic & medicinal chemistry letters, 5(16), 1995, pp. 1779-1784
RPR113228, A NOVEL FARNESYL-PROTEIN TRANSFERASE INHIBITOR PRODUCED BYCHRYSOSPORIUM-LOBATUM
Authors: VANDERPYL D CANS P DEBERNARD JJ HERMAN F LELIEVRE Y TAHRAOUI L VUILHORGNE M LEBOUL J
Citation: D. Vanderpyl et al., RPR113228, A NOVEL FARNESYL-PROTEIN TRANSFERASE INHIBITOR PRODUCED BYCHRYSOSPORIUM-LOBATUM, Journal of antibiotics, 48(7), 1995, pp. 736-737
SYNTHESIS OF C2-SYMMETRICAL INHIBITORS OF THE HIV-1 PROTEASE, WITH N,N'-SUBSTITUTED ETHYLENEDIAMIDE AND ETHYLENEDIAMINE LINKERS
Authors: MAZALEYRAT JP RAGE I SAVRDA J MOUNA M WAKSELMAN M BOULAY R LELIEVRE Y
Citation: Jp. Mazaleyrat et al., SYNTHESIS OF C2-SYMMETRICAL INHIBITORS OF THE HIV-1 PROTEASE, WITH N,N'-SUBSTITUTED ETHYLENEDIAMIDE AND ETHYLENEDIAMINE LINKERS, Bioorganic & medicinal chemistry letters, 4(5), 1994, pp. 653-656
ANTI-HIV ACTIVITY OF N-(2,3-DIHALOGENOPROPYL)-GLYCINE AND N-ALLYL-GLYCINE CONTAINING PENTAPEPTIDES
Authors: WAKSELMAN M MOUNA AM XIE J MAZALEYRAT JP BOULAY R LELIEVRE Y BOUSSEAU A NACHMANSOHN C HENIN Y
Citation: M. Wakselman et al., ANTI-HIV ACTIVITY OF N-(2,3-DIHALOGENOPROPYL)-GLYCINE AND N-ALLYL-GLYCINE CONTAINING PENTAPEPTIDES, Bioorganic & medicinal chemistry letters, 4(21), 1994, pp. 2533-2537
PEPTOID MIMICS OF A C-2-SYMMETRICAL INHIBITOR OF THE HIV-1 PROTEASE
Authors: MAZALEYRAT JP RAGE I MOUNA AM SAVRDA J WAKSELMAN M BOULAY R LELIEVRE Y
Citation: Jp. Mazaleyrat et al., PEPTOID MIMICS OF A C-2-SYMMETRICAL INHIBITOR OF THE HIV-1 PROTEASE, Bioorganic & medicinal chemistry letters, 4(11), 1994, pp. 1281-1284
SENSITIVE, HYDROSOLUBLE, MACROMOLECULAR FLUOROGENIC SUBSTRATES FOR HUMAN IMMUNODEFICIENCY VIRUS-1 PROTEINASE
Authors: ANJUERE F MONSIGNY M LELIEVRE Y MAYER R
Citation: F. Anjuere et al., SENSITIVE, HYDROSOLUBLE, MACROMOLECULAR FLUOROGENIC SUBSTRATES FOR HUMAN IMMUNODEFICIENCY VIRUS-1 PROTEINASE, Biochemical journal, 291, 1993, pp. 869-873
Risultati: 1-9 |