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Results: 1-13 |
Results: 13
STRUCTURAL INSIGHT INTO THE BINDING MOTIFS FOR THE CALCIUM-ION AND THE NONCATALYTIC ZINC IN MATRIX METALLOPROTEASES
Authors: MASSOVA I KOTRA LP MOBASHERY S
Citation: I. Massova et al., STRUCTURAL INSIGHT INTO THE BINDING MOTIFS FOR THE CALCIUM-ION AND THE NONCATALYTIC ZINC IN MATRIX METALLOPROTEASES, Bioorganic & medicinal chemistry letters, 8(7), 1998, pp. 853-858
MATRIX METALLOPROTEINASES - STRUCTURES, EVOLUTION, AND DIVERSIFICATION
Authors: MASSOVA I KOTRA LP FRIDMAN R MOBASHERY S
Citation: I. Massova et al., MATRIX METALLOPROTEINASES - STRUCTURES, EVOLUTION, AND DIVERSIFICATION, The FASEB journal, 12(12), 1998, pp. 1075-1095
SELECTION AND CHARACTERIZATION OF BETA-LACTAM-BETA-3-LACTAMASE INACTIVATOR-RESISTANT MUTANTS FOLLOWING PCR MUTAGENESIS OF THE TEM-1 BETA-LACTAMASE GENE
Authors: VAKULENKO SB GERYK B KOTRA LP MOBASHERY S LERNER SA
Citation: Sb. Vakulenko et al., SELECTION AND CHARACTERIZATION OF BETA-LACTAM-BETA-3-LACTAMASE INACTIVATOR-RESISTANT MUTANTS FOLLOWING PCR MUTAGENESIS OF THE TEM-1 BETA-LACTAMASE GENE, Antimicrobial agents and chemotherapy, 42(7), 1998, pp. 1542-1548
BETA-LACTAM ANTIBIOTICS, BETA-LACTAMASES AND BACTERIAL-RESISTANCE
Authors: KOTRA LP MOBASHERY S
Citation: Lp. Kotra et S. Mobashery, BETA-LACTAM ANTIBIOTICS, BETA-LACTAMASES AND BACTERIAL-RESISTANCE, Bulletin de l'Institut Pasteur, 96(3), 1998, pp. 139-150
SYNTHESIS OF 2,3-DIDEOXY-2,2-DIFLUORO-L-GLYCERO-PENTOFURANOSYL NUCLEOSIDES
Authors: KOTRA LP NEWTON MG CHU CK
Citation: Lp. Kotra et al., SYNTHESIS OF 2,3-DIDEOXY-2,2-DIFLUORO-L-GLYCERO-PENTOFURANOSYL NUCLEOSIDES, Carbohydrate research, 306(1-2), 1998, pp. 69-80
STRUCTURAL BASIS FOR CLINICAL LONGEVITY OF CARBAPENEM ANTIBIOTICS IN THE FACE OF CHALLENGE BY THE COMMON CLASS-A BETA-LACTAMASES FROM THE ANTIBIOTIC-RESISTANT BACTERIA
Authors: MAVEYRAUD L MOUREY L KOTRA LP PEDELACQ JD GUILLET V MOBASHERY S SAMAMA JP
Citation: L. Maveyraud et al., STRUCTURAL BASIS FOR CLINICAL LONGEVITY OF CARBAPENEM ANTIBIOTICS IN THE FACE OF CHALLENGE BY THE COMMON CLASS-A BETA-LACTAMASES FROM THE ANTIBIOTIC-RESISTANT BACTERIA, Journal of the American Chemical Society, 120(38), 1998, pp. 9748-9752
4-AZIDO-2-PYRIMIDINONE NUCLEOSIDES AND RELATED CHEMISTRY
Authors: KOTRA LP WANG PP BARTLETT MG SHANMUGANATHAN K XU ZS CAVALCANTI S NEWTON MG CHU CK
Citation: Lp. Kotra et al., 4-AZIDO-2-PYRIMIDINONE NUCLEOSIDES AND RELATED CHEMISTRY, Journal of organic chemistry, 62(21), 1997, pp. 7267-7271
STRUCTURE-ACTIVITY-RELATIONSHIPS OF 2'-DEOXY-2',2'-DIFLUORO-L-ERYTHRO-PENTOFURANOSYL NUCLEOSIDES
Authors: KOTRA LP XIANG YJ NEWTON MG SCHINAZI RF CHENG YC CHU CK
Citation: Lp. Kotra et al., STRUCTURE-ACTIVITY-RELATIONSHIPS OF 2'-DEOXY-2',2'-DIFLUORO-L-ERYTHRO-PENTOFURANOSYL NUCLEOSIDES, Journal of medicinal chemistry, 40(22), 1997, pp. 3635-3644
DESIGN AND SYNTHESIS OF 2'-HYDROXYETHYLCYCLOPROPYL CARBOCYCLIC NUCLEOSIDES
Authors: YANG TF KIM H KOTRA LP CHU CK
Citation: Tf. Yang et al., DESIGN AND SYNTHESIS OF 2'-HYDROXYETHYLCYCLOPROPYL CARBOCYCLIC NUCLEOSIDES, Tetrahedron letters, 37(49), 1996, pp. 8849-8852
SYNTHESIS, BIOTRANSFORMATION, AND PHARMACOKINETIC STUDIES OF 9-(BETA-D-ARABINOFURANOSYL)-6-AZIDOPURINE - A PRODRUG FOR ARA-A DESIGNED TO UTILIZE THE AZIDE REDUCTION PATHWAY
Authors: KOTRA LP MANOUILOV KK CRETTONSCOTT E SOMMADOSSI JP BOUDINOT FD SCHINAZI RF CHU CK
Citation: Lp. Kotra et al., SYNTHESIS, BIOTRANSFORMATION, AND PHARMACOKINETIC STUDIES OF 9-(BETA-D-ARABINOFURANOSYL)-6-AZIDOPURINE - A PRODRUG FOR ARA-A DESIGNED TO UTILIZE THE AZIDE REDUCTION PATHWAY, Journal of medicinal chemistry, 39(26), 1996, pp. 5202-5207
SYNTHESIS AND ANTI-HIV ACTIVITIES OF XY-2',2''-DIFLUORO-BETA-L-RIBOFURANOSYL-PYRIMIDINE AND -DEOXY-2',2''-DIFLUORO-BETA-L-RIBOFURANOSYL-PURINE NUCLEOSIDES
Authors: XIANG YJ KOTRA LP CHU CK
Citation: Yj. Xiang et al., SYNTHESIS AND ANTI-HIV ACTIVITIES OF XY-2',2''-DIFLUORO-BETA-L-RIBOFURANOSYL-PYRIMIDINE AND -DEOXY-2',2''-DIFLUORO-BETA-L-RIBOFURANOSYL-PURINE NUCLEOSIDES, Bioorganic & medicinal chemistry letters, 5(7), 1995, pp. 743-748
LYMPHATIC TARGETING OF ANTI-HIV NUCLEOSIDES - DISTRIBUTION OF 3'-AZIDO-3'-DEOXYTHYMIDINE (AZT) AND 3'-AZIDO-2',3'-DIDEOXYURIDINE (AZDU) AFTER ADMINISTRATION OF DIPALMITOYLPHOSPHATIDYL PRODRUGS TO MICE
Authors: MANOUILOV KK FEDOROV II BOUDINOT FD WHITE CA KOTRA LP SCHINAZI RF HONG CII CHU CK
Citation: Kk. Manouilov et al., LYMPHATIC TARGETING OF ANTI-HIV NUCLEOSIDES - DISTRIBUTION OF 3'-AZIDO-3'-DEOXYTHYMIDINE (AZT) AND 3'-AZIDO-2',3'-DIDEOXYURIDINE (AZDU) AFTER ADMINISTRATION OF DIPALMITOYLPHOSPHATIDYL PRODRUGS TO MICE, Antiviral chemistry & chemotherapy, 6(4), 1995, pp. 230-238
SYNTHESIS OF [4-(HYDROXY)TETRAHYDROFURAN-2-YL]NUCLEOSIDES AS A NOVEL CLASS OF URIDINE PHOSPHORYLASE INHIBITORS
Authors: YANG TF KOTRA LP TENG Q NAGUIB FNM SOMMADOSSI JP ELKOUNI M CHU CK
Citation: Tf. Yang et al., SYNTHESIS OF [4-(HYDROXY)TETRAHYDROFURAN-2-YL]NUCLEOSIDES AS A NOVEL CLASS OF URIDINE PHOSPHORYLASE INHIBITORS, Tetrahedron letters, 36(7), 1995, pp. 983-986
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