triazoles has been researched along with s 1360 in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 15 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Stephenson, J | 1 |
Billich, A | 1 |
De Clercq, E; De Maeyer, M; Debyser, Z; Engelborghs, Y; Fikkert, V; Gurnari, C; Hantson, A; Michiels, M; Pannecouque, C; Van Maele, B; Van Remoortel, B; Vercammen, J; Witvrouw, M | 1 |
Fujishita, T; Rosemond, MJ; St John-Williams, L; Walsh, JS; Yamaguchi, T | 1 |
Johnson, AA; Marchand, C; Pommier, Y | 1 |
Dayam, R; Neamati, N | 1 |
De Clercq, E; De Maeyer, M; Debyser, Z; Fikkert, V; Hombrouck, A; Pannecouque, C; Van Remoortel, B; Witvrouw, M | 1 |
Clement, O; Dayam, R; Neamati, N; Sanchez, T; Sei, S; Shoemaker, R | 1 |
Dayam, R; Neamati, N; Sanchez, T | 1 |
Wang, C; Zhao, GS | 1 |
Alves, CN; Andrés, J; Castillo, R; Martí, S; Moliner, V; Silla, E; Tuñón, I | 1 |
Al-Mawsawi, LQ; Dayam, R; Neamati, N | 1 |
Chen, JM; Chen, X; Hung, M; Jin, H; Jones, GS; Kim, CU; Qi, X; Swaminathan, S; Tsiang, M; Yu, F; Zeynalzadegan, A | 1 |
Foster, SA; Fujishita, T; Fujiwara, T; Garvey, EP; Johns, BA; Kanamori-Koyama, M; Kawauchi, S; Kobayashi, M; Miki, S; Nakahara, K; Noshi, T; Sato, A; Seki, T; Suyama, A; Underwood, MR; Wakasa-Morimoto, C; Yoshinaga, T | 1 |
Barreca, ML; Chimirri, A; De Luca, L; Iraci, N | 1 |
3 review(s) available for triazoles and s 1360
Article | Year |
---|---|
S-1360 Shionogi-GlaxoSmithKline.
Topics: Anti-HIV Agents; Clinical Trials, Phase I as Topic; Clinical Trials, Phase II as Topic; Furans; HIV Infections; HIV Integrase Inhibitors; Humans; Triazoles | 2003 |
HIV-1 integrase inhibitors: a decade of research and two drugs in clinical trial.
Topics: Acetoacetates; Anti-HIV Agents; Biological Factors; Caffeic Acids; Clinical Trials as Topic; Furans; HIV Integrase; HIV Integrase Inhibitors; HIV-1; Humans; Indoles; Models, Molecular; Molecular Structure; Oligonucleotides; Pyrroles; Reverse Transcriptase Inhibitors; Succinates; Tetrazoles; Triazoles | 2004 |
[Advances in the study of HIV-1 integrase inhibitor of aryl beta-diketoacids].
Topics: Animals; Anti-HIV Agents; Furans; HIV Integrase Inhibitors; HIV-1; Humans; Keto Acids; Molecular Structure; Naphthyridines; Triazoles | 2006 |
12 other study(ies) available for triazoles and s 1360
Article | Year |
---|---|
Researchers explore new anti-HIV agents.
Topics: Anti-HIV Agents; CCR5 Receptor Antagonists; Clinical Trials as Topic; Cyclic N-Oxides; Drugs, Investigational; Enfuvirtide; Furans; HIV; HIV Envelope Protein gp120; HIV Envelope Protein gp41; HIV Infections; HIV Integrase Inhibitors; Humans; Nitriles; Oximes; Peptide Fragments; Piperazines; Piperidines; Pyridazines; Pyridines; Pyrimidines; Reverse Transcriptase Inhibitors; Triazoles | 2002 |
Development of resistance against diketo derivatives of human immunodeficiency virus type 1 by progressive accumulation of integrase mutations.
Topics: Acetoacetates; Anti-HIV Agents; Cell Line; Drug Resistance, Viral; Furans; HIV Integrase; HIV Integrase Inhibitors; HIV-1; Humans; Models, Molecular; Mutation; Recombination, Genetic; Triazoles; Virus Integration; Virus Replication | 2003 |
Enzymology of a carbonyl reduction clearance pathway for the HIV integrase inhibitor, S-1360: role of human liver cytosolic aldo-keto reductases.
Topics: Alcohol Oxidoreductases; Aldehyde Reductase; Aldo-Keto Reductases; Anti-HIV Agents; Carbon Radioisotopes; Cytosol; Enzyme Inhibitors; Furans; HIV Integrase Inhibitors; Humans; Liver; Microsomes, Liver; Mitochondria, Liver; Oxidation-Reduction; Triazoles | 2004 |
Active site binding modes of the beta-diketoacids: a multi-active site approach in HIV-1 integrase inhibitor design.
Topics: Anti-HIV Agents; Binding Sites; Carboxylic Acids; Computer Simulation; Drug Design; Drug Resistance; Furans; HIV Integrase; HIV Integrase Inhibitors; Molecular Conformation; Protein Binding; Protein Conformation; Structure-Activity Relationship; Triazoles | 2004 |
Multiple mutations in human immunodeficiency virus-1 integrase confer resistance to the clinical trial drug S-1360.
Topics: Anti-HIV Agents; Cells, Cultured; Clone Cells; Drug Resistance, Viral; Furans; HIV Infections; HIV Integrase; HIV-1; Humans; Mutation; Phenotype; Polymerase Chain Reaction; Triazoles; Virus Replication | 2004 |
Beta-diketo acid pharmacophore hypothesis. 1. Discovery of a novel class of HIV-1 integrase inhibitors.
Topics: Anti-HIV Agents; Cells, Cultured; Drug Design; Drug Evaluation, Preclinical; Furans; HIV Integrase; HIV Integrase Inhibitors; Humans; Models, Molecular; Molecular Structure; Rhodanine; Salicylic Acid; Structure-Activity Relationship; T-Lymphocytes; Triazoles | 2005 |
Diketo acid pharmacophore. 2. Discovery of structurally diverse inhibitors of HIV-1 integrase.
Topics: Cell Line; Databases, Factual; Drug Design; Furans; HIV Integrase; HIV Integrase Inhibitors; Humans; Hydrogen Bonding; Keto Acids; Models, Molecular; Structure-Activity Relationship; Triazoles | 2005 |
Calculation of binding energy using BLYP/MM for the HIV-1 integrase complexed with the S-1360 and two analogues.
Topics: Amino Acid Sequence; Amino Acid Substitution; Crystallography, X-Ray; Furans; HIV Integrase; HIV Integrase Inhibitors; Humans; Lysine; Magnesium; Models, Chemical; Propane; Protein Conformation; Pyrroles; Structure-Activity Relationship; Triazoles | 2007 |
Substituted 2-pyrrolinone inhibitors of HIV-1 integrase.
Topics: Furans; HIV Integrase; HIV Integrase Inhibitors; Humans; Molecular Structure; Organic Chemicals; Pyrroles; Pyrrolidinones; Quinolones; Raltegravir Potassium; Triazoles | 2007 |
Modeling, analysis, and validation of a novel HIV integrase structure provide insights into the binding modes of potent integrase inhibitors.
Topics: Acetoacetates; Binding Sites; Crystallography, X-Ray; DNA, Viral; Furans; HIV Integrase; HIV Integrase Inhibitors; HIV-1; Hydrophobic and Hydrophilic Interactions; Magnesium; Models, Chemical; Models, Molecular; Mutation; Naphthyridines; Nucleic Acid Conformation; Protein Binding; Protein Conformation; Protein Structure, Secondary; Protein Structure, Tertiary; Pyrroles; Reproducibility of Results; Triazoles | 2008 |
Secondary mutations in viruses resistant to HIV-1 integrase inhibitors that restore viral infectivity and replication kinetics.
Topics: Anti-HIV Agents; Furans; HIV Integrase; HIV-1; Humans; Jurkat Cells; Mutation, Missense; Triazoles; Virus Replication | 2009 |
Induced-fit docking approach provides insight into the binding mode and mechanism of action of HIV-1 integrase inhibitors.
Topics: Acetoacetates; Anti-HIV Agents; Binding Sites; Computer Simulation; Drug Design; Furans; HIV Integrase; HIV Integrase Inhibitors; Humans; Mutation; Naphthyridines; Pyrroles; Pyrrolidinones; Quinolones; Raltegravir Potassium; Triazoles | 2009 |