Triazoles

Naphthoquinoidal [1,2,3]-triazole, a new structural moiety active against Trypanosoma cruzi

Organic Chemistry / Treatment / Drug development / Macromolecular X-Ray Crystallography / In Vitro / Animals / Naphthoquinones / Chagas disease / European / Hydrogen Bonding / Trypanosoma Cruzi / Trypanocidal Agents / Triazoles / Structure activity Relationship / Cations / Chemical Synthesis / Molecular Structure / Animals / Naphthoquinones / Chagas disease / European / Hydrogen Bonding / Trypanosoma Cruzi / Trypanocidal Agents / Triazoles / Structure activity Relationship / Cations / Chemical Synthesis / Molecular Structure

A novel nucleoside analog, 1-β-d-ribofuranosyl-3-ethynyl-[1,2,4]triazole (ETAR), exhibits efficacy against a broad range of flaviviruses in vitro

Medical Microbiology / Dengue Virus / Cercopithecus aethiops / Yellow fever / Animals / Animal Model / Guanosine Triphosphate / Flavivirus / Microbial Sensitivity Tests / Mechanism of action / Antiviral / Imidazoles / Triazoles / Nucleosides / Vero cells / Ribavirin / Antiviral Agents / West Nile / Animal Model / Guanosine Triphosphate / Flavivirus / Microbial Sensitivity Tests / Mechanism of action / Antiviral / Imidazoles / Triazoles / Nucleosides / Vero cells / Ribavirin / Antiviral Agents / West Nile

Naphthoquinoidal [1,2,3]-triazole, a new structural moiety active against Trypanosoma cruzi

Organic Chemistry / Drug development / Macromolecular X-Ray Crystallography / Animals / Naphthoquinones / Chagas disease / European / Hydrogen Bonding / Trypanosoma Cruzi / Trypanocidal Agents / Triazoles / Structure activity Relationship / Cations / Molecular Structure / Chagas disease / European / Hydrogen Bonding / Trypanosoma Cruzi / Trypanocidal Agents / Triazoles / Structure activity Relationship / Cations / Molecular Structure

Physiological testosterone levels enhance chondrogenic extracellular matrix synthesis by male intervertebral disc cells in vitro, but not by mesenchymal stem cells

Extracellular Matrix / Cell Differentiation / Mesenchymal stem cells / Humans / Testosterone / Nitriles / Female / Male / Intervertebral disc / Clinical Sciences / Middle Aged / Adult / Sex Factors / Transforming Growth Factor Beta / Chondrogenesis / Triazoles / Cell Survival / Neurosciences / Mesenchymal Stromal Cells / Nitriles / Female / Male / Intervertebral disc / Clinical Sciences / Middle Aged / Adult / Sex Factors / Transforming Growth Factor Beta / Chondrogenesis / Triazoles / Cell Survival / Neurosciences / Mesenchymal Stromal Cells

beta-1,2,3-Triazolyl-nucleosides as nicotinamide riboside mimics

Sirtuins / Molecular Mimicry / Triazoles / Nucleosides / Nucleotides / Biochemistry and cell biology / Molecular Structure / Biochemistry and cell biology / Molecular Structure

Clinical challenge: fatal mucormycotic osteomyelitis caused by Rhizopus microsporus despite aggressive multimodal treatment

Microbiology / Medical Microbiology / Humans / Male / Mucormycosis / Osteomyelitis / Clinical Sciences / Aged / Bone Marrow Transplantation / Antifungal Agents / Triazoles / Osteomyelitis / Clinical Sciences / Aged / Bone Marrow Transplantation / Antifungal Agents / Triazoles

2,6-Diphenylthiazolo[3,2-b][1,2,4]triazoles as telomeric G-quadruplex stabilizers

Organic Chemistry / Macromolecular X-Ray Crystallography / Fluorescence Resonance Energy Transfer / Computer Simulation / Drug Design / Telomere / Triazoles / Thiazoles / Transition Temperature / Telomere / Triazoles / Thiazoles / Transition Temperature

Naphthoquinoidal [1,2,3]-triazole, a new structural moiety active against Trypanosoma cruzi

Organic Chemistry / Treatment / Drug development / Macromolecular X-Ray Crystallography / In Vitro / Animals / Naphthoquinones / Chagas disease / European / Hydrogen Bonding / Trypanosoma Cruzi / Trypanocidal Agents / Triazoles / Structure activity Relationship / Cations / Chemical Synthesis / Molecular Structure / Animals / Naphthoquinones / Chagas disease / European / Hydrogen Bonding / Trypanosoma Cruzi / Trypanocidal Agents / Triazoles / Structure activity Relationship / Cations / Chemical Synthesis / Molecular Structure

Angio-oedema induced by dual dipeptidyl peptidase inhibitor and angiotensin II receptor blocker: a first case report

Treatment Outcome / Humans / Female / Clinical Sciences / Aged / Triazoles / Angioedema / Type 2 Diabetes Mellitus / Triazoles / Angioedema / Type 2 Diabetes Mellitus

In vitro activities of new and established triazoles against opportunistic filamentous and dimorphic fungi

Medical Microbiology / Fungi / Medical Mycology / Humans / Voriconazole / Antifungal Agents / Microbial Sensitivity Tests / Species Specificity / Triazoles / Thiazoles / Medical / Antifungal Agents / Microbial Sensitivity Tests / Species Specificity / Triazoles / Thiazoles / Medical

Broad-Spectrum Antiviral Activity of Virazole: 1-f8- D-Ribofuranosyl- 1,2,4-triazole- 3-carboxamide

Science / Multidisciplinary / DNA viruses / RNA viruses / Tissue culture / Mice / Animals / Vesicular Stomatitis Virus / Cytomegalovirus / Spectrum / Amides / Vaccinia Virus / Microbial Sensitivity Tests / Rabbits / Triazoles / Virus infection / Rhinovirus / Antiviral Activity / Nucleosides / Virus diseases / Rabies Virus / Antiviral Agents / Poliovirus / Mice / Animals / Vesicular Stomatitis Virus / Cytomegalovirus / Spectrum / Amides / Vaccinia Virus / Microbial Sensitivity Tests / Rabbits / Triazoles / Virus infection / Rhinovirus / Antiviral Activity / Nucleosides / Virus diseases / Rabies Virus / Antiviral Agents / Poliovirus

Synthesis of Novel Derivatives of 4-Amino-3-(2-Furyl)-5-Mercapto-1,2,4-Triazole as Potential HIV-1 NNRTIs

Organic Chemistry / HIV / Cell line / Humans / Molecules / Triazoles

Discovery of triazolone derivatives as novel, potent stearoyl-CoA desaturase-1 (SCD1) inhibitors

Organic Chemistry / Drug Discovery / Humans / Metabolic diseases / Mice / Animals / Lipid metabolism / Rats / Bioorganic and medicinal Chemistry / Triazoles / Structure activity Relationship / Stearoyl-CoA desaturase / Animals / Lipid metabolism / Rats / Bioorganic and medicinal Chemistry / Triazoles / Structure activity Relationship / Stearoyl-CoA desaturase

Discovery of triazolone derivatives as novel, potent stearoyl-CoA desaturase-1 (SCD1) inhibitors

Organic Chemistry / Drug Discovery / Humans / Metabolic diseases / Mice / Animals / Lipid metabolism / Rats / Bioorganic and medicinal Chemistry / Triazoles / Structure activity Relationship / Stearoyl-CoA desaturase / Animals / Lipid metabolism / Rats / Bioorganic and medicinal Chemistry / Triazoles / Structure activity Relationship / Stearoyl-CoA desaturase

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