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Antimycobacterial activity of novel 1-(5-cyclobutyl-1,3-oxazol-2-yl)-3-(sub)phenyl/pyridylthiourea compounds endowed with high activity toward multidrug-resistant Mycobacterium tuberculosis.
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- Journal of Antimicrobial Chemotherapy (JAC), 2007, v. 59, n. 6, p. 1194, doi. 10.1093/jac/dkm085
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- Publication type:
- Article
Design, Synthesis, and in vitro antitubercular activity of 1,2,3‐triazolyl‐dihydroquinoline derivatives.
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- Chemical Biology & Drug Design, 2018, v. 92, n. 1, p. 1315, doi. 10.1111/cbdd.13196
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- Article
Inhibition of tyrosinase by 4 H-chromene analogs: Synthesis, kinetic studies, and computational analysis.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 5, p. 804, doi. 10.1111/cbdd.13001
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- Article
Design, synthesis, and in vitro antituberculosis activity of benzo[6,7]cyclohepta[1,2- b]pyridine-1,3,4-oxadiazole derivatives.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 4, p. 496, doi. 10.1111/cbdd.12969
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- Article
Design and Development of Mycobacterium tuberculosis Lysine ɛ-Aminotransferase Inhibitors for Latent Tuberculosis Infection.
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- Chemical Biology & Drug Design, 2016, v. 87, n. 2, p. 265, doi. 10.1111/cbdd.12655
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- Article
Targeting NAMPT for Therapeutic Intervention in Cancer.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 881, doi. 10.1111/cbdd.12562
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- Article
Design and Biological Evaluation of Furan/Pyrrole/Thiophene-2-carboxamide Derivatives as Efficient DNA GyraseB Inhibitors of Staphylococcus aureus.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 918, doi. 10.1111/cbdd.12529
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- Article
Discovery and Structure Optimization of a Series of Isatin Derivatives as Mycobacterium tuberculosis Chorismate Mutase Inhibitors.
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- Chemical Biology & Drug Design, 2014, v. 83, n. 4, p. 498, doi. 10.1111/cbdd.12265
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- Article
Discovery of Novel 1,2,4-Triazol-5-Ones as Tumor Necrosis Factor-Alpha Inhibitors for the Treatment of Neuropathic Pain.
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- Chemical Biology & Drug Design, 2012, v. 80, n. 6, p. 961, doi. 10.1111/cbdd.12049
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- Article
Synthesis and Antimycobacterial Evaluation of Novel Phthalazin-4-ylacetamides Against log- and Starved Phase Cultures.
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- Chemical Biology & Drug Design, 2010, v. 75, n. 4, p. 381, doi. 10.1111/j.1747-0285.2010.00947.x
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- Article
Anticancer Potential of N‐Sulfonyl Noscapinoids: Synthesis and Evaluation.
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- ChemistrySelect, 2020, v. 5, n. 10, p. 2972, doi. 10.1002/slct.202000142
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- Article
Design, Synthesis and Molecular Docking Studies of Novel Triazole‐Chromene Conjugates as Antitubercular, Antioxidant and Antifungal Agents.
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- ChemistrySelect, 2018, v. 3, n. 46, p. 13113, doi. 10.1002/slct.201801859
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- Publication type:
- Article
Synthesis, crystal structure and antimycobacterial activities of 4-indolyl-1,4-dihydropyridine derivatives possessing various ester groups.
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- Research on Chemical Intermediates, 2017, v. 43, n. 12, p. 7471, doi. 10.1007/s11164-017-3087-0
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- Article
Synthesis of new pyrazole-triazole hybrids by click reaction using a green solvent and evaluation of their antitubercular and antibacterial activity.
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- Research on Chemical Intermediates, 2016, v. 42, n. 4, p. 3721, doi. 10.1007/s11164-015-2241-9
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- Article
Synthesis of Disulfide‐Bridged N‐Phenyl‐N′‐(alkyl/aryl/heteroaryl)urea Derivatives and Evaluation of Their Antimicrobial Activities.
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- Chemistry & Biodiversity, 2019, v. 16, n. 12, p. N.PAG, doi. 10.1002/cbdv.201900461
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- Article
Structure-based design of diverse inhibitors of Mycobacterium tuberculosis N-acetylglucosamine-1-phosphate uridyltransferase: combined molecular docking, dynamic simulation, and biological activity.
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- Journal of Molecular Modeling, 2015, v. 21, n. 7, p. 174, doi. 10.1007/s00894-015-2704-3
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- Article
Novel fluoroquinolones containing 2‐arylamino‐2‐oxoethyl fragment: Design, synthesis, evaluation of antibacterial and antituberculosis activities and molecular modeling studies.
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- Journal of Heterocyclic Chemistry, 2022, v. 59, n. 5, p. 909, doi. 10.1002/jhet.4430
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- Article
Synthesis of isoniazid‐1,2,3‐triazole conjugates: Antitubercular, antimicrobial evaluation and molecular docking study.
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- Journal of Heterocyclic Chemistry, 2020, v. 57, n. 10, p. 3544, doi. 10.1002/jhet.4072
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- Article
Design and Synthesis of New Aryloxy‐linked Dimeric 1,2,3‐Triazoles via Click Chemistry Approach: Biological Evaluation and Molecular Docking Study.
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- Journal of Heterocyclic Chemistry, 2019, v. 56, n. 8, p. 2144, doi. 10.1002/jhet.3608
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- Publication type:
- Article
Heteroaryl-substuted semicarbazones: Synthesis and anticonvulsant activity of N-(3-methylpyridin-2-yl)-substituted semicarbazones.
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- Journal of Heterocyclic Chemistry, 2006, v. 43, n. 5, p. 1287, doi. 10.1002/jhet.5570430522
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- Article
Targeting multiple response regulators of Mycobacterium tuberculosis augments the host immune response to infection.
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- Scientific Reports, 2016, p. 25851, doi. 10.1038/srep25851
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- Article
Advancing host-directed therapy for tuberculosis/MDR-TB: Development of novel AKT inhibitors as an adjunctive treatment for tuberculosis.
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- International Journal of Mycobacteriology, 2021, v. 10, p. 70, doi. 10.4103/2212-5531.307123
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- Article
Identification and Development of Novel Indazole Derivatives as Potent Bacterial Peptidoglycan Synthesis Inhibitors.
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- International Journal of Mycobacteriology, 2018, v. 7, n. 1, p. 76, doi. 10.4103/ijmy.ijmy_201_17
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- Article
Design and development of novel inhibitors for the treatment of latent tuberculosis.
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- International Journal of Mycobacteriology, 2016, v. 5, p. S121, doi. 10.1016/j.ijmyco.2016.09.006
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- Article
Benzothiazinone-piperazine derivatives as efficient Mycobacterium tuberculosis DNA gyrase inhibitors.
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- International Journal of Mycobacteriology, 2015, v. 4, n. 2, p. 104, doi. 10.1016/j.ijmyco.2015.02.002
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- Publication type:
- Article
Optimization and validation of Mycobacterium marinum-induced adult zebrafish model for evaluation of oral anti-tuberculosis drugs.
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- International Journal of Mycobacteriology, 2014, v. 3, n. 4, p. 259, doi. 10.1016/j.ijmyco.2014.10.001
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- Article
Investigating structure–activity relationship and mechanism of action of antitubercular 1-(4-chlorophenyl)-4-(4-hydroxy-3-methoxy-5-nitrobenzylidene) pyrazolidine-3,5-dione [CD59].
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- International Journal of Mycobacteriology, 2014, v. 3, n. 2, p. 117, doi. 10.1016/j.ijmyco.2014.02.006
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- Article
A Novel, Potent, Small Molecule AKT Inhibitor Exhibits Efficacy against Lung Cancer Cells In Vitro.
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- Cancer Research & Treatment, 2015, v. 47, n. 4, p. 913, doi. 10.4143/crt.2014.057
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- Article
Novel Thiazolidinone-Azole Hybrids: Design, Synthesis and Antimycobacterial Activity Studies.
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- Iranian Journal of Pharmaceutical Research, 2016, v. 15, n. 4, p. 783
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- Publication type:
- Article
Synthesis and anti-mycobacterial activity of 4-(4-phenyl-1 H-1,2,3-triazol-1-yl)salicylhydrazones: revitalizing an old drug.
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- Archives of Pharmacal Research, 2017, v. 40, n. 2, p. 168, doi. 10.1007/s12272-016-0882-x
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- Article
Polymer-gold nanoparticle composite films for topical application: Evaluation of physical properties and antibacterial activity.
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- Polymer Composites, 2017, v. 38, n. 12, p. 2829, doi. 10.1002/pc.23885
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- Article
The Small Molecule Indirubin-3′-Oxime Inhibits Protein Kinase R: Antiapoptotic and Antioxidant Effect in Rat Cardiac Myocytes.
- Published in:
- Pharmacology, 2016, v. 97, n. 1/2, p. 25, doi. 10.1159/000441727
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- Publication type:
- Article
Newer N-Phthaloyl GABA Derivatives with Antiallodynic and Antihyperalgesic Activities in Both Sciatic Nerve and Spinal Nerve Ligation Models of Neuropathic Pain.
- Published in:
- Pharmacology, 2007, v. 81, n. 1, p. 21, doi. 10.1159/000107711
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- Article
Discovery of potent antimycobacterial agents targeting lumazine synthase (RibH) of Mycobacterium tuberculosis.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-63051-6
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- Article
Structural Models for the Design of PKMzeta Inhibitors with Neurobiological Indications.
- Published in:
- Molecular Informatics, 2015, v. 34, n. 10, p. 665, doi. 10.1002/minf.201500003
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- Article
Design of Novel Mycobacterium tuberculosis Pantothenate Synthetase Inhibitors: Virtual Screening, Synthesis and In Vitro Biological Activities.
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- Molecular Informatics, 2015, v. 34, n. 2/3, p. 147, doi. 10.1002/minf.201400120
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- Publication type:
- Article
Discovery of Novel Mycobacterial DNA Gyrase B Inhibitors: In Silico and In Vitro Biological Evaluation.
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- Molecular Informatics, 2014, v. 33, n. 9, p. 597, doi. 10.1002/minf.201400058
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- Publication type:
- Article
Multiple e-Pharmacophore Modeling Combined with High-Throughput Virtual Screening and Docking to Identify Potential Inhibitors of β-Secretase(BACE1).
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- Molecular Informatics, 2013, v. 32, n. 4, p. 385, doi. 10.1002/minf.201200169
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- Article
Erratum: First‐in‐class pyrido[2,3‐d]pyrimidine‐2,4(1H,3H)‐diones against leishmaniasis and tuberculosis: Rationale, in vitro, ex vivo studies and mechanistic insights.
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- 2022
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- Publication type:
- Correction Notice
First‐in‐class pyrido[2,3‐d]pyrimidine‐2,4(1H,3H)‐diones against leishmaniasis and tuberculosis: Rationale, in vitro, ex vivo studies and mechanistic insights.
- Published in:
- Archiv der Pharmazie, 2022, v. 355, n. 4, p. 1, doi. 10.1002/ardp.202100440
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- Article
3‐Aryl‐substituted imidazo[1,2‐a]pyridines as antituberculosis agents.
- Published in:
- Archiv der Pharmazie, 2021, v. 354, n. 10, p. 1, doi. 10.1002/ardp.202000419
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- Article
Synthesis and antimicrobial evaluation of new nitric oxide‐donating fluoroquinolone/oxime hybrids.
- Published in:
- Archiv der Pharmazie, 2021, v. 354, n. 1, p. 1, doi. 10.1002/ardp.202000180
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- Article
Synthesis of novel 4,5‐dihydropyrrolo[1,2‐a]quinoxalines, pyrrolo[1,2‐a]quinoxalin]‐2‐ones and their antituberculosis and anticancer activity.
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- Archiv der Pharmazie, 2020, v. 353, n. 12, p. 1, doi. 10.1002/ardp.202000192
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- Article
Unfortunately, in the article Synthesis of novel 4,5‐dihydropyrrolo[1,2‐a]quinoxalines, pyrrolo[1,2‐a]quinoxalin]‐2‐ones and their antituberculosis and anticancer activity.
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- 2020
- By:
- Publication type:
- Correction Notice
Pyrazole–coumarin and pyrazole–quinoline chalcones as potential antitubercular agents.
- Published in:
- Archiv der Pharmazie, 2020, v. 353, n. 8, p. 1, doi. 10.1002/ardp.202000077
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- Article
Targeting HIV‐TB coinfection by developing novel piperidin‐4‐substituted imines: Design, synthesis, in vitro and in silico studies.
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- Archiv der Pharmazie, 2019, v. 352, n. 6, p. 1, doi. 10.1002/ardp.201800358
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- Publication type:
- Article
Divergent downstream biosynthetic pathways are supported by L-cysteine synthases of Mycobacterium tuberculosis.
- Published in:
- eLife, 2024, p. 1, doi. 10.7554/eLife.91970
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- Publication type:
- Article
Inhibition of protein kinase R protects against palmitic acid–induced inflammation, oxidative stress, and apoptosis through the JNK/NF‐kB/NLRP3 pathway in cultured H9C2 cardiomyocytes.
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- Journal of Cellular Biochemistry, 2019, v. 120, n. 3, p. 3651, doi. 10.1002/jcb.27643
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- Article
5-Methyl-4-thiazolidinones: Synthesis and evaluation as antitubercular agents.
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- Journal of Research in Pharmacy, 2020, v. 24, n. 1, p. 30, doi. 10.35333/jrp.2020.110
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- Article
Depletion of M. tuberculosis GlmU from Infected Murine Lungs Effects the Clearance of the Pathogen.
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- PLoS Pathogens, 2015, v. 11, n. 10, p. 1, doi. 10.1371/journal.ppat.1005235
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- Article