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Novel gene similar to nitrite reductase (NO forming) plays potentially important role in the latency of tuberculosis.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-99346-1
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- Article
Superoxide Generation and Its Involvement in the Growth of Mycobacterium smegmatis.
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- Frontiers in Microbiology, 2017, v. 8, p. 1, doi. 10.3389/fmicb.2017.00105
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Synthesis, biological evaluation, and molecular docking studies of novel 3-aryl-5-(alkyl-thio)-1 H-1,2,4-triazoles derivatives targeting Mycobacterium tuberculosis.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 6, p. 1206, doi. 10.1111/cbdd.13040
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Synthesis and biological evaluation of 1,2,4-triazole-3-thione and 1,3,4-oxadiazole-2-thione as antimycobacterial agents.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 2, p. 200, doi. 10.1111/cbdd.12939
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- Article
Targeting Dormant Tuberculosis Bacilli: Results for Molecules with a Novel Pyrimidone Scaffold.
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- Chemical Biology & Drug Design, 2015, v. 85, n. 2, p. 201, doi. 10.1111/cbdd.12373
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- Article
Exploring the Pharmacological Potentials of Biosurfactant Derived from Planococcus maritimus SAMP MCC 3013.
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- Current Microbiology, 2020, v. 77, n. 3, p. 452, doi. 10.1007/s00284-019-01850-1
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- Article
Design and Synthesis of 2‐Amino‐thiophene‐proline‐conjugates and Their Anti‐tubercular Activity against Mycobacterium Tuberculosis H37Ra.
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- ChemistrySelect, 2019, v. 4, n. 9, p. 2851, doi. 10.1002/slct.201803370
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- Article
Design, Synthesis and Biological Screening of Novel 1,3,4‐Oxadiazoles as Antitubercular Agents.
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- ChemistrySelect, 2018, v. 3, n. 47, p. 13304, doi. 10.1002/slct.201802227
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- Article
Novel 2,4‐Dimethyl‐5‐((E)‐3‐phenyl‐3‐oxoprop‐1‐enyl)‐1H‐pyrrole‐3‐carboxylic Acid Derivatives: New Leads in Cancer and Bacterial Chemotherapy.
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- ChemistrySelect, 2018, v. 3, n. 33, p. 9571, doi. 10.1002/slct.201801458
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Synthesis and biological evaluation of novel triazole-biscoumarin conjugates as potential antitubercular and anti-oxidant agents.
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- Research on Chemical Intermediates, 2018, v. 44, n. 10, p. 6283, doi. 10.1007/s11164-018-3490-1
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- Article
Synthesis and biological evaluation of new 2-aryl-4-((4-aryl-1 H-1,2,3-triazol-1-yl)methyl)thiazole derivatives.
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- Research on Chemical Intermediates, 2018, v. 44, n. 2, p. 1247, doi. 10.1007/s11164-017-3164-4
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- Article
Click-chemistry-based multicomponent condensation approach for design and synthesis of spirochromene-tethered 1,2,3-triazoles as potential antitubercular agents.
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- Research on Chemical Intermediates, 2017, v. 43, n. 10, p. 5675, doi. 10.1007/s11164-017-2955-y
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- Article
[EtNH][HSO] catalyzed efficient synthesis of 5-arylidene-rhodanine conjugates and their antitubercular activity.
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- Research on Chemical Intermediates, 2016, v. 42, n. 8, p. 6607, doi. 10.1007/s11164-016-2484-0
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- Article
Synthesis, biological evaluation and molecular docking studies of N-acylheteroaryl hydrazone derivatives as antioxidant and anti-inflammatory agents.
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- Research on Chemical Intermediates, 2016, v. 42, n. 3, p. 2707, doi. 10.1007/s11164-015-2176-1
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- Article
Synthesis and antimycobacterial screening of new 4‐(4‐(1‐benzyl‐1H‐1,2,3‐triazol‐4‐yl)‐1‐phenyl‐1H‐pyrazol‐3‐yl)quinoline derivatives.
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- Journal of Heterocyclic Chemistry, 2020, v. 57, n. 11, p. 3918, doi. 10.1002/jhet.4101
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- Article
Synthesis and biological evaluation of new 4‐(4‐(1‐benzyl‐1H‐1,2,3‐triazol‐4‐yl)phenyl)‐2‐phenylthiazole derivatives.
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- Journal of Heterocyclic Chemistry, 2019, v. 56, n. 11, p. 3093, doi. 10.1002/jhet.3708
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- Article
Microwave‐Assisted Synthesis and Antituberculosis Screening of Some 4‐((3‐(Trifluoromethyl)‐5,6‐dihydro‐[1,2,4]triazolo[4,3‐a]pyrazin‐7(8H)‐l)methyl)benzenamine Hybrids.
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- Journal of Heterocyclic Chemistry, 2019, v. 56, n. 2, p. 434, doi. 10.1002/jhet.3416
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Synthesis and Antitubercular activity of New Thiazolidinones with Pyrazinyl and Thiazolyl Scaffolds.
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- Journal of Heterocyclic Chemistry, 2017, v. 54, n. 1, p. 125, doi. 10.1002/jhet.2552
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- Article
Synthesis of Novel Triazole-incorporated Isatin Derivatives as Antifungal, Antitubercular, and Antioxidant Agents and Molecular Docking Study.
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- Journal of Heterocyclic Chemistry, 2017, v. 54, n. 1, p. 413, doi. 10.1002/jhet.2598
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- Article
Phytogenic silver, gold, and bimetallic nanoparticles as novel antitubercular agents.
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- International Journal of Nanomedicine, 2016, v. 11, p. 1889, doi. 10.2147/IJN.S102488
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- Article
Synthesis and biological evaluation of some bicyclic [2-(2,4-dimethylphenylthio)phenyl] aniline and its amide derivatives as potential antitubercular agents.
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- Journal of Chemical Sciences, 2018, v. 130, n. 3, p. 0, doi. 10.1007/s12039-018-1424-5
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- Article
Synthesis and biological evaluation of some new tricyclic pyrrolo[3,2‐e]tetrazolo[1,5‐c]pyrimidine derivatives as potential antitubercular agents.
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- Archiv der Pharmazie, 2018, v. 351, n. 8, p. 1, doi. 10.1002/ardp.201800040
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Design, synthesis, and pharmacological evaluation of fluorinated azoles as anti‐tubercular agents.
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- Archiv der Pharmazie, 2018, v. 351, n. 2, p. 1, doi. 10.1002/ardp.201700294
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- Article
Evidence of nitrite acting as a stable and robust inducer of non-cultivability in Mycobacterium tuberculosis with physiological relevance.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-45652-8
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- Article
Two Chitotriose-Specific Lectins Show Anti-Angiogenesis, Induces Caspase-9-Mediated Apoptosis and Early Arrest of Pancreatic Tumor Cell Cycle.
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- PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0146110
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Internet of Music Things: an edge computing paradigm for opportunistic crowdsensing.
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- Journal of Supercomputing, 2018, v. 74, n. 11, p. 6069, doi. 10.1007/s11227-018-2511-6
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Conventional and microwave‐assisted organic synthesis of novel antimycobacterial agents bearing furan and pyridine hybrids.
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- Drug Development Research, 2022, v. 83, n. 2, p. 416, doi. 10.1002/ddr.21872
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Design, Synthesis, and in vitro Biological Evaluation of ROS‐Generating Phenanthridin‐trione‐Epoxide Conjugates as Agents against Mycobacterium tuberculosis.
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- ChemistrySelect, 2023, v. 8, n. 25, p. 1, doi. 10.1002/slct.202300416
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- Article
Ultrasound Assisted Synthesis of 4-(Benzyloxy)-N-(3-chloro-2-(substitutedphenyl)-4-oxoazetidin-1-yl) Benzamide as Challenging Anti-Tubercular Scaffold.
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- Molecules, 2018, v. 23, n. 8, p. 1945, doi. 10.3390/molecules23081945
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Qualitative and quantitative proteomic analysis of vitamin C induced changes in Mycobacterium smegmatis.
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- Frontiers in Microbiology, 2015, p. 1, doi. 10.3389/fmicb.2015.00451
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Using diphenyleneiodonium to induce a viable but non-culturable phenotype in Mycobacterium tuberculosis and its metabolomics analysis.
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- PLoS ONE, 2019, v. 14, n. 8, p. 1, doi. 10.1371/journal.pone.0220628
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Detection of a target protein (GroEl2) in Mycobacterium tuberculosis using a derivative of 1,2,4-triazolethiols.
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- Molecular Diversity, 2022, v. 26, n. 5, p. 2535, doi. 10.1007/s11030-021-10351-y
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2D-QSAR modeling and two-fold classification of 1,2,4-triazole derivatives for antitubercular potency against the dormant stage of Mycobacterium tuberculosis.
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- Molecular Diversity, 2022, v. 26, n. 2, p. 1227, doi. 10.1007/s11030-021-10254-y
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Anti-proliferative effect of novel primary cetyl alcohol derived sophorolipids against human cervical cancer cells HeLa.
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- PLoS ONE, 2017, v. 12, n. 4, p. 1, doi. 10.1371/journal.pone.0174241
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Synthesis and antimycobacterial screening of a novel series of a-amino acids containing thiazole linker.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 64, doi. 10.24820/ark.5550190.p011.831
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