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Synthesis of Oxaspirocyclohexadienones via Lewis‐Acid Catalyzed [2+3]‐Annulations of p‐Quinone Methides and Iodonium Ylides

Advanced synthesis & catalysis, 2024-08, Vol.366 (15), p.3283-3289

2024

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Tweaking host immune responses for novel therapeutic approaches against Mycobacterium tuberculosis

Drug discovery today, 2023-09, Vol.28 (9), p.103693-103693, Article 103693

2023

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Editorial: Approaches to Address Resistance, Drug Discovery, and Vaccine Development in Mycobacterium tuberculosis : Challenges and Opportunities

Frontiers in microbiology, 2022-04, Vol.13, p.871464-871464

2022

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Capsaicin, a novel inhibitor of the NorA efflux pump, reduces the intracellular invasion of Staphylococcus aureus

Journal of antimicrobial chemotherapy, 2012-10, Vol.67 (10), p.2401-2408

2012

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Antitubercular activity of 2-mercaptobenzothiazole derivatives targeting Mycobacterium tuberculosis type II NADH dehydrogenase

RSC medicinal chemistry, 2024-05, Vol.15 (5), p.1664-1674

2024

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Cytochrome bd oxidase: an emerging anti-tubercular drug target

RSC medicinal chemistry, 2024-03, Vol.15 (3), p.769-787

2024

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Targeting the Mycobacterium ulcerans cytochrome bc 1 :aa 3 for the treatment of Buruli ulcer

Nature communications, 2018-12, Vol.9 (1), p.1-9

2018

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Discovery of a Novel Mycobacterial F‐ATP Synthase Inhibitor and its Potency in Combination with Diarylquinolines

Angewandte Chemie International Edition, 2020-08, Vol.59 (32), p.13295-13304

International ed. in English, 2020

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Exploring rhodanine linked enamine–carbohydrazide derivatives as mycobacterial carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and molecular docking studies

Archiv der Pharmazie (Weinheim), 2024-07, Vol.357 (7), p.e2400064-n/a

2024

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M. tuberculosis relies on trace oxygen to maintain energy homeostasis and survive in hypoxic environments

Cell reports (Cambridge), 2023-05, Vol.42 (5), p.112444-112444, Article 112444

2023

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Piperine as an inhibitor of the MdeA efflux pump of Staphylococcus aureus

Journal of medical microbiology, 2011-10, Vol.60 (10), p.1472-1478

2011

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Exploration of 3‐aryl pyrazole‐tethered sulfamoyl carboxamides as carbonic anhydrase inhibitors

Archiv der Pharmazie (Weinheim), 2023-11, Vol.356 (11), p.e2300309-e2300309

2023

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Synthesis and pharmacological evaluation of 1,3-diaryl substituted pyrazole based (thio)urea derivatives as potent antimicrobial agents against multi-drug resistant Staphylococcus aureus and Mycobacterium tuberculosis

RSC medicinal chemistry, 2023-07, Vol.14 (7), p.1296-1308

2023

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GaMF1.39's antibiotic efficacy and its enhanced antitubercular activity in combination with clofazimine, Telacebec, ND-011992, or TBAJ-876

Microbiology spectrum, 2023-12, Vol.11 (6), p.e0228223-e0228223

2023

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Discovery of a Novel Mycobacterial F‐ATP Synthase Inhibitor and its Potency in Combination with Diarylquinolines

Angewandte Chemie, 2020-08, Vol.132 (32), p.13397-13406

2020

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Synthesis and Antitubercular Activity of Berberine Derivatives

Chemistry of natural compounds, 2014-05, Vol.50 (2), p.321-325

2014

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P-glycoprotein inhibitors as an adjunct therapy for TB

Drug discovery today, 2024-09, Vol.29 (9), p.104108, Article 104108

2024

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Turbidity-Based MIC Assay and Characterization of Spontaneous Drug Resistant Mutants in Mycobacterium ulcerans

Methods in molecular biology (Clifton, N.J.), 2022, Vol.2387, p.209

2022

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Role of transcription termination factor Rho in anti-tuberculosis drug discovery

Drug discovery today, 2023-03, Vol.28 (3), p.103490-103490, Article 103490

2023

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Exploring and exploiting the host cell autophagy during Mycobacterium tuberculosis infection

European journal of clinical microbiology & infectious diseases, 2023-11, Vol.42 (11), p.1297-1315

2023

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Design, Synthesis, Evaluation of Antitubercular Activity and Insilco Studies of Novel 1,5-Naphthyridin-2(1H)-one Pendent 1,2,3-Triazoles

Chemistry & biodiversity, 2024-08, p.e202401491

2024

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A comprehensive review of genomics, transcriptomics, proteomics, and metabolomic insights into the differentiation of Pseudomonas aeruginosa from the planktonic to biofilm state: A multi-omics approach

International journal of biological macromolecules, 2024-02, Vol.257 (Pt 1), p.128563-128563, Article 128563

2024

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Unravelling the flexibility of Mycobacterium tuberculosis: an escape way for the bacilli

Journal of medical microbiology, 2023-06, Vol.72 (6)

2023

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Antitubercular activity of 2-mercaptobenzothiazole derivatives targeting type II NADH dehydrogenase

RSC medicinal chemistry, 2024-05, Vol.15 (5), p.1664-1674

2024

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Toward a Single-Dose Cure for Buruli Ulcer

Antimicrobial agents and chemotherapy, 2020-08, Vol.64 (9)

2020

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Synthesis of Oxaspirocyclohexadienones via Lewis‐Acid Catalyzed [2+3]‐Annulations of p‐Quinone Methides and Iodonium Ylides

Tweaking host immune responses for novel therapeutic approaches against Mycobacterium tuberculosis

Editorial: Approaches to Address Resistance, Drug Discovery, and Vaccine Development in Mycobacterium tuberculosis : Challenges and Opportunities

Capsaicin, a novel inhibitor of the NorA efflux pump, reduces the intracellular invasion of Staphylococcus aureus

Antitubercular activity of 2-mercaptobenzothiazole derivatives targeting Mycobacterium tuberculosis type II NADH dehydrogenase

Cytochrome bd oxidase: an emerging anti-tubercular drug target

Targeting the Mycobacterium ulcerans cytochrome bc 1 :aa 3 for the treatment of Buruli ulcer

Discovery of a Novel Mycobacterial F‐ATP Synthase Inhibitor and its Potency in Combination with Diarylquinolines

Exploring rhodanine linked enamine–carbohydrazide derivatives as mycobacterial carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and molecular docking studies

M. tuberculosis relies on trace oxygen to maintain energy homeostasis and survive in hypoxic environments

Piperine as an inhibitor of the MdeA efflux pump of Staphylococcus aureus

Exploration of 3‐aryl pyrazole‐tethered sulfamoyl carboxamides as carbonic anhydrase inhibitors

Synthesis and pharmacological evaluation of 1,3-diaryl substituted pyrazole based (thio)urea derivatives as potent antimicrobial agents against multi-drug resistant Staphylococcus aureus and Mycobacterium tuberculosis

GaMF1.39's antibiotic efficacy and its enhanced antitubercular activity in combination with clofazimine, Telacebec, ND-011992, or TBAJ-876

Discovery of a Novel Mycobacterial F‐ATP Synthase Inhibitor and its Potency in Combination with Diarylquinolines

Synthesis and Antitubercular Activity of Berberine Derivatives

P-glycoprotein inhibitors as an adjunct therapy for TB

Turbidity-Based MIC Assay and Characterization of Spontaneous Drug Resistant Mutants in Mycobacterium ulcerans

Role of transcription termination factor Rho in anti-tuberculosis drug discovery

Exploring and exploiting the host cell autophagy during Mycobacterium tuberculosis infection

Design, Synthesis, Evaluation of Antitubercular Activity and Insilco Studies of Novel 1,5-Naphthyridin-2(1H)-one Pendent 1,2,3-Triazoles

A comprehensive review of genomics, transcriptomics, proteomics, and metabolomic insights into the differentiation of Pseudomonas aeruginosa from the planktonic to biofilm state: A multi-omics approach

Unravelling the flexibility of Mycobacterium tuberculosis: an escape way for the bacilli

Antitubercular activity of 2-mercaptobenzothiazole derivatives targeting type II NADH dehydrogenase

Toward a Single-Dose Cure for Buruli Ulcer

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