Results 101 to 110 of about 3,184,601 (122)
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Journal of Medicinal Chemistry, 2021
The benzothiazinone (BTZ) scaffold compound PBTZ169 kills Mycobacterium tuberculosis by inhibiting the essential flavoenzyme DprE1, consequently blocking the synthesis of the cell wall component arabinans.
Dongguang Fan+10 more
semanticscholar +1 more source
The benzothiazinone (BTZ) scaffold compound PBTZ169 kills Mycobacterium tuberculosis by inhibiting the essential flavoenzyme DprE1, consequently blocking the synthesis of the cell wall component arabinans.
Dongguang Fan+10 more
semanticscholar +1 more source
Pyrazole-coumarin and pyrazole-quinoline chalcones as potential antitubercular agents.
Archiv der Pharmazie, 2020Pyrazole, coumarin, and quinoline are medicinally important moieties. In this study, two series of novel pyrazole-coumarin chalcones and pyrazole-quinoline chalcones were synthesized using multiple-step reactions.
Gautam Kumar+3 more
semanticscholar +1 more source
Current Computer - Aided Drug Design, 2020
BACKGROUND A series of new six thiazolyl-2-amine based Schiff base derivatives (4a-4f) were synthesized by a sequential multistep reactions starting with Salicylaldehyde.
Bhagwat Jadhav+5 more
semanticscholar +1 more source
BACKGROUND A series of new six thiazolyl-2-amine based Schiff base derivatives (4a-4f) were synthesized by a sequential multistep reactions starting with Salicylaldehyde.
Bhagwat Jadhav+5 more
semanticscholar +1 more source
Drug development research (Print), 2020
Tuberculosis (TB), a chronic infectious disease, is one of the greatest risks to human beings and 10 million people were diagnosed with TB and 1.6 million died from this disease in 2017. In addition, with the emergence of multidrug‐resistant tuberculosis
Mi Yan+9 more
semanticscholar +1 more source
Tuberculosis (TB), a chronic infectious disease, is one of the greatest risks to human beings and 10 million people were diagnosed with TB and 1.6 million died from this disease in 2017. In addition, with the emergence of multidrug‐resistant tuberculosis
Mi Yan+9 more
semanticscholar +1 more source
Brevifoliol and its Analogs: A New Class of Antitubercular Agents.
Current Topics in Medicinal Chemistry, 2020Brevifoliol is an abeo-taxane isolated from the Taxus wallichiana needles, eighteen semi-synthetic esters derivatives of brevifoliol were prepared by Steglich esterification and screened for their anti-tubercular potential against Mycobacterium ...
Balakishan Bhukya+7 more
semanticscholar +1 more source
Future Medicinal Chemistry, 2019
AIM In recent times, heterocyclic chemotypes are being explored for the development of new antimycobacterials that target the drug-resistant tuberculosis.
Vitthal B. Makane+9 more
semanticscholar +1 more source
AIM In recent times, heterocyclic chemotypes are being explored for the development of new antimycobacterials that target the drug-resistant tuberculosis.
Vitthal B. Makane+9 more
semanticscholar +1 more source
Journal of Molecular Structure, 2023
Chethana B. Krishnamurthy+3 more
semanticscholar +1 more source
Chethana B. Krishnamurthy+3 more
semanticscholar +1 more source
New Journal of Chemistry, 2019
Thiazolidinone–sulfonamide hybrids emerged as promising anticancer and antitubercular agents, and their anticancer activity was confirmed by docking studies.
A. Sunil Kumar+9 more
semanticscholar +1 more source
Thiazolidinone–sulfonamide hybrids emerged as promising anticancer and antitubercular agents, and their anticancer activity was confirmed by docking studies.
A. Sunil Kumar+9 more
semanticscholar +1 more source
Usnic Acid Enaminone-Coupled 1,2,3-Triazoles as Antibacterial and Antitubercular Agents.
Journal of Natural Products, 2019(+)-Usnic acid, a product of secondary metabolism in lichens, has displayed a broad range of biological properties such as antitumor, antimicrobial, antiviral, anti-inflammatory, and insecticidal activities. Interested by these pharmacological activities
P. Bangalore+8 more
semanticscholar +1 more source