Results 201 to 210 of about 37,127 (212)
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Synthetic Communications, 2019
In a search of new potentially active antitubercular agents here we have synthesized 3-substituted phenyl-2-(4-(tetrazolo[1,5-a]quinolin-4-ylmethoxy)phenyl)thiazolidin-4-ones (8a-l) and evaluated their antibacterial, particularly antitubercular activity.
Amarsinh R. Deshmukh +5 more
semanticscholar +1 more source
In a search of new potentially active antitubercular agents here we have synthesized 3-substituted phenyl-2-(4-(tetrazolo[1,5-a]quinolin-4-ylmethoxy)phenyl)thiazolidin-4-ones (8a-l) and evaluated their antibacterial, particularly antitubercular activity.
Amarsinh R. Deshmukh +5 more
semanticscholar +1 more source
Dry powder inhalers of antitubercular drugs.
Tuberculosis, 2022Nidhi Nainwal +2 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
, 2020
Decaprenylphosphoryl-β-D-ribose epimerase (DprE1), a flavoprotein enzyme engaged in the biosynthesis of decaprenylphosphoryl-β-D-arabinofuranose (DPA), is the only contributor of arabinose residues which is fundamental for the mycobacterium cell wall ...
N. Ganesh +4 more
semanticscholar +1 more source
Decaprenylphosphoryl-β-D-ribose epimerase (DprE1), a flavoprotein enzyme engaged in the biosynthesis of decaprenylphosphoryl-β-D-arabinofuranose (DPA), is the only contributor of arabinose residues which is fundamental for the mycobacterium cell wall ...
N. Ganesh +4 more
semanticscholar +1 more source
Infectious Diseases - Drug Targets, 2019
A series of new pyrazolines containing 2,5-dichloro-3-acetylthiophene chalcone moiety (PZT1-PZT20) have been synthesized, characterized by 1HNMR and 13CNMR and evaluated for them in vitro antitubercular activity against M.
B. V. Lokesh, Y. Prasad, A. Shaik
semanticscholar +1 more source
A series of new pyrazolines containing 2,5-dichloro-3-acetylthiophene chalcone moiety (PZT1-PZT20) have been synthesized, characterized by 1HNMR and 13CNMR and evaluated for them in vitro antitubercular activity against M.
B. V. Lokesh, Y. Prasad, A. Shaik
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
Antitubercular properties of thiazolidin-4-ones - A review.
European journal of medicinal chemistry, 2021Nazar Trotsko
semanticscholar +1 more source

