Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Neha Agre"'
Autor:
Neha Agre, Nilesh Tawari, Arundhati Maitra, Antima Gupta, Tulika Munshi, Mariam Degani, Sanjib Bhakta
Publikováno v:
Antibiotics, Vol 9, Iss 7, p 368 (2020)
In this study, the inhibitory potential of 3-(5-nitrofuran-2-yl)prop-2-en-1-one derivatives was evaluated against a panel of bacteria, as well as mammalian cell lines to determine their therapeutic index. In addition, we investigated the mechanism of
Externí odkaz:
https://doaj.org/article/970cd61708f2432691922a9b3840b1ce
Autor:
Arundhati Maitra, Tulika Munshi, Mihir Khambete, Antima Gupta, Sanjib Bhakta, Mariam S. Degani, Neha Agre
Publikováno v:
Chemical Biology & Drug Design. 95:192-199
We report the biological evaluation of 5-(5-nitrothiophen-2-yl)-4,5-dihydro-1H-pyrazole derivatives against bacteria, eukaryotic cell lines and the assessment of their mechanisms of action to determine their prospects of being developed into potent a
Autor:
Antima Gupta, Neha Agre, Tulika Munshi, Arundhati Maitra, Sanjib Bhakta, Nilesh R. Tawari, Mariam S. Degani
Publikováno v:
Antibiotics
Volume 9
Issue 7
Antibiotics, Vol 9, Iss 368, p 368 (2020)
Volume 9
Issue 7
Antibiotics, Vol 9, Iss 368, p 368 (2020)
In this study, the inhibitory potential of 3-(5-nitrofuran-2-yl)prop-2-en-1-one derivatives was evaluated against a panel of bacteria, as well as mammalian cell lines to determine their therapeutic index. In addition, we investigated the mechanism of
Publikováno v:
Medicinal Chemistry of Neglected and Tropical Diseases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbfeedfd059f1426e30dff79acd23e71
https://doi.org/10.1201/9781351011655-8
https://doi.org/10.1201/9781351011655-8
Publikováno v:
Publons
Quantitative three dimensional structure activity relationship (3D-QSAR) studies were performed on phenothiazine derivatives as Butyrylcholinesterase (BuChE) inhibitors. Pharmacophore Alignment and Scoring Engine (PHASE) was used to develop predictiv
Publikováno v:
Archiv der Pharmazie. 352:1900068
5-Substituted-6-acetyl-2-amino-7-methyl-5,8-dihydropyrido[2,3-d]pyrimidin-4(3H)-one derivatives were synthesized and evaluated against Mycobacterium tuberculosis H37Rv, Mycobacterium aurum, Escherichia coli, and Staphylococcus aureus as well as a hum