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Abhay Bavishi

Researcher at Saurashtra University

Publications -  12
Citations -  315

Abhay Bavishi is an academic researcher from Saurashtra University. The author has contributed to research in topics: Pyrazole & Moiety. The author has an hindex of 6, co-authored 12 publications receiving 272 citations.

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Diversity oriented design of various hydrazides and their in vitro evaluation against Mycobacterium tuberculosis H37Rv strains.

TL;DR: In this article, the authors describe the syntheses of various hydrazides of comarins, quinolones and pyrroles and screening against M. tuberculosis (Mtb) H37Rv by using rifampin as a standard drug.
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Synthesis and in vitro anti-HIV activity of N-1,3-benzo[d]thiazol-2-yl-2-(2-oxo-2H-chromen-4-yl)acetamide derivatives using MTT method.

TL;DR: A series of novel N-1,3-benzo[d]thiazol-2-yl-2-(2-oxo-2H-chromen-4-yl)acetamide derivatives has been synthesized and six compounds have been exhibits potent anti-HIV activity against MT-4 cells.
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Synthesis of some novel benzofuran-2-yl(4,5-dihyro-3,5-substituted diphenylpyrazol-1-yl) methanones and studies on the antiproliferative effects and reversal of multidrug resistance of human MDR1-gene transfected mouse lymphoma cells in vitro.

TL;DR: The main significance of the process is easy workup process, short reaction time and high yield of the new compounds for biological interest, however, the studies on genetically modified multidrug resistant cancer cells are costly and time consuming.
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Synthesis and 3D-QSAR study of 1,4-dihydropyridine derivatives as MDR cancer reverters.

TL;DR: 3D contour maps as a result of 3D-QSAR were utilized to identify some novel features that can be incorporated into the 1,4-dihydropyridine framework to enhance the activity.
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Synthesis and biological evaluation of 4-styrylcoumarin derivatives as inhibitors of TNF-α and IL-6 with anti-tubercular activity

TL;DR: A series of 4-styrylcoumarin have been synthesized by Knoevenagel condensation between substituted 4-methylcou marin-3-carbonitrile and different heterocyclic or aromatic aldehydes and their anti-inflammatory activity and anti-tubercular activity were evaluated.