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Shrikant S. Gawande

Researcher at Swami Ramanand Teerth Marathwada University

Publications -  7
Citations -  598

Shrikant S. Gawande is an academic researcher from Swami Ramanand Teerth Marathwada University. The author has contributed to research in topics: Biological activity & DPPH. The author has an hindex of 7, co-authored 7 publications receiving 522 citations.

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Synthesis and biological evaluation of simple methoxylated chalcones as anticancer, anti-inflammatory and antioxidant agents

TL;DR: 3s was obtained as lead compound with promising anticancer, anti-inflammatory and antioxidant activities and was confirmed to be nontoxic by in vitro cytotoxicity study.
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Synthesis and biological evaluation of a novel series of pyrazole chalcones as anti-inflammatory, antioxidant and antimicrobial agents.

TL;DR: The structure-activity relationship (SAR) and in silico drug relevant properties (HBD, HBA, PSA, cLogP, molecular weight, E(HOMO) and E(LUMO)) further confirmed that the compounds are potential lead compounds for future drug discovery study.
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Synthesis and biological screening of a combinatorial library of β-chlorovinyl chalcones as anticancer, anti-inflammatory and antimicrobial agents

TL;DR: A combinatorial library of beta-chlorovinyl chalcones synthesized by Claisen-Schmidt condensation reaction revealed promising anti-inflammatory activity and promising antimicrobial activity against selected pathogenic bacteria and fungi.
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Synthesis of new heterocyclic hybrids based on pyrazole and thiazolidinone scaffolds as potent inhibitors of tyrosinase.

TL;DR: The inhibition mechanism analysis of 5h and 5g thiazolidinone derivatives demonstrated that the inhibitory effects of the compounds on tyrosinase were reversible and competitive.
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Silica supported perchloric acid (HClO4-SiO2): a green, reusable, and highly efficient heterogeneous catalyst for the synthesis of thioethers under solvent-free conditions at room temperature

TL;DR: In this paper, a highly efficient and clean procedure is described for the synthesis of thioethers with excellent yields under solvent-free conditions at room temperature using a catalytic amount of HClO4-SiO2.