Search Results - "Amrutkar, Suyog"
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Imine/amide–imidazole conjugates derived from 5-amino-4-cyano-N1-substituted benzyl imidazole: Microwave-assisted synthesis and anticancer activity via selective topoisomerase-II-α inhibition
Published in Bioorganic & medicinal chemistry (01-09-2015)“…[Display omitted] Microwave-accelerated synthesis and anticancer activity of novel imine/amide–imidazole conjugates derived from 5-amino-4-cyano-N1-substituted…”
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Switch in Site of Inhibition: A Strategy for Structure-Based Discovery of Human Topoisomerase IIα Catalytic Inhibitors
Published in ACS medicinal chemistry letters (09-04-2015)“…A study of structure-based modulation of known ligands of hTopoIIα, an important enzyme involved in DNA processes, coupled with synthesis and in vitro assays…”
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One-pot synthesis of (R)-1-(1-naphthyl)ethanol by stereoinversion using Candida parapsilosis
Published in Tetrahedron letters (19-06-2013)“…(R)-1-(1-Naphthyl)ethanol is an essential chiral substrate for the synthesis of nonactin and dihydro-[1H]-quinoline-2-one derivatives. Stereoinversion of…”
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Scaffold-Hopping of Aurones: 2‑Arylideneimidazo[1,2‑a]pyridinones as Topoisomerase IIα-Inhibiting Anticancer Agents
Published in ACS medicinal chemistry letters (08-12-2016)“…Scaffold-hopping of bioactive natural product aurones has been studied for the first time. 2-Arylideneimidazo[1,2-a]pyridinones as potential topoisomerase…”
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Anticancer activity of dihydropyrazolo[1,5‐c]quinazolines against rat C6 glioma cells via inhibition of topoisomerase II
Published in Archiv der Pharmazie (Weinheim) (01-06-2018)“…The design and synthesis of dihydropyrazolo[1,5‐c]quinazolines (1a–h) as human topoisomerase II (TopoII) catalytic inhibitors are reported. The compounds were…”
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Sulfinate Based Selective Labeling of 5‑Hydroxymethylcytosine: Application to Biotin Pull Down Assay
Published in Bioconjugate chemistry (21-02-2018)“…We developed an enzyme-free, chemical method to selectively label the epigenetic base, 5-hydroxymethylcytosine (hmC) with versatile sulfinate reagents in…”
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Scaffold-hopping of bioactive flavonoids: Discovery of aryl-pyridopyrimidinones as potent anticancer agents that inhibit catalytic role of topoisomerase IIα
Published in European journal of medicinal chemistry (21-10-2016)“…A strategy of scaffold-hopping of bioactive natural products, flavones and isoflavones, leading to target-based discovery of potent anticancer agents has been…”
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E-pharmacophore guided discovery of pyrazolo[1,5-c]quinazolines as dual inhibitors of topoisomerase-I and histone deacetylase
Published in Bioorganic chemistry (01-01-2020)“…[Display omitted] •Non-camptothecin analogues among 11 motifs of pyrazoloquinazolines are reported.•E-pharmacophore drug design guided discovery of…”
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