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Journal ArticleDOI

One-pot synthesis and molecular docking of some new spiropyranindol-2-one derivatives as immunomodulatory agents and in vitro antimicrobial potential with DNA gyrase inhibitor

TLDR
The most potent compounds showed an increase in the intracellular killing activity of neutrophils which confirmed the immunostimulatory power, and compounds 7f showed the much better than norfloxacin with higher potency results.
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This article is published in European Journal of Medicinal Chemistry.The article was published on 2020-02-15. It has received 59 citations till now. The article focuses on the topics: DNA gyrase & Norfloxacin.

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Oxindole and its derivatives: A review on recent progress in biological activities.

TL;DR: In this paper, the authors provide a description of the general chemistry based on existing corresponding structureactivity relationships (SARs) and compile all recent developmentary studies on oxindole-derived compounds as a successful pharmaceutical agent.
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Antimicrobial evaluation of thiadiazino and thiazolo quinoxaline hybrids as potential DNA gyrase inhibitors; design, synthesis, characterization and morphological studies

TL;DR: The most potent compounds 2, 7, 9, 10, 12 and 13c were exhibited bactericidal activity, in addition to fungistatic activity by dead live assay, and showed a significant result against all multi-drug resistance (MDRB) used especially compound 13c that displayed the best results with MICs of MDRB.
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Discovery of New Schiff Bases Tethered Pyrazole Moiety: Design, Synthesis, Biological Evaluation, and Molecular Docking Study as Dual Targeting DHFR/DNA Gyrase Inhibitors with Immunomodulatory Activity.

TL;DR: Immunomodulatory activities showed that the promising Schiff bases increase the immunomodulator effect of defense cell and the Schiff base 8a is the highest one by (Intra. killing activity = 136.5 ± 0.3%) having a pyrazole moiety as well as amide function (O=C-NH2) and piperidinyl core.
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Design, synthesis, in vitro antimicrobial evaluation and molecular docking studies of indol-2-one tagged with morpholinosulfonyl moiety as DNA gyrase inhibitors.

TL;DR: A series of Schiff bases 3, 5, 7 and hydrazones 9 were achieved via reaction of 5-(morpholinosulfonyl)indol-2,3-dione with appropriate amines and/or hydrazide derivatives and enabled a better understanding of their structural features.
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Design, synthesis, antiproliferative evaluation, and molecular docking study of new quinoxaline derivatives as apoptotic inducers and EGFR inhibitors

TL;DR: A new series of quinoxaline derivatives synthesized and pharmacologically evaluated against (HepG-2, HCT-116, and MCF-7) cell lines and revealed that it increases apoptotic cells and induced cell cycle arrest at pre-G1 and G2/M phases.
References
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Journal ArticleDOI

Multicomponent Reaction Discovery: Three-Component Synthesis of Spirooxindoles

TL;DR: The Lewis acid-catalyzed, three-component reaction of isatin and two 1,3-dicarbonyl compounds is reported, with high efficiency under mild reaction conditions and with good functional group tolerance to afford spirooxindole pyranochromenedione derivatives.
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Synthesis and antimicrobial activity of some novel derivatives of benzofuran part 1. Synthesis and antimicrobial activity of (benzofuran-2-yl)(3-phenyl-3-methylcyclobutyl) ketoxime derivatives

TL;DR: (benzofuran-2-yl)(3-phenyl-3-methyl cyclobutyl)-O-benzylketoxime 6a showed good antimicrobial effect against C. albicans ATCC 10231 and was found the most active derivative against S. aureus ATCC 6538.
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Cyclopiamines A and B, novel oxindole metabolites of Penicillium cyclopium westling

TL;DR: In this article, the isolation of two new oxindole alkaloids, cyclopiamine A and B, from Penicillium cyclopium, is described.
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Inhibition of DNA gyrase and DNA topoisomerase IV of Staphylococcus aureus and Escherichia coli by aminocoumarin antibiotics

TL;DR: Insight is provided about the substituents that are important for the inhibitory activity of aminocoumarins against the target enzymes, which will facilitate the rational design of improved antibiotics.
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Synthesis of (+/-)-strychnofoline via a highly convergent selective annulation reaction.

TL;DR: A recently developed MgI(2)-mediated ring-expansion reaction of spiro[cyclopropan-1,3'-oxindole] with a cyclic disubstituted aldimine results in a single diastereoisomer, possessing the same stereochemical pattern found in strychnofoline.
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