scispace - formally typeset
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.
About
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.

read more

Citations
More filters
Journal ArticleDOI

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.
Journal ArticleDOI

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.
Journal ArticleDOI

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.
Journal ArticleDOI

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.
Journal ArticleDOI

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
More filters
Journal ArticleDOI

Synthesis of New Thiazole, Bithiazolidinone and Pyrano[2,3- d ]thiazole Derivatives as Potential Antimicrobial Agents

TL;DR: In this paper, a series of thiazole derivatives containing furan moiety 3, 7, 8a,b, 10a-c and 12 were prepared via the reaction of 2-cyano-N-(furan-2-ylmethyl)acetamide (1) with phenyl isothiocyanate and α-halocarbonyl compounds.
Journal ArticleDOI

Antibacterial evaluation and mode of action study of BIMQ, a novel bacterial cell division inhibitor.

TL;DR: The biochemical studies prove that the new indolyl quinolinium compound is able to disrupt FtsZ polymerization effectively through a stimulatory mechanism and can delay the development of drug resistance mutants.
Journal ArticleDOI

Synthesis and structure-activity relationships of novel 9-oxime acylides with improved bactericidal activity.

TL;DR: This study suggests that the 9-oxime acylides possess a bactericidal mechanism that is different from the traditional near-complete inhibition of protein synthesis, which provides a foundation for the rational design of macrolide antibiotics.
Journal Article

[Tetracyclines: bacteriostatic or bactericidal drugs? In vitro studies with rolitetracycline, minocycline and doxycycline (author's transl)].

TL;DR: Minimal bacteriostatic and minimal bactericidal concentrations of rolitetracycline, minocycline and doxycycline on 20 different E. coli serotypes and 16 staphylococcus aureus strains have been compared in bouillon and serum to find out whether these concentrations can be improved by addition of serum.
Related Papers (5)