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Journal ArticleDOI

Synthesis and Antibacterial Activity Studies of 8,9‐Dihydro [7h] Benzo 1,2,4‐Oxadiazoles and its Coumarin Derivatives

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TLDR
In this paper, the synthesis, characterization, and antibacterial active studies of 12 coumarin derivatives were described by using 4-carbonyl chloride with 1,2-dichloroethane as a solvent, in moderate to good yields.
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This article is published in Journal of Heterocyclic Chemistry.The article was published on 2017-09-18. It has received 11 citations till now. The article focuses on the topics: Antibacterial activity.

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Journal ArticleDOI

Coumarin-containing hybrids and their antibacterial activities.

TL;DR: This review outlines the advances in coumarin‐containing hybrids with antibacterial potential in the recent 5 years and the structure–activity relationships are also discussed.
Journal ArticleDOI

Design and synthesis of purine connected piperazine derivatives as novel inhibitors of Mycobacterium tuberculosis.

TL;DR: A series of novel purine linked piperazine derivatives were synthesized to identify new, potent inhibitors of Mycobacterium tuberculosis, designed to target MurB disrupting the biosynthesis of the peptidoglycan and exert antiproliferative effects.
Journal ArticleDOI

Design and Synthesis of "Chloropicolinate Amides and Urea Derivatives" as Novel Inhibitors for Mycobacterium tuberculosis.

TL;DR: A series of 30 diamino phenyl chloropicolinate fettered carboxamides, urea, and thiourea derivatives were synthesized by coupling of methyl 4-amino-6-(2-aminophenyl)-3-chloropyridine-2-carboxylate with different acid chlorides and urea derivatives, respectively as mentioned in this paper.
References
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Journal ArticleDOI

A new therapeutic approach in Alzheimer disease: some novel pyrazole derivatives as dual MAO-B inhibitors and antiinflammatory analgesics.

TL;DR: A novel series of 1-thiocarbamoyl-3-substituted phenyl-5-(2-pyrrolyl)-4,5-dihydro-(1H)-pyrazole derivatives as promising MAO-B inhibitors was synthesized and investigated for the ability to inhibit selectively the activity of the A and B isoforms of monoamine oxidation.
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Design, synthesis, and evaluation of Phe-Gly mimetics: heterocyclic building blocks for pseudopeptides.

TL;DR: Enantiopure heterocyclic Boc-protected Phe-Gly dipeptidomimetics containing 1,3, 4-oxadiazole, 1,2,4-ox adenosine ring systems have been synthesized as building blocks in the synthesis of pseudopeptides.
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Synthesis and antimicrobial studies on novel sulfonamides containing 4-azidomethyl coumarin.

TL;DR: A series of new and novel coumarin-6-sulfonamides with a free C4-azidomethyl group have been synthesized as antimicrobials as well as screened for their in vitro anti-bacterial and anti-fungal activities.
Journal ArticleDOI

Synthesis, characterization and antimicrobial activity of new aliphatic sulfonamide.

TL;DR: The authors' aliphatic sulfonamides have highest powerful antibacterial activity for Gram-negative bacteria than Gram-positive bacteria and antib bacterial activity decreases as the length of the carbon chain increases.
Journal ArticleDOI

Synthesis and biological activity of 1,2,4-oxadiazole derivatives: highly potent and efficacious agonists for cortical muscarinic receptors.

TL;DR: The synthesis and biochemical evaluation of novel 1,2,4-oxadiazole-based muscarinic agonists which can readily penetrate into the CNS is reported and efficacy and affinity are influenced by the geometry between the cationic head.
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