Articles with "synthesis anti" as a keyword



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Synthesis, anti‐inflammatory activity, and molecular docking studies of some novel Mannich bases of the 1,3,4‐oxadiazole‐2(3H)‐thione scaffold

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Published in 2020 at "Archiv der Pharmazie"

DOI: 10.1002/ardp.202000061

Abstract: A series of novel ibuprofen and salicylic acid‐based 3,5‐disubstituted‐1,3,4‐oxadiazole‐2(3H)‐thione derivatives was synthesized, and they were evaluated as potential anti‐inflammatory agents. Following the structure identification studies employing IR, 1H nuclear magnetic resonance (NMR), 13C NMR, and… read more here.

Keywords: anti inflammatory; docking studies; oxadiazole thione; synthesis anti ... See more keywords
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Synthesis, anti‐TB activities, and molecular docking studies of 4‐(1,2,3‐triazoyl)arylmethanone derivatives

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Published in 2022 at "Journal of Biochemical and Molecular Toxicology"

DOI: 10.1002/jbt.22998

Abstract: Infectious diseases such as tuberculosis (TB) are leading causes of human death. Antibiotics are effective molecules to combat bacterial infections by affecting the processes required for bacterial cell growth and proliferation. The development of new… read more here.

Keywords: molecular docking; triazoyl arylmethanone; anti activities; arylmethanone derivatives ... See more keywords
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Synthesis and anti-inflammatory activities of novel dihydropyranoaurone derivatives

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Published in 2017 at "Archives of Pharmacal Research"

DOI: 10.1007/s12272-017-0910-5

Abstract: A novel series of dihydropyranoaurone derivatives were synthesized and evaluated as potential anti-inflammatory agents. Late-stage derivatization by versatile piperazine-catalyzed aldol reaction between dihydropyanobenzofuran intermediate 2 and diverse aldehydes readily afforded the novel dihydropyranoaurone analogs. Evaluation… read more here.

Keywords: anti inflammatory; dihydropyranoaurone derivatives; dihydropyranoaurone; novel dihydropyranoaurone ... See more keywords
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Synthesis and anti-mitotic activity of 6,7-dihydro-4H-isothiazolo[4,5-b]pyridin-5-ones: In vivo and cell-based studies.

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Published in 2017 at "European journal of medicinal chemistry"

DOI: 10.1016/j.ejmech.2016.09.075

Abstract: A series of 3,7-diaryl-6,7-dihydroisothiazolo [4,5-b]pyridin-5(4H)-ones 8 and 9 was synthesized by multicomponent condensation of 3-aryl-5-isothiazolecarboxylic acid esters 4a-f with aromatic (or thienyl) aldehydes 7 and Meldrum's acid in an acidic medium. The targeted compounds were… read more here.

Keywords: pyridin ones; cell based; synthesis anti; cell ... See more keywords
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Synthesis and anti-mitotic activity of 2,4- or 2,6-disubstituted- and 2,4,6-trisubstituted-2H-pyrazolo[4,3-c]pyridines.

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Published in 2018 at "European journal of medicinal chemistry"

DOI: 10.1016/j.ejmech.2018.03.037

Abstract: An efficient synthetic route for the synthesis of 2H-pyrazolo[4,3-c]pyridines, primarily varying by the substituents at the 2-, 4- and 6-positions, is described here. A Sonogashira-type cross-coupling reaction was employed to yield 3-alkynyl-1H-pyrazole-4-carbaldehydes, ethanones and propanones… read more here.

Keywords: anti mitotic; pyrazolo pyridines; synthesis anti; mitotic activity ... See more keywords
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Synthesis of anti-tubercular marine alkaloids denigrins A and B

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Published in 2018 at "Tetrahedron Letters"

DOI: 10.1016/j.tetlet.2018.06.013

Abstract: Abstract The first synthesis of anti-tubercular marine alkaloids denigrins A and B were accomplished in three and five steps and 62% and 31% overall yields respectively, from maleic anhydride. The key features of the synthesis… read more here.

Keywords: marine alkaloids; synthesis anti; anti tubercular; alkaloids denigrins ... See more keywords
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Synthesis, Anti-Plasmodial Activities, and Mechanistic Insights of 4-Aminoquinoline-Triazolopyrimidine Hybrids.

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Published in 2022 at "ACS medicinal chemistry letters"

DOI: 10.1021/acsmedchemlett.2c00078

Abstract: In the search of new antiplasmodial agents, a multitargeted approach was used in the synthesis of triazolopyrimidine- and 4-aminoquinolines-based hybrids. In vitro antiplasmodial evaluation on chloroquine-sensitive (3D7) and -resistant (W2) P. falciparum strains identified triazolopyrimidine-4-aminoquinoline… read more here.

Keywords: insights aminoquinoline; anti plasmodial; plasmodial activities; activities mechanistic ... See more keywords
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Synthesis, anti-proliferative and apoptosis-inducing studies of palladacycles containing a diphosphine and a Sn,As-based chelate ligand.

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Published in 2019 at "Dalton transactions"

DOI: 10.1039/c8dt03875a

Abstract: Cleavage of the bromide bridges in [Pd2(μ-Br)2{κ2(Sn,As)-2-MeBrSnC6F4AsPh2}2] (1) by diphosphine ligands gave the mono- and dinuclear palladacycles [Pd(L)Br{κ2(Sn,As)-2-MeBrSnC6F4AsPh2}] [L = dppe (2) dppm (3), ortho-dppBz (4)] and [Pd2Br2(para-dppBz){κ2(Sn,As)-2-MeBrSnC6F4AsPh2}2] (5). The interactions of these complexes with… read more here.

Keywords: anti proliferative; apoptosis inducing; proliferative apoptosis; synthesis anti ... See more keywords
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Synthesis, anti-mycobacterial and cytotoxic evaluation of substituted isoindoline-1,3-dione-4-aminoquinolines coupled via alkyl/amide linkers

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Published in 2019 at "RSC Advances"

DOI: 10.1039/c8ra10532d

Abstract: A series of secondary amine-substituted isoindoline-1,3-dione-4-aminoquinolines were prepared via microwave heating and assayed for their anti-mycobacterial activities. read more here.

Keywords: anti mycobacterial; synthesis anti; isoindoline dione; dione aminoquinolines ... See more keywords
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Synthesis and anti-osteoporosis activity of novel Teriparatide glycosylation derivatives

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Published in 2020 at "RSC Advances"

DOI: 10.1039/d0ra05136e

Abstract: Osteoporosis is a metabolic bone disease that is characterized by low bone mass and micro-architectural deterioration of bones. The mechanism underlying this disease implicates an imbalance between bone resorption and bone remodeling. In 2002, the… read more here.

Keywords: anti osteoporosis; synthesis anti; glycosylation derivatives; teriparatide ... See more keywords
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Microwave synthesis, anti-oxidant and anti-tumor activity of some nucleosides derived 2-oxonicotinonitrile

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Published in 2019 at "Synthetic Communications"

DOI: 10.1080/00397911.2019.1672747

Abstract: Abstract A facile and convenient synthesis of novel cyclic and acyclic nucleoside derivatives incorporating 2-oxo-1,2-dihydropyridine-3-carbonitrile moiety has been described. The aglycons 3a,b were coupled with different activated halosugars such as glucosyl, galactosyl, lactosyl bromides and… read more here.

Keywords: anti oxidant; anti tumor; synthesis anti; microwave synthesis ... See more keywords