Search Results - "Nayak, V. Lakshma"
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Synthesis and biological evaluation of cis-restricted triazole/tetrazole mimics of combretastatin-benzothiazole hybrids as tubulin polymerization inhibitors and apoptosis inducers
Published in Bioorganic & medicinal chemistry (01-02-2017)“…[Display omitted] A series of colchicine site binding tubulin inhibitors were synthesized by the modification of the combretastatin pharmacophore. The ring B…”
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Design, synthesis and biological evaluation of N-((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)-1,3-diphenyl-1H-pyrazole-4-carboxamides as CDK1/Cdc2 inhibitors
Published in European journal of medicinal chemistry (21-10-2016)“…A series of new (N-((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)-1,3-diphenyl-1H-pyrazole-4-carboxamide derivatives (8–35) were designed, synthesized and evaluated…”
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Design, synthesis and anticancer properties of novel oxa/azaspiro[4,5]trienones as potent apoptosis inducers through mitochondrial disruption
Published in European journal of medicinal chemistry (28-08-2015)“…A series of twenty seven oxa/azaspiro[4,5]trienone derivatives were synthesized and their anticancer properties have been explored. GI50 values of all these…”
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Comprehensive Analysis of Secondary Metabolites in Usnea longissima (Lichenized Ascomycetes, Parmeliaceae) Using UPLC-ESI-QTOF-MS/MS and Pro-Apoptotic Activity of Barbatic Acid
Published in Molecules (Basel, Switzerland) (18-06-2019)“…Considering the importance of ultra-performance liquid chromatography-electrospray ionization-quadrupole time of flight-tandem mass spectrometry…”
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Design, synthesis and biological evaluation of novel cationic liposomes loaded with melphalan for the treatment of cancer
Published in Bioorganic & medicinal chemistry letters (01-01-2024)“…[Display omitted] Therapeutically active lipids in drug delivery systems offer customization for enhanced pharmaceutical and biological effects, improving…”
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Design and synthesis of DNA-intercalative naphthalimide-benzothiazole/cinnamide derivatives: cytotoxicity evaluation and topoisomerase-IIα inhibition
Published in MedChemComm (01-01-2019)“…A new series of different naphthalimide-benzothiazole/cinnamide derivatives were designed, synthesized and tested for their cytotoxicity on selected human…”
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Synthesis and biological evaluation of Schizandrin derivatives as potential anti-cancer agents
Published in European journal of medicinal chemistry (10-04-2018)“…A new series of Schizandrin (1) derivatives were synthesized utilizing the C-9 position of the Schizandrin core and evaluated for their cytotoxic activities…”
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Synthesis and biological evaluation of imidazo[2,1-b]thiazole-benzimidazole conjugates as microtubule-targeting agents
Published in Bioorganic chemistry (01-04-2018)“…[Display omitted] •Imidazo[2,1-b]thiazole linked benzimidazole conjugates (6a–u) showed cytotoxic activity.•Compound 6d showed significant cytotoxic activity…”
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Synthesis and anticancer activity of oxindole derived imidazo[1,5-a]pyrazines
Published in European journal of medicinal chemistry (01-06-2011)“…A series of oxindole derivatives of imidazo[1,5-a]pyrazines were prepared and confirmed by 1H NMR, mass and HRMS data. These compounds were evaluated for their…”
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Design and Synthesis of C3-Pyrazole/Chalcone-Linked Beta-Carboline Hybrids: Antitopoisomerase I, DNA-Interactive, and Apoptosis-Inducing Anticancer Agents
Published in ChemMedChem (01-09-2014)“…A series of β‐carboline hybrids bearing a substituted phenyl and a chalcone/(N‐acetyl)‐pyrazole moiety at the C1 and C3 positions, respectively, was designed,…”
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Methyl angolensate and mexicanolide-type limonoids from the seeds of Cipadessa baccifera
Published in Phytochemistry (Oxford) (01-02-2014)“…Six new methyl angolensate type (1–6) and three new mexicanolide-type (7–9) limonoids, along with six known limonoids (10–15), were isolated from the seeds of…”
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Synthesis and biological evaluation of imidazo[1,5-a]pyridine-benzimidazole hybrids as inhibitors of both tubulin polymerization and PI3K/Akt pathway
Published in Organic & biomolecular chemistry (28-12-2014)“…A series of imidazo[1,5-a]pyridine-benzimidazole hybrids (5a–aa) were prepared and evaluated for their cytotoxic activity against a panel of sixty human tumor…”
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Synthesis and biological evaluation of bergenin-1,2,3-triazole hybrids as novel class of anti-mitotic agents
Published in Bioorganic chemistry (01-10-2019)“…A series of bergenin-triazole hybrids were synthesized based on “Click” reaction and tested for cytotoxic activities. Among the congeners, 4j showed potent…”
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Synthesis and biological evaluation of 1-benzyl-N-(2-(phenylamino)pyridin-3-yl)-1H-1,2,3-triazole-4-carboxamides as antimitotic agents
Published in Bioorganic chemistry (01-03-2019)“…[Display omitted] •Conjugates (7a–7al) were design, synthesized and evaluated for their cytotoxic activity.•Conjugates 7a, 7b, 7c, 7f, 7h, 7j, 7m, 7n exhibited…”
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Rational design and synthesis of 2-anilinopyridinyl-benzothiazole Schiff bases as antimitotic agents
Published in Bioorganic & medicinal chemistry letters (01-06-2017)“…[Display omitted] Based on our previous results and literature precedence, a series of 2-anilinopyridinyl-benzothiazole Schiff bases were rationally designed…”
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Synthesis and biological evaluation of new bisindole-imidazopyridine hybrids as apoptosis inducers
Published in Bioorganic chemistry (01-06-2019)“…[Display omitted] •Imidazo[1,5-a]pyridine-bisindole conjugates(5a-t) as apoptis inducedrs.•Conjugate 5k IC50 value 1.6 µM againt Lung cancer cell line.•Arrest…”
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Design, synthesis and biological evaluation of imidazopyridine-propenone conjugates as potent tubulin inhibitors
Published in MedChemComm (01-05-2017)“…A library of imidazopyridine-propenone conjugates ( ) were synthesized and evaluated for their antitumor activity against four human cancer cell lines, namely,…”
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Synthesis of a terphenyl substituted 4-aza-2,3-didehydropodophyllotoxin analogues as inhibitors of tubulin polymerization and apoptosis inducers
Published in Bioorganic & medicinal chemistry (01-05-2014)“…A series of terphenyl based 4-aza-2,3-didehydropodophyllotoxin conjugates (8a–r) were synthesized by a straightforward one-step multicomponent synthesis that…”
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Benzo[b]furan derivatives induces apoptosis by targeting the PI3K/Akt/mTOR signaling pathway in human breast cancer cells
Published in Bioorganic chemistry (01-06-2016)“…Benzo[b]furan derivatives (26 and 36) showed significant antiproliferative activity against human breast cancer cell line, MCF-7. These benzo[b]furan…”
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Synthesis of chalcone-amidobenzothiazole conjugates as antimitotic and apoptotic inducing agents
Published in Bioorganic & medicinal chemistry (01-06-2012)“…A series of chalcone-amidobenzothiazole conjugates (9a–k and 10a,b) have been synthesized and evaluated for their anticancer activity. All these compounds…”
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