Search Results - "Shaik, Siddiq Pasha"
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Iodine-mediated C-N and N-N bond formation: a facile one-pot synthetic approach to 1,2,3-triazoles under metal-free and azide-free conditions
Published in RSC advances (28-08-2019)“…A novel strategy towards the synthesis of 1,4-disubstituted 1,2,3-triazoles via C-N and N-N bond formation has been demonstrated under transition metal-free…”
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2
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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3
Zinc Dependent Histone Deacetylase Inhibitors in Cancer Therapeutics: Recent Update
Published in Current medicinal chemistry (01-01-2019)“…Histone deacetylases (HDAC) are an important class of enzymes that play a pivotal role in epigenetic regulation of gene expression that modifies the terminal…”
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4
One‐Pot Synthesis of Naphtho[1′,2′:4,5]imidazo[1,2‐a]pyridin‐5‐yl(aryl)methanones through Sequential Sonogashira Coupling/Alkyne–Carbonyl Metathesis
Published in European journal of organic chemistry (25-07-2017)“…An efficient one‐pot route for the construction of naphtho[1′,2′:4,5]imidazo[1,2‐a]pyridin‐5‐yl(aryl)methanones and…”
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5
Efficient and green sulfamic acid catalyzed synthesis of new 1,2-dihydroquinazoline derivatives with antibacterial potential
Published in Arabian journal of chemistry (01-12-2019)“…[Display omitted] A simple, efficient and eco-friendly method for the synthesis of 1,2-dihydroquinazolines has been developed using three-component reaction of…”
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6
Iodine-catalyzed Csp3-H functionalization of methylhetarenes: One-pot synthesis and cytotoxic evaluation of heteroarenyl-benzimidazoles and benzothiazole
Published in Bioorganic & medicinal chemistry letters (01-09-2017)“…[Display omitted] An efficient one-pot synthetic procedure has been developed for the preparation of heteroarenyl-benzimidazoles via oxidative Csp3-H…”
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7
Design and synthesis of imidazo[2,1-b]thiazole linked triazole conjugates: Microtubule-destabilizing agents
Published in European journal of medicinal chemistry (27-01-2017)“…A series of imidazo[2,1-b]thiazole linked triazole conjugates were synthesized by using Huisgen 1,3-dipolar cyclo-addition reaction (click chemistry approach)…”
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8
Benzimidazole-linked pyrazolo[1,5-a]pyrimidine conjugates: synthesis and detail evaluation as potential anticancer agents
Published in Molecular diversity (01-06-2023)“…A library of benzimidazole briged pyrazolo[1,5- a ]pyrimidine ( 6a-q ) was designed, synthesized and subjected for evaluation for cytotoxic potential…”
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Transition‐Metal‐Free Oxidative Cross‐Coupling of Methylhetarenes with Imidazoheterocycles towards Efficient C(sp2)−H Carbonylation
Published in Asian journal of organic chemistry (01-07-2017)“…An efficient method for the oxidative cross‐coupling of methylhetarenes with imidazoheterocycles by employing an eco‐friendly iodine/DMSO reagent system has…”
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10
Design and synthesis of 1,2,3-triazolo linked benzo[d]imidazo[2,1-b]thiazole conjugates as tubulin polymerization inhibitors
Published in Bioorganic & medicinal chemistry (01-07-2017)“…[Display omitted] •1,2,3-Triazolo linked benzo[d]imidazo[2,1-b]thiazole conjugates (5a–v) showed antiproliferative activity.•Conjugates 5f and 5k arrested in…”
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11
Sulfamic acid promoted one-pot three-component synthesis and cytotoxic evaluation of spirooxindoles
Published in Bioorganic & medicinal chemistry letters (15-05-2015)“…[Display omitted] A simple, mild and efficient method for the synthesis of pyrazolopyridine based spirooxindoles by the three-component reaction has been…”
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12
Synthesis and biological evaluation of imidazopyridinyl-1,3,4-oxadiazole conjugates as apoptosis inducers and topoisomerase IIα inhibitors
Published in Bioorganic chemistry (01-12-2016)“…A series of imidazopyridinyl-1,3,4-oxadiazole conjugates were synthesized and evaluated for their anticancer potential against a panel of sixty human tumor…”
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13
2-Arylaminobenzothiazole-arylpropenone conjugates as tubulin polymerization inhibitorsThe authors declare no competing interests
Published 24-05-2017“…A new series of 2-arylaminobenzothiazole-arylpropenone conjugates 5 - 6 ( a - r ) was designed, synthesized and investigated for their cytotoxic potency…”
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14
2-Arylaminobenzothiazole-arylpropenone conjugates as tubulin polymerization inhibitors† †The authors declare no competing interests
Published in MedChemComm (07-03-2017)“…A new series of 2-arylaminobenzothiazole-arylpropenone conjugates were designed based on 5F-203, synthesized and evaluated for their cytotoxic potency as well…”
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15
Molecular Iodine‐Promoted Transimination for the Synthesis of 6‐Phenylpyrido[2′,1′:2,3]imidazo[4,5‐c]quinoline and 6‐(Pyridin‐2‐yl)pyrido[2′,1′:2,3]imidazo[4,5‐c]quinolines
Published in Asian journal of organic chemistry (01-12-2017)“…An unprecedented, efficient I2‐mediated approach for the synthesis of 6‐phenylpyrido[2′,1′:2,3]imidazo[4,5‐c]quinoline heterocyclic skeletons has been achieved…”
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16
Design, Synthesis and Biological Evaluation of 2‐Anilinopyridyl‐Linked Oxindole Conjugates as Potent Tubulin Polymerisation Inhibitors
Published in ChemistrySelect (Weinheim) (31-10-2017)“…A series of 2‐anilinopyridyl linked oxindole conjugates (6 a‐ad) were synthesized andevaluated for their antiproliferative activity against a panel of four…”
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17
2-Arylaminobenzothiazole-arylpropenone conjugates as tubulin polymerization inhibitors
Published in MedChemComm (01-05-2017)“…A new series of 2-arylaminobenzothiazole-arylpropenone conjugates - ( - ) was designed, synthesized and investigated for their cytotoxic potency against the…”
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18
Iodine-catalyzed C sp3 -H functionalization of methylhetarenes: One-pot synthesis and cytotoxic evaluation of heteroarenyl-benzimidazoles and benzothiazole
Published in Bioorganic & medicinal chemistry letters (01-09-2017)“…An efficient one-pot synthetic procedure has been developed for the preparation of heteroarenyl-benzimidazoles via oxidative C -H functionalization with…”
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