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Homochiral drugs: a demanding tendency of the pharmaceutical industry

Current medicinal chemistry, 2009-06, Vol.16 (16), p.2064-2074

2009

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Synthesis and Biological Evaluation of 2‑(Alkoxycarbonyl)-3-Anilinobenzo[b]thiophenes and Thieno[2,3‑b]pyridines as New Potent Anticancer Agents

Journal of medicinal chemistry, 2013-03, Vol.56 (6), p.2606-2618

2013

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Design, synthesis and biological evaluation of novel vicinal diaryl-substituted 1H-Pyrazole analogues of combretastatin A-4 as highly potent tubulin polymerization inhibitors

European journal of medicinal chemistry, 2019-11, Vol.181, p.111577-111577, Article 111577

2019

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Anticancer and Structure Activity Relationship of Non-Symmetrical Choline Kinase Inhibitors

Pharmaceutics, 2021-08, Vol.13 (9), p.1360

2021

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Design, synthesis and biological evaluation of 3,5-disubstituted 2-amino thiophene derivatives as a novel class of antitumor agents

Bioorganic & medicinal chemistry, 2014-09, Vol.22 (18), p.5097-5109

2014

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One-pot synthesis and biological evaluation of 2-pyrrolidinyl-4-amino-5-(3′,4′,5′-trimethoxybenzoyl)thiazole: A unique, highly active antimicrotubule agent

European journal of medicinal chemistry, 2011-12, Vol.46 (12), p.6015-6024

2011

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Design, synthesis and biological evaluation of 2-alkoxycarbonyl-3-anilinoindoles as a new class of potent inhibitors of tubulin polymerization

Bioorganic chemistry, 2020-04, Vol.97, p.103665-103665, Article 103665

2020

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2-Alkoxycarbonyl-3-arylamino-5-substituted thiophenes as a novel class of antimicrotubule agents: Design, synthesis, cell growth and tubulin polymerization inhibition

European journal of medicinal chemistry, 2018-01, Vol.143, p.683-698

2018

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Follicular Dendritic Cells Are Related to Bone Marrow Stromal Cell Progenitors and to Myofibroblasts

Journal of Immunology, 2006-07, Vol.177 (1), p.280-289

2006

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Synthesis and Antitumor Molecular Mechanism of Agents Based on Amino 2-(3′,4′,5′-Trimethoxybenzoyl)benzo[b]furan: Inhibition of Tubulin and Induction of Apoptosis

ChemMedChem, 2011-10, Vol.6 (10), p.1841-1853

2011

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Synthesis and biological effects of novel 2-amino-3-(4-chlorobenzoyl)-4-substituted thiophenes as allosteric enhancers of the A1 adenosine receptor

European journal of medicinal chemistry, 2013-09, Vol.67, p.409-427

2013

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Design, Synthesis and Biological Evaluation of Hybrid Molecules Containing Conjugated Styryl Ketone and α-Bromoacryloyl Moieties

Letters in drug design & discovery, 2012-02, Vol.9 (2), p.140-152

2012

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Synthesis and Evaluation of 1,5-Disubstituted Tetrazoles as Rigid Analogues of Combretastatin A-4 with Potent Antiproliferative and Antitumor Activity

Journal of medicinal chemistry, 2012-01, Vol.55 (1), p.475-488

2012

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A facile synthesis of diaryl pyrroles led to the discovery of potent colchicine site antimitotic agents

European journal of medicinal chemistry, 2021-03, Vol.214, p.113229, Article 113229

2021

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Design, synthesis and biological evaluation of 3-substituted-2-oxindole hybrid derivatives as novel anticancer agents

European journal of medicinal chemistry, 2017-07, Vol.134, p.258-270

2017

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Synthesis, Antimitotic and Antivascular Activity of 1‑(3′,4′,5′-Trimethoxybenzoyl)-3-arylamino-5-amino-1,2,4-triazoles

Journal of medicinal chemistry, 2014-08, Vol.57 (15), p.6795-6808

2014

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Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione

European journal of medicinal chemistry, 2013-05, Vol.63, p.544-557

2013

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Design, Synthesis, in Vitro, and in Vivo Anticancer and Antiangiogenic Activity of Novel 3‑Arylaminobenzofuran Derivatives Targeting the Colchicine Site on Tubulin

Journal of medicinal chemistry, 2015-04, Vol.58 (7), p.3209-3222

2015

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Synthesis and biological evaluation of 2-substituted-4-(3′,4′,5′-trimethoxyphenyl)-5-aryl thiazoles as anticancer agents

Bioorganic & medicinal chemistry, 2012-12, Vol.20 (24), p.7083-7094

2012

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Syntheses of 2,3-Dihydro-1,4-Benzodioxins and Bioisosteres as Structural Motifs for Biologically Active Compounds

Current organic chemistry, 2011-03, Vol.15 (6), p.869-887

2011

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Synthesis and Biological Evaluation of 2-Methyl-4,5-Disubstituted Oxazoles as a Novel Class of Highly Potent Antitubulin Agents

Scientific reports, 2017-04, Vol.7 (1), p.46356-46356, Article 46356

2017

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Discovery and Optimization of a Series of 2-Aryl-4-Amino-5-(3′,4′,5′-trimethoxybenzoyl)Thiazoles as Novel Anticancer Agents

Journal of medicinal chemistry, 2012-06, Vol.55 (11), p.5433-5445

2012

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Allosteric modulation of A1-adenosine receptor: a review

Drug discovery today. Technologies, 2013, Vol.10 (2), p.e285-e296

2013

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Design, synthesis and biological evaluation of arylcinnamide hybrid derivatives as novel anticancer agents

European journal of medicinal chemistry, 2014-06, Vol.81, p.394-407

2014

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Contractile Activity of Human Decidual Stromal Cells

The journal of clinical endocrinology and metabolism, 2003-02, Vol.88 (2), p.844-849

2003

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Homochiral drugs: a demanding tendency of the pharmaceutical industry

Synthesis and Biological Evaluation of 2‑(Alkoxycarbonyl)-3-Anilinobenzo[b]thiophenes and Thieno[2,3‑b]pyridines as New Potent Anticancer Agents

Design, synthesis and biological evaluation of novel vicinal diaryl-substituted 1H-Pyrazole analogues of combretastatin A-4 as highly potent tubulin polymerization inhibitors

Anticancer and Structure Activity Relationship of Non-Symmetrical Choline Kinase Inhibitors

Design, synthesis and biological evaluation of 3,5-disubstituted 2-amino thiophene derivatives as a novel class of antitumor agents

One-pot synthesis and biological evaluation of 2-pyrrolidinyl-4-amino-5-(3′,4′,5′-trimethoxybenzoyl)thiazole: A unique, highly active antimicrotubule agent

Design, synthesis and biological evaluation of 2-alkoxycarbonyl-3-anilinoindoles as a new class of potent inhibitors of tubulin polymerization

2-Alkoxycarbonyl-3-arylamino-5-substituted thiophenes as a novel class of antimicrotubule agents: Design, synthesis, cell growth and tubulin polymerization inhibition

Follicular Dendritic Cells Are Related to Bone Marrow Stromal Cell Progenitors and to Myofibroblasts

Synthesis and Antitumor Molecular Mechanism of Agents Based on Amino 2-(3′,4′,5′-Trimethoxybenzoyl)benzo[b]furan: Inhibition of Tubulin and Induction of Apoptosis

Synthesis and biological effects of novel 2-amino-3-(4-chlorobenzoyl)-4-substituted thiophenes as allosteric enhancers of the A1 adenosine receptor

Design, Synthesis and Biological Evaluation of Hybrid Molecules Containing Conjugated Styryl Ketone and α-Bromoacryloyl Moieties

Synthesis and Evaluation of 1,5-Disubstituted Tetrazoles as Rigid Analogues of Combretastatin A-4 with Potent Antiproliferative and Antitumor Activity

A facile synthesis of diaryl pyrroles led to the discovery of potent colchicine site antimitotic agents

Design, synthesis and biological evaluation of 3-substituted-2-oxindole hybrid derivatives as novel anticancer agents

Synthesis, Antimitotic and Antivascular Activity of 1‑(3′,4′,5′-Trimethoxybenzoyl)-3-arylamino-5-amino-1,2,4-triazoles

Anticancer activity of novel hybrid molecules containing 5-benzylidene thiazolidine-2,4-dione

Design, Synthesis, in Vitro, and in Vivo Anticancer and Antiangiogenic Activity of Novel 3‑Arylaminobenzofuran Derivatives Targeting the Colchicine Site on Tubulin

Synthesis and biological evaluation of 2-substituted-4-(3′,4′,5′-trimethoxyphenyl)-5-aryl thiazoles as anticancer agents

Syntheses of 2,3-Dihydro-1,4-Benzodioxins and Bioisosteres as Structural Motifs for Biologically Active Compounds

Synthesis and Biological Evaluation of 2-Methyl-4,5-Disubstituted Oxazoles as a Novel Class of Highly Potent Antitubulin Agents

Discovery and Optimization of a Series of 2-Aryl-4-Amino-5-(3′,4′,5′-trimethoxybenzoyl)Thiazoles as Novel Anticancer Agents

Allosteric modulation of A1-adenosine receptor: a review

Design, synthesis and biological evaluation of arylcinnamide hybrid derivatives as novel anticancer agents

Contractile Activity of Human Decidual Stromal Cells

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