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Synthesis of new 4-aminoquinolines and quinoline–acridine hybrids as antimalarial agents

Bioorganic & medicinal chemistry letters, 2010-12, Vol.20 (23), p.7059-7063

2010

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Cyanuric Chloride Catalyzed Mild Protocol for Synthesis of Biologically Active Dihydro/Spiro Quinazolinones and Quinazolinone-glycoconjugates

Journal of organic chemistry, 2012-01, Vol.77 (2), p.929-937

2012

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Bis and tris indole alkaloids from marine organisms: new leads for drug discovery

Current medicinal chemistry, 2007-07, Vol.14 (16), p.1789-1803

2007

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Design and Synthesis of a New Class of 4-Aminoquinolinyl- and 9-Anilinoacridinyl Schiff Base Hydrazones as Potent Antimalarial Agents

Chemical biology & drug design, 2014-08, Vol.84 (2), p.175-181

2014

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Discovery of a New Class of Natural Product-Inspired Quinazolinone Hybrid as Potent Antileishmanial agents

Journal of medicinal chemistry, 2013-06, Vol.56 (11), p.4374-4392

2013

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Synthesis and bioevaluation of hybrid 4-aminoquinoline triazines as a new class of antimalarial agents

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (24), p.6530-6533

2008

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Synthesis of oxalamide and triazine derivatives as a novel class of hybrid 4-aminoquinoline with potent antiplasmodial activity

Bioorganic & medicinal chemistry, 2009-09, Vol.17 (17), p.6451-6462

2009

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Dihydrofolate reductase as a therapeutic target for infectious diseases: opportunities and challenges

Future medicinal chemistry, 2012-06, Vol.4 (10), p.1335-1365

2012

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Synthesis of 9-anilinoacridine triazines as new class of hybrid antimalarial agents

Bioorganic & medicinal chemistry letters, 2009-12, Vol.19 (24), p.6996-6999

2009

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A Ligand-Free Pd-Catalyzed Cascade Reaction: An Access to the Highly Diverse Isoquinolin-1(2H)-one Derivatives via Isocyanide and Ugi-MCR Synthesized Amide Precursors

Organic letters, 2012-06, Vol.14 (12), p.3126-3129

2012

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Skeletal Diverse Synthesis of N-Fused Polycyclic Heterocycles via the Sequence of Ugi-Type MCR and CuI-Catalyzed Coupling/Tandem Pictet–Spengler Reaction

Journal of organic chemistry, 2012-02, Vol.77 (3), p.1414-1421

2012

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Synthesis and biological evaluation of indolyl glyoxylamides as a new class of antileishmanial agents

Bioorganic & medicinal chemistry letters, 2010-11, Vol.20 (21), p.6191-6194

2010

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Synthesis of novel β-carboline based chalcones with high cytotoxic activity against breast cancer cells

Bioorganic & medicinal chemistry letters, 2014-07, Vol.24 (13), p.2820-2824

2014

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Synthesis of Perspicamide A and Related Diverse Analogues: Their Bioevaluation as Potent Antileishmanial Agents

Journal of organic chemistry, 2013-02, Vol.78 (4), p.1534-1546

2013

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Discovery of Novel Antileishmanial Agents in an Attempt to Synthesize Pentamidine−Aplysinopsin Hybrid Molecule

Journal of medicinal chemistry, 2009-10, Vol.52 (19), p.5793-5802

2009

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Synthesis and biological evaluation of new [1,2,4]triazino[5,6- b]indol-3-ylthio-1,3,5-triazines and [1,2,4]triazino[5,6- b]indol-3-ylthio-pyrimidines against Leishmania donovani

European journal of medicinal chemistry, 2010-06, Vol.45 (6), p.2359-2365

2010

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Discovery of new 1,3,5-triazine scaffolds with potent activity against Mycobacterium tuberculosis H37Rv

European journal of medicinal chemistry, 2010-08, Vol.45 (8), p.3335-3345

2010

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Synthesis of novel thiourea, thiazolidinedione and thioparabanic acid derivatives of 4-aminoquinoline as potent antimalarials

Bioorganic & medicinal chemistry letters, 2009-05, Vol.19 (9), p.2570-2573

2009

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4-Anilinoquinoline triazines: A novel class of hybrid antimalarial agents

European journal of medicinal chemistry, 2011-02, Vol.46 (2), p.676-690

2011

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Synthesis and cytotoxicity evaluation of (tetrahydro-β-carboline)-1,3,5-triazine hybrids as anticancer agents

European journal of medicinal chemistry, 2010-06, Vol.45 (6), p.2265-2276

2010

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Access to Indole- And Pyrrole-Fused Diketopiperazines via Tandem Ugi-4CR/Intramolecular Cyclization and Its Regioselective Ring-Opening by Intermolecular Transamidation

Journal of organic chemistry, 2012-11, Vol.77 (22), p.10211-10227

2012

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Substituted quinolinyl chalcones and quinolinyl pyrimidines as a new class of anti-infective agents

European journal of medicinal chemistry, 2009-05, Vol.44 (5), p.2081-2091

2009

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Synthesis and antileishmanial activity of novel 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines

European journal of medicinal chemistry, 2009-06, Vol.44 (6), p.2473-2481

2009

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Base mediated 7-exo-dig intramolecular cyclization of Ugi-propargyl precursors: a highly efficient and regioselective synthetic approach toward diverse 1,4-benzoxazepine-5(2H)-ones

Organic & biomolecular chemistry, 2014-08, Vol.12 (29), p.5346-5350

2014

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Discovery of Triazine Mimetics As Potent Antileishmanial Agents

ACS medicinal chemistry letters, 2013-11, Vol.4 (11), p.1108-1113

2013

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Synthesis of new 4-aminoquinolines and quinoline–acridine hybrids as antimalarial agents

Cyanuric Chloride Catalyzed Mild Protocol for Synthesis of Biologically Active Dihydro/Spiro Quinazolinones and Quinazolinone-glycoconjugates

Bis and tris indole alkaloids from marine organisms: new leads for drug discovery

Design and Synthesis of a New Class of 4-Aminoquinolinyl- and 9-Anilinoacridinyl Schiff Base Hydrazones as Potent Antimalarial Agents

Discovery of a New Class of Natural Product-Inspired Quinazolinone Hybrid as Potent Antileishmanial agents

Synthesis and bioevaluation of hybrid 4-aminoquinoline triazines as a new class of antimalarial agents

Synthesis of oxalamide and triazine derivatives as a novel class of hybrid 4-aminoquinoline with potent antiplasmodial activity

Dihydrofolate reductase as a therapeutic target for infectious diseases: opportunities and challenges

Synthesis of 9-anilinoacridine triazines as new class of hybrid antimalarial agents

A Ligand-Free Pd-Catalyzed Cascade Reaction: An Access to the Highly Diverse Isoquinolin-1(2H)-one Derivatives via Isocyanide and Ugi-MCR Synthesized Amide Precursors

Skeletal Diverse Synthesis of N-Fused Polycyclic Heterocycles via the Sequence of Ugi-Type MCR and CuI-Catalyzed Coupling/Tandem Pictet–Spengler Reaction

Synthesis and biological evaluation of indolyl glyoxylamides as a new class of antileishmanial agents

Synthesis of novel β-carboline based chalcones with high cytotoxic activity against breast cancer cells

Synthesis of Perspicamide A and Related Diverse Analogues: Their Bioevaluation as Potent Antileishmanial Agents

Discovery of Novel Antileishmanial Agents in an Attempt to Synthesize Pentamidine−Aplysinopsin Hybrid Molecule

Synthesis and biological evaluation of new [1,2,4]triazino[5,6- b]indol-3-ylthio-1,3,5-triazines and [1,2,4]triazino[5,6- b]indol-3-ylthio-pyrimidines against Leishmania donovani

Discovery of new 1,3,5-triazine scaffolds with potent activity against Mycobacterium tuberculosis H37Rv

Synthesis of novel thiourea, thiazolidinedione and thioparabanic acid derivatives of 4-aminoquinoline as potent antimalarials

4-Anilinoquinoline triazines: A novel class of hybrid antimalarial agents

Synthesis and cytotoxicity evaluation of (tetrahydro-β-carboline)-1,3,5-triazine hybrids as anticancer agents

Access to Indole- And Pyrrole-Fused Diketopiperazines via Tandem Ugi-4CR/Intramolecular Cyclization and Its Regioselective Ring-Opening by Intermolecular Transamidation

Substituted quinolinyl chalcones and quinolinyl pyrimidines as a new class of anti-infective agents

Synthesis and antileishmanial activity of novel 2,4,6-trisubstituted pyrimidines and 1,3,5-triazines

Base mediated 7-exo-dig intramolecular cyclization of Ugi-propargyl precursors: a highly efficient and regioselective synthetic approach toward diverse 1,4-benzoxazepine-5(2H)-ones

Discovery of Triazine Mimetics As Potent Antileishmanial Agents

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