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Synthesis and in vitro antiproliferative activity of new 1,3,4-oxadiazole derivatives possessing sulfonamide moiety

European journal of medicinal chemistry, 2015-01, Vol.90, p.45-52

2015

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Novel Quinolinylaminoisoquinoline Bioisosteres of Sorafenib as Selective RAF1 Kinase Inhibitors: Design, Synthesis, and Antiproliferative Activity against Melanoma Cell Line

Chemical and Pharmaceutical Bulletin, 2013/07/01, Vol.61(7), pp.747-756

2013

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Synthesis and broad-spectrum antiproliferative activity of diarylamides and diarylureas possessing 1,3,4-oxadiazole derivatives

Bioorganic & medicinal chemistry letters, 2015-04, Vol.25 (8), p.1692-1699

2015

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Structural optimization of imidazothiazole derivatives affords a new promising series as B-Raf V600E inhibitors; synthesis, in vitro assay and in silico screening

Bioorganic chemistry, 2020-07, Vol.100, p.103967, Article 103967

2020

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Synthesis, in vitro Antiproliferative and Antiinflammatory Activities, and Kinase Inhibitory effects of New 1,3,4-triarylpyrazole Derivatives

Anti-cancer agents in medicinal chemistry, 2017, Vol.17 (1), p.75-84

2017

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Synthesis of New Triarylpyrazole Derivatives Possessing Terminal Sulfonamide Moiety and Their Inhibitory Effects on PGE₂ and Nitric Oxide Productions in Lipopolysaccharide-Induced RAW 264.7 Macrophages

Molecules (Basel, Switzerland), 2018-10, Vol.23 (10), p.2556

2018

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Design, synthesis, in vitro potent antiproliferative activity, and kinase inhibitory effects of new triarylpyrazole derivatives possessing different heterocycle terminal moieties

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.1534-1543

2019

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Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines. Part 2

Bioorganic & medicinal chemistry letters, 2012-07, Vol.22 (13), p.4362-4367

2012

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FMS Kinase Inhibitors: Current Status and Future Prospects

Medicinal research reviews, 2013-05, Vol.33 (3), p.599-636

2013

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Synthesis and inhibitory effects of triarylpyrazoles on LPS-induced NO and PGE2 productions in RAW 264.7 macrophages

Medicinal chemistry research, 2017-09, Vol.26 (9), p.2161-2171

2017

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Subtle Ligand/Media Effects. Modulation of cis/trans Isomerism in Hydrogen Peroxide Oxidation of Pt(II) to Pt(IV) Complexes

Bulletin of the Chemical Society of Japan, 2003-01, Vol.76 (1), p.107-110

2003

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Comprehensive impurity profiling and quantification of Sudan III dyes by gas chromatography/mass spectrometry

Journal of Chromatography A, 2013-07, Vol.1297, p.186-195

2013

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Design, synthesis and biological evaluation of new potent and highly selective ROS1-tyrosine kinase inhibitor

Bioorganic & medicinal chemistry letters, 2009-08, Vol.19 (16), p.4720-4723

2009

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Aminostyrylbenzofuran derivatives as potent inhibitors for Aβ fibril formation

Bioorganic & medicinal chemistry, 2008-10, Vol.18 (20), p.5591-5593

2008

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Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines

European journal of medicinal chemistry, 2011-08, Vol.46 (8), p.3218-3226

2011

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Unique Nanometer-Thick Layered Network

Chemistry letters, 2002-05, Vol.31 (5), p.500-501

2002

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New diarylureas and diarylamides possessing acet(benz)amidophenyl scaffold: Design, synthesis, and antiproliferative activity against melanoma cell line

Bioorganic & medicinal chemistry letters, 2012-05, Vol.22 (9), p.3269-3273

2012

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Structure based design and syntheses of amino-1H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells

Bioorganic & medicinal chemistry, 2011-03, Vol.19 (6), p.1915-1923

2011

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Synthesis and antibacterial activities of novel oxazolidinones having cyclic sulfonamide moieties

Bioorganic & medicinal chemistry letters, 2008-11, Vol.18 (21), p.5815-5818

2008

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Synthesis of pyrrolo[2,3- d]pyrimidine derivatives and their antiproliferative activity against melanoma cell line

Bioorganic & medicinal chemistry letters, 2009-12, Vol.19 (23), p.6538-6543

2009

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1,4-Dihydropyrazolo[4,3-d]imidazole phenyl derivatives: A novel type II Raf kinase inhibitors

Bioorganic & medicinal chemistry letters, 2010-06, Vol.20 (12), p.3805-3808

2010

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Discovery and initial SAR of pyrimidin-4-yl-1H-imidazole derivatives with antiproliferative activity against melanoma cell lines

Bioorganic & medicinal chemistry letters, 2010-03, Vol.20 (5), p.1573-1577

2010

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Development and Therapeutic Potential of NUAKs Inhibitors

Journal of medicinal chemistry, 2021-01, Vol.64 (1), p.2-25

2021

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Synthesis and Biological Activity of New 4-(Pyridin-4-yl)-(3-methoxy-5-methylphenyl)-1H-pyrazoles Derivatives as ROS Receptor Tyrosine Kinase Inhibitors

Bulletin of the Korean Chemical Society, 2012, 33(11), , pp.3629-3634

2012

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Coligand Effects on Bonding Mode. Synthesis and Properties of (Diallylmalonato)platinum(II) Complexes of P vs. N Donating Ligand

Bulletin of the Chemical Society of Japan, 1999-09, Vol.72 (9), p.2091-2096

1999

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Synthesis and in vitro antiproliferative activity of new 1,3,4-oxadiazole derivatives possessing sulfonamide moiety

Novel Quinolinylaminoisoquinoline Bioisosteres of Sorafenib as Selective RAF1 Kinase Inhibitors: Design, Synthesis, and Antiproliferative Activity against Melanoma Cell Line

Synthesis and broad-spectrum antiproliferative activity of diarylamides and diarylureas possessing 1,3,4-oxadiazole derivatives

Structural optimization of imidazothiazole derivatives affords a new promising series as B-Raf V600E inhibitors; synthesis, in vitro assay and in silico screening

Synthesis, in vitro Antiproliferative and Antiinflammatory Activities, and Kinase Inhibitory effects of New 1,3,4-triarylpyrazole Derivatives

Synthesis of New Triarylpyrazole Derivatives Possessing Terminal Sulfonamide Moiety and Their Inhibitory Effects on PGE₂ and Nitric Oxide Productions in Lipopolysaccharide-Induced RAW 264.7 Macrophages

Design, synthesis, in vitro potent antiproliferative activity, and kinase inhibitory effects of new triarylpyrazole derivatives possessing different heterocycle terminal moieties

Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines. Part 2

FMS Kinase Inhibitors: Current Status and Future Prospects

Synthesis and inhibitory effects of triarylpyrazoles on LPS-induced NO and PGE2 productions in RAW 264.7 macrophages

Subtle Ligand/Media Effects. Modulation of cis/trans Isomerism in Hydrogen Peroxide Oxidation of Pt(II) to Pt(IV) Complexes

Comprehensive impurity profiling and quantification of Sudan III dyes by gas chromatography/mass spectrometry

Design, synthesis and biological evaluation of new potent and highly selective ROS1-tyrosine kinase inhibitor

Aminostyrylbenzofuran derivatives as potent inhibitors for Aβ fibril formation

Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines

Unique Nanometer-Thick Layered Network

New diarylureas and diarylamides possessing acet(benz)amidophenyl scaffold: Design, synthesis, and antiproliferative activity against melanoma cell line

Structure based design and syntheses of amino-1H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells

Synthesis and antibacterial activities of novel oxazolidinones having cyclic sulfonamide moieties

Synthesis of pyrrolo[2,3- d]pyrimidine derivatives and their antiproliferative activity against melanoma cell line

1,4-Dihydropyrazolo[4,3-d]imidazole phenyl derivatives: A novel type II Raf kinase inhibitors

Discovery and initial SAR of pyrimidin-4-yl-1H-imidazole derivatives with antiproliferative activity against melanoma cell lines

Development and Therapeutic Potential of NUAKs Inhibitors

Synthesis and Biological Activity of New 4-(Pyridin-4-yl)-(3-methoxy-5-methylphenyl)-1H-pyrazoles Derivatives as ROS Receptor Tyrosine Kinase Inhibitors

Coligand Effects on Bonding Mode. Synthesis and Properties of (Diallylmalonato)platinum(II) Complexes of P vs. N Donating Ligand

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