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2-[(4,6-Diaminopyrimidin-2-yl)sulfanyl]- N -(4-methoxyphenyl)acetamide

IUCrData, 2018-04, Vol.3 (4), p.x180600, Article x180600

2018

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Bioactive phenylpropanoid analogues from Piper betle L. var. birkoli leaves

Natural product research, 2017-11, Vol.31 (22), p.2604-2611

2017

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ChemInform Abstract: Progress and Prospects on DENV Protease Inhibitors

ChemInform, 2016-06, Vol.47 (27), p.no-no

2016

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Chikungunya epidemiological survey and Current available inhibitors

Journal of Pharmaceutical Chemistry, 2014-10, Vol.1 (3), p.59-67

2014

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Chiral HPLC Method for the Novel Triazole Antitubercular Compound MSDRT 12

Chromatographia, 2014, Vol.77 (5-6), p.511-516

2014

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Cink4T, a quinazolinone-based dual inhibitor of Cdk4 and tubulin polymerization, identified via ligand-based virtual screening, for efficient anticancer therapy

European journal of medicinal chemistry, 2019-03, Vol.165, p.115-132

2019

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Comparative Computational Studies on Selective CytochromeP450 1B1 Inhibitors

Bioautomation, 2020-09, Vol.24 (3), p.213-224

2020

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Comparative Shape and Electrostatic Study of Highly Potent and Selective CYP1B1 Inhibitor: Assessment of Active Site of CYP1B1 by Binding Mode Analysis Using Site Map Tool

Indian journal of pharmaceutical education & research, 2018-01, Vol.52 (1), p.159-165

2018

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Computer-Aided Structure Based Drug Design Approaches for the Discovery of New Anti-CHIKV Agents

Current computer-aided drug design, 2017-12, Vol.13 (4), p.346

2017

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A Critical Observation on the Design and Development of Reported Peptide Inhibitors of DENV NS2B-NS3 Protease in the Last Two Decades

Mini reviews in medicinal chemistry, 2022-01, Vol.22 (8), p.1108-1130

2022

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Crystal structures and Hirshfeld surface analyses of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(pyridin-2-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(pyrazin-2-yl)acetamide

Acta crystallographica. Section E, Crystallographic communications, 2018-05, Vol.74 (Pt 5), p.718-723

2018

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Crystal structures of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(2,4-di-methyl-phen-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(3-meth-oxy-phen-yl)acetamide

Acta crystallographica. Section E, Crystallographic communications, 2017-07, Vol.73 (Pt 7), p.996-1000

2017

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Crystal structures of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(naphthalen-1-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(4-fluoro-phen-yl)acetamide

Acta crystallographica. Section E, Crystallographic communications, 2017-02, Vol.73 (Pt 2), p.306-309

2017

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Crystal structures of N -(4-chloro-phen-yl)-2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]acetamide and N -(3-chloro-phen-yl)-2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]acetamide

Acta crystallographica. Section E, Crystallographic communications, 2017-04, Vol.73 (Pt 4), p.467-471

2017

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Design, synthesis and anticancer activity of piperazine hydroxamates and their histone deacetylase (HDAC) inhibitory activity

Bioorganic & medicinal chemistry letters, 2010-07, Vol.20 (13), p.3906-3910

2010

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Design, synthesis and MAO inhibitory activity of 2-（arylmethylidene）-2,3-dihydro-1-benzofuran-3-one derivatives

中国化学快报：英文版, 2017, Vol.28 (7), p.1528-1532

Vishnu Nayak Badavath Chandrani Nath Narayana Murthy Ganta Gulberk Ucar Barij Nayan Sinha Venkatesan Jayaprakash

2017

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Design, synthesis and MAO inhibitory activity of 2-(arylmethylidene)-2,3-dihydro-1-benzofuran-3-one derivatives

Chinese chemical letters, 2017-07, Vol.28 (7), p.1528-1532

2017

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Design, synthesis, optimization and antiviral activity of a class of hybrid dengue virus E protein inhibitors

Bioorganic & medicinal chemistry letters, 2015-04, Vol.25 (8), p.1747-1752

2015

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Development of selective and reversible pyrazoline based MAO-A inhibitors: Synthesis, biological evaluation and docking studies

Bioorganic & medicinal chemistry, 2010-03, Vol.18 (5), p.1875-1881

2010

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Effect of substitution at N″-position of N′-hydroxy-N-amino guanidines on tumor cell growth

Bioorganic & medicinal chemistry letters, 2012-08, Vol.22 (15), p.4934-4938

2012

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Ficus religiosa L. bark extracts inhibit human rhinovirus and respiratory syncytial virus infection in vitro

Journal of ethnopharmacology, 2015-12, Vol.176, p.252-257

2015

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Fragment and knowledge-based design of selective GSK-3β inhibitors using virtual screening models

European journal of medicinal chemistry, 2009-06, Vol.44 (6), p.2361-2371

2009

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Fragment and knowledge-based design of selective GSK-3beta inhibitors using virtual screening models

European journal of medicinal chemistry, 2009-06, Vol.44 (6), p.2361-2371

2009

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Histone deacetylase inhibitors: a review on class-I specific inhibition

Mini reviews in medicinal chemistry, 2015-01, Vol.15 (9), p.731-750

2015

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Identification of Dengue NS2B-NS3 Protease Inhibitors Through High-Throughput Virtual Screening—Impacts on Drug Development Against the Dengue Virus

Human Viruses: Diseases, Treatments and Vaccines, 2021, p.93-120

2021

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2-[(4,6-Diaminopyrimidin-2-yl)sulfanyl]- N -(4-methoxyphenyl)acetamide

Bioactive phenylpropanoid analogues from Piper betle L. var. birkoli leaves

ChemInform Abstract: Progress and Prospects on DENV Protease Inhibitors

Chikungunya epidemiological survey and Current available inhibitors

Chiral HPLC Method for the Novel Triazole Antitubercular Compound MSDRT 12

Cink4T, a quinazolinone-based dual inhibitor of Cdk4 and tubulin polymerization, identified via ligand-based virtual screening, for efficient anticancer therapy

Comparative Computational Studies on Selective CytochromeP450 1B1 Inhibitors

Comparative Shape and Electrostatic Study of Highly Potent and Selective CYP1B1 Inhibitor: Assessment of Active Site of CYP1B1 by Binding Mode Analysis Using Site Map Tool

Computer-Aided Structure Based Drug Design Approaches for the Discovery of New Anti-CHIKV Agents

A Critical Observation on the Design and Development of Reported Peptide Inhibitors of DENV NS2B-NS3 Protease in the Last Two Decades

Crystal structures and Hirshfeld surface analyses of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(pyridin-2-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(pyrazin-2-yl)acetamide

Crystal structures of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(2,4-di-methyl-phen-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(3-meth-oxy-phen-yl)acetamide

Crystal structures of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(naphthalen-1-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(4-fluoro-phen-yl)acetamide

Crystal structures of N -(4-chloro-phen-yl)-2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]acetamide and N -(3-chloro-phen-yl)-2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]acetamide

Design, synthesis and anticancer activity of piperazine hydroxamates and their histone deacetylase (HDAC) inhibitory activity

Design, synthesis and MAO inhibitory activity of 2-（arylmethylidene）-2,3-dihydro-1-benzofuran-3-one derivatives

Design, synthesis and MAO inhibitory activity of 2-(arylmethylidene)-2,3-dihydro-1-benzofuran-3-one derivatives

Design, synthesis, optimization and antiviral activity of a class of hybrid dengue virus E protein inhibitors

Development of selective and reversible pyrazoline based MAO-A inhibitors: Synthesis, biological evaluation and docking studies

Effect of substitution at N″-position of N′-hydroxy-N-amino guanidines on tumor cell growth

Ficus religiosa L. bark extracts inhibit human rhinovirus and respiratory syncytial virus infection in vitro

Fragment and knowledge-based design of selective GSK-3β inhibitors using virtual screening models

Fragment and knowledge-based design of selective GSK-3beta inhibitors using virtual screening models

Histone deacetylase inhibitors: a review on class-I specific inhibition

Identification of Dengue NS2B-NS3 Protease Inhibitors Through High-Throughput Virtual Screening—Impacts on Drug Development Against the Dengue Virus

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