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Synthesis of 3(N(1,3dioxo 1H Benzo[de]isoquinolin-2(3h)-Yl)alkyl)-2-(4-Substituted) Phenylthiazolidine-4-Carboxylic Acid

Chemical Science Transactions

2016

English

Antiproliferative Benzoindazolequinones as Potential Cyclooxygenase-2 Inhibitors

Theoretical Chemistry

Pharmaceutical Science

English

2-Guanidinoquinazolines as New Inhibitors of the STAT3 Pathway

Bioorganic and Medicinal Chemistry Letters

Clinical Biochemistry

Pharmaceutical Science

Drug Discovery

2014

English

Synthesis, Spectral Analysis and Antibacterial Evaluation of 5-Substituted-1,3,4-Oxadiazol-2-Yl 4-(4-Methylpiperidin-1-Ylsulfonyl)benzyl Sulfides

Journal of the Chilean Chemical Society

Chemistry

2017

English

Antifungal Styryloquinolines as Candida Albicans Efflux Pump Inhibitors: Styryloquinolines Are ABC Transporter Inhibitors

Theoretical Chemistry

Pharmaceutical Science

English

Synthesis of Structurally Diverse N-Substituted Quaternary Carbon Containing Small Molecules From Α,α-Disubstituted Propargyl Amino Esters

Chemistry - A European Journal

English

Clinical Impact of Checkpoint Inhibitors as Novel Cancer Therapies

Drugs

Pharmacology

2014

English

Figure 2: Outline for the Synthesis of Different N-Substituted Derivatives, 5a–j, of N-(4-Methoxyphenethyl)-4-Methylbenzensulfonamide (3).

English

Amino Acid Sequence Elucidation of Human Acrosin-Trypsin Inhibitor (HUSI-II) Reveals That Kazal-Type Proteinase Inhibitors Are Structurally Related to Β-Subunits of Glycoprotein Hormones

English

Molecular Docking Studies of Arbutin Derivatives as Tyrosinase Inhibitors

International Journal of Bioscience, Biochemistry and Bioinformatics

2019

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Synthesis of 3(N(1,3dioxo 1H Benzo[de]isoquinolin-2(3h)-Yl)alkyl)-2-(4-Substituted) Phenylthiazolidine-4-Carboxylic Acid

Antiproliferative Benzoindazolequinones as Potential Cyclooxygenase-2 Inhibitors

2-Guanidinoquinazolines as New Inhibitors of the STAT3 Pathway

Synthesis, Spectral Analysis and Antibacterial Evaluation of 5-Substituted-1,3,4-Oxadiazol-2-Yl 4-(4-Methylpiperidin-1-Ylsulfonyl)benzyl Sulfides

Antifungal Styryloquinolines as Candida Albicans Efflux Pump Inhibitors: Styryloquinolines Are ABC Transporter Inhibitors

Synthesis of Structurally Diverse N-Substituted Quaternary Carbon Containing Small Molecules From Α,α-Disubstituted Propargyl Amino Esters

Clinical Impact of Checkpoint Inhibitors as Novel Cancer Therapies

Figure 2: Outline for the Synthesis of Different N-Substituted Derivatives, 5a–j, of N-(4-Methoxyphenethyl)-4-Methylbenzensulfonamide (3).

Amino Acid Sequence Elucidation of Human Acrosin-Trypsin Inhibitor (HUSI-II) Reveals That Kazal-Type Proteinase Inhibitors Are Structurally Related to Β-Subunits of Glycoprotein Hormones

Molecular Docking Studies of Arbutin Derivatives as Tyrosinase Inhibitors