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Anti-diabetic xanthones from the bark of Garcinia xanthochymus

Bioorganic & medicinal chemistry letters, 2017-08, Vol.27 (15), p.3301-3304

2017

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Triterpenoids from the bark of Entandrophragma angolense

Natural product research, 2023, Vol.37 (2), p.240-247

2023

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Risks of Major Long‐Term Side Effects Associated with Androgen‐Deprivation Therapy in Men with Prostate Cancer

Pharmacotherapy, 2018-10, Vol.38 (10), p.999-1009

2018

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A new 26-norlanostane from Phlogacanthus turgidus growing in Vietnam

Journal of asian natural products research, 2022-02, Vol.24 (2), p.196-202

2022

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Cyclophostin and Cyclipostins analogues, new promising molecules to treat mycobacterial-related diseases

International journal of antimicrobial agents, 2018-04, Vol.51 (4), p.651-654

2018

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Two furanoxanthones from the bark of Cratoxylum cochinchinense

Phytochemistry letters, 2022-10, Vol.51, p.63-66

2022

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Liposomal Sphingomyelin Influences the Cellular Lipid Profile of Human Lymphoblastic Leukemia Cells without Effect on P‑Glycoprotein Activity

Molecular pharmaceutics, 2013-03, Vol.10 (3), p.1020-1034

2013

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Crystal Structures for HIV-1 Reverse Transcriptase in Complexes with Three Pyridinone Derivatives: A New Class of Non-Nucleoside Inhibitors Effective against a Broad Range of Drug-Resistant Strains

Journal of medicinal chemistry, 2005-12, Vol.48 (24), p.7582-7591

2005

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Identification of potential drug name confusion errors in the Sentinel System

Pharmacoepidemiology and drug safety, 2019-10, Vol.28 (10), p.1405-1410

2019

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Cost-Effectiveness of Adding Androgen Deprivation Therapy to Radiation Therapy for Men with Advanced Prostate Cancer from a U.S. Payer's Perspective

Journal of managed care & specialty pharmacy, 2019-02, Vol.25 (2), p.225-234

2019

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Design, Synthesis, and Biological Evaluation of Polyaminocarboxylate Ligand‐Based Theranostic Conjugates for Antibody‐Targeted Cancer Therapy and Near‐Infrared Optical Imaging

ChemMedChem, 2018-12, Vol.13 (24), p.2606-2617

2018

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Design, synthesis, and in vivo activity of novel inhibitors of delta-5 desaturase for the treatment of metabolic syndrome

Bioorganic & medicinal chemistry letters, 2015-09, Vol.25 (18), p.3836-3839

2015

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Retinal Anatomy and Pathology

Developments in ophthalmology, 2016, Vol.55, p.7

2016

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A Potent and Selective AMPK Activator That Inhibits de Novo Lipogenesis

ACS medicinal chemistry letters, 2010-12, Vol.1 (9), p.478-482

2010

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4-Benzyl and 4-Benzoyl-3-dimethylaminopyridin-2(1H)-ones: In Vitro Evaluation of New C-3-Amino-Substituted and C-5,6-Alkyl-Substituted Analogues against Clinically Important HIV Mutant Strains

Journal of medicinal chemistry, 2005-03, Vol.48 (6), p.1948-1964

2005

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Randomised clinical trial: alisporivir combined with peginterferon and ribavirin in treatment‐naïve patients with chronic HCV genotype 1 infection (ESSENTIAL II)

Alimentary pharmacology & therapeutics, 2015-10, Vol.42 (7), p.829-844

2015

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Antithrombin activity of medicinal plants from central Florida

Journal of ethnopharmacology, 2002-07, Vol.81 (2), p.277-280

2002

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Triple-Helix Directed Cleavage of Double-Stranded DNA by Benzoquinoquinoxaline-1,10-phenanthroline Conjugates

Chembiochem : a European journal of chemical biology, 2004-11, Vol.5 (11), p.1550-1557

2004

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Ketorolac amide prodrugs for transdermal delivery: stability and in vitro rat skin permeation studies

International journal of pharmaceutics, 2005-04, Vol.293 (1), p.193-202

2005

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(3R,5S,E)-7-(4-(4-Fluorophenyl)-6-isopropyl-2-(methyl(1-methyl-1H-1,2,4-triazol-5-yl)amino)pyrimidin-5-yl)-3,5-dihydroxyhept-6-enoic Acid (BMS-644950): A Rationally Designed Orally Efficacious 3-Hydroxy-3-methylglutaryl Coenzyme-A Reductase Inhibitor with Reduced Myotoxicity Potential

Journal of medicinal chemistry, 2008-05, Vol.51 (9), p.2722-2733

2008

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3-Iodo-4-phenoxypyridinones (IOPY's), a new family of highly potent non-nucleoside inhibitors of HIV-1 reverse transcriptase

Bioorganic & medicinal chemistry letters, 2003-12, Vol.13 (24), p.4309-4312

2003

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Synthesis and Evaluation of “AZT-HEPT”, “AZT-Pyridinone”, and “ddC-HEPT” Conjugates as Inhibitors of HIV Reverse Transcriptase

Journal of medicinal chemistry, 2000-05, Vol.43 (10), p.1927-1939

2000

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4-Benzyl- and 4-Benzoyl-3-dimethylaminopyridin-2(1H)-ones, a New Family of Potent Anti-HIV Agents: Optimization and in Vitro Evaluation against Clinically Important HIV Mutant Strains

Journal of medicinal chemistry, 2004-10, Vol.47 (22), p.5501-5514

2004

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Benzoindoloquinolines interact with DNA tetraplexes and inhibit telomerase

Bioorganic & medicinal chemistry letters, 2002-04, Vol.12 (7), p.1071-1074

2002

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Optimization of Triple-Helix-Directed DNA Cleavage by Benzoquinoquinoxaline-Ethylenediaminetetraacetic Acid Conjugates

Chembiochem : a European journal of chemical biology, 2003-09, Vol.4 (9), p.856-862

2003

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Anti-diabetic xanthones from the bark of Garcinia xanthochymus

Triterpenoids from the bark of Entandrophragma angolense

Risks of Major Long‐Term Side Effects Associated with Androgen‐Deprivation Therapy in Men with Prostate Cancer

A new 26-norlanostane from Phlogacanthus turgidus growing in Vietnam

Cyclophostin and Cyclipostins analogues, new promising molecules to treat mycobacterial-related diseases

Two furanoxanthones from the bark of Cratoxylum cochinchinense

Liposomal Sphingomyelin Influences the Cellular Lipid Profile of Human Lymphoblastic Leukemia Cells without Effect on P‑Glycoprotein Activity

Crystal Structures for HIV-1 Reverse Transcriptase in Complexes with Three Pyridinone Derivatives: A New Class of Non-Nucleoside Inhibitors Effective against a Broad Range of Drug-Resistant Strains

Identification of potential drug name confusion errors in the Sentinel System

Cost-Effectiveness of Adding Androgen Deprivation Therapy to Radiation Therapy for Men with Advanced Prostate Cancer from a U.S. Payer's Perspective

Design, Synthesis, and Biological Evaluation of Polyaminocarboxylate Ligand‐Based Theranostic Conjugates for Antibody‐Targeted Cancer Therapy and Near‐Infrared Optical Imaging

Design, synthesis, and in vivo activity of novel inhibitors of delta-5 desaturase for the treatment of metabolic syndrome

Retinal Anatomy and Pathology

A Potent and Selective AMPK Activator That Inhibits de Novo Lipogenesis

4-Benzyl and 4-Benzoyl-3-dimethylaminopyridin-2(1H)-ones: In Vitro Evaluation of New C-3-Amino-Substituted and C-5,6-Alkyl-Substituted Analogues against Clinically Important HIV Mutant Strains

Randomised clinical trial: alisporivir combined with peginterferon and ribavirin in treatment‐naïve patients with chronic HCV genotype 1 infection (ESSENTIAL II)

Antithrombin activity of medicinal plants from central Florida

Triple-Helix Directed Cleavage of Double-Stranded DNA by Benzoquinoquinoxaline-1,10-phenanthroline Conjugates

Ketorolac amide prodrugs for transdermal delivery: stability and in vitro rat skin permeation studies

(3R,5S,E)-7-(4-(4-Fluorophenyl)-6-isopropyl-2-(methyl(1-methyl-1H-1,2,4-triazol-5-yl)amino)pyrimidin-5-yl)-3,5-dihydroxyhept-6-enoic Acid (BMS-644950): A Rationally Designed Orally Efficacious 3-Hydroxy-3-methylglutaryl Coenzyme-A Reductase Inhibitor with Reduced Myotoxicity Potential

3-Iodo-4-phenoxypyridinones (IOPY's), a new family of highly potent non-nucleoside inhibitors of HIV-1 reverse transcriptase

Synthesis and Evaluation of “AZT-HEPT”, “AZT-Pyridinone”, and “ddC-HEPT” Conjugates as Inhibitors of HIV Reverse Transcriptase

4-Benzyl- and 4-Benzoyl-3-dimethylaminopyridin-2(1H)-ones, a New Family of Potent Anti-HIV Agents: Optimization and in Vitro Evaluation against Clinically Important HIV Mutant Strains

Benzoindoloquinolines interact with DNA tetraplexes and inhibit telomerase

Optimization of Triple-Helix-Directed DNA Cleavage by Benzoquinoquinoxaline-Ethylenediaminetetraacetic Acid Conjugates

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