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5-Aminoisoquinolin-1-one (5-AIQ), a Water-Soluble Inhibitor of the Poly(ADP-Ribose)Polymerases (PARPs)

Current medicinal chemistry, 2015-01, Vol.22 (33), p.3807

Threadgill, Michael D

2015

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Structure-activity relationships of 2-arylquinazolin-4-ones as highly selective and potent inhibitors of the tankyrases

European journal of medicinal chemistry, 2016-08, Vol.118, p.316-327

2016

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A neoclerodane orthoester and other new neoclerodane diterpenoids from Teucrium yemense chemistry and effect on secretion of insulin

Scientific reports, 2021-04, Vol.11 (1), p.8074-8074, Article 8074

2021

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Design, Synthesis, and Evaluation in Vitro of Quinoline-8-carboxamides, a New Class of Poly(adenosine-diphosphate-ribose)polymerase-1 (PARP-1) Inhibitor

Journal of medicinal chemistry, 2009-02, Vol.52 (3), p.868-877

2009

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Design and Discovery of 2‑Arylquinazolin-4-ones as Potent and Selective Inhibitors of Tankyrases

ACS medicinal chemistry letters, 2013-12, Vol.4 (12), p.1173-1177

2013

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Chemopreventive Efficacy and Pharmacokinetics of Curcumin in the Min/+ Mouse, a Model of Familial Adenomatous Polyposis

Cancer epidemiology, biomarkers & prevention, 2002-06, Vol.11 (6), p.535-540

2002

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Macrolides from rare actinomycetes: Structures and bioactivities

International journal of antimicrobial agents, 2022-02, Vol.59 (2), p.106523-106523, Article 106523

2022

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25th Conference of GP2A

Pharmaceuticals (Basel, Switzerland), 2017-12, Vol.10 (4), p.97

2017

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Racemases and epimerases operating through a 1,1-proton transfer mechanism: reactivity, mechanism and inhibition

Chemical Society reviews, 2021-05, Vol.5 (1), p.5952-5984

2021

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Observation by NMR of cationic Wheland-like intermediates in the deiodination of protected 1-iodonaphthalene-2,4-diamines in acidic media

Organic & biomolecular chemistry, 2013-09, Vol.11 (36), p.6208-6214

2013

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Thiourea-functionalized aminoglutethimide derivatives as anti-leishmanial agents

Future medicinal chemistry, 2024-07, p.1-13

2024

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Derivatives of a PARP Inhibitor TIQ-A through the Synthesis of 8-Alkoxythieno[2,3- c ]isoquinolin-5(4 H )-ones

ACS omega, 2020-06, Vol.5 (22), p.13447-13453

2020

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Isolation, identification and quantitation of hydroxycinnamic acid conjugates, potential platform chemicals, in the leaves and stems of Miscanthus x giganteus using LC-ESI-MSn

Phytochemistry (Oxford), 2011-12, Vol.72 (18), p.2376-2384

2011

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Structure-based design, synthesis and preliminary evaluation of selective inhibitors of dihydrofolate reductase from Mycobacterium tuberculosis

Bioorganic & medicinal chemistry, 2007-07, Vol.15 (13), p.4552-4576

2007

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Poly(ADP-ribose)polymerase inhibition - where now?

Current medicinal chemistry, 2005-01, Vol.12 (20), p.2373

2005

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Correction to “Compounds Related to Saudin and Three New Series of Diterpenoids from Clutia lanceolata”

Journal of natural products (Washington, D.C.), 2023-10, Vol.86 (10), p.2421-2422

2023

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Compounds Related to Saudin and Three New Series of Diterpenoids from Clutia lanceolata

Journal of natural products (Washington, D.C.), 2023-05, Vol.86 (5), p.1129-1149

2023

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Oxidative Phenols in Forage Crops Containing Polyphenol Oxidase Enzymes

Journal of agricultural and food chemistry, 2010-02, Vol.58 (3), p.1371-1382

2010

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Highly Potent and Isoform Selective Dual Site Binding Tankyrase/Wnt Signaling Inhibitors That Increase Cellular Glucose Uptake and Have Antiproliferative Activity

Journal of medicinal chemistry, 2017-01, Vol.60 (2), p.814-820

2017

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Inhibitors of poly(ADP-ribose) polymerase modulate signal transduction pathways and secondary damage in experimental spinal cord trauma

The Journal of pharmacology and experimental therapeutics, 2005-02, Vol.312 (2), p.449

2005

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Two-Step Synthesis of Paracetamol (Acetaminophen), a Practical Illustration of Carbonyl Reactivity for Year-One Biosciences Students

Journal of chemical education, 2023-10, Vol.100 (10), p.3955-3959

2023

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New flavonoids from the Saudi Arabian plant Retama raetam which stimulates secretion of insulin and inhibits α-glucosidase

Organic & biomolecular chemistry, 2019-01, Vol.17 (5), p.1266-1276

2019

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α-Methylacyl-CoA racemase (AMACR): Metabolic enzyme, drug metabolizer and cancer marker P504S

Progress in lipid research, 2013-04, Vol.52 (2), p.220-230

2013

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A novel colorimetric assay for α-methylacyl-CoA racemase 1A (AMACR; P504S) utilizing the elimination of 2,4-dinitrophenolate

Chemical communications (Cambridge, England), 2017-05, Vol.53 (37), p.5087-5090

2017

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Structure-based design, synthesis and evaluation in vitro of arylnaphthyridinones, arylpyridopyrimidinones and their tetrahydro derivatives as inhibitors of the tankyrases

Bioorganic & medicinal chemistry, 2015-07, Vol.23 (13), p.3013-3032

2015

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5-Aminoisoquinolin-1-one (5-AIQ), a Water-Soluble Inhibitor of the Poly(ADP-Ribose)Polymerases (PARPs)

Structure-activity relationships of 2-arylquinazolin-4-ones as highly selective and potent inhibitors of the tankyrases

A neoclerodane orthoester and other new neoclerodane diterpenoids from Teucrium yemense chemistry and effect on secretion of insulin

Design, Synthesis, and Evaluation in Vitro of Quinoline-8-carboxamides, a New Class of Poly(adenosine-diphosphate-ribose)polymerase-1 (PARP-1) Inhibitor

Design and Discovery of 2‑Arylquinazolin-4-ones as Potent and Selective Inhibitors of Tankyrases

Chemopreventive Efficacy and Pharmacokinetics of Curcumin in the Min/+ Mouse, a Model of Familial Adenomatous Polyposis

Macrolides from rare actinomycetes: Structures and bioactivities

25th Conference of GP2A

Racemases and epimerases operating through a 1,1-proton transfer mechanism: reactivity, mechanism and inhibition

Observation by NMR of cationic Wheland-like intermediates in the deiodination of protected 1-iodonaphthalene-2,4-diamines in acidic media

Thiourea-functionalized aminoglutethimide derivatives as anti-leishmanial agents

Derivatives of a PARP Inhibitor TIQ-A through the Synthesis of 8-Alkoxythieno[2,3- c ]isoquinolin-5(4 H )-ones

Isolation, identification and quantitation of hydroxycinnamic acid conjugates, potential platform chemicals, in the leaves and stems of Miscanthus x giganteus using LC-ESI-MSn

Structure-based design, synthesis and preliminary evaluation of selective inhibitors of dihydrofolate reductase from Mycobacterium tuberculosis

Poly(ADP-ribose)polymerase inhibition - where now?

Correction to “Compounds Related to Saudin and Three New Series of Diterpenoids from Clutia lanceolata”

Compounds Related to Saudin and Three New Series of Diterpenoids from Clutia lanceolata

Oxidative Phenols in Forage Crops Containing Polyphenol Oxidase Enzymes

Highly Potent and Isoform Selective Dual Site Binding Tankyrase/Wnt Signaling Inhibitors That Increase Cellular Glucose Uptake and Have Antiproliferative Activity

Inhibitors of poly(ADP-ribose) polymerase modulate signal transduction pathways and secondary damage in experimental spinal cord trauma

Two-Step Synthesis of Paracetamol (Acetaminophen), a Practical Illustration of Carbonyl Reactivity for Year-One Biosciences Students

New flavonoids from the Saudi Arabian plant Retama raetam which stimulates secretion of insulin and inhibits α-glucosidase

α-Methylacyl-CoA racemase (AMACR): Metabolic enzyme, drug metabolizer and cancer marker P504S

A novel colorimetric assay for α-methylacyl-CoA racemase 1A (AMACR; P504S) utilizing the elimination of 2,4-dinitrophenolate

Structure-based design, synthesis and evaluation in vitro of arylnaphthyridinones, arylpyridopyrimidinones and their tetrahydro derivatives as inhibitors of the tankyrases

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