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Getting physical in drug discovery II: the impact of chromatographic hydrophobicity measurements and aromaticity

Drug discovery today, 2011-09, Vol.16 (17), p.822-830

2011

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Getting physical in drug discovery: a contemporary perspective on solubility and hydrophobicity

Drug discovery today, 2010-08, Vol.15 (15), p.648-655

2010

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Development of GSK's acid and base selection guides

Green chemistry : an international journal and green chemistry resource : GC, 2015-02, Vol.17 (2), p.945-949

2015

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Use of Calculated Physicochemical Properties to Enhance Quantitative Response When Using Charged Aerosol Detection

Analytical chemistry (Washington), 2017-02, Vol.89 (3), p.1772-1777

2017

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Retention of Ionizable Compounds on HPLC. 8. Influence of Mobile-Phase pH Change on the Chromatographic Retention of Acids and Bases during Gradient Elution

Analytical chemistry (Washington), 2001-10, Vol.73 (20), p.4937-4945

2001

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Estimating Unbound Volume of Distribution and Tissue Binding by In Vitro HPLC-Based Human Serum Albumin and Immobilised Artificial Membrane-Binding Measurements

Journal of pharmaceutical sciences, 2011-03, Vol.100 (3), p.849-862

2011

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Synthesis and Structure–Activity Relationships of Indazole Arylsulfonamides as Allosteric CC-Chemokine Receptor 4 (CCR4) Antagonists

Journal of medicinal chemistry, 2013-03, Vol.56 (5), p.1946-1960

2013

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Dimeric Zanamivir Conjugates with Various Linking Groups Are Potent, Long-Lasting Inhibitors of Influenza Neuraminidase Including H5N1 Avian Influenza

Journal of medicinal chemistry, 2005-04, Vol.48 (8), p.2964-2971

2005

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Discovery of 4-[3-(trans-3-Dimethylaminocyclobutyl)-1H-indol-5-ylmethyl]- (4S)-oxazolidin-2-one (4991W93), a 5HT1B/1D Receptor Partial Agonist and a Potent Inhibitor of Electrically Induced Plasma Extravasation

Journal of medicinal chemistry, 2001-03, Vol.44 (5), p.681-693

2001

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Identification of GSK3186899/DDD853651 as a Preclinical Development Candidate for the Treatment of Visceral Leishmaniasis

Journal of medicinal chemistry, 2019-02, Vol.62 (3), p.1180-1202

2019

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Computer-Aided Design and Synthesis of 5-Substituted Tryptamines and Their Pharmacology at the 5-HT1D Receptor: Discovery of Compounds with Potential Anti-Migraine Properties

Journal of medicinal chemistry, 1995-09, Vol.38 (18), p.3566-3580

1995

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Development of GSK's acid and base selection guidesElectronic supplementary information (ESI) available. See DOI: 10.1039/c4gc01481b

2015-02

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Inotropic 'A' ring substituted sulmazole and isomazole analogs

Journal of medicinal chemistry, 1990-08, Vol.33 (8), p.2231-2239

1990

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Discovery of 4-[3-( trans -3-Dimethylaminocyclobutyl)-1 H -indol-5-ylmethyl]- (4 S )-oxazolidin-2-one (4991W93), a 5HT 1B/1D Receptor Partial Agonist and a Potent Inhibitor of Electrically Induced Plasma Extravasation

Journal of medicinal chemistry, 2001-03, Vol.44 (5), p.681-693

2001

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Cardiotonic 'C' Ring Modified Isomazole Analogues

Archiv der Pharmazie (Weinheim), 1990, Vol.323 (8), p.507-512

1990

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Principles of Method Selection in Partition Studies

Quantitative structure-activity relationships, 1989, Vol.8 (4), p.288-296

1989

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A new Method for the Calculation of Partition Coefficients from Experimental Data for Both Mixtures and Pure Compounds

Quantitative structure-activity relationships, 1992, Vol.11 (4), p.505-509

1992

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Description and evaluation of the UKCA stratosphere–troposphere chemistry scheme (StratTrop vn 1.0) implemented in UKESM1

Geoscientific Model Development, 2020-03, Vol.13 (3), p.1223-1266

2020

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Treatment of Subclinical Hypothyroidism or Hypothyroxinemia in Pregnancy

The New England journal of medicine, 2017-03, Vol.376 (9), p.815-825

2017

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Labor Induction versus Expectant Management in Low-Risk Nulliparous Women

The New England journal of medicine, 2018-08, Vol.379 (6), p.513-523

2018

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Prediction of DNA Repair Inhibitor Response in Short-Term Patient-Derived Ovarian Cancer Organoids

Cancer discovery, 2018-11, Vol.8 (11), p.1404-1421

2018

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Enhanced stability of tristetraprolin mRNA protects mice against immune-mediated inflammatory pathologies

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (7), p.1865-1870

2016

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Antenatal Betamethasone for Women at Risk for Late Preterm Delivery

The New England journal of medicine, 2016-04, Vol.374 (14), p.1311-1320

2016

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Metabolomic analysis of pressure-overloaded and infarcted mouse hearts

Circulation. Heart failure, 2014-07, Vol.7 (4), p.634-642

2014

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Getting physical in drug discovery II: the impact of chromatographic hydrophobicity measurements and aromaticity

Getting physical in drug discovery: a contemporary perspective on solubility and hydrophobicity

Development of GSK's acid and base selection guides

Use of Calculated Physicochemical Properties to Enhance Quantitative Response When Using Charged Aerosol Detection

Retention of Ionizable Compounds on HPLC. 8. Influence of Mobile-Phase pH Change on the Chromatographic Retention of Acids and Bases during Gradient Elution

Discovery and Optimization of 5‑Amino-1,2,3-triazole-4-carboxamide Series against Trypanosoma cruzi

Estimating Unbound Volume of Distribution and Tissue Binding by In Vitro HPLC-Based Human Serum Albumin and Immobilised Artificial Membrane-Binding Measurements

Synthesis and Structure–Activity Relationships of Indazole Arylsulfonamides as Allosteric CC-Chemokine Receptor 4 (CCR4) Antagonists

Dimeric Zanamivir Conjugates with Various Linking Groups Are Potent, Long-Lasting Inhibitors of Influenza Neuraminidase Including H5N1 Avian Influenza

Discovery of 4-[3-(trans-3-Dimethylaminocyclobutyl)-1H-indol-5-ylmethyl]- (4S)-oxazolidin-2-one (4991W93), a 5HT1B/1D Receptor Partial Agonist and a Potent Inhibitor of Electrically Induced Plasma Extravasation

Identification of GSK3186899/DDD853651 as a Preclinical Development Candidate for the Treatment of Visceral Leishmaniasis

Computer-Aided Design and Synthesis of 5-Substituted Tryptamines and Their Pharmacology at the 5-HT1D Receptor: Discovery of Compounds with Potential Anti-Migraine Properties

Development of GSK's acid and base selection guidesElectronic supplementary information (ESI) available. See DOI: 10.1039/c4gc01481b

Inotropic 'A' ring substituted sulmazole and isomazole analogs

Discovery of 4-[3-( trans -3-Dimethylaminocyclobutyl)-1 H -indol-5-ylmethyl]- (4 S )-oxazolidin-2-one (4991W93), a 5HT 1B/1D Receptor Partial Agonist and a Potent Inhibitor of Electrically Induced Plasma Extravasation

Cardiotonic 'C' Ring Modified Isomazole Analogues

Principles of Method Selection in Partition Studies

A new Method for the Calculation of Partition Coefficients from Experimental Data for Both Mixtures and Pure Compounds

Description and evaluation of the UKCA stratosphere–troposphere chemistry scheme (StratTrop vn 1.0) implemented in UKESM1

Treatment of Subclinical Hypothyroidism or Hypothyroxinemia in Pregnancy

Labor Induction versus Expectant Management in Low-Risk Nulliparous Women

Prediction of DNA Repair Inhibitor Response in Short-Term Patient-Derived Ovarian Cancer Organoids

Enhanced stability of tristetraprolin mRNA protects mice against immune-mediated inflammatory pathologies

Antenatal Betamethasone for Women at Risk for Late Preterm Delivery

Metabolomic analysis of pressure-overloaded and infarcted mouse hearts

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