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The Chemical Basis of Serine Palmitoyltransferase Inhibition by Myriocin

Journal of the American Chemical Society, 2013-09, Vol.135 (38), p.14276-14285

2013

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A Residue-Resolved Bayesian Approach to Quantitative Interpretation of Hydrogen–Deuterium Exchange from Mass Spectrometry: Application to Characterizing Protein–Ligand Interactions

The journal of physical chemistry. B, 2017-04, Vol.121 (15), p.3493-3501

2017

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5-(4-Chlorophenyl)-4-methyl-3-(1-(2- phenylethyl)piperidin-4-yl)isoxazole: A Potent, Selective Antagonist at Human Cloned Dopamine D4 Receptors

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.1943-1945

1996

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Selection of heterocycles for drug design

Journal of molecular graphics & modelling, 2004-09, Vol.23 (1), p.51-58

2004

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Identification of a Novel, Selective GABAA α5 Receptor Inverse Agonist Which Enhances Cognition

Journal of medicinal chemistry, 2003-05, Vol.46 (11), p.2227-2240

2003

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N-Arylsulfonylindole Derivatives as Serotonin 5-HT6 Receptor Ligands

Journal of medicinal chemistry, 2001-11, Vol.44 (23), p.3881-3895

2001

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Controlled Modification of Acidity in Cholecystokinin B Receptor Antagonists: N-(1,4-Benzodiazepin-3-yl)-N ‘-[3-(tetrazol-5-ylamino)phenyl]ureas

Journal of medicinal chemistry, 1996-02, Vol.39 (4), p.842-849

1996

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A method for including protein flexibility in protein-ligand docking: improving tools for database mining and virtual screening

Journal of molecular graphics & modelling, 2000-06, Vol.18 (3), p.247-257

Broughton, Howard B.

2000

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Molecular binding interactions: their estimation and rationalization in QSARs in terms of theoretically derived parameters

TheScientificWorld, 2002, Vol.2, p.1776-1660

2002

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Fluorination of 3-(3-(Piperidin-1-yl)propyl)indoles and 3-(3-(Piperazin-1-yl)propyl)indoles Gives Selective Human 5-HT1D Receptor Ligands with Improved Pharmacokinetic Profiles

Journal of medicinal chemistry, 1999-06, Vol.42 (12), p.2087-2104

1999

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3-[[4-(4-Chlorophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine: An Antagonist with High Affinity and Selectivity for the Human Dopamine D4 Receptor

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.1941-1942

1996

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Stereocontrolled Synthesis of Cyclopropanol Amino Acids from Allylic Sulfones: Conformationally Restricted Building Blocks

Organic letters, 2003-10, Vol.5 (20), p.3687-3690

2003

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6,7-Dihydro-2-benzothiophen-4(5H)-ones: A Novel Class of GABA-A α5 Receptor Inverse Agonists

Journal of medicinal chemistry, 2002-03, Vol.45 (6), p.1176-1179

2002

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Chemistry of Epoxysulfones: Straightforward Synthesis of Versatile Chiral Building Blocks

Organic letters, 2003-11, Vol.5 (23), p.4361-4364

2003

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New Selective Cytotoxic Diterpenylquinones and Diterpenylhydroquinones

Journal of medicinal chemistry, 2001-04, Vol.44 (8), p.1257-1267

2001

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Structure and mechanism of inositol monophosphatase

FEBS Letters, 1995-03, Vol.361 (1), p.1-7

1995

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4-Heterocyclylpiperidines as Selective High-Affinity Ligands at the Human Dopamine D4 Receptor

Journal of medicinal chemistry, 1997-07, Vol.40 (15), p.2374-2385

1997

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Development of Peptide 3D Structure Mimetics: Rational Design of Novel Peptoid Cholecystokinin Receptor Antagonists

Journal of medicinal chemistry, 2000-09, Vol.43 (19), p.3505-3517

2000

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3-[3-(Piperidin-1-yl)propyl]indoles as Highly Selective h5-HT1D Receptor Agonists

Journal of medicinal chemistry, 1999-12, Vol.42 (24), p.4981-5001

1999

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Molecular modeling

Current opinion in chemical biology, 1997-10, Vol.1 (3), p.392-398

Broughton, Howard B

1997

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5-(Piperidin-2-yl)- and 5-(Homopiperidin-2-yl)-1,4-benzodiazepines: High-Affinity, Basic Ligands for the Cholecystokinin-B Receptor

Journal of medicinal chemistry, 1997-08, Vol.40 (16), p.2491-2501

1997

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Synthesis of 2-Amino-5-arylthiazoles by Palladium-Catalyzed Arylation at the C5 Position with Aryl Iodides

Synlett, 2007-12, Vol.2007 (19), p.2957-2960

2007

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The Synthesis of Azadirachtin: A Potent Insect Antifeedant

Chemistry : a European journal, 2008-11, Vol.14 (34), p.10683-10704

2008

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A new class of chiral pyrrolidine for asymmetric Michael addition reactions. New mechanism via simple 4+2 type attack of the enamine on the trans-nitrostyrene

Tetrahedron, 2007-01, Vol.63 (3), p.740-747

2007

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The Chemical Basis of Serine Palmitoyltransferase Inhibition by Myriocin

A Residue-Resolved Bayesian Approach to Quantitative Interpretation of Hydrogen–Deuterium Exchange from Mass Spectrometry: Application to Characterizing Protein–Ligand Interactions

Defining Target Engagement Required for Efficacy In Vivo at the Retinoic Acid Receptor-Related Orphan Receptor C2 (RORγt)

5-(4-Chlorophenyl)-4-methyl-3-(1-(2- phenylethyl)piperidin-4-yl)isoxazole: A Potent, Selective Antagonist at Human Cloned Dopamine D4 Receptors

Selection of heterocycles for drug design

Identification of a Novel, Selective GABAA α5 Receptor Inverse Agonist Which Enhances Cognition

N-Arylsulfonylindole Derivatives as Serotonin 5-HT6 Receptor Ligands

Controlled Modification of Acidity in Cholecystokinin B Receptor Antagonists: N-(1,4-Benzodiazepin-3-yl)-N ‘-[3-(tetrazol-5-ylamino)phenyl]ureas

A method for including protein flexibility in protein-ligand docking: improving tools for database mining and virtual screening

Molecular binding interactions: their estimation and rationalization in QSARs in terms of theoretically derived parameters

Fluorination of 3-(3-(Piperidin-1-yl)propyl)indoles and 3-(3-(Piperazin-1-yl)propyl)indoles Gives Selective Human 5-HT1D Receptor Ligands with Improved Pharmacokinetic Profiles

3-[[4-(4-Chlorophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine: An Antagonist with High Affinity and Selectivity for the Human Dopamine D4 Receptor

Stereocontrolled Synthesis of Cyclopropanol Amino Acids from Allylic Sulfones: Conformationally Restricted Building Blocks

6,7-Dihydro-2-benzothiophen-4(5H)-ones: A Novel Class of GABA-A α5 Receptor Inverse Agonists

Chemistry of Epoxysulfones: Straightforward Synthesis of Versatile Chiral Building Blocks

New Selective Cytotoxic Diterpenylquinones and Diterpenylhydroquinones

Structure and mechanism of inositol monophosphatase

4-Heterocyclylpiperidines as Selective High-Affinity Ligands at the Human Dopamine D4 Receptor

Development of Peptide 3D Structure Mimetics: Rational Design of Novel Peptoid Cholecystokinin Receptor Antagonists

3-[3-(Piperidin-1-yl)propyl]indoles as Highly Selective h5-HT1D Receptor Agonists

Molecular modeling

5-(Piperidin-2-yl)- and 5-(Homopiperidin-2-yl)-1,4-benzodiazepines: High-Affinity, Basic Ligands for the Cholecystokinin-B Receptor

Synthesis of 2-Amino-5-arylthiazoles by Palladium-Catalyzed Arylation at the C5 Position with Aryl Iodides

The Synthesis of Azadirachtin: A Potent Insect Antifeedant

A new class of chiral pyrrolidine for asymmetric Michael addition reactions. New mechanism via simple 4+2 type attack of the enamine on the trans-nitrostyrene

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