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Factors Contributing to Aromatic Stacking in Water: Evaluation in the Context of DNA

Journal of the American Chemical Society, 2000-03, Vol.122 (10), p.2213-2222

2000

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Experimental Measurement of Aromatic Stacking Affinities in the Context of Duplex DNA

Journal of the American Chemical Society, 1996-08, Vol.118 (34), p.8182-8183

1996

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Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 2. Discovery of 7-azaspiro[3.5]nonane urea PF-04862853, an orally efficacious inhibitor of fatty acid amide hydrolase (FAAH) for pain

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6545-6553

2011

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Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 1: Identification of 7-azaspiro[3.5]nonane and 1-oxa-8-azaspiro[4.5]decane as lead scaffolds

Bioorganic & medicinal chemistry letters, 2011-11, Vol.21 (21), p.6538-6544

2011

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Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA

Journal of the American Chemical Society, 1995-02, Vol.117 (7), p.1863-1872

1995

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Thienopyrimidine-based P2Y12 platelet aggregation inhibitors

Bioorganic & medicinal chemistry letters, 2009-10, Vol.19 (20), p.5919-5923

2009

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Structure-based design and synthesis of pyrazinones containing novel P1 'side pocket' moieties as inhibitors of TF/VIIa

Bioorganic & medicinal chemistry letters, 2005-06, Vol.15 (12), p.3006-3011

2005

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Aromatic Nonpolar Nucleosides as Hydrophobic Isosteres of Pyrimidine and Purine Nucleosides

Journal of organic chemistry, 1994-12, Vol.59 (24), p.7238-7242

1994

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Controlling the intracellular localization of fluorescent polyamide analogues in cultured cells

Bioorganic & medicinal chemistry letters, 2003-05, Vol.13 (9), p.1565-1570

2003

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Aromatic Nonpolar Nucleosides as Hydrophobic Isosteres of Pyrimidines and Purine Nucleosides

Journal of organic chemistry, 1994-12, Vol.59 (24), p.7238-7242

1994

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Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA

Journal of the American Chemical Society, 1995-02, Vol.117 (7), p.1863-1872

1995

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Discovery of imidazole glycerol phosphate dehydratase inhibitors through 3-D database searching

Bioorganic & medicinal chemistry letters, 2002-07, Vol.12 (13), p.1743-1746

2002

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Formation of Stable DNA Loops by Incorporation of Nonpolar, Non-Hydrogen-Bonding Nucleoside Isosteres

Angewandte Chemie (International ed.), 1996-04, Vol.35 (7), p.743-746

1996

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Aromatic Nonpolar Nucleosides as Hydrophobic Isosteres of Pyrimidine and Purine Nucleosides. [Erratum to document cited in CA122:10456]

Journal of organic chemistry, 1995-12, Vol.60 (25), p.8326-8326

1995

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Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA J. Am. Chem. Soc. 1995, 117, 1863−1872

Journal of the American Chemical Society, 1996-01, Vol.118 (4), p.931-931

1996

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Thienopyrimidine-based P2Y sub(12) platelet aggregation inhibitors

Bioorganic & medicinal chemistry letters, 2009-10, Vol.19 (20), p.5919-5923

2009

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Thienopyrimidine-based P2Y 12 platelet aggregation inhibitors

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (20), p.5919-5923

2009

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Structure-based design and synthesis of pyrazinones containing novel P 1 ‘side pocket’ moieties as inhibitors of TF/VIIa

Bioorganic & medicinal chemistry letters, 2005-06, Vol.15 (12), p.3006-3011

2005

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Design and synthesis of β-carboxamido phosphonates as potent inhibitors of imidazole glycerol phosphate dehydratase

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (14), p.2053-2058

1999

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Stabile DNA‐Schleifen durch Einbau unpolarer und keine Wasserstoffbrücken bildender Nucleosid‐Isostere

Angewandte Chemie, 1996-04, Vol.108 (7), p.834-837

1996

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Discovery of Imidazole Glycerol Phosphate Dehydratase Inhibitors Through 3-D Database Searching

ChemInform, 2002-10, Vol.33 (42), p.250-250

2002

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ChemInform Abstract: Design and Synthesis of β-Carboxamido Phosphonates as Potent Inhibitors of Imidazole Glycerol Phosphate Dehydratase

ChemInform, 1999-10, Vol.30 (43), p.no-no

1999

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Stabile DNA-Schleifen durch Einbau unpolarer und keine Wasserstoffbrücken bildender Nucleosid-Isostere

Angewandte Chemie, 1996-04, Vol.108 (7), p.834-837

1996

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Synaptopathies: synaptic dysfunction in neurological disorders – A review from students to students

Journal of neurochemistry, 2016-09, Vol.138 (6), p.785-805

2016

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Factors Contributing to Aromatic Stacking in Water: Evaluation in the Context of DNA

Experimental Measurement of Aromatic Stacking Affinities in the Context of Duplex DNA

Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 2. Discovery of 7-azaspiro[3.5]nonane urea PF-04862853, an orally efficacious inhibitor of fatty acid amide hydrolase (FAAH) for pain

Discovery of novel spirocyclic inhibitors of fatty acid amide hydrolase (FAAH). Part 1: Identification of 7-azaspiro[3.5]nonane and 1-oxa-8-azaspiro[4.5]decane as lead scaffolds

Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA

Thienopyrimidine-based P2Y12 platelet aggregation inhibitors

Structure-based design and synthesis of pyrazinones containing novel P1 'side pocket' moieties as inhibitors of TF/VIIa

Aromatic Nonpolar Nucleosides as Hydrophobic Isosteres of Pyrimidine and Purine Nucleosides

Controlling the intracellular localization of fluorescent polyamide analogues in cultured cells

Discovery of an Oral Potent Selective Inhibitor of Hematopoietic Prostaglandin D Synthase (HPGDS)

Aromatic Nonpolar Nucleosides as Hydrophobic Isosteres of Pyrimidines and Purine Nucleosides

Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA

Discovery of imidazole glycerol phosphate dehydratase inhibitors through 3-D database searching

Formation of Stable DNA Loops by Incorporation of Nonpolar, Non-Hydrogen-Bonding Nucleoside Isosteres

Aromatic Nonpolar Nucleosides as Hydrophobic Isosteres of Pyrimidine and Purine Nucleosides. [Erratum to document cited in CA122:10456]

Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA J. Am. Chem. Soc. 1995, 117, 1863−1872

Thienopyrimidine-based P2Y sub(12) platelet aggregation inhibitors

Thienopyrimidine-based P2Y 12 platelet aggregation inhibitors

Structure-based design and synthesis of pyrazinones containing novel P 1 ‘side pocket’ moieties as inhibitors of TF/VIIa

Design and synthesis of β-carboxamido phosphonates as potent inhibitors of imidazole glycerol phosphate dehydratase

Stabile DNA‐Schleifen durch Einbau unpolarer und keine Wasserstoffbrücken bildender Nucleosid‐Isostere

Discovery of Imidazole Glycerol Phosphate Dehydratase Inhibitors Through 3-D Database Searching

ChemInform Abstract: Design and Synthesis of β-Carboxamido Phosphonates as Potent Inhibitors of Imidazole Glycerol Phosphate Dehydratase

Stabile DNA-Schleifen durch Einbau unpolarer und keine Wasserstoffbrücken bildender Nucleosid-Isostere

Synaptopathies: synaptic dysfunction in neurological disorders – A review from students to students

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