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Structure of the Francisella response regulator QseB receiver domain, and characterization of QseB inhibition by antibiofilm 2‐aminoimidazole‐based compounds

Molecular microbiology, 2017-10, Vol.106 (2), p.223-235

2017

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Discovery and in vitro evaluation of potent kinase inhibitors: Pyrido[1′,2′:1,5]pyrazolo[3,4- d]pyrimidines

Bioorganic & medicinal chemistry letters, 2005-08, Vol.15 (16), p.3778-3781

2005

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Development of Dihydropyridone Indazole Amides as Selective Rho-Kinase Inhibitors

Journal of medicinal chemistry, 2007-01, Vol.50 (1), p.6-9

2007

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Pyrazolo[1,5-a]pyridines as p38 Kinase Inhibitors

Organic letters, 2005-10, Vol.7 (21), p.4753-4756

2005

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The identification of pyrazolo[1,5- a]pyridines as potent p38 kinase inhibitors

Bioorganic & medicinal chemistry, 2008-10, Vol.18 (20), p.5428-5430

2008

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The discovery of potent cRaf1 kinase inhibitors

Bioorganic & medicinal chemistry letters, 2000-02, Vol.10 (3), p.223-226

2000

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Synthesis of Ultra-Short-Acting Neuromuscular Blocker GW 0430: A Remarkably Stereo- and Regioselective Synthesis of Mixed Tetrahydroisoquinolinium Chlorofumarates

Organic letters, 1999-12, Vol.1 (12), p.1993-1996

1999

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Total Synthesis of Baccatin III and Taxol

Journal of the American Chemical Society, 1996-03, Vol.118 (12), p.2843-2859

1996

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Pyrazolo[1,5- a]pyridines: synthetic approaches to a novel class of antiherpetics

Tetrahedron, 2003-11, Vol.59 (45), p.9001-9011

2003

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(1 H-Imidazo[4,5- c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors

Bioorganic & medicinal chemistry letters, 2005-07, Vol.15 (14), p.3402-3406

2005

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Synthesis of competent nucleophiles for delivering the A ring of taxol

Journal of organic chemistry, 1993-08, Vol.58 (18), p.4989-4992

1993

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Identification and Structure–Activity Studies of Novel Ultrashort-Acting Benzodiazepine Receptor Agonists

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (21), p.3215-3218

2002

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Neuromuscular Blocking Activity and Therapeutic Potential of Mixed-Tetrahydroisoquinolinium Halofumarates and Halosuccinates in Rhesus Monkeys

Journal of medicinal chemistry, 2003-06, Vol.46 (12), p.2502-2515

2003

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Structure of the Francisella response regulator QseB receiver domain, and characterization of QseB inhibition by antibiofilm 2-aminoimidazole-based compounds: Inhibition of response regulator QseB by antibiofilm compounds

Molecular microbiology, 2017-08, Vol.106 (2)

2017

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Synthetic studies on the ginkgolides: total synthesis of (.+-.)-bilobalide

Journal of the American Chemical Society, 1993-04, Vol.115 (8), p.3146-3155

1993

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A concise synthesis of a highly functionalized C-aryl taxol analog by an intramolecular Heck olefination reaction

Tetrahedron letters, 1993-11, Vol.34 (45), p.7253-7256

1993

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Corrigendum to “(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors” [Bioorg. Med. Chem. Lett. 15 (2005) 3402–3406]

Bioorganic & medicinal chemistry letters, 2015-03, Vol.25 (5), p.1151-1151

2015

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A total synthesis of (.+-.)-bilobalide

Journal of the American Chemical Society, 1992-06, Vol.114 (13), p.5445-5447

1992

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A Novel Intramolecular Heck Reaction: Synthesis of a Cholesterol - Baccatin III Hybrid

Angewandte Chemie (International ed.), 1995-03, Vol.34 (4), p.452-455

1995

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Improvement in word recognition following treatment failure for sudden sensorineural hearing loss

World Journal of Otorhinolaryngology-Head and Neck Surgery, 2016-09, Vol.2 (3), p.168-174

2016

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Discovery and in vitro evaluation of potent kinase inhibitors : Pyrido[1',2':1,5]pyrazolo[3,4-d]pyrimidines: G-protein-coupled receptors in drug discovery

Bioorganic & medicinal chemistry letters, 2005, Vol.15 (16), p.3778-3781

2005

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Discovery and in vitro Evaluation of Potent Kinase Inhibitors: Pyrido[1′,2′:1,5]pyrazolo[3,4-d]pyrimidines

ChemInform, 2006-01, Vol.37 (4), p.no-no

2006

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A prodrug approach to the design of cRaf1 kinase inhibitors with improved cellular activity

Anti-cancer drug design, 2001-02, Vol.16 (1), p.1

2001

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Eine neuartige, intramolekulare Heck-Reaktion: Synthese eines Cholesterin-Baccatin-III-Hybrids

Angewandte Chemie, 1995-02, Vol.107 (4), p.495-498

1995

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Structure of the Francisella response regulator QseB receiver domain, and characterization of QseB inhibition by antibiofilm 2‐aminoimidazole‐based compounds

Discovery and in vitro evaluation of potent kinase inhibitors: Pyrido[1′,2′:1,5]pyrazolo[3,4- d]pyrimidines

Development of Dihydropyridone Indazole Amides as Selective Rho-Kinase Inhibitors

Pyrazolo[1,5-a]pyridines as p38 Kinase Inhibitors

Discovery of Aminofurazan-azabenzimidazoles as Inhibitors of Rho-Kinase with High Kinase Selectivity and Antihypertensive Activity

The identification of pyrazolo[1,5- a]pyridines as potent p38 kinase inhibitors

The discovery of potent cRaf1 kinase inhibitors

Synthesis of Ultra-Short-Acting Neuromuscular Blocker GW 0430: A Remarkably Stereo- and Regioselective Synthesis of Mixed Tetrahydroisoquinolinium Chlorofumarates

Total Synthesis of Baccatin III and Taxol

Pyrazolo[1,5- a]pyridines: synthetic approaches to a novel class of antiherpetics

(1 H-Imidazo[4,5- c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors

Synthesis of competent nucleophiles for delivering the A ring of taxol

Identification and Structure–Activity Studies of Novel Ultrashort-Acting Benzodiazepine Receptor Agonists

Neuromuscular Blocking Activity and Therapeutic Potential of Mixed-Tetrahydroisoquinolinium Halofumarates and Halosuccinates in Rhesus Monkeys

Structure of the Francisella response regulator QseB receiver domain, and characterization of QseB inhibition by antibiofilm 2-aminoimidazole-based compounds: Inhibition of response regulator QseB by antibiofilm compounds

Synthetic studies on the ginkgolides: total synthesis of (.+-.)-bilobalide

A concise synthesis of a highly functionalized C-aryl taxol analog by an intramolecular Heck olefination reaction

Corrigendum to “(1H-Imidazo[4,5-c]pyridin-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: A novel class of potent MSK-1-inhibitors” [Bioorg. Med. Chem. Lett. 15 (2005) 3402–3406]

A total synthesis of (.+-.)-bilobalide

A Novel Intramolecular Heck Reaction: Synthesis of a Cholesterol - Baccatin III Hybrid

Improvement in word recognition following treatment failure for sudden sensorineural hearing loss

Discovery and in vitro evaluation of potent kinase inhibitors : Pyrido[1',2':1,5]pyrazolo[3,4-d]pyrimidines: G-protein-coupled receptors in drug discovery

Discovery and in vitro Evaluation of Potent Kinase Inhibitors: Pyrido[1′,2′:1,5]pyrazolo[3,4-d]pyrimidines

A prodrug approach to the design of cRaf1 kinase inhibitors with improved cellular activity

Eine neuartige, intramolekulare Heck-Reaktion: Synthese eines Cholesterin-Baccatin-III-Hybrids

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