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Controlling postoperative use of i.v. acetaminophen at an academic medical center

American journal of health-system pharmacy, 2018-04, Vol.75 (8), p.548-555

2018

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Experimental solubility profiling of marketed CNS drugs, exploring solubility limit of CNS discovery candidate

Bioorganic & medicinal chemistry letters, 2010-12, Vol.20 (24), p.7312-7316

2010

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Calcium-Dependent K-Channels in Guinea Pig and Human Urinary Bladder

Biochemical and biophysical research communications, 1995-08, Vol.213 (2), p.404-409

1995

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4-Sulfonamidoanilide tertiary carbinols: A novel series of potassium channel openers

Bioorganic & medicinal chemistry letters, 1997-04, Vol.7 (7), p.775-778

1997

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Real-Time in situ Raman Analysis of Microwave-Assisted Organic Reactions

Applied spectroscopy, 2004-01, Vol.58 (1), p.41-46

2004

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Pyridazinoquinolinetriones as NMDA Glycine-Site Antagonists with Oral Antinociceptive Activity in a Model of Neuropathic Pain

Journal of medicinal chemistry, 2007-06, Vol.50 (13), p.3113-3131

2007

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Zeneca ZD6169 and its analogs from a novel series of anilide tertiary carbinols: in vitro KATP channel opening activity in bladder detrusor

Pharmacology, 1995, Vol.51 (1), p.33-42

1995

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K-channel opening activity of ZD6169 and its analogs: effect on 86Rb efflux and 3H-P1075 binding in bladder smooth muscle

Pharmacology, 1995-06, Vol.50 (6), p.388-397

1995

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Synthetic Strategies Towards the Total Synthesis of Phyllanthocin and Breynolide. Application of Stereochemically Linear and Convergent Strategies

Chemical and Pharmaceutical Bulletin, 1999/12/15, Vol.47(12), pp.1671-1678

1999

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ZENECA ZD6169: a novel KATP channel opener with in vivo selectivity for urinary bladder

The Journal of pharmacology and experimental therapeutics, 1995-08, Vol.274 (2), p.884

1995

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Synthesis of 7-chloro-2,3-dihydro-2-[1-(pyridinyl)alkyl]-pyridazino[4,5-b]quinoline-1,4,10(5h )-triones as NMDA glycine-site antagonists

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (20), p.3553-3556

2003

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Total synthesis of (.+-.)-breynolide, an aglycon derivative of the orally active hypocholesterolemic agent breynin A

Journal of the American Chemical Society, 1992-11, Vol.114 (24), p.9419-9434

1992

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Enantioselective synthesis of (+)-kjellmanianone

Tetrahedron, 1991, Vol.47 (2), p.173-182

1991

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Total synthesis of (.+-.)-breynolide: an aglycon derivative of a potent, orally active hypocholesterolemic agent

Journal of the American Chemical Society, 1991-05, Vol.113 (10), p.4037-4038

1991

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N-Aryl-3,3,3-trifluoro-2-hydroxy-2-methylpropanamides: KATP Potassium Channel Openers. Modifications on the Western Region

Journal of medicinal chemistry, 1996-11, Vol.39 (23), p.4592-4601

1996

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Coordination compounds with a biomimetic N2S2 ligand, resulting in long metal-thioether bonds. The crystal and molecular structure of [1,7-bis(5-methyl-4-imidazolyl)-2,6-dithiaheptane] bis (thiocyanato-N) cobalt (II)

Polyhedron, 1989, Vol.8 (15), p.1965-1970

1989

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Phyllanthoside-phyllanthostatin synthetic studies. VI: An augmented spiroketalization tactic for thr total synthesis of phyllanthocin

Tetrahedron letters, 1989, Vol.30 (52), p.7325-7328

1989

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Phyllanthoside-phyllanthostatin synthetic studies. VII, Total synthesis of (+)-phyllanthocin and (+)-phyllanthocindiol

Journal of the American Chemical Society, 1991, Vol.113 (6), p.2071-2092

1991

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Reactions of o-quinone monoimides with sulfoxides, diazoalkanes, and triphenylphosphine

Journal of organic chemistry, 1986-03, Vol.51 (6), p.829-833

1986

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Progress in Understanding and Treating SCN2A-Mediated Disorders

Trends in neurosciences (Regular ed.), 2018-07, Vol.41 (7), p.442-456

2018

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ChemInform Abstract: 4-Sulfonamidoanilide Tertiary Carbinols: A Novel Series of Potassium Channel Openers

ChemInform, 1997-08, Vol.28 (34), p.no-no

1997

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ChemInform Abstract: Total Synthesis of (.+-.)-Breynolide: An Aglycon Derivative of a Potent, Orally Active Hypocholesterolemic Agent

ChemInform, 1991-08, Vol.22 (34), p.no-no

1991

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ChemInform Abstract: Phyllanthoside-Phyllanthostatin Synthetic Studies. Part 7. Total Synthesis of (+)-Phyllanthocin and (+)-Phyllanthocindiol

ChemInform, 1991-07, Vol.22 (30), p.no-no

1991

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The contribution of Na V 1.6 to the efficacy of voltage-gated sodium channel inhibitors in wild type and Na V 1.6 gain-of-function (GOF) mouse seizure control

British journal of pharmacology, 2024-10, Vol.181 (20), p.3993-4011

2024

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The contribution of NaV1.6 to the efficacy of voltage‐gated sodium channel inhibitors in wild type and NaV1.6 gain‐of‐function (GOF) mouse seizure control

British journal of pharmacology, 2024-10, Vol.181 (20), p.3993-4011

2024

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Controlling postoperative use of i.v. acetaminophen at an academic medical center

Experimental solubility profiling of marketed CNS drugs, exploring solubility limit of CNS discovery candidate

Calcium-Dependent K-Channels in Guinea Pig and Human Urinary Bladder

4-Sulfonamidoanilide tertiary carbinols: A novel series of potassium channel openers

Real-Time in situ Raman Analysis of Microwave-Assisted Organic Reactions

Pyridazinoquinolinetriones as NMDA Glycine-Site Antagonists with Oral Antinociceptive Activity in a Model of Neuropathic Pain

Zeneca ZD6169 and its analogs from a novel series of anilide tertiary carbinols: in vitro KATP channel opening activity in bladder detrusor

K-channel opening activity of ZD6169 and its analogs: effect on 86Rb efflux and 3H-P1075 binding in bladder smooth muscle

Synthetic Strategies Towards the Total Synthesis of Phyllanthocin and Breynolide. Application of Stereochemically Linear and Convergent Strategies

ZENECA ZD6169: a novel KATP channel opener with in vivo selectivity for urinary bladder

Synthesis of 7-chloro-2,3-dihydro-2-[1-(pyridinyl)alkyl]-pyridazino[4,5-b]quinoline-1,4,10(5h )-triones as NMDA glycine-site antagonists

Total synthesis of (.+-.)-breynolide, an aglycon derivative of the orally active hypocholesterolemic agent breynin A

Enantioselective synthesis of (+)-kjellmanianone

Total synthesis of (.+-.)-breynolide: an aglycon derivative of a potent, orally active hypocholesterolemic agent

N-Aryl-3,3,3-trifluoro-2-hydroxy-2-methylpropanamides: KATP Potassium Channel Openers. Modifications on the Western Region

Coordination compounds with a biomimetic N2S2 ligand, resulting in long metal-thioether bonds. The crystal and molecular structure of [1,7-bis(5-methyl-4-imidazolyl)-2,6-dithiaheptane] bis (thiocyanato-N) cobalt (II)

Phyllanthoside-phyllanthostatin synthetic studies. VI: An augmented spiroketalization tactic for thr total synthesis of phyllanthocin

Phyllanthoside-phyllanthostatin synthetic studies. VII, Total synthesis of (+)-phyllanthocin and (+)-phyllanthocindiol

Reactions of o-quinone monoimides with sulfoxides, diazoalkanes, and triphenylphosphine

Progress in Understanding and Treating SCN2A-Mediated Disorders

ChemInform Abstract: 4-Sulfonamidoanilide Tertiary Carbinols: A Novel Series of Potassium Channel Openers

ChemInform Abstract: Total Synthesis of (.+-.)-Breynolide: An Aglycon Derivative of a Potent, Orally Active Hypocholesterolemic Agent

ChemInform Abstract: Phyllanthoside-Phyllanthostatin Synthetic Studies. Part 7. Total Synthesis of (+)-Phyllanthocin and (+)-Phyllanthocindiol

The contribution of Na V 1.6 to the efficacy of voltage-gated sodium channel inhibitors in wild type and Na V 1.6 gain-of-function (GOF) mouse seizure control

The contribution of NaV1.6 to the efficacy of voltage‐gated sodium channel inhibitors in wild type and NaV1.6 gain‐of‐function (GOF) mouse seizure control

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