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0.45% saline and 5% dextrose in water, but not 0.9% saline or 5% dextrose in 0.9% saline, worsen brain edema two hours after closed head trauma in rats two hours after closed head trauma in rats

Anesthesia and analgesia, 1998, Vol.86 (6), p.1225-1229

1998

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1-{1-[4-[(N-acetyl-4-piperidinyl)oxy]-2-methoxybenzoyl]piperidin-4-yl}-4H-3,1-benzoxazin-2(1H)-one (L-371,257) : a new, orally bioavailable, non-peptide oxytocin antagonist

Journal of medicinal chemistry, 1995-11, Vol.38 (23), p.4634-4636

1995

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1-2-(2,2,2-Trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (10), p.3125-3128

2010

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1,2,5,6-tetrahydropyridine oxime ethers incorporating electron withdrawing groups are potent and selective muscarinic agonists

Bioorganic & medicinal chemistry letters, 1994-02, Vol.4 (4), p.557-562

1994

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1-[2-[(5-Cyanopyridin-2-yl)amino]-ethylamino]acetyl-2-(S)-pyrrolidine-carbonitri le: A potent, selective, and orally bioavailable Dipeptidyl peptidase IV inhibitor with antihyperglycemic properties

Journal of medicinal chemistry, 2002, Vol.45 (12), p.2362-2365

2002

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1,2-Diarylcyclopentenes as Selective Cyclooxygenase-2 Inhibitors and Orally Active Anti-inflammatory Agents

Journal of medicinal chemistry, 1995-10, Vol.38 (22), p.4570-4578

1995

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1-(3-Cyanobenzylpiperidin-4-yl)-5-methyl-4-phenyl-1,3-dihydroimidazol-2-one : A selective high-affinity antagonist for the human dopamine D4receptor with excellent selectivity over ion channels

Journal of medicinal chemistry, 1999, Vol.42 (14), p.2706-2715

1999

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1,3-dialkyltriazenes : reactie intermediates and DNA alkylation

Chemical research in toxicology, 1991, Vol.4 (3), p.334-340

1991

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1,3-dioxane-4,6-dione-5-carboxamide-based inhibitors of human group IIa phospholipase A2 : X-ray structure of the complex and interfacial selection of inhibitors from a structural library

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (8), p.1097-1102

1999

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1,4-Benzodiazepin-2-one derived neurokinin-1 receptor antagonists

Bioorganic & medicinal chemistry letters, 1997-08, Vol.7 (15), p.2037-2042

1997

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1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione and related compounds as potent antifungal and antimicrobial agents

Bioorganic & medicinal chemistry letters, 1997-12, Vol.7 (24), p.3153-3158

1997

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1-(4-(Naphthalen-2-yl)pyrimidin-2-yl)piperidin-4-ylmethanamine: A Wingless β-Catenin Agonist That Increases Bone Formation Rate

Journal of medicinal chemistry, 2009, Vol.52 (22), p.6962-6965

2009

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1,4-substituted indoles: a potent and selective class of angiotensin II receptor antagonists

Bioorganic & medicinal chemistry letters, 1994-01, Vol.4 (1), p.145-150

1994

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1-653 resists degradation in rats

Anesthesia and analgesia, 1988, Vol.67 (6), p.534-538

1988

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'1-8 interferon inducible gene family' : putative colon carcinoma-associated antigens

British journal of cancer, 2007-12, Vol.97 (12), p.1655-1663

2007

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IL-1β in bronchial lavage fluid is a non-invasive marker that predicts the viability of the pulmonary graft from the non-heart-beating donor

The Journal of heart and lung transplantation, 2005, Vol.24 (1), p.20-28

2005

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IL-1β induced protein changes in diabetes prone BB rat islets of Langerhans identified by proteome analysis

Diabetologia, 2002-11, Vol.45 (11), p.1550-1561

2002

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IL‐1β induces stabilization of IL‐8 mRNA in malignant breast cancer cells via the 3′ untranslated region: Involvement of divergent RNA‐binding factors HuR, KSRP and TIAR

International journal of cancer, 2005-03, Vol.113 (6), p.911-919

2005

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1 NMR spectroscopy characterization of perchloric acid extracts from breast carcinomas and non-involved breast tissue

NMR in biomedicine, 1994, Vol.7 (4), p.181-194

1994

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(-)-1-Norvincorine, a new alkaloid from Vinca minor

Planta medica, 1987-02, Vol.53 (1), p.120-120

1987

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1-Oxa-3,8-diazaspiro[4.5]decan-2-one derivatives with a potent inhibitory effect on neural Ca-uptake and protecting action against TET-induced brain edema and memory and learning deficits

European journal of medicinal chemistry, 1997, Vol.32 (1), p.27-38

1997

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1-phenyl-3-amino-1,2,3,4-tetrahydronaphthalenes and related derivatives as ligands for the neuromodulatory σ3 receptor : further structure-activity relationships

Journal of medicinal chemistry, 1995-09, Vol.38 (19), p.3857-3864

1995

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A 1-Year Study of Brimonidine Twice Daily in Glaucoma and Ocular Hypertension: A Controlled, Randomized, Multicenter Clinical Trial

Archives of ophthalmology (1960), 1997-07, Vol.115 (7), p.847

Schuman, Joel S.

1997

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10-Deacetylbaccatin III Analogues from Taxus baccata

Journal of natural products (Washington, D.C.), 1995-10, Vol.58 (10), p.1508-1514

1995

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10-Ketomorphinan and 3-Substituted-3-desoxymorphinan Analogues as Mixed κ and μ Opioid Ligands: Synthesis and Biological Evaluation of Their Binding Affinity at Opioid Receptors

Journal of medicinal chemistry, 2004-01, Vol.47 (1), p.165-174

2004

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0.45% saline and 5% dextrose in water, but not 0.9% saline or 5% dextrose in 0.9% saline, worsen brain edema two hours after closed head trauma in rats two hours after closed head trauma in rats

1-{1-[4-[(N-acetyl-4-piperidinyl)oxy]-2-methoxybenzoyl]piperidin-4-yl}-4H-3,1-benzoxazin-2(1H)-one (L-371,257) : a new, orally bioavailable, non-peptide oxytocin antagonist

1-2-(2,2,2-Trifluoroethoxy)ethyl-1H-pyrazolo[4,3-d]pyrimidines as potent phosphodiesterase 5 (PDE5) inhibitors

1,2,5,6-tetrahydropyridine oxime ethers incorporating electron withdrawing groups are potent and selective muscarinic agonists

1-[2-[(5-Cyanopyridin-2-yl)amino]-ethylamino]acetyl-2-(S)-pyrrolidine-carbonitri le: A potent, selective, and orally bioavailable Dipeptidyl peptidase IV inhibitor with antihyperglycemic properties

1,2-Diarylcyclopentenes as Selective Cyclooxygenase-2 Inhibitors and Orally Active Anti-inflammatory Agents

1-(3-Cyanobenzylpiperidin-4-yl)-5-methyl-4-phenyl-1,3-dihydroimidazol-2-one : A selective high-affinity antagonist for the human dopamine D4receptor with excellent selectivity over ion channels

1,3-dialkyltriazenes : reactie intermediates and DNA alkylation

1,3-dioxane-4,6-dione-5-carboxamide-based inhibitors of human group IIa phospholipase A2 : X-ray structure of the complex and interfacial selection of inhibitors from a structural library

1,4-Benzodiazepin-2-one derived neurokinin-1 receptor antagonists

1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione and related compounds as potent antifungal and antimicrobial agents

1-(4-(Naphthalen-2-yl)pyrimidin-2-yl)piperidin-4-ylmethanamine: A Wingless β-Catenin Agonist That Increases Bone Formation Rate

1,4-substituted indoles: a potent and selective class of angiotensin II receptor antagonists

1-653 resists degradation in rats

'1-8 interferon inducible gene family' : putative colon carcinoma-associated antigens

IL-1β in bronchial lavage fluid is a non-invasive marker that predicts the viability of the pulmonary graft from the non-heart-beating donor

IL-1β induced protein changes in diabetes prone BB rat islets of Langerhans identified by proteome analysis

IL‐1β induces stabilization of IL‐8 mRNA in malignant breast cancer cells via the 3′ untranslated region: Involvement of divergent RNA‐binding factors HuR, KSRP and TIAR

1 NMR spectroscopy characterization of perchloric acid extracts from breast carcinomas and non-involved breast tissue

(-)-1-Norvincorine, a new alkaloid from Vinca minor

1-Oxa-3,8-diazaspiro[4.5]decan-2-one derivatives with a potent inhibitory effect on neural Ca-uptake and protecting action against TET-induced brain edema and memory and learning deficits

1-phenyl-3-amino-1,2,3,4-tetrahydronaphthalenes and related derivatives as ligands for the neuromodulatory σ3 receptor : further structure-activity relationships

A 1-Year Study of Brimonidine Twice Daily in Glaucoma and Ocular Hypertension: A Controlled, Randomized, Multicenter Clinical Trial

10-Deacetylbaccatin III Analogues from Taxus baccata

10-Ketomorphinan and 3-Substituted-3-desoxymorphinan Analogues as Mixed κ and μ Opioid Ligands: Synthesis and Biological Evaluation of Their Binding Affinity at Opioid Receptors

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