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Phosphodiesterase Inhibitors for Cognitive Enhancement

Current pharmaceutical design, 2005-10, Vol.11 (26), p.3329-3334

2005

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No evidence of potentiation of buprenorphine by milnacipran in healthy subjects using a nociceptive test battery

European journal of pain, 2017-03, Vol.21 (3), p.494-506

2017

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Phosphodiesterase inhibitors for cognitive enhancement

Current pharmaceutical design, 2005-01, Vol.11 (26), p.3329

2005

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Characterization of antiallodynic actions of ALE-0540, a novel nerve growth factor receptor antagonist, in the rat

The Journal of pharmacology and experimental therapeutics, 1999-06, Vol.289 (3), p.1271

1999

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Total synthesis of (-)-tetrahydrolipstatin

Journal of organic chemistry, 1993-12, Vol.58 (27), p.7768-7781

1993

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N-(1-Benzylpyrrolidin-3-yl)arylbenzamides as potent and selective human dopamine D 4 antagonists

Bioorganic & medicinal chemistry letters, 2004-10, Vol.14 (19), p.4847-4850

2004

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Efficient syntheses for optically pure stereogenically labile 4-substituted-2-hydroxytetronic acids

Journal of organic chemistry, 1990-02, Vol.55 (3), p.1112-1114

1990

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(R)-3-(N-methylpyrrolidin-2-ylmethyl)-5-(1,2,3,6-tetrahydropyridin-4-yl)-1h-indole derivatives as high affinity h5-HT1B/1D ligands

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (20), p.3419-3421

2003

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3-(2-Pyrrolidin-1-ylethyl)-5-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives as high affinity human 5-HT1B/1D ligands

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (3), p.727-729

2004

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Synthesis of some 1,3,6-trioxygenated isopentenylated xanthones: Constitution of garcinone A

Tetrahedron, 1984, Vol.40 (17), p.3303-3312

1984

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Serum lipoprotein and apoprotein concentrations in 4-(4-chlorophenyl)-2-hydroxytetronic acid and clofibrate-treated cholesterol and cholic acid-fed rats

Lipids, 1989-01, Vol.24 (1), p.25-32

1989

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1-(Bicyclopiperazinyl)ethylindoles and 1-(homopiperazinyl)ethyl-indoles as highly selective and potent 5-HT7 receptor ligands

Bioorganic & medicinal chemistry letters, 2002-09, Vol.12 (17), p.2451-2454

2002

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Synthetic aci-reductones: 3,4-dihydroxy-2H-1-benzopyran-2-ones and their cis- and trans-4a,5,6,7,8,8a-hexahydro diastereomers. Antiaggregatory, antilipidemic, and redox properties compared to those of the 4-substituted 2-hydroxytetronic acids

Journal of medicinal chemistry, 1988-07, Vol.31 (7), p.1437-1445

1988

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Structural features associated with reactive metabolite formation in clozapine analogues

Chemico-biological interactions, 1997-05, Vol.104 (2), p.117-129

1997

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Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-bioavailable 5-HT1D agonists

Bioorganic & medicinal chemistry letters, 2003-12, Vol.13 (24), p.4409-4413

2003

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Synthetic approaches to 4-spiro-2-hydroxytetronic acids

Journal of organic chemistry, 1987-05, Vol.52 (11), p.2324-2327

1987

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A remarkably facile and stereochemically controlled fragmentation reaction in the hygrolide group of macrolide antibiotics

Tetrahedron letters, 1996-12, Vol.37 (50), p.9001-9004

1996

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Synthesis of 6-carboxy-2,2-dimethylchromans and chromenes

Tetrahedron, 1982, Vol.38 (24), p.3673-3677

1982

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ChemInform Abstract: A Remarkably Facile and Stereochemically Controlled Fragmentation Reaction in the Hygrolide Group of Macrolide Antibiotics

ChemInform, 1997-04, Vol.28 (14), p.no-no

1997

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ChemInform Abstract: Total Synthesis of (-)-Tetrahydrolipstatin

ChemInform, 1994-05, Vol.25 (21), p.no-no

1994

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ChemInform Abstract: Efficient Syntheses for Optically Pure Stereogenically Labile 4‐Substituted 2‐Hydroxytetronic Acids

ChemInform, 1990-07, Vol.21 (27), p.no-no

1990

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ChemInform Abstract: Synthetic Approaches to 4‐Spiro‐2‐hydroxytetronic Acids

ChemInform, 1987-11, Vol.18 (45), p.no-no

1987

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ChemInform Abstract: A NEW ROUTE TOWARDS THE SYNTHESIS OF DIHYDROPYRANOXANTHONES

Chemischer Informationsdienst, 1985-06, Vol.16 (23)

1985

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ChemInform Abstract: SYNTHESIS OF SOME 1,3,6‐TRIOXYGENATED ISOPENTENYLATED XANTHONES. CONSTITUTION OF GARCINONE A

Chemischer Informationsdienst, 1985-02, Vol.16 (7)

1985

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ChemInform Abstract: SYNTHESIS OF CARBOXY‐2,2‐DIMETHYLCHROMANS AND CHROMENES

Chemischer Informationsdienst, 1984-04, Vol.15 (16)

1984

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Phosphodiesterase Inhibitors for Cognitive Enhancement

No evidence of potentiation of buprenorphine by milnacipran in healthy subjects using a nociceptive test battery

Phosphodiesterase inhibitors for cognitive enhancement

Characterization of antiallodynic actions of ALE-0540, a novel nerve growth factor receptor antagonist, in the rat

Total synthesis of (-)-tetrahydrolipstatin

N-(1-Benzylpyrrolidin-3-yl)arylbenzamides as potent and selective human dopamine D 4 antagonists

Efficient syntheses for optically pure stereogenically labile 4-substituted-2-hydroxytetronic acids

(R)-3-(N-methylpyrrolidin-2-ylmethyl)-5-(1,2,3,6-tetrahydropyridin-4-yl)-1h-indole derivatives as high affinity h5-HT1B/1D ligands

3-(2-Pyrrolidin-1-ylethyl)-5-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole derivatives as high affinity human 5-HT1B/1D ligands

Synthesis of some 1,3,6-trioxygenated isopentenylated xanthones: Constitution of garcinone A

Serum lipoprotein and apoprotein concentrations in 4-(4-chlorophenyl)-2-hydroxytetronic acid and clofibrate-treated cholesterol and cholic acid-fed rats

1-(Bicyclopiperazinyl)ethylindoles and 1-(homopiperazinyl)ethyl-indoles as highly selective and potent 5-HT7 receptor ligands

Synthetic aci-reductones: 3,4-dihydroxy-2H-1-benzopyran-2-ones and their cis- and trans-4a,5,6,7,8,8a-hexahydro diastereomers. Antiaggregatory, antilipidemic, and redox properties compared to those of the 4-substituted 2-hydroxytetronic acids

Structural features associated with reactive metabolite formation in clozapine analogues

Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-bioavailable 5-HT1D agonists

Synthetic approaches to 4-spiro-2-hydroxytetronic acids

A remarkably facile and stereochemically controlled fragmentation reaction in the hygrolide group of macrolide antibiotics

Synthesis of 6-carboxy-2,2-dimethylchromans and chromenes

ChemInform Abstract: A Remarkably Facile and Stereochemically Controlled Fragmentation Reaction in the Hygrolide Group of Macrolide Antibiotics

ChemInform Abstract: Total Synthesis of (-)-Tetrahydrolipstatin

ChemInform Abstract: Efficient Syntheses for Optically Pure Stereogenically Labile 4‐Substituted 2‐Hydroxytetronic Acids

ChemInform Abstract: Synthetic Approaches to 4‐Spiro‐2‐hydroxytetronic Acids

ChemInform Abstract: A NEW ROUTE TOWARDS THE SYNTHESIS OF DIHYDROPYRANOXANTHONES

ChemInform Abstract: SYNTHESIS OF SOME 1,3,6‐TRIOXYGENATED ISOPENTENYLATED XANTHONES. CONSTITUTION OF GARCINONE A

ChemInform Abstract: SYNTHESIS OF CARBOXY‐2,2‐DIMETHYLCHROMANS AND CHROMENES

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