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Novel inhibitors of fatty acid amide hydrolase

Bioorganic & medicinal chemistry letters, 2007-06, Vol.17 (12), p.3287-3291

2007

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Oxime Carbamate—Discovery of a series of novel FAAH inhibitors

Bioorganic & medicinal chemistry letters, 2010-02, Vol.20 (3), p.1272-1277

2010

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Dihydropyridine neuropeptide Y Y1 receptor antagonists 2: bioisosteric urea replacements

Bioorganic & medicinal chemistry, 2004-01, Vol.12 (2), p.507-521

2004

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Transvaginal Ultrasound Measurement of Endometrial Thickness as a Biomarker for Estrogen Exposure

Cancer epidemiology, biomarkers & prevention, 2004-09, Vol.13 (9), p.1459-1465

2004

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Synthesis, biological profile, and quantitative structure-activity relationship of a series of novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors

Journal of medicinal chemistry, 1990-11, Vol.33 (11), p.2982-2999

1990

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Selective inhibition of cholesterol synthesis in liver versus extrahepatic tissues by HMG-CoA reductase inhibitors

Journal of lipid research, 1990-07, Vol.31 (7), p.1271-1282

1990

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Hormone Replacement Therapy Formulations and Risk of Epithelial Ovarian Carcinoma

Gynecologic oncology, 2002-08, Vol.86 (2), p.118-123

2002

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A potent, tissue-selective, synthetic inhibitor of HMG-CoA reductase

Journal of medicinal chemistry, 1989-09, Vol.32 (9), p.2038-2041

1989

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Paclitaxel and Carboplatin for Recurrent or Persistent Cancer of the Cervix

Cancer investigation, 2004, Vol.22 (3), p.368-373

2004

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Dopamine agonists in the treatment of Parkinson s disease past, present and future

Current pharmaceutical design, 2000-08, Vol.6 (12), p.1211

Sit, S Y

2000

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Dinapsoline: characterization of a D1 dopamine receptor agonist in a rat model of Parkinson's disease

The Journal of pharmacology and experimental therapeutics, 2001-02, Vol.296 (2), p.338

2001

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Synthesis of tetrazol-1-yl analogs of HMG-COA reductase inhibitor BMS180431 (formerly BMY21950)

Bioorganic & medicinal chemistry letters, 1992-09, Vol.2 (9), p.1085-1088

1992

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3-Thio-quinolinone maxi-K openers for the treatment of erectile dysfunction

Bioorganic & medicinal chemistry letters, 2004-10, Vol.14 (20), p.5089-5093

2004

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ChemInform Abstract: 3-Hydroxyquinolin-2-ones: Inhibitors of (3H)-Glycine Binding to the Site Associated with the NMDA Receptor

ChemInform, 1996-07, Vol.27 (28), p.no-no

1996

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Dihydropyridine neuropeptide Y Y 1 receptor antagonists 2

Bioorganic & medicinal chemistry, 2004-01, Vol.12 (2), p.507-521

2004

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Chemotherapy for Malignant Mixed Müllerian Tumors of the Ovary

Gynecologic oncology, 2000-11, Vol.79 (2), p.196-200

2000

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A preparation of bromoolefins from carbonyl compounds

Tetrahedron letters, 1981, Vol.22 (38), p.3745-3748

1981

Volltextzugriff (PDF)

Synthesis and SAR exploration of dinapsoline analogues

Bioorganic & medicinal chemistry, 2004-02, Vol.12 (4), p.715-734

2004

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3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase: Molecular Modeling, Three-Dimensional Structure-Activity Relationships, Inhibitor Design

Quantitative structure-activity relationships, 1991, Vol.10 (1), p.30-35

1991

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Novel Dihydropyrazine Analogues as NPY Antagonists

Bioorganic & medicinal chemistry letters, 2002-02, Vol.12 (3), p.337-340

2002

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(+)-Dinapsoline: An Efficient Synthesis and Pharmacological Profile of a Novel Dopamine Agonist

Journal of medicinal chemistry, 2002-08, Vol.45 (17), p.3660-3668

2002

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Regiospecific Functionalization of 1,3-Dihydro-2H-benzimidazol-2-one and Structurally Related Cyclic Urea Derivatives

Journal of organic chemistry, 1995-03, Vol.60 (6), p.1565-1582

1995

Volltextzugriff (PDF)

3-Hydroxy-quinolin-2-ones: Inhibitors of [ 3H]-glycine binding to the site associated with the NMDA receptor

Bioorganic & medicinal chemistry letters, 1996-03, Vol.6 (5), p.499-504

1996

Volltextzugriff (PDF)

Detection of Heterozygous XY Complete Hydatidiform Mole by Chromosome in Situ Hybridization

Gynecologic oncology, 1994-12, Vol.55 (3), p.386-392

1994

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N-Benzylated benzimidazol-2-one derivatives: activators of large-conductance Ca2+-dependent K+ channels

Bioorganic & medicinal chemistry letters, 1996-07, Vol.6 (14), p.1641-1646

1996

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Novel inhibitors of fatty acid amide hydrolase

Oxime Carbamate—Discovery of a series of novel FAAH inhibitors

Dihydropyridine neuropeptide Y Y1 receptor antagonists 2: bioisosteric urea replacements

Transvaginal Ultrasound Measurement of Endometrial Thickness as a Biomarker for Estrogen Exposure

Synthesis, biological profile, and quantitative structure-activity relationship of a series of novel 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors

Selective inhibition of cholesterol synthesis in liver versus extrahepatic tissues by HMG-CoA reductase inhibitors

Hormone Replacement Therapy Formulations and Risk of Epithelial Ovarian Carcinoma

A potent, tissue-selective, synthetic inhibitor of HMG-CoA reductase

Paclitaxel and Carboplatin for Recurrent or Persistent Cancer of the Cervix

Dopamine agonists in the treatment of Parkinson s disease past, present and future

Dinapsoline: characterization of a D1 dopamine receptor agonist in a rat model of Parkinson's disease

Synthesis of tetrazol-1-yl analogs of HMG-COA reductase inhibitor BMS180431 (formerly BMY21950)

3-Thio-quinolinone maxi-K openers for the treatment of erectile dysfunction

ChemInform Abstract: 3-Hydroxyquinolin-2-ones: Inhibitors of (3H)-Glycine Binding to the Site Associated with the NMDA Receptor

Dihydropyridine neuropeptide Y Y 1 receptor antagonists 2

Chemotherapy for Malignant Mixed Müllerian Tumors of the Ovary

A preparation of bromoolefins from carbonyl compounds

Synthesis and SAR exploration of dinapsoline analogues

3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase: Molecular Modeling, Three-Dimensional Structure-Activity Relationships, Inhibitor Design

Novel Dihydropyrazine Analogues as NPY Antagonists

(+)-Dinapsoline: An Efficient Synthesis and Pharmacological Profile of a Novel Dopamine Agonist

Regiospecific Functionalization of 1,3-Dihydro-2H-benzimidazol-2-one and Structurally Related Cyclic Urea Derivatives

3-Hydroxy-quinolin-2-ones: Inhibitors of [ 3H]-glycine binding to the site associated with the NMDA receptor

Detection of Heterozygous XY Complete Hydatidiform Mole by Chromosome in Situ Hybridization

N-Benzylated benzimidazol-2-one derivatives: activators of large-conductance Ca2+-dependent K+ channels

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