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Endocrinological properties of two novel nonsteroidal progesterone receptor modulators, CP8816 and CP8863

The Journal of pharmacology and experimental therapeutics, 2005-05, Vol.313 (2), p.916

2005

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Anxiolytic-like profiles of histamine H3 receptor agonists in animal models of anxiety: a comparative study with antidepressants and benzodiazepine anxiolytic

Psychopharmacologia, 2009-08, Vol.205 (2), p.177-187

2009

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Total synthesis of progesterone receptor ligands, (−)-PF1092A, B and C

Tetrahedron letters, 1997-02, Vol.38 (8), p.1439-1442

1997

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Synthesis and structure-activity relationships of new non-steroidal progesterone receptor ligands

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (13), p.1837-1842

1999

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Discovery of Progesterone Receptor Agonists and Antagonists inspired by the Fungal Metabolite PF1092C

Journal of Synthetic Organic Chemistry, Japan, 2006/05/01, Vol.64(5), pp.559-572

2006

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Role of Hydrophobic Substituents on the Terminal Nitrogen of Histamine in Receptor Binding and Agonist Activity: Development of an Orally Active Histamine Type 3 Receptor Agonist and Evaluation of Its Antistress Activity in Mice

Journal of medicinal chemistry, 2010-05, Vol.53 (9), p.3840-3844

2010

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Synthesis of (±)-PF1092A, B, and C; New Nonsteroidal Progesterone Receptor Ligands

The Journal of Antibiotics, 1997/04/25, Vol.50(4), pp.360-362

1997

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Nonsteroidal progesterone receptor ligands (II); synthesis and SAR of new tetrahydrobenzindolone derivatives

Bioorganic & medicinal chemistry, 2006-07, Vol.14 (14), p.4862-4878

2006

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Nonsteroidal progesterone receptor ligands (I): Synthesis and SAR of new tetrahydronaphthofuranone derivatives

Bioorganic & medicinal chemistry, 2006-07, Vol.14 (14), p.4850-4861

2006

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New Bellenamine Homologs Inhibiting Human Immunodeficiency Virus Type 1 Infectivity

The Journal of Antibiotics, 1996/01/25, Vol.49(1), pp.113-114

1996

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CP8668, a novel orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzindolone skeleton

European journal of pharmacology, 2003-02, Vol.461 (1), p.73-78

2003

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Erratum to “CP8668, a novel orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzindolone skeleton” [Eur. J. Pharmacol. 461 (2003) 73–78]

European journal of pharmacology, 2003-04, Vol.465 (3), p.299-299

2003

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In vitro and in vivo characterization of novel nonsteroidal progesterone receptor antagonists derived from the fungal metabolite PF1092C

The Journal of steroid biochemistry and molecular biology, 2002-10, Vol.82 (2), p.217-223

2002

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Fungal metabolites, PF1092 compounds and their derivatives, are nonsteroidal and selective progesterone receptor modulators

European journal of pharmacology, 2001-11, Vol.430 (2), p.159-165

2001

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Discovery of Progesterone Receptor Agonists and Antagonists Inspired by the Fungal Metabolite PF1092C

ChemInform, 2006-10, Vol.37 (42), p.no-no

2006

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Endocrinological properties of two novel nonsteroidal progesterone receptor modulators, CP8816 and CP8863

Anxiolytic-like profiles of histamine H3 receptor agonists in animal models of anxiety: a comparative study with antidepressants and benzodiazepine anxiolytic

Total synthesis of progesterone receptor ligands, (−)-PF1092A, B and C

Synthesis and structure-activity relationships of new non-steroidal progesterone receptor ligands

Discovery of Progesterone Receptor Agonists and Antagonists inspired by the Fungal Metabolite PF1092C

Role of Hydrophobic Substituents on the Terminal Nitrogen of Histamine in Receptor Binding and Agonist Activity: Development of an Orally Active Histamine Type 3 Receptor Agonist and Evaluation of Its Antistress Activity in Mice

Synthesis of (±)-PF1092A, B, and C; New Nonsteroidal Progesterone Receptor Ligands

Nonsteroidal progesterone receptor ligands (II); synthesis and SAR of new tetrahydrobenzindolone derivatives

Nonsteroidal progesterone receptor ligands (I): Synthesis and SAR of new tetrahydronaphthofuranone derivatives

New Bellenamine Homologs Inhibiting Human Immunodeficiency Virus Type 1 Infectivity

CP8668, a novel orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzindolone skeleton

Erratum to “CP8668, a novel orally active nonsteroidal progesterone receptor modulator with tetrahydrobenzindolone skeleton” [Eur. J. Pharmacol. 461 (2003) 73–78]

In vitro and in vivo characterization of novel nonsteroidal progesterone receptor antagonists derived from the fungal metabolite PF1092C

Fungal metabolites, PF1092 compounds and their derivatives, are nonsteroidal and selective progesterone receptor modulators

Discovery of Progesterone Receptor Agonists and Antagonists Inspired by the Fungal Metabolite PF1092C

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