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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.916-920

2005

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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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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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Application of Polymer Supported Base in Solid Phase Synthesis: Convenient Synthesis of N -Aryl- N ′-benzyl Piperazine Derivatives

Chemistry letters, 1999-02, Vol.28 (2), p.103-104

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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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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Cladinose Analogues of Sixteen-membered Macrolide Antibiotics.IV. Improved Therapeutic Effects of 4-O-Acyl-L-cladinose Analogues of Sixteen-membered Macrolide Antibiotics

Journal of antibiotics, 1997, Vol.50 (2), p.150-161

1997

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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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A NEW AMINOTHIAZOLYLCEPHALOSPORIN HAVING 1-CARBOXYETHOXYIMINO GROUP, ME1228

The Journal of Antibiotics, 1990/01/25, Vol.43(1), pp.62-69

1990

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Peptidyl α-keto thiazole as potent thrombin inhibitors

Bioorganic & medicinal chemistry letters, 1997-03, Vol.7 (5), p.533-538

1997

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Synthesis and Structure-Activity Relationships of Peptidyl .alpha.-Keto Heterocycles as Novel Inhibitors of Prolyl Endopeptidase

Journal of medicinal chemistry, 1994-10, Vol.37 (21), p.3492-3502

1994

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SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF NOVEL 2-METHYL-1-OXACEPHALOSPORINS

The Journal of Antibiotics, 1990/04/25, Vol.43(4), pp.357-371

1990

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Wittig reaction in benzene-aqueous alkaline solution

Tetrahedron letters, 1974, Vol.15 (30), p.2587-2590

1974

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Synthesis of a novel 2.BETA.-methyl-1-oxacephalosporin, OCP-9-176

Journal of antibiotics, 1988, Vol.41 (8), p.1154-1157

1988

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Micellar Effect of Lauryldimethylsulfonium Halides on the Hydrolysis of p-Nitrophenyl Decanoate

Bulletin of the Chemical Society of Japan, 1974-03, Vol.47 (3), p.771-772

1974

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α-Ketothiazole inhibitors of prolyl endopeptidase

Bioorganic & medicinal chemistry letters, 1994-03, Vol.4 (6), p.831-834

1994

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Cladinose Analogues of Sixteen-membered Macrolide Antibiotics: IV. Improved Therapeutic Effects of 4-O-Acyl-L-cladinose Analogues of Sixteen-membered Macrolide Antibiotics

The Journal of Antibiotics, 1997/02/25, Vol.50(2), pp.150-161

1997

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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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SYNTHESIS OF A NOVEL 2β-METHYL-1-OXACEPHALOSPORIN, OCP-9-176

The Journal of Antibiotics, 1988/08/25, Vol.41(8), pp.1154-1157

1988

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Novel 2-Methyl-1-oxacephalosporins 1. Synthesis of 2-Methyl-3-nor-1-oxacephem Nucleus

Heterocycles, 1990-05, Vol.31 (5), p.791

1990

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

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

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

Application of Polymer Supported Base in Solid Phase Synthesis: Convenient Synthesis of N -Aryl- N ′-benzyl Piperazine Derivatives

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

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

Cladinose Analogues of Sixteen-membered Macrolide Antibiotics.IV. Improved Therapeutic Effects of 4-O-Acyl-L-cladinose Analogues of Sixteen-membered Macrolide Antibiotics

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

A NEW AMINOTHIAZOLYLCEPHALOSPORIN HAVING 1-CARBOXYETHOXYIMINO GROUP, ME1228

Peptidyl α-keto thiazole as potent thrombin inhibitors

Synthesis and Structure-Activity Relationships of Peptidyl .alpha.-Keto Heterocycles as Novel Inhibitors of Prolyl Endopeptidase

SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF NOVEL 2-METHYL-1-OXACEPHALOSPORINS

Wittig reaction in benzene-aqueous alkaline solution

Synthesis of a novel 2.BETA.-methyl-1-oxacephalosporin, OCP-9-176

Micellar Effect of Lauryldimethylsulfonium Halides on the Hydrolysis of p-Nitrophenyl Decanoate

α-Ketothiazole inhibitors of prolyl endopeptidase

Cladinose Analogues of Sixteen-membered Macrolide Antibiotics: IV. Improved Therapeutic Effects of 4-O-Acyl-L-cladinose Analogues of Sixteen-membered Macrolide Antibiotics

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

SYNTHESIS OF A NOVEL 2β-METHYL-1-OXACEPHALOSPORIN, OCP-9-176

Novel 2-Methyl-1-oxacephalosporins 1. Synthesis of 2-Methyl-3-nor-1-oxacephem Nucleus

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