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Induction of hepatitis A virus-neutralizing antibody by a virus-specific synthetic peptide

Journal of Virology, 1985-09, Vol.55 (3), p.836-839

1985

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Nonpeptide oxytocin antagonists: Analogs of L-371,257 with improved potency

Bioorganic & medicinal chemistry letters, 1999-05, Vol.9 (9), p.1311-1316

1999

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Renin inhibitors. Syntheses of subnanomolar, competitive, transition-state analog inhibitors containing a novel analog of statine

Journal of medicinal chemistry, 1985-12, Vol.28 (12), p.1779-1790

1985

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Nonpeptide oxytocin antagonists: Potent, orally bioavailable analogs of L-371,257 containing A 1- R-(pyridyl)ethyl ether terminus

Bioorganic & medicinal chemistry letters, 1998-11, Vol.8 (21), p.3081-3086

1998

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Development of a novel class of cyclic hexapeptide oxytocin antagonists based on a natural product

Journal of medicinal chemistry, 1992-10, Vol.35 (21), p.3905-3918

1992

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Conformationally constrained tachykinin analogs which are selective ligands for the eledoisin binding site

Molecular pharmacology, 1986-01, Vol.29 (1), p.34-38

1986

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A super active cyclic hexapeptide analog of somatostatin

Life sciences (1973), 1984-01, Vol.34 (14), p.1371-1378

1984

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The selectivity of statine-based inhibitors against various human aspartic proteinases

Biochemical journal, 1990-02, Vol.265 (3), p.871-878

1990

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Angiotensin-converting enzyme inhibitors: synthesis and biological activity of acyl tripeptide analogues of enalapril

Journal of medicinal chemistry, 1985-01, Vol.28 (4), p.434-442

1985

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Design and discovery in the development of long-acting renin inhibitors

Biochemical Society transactions, 1990-12, Vol.18 (6), p.1291-1294

1990

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Use of N-Fmoc amino acid chlorides and activated 2-(fluorenylmethoxy)-5(4H)-oxazolones in solid-phase peptide synthesis. Efficient syntheses of highly N-alkylated cyclic hexapeptide oxytocin antagonists related to L-365,209

Journal of organic chemistry, 1992-07, Vol.57 (16), p.4394-4400

1992

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Protected lactam-bridged dipeptides for use as conformational constraints in peptides

Journal of organic chemistry, 1982-01, Vol.47 (1), p.104-109

1982

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Bioactive Conformation of Luteinizing Hormone-Releasing Hormone: Evidence from a Conformationally Constrained Analog

Science (American Association for the Advancement of Science), 1980-11, Vol.210 (4470), p.656-658

1980

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Conformational modifications of cyclic hexapeptide somatostatin analogs

International Journal of Peptide and Protein Research, 1984-02, Vol.23 (2), p.142-150

1984

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A potent cyclic hexapeptide analogue of somatostatin

Nature (London), 1981-07, Vol.292 (5818), p.55-58

1981

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A series of 5-(5,6)-dihydrouracil substituted 8-hydroxy-[1,6]naphthyridine-7-carboxylic acid 4-fluorobenzylamide inhibitors of HIV-1 integrase and viral replication in cells

Bioorganic & medicinal chemistry letters, 2005-10, Vol.15 (20), p.4550-4554

2005

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Renin inhibitors containing conformationally restricted P1-P1' dipeptide mimetics

Journal of medicinal chemistry, 1991-03, Vol.34 (3), p.887-900

1991

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Synthesis of new peptides based on models of receptor-bound conformation

Psychopharmacology series, 1987, Vol.3, p.12

1987

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Nanomolar-affinity, non-peptide oxytocin receptor antagonists

Journal of medicinal chemistry, 1993-12, Vol.36 (25), p.3993-4005

1993

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Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation

Bioorganic & medicinal chemistry, 1994-09, Vol.2 (9), p.971-985

1994

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Synthesis of 9-fluorenylmethyloxycarbonyl-protected N-alkyl amino acids by reduction of oxazolidinones

Journal of organic chemistry, 1983-01, Vol.48 (1), p.77-81

1983

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1-7,7-Dimethyl-2(S)-(2(S)-amino-4-(methylsulfonyl)butyramido)bicyclo[2.2.1]-heptan-1(S)-ylmethylsulfonyl-4-(2-methylphenyl)piperazine (L-368,899) : an orally bioavailable, non-peptide oxytocin antagonist with potential utility for managing preterm labor

Journal of medicinal chemistry, 1994, Vol.37 (5), p.565-571

1994

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Cyclic hexapeptide oxytocin antagonists. Potency-, selectivity-, and solubility-enhancing modifications

Journal of medicinal chemistry, 1990-07, Vol.33 (7), p.1843-1845

1990

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Interaction of Mouse Submaxillary Gland Renin with a Statine-Containing Subnanomolar, Competitive Inhibitor

Journal of enzyme inhibition, 1985, Vol.1 (1), p.13-23

1985

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Renin inhibitors containing conformationally restricted P1P1' dipeptide mimetics

Journal of medicinal chemistry, 1991, Vol.34 (3), p.887-900

1991

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Induction of hepatitis A virus-neutralizing antibody by a virus-specific synthetic peptide

Nonpeptide oxytocin antagonists: Analogs of L-371,257 with improved potency

Renin inhibitors. Syntheses of subnanomolar, competitive, transition-state analog inhibitors containing a novel analog of statine

Nonpeptide oxytocin antagonists: Potent, orally bioavailable analogs of L-371,257 containing A 1- R-(pyridyl)ethyl ether terminus

Development of a novel class of cyclic hexapeptide oxytocin antagonists based on a natural product

Conformationally constrained tachykinin analogs which are selective ligands for the eledoisin binding site

A super active cyclic hexapeptide analog of somatostatin

The selectivity of statine-based inhibitors against various human aspartic proteinases

Angiotensin-converting enzyme inhibitors: synthesis and biological activity of acyl tripeptide analogues of enalapril

Design and discovery in the development of long-acting renin inhibitors

Use of N-Fmoc amino acid chlorides and activated 2-(fluorenylmethoxy)-5(4H)-oxazolones in solid-phase peptide synthesis. Efficient syntheses of highly N-alkylated cyclic hexapeptide oxytocin antagonists related to L-365,209

Protected lactam-bridged dipeptides for use as conformational constraints in peptides

Bioactive Conformation of Luteinizing Hormone-Releasing Hormone: Evidence from a Conformationally Constrained Analog

Conformational modifications of cyclic hexapeptide somatostatin analogs

A potent cyclic hexapeptide analogue of somatostatin

A series of 5-(5,6)-dihydrouracil substituted 8-hydroxy-[1,6]naphthyridine-7-carboxylic acid 4-fluorobenzylamide inhibitors of HIV-1 integrase and viral replication in cells

Renin inhibitors containing conformationally restricted P1-P1' dipeptide mimetics

Synthesis of new peptides based on models of receptor-bound conformation

Nanomolar-affinity, non-peptide oxytocin receptor antagonists

Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation

Synthesis of 9-fluorenylmethyloxycarbonyl-protected N-alkyl amino acids by reduction of oxazolidinones

1-7,7-Dimethyl-2(S)-(2(S)-amino-4-(methylsulfonyl)butyramido)bicyclo[2.2.1]-heptan-1(S)-ylmethylsulfonyl-4-(2-methylphenyl)piperazine (L-368,899) : an orally bioavailable, non-peptide oxytocin antagonist with potential utility for managing preterm labor

Cyclic hexapeptide oxytocin antagonists. Potency-, selectivity-, and solubility-enhancing modifications

Interaction of Mouse Submaxillary Gland Renin with a Statine-Containing Subnanomolar, Competitive Inhibitor

Renin inhibitors containing conformationally restricted P1P1' dipeptide mimetics

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