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Rho Signaling Pathway Targeted to Promote Spinal Cord Repair

The Journal of neuroscience, 2002-08, Vol.22 (15), p.6570-6577

2002

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Mimicry of Peptide Backbone Geometry and Heteroatomic Side-Chain Functionality: Synthesis of Enantiopure Indolizidin-2-one Amino Acids Possessing Alcohol, Acid, and Azide Functional Groups

Journal of organic chemistry, 2001-02, Vol.66 (4), p.1171-1180

2001

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VRQ397 (CRAVKY): a novel noncompetitive V2 receptor antagonist

American journal of physiology. Regulatory, integrative and comparative physiology, 2009-10, Vol.297 (4), p.R1009-R1018

2009

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Synthesis of Enantiopure 7-[3-Azidopropyl]indolizidin-2-one Amino Acid. A Constrained Mimic of the Peptide Backbone Geometry and Heteroatomic Side-Chain Functionality of the Ala-Lys Dipeptide

Journal of organic chemistry, 2001-02, Vol.66 (4), p.1181-1185

2001

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Design, synthesis, and conformational analysis of azacycloalkane amino acids as conformationally constrained probes for mimicry of peptide secondary structures

BIOPOLYM, 2000, Vol.55 (2), p.101-122

2000

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Poly-(ProΨ[CH(OAc)CH2]Aib)3 a Protected Trimer of Pro-Aib Hydroxyethylene Isosteres

Advances in experimental medicine and biology, 2009, Vol.611, p.171-172

2009

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Rigid Dipeptide Surrogates: Syntheses of Enantiopure Quinolizidinone and Pyrroloazepinone Amino Acids from a Common Diaminodicarboxylate Precursor

Journal of organic chemistry, 2000-04, Vol.65 (7), p.2163-2171

2000

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Exploring the relationship between turn geometry and allosteric antagonism of peptide mimic ligands for the prostaglandin F2alpha receptor

Advances in experimental medicine and biology, 2009, Vol.611, p.271

2009

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N-(9-(9-Phenylfluorenyl))homoserine-Derived Cyclic Sulfamidates: Novel Chiral Educts for the Synthesis of Enantiopure γ-Substituted α-Amino Acids

Organic letters, 2001-09, Vol.3 (19), p.2965-2968

2001

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PepLook: An innovative in silico tool for determination of structure, polymorphism and stability of peptides

Advances in experimental medicine and biology, 2009, Vol.611, p.459-460

2009

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Racemization in the Use of N-(9-(9-Phenylfluorenyl))Serine-Derived Cyclic Sulfamidates in the Synthesis of δ-Keto α-Amino Carboxylates and Prolines

Organic letters, 2000-08, Vol.2 (17), p.2595-2598

2000

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Amino acid-azetidine chimeras: synthesis of enantiopure 3-substituted azetidine-2-carboxylic acids

The journal of peptide research, 2005-02, Vol.65 (2), p.298-310

2005

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Exploring relationships between mimic configuration, peptide conformation and biological activity in indolizidin-2-one amino acid analogs of gramicidin S

The journal of peptide research, 2002-10, Vol.60 (4), p.198-214

2002

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A study of the relationship between biological activity and prolyl amide isomer geometry in oxytocin using 5-tert-butylproline to augment the Cys(6)-Pro(7) amide cis-isomer population

Journal of medicinal chemistry, 2000-04, Vol.43 (8), p.1448-1455

2000

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Aza-scanning of the Potent Melanocortin Receptor Agonist Ac-His-d-Phe-Arg-Trp-NH2

Chemical biology & drug design, 2006-04, Vol.67 (4), p.275-283

2006

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An examination of the steric effects of 5-tert-butylproline on the conformation of polyproline and the cooperative nature of type II to type I helical interconversion

BIOPOLYM, 2000-03, Vol.53 (3), p.249-256

2000

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Functional Selectivity Revealed by N‑Methylation Scanning of Human Urotensin II and Related Peptides

Journal of medicinal chemistry, 2019-02, Vol.62 (3), p.1455-1467

2019

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Enantioselective synthesis of β-amino acids based on BINAP—ruthenium(II) catalyzed hydrogenation

Tetrahedron: asymmetry, 1991, Vol.2 (7), p.543-554

1991

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The influence of steric interactions on the conformation and biology of oxytocin. Synthesis and analysis of penicillamine(6)-oxytocin and penicillamine(6)-5-tert-butylproline(7)-oxytocin analogs

The journal of peptide research, 2001-09, Vol.58 (3), p.263-273

2001

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Probing Opioid Receptor Interactions with Azacycloalkane Amino Acids. Synthesis of a Potent and Selective ORL1 Antagonist

Journal of medicinal chemistry, 2002-11, Vol.45 (24), p.5353-5357

2002

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Probing opioid receptor-ligand interactions by employment of indolizidin-9-one amino acid as a constrained Gly(2)-Gly(3) surrogate in a leucine-enkephalin mimic

The journal of peptide research, 2001-04, Vol.57 (4), p.337-344

2001

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5-tert-Butylproline

Journal of organic chemistry, 1996-12, Vol.61 (26), p.9447-9454

1996

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Synthesis and reactivity of cyclic sulfamidites and sulfamidates

Tetrahedron, 2003-04, Vol.59 (15), p.2581-2616

2003

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Systematic Study of the Synthesis of Macrocyclic Dipeptide β-Turn Mimics Possessing 8-, 9-, and 10- Membered Rings by Ring-Closing Metathesis

Journal of organic chemistry, 2005-05, Vol.70 (10), p.3838-3844

2005

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Synthesis and pharmacology of new enantiopure delta(3)-4-arylkainoids

Bioorganic & medicinal chemistry letters, 2000-04, Vol.10 (8), p.771

2000

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Rho Signaling Pathway Targeted to Promote Spinal Cord Repair

Mimicry of Peptide Backbone Geometry and Heteroatomic Side-Chain Functionality: Synthesis of Enantiopure Indolizidin-2-one Amino Acids Possessing Alcohol, Acid, and Azide Functional Groups

VRQ397 (CRAVKY): a novel noncompetitive V2 receptor antagonist

Synthesis of Enantiopure 7-[3-Azidopropyl]indolizidin-2-one Amino Acid. A Constrained Mimic of the Peptide Backbone Geometry and Heteroatomic Side-Chain Functionality of the Ala-Lys Dipeptide

Design, synthesis, and conformational analysis of azacycloalkane amino acids as conformationally constrained probes for mimicry of peptide secondary structures

Poly-(ProΨ[CH(OAc)CH2]Aib)3 a Protected Trimer of Pro-Aib Hydroxyethylene Isosteres

Rigid Dipeptide Surrogates: Syntheses of Enantiopure Quinolizidinone and Pyrroloazepinone Amino Acids from a Common Diaminodicarboxylate Precursor

Exploring the relationship between turn geometry and allosteric antagonism of peptide mimic ligands for the prostaglandin F2alpha receptor

N-(9-(9-Phenylfluorenyl))homoserine-Derived Cyclic Sulfamidates: Novel Chiral Educts for the Synthesis of Enantiopure γ-Substituted α-Amino Acids

PepLook: An innovative in silico tool for determination of structure, polymorphism and stability of peptides

Racemization in the Use of N-(9-(9-Phenylfluorenyl))Serine-Derived Cyclic Sulfamidates in the Synthesis of δ-Keto α-Amino Carboxylates and Prolines

Amino acid-azetidine chimeras: synthesis of enantiopure 3-substituted azetidine-2-carboxylic acids

Exploring relationships between mimic configuration, peptide conformation and biological activity in indolizidin-2-one amino acid analogs of gramicidin S

A study of the relationship between biological activity and prolyl amide isomer geometry in oxytocin using 5-tert-butylproline to augment the Cys(6)-Pro(7) amide cis-isomer population

Aza-scanning of the Potent Melanocortin Receptor Agonist Ac-His-d-Phe-Arg-Trp-NH2

An examination of the steric effects of 5-tert-butylproline on the conformation of polyproline and the cooperative nature of type II to type I helical interconversion

Functional Selectivity Revealed by N‑Methylation Scanning of Human Urotensin II and Related Peptides

Enantioselective synthesis of β-amino acids based on BINAP—ruthenium(II) catalyzed hydrogenation

The influence of steric interactions on the conformation and biology of oxytocin. Synthesis and analysis of penicillamine(6)-oxytocin and penicillamine(6)-5-tert-butylproline(7)-oxytocin analogs

Probing Opioid Receptor Interactions with Azacycloalkane Amino Acids. Synthesis of a Potent and Selective ORL1 Antagonist

Probing opioid receptor-ligand interactions by employment of indolizidin-9-one amino acid as a constrained Gly(2)-Gly(3) surrogate in a leucine-enkephalin mimic

5-tert-Butylproline

Synthesis and reactivity of cyclic sulfamidites and sulfamidates

Systematic Study of the Synthesis of Macrocyclic Dipeptide β-Turn Mimics Possessing 8-, 9-, and 10- Membered Rings by Ring-Closing Metathesis

Synthesis and pharmacology of new enantiopure delta(3)-4-arylkainoids

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