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Preclinical Evaluation of Antiangiogenic Thrombospondin-1 Peptide Mimetics, ABT-526 and ABT-510, in Companion Dogs with Naturally Occurring Cancers

Clinical cancer research, 2006-12, Vol.12 (24), p.7444-7455

2006

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Thrombospondin-1 Mimetic Peptide Inhibitors of Angiogenesis and Tumor Growth: Design, Synthesis, and Optimization of Pharmacokinetics and Biological Activities

Journal of medicinal chemistry, 2005-04, Vol.48 (8), p.2838-2846

2005

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Inhibition of tumor growth by systemic treatment with thrombospondin‐1 peptide mimetics

International journal of cancer, 2002-04, Vol.98 (5), p.682-689

2002

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Effect of N-methyl substitution of the peptide bonds in luteinizing hormone-releasing hormone agonists

Journal of medicinal chemistry, 1993-02, Vol.36 (3), p.363-369

1993

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Refolding of misfolded mutant GPCR: Post-translational pharmacoperone action in vitro

Molecular and cellular endocrinology, 2007-06, Vol.272 (1), p.77-85

2007

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Nonpeptide Luteinizing Hormone-Releasing Hormone Antagonists Derived from Erythromycin A: Design, Synthesis, and Biological Activity of Cladinose Replacement Analogues

Journal of medicinal chemistry, 2004-02, Vol.47 (5), p.1085-1097

2004

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Elimination of antibacterial activities of non-peptide luteinizing hormone-releasing hormone (LHRH) antagonists derived from erythromycin A

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (6), p.1599-1602

2004

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In vitro and in vivo Activities of Reduced-Size Antagonists of Luteinizing Hormone-Releasing Hormone

Journal of medicinal chemistry, 1994-03, Vol.37 (5), p.701-705

1994

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3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives: inhibitors of immune complex induced inflammation

Journal of medicinal chemistry, 1988-09, Vol.31 (9), p.1719-1728

1988

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Pharmacological and endocrine characterization of A-198401, an orally active GnRH antagonist, in intact and castrate male rat models

Drug development research, 2001-03, Vol.52 (3), p.485-491

2001

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Condensations of 4-methyl-4-dichloromethyl-2,5-cyclohexadienone

Journal of the American Chemical Society, 1969-04, Vol.91 (9), p.2299-2307

1969

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Semisynthetic cephalosporins. IV Synthesis and structure activity relationships of parenterarry active 7-(4-(substituted methyl)phenyl)acetamido-3-cephem-4-carboxylic acids

Journal of antibiotics, 1981, Vol.34 (10), p.1311-1317

1981

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Differential orientation of a GnRH agonist and antagonist in the pituitary GnRH receptor

Endocrinology (Philadelphia), 1993-08, Vol.133 (2), p.942-945

1993

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Stabilization of the N-terminal residues of luteinizing hormone-releasing hormone agonists and the effect on pharmacokinetics

Journal of medicinal chemistry, 1992-10, Vol.35 (21), p.3890-3894

1992

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Active reduced-size hexapeptide analogs of luteinizing hormone-releasing hormone

Journal of medicinal chemistry, 1989-10, Vol.32 (10), p.2340-2344

1989

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Quantitative structure-activity relationship of inhibitors of immune complex-induced inflammation: 1-Phenyl-3-aminopyrazoline derivatives

Journal of pharmaceutical sciences, 1990-07, Vol.79 (7), p.609-613

1990

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The effect of NMeTyr5 substitution in luteinizing hormone-releasing hormone antagonists

Journal of medicinal chemistry, 1993-04, Vol.36 (7), p.928-933

1993

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Inhibitors of Immune Complex-Induced Inflammation: 3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile Derivatives

Journal of pharmaceutical sciences, 1989-06, Vol.78 (6), p.494-498

1989

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1 - Synthetic Approaches to Incorporation of Novel Amino Acids into Gonadotropin-Releasing Hormone Peptides

Methods in Neurosciences, 1993, Vol.13, p.3-18

1993

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Inhibitors of Immune Complex-Induced Inflammation: 5-Substituted 3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile Derivatives

Journal of pharmaceutical sciences, 1990-08, Vol.79 (8), p.682-684

1990

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2-[(Phenylthio)methyl]pyridine derivatives: new antiinflammatory agents

Journal of medicinal chemistry, 1983-02, Vol.26 (2), p.218-222

1983

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Transformations of 1-methyl-1-(dichloromethyl)cyclohexane derivatives

Journal of organic chemistry, 1970-06, Vol.35 (6), p.2092-2095

1970

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SEMISYNTHETIC CEPHALOSPORINS. IV: SYNTHESIS AND STRUCTURE ACTIVITY RELATIONSHIPS OF PARENTERALLY ACTIVE 7-[4-(SUBSTITUTED METHYL)PHENYL]- ACETAMIDO-3-CEPHEM-4-CARBOXYLIC ACIDS

The Journal of Antibiotics, 1981, Vol.34(10), pp.1311-1317

1981

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Preclinical Evaluation of Antiangiogenic Thrombospondin-1 Peptide Mimetics, ABT-526 and ABT-510, in Companion Dogs with Naturally Occurring Cancers

Thrombospondin-1 Mimetic Peptide Inhibitors of Angiogenesis and Tumor Growth: Design, Synthesis, and Optimization of Pharmacokinetics and Biological Activities

Inhibition of tumor growth by systemic treatment with thrombospondin‐1 peptide mimetics

Effect of N-methyl substitution of the peptide bonds in luteinizing hormone-releasing hormone agonists

Refolding of misfolded mutant GPCR: Post-translational pharmacoperone action in vitro

Nonpeptide Luteinizing Hormone-Releasing Hormone Antagonists Derived from Erythromycin A: Design, Synthesis, and Biological Activity of Cladinose Replacement Analogues

Elimination of antibacterial activities of non-peptide luteinizing hormone-releasing hormone (LHRH) antagonists derived from erythromycin A

In vitro and in vivo Activities of Reduced-Size Antagonists of Luteinizing Hormone-Releasing Hormone

3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives: inhibitors of immune complex induced inflammation

Pharmacological and endocrine characterization of A-198401, an orally active GnRH antagonist, in intact and castrate male rat models

Condensations of 4-methyl-4-dichloromethyl-2,5-cyclohexadienone

Semisynthetic cephalosporins. IV Synthesis and structure activity relationships of parenterarry active 7-(4-(substituted methyl)phenyl)acetamido-3-cephem-4-carboxylic acids

Differential orientation of a GnRH agonist and antagonist in the pituitary GnRH receptor

Stabilization of the N-terminal residues of luteinizing hormone-releasing hormone agonists and the effect on pharmacokinetics

Active reduced-size hexapeptide analogs of luteinizing hormone-releasing hormone

Quantitative structure-activity relationship of inhibitors of immune complex-induced inflammation: 1-Phenyl-3-aminopyrazoline derivatives

The effect of NMeTyr5 substitution in luteinizing hormone-releasing hormone antagonists

Inhibitors of Immune Complex-Induced Inflammation: 3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile Derivatives

1 - Synthetic Approaches to Incorporation of Novel Amino Acids into Gonadotropin-Releasing Hormone Peptides

Inhibitors of Immune Complex-Induced Inflammation: 5-Substituted 3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile Derivatives

2-[(Phenylthio)methyl]pyridine derivatives: new antiinflammatory agents

Transformations of 1-methyl-1-(dichloromethyl)cyclohexane derivatives

SEMISYNTHETIC CEPHALOSPORINS. IV: SYNTHESIS AND STRUCTURE ACTIVITY RELATIONSHIPS OF PARENTERALLY ACTIVE 7-[4-(SUBSTITUTED METHYL)PHENYL]- ACETAMIDO-3-CEPHEM-4-CARBOXYLIC ACIDS

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