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Novel Benzodiazepine Photoaffinity Probe Stereoselectively Labels a Site Deep within the Membrane-Spanning Domain of the Cholecystokinin Receptor

Journal of medicinal chemistry, 2006-02, Vol.49 (3), p.850-863

2006

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Optimization of 3-(1H-Indazol-3-ylmethyl)-1,5-benzodiazepines as Potent, Orally Active CCK-A Agonists

Journal of medicinal chemistry, 1997-08, Vol.40 (17), p.2706-2725

1997

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Discovery of 1,5-Benzodiazepines with Peripheral Cholecystokinin (CCK-A) Receptor Agonist Activity. 1. Optimization of the Agonist “Trigger”

Journal of medicinal chemistry, 1996-01, Vol.39 (2), p.562-569

1996

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1,4-Benzodiazepine Peripheral Cholecystokinin (CCK-A) Receptor Agonists

Bioorganic & medicinal chemistry letters, 2001-05, Vol.11 (9), p.1145-1148

2001

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Synthetic charybdotoxin-iberiotoxin chimeric peptides define toxin binding sites on calcium-activated and voltage-dependent potassium channels

Biochemistry (Easton), 1993-03, Vol.32 (9), p.2363-2370

1993

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3-[2-(N-Phenylacetamide)]-1,5-benzodiazepines: Orally Active, Binding Selective CCK-A Agonists

Journal of medicinal chemistry, 1996-07, Vol.39 (15), p.3030-3034

1996

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3-(1H-Indazol-3-ylmethyl)-1,5-benzodiazepines: CCK-A Agonists That Demonstrate Oral Activity as Satiety Agents

Journal of medicinal chemistry, 1996-07, Vol.39 (14), p.2655-2658

1996

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Modification of Receptor Selectivity and Functional Activity in Cholecystokinin Peptoid Ligands

Journal of medicinal chemistry, 1995-08, Vol.38 (17), p.3384-3390

1995

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Synthesis and evaluation of potent and selective beta(3) adrenergic receptor agonists containing acylsulfonamide, sulfonylsulfonamide, and sulfonylurea carboxylic acid isosteres

Journal of medicinal chemistry, 2002-01, Vol.45 (3), p.567-583

2002

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Allele-specific activation of genetically engineered receptors

The Journal of biological chemistry, 1991-01, Vol.266 (1), p.5-8

1991

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Biarylaniline phenethanolamines as potent and selective beta3 adrenergic receptor agonists

Journal of medicinal chemistry, 2006-05, Vol.49 (9), p.2758

2006

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Discovery of 1,5-Benzodiazepines with Peripheral Cholecystokinin (CCK-A) Receptor Agonist Activity (II): Optimization of the C3 Amino Substituent

Journal of medicinal chemistry, 1996-12, Vol.39 (26), p.5236-5245

1996

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Immunogenicity of synthetic HIV-1 gp120 V3-loop peptide-conjugate immunogens

Vaccine, 1994, Vol.12 (5), p.445-451

1994

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D-Isomeric replacements within the 6-9 core sequence of ac-[Nle4]-α-MSH4-11-NH2: A topological model for the solution conformation of α-melanotropin

Biopolymers, 1986-11, Vol.25 (11), p.2029-2042

1986

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Synthesis and biological evaluation of Nα-hydroxysulfonyl-[Nle28,31]-CCK26-33

Life sciences (1973), 1986-11, Vol.39 (18), p.1623-1629

1986

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Analogs of oxytocin containing a modified peptide bond

International Journal of Peptide and Protein Research, 1987-09, Vol.30 (3), p.318-322

1987

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Cholecystokinic activity of Nα-hydroxysulfonyl-[Nle28,31]CCK26-33 analogues modified at the C-terminal residue

International Journal of Peptide and Protein Research, 1988-06, Vol.31 (6), p.514-519

1988

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Dermal Sensory Regenerative Peripheral Nerve Interface for Reestablishing Sensory Nerve Feedback in Peripheral Afferents in the Rat

Plastic and reconstructive surgery (1963), 2023-05, Vol.151 (5), p.804e-813e

2023

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Silibinin inhibits ethanol metabolism and ethanol-dependent cell proliferation in an in vitro model of hepatocellular carcinoma

Cancer letters, 2010-05, Vol.291 (1), p.120-129

2010

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Assessment of Risk for Exposure to Bats in Sleeping Quarters Before and During Remediation — Kentucky, 2012

MMWR. Morbidity and mortality weekly report, 2013-05, Vol.62 (19), p.382-384

2013

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Novel Benzodiazepine Photoaffinity Probe Stereoselectively Labels a Site Deep within the Membrane-Spanning Domain of the Cholecystokinin Receptor

Optimization of 3-(1H-Indazol-3-ylmethyl)-1,5-benzodiazepines as Potent, Orally Active CCK-A Agonists

Discovery of 1,5-Benzodiazepines with Peripheral Cholecystokinin (CCK-A) Receptor Agonist Activity. 1. Optimization of the Agonist “Trigger”

1,4-Benzodiazepine Peripheral Cholecystokinin (CCK-A) Receptor Agonists

Synthetic charybdotoxin-iberiotoxin chimeric peptides define toxin binding sites on calcium-activated and voltage-dependent potassium channels

3-[2-(N-Phenylacetamide)]-1,5-benzodiazepines: Orally Active, Binding Selective CCK-A Agonists

3-(1H-Indazol-3-ylmethyl)-1,5-benzodiazepines: CCK-A Agonists That Demonstrate Oral Activity as Satiety Agents

Modification of Receptor Selectivity and Functional Activity in Cholecystokinin Peptoid Ligands

Synthesis and evaluation of potent and selective beta(3) adrenergic receptor agonists containing acylsulfonamide, sulfonylsulfonamide, and sulfonylurea carboxylic acid isosteres

Allele-specific activation of genetically engineered receptors

Biarylaniline phenethanolamines as potent and selective beta3 adrenergic receptor agonists

Discovery of 1,5-Benzodiazepines with Peripheral Cholecystokinin (CCK-A) Receptor Agonist Activity (II): Optimization of the C3 Amino Substituent

Immunogenicity of synthetic HIV-1 gp120 V3-loop peptide-conjugate immunogens

D-Isomeric replacements within the 6-9 core sequence of ac-[Nle4]-α-MSH4-11-NH2: A topological model for the solution conformation of α-melanotropin

Synthesis and biological evaluation of Nα-hydroxysulfonyl-[Nle28,31]-CCK26-33

Analogs of oxytocin containing a modified peptide bond

Cholecystokinic activity of Nα-hydroxysulfonyl-[Nle28,31]CCK26-33 analogues modified at the C-terminal residue

Dermal Sensory Regenerative Peripheral Nerve Interface for Reestablishing Sensory Nerve Feedback in Peripheral Afferents in the Rat

Silibinin inhibits ethanol metabolism and ethanol-dependent cell proliferation in an in vitro model of hepatocellular carcinoma

Assessment of Risk for Exposure to Bats in Sleeping Quarters Before and During Remediation — Kentucky, 2012

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