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Katie T Freeman

Showing results (1-10 of 36) with videos related to

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ACS Medicinal Chemistry Letters|October 16, 2020
Peptoid NPhe<sup>4</sup> in AGRP-Based c[Pro<sup>1</sup>-Arg<sup>2</sup>-Phe<sup>3</sup>-Phe<sup>4</sup>-Xxx<sup>5</sup>-Ala<sup>6</sup>-Phe<sup>7</sup>-DPro<sup>8</sup>] Scaffolds Maintain Mouse MC4R Antagonist PotencyMark D Ericson, Katie T Freeman, Carrie Haskell-Luevano
Bioorganic & Medicinal Chemistry Letters|October 5, 2015
A fragment of the Escherichia coli ClpB heat-shock protein is a micromolar melanocortin 1 receptor agonistMark D Ericson, Sathya M Schnell, Katie T Freeman, et al.
ACS Medicinal Chemistry Letters|March 19, 2020
Single Nucleotide Polymorphisms in the Melanocortin His-Phe-Arg-Trp Sequences Decrease Tetrapeptide Potency and EfficacyMarshall D Winget, Mark D Ericson, Katie T Freeman, et al.
Journal of Medicinal Chemistry|January 4, 2017
A Macrocyclic Agouti-Related Protein/[Nle<sup>4</sup>,DPhe<sup>7</sup>]α-Melanocyte Stimulating Hormone Chimeric Scaffold Produces Subnanomolar Melanocortin Receptor LigandsMark D Ericson, Katie T Freeman, Sathya M Schnell, et al.
Journal of Medicinal Chemistry|July 24, 2018
Synergistic Multiresidue Substitutions of a Macrocyclic c[Pro-Arg-Phe-Phe-Asn-Ala-Phe-dPro] Agouti-Related Protein (AGRP) Scaffold Yield Potent and >600-Fold MC4R versus MC3R Selective Melanocortin Receptor AntagonistsKatlyn A Fleming, Katie T Freeman, Mark D Ericson, et al.
ACS Medicinal Chemistry Letters|January 25, 2021
Multiresidue Tetrapeptide Substitutions Yield a 140-fold Selective Melanocortin-3 over Melanocortin-4 Receptor AgonistMark D Ericson, Romessa Shaikh, Courtney M Larson, et al.
ACS Pharmacology & Translational Science|January 16, 2025
Recommended Opioid Receptor Tool Compounds: Comparative <i>In Vitro</i> for Receptor Selectivity Profiles and <i>In Vivo</i> for Pharmacological Antinociceptive ProfilesLinh T Tran, Katie T Freeman, Mary M Lunzer, et al.
Journal of Medicinal Chemistry|August 17, 2017
Structure-Activity Relationship Studies on a Macrocyclic Agouti-Related Protein (AGRP) Scaffold Reveal Agouti Signaling Protein (ASP) Residue Substitutions Maintain Melanocortin-4 Receptor Antagonist Potency and Result in Inverse Agonist Pharmacology at the Melanocortin-5 ReceptorMark D Ericson, Katie T Freeman, Sathya M Schnell, et al.
ACS Chemical Neuroscience|June 21, 2018
Arg-Phe-Phe d-Amino Acid Stereochemistry Scan in the Macrocyclic Agouti-Related Protein Antagonist Scaffold c[Pro-Arg-Phe-Phe-Xxx-Ala-Phe-DPro] Results in Unanticipated Melanocortin-1 Receptor Agonist ProfilesMark D Ericson, Zoe M Koerperich, Katie T Freeman, et al.
ACS Omega|August 15, 2022
Incorporation of Indoylated Phenylalanine Yields a Sub-Micromolar Selective Melanocortin-4 Receptor Antagonist TetrapeptideMark D Ericson, Courtney M Larson, Katie T Freeman, et al.
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Showing results (1-10 of 36) with videos related to

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ACS Medicinal Chemistry Letters|October 16, 2020
Peptoid NPhe<sup>4</sup> in AGRP-Based c[Pro<sup>1</sup>-Arg<sup>2</sup>-Phe<sup>3</sup>-Phe<sup>4</sup>-Xxx<sup>5</sup>-Ala<sup>6</sup>-Phe<sup>7</sup>-DPro<sup>8</sup>] Scaffolds Maintain Mouse MC4R Antagonist PotencyMark D Ericson, Katie T Freeman, Carrie Haskell-Luevano
Bioorganic & Medicinal Chemistry Letters|October 5, 2015
A fragment of the Escherichia coli ClpB heat-shock protein is a micromolar melanocortin 1 receptor agonistMark D Ericson, Sathya M Schnell, Katie T Freeman, et al.
ACS Medicinal Chemistry Letters|March 19, 2020
Single Nucleotide Polymorphisms in the Melanocortin His-Phe-Arg-Trp Sequences Decrease Tetrapeptide Potency and EfficacyMarshall D Winget, Mark D Ericson, Katie T Freeman, et al.
Journal of Medicinal Chemistry|January 4, 2017
A Macrocyclic Agouti-Related Protein/[Nle<sup>4</sup>,DPhe<sup>7</sup>]α-Melanocyte Stimulating Hormone Chimeric Scaffold Produces Subnanomolar Melanocortin Receptor LigandsMark D Ericson, Katie T Freeman, Sathya M Schnell, et al.
Journal of Medicinal Chemistry|July 24, 2018
Synergistic Multiresidue Substitutions of a Macrocyclic c[Pro-Arg-Phe-Phe-Asn-Ala-Phe-dPro] Agouti-Related Protein (AGRP) Scaffold Yield Potent and >600-Fold MC4R versus MC3R Selective Melanocortin Receptor AntagonistsKatlyn A Fleming, Katie T Freeman, Mark D Ericson, et al.
ACS Medicinal Chemistry Letters|January 25, 2021
Multiresidue Tetrapeptide Substitutions Yield a 140-fold Selective Melanocortin-3 over Melanocortin-4 Receptor AgonistMark D Ericson, Romessa Shaikh, Courtney M Larson, et al.
ACS Pharmacology & Translational Science|January 16, 2025
Recommended Opioid Receptor Tool Compounds: Comparative <i>In Vitro</i> for Receptor Selectivity Profiles and <i>In Vivo</i> for Pharmacological Antinociceptive ProfilesLinh T Tran, Katie T Freeman, Mary M Lunzer, et al.
Journal of Medicinal Chemistry|August 17, 2017
Structure-Activity Relationship Studies on a Macrocyclic Agouti-Related Protein (AGRP) Scaffold Reveal Agouti Signaling Protein (ASP) Residue Substitutions Maintain Melanocortin-4 Receptor Antagonist Potency and Result in Inverse Agonist Pharmacology at the Melanocortin-5 ReceptorMark D Ericson, Katie T Freeman, Sathya M Schnell, et al.
ACS Chemical Neuroscience|June 21, 2018
Arg-Phe-Phe d-Amino Acid Stereochemistry Scan in the Macrocyclic Agouti-Related Protein Antagonist Scaffold c[Pro-Arg-Phe-Phe-Xxx-Ala-Phe-DPro] Results in Unanticipated Melanocortin-1 Receptor Agonist ProfilesMark D Ericson, Zoe M Koerperich, Katie T Freeman, et al.
ACS Omega|August 15, 2022
Incorporation of Indoylated Phenylalanine Yields a Sub-Micromolar Selective Melanocortin-4 Receptor Antagonist TetrapeptideMark D Ericson, Courtney M Larson, Katie T Freeman, et al.
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