Sathya M. Schnell - Concepedia

Author

Sathya M. Schnell

University of Minnesota

Also Known As

Sathya M. Schnell, Sathya Schnell

Publications

320

Citations

H-Index

Concepts

All Affiliations

University of Minnesota Georgetown University Nova Southeastern University University of Florida

About

Sathya M. Schnell is an author at University of Minnesota specializing in medicine, molecular biology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	114
2	Natural Sciences	3	3	76
3	Biochemistry	3	3	76
4	Chemical Biology	1	1	42
5	Endocrinology	1	1	17

Sathya M. Schnell

Publications

196

Citations

H-Index

Page 1

	Year	Citations
An in Vitro and in Vivo Investigation of Bivalent Ligands That Display Preferential Binding and Functional Activity for Different Melanocortin Receptor Homodimers Cody J. Lensing, Katie T. Freeman, Sathya M. Schnell, Journal of Medicinal Chemistry Different Bivalent LigandsMolecular BiologyLead IdentificationPharmacotherapyChemical Biology	2016	42
A fragment of the Escherichia coli ClpB heat-shock protein is a micromolar melanocortin 1 receptor agonist Mark D. Ericson, Sathya M. Schnell, Katie T. Freeman, Bioorganic & Medicinal Chemistry Letters Protein FunctionSignal TransductionMicromolar Melanocortin 1Molecular RegulationReceptor (Biochemistry)	2015	38
1,2,3-Triazole Rings as a Disulfide Bond Mimetic in Chimeric AGRP-Melanocortin Peptides: Design, Synthesis, and Functional Characterization Srinivasa R. Tala, Anamika Singh, Cody J. Lensing, ACS Chemical Neuroscience	2017	28
Developing a Biased Unmatched Bivalent Ligand (BUmBL) Design Strategy to Target the GPCR Homodimer Allosteric Signaling (cAMP over β-Arrestin 2 Recruitment) Within the Melanocortin Receptors Cody J. Lensing, Katie T. Freeman, Sathya M. Schnell, Journal of Medicinal Chemistry	2018	22
A Macrocyclic Agouti-Related Protein/[Nle<sup>4</sup>,DPhe<sup>7</sup>]α-Melanocyte Stimulating Hormone Chimeric Scaffold Produces Subnanomolar Melanocortin Receptor Ligands Mark D. Ericson, Katie T. Freeman, Sathya M. Schnell, Journal of Medicinal Chemistry Molecular PharmacologySignal TransductionAntagonist PotencyBiochemistryMelanocortin System	2017	17
A Direct in Vivo Comparison of the Melanocortin Monovalent Agonist Ac-His-DPhe-Arg-Trp-NH<sub>2</sub> versus the Bivalent Agonist Ac-His-DPhe-Arg-Trp-PEDG20-His-DPhe-Arg-Trp-NH<sub>2</sub>: A Bivalent Advantage Cody J. Lensing, Danielle N. Adank, Stacey L. Wilber, ACS Chemical Neuroscience	2017	17
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 Receptor Mark D. Ericson, Katie T. Freeman, Sathya M. Schnell, Journal of Medicinal Chemistry Melanocortin SystemPeptide ScienceInverse Agonist PharmacologyMolecular PharmacologyAla Substitution	2017	17
Discovery of Mixed Pharmacology Melanocortin-3 Agonists and Melanocortin-4 Receptor Tetrapeptide Antagonist Compounds (TACOs) Based on the Sequence Ac-Xaa<sup>1</sup>-Arg-(pI)DPhe-Xaa<sup>4</sup>-NH<sub>2</sub> Skye R. Doering, Katie T. Freeman, Sathya M. Schnell, Journal of Medicinal Chemistry	2017	15

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