12 articles for MA Giulianotti
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis and biological evaluations of novel endomorphin analogues containinga-hydroxy-ß-phenylalanine (AHPBA) displaying mixedµ/d opioid receptor agonist andd opioid receptor antagonist activities.

Zhejiang University
Identification of tetrapeptides from a mixture based positional scanning library that can restore nM full agonist function of the L106P, I69T, I102S, A219V, C271Y, and C271R human melanocortin-4 polymorphic receptors (hMC4Rs).

University of Florida
Scaffold ranking and positional scanning utilized in the discovery of nAChR-selective compounds suitable for optimization studies.

Torrey Pines Institute For Molecular Studies
Conformation-opioid activity relationships of bicyclic guanidines from 3D similarity analysis.

Torrey Pines Institute For Molecular Studies
Synthesis and biological evaluation of 2-indolinone derivatives as potential antitumor agents.

Zhejiang University
Identification, structure-activity relationships and molecular modeling of potent triamine and piperazine opioid ligands.

Institute For Molecular Studies
Discovery of a novel protein kinase B inhibitor by structure-based virtual screening.

Torrey Pines Institute For Molecular Studies
Discovery of Nanomolar Melanocortin-3 Receptor (MC3R)-Selective Small Molecule Pyrrolidine Bis-Cyclic Guanidine Agonist Compounds Via a High-Throughput "Unbiased" Screening Campaign.

University of Minnesota
Functional Mixture-Based Positional Scan Identifies a Library of Antagonist Tetrapeptide Sequences (LAtTeS) with Nanomolar Potency for the Melanocortin-4 Receptor and Equipotent with the Endogenous AGRP(86-132) Antagonist.

University of Minnesota
Discovery of Polypharmacological Melanocortin-3 and -4 Receptor Probes and Identification of a 100-Fold Selective nM MC3R Agonist versus a μM MC4R Partial Agonist.

University of Minnesota
Discovery of Mixed Pharmacology Melanocortin-3 Agonists and Melanocortin-4 Receptor Tetrapeptide Antagonist Compounds (TACOs) Based on the Sequence Ac-Xaa

University of Minnesota
Highly Selective and Potentα4β2 nAChR Antagonist Inhibits Nicotine Self-Administration and Reinstatement in Rats.

Torrey Pines Institute For Molecular Studies