scispace - formally typeset
V

Victor J. Hruby

Researcher at University of Arizona

Publications -  1129
Citations -  43368

Victor J. Hruby is an academic researcher from University of Arizona. The author has contributed to research in topics: Receptor & Agonist. The author has an hindex of 88, co-authored 1126 publications receiving 42159 citations. Previous affiliations of Victor J. Hruby include University of Northern Colorado & Scripps Research Institute.

Papers
More filters
Journal ArticleDOI

A new type of synthetic peptide library for identifying ligand-binding activity

TL;DR: The simple methodology greatly enhances the production and rapid evaluation of random libraries of millions of peptides so that acceptor-binding ligands of high affinity can be rapidly identified and sequenced, on the basis of a "one-bead, one-peptide9 approach.
Journal ArticleDOI

Role of melanocortinergic neurons in feeding and the agouti obesity syndrome

TL;DR: The authors' data show that melanocortinergic neurons exert a tonic inhibition of feeding behaviour, and chronic disruption of this inhibitory signal is a likely explanation of the agouti obesity syndrome.
Journal Article

Role of melanocortinergic neurons in feeding and the agouti obesity syndrome

TL;DR: In this article, cyclic melanocortin analogues were identified that are potent agonists or antagonists of the neural MC3 and MC4 receptors, thus explaining the inhibitory effect of agouti on eumelanin pigment synthesis.
Journal ArticleDOI

Bis-penicillamine enkephalins possess highly improved specificity toward delta opioid receptors.

TL;DR: The conformationally restricted, cyclic, disulfide-containing, enkephalin analogs and the bis-Pen-containing analogs provide an order of magnitude increase in delta receptor selectivity.
Journal ArticleDOI

4-Norleucine, 7-D-phenylalanine-alpha-melanocyte-stimulating hormone: a highly potent alpha-melanotropin with ultralong biological activity.

TL;DR: This Nle4, D-Phe7 synthetic analogue of alpha-MSH is a very porent melanotropin, 26 times as potent as alpha- MSH in the adenylate cyclase assay, and the resistance of the peptide to enzymatic degradation and its extraordinarily potent and prolonged biological activity should make this analogue ofalpha-MSh an important molecular probe for studying the melanotropic receptors of both normal and abnormal (melanoma) melanocytes.