Endogenous opiates and behavior: 2012

RJ Bodnar - Peptides, 2013 - Elsevier
This paper is the thirty-fifth consecutive installment of the annual review of research
concerning the endogenous opioid system. It summarizes papers published during 2012 …

Cell-Penetrating Peptides Selectively Cross the Blood-Brain Barrier In Vivo

S Stalmans, N Bracke, E Wynendaele, B Gevaert… - PloS one, 2015 - journals.plos.org
Cell-penetrating peptides (CPPs) are a group of peptides, which have the ability to cross cell
membrane bilayers. CPPs themselves can exert biological activity and can be formed …

The μ opioid receptor and ligands acting at the μ opioid receptor, as therapeutics and potential therapeutics

M Spetea, M Faheem Asim, G Wolber… - Current …, 2013 - ingentaconnect.com
Although the μ opioid receptor (MOR) was pharmacologically and biochemically identified in
binding studies forty years ago, its structure, function, and true complexity only have …

Pd (II)-catalyzed [5+ 2] rollover annulation and lactonization of 1-benzylpyrazoles with 4-hydroxy-2-alkynoates

SR Kancharla, R Bantu, B Sridhar, AV Narsaiah… - Tetrahedron, 2024 - Elsevier
Abstract The first Pd-catalyzed [5+ 2] rollover annulation of 1-benzylpyrazoles has been
developed to afford a novel class of 1H-benzo [e] furo [3, 4-c] pyrazolo [1, 5-a] azepin-3 (8H) …

Synthesis of 2-spiropseudoindoxyls via an intramolecular nitroalkyne redox–dipolar cycloaddition cascade

N Marien, B Brigou, B Pinter, F De Proft… - Organic letters, 2015 - ACS Publications
Novel spiropseudoindoxyls were synthesized in high yields via a fully regioselective Au (III)-
catalyzed cycloisomerization of easily obtainable o-nitrophenylpropiolamides, followed by …

A bifunctional-biased mu-opioid agonist–neuropeptide FF receptor antagonist as analgesic with improved acute and chronic side effects

AD La Rochelle, K Guillemyn, M Dumitrascuta… - Pain, 2018 - journals.lww.com
Opioid analgesics, such as morphine, oxycodone, and fentanyl, are the cornerstones for
treating moderate to severe pain. However, on chronic administration, their efficiency is …

Biodegradable amphipathic peptide hydrogels as extended-release system for opioid peptides

C Martin, M Dumitrascuta, M Mannes… - Journal of medicinal …, 2018 - ACS Publications
Chronic pain is currently treated with opioids that offer unsatisfactory long-term analgesia
and produce serious side effects. There is a clear need for alternative therapies. Herein …

Side chain cyclized aromatic amino acids: great tools as local constraints in peptide and peptidomimetic design

O Van der Poorten, A Knuhtsen… - Journal of Medicinal …, 2016 - ACS Publications
Constraining the conformation of flexible peptides is a proven strategy to increase potency,
selectivity, and metabolic stability. The focus has mostly been on constraining the backbone …

Mimicking of Arginine by Functionalized Nω-Carbamoylated Arginine As a New Broadly Applicable Approach to Labeled Bioactive Peptides: High Affinity …

M Keller, KK Kuhn, J Einsiedel… - Journal of Medicinal …, 2016 - ACS Publications
Derivatization of biologically active peptides by conjugation with fluorophores or
radionuclide-bearing moieties is an effective and commonly used approach to prepare …

Asymmetric Synthesis of 1-Benzazepine Derivatives via Copper-Catalyzed Intramolecular Reductive Cyclization

DX Li, Y Park, W Yoon, H Yun, J Yun - Organic letters, 2019 - ACS Publications
An asymmetric construction of enantioenriched 2, 3-substituted-1-benzazepine derivatives
containing a cyclic tertiary amine moiety was developed by copper-catalyzed reductive …