Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anthony F. Nastase"'
Autor:
Aaron M. Bender, Thomas J Fernandez, John R. Traynor, Emily M. Jutkiewicz, Henry I. Mosberg, Nicholas W. Griggs, Jessica P. Anand, Anthony F. Nastase, Deanna Montgomery
Publikováno v:
Journal of Medicinal Chemistry. 62:4193-4203
Short-acting μ-opioid receptor (MOR) agonists have long been used for the treatment of severe, breakthrough pain. However, selective MOR agonists including fentanyl and morphine derivatives are limited clinically due to high risks of dependence, tol
Autor:
Emily M. Jutkiewicz, Nicholas W. Griggs, Henry I. Mosberg, Jessica P. Anand, Anthony F. Nastase, Deanna Montgomery, Kelsey E Kochan, John R. Traynor
Publikováno v:
British Journal of Pharmacology. 175:2013-2027
BACKGROUND AND PURPOSE Agonists at μ-opioid receptors (μ-receptors) are used for pain management but produce adverse effects including tolerance, dependence and euphoria. The co-administration of a μ-receptor agonist with a δ-opioid receptor (δ-
Autor:
Anthony F. Nastase, Jessica P. Anand, Tyler J. Trask, Henry I. Mosberg, Emily M. Jutkiewicz, Thomas J Fernandez, Nicholas W. Griggs, John R. Traynor, Aubrie A. Harland
Publikováno v:
ACS Chem Neurosci
The use of opioids for the treatment of pain, while largely effective, is limited by detrimental side effects including analgesic tolerance, physical dependence, and euphoria, which may lead to opioid abuse. Studies have shown that compounds with a
Autor:
Nicholas W. Griggs, Thomas J Fernandez, John R. Traynor, Anthony F. Nastase, Jessica P. Anand, Emily J. Jutkiewicz, Henry I. Mosberg
Publikováno v:
The FASEB Journal. 32
Autor:
Jessica P, Anand, Kelsey E, Kochan, Anthony F, Nastase, Deanna, Montgomery, Nicholas W, Griggs, John R, Traynor, Henry I, Mosberg, Emily M, Jutkiewicz
Publikováno v:
British journal of pharmacology. 175(11)
BACKGROUND AND PURPOSE: Agonists at μ‐opioid receptors (μ‐receptors) are used for pain management but produce adverse effects including tolerance, dependence and euphoria. The co‐administration of a μ‐receptor agonist with a δ‐opioid re
Autor:
Donald B. Boyd, Anthony F. Nastase
Publikováno v:
Journal of chemical information and modeling. 52(12)
Beta-site amyloid precursor protein cleaving enzyme-1 (BACE1) is a target of interest for treating patients with Alzheimer's disease (AD). Inhibition of BACE1 may prevent amyloid-ß (Aß) plaque formation and the development or progression of Alzheim