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Minimizing HCN in DIC/Oxyma mediated amide bond forming reactions
POxAP Precatalysts and the Negishi Cross-Coupling Reaction
Aminoguanidine Hydrazone Derivatives as Nonpeptide NPFF1 Receptor Antagonists Reverse Opioid Induced Hyperalgesia
Effects of systematic N-terminus deletions and benzoylations of endogenous RF-amide peptides on NPFF1R, NPFF2R, GPR10, GPR54 and GPR103
Development of sub-nanomolar dipeptidic ligands of neuropeptide FF receptors
Trisubstitution of pyridine through sequential and regioselective palladium cross-coupling reactions affording analogs of known GPR54 antagonists
Rapid and scalable synthesis of innovative unnatural α,β or γ-amino acids functionalized with tertiary amines on their side-chains.
Neuropeptide FF and prolactin-releasing peptide decrease cortical excitability through activation of NPFF receptors.
Diastereoselective Synthesis of Nonplanar 3-Amino-1,2,4-oxadiazine Scaffold: Structure Revision of Alchornedine
Development of Dipeptidic hGPR54 Agonists.
RF-amide neuropeptides and their receptors in Mammals: Pharmacological properties, drug development and main physiological functions
Evolution of coumaroyl conjugate 3‐hydroxylases in land plants: Lignin biosynthesis and defense
Endogenous mammalian RF-amide peptides, including PrRP, kisspeptin and 26RFa, modulate nociception and morphine analgesia via NPFF receptors
The neuroprotector kynurenic acid increases neuronal cell survival through neprilysin induction.
The translocator protein ligand XBD173 improves clinical symptoms and neuropathological markers in the SJL/J mouse model of multiple sclerosis
TSPO Ligands Boost Mitochondrial Function and Pregnenolone Synthesis
The effect of neuropeptide FF in the amygdala kindling model.
Design and synthesis of 3-aminophthalazine derivatives and structural analogues as PDE5 inhibitors: anti-allodynic effect against neuropathic pain in a mouse model
Phenylpyridine-2-ylguanidines and rigid mimetics as novel inhibitors of TNFα overproduction: Beneficial action in models of neuropathic pain and of acute lung inflammation
A bifunctional-biased mu-opioid agonist–neuropeptide FF receptor antagonist as analgesic with improved acute and chronic side effects

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