Results 131 to 140 of about 11,769 (169)
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The location, physiology, pathology of hippocampus Melatonin MT2 receptor and MT2-selective modulators

European Journal of Medicinal Chemistry, 2023
Melatonin, a neurohormone secreted by the pineal gland and regulated by the suprachiasmatic nucleus (SCN) of the hypothalamus, is synthesized and directly released into the cerebrospinal fluid (CSF) of the third ventricle (3rdv), where it undergoes rapid absorption by surrounding tissues to exert its physiological function.
Yueqin, Feng   +3 more
openaire   +2 more sources

MT2 Inhibits Osteoclastogenesis by Scavenging Ros

Acta Endocrinologica (Bucharest), 2023
Reactive oxygen species (ROS) produced under oxidative stress is important for osteoclastogenesis. As a major member of the metallothionein (MT) family, metallothionein2 (MT2) can scavenge ROS in osteoblasts. However, the role of MT2 in osteoclastogenesis and ROS production in osteoclast precursors (OCPs) is unknown.In this study, we first investigated
S, Wei   +7 more
openaire   +2 more sources

Puchok-MT2 diagnostic esophagoscope

Biomedical Engineering, 1979
The proximal part contains a zoom eyepiece, a handle for managing the distal end, buttons for controlling the supply of water and air, means of withdrawing secretions, and a hole for passing biopsy probes. Secretions are withdrawn automatically when an aspirator is connected. Distance marks are made at intervals of 50 mm on the working part.
A. N. Moll   +3 more
openaire   +1 more source

MPEC 2023-M101 : 2023 MT2

2023
The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
openaire   +1 more source

Tetrahydroisoquinoline derivatives as melatonin MT2 receptor antagonists

Bioorganic & Medicinal Chemistry Letters, 2004
A series of tetrahydroisoquinolines has yielded potent MT(2) receptor antagonists, which are selective versus the MT(1) receptor.
George N, Karageorge   +6 more
openaire   +2 more sources

Indanyl piperazines as melatonergic MT2 selective agents

Bioorganic & Medicinal Chemistry Letters, 2003
Optimization of a benzyl piperazine pharmacophore produced N-acyl-4-indanyl-piperazines that bind with high affinity to melatonergic MT(2) receptors. (R)-4-(2,3-dihydro-6-methoxy-1H-inden-1-yl)-N-ethyl-1-piperazine-carboxamide fumarate (13) is a water soluble, selective MT(2) agonist, which produces advances in circadian phase in rats at doses of 1-56 ...
Ronald J, Mattson   +10 more
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The molecules recognized by anti-MT2 alloantisera and anti-MT2-like (DRw52) monoclonal antibodies are different

Human Immunology, 1985
The human class II alloantigens include the HLA-DR, DQ, and MT determinants. Previous reports in the literature suggest that while the DQ determinants appear to be on a molecule separate from DR, the MT determinants are variably present on DR or DQ molecules. We have previously reported, using the homozygous DR5 cell line Swei, that the MT4 determinant
J, Schiffenbauer, C, Bono, B D, Schwartz
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Preferential Formation of MT1/MT2 Melatonin Receptor Heterodimers with Distinct Ligand Interaction Properties Compared with MT2 Homodimers

Molecular Pharmacology, 2004
Heterodimerization has been documented for several members of the G protein-coupled receptor (GPCR) superfamily, including the closely related MT(1) and MT(2) melatonin receptors. However, the relative abundance of hetero-versus homodimers and the specific properties, which can be attributed to each form, are difficult to determine.
Mohammed A, Ayoub   +3 more
openaire   +2 more sources

Investigational Selective Melatoninergic Ligands for Receptor Subtype MT2

Mini-Reviews in Medicinal Chemistry, 2013
Melatonin, an endogenous ligand for melatonin receptor, plays an important role in modulating various physiological activities through acting on different subtypes MT1, MT2 or the binding site MT3. The distinct roles of the receptor subtypes provide great potential for receptor-specific pharmacological agents. Melatonin has no subtypeselectivity, so it
Ning, Wan   +5 more
openaire   +2 more sources

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