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Melatonin receptors are G protein-coupled receptors (GPCR) which bind melatonin. [1] Three types of melatonin receptors have been cloned.The MT 1 (or Mel 1A or MTNR1A) and MT 2 (or Mel 1B or MTNR1B) receptor subtypes are present in humans and other mammals, [2] while an additional melatonin receptor subtype MT 3 (or Mel 1C or MTNR1C) has been identified in amphibia and birds. [3]
17773 Ensembl ENSG00000168412 ENSMUSG00000054764 UniProt P48039 Q61184 RefSeq (mRNA) NM_005958 NM_008639 RefSeq (protein) NP_005949 NP_032665 Location (UCSC) Chr 4: 186.53 – 186.56 Mb Chr 8: 45.52 – 45.54 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Melatonin receptor type 1A is a protein that in humans is encoded by the MTNR1A gene. Function This gene encodes the MT 1 protein ...
244701 Ensembl ENSG00000134640 ENSMUSG00000050901 UniProt P49286 Q8CIQ6 Q3SXF8 RefSeq (mRNA) NM_005959 NM_145712 RefSeq (protein) NP_005950 NP_663758 Location (UCSC) Chr 11: 92.97 – 92.99 Mb Chr 9: 15.74 – 15.79 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Melatonin receptor 1B, also known as MTNR1B, is a protein that in humans is encoded by the MTNR1B gene. Function This gene ...
The melatonin receptors are G protein-coupled receptors and are expressed in various tissues of the body. There are two subtypes of the receptor in humans, melatonin receptor 1 (MT 1) and melatonin receptor 2 (MT 2). [2] Melatonin and melatonin receptor agonists, on market or in clinical trials, all bind to and activate both receptor types. [1]
Ramelteon is a melatonin receptor agonist with both high affinity for melatonin MT 1 and MT 2 receptors and selectivity over the non-human MT 3 receptor. Ramelteon demonstrates full agonist activity in vitro in cells expressing human MT 1 or MT 2 receptors, and high selectivity for human MT 1 and MT 2 receptors compared to the non-human MT 3 ...
Agomelatine acts as a highly potent and selective melatonin MT 1 and MT 2 receptor agonist (K i = 0.1 nM and 0.12 nM, respectively) and also as a relatively weak serotonin 5-HT 2B and 5-HT 2C receptor antagonist (K i = 660 nM and 631 nM, respectively; ~6,000-fold lower than for the melatonin receptors).
TIK-301 (LY-156735) is an agonist for the melatonin receptors MT 1 and MT 2 that is under development for the treatment of insomnia and other sleep disorders. [1] Its agonist action on MT 1 and MT 2 receptors in the suprachiasmatic nucleus in the brain enables its action as a chronobiotic.
Stimulation of the melanocortin-4 receptor causes a decrease in appetite and an increase in metabolism of fat and lean body mass, even in a relatively starved state. [21] Conversely, damage to this receptor has been shown to result in morbid obesity, and is the most commonly known cause of monogenic morbid obesity. [ 22 ]