Home GPCR & G Protein MT Receptor agonist Ramelteon For research use only.

Ramelteon

Synonyms: TAK-375

Ramelteon (TAK-375) is a novel melatonin receptor agonist for human MT1 and MT2 receptors and chick forebrain melatonin receptors with Ki of 14 pM, 112 pM and 23.1 pM, respectively.

Ramelteon Chemical Structure

Ramelteon Chemical Structure

CAS: 196597-26-9

Selleck's Ramelteon has been cited by 7 Publications

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Purity & Quality Control

Batch: Purity: 99.92%
99.92

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Biological Activity

Description Ramelteon (TAK-375) is a novel melatonin receptor agonist for human MT1 and MT2 receptors and chick forebrain melatonin receptors with Ki of 14 pM, 112 pM and 23.1 pM, respectively.
Features A tricyclic synthetic analog of melatonin.
Targets
MT1 receptor [1]
(Cell-free assay)		 MT receptor (chicken) [1]
(Cell-free assay)		 MT2 receptor [1]
(Cell-free assay)
14 pM(Ki) 23.1 pM(Ki) 112 pM(Ki)
In vitro
In vitro Ramelteon inhibits forskolin-stimulated cAMP production with IC50 of 21.2 pM in CHO cells. [1] Ramelteon has high affinity with recombinant human MT1 and MT2 receptors with pKi of 10.05 and 9.70, respectively. Ramelteon inhibits Xenopus laevis melanophore pigment granule aggregation with pEC50 of 11.48. [2] Ramelteon (1 nM) increases ERK1/2 phosphorylation not only in MT1/MT2 cerebellar granule cells but also in cerebellar granule cells expressing only one of the two melatonin receptors. 4P-PDOT blocks the stimulatory action of Ramelteon (1 nM) in MT1 KO cerebellar granule cells, while luzindole attenuates the action of Ramelteon (1 nM) in MT2 KO cerebellar granule cells. Ramelteon (100 μM) induces any pigment dispersion while melatonin completely disperses aggregated melanophores at 10 μM. [3]
In Vivo
In vivo Ramelteon (10 mg/kg, i/p) significantly reduces NREM sleep latency in rat and also produces a short-lasting increase in nonrapid eye movement (NREM) sleep duration, but the NREM power spectrum is unaltered. [2] Ramelteon (0.1 mg/kg and 1 mg/kg, p.o.) accelerates reentrainment of running wheel activity rhythm to the new lightdark cycle in rats without affecting learning or memory. [4] Ramelteon (0.03 mg/kg and 0.3 mg/kg, p.o.) significantly shortens latency to sleep onset and significantly increases total duration of sleep in freely moving monkeys without affecting the general behavior of the monkeys. [5]
Animal Research Animal Models estrogen-deficient ovariectomized (OVX) rats
Dosages 1 mg/kg
Administration Orally
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT03931070 Completed Delirium Rhode Island Hospital May 9 2019 Phase 4
NCT02560324 Completed Tobacco Use Disorder University of Pennsylvania|National Institute on Drug Abuse (NIDA)|National Institutes of Health (NIH) September 2015 Phase 2
NCT02969343 Completed Central Line-Associated Bloodstream Infection (CLABSI)|Venous Thromboembolism|Patient Fall|Catheter-Associated Infection|Severe Hypoglycemia|Opioid-Related Severe Adverse Drug Event|Hospital Acquired Pressure Ulcer|Adverse Drug Event|Severe Hospital Acquired Delerium|Rapid Response Related to Arrhythmia Brigham and Women''s Hospital|Northeastern University April 2015 Not Applicable
NCT00568789 Completed Insomnia Takeda June 2006 Phase 4

Chemical lnformation & Solubility

Molecular Weight 259.34 Formula

C16H21NO2
CAS No. 196597-26-9 SDF Download Ramelteon SDF
Smiles CCC(=O)NCCC1CCC2=C1C3=C(C=C2)OCC3
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 51 mg/mL ( (196.65 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 51 mg/mL

Water : Insoluble


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In vivo
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