SKU:K1360 | M. Wt:259.34 | ||
Formula:C16H21NO2 | Solubility:No | ||
Purity:>99% | Storage:2 years at -20 degrees centigrade | ||
CAS No.:196597-26-9 | Synonyms:Rozerem, TAK-375 | ||
Chemical NameN/A |
供货周期: | 一周 |
品牌: | |
规格: | 2mg |
货号: | K1360 |
CAS号: | 196597-26-9 |
SKU:K1360 | M. Wt:259.34 | ||
Formula:C16H21NO2 | Solubility:No | ||
Purity:>99% | Storage:2 years at -20 degrees centigrade | ||
CAS No.:196597-26-9 | Synonyms:Rozerem, TAK-375 | ||
Chemical NameN/A |
Description | Ramelteon(TAK-375) | |||||
---|---|---|---|---|---|---|
Targets | MT1 receptor | MT2 receptor | MT receptor (chicken) | |||
IC50 | 14 pM (Ki) | 112 pM (Ki) | 23.1 pM (Ki) | |||
In vitro | Ramelteon (TAK-375) can inhibit MT1 receptor and MT2 receptor with Ki of 14 pM and 112 pM. Ramelteon has high affinity with recombinant human MT1 and MT2 receptors with pKi of 10.05 and 9.70. 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. | |||||
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. | |||||
Clinical Trials | N/A | |||||
Features | N/A |
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