Ramelteon-d5

Ramelteon-d5 Suppliers list
Company Name: Adamas Reagent, Ltd.  
Tel: 400-6009262 15618770481
Email: yhx@titansci.com
Company Name: Artis Biotech Co. Ltd.  
Tel: 18108108965 18108108965
Email: sales@artisbio.com
Company Name: Shanghai Hongye Biotechnology Co. Ltd  
Tel: 400-9205774 400-920-5774
Email: sales@glpbio.cn
Company Name: Hefei Molake Biotechnology Co., Ltd.  
Tel: 0551-66336380 18956014586
Email: 983438788@qq.com
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com

Ramelteon-d5 manufacturers

  • Ramelteon-D5
  • Ramelteon-D5 pictures
  • $3420.00
  • 2026-05-11
  • CAS:1134159-63-9
  • Purity:
  • Supply Ability: 10g
Ramelteon-d5 Basic information
Product Name:Ramelteon-d5
Synonyms:Ramelteon-d5;N-{2-[(8S)-1H,2H,6H,7H,8H-indeno[5,4-b]furan-8-yl]ethyl}(2H?)propanamide
CAS:1134159-63-9
MF:C16H21NO2
MW:259.35
EINECS:
Product Categories:
Mol File:1134159-63-9.mol
Ramelteon-d5 Structure
Ramelteon-d5 Chemical Properties
Safety Information
MSDS Information
Ramelteon-d5 Usage And Synthesis
UsesRamelteon-d5 is deuterium labeled Ramelteon. Ramelteon is a potent, highly selective, and orally active agonist of MT1/MT2 with Ki values of 14 and 112 pM, respectively. Ramelteon has the potential for the research of insomnia. Ramelteon consistently reduces sleep onset after long-term treatment, with no next-morning residual effects or rebound insomnia or withdrawal symptoms upon discontinuation[1][2].
IC 50MT2; MT1
References[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Kato K, et al. Neurochemical properties of ramelteon (TAK-375), a selective MT1/MT2 receptor agonist. Neuropharmacology. 2005;48(2):301-310. DOI:10.1016/j.neuropharm.2004.09.007
[3] Mayer G, et al. Efficacy and safety of 6-month nightly ramelteon administration in adults with chronic primary insomnia. Sleep. 2009;32(3):351-360. DOI:10.1093/sleep/32.3.351
[4] Hirai K, et al. Ramelteon (TAK-375) accelerates reentrainment of circadian rhythm after a phase advance of the light-dark cycle in rats. J Biol Rhythms. 2005;20(1):27-37. DOI:10.1177/0748730404269890
[5] Miyamoto M, et al. The sleep-promoting action of ramelteon (TAK-375) in freely moving cats. Sleep. 2004;27(7):1319-1325. DOI:10.1093/sleep/27.7.1319
Ramelteon-d5 Preparation Products And Raw materials
Tag:Ramelteon-d5(1134159-63-9) Related Product Information
3-(6,7-Dibromo-2,3-dihydrobenzofuran-5-yl)propanoic Acid Ramelteon Impurity 14 (E)-2-(1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-ylidene)ethylamine 4-Hydroxy Ramelteon Ramelteon Metabolite M-II PropanaMide, N-[2-(1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-ylidene)ethyl]- (R)-Ramelteon (S)-(+)-Ibuprofen Ramelteon Impurity 10 Ramelteon Impurity 1 HCl Acetonitrile, (1,2,6,7-tetrahydro-8H-indeno[5,4-b]furan-8-ylidene)-, (2E)- (R)-2-(2,6,7,8-tetrahydro-1H-indeno[5,4-b]furan-8-yl)acetic acid (S)-2-(2,6,7,8-tetrahydro-1H-indeno[5,4-b]furan-8-yl)acetic acid Ramelteon Impurity 6 Despropionyl Ramelteon Hydrochloride Ramelteon Impurity 22 2-(1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-yl)ethylaMine hydrochloride Ramelteon