1246812-22-5
1246812-22-5
Chemical Structure
Ramelteon metabolite M-II-d3
- CAS No.: 1246812-22-5
- Formula:C16H18D3NO3
- Molecular Weight:278.36
IUPAC Name: 2-hydroxy-N-(2-((S)-1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-yl)ethyl)propanamide
InChIKey: FGFNIJYHXMJYJN-PJCDIQNWSA-N
SMILES: [2H]C([2H])([2H])C(O)C(NCC[C@H]1C2=C(CC1)C=CC3=C2CCO3)=O
Biological Activity: Ramelteon metabolite M-II-d3 is the deuterium labeled Ramelteon metabolite M-II. Ramelteon metabolite M-II is the major metabolite of Ramelteon, with IC50s of 208 pM, 1470 pM for human melatonin receptors (MT1 or MT2). Ramelteon is a selective melatonin agonist[1][2].
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Ramelteon metabolite M-II-d3 | 99.78% | Ramelteon metabolite M-II-d3 is the deuterium labeled Ramelteon metabolite M-II. Ramelteon metabolite M-II is the major metabolite of Ramelteon, with IC50s of 208 pM, 1470 pM for human melatonin receptors (MT1 or MT2). Ramelteon is a selective melatonin agonist. | ||||||||||||||||||||
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Ramelteon metabolite M-II (Standard) | ≥98% | Ramelteon metabolite M-II (Standard) is the analytical standard of Ramelteon metabolite M-II (HY-103005). This product is intended for research and analytical applications. Ramelteon metabolite M-II is the major metabolite of Ramelteon, with IC50s of 208 pM, 1470 pM for human melatonin receptors (MT1 or MT2). Ramelteon is a selective melatonin agonist. | ||||||||||||||||||||
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Ramelteon metabolite M-II | 98.84% | Ramelteon metabolite M-II is the major metabolite of Ramelteon, with IC50s of 208 pM, 1470 pM for human melatonin receptors (MT1 or MT2). Ramelteon is a selective melatonin agonist. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.87
HY-75256RRamelteon impurity 10 (Standard) -
Similarity Score 0.87
HY-A0014RRamelteon (Standard) -
Similarity Score 0.87
HY-I0603(R)-Ramelteon -
Similarity Score 0.86
HY-75256S(Rac)-Remelteon-d3 -
Similarity Score 0.86
HY-A0014S1Ramelteon-d3 -
Similarity Score 0.83
HY-A0014SRamelteon-d5 -
Similarity Score 0.81
HY-75256Ramelteon impurity 10 -
Similarity Score 0.78
![(S)-2-(2,6,7,8-Tetrahydro-1H-indeno[5,4-b]furan-8-yl)ethanamine hydrochloride Chemical Structure](//file.medchemexpress.com/product_pic/hy-75074.gif)
HY-75074(S)-2-(2,6,7,8-Tetrahydro-1H-indeno[5,4-b]furan-8-yl)ethanamine hydrochloride -
Similarity Score 0.78
![1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-ethanamine hydrochloride Chemical Structure](//file.medchemexpress.com/product_pic/hy-75253a.gif)
HY-75253A1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-ethanamine hydrochloride -
Explore the MedChemAI to find more analogs
![(S)-2-(2,6,7,8-Tetrahydro-1H-indeno[5,4-b]furan-8-yl)ethanamine hydrochloride Chemical Structure](http://file.medchemexpress.com/product_pic/hy-75074.gif)
![1,6,7,8-Tetrahydro-2H-indeno[5,4-b]furan-8-ethanamine hydrochloride Chemical Structure](http://file.medchemexpress.com/product_pic/hy-75253a.gif)
References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief]
- [2]. Nishiyama K, et al. Pharmacological characterization of M-II, the major human metabolite of ramelteon. Pharmacology. 2014;93(3-4):197-201. [Content Brief]
