CAS 896736-21-3
:2-hydroxy-N-[2-[(8S)-2,6,7,8-tetrahydro-1H-cyclopenta[e]benzofuran-8-yl]ethyl]propanamide
Description:
2-hydroxy-N-[2-[(8S)-2,6,7,8-tetrahydro-1H-cyclopenta[e]benzofuran-8-yl]ethyl]propanamide, with the CAS number 896736-21-3, is a synthetic organic compound characterized by its complex structure, which includes a hydroxy group, an amide functional group, and a bicyclic system derived from cyclopenta[e]benzofuran. This compound features a chiral center, indicated by the (8S) configuration, which contributes to its stereochemical properties and potential biological activity. The presence of the hydroxy group suggests it may exhibit hydrogen bonding capabilities, influencing its solubility and reactivity. The bicyclic structure may impart unique pharmacological properties, making it of interest in medicinal chemistry. Additionally, the compound's amide linkage can affect its stability and interactions with biological targets. Overall, this substance may be explored for its potential applications in drug development, particularly in areas related to neuropharmacology or other therapeutic fields, although specific biological activities would require further investigation.
Formula:C16H21NO3
InChI:InChI=1/C16H21NO3/c1-10(18)16(19)17-8-6-12-3-2-11-4-5-14-13(15(11)12)7-9-20-14/h4-5,10,12,18H,2-3,6-9H2,1H3,(H,17,19)/t10?,12-/m0/s1
SMILES:CC(C(=NCC[C@@H]1CCc2ccc3c(CCO3)c12)O)O
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Found 5 products.
(R,S)-hydroxy Ramelteon Metabolite M-II
CAS:Formula:C16H21NO3Color and Shape:SolidMolecular weight:275.3428Ramelteon metabolite M-II
CAS:Ramelteon M-II binds MT1/MT2 with IC50s: 208/1470 pM; it's the main metabolite and a melatonin receptor agonist.Formula:C16H21NO3Purity:98%Color and Shape:SolidMolecular weight:275.34Ramelteon Metabolite M-II
CAS:Formula:C16H21NO3Color and Shape:White To Off-White SolidMolecular weight:275.35Ramelteon Metabolite M-II (mixture of R and S at the hydroxy position)
CAS:Controlled Product<p>Applications The major metabolite of Ramelteon in serum (M-II).<br>References Karim, A., et al.: J. Clin. Pharmacol., 44, 1210 (2004), Prescott, E., et al.: Drug Metab. Rev., 36, 203 (2004), Kato, K., et al.: Neuropharmacology, 48, 301 (2005), Karim, A., et al.: J. Clin. Pharmacol., 46, 140 (2006),<br></p>Formula:C16H21NO3Color and Shape:NeatMolecular weight:275.34(R)-Ramelteon Metabolite M-II
CAS:Controlled Product<p>Applications R-Ramelteon Metabolite M-II is a metabolite of Ramelteon in serum (M-II).<br>References Karim, A., et al.: J. Clin. Pharmacol., 44, 1210 (2004); Prescott, E., et al.: Drug Metab. Rev., 36, 203 (2004); Kato, K., et al.: Neuropharmacology, 48, 301 (2005); Karim, A., et al.: J. Clin. Pharmacol., 46, 140 (2006)<br></p>Formula:C11H18O4SColor and Shape:NeatMolecular weight:246.323



