(3S,6R)-6-(dimethylamino)-4,4-diphenylheptan-3-yl acetate hydrochloride

• ChemBase编号: 159352
• 分子式: C23H32ClNO2
• 平均质量: 389.95868
• 单一同位素质量: 389.21215695
• SMILES: C([C@@H](C(C[C@H](N(C)C)C)(c1ccccc1)c1ccccc1)OC(=O)C)C.Cl
• Canonical SMILES: CC[C@@H](C(c1ccccc1)(c1ccccc1)C[C@H](N(C)C)C)OC(=O)C.Cl
• InChI: InChI=1S/C23H31NO2.ClH/c1-6-22(26-19(3)25)23(17-18(2)24(4)5,20-13-9-7-10-14-20)21-15-11-8-12-16-21;/h7-16,18,22H,6,17H2,1-5H3;1H/t18-,22+;/m1./s1
• InChIKey: UXBPQRGCVJOTNT-MYXGOWFTSA-N

名称和登记号

名称

• IUPAC标准名: (3S,6R)-6-(dimethylamino)-4,4-diphenylheptan-3-yl acetate hydrochloride
• IUPAC传统名: betacetylmethadol hydrochloride
• 别名: Betacetylmethadol Hydrochloride; (3S,6R)-(-)-6-(Dimethylamino)-4,4-diphenyl-3-heptanol Acetate (Ester) Hydrochloride; (αS)-β-[(2R)-2-(Dimethylamino)propyl]-α-ethyl-β-phenylbenzeneethanol Acetate (Ester) Hydrochloride; β-3-Acetoxy-6-dimethylamino-4,4-diphenylheptane Hydrochloride; [S-(R*,S*)]-β-[2-(Dimethylamino)propyl]-α-ethyl-β-phenylbenzeneethanol Acetate (Ester) Hydrochloride; (αR)-β-[(2R)-2-(dimethylamino)propyl]-α-ethyl-β-phenylbenzeneethanol 1-Acetate Hydrochloride; α-Acetylmethadol hydrochloride; R-(R*,R*)]-β-[2-(dimethylamino)propyl]-α-ethyl-β-phenylbenzeneethanol Acetate (Ester) Hydrochloride; α-d-Acetylmethadol hydrochloride; (+)-α-Acetylmethadol Hydrochloride

登记号

• CAS号: 53757-35-0; 61443-60-5
• PubChem SID: 162253487
• PubChem CID: 66968112

理论计算性质

• 质子受体: 2
• 质子供体: 0
• LogD (pH = 5.5): 1.4385403
• LogD (pH = 7.4): 2.4523962
• Log P: 4.8847694
• 摩尔折射率: 117.8576 cm^3
• 极化性: 42.51397 Å^3
• 极化表面积: 29.54 Å^2
• 可自由旋转的化学键: 9
• 里宾斯基五规则: true

详细说明

Toronto Research Chemicals - A186320

The enantiomer of (-)-α-Acetylmethadol (A186325), a synthetic opioid similar in structure to Methadone (M225865) used in the treatment of opiate dependence. (+)-α-Acetylmethadol is more effective than (-)-α-Acetylmethadol in competing for both 3H-ligands

Toronto Research Chemicals - B323500

A synthetic opioid similar in structure to Methadone (M225865). It acts as a μ-opioid receptor agonist and evokes heroin-like discriminative stimulus effects.

参考文献

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• Xiao, Y. et al.: J. Pharmacol. Exp. Therap., 299, 366 (1974)
• Horng, J.S. et al.: Res. Comm. Chem. Pathol. Pharmacol., 14, 621 (1974)
• Newman, J.L. et al.: Psychopharmacol., 164, 108 (2002)
• Brase, D.A. et al.: Biochem. Pharmacol., 25, 1684 (2002)