({3-[3-(piperidin-1-ylmethyl)phenoxy]propyl}carbamoyl)methyl acetate hydrochloride

• ChemBase编号: 177482
• 分子式: C19H29ClN2O4
• 平均质量: 384.89756
• 单一同位素质量: 384.1815851
• SMILES: c1c(cc(cc1)CN1CCCCC1)OCCCNC(=O)COC(=O)C.Cl
• Canonical SMILES: O=C(COC(=O)C)NCCCOc1cccc(c1)CN1CCCCC1.Cl
• InChI: InChI=1S/C19H28N2O4.ClH/c1-16(22)25-15-19(23)20-9-6-12-24-18-8-5-7-17(13-18)14-21-10-3-2-4-11-21;/h5,7-8,13H,2-4,6,9-12,14-15H2,1H3,(H,20,23);1H
• InChIKey: FEWCTJHCXOHWNL-UHFFFAOYSA-N

名称和登记号

名称

• IUPAC标准名: ({3-[3-(piperidin-1-ylmethyl)phenoxy]propyl}carbamoyl)methyl acetate hydrochloride
• IUPAC传统名: roxatidine acetate hydrochloride
• 别名: 2-(Acetyloxy)-N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]acetamide Hydrochloride; Altat; Gastralgin; HOE 760; Neo H2; Roxit; TZU 0460; Roxatidine Acetate Hydrochloride; Roxatidine acetate HCl

登记号

• CAS号: 93793-83-0
• PubChem SID: 164233392
• PubChem CID: 56704

理论计算性质

• Acid pKa: 14.8782835
• 质子受体: 4
• 质子供体: 1
• LogD (pH = 5.5): -1.7924889
• LogD (pH = 7.4): -0.12762822
• Log P: 1.3130374
• 摩尔折射率: 96.3186 cm^3
• 极化性: 37.719524 Å^3
• 极化表面积: 67.87 Å^2
• 可自由旋转的化学键: 10
• 里宾斯基五规则: true

分子性质

理化性质

• 溶解度: DMSO; Methanol; Water
• 外观: White Solid
• 熔点: 147-149°C

安全信息

• 保存条件: Refrigerator

药理学性质

• 作用靶点: Histamine Receptor

产品相关信息

• 成盐信息: HCl

详细说明

Toronto Research Chemicals - R700870

A histamine H2-receptor antagonist. It is used to inhibit gastric acid secretion; an antiulcer agent.

参考文献

• Tarutani, M. et al.: Arzneim.-Forsch., 35, 703 (1985)
• Yagita, M. et al.: Therap. Res., 7, 96 (1985)
• Asai, M. et al.: Gek. Yak., 50, 922 (1985)