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69010-88-4 分子结构
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1-(tert-butylamino)-3-[(2-methyl-1H-indol-4-yl)oxy]propan-2-yl benzoate

ChemBase编号:6407
分子式:C23H28N2O3
平均质量:380.48002
单一同位素质量:380.20999277
SMILES和InChIs

SMILES:
O(C(CNC(C)(C)C)COc1c2c([nH]c(c2)C)ccc1)C(=O)c1ccccc1
Canonical SMILES:
O=C(c1ccccc1)OC(COc1cccc2c1cc([nH]2)C)CNC(C)(C)C
InChI:
InChI=1S/C23H28N2O3/c1-16-13-19-20(25-16)11-8-12-21(19)27-15-18(14-24-23(2,3)4)28-22(26)17-9-6-5-7-10-17/h5-13,18,24-25H,14-15H2,1-4H3
InChIKey:
UUOJIACWOAYWEZ-UHFFFAOYSA-N

引用这个纪录

CBID:6407 http://www.chembase.cn/molecule-6407.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
1-(tert-butylamino)-3-[(2-methyl-1H-indol-4-yl)oxy]propan-2-yl benzoate
IUPAC传统名
bopindolol
商标名
Sandonorm
别名
Bopindolol
1-[(1,1-Dimethylethyl)amino]-3-[(2-methyl-1H-indol-4-yl)oxy]-2-propanol 2-Benzoate
(±)-1-[(1,1-Dimethylethyl)amino]-3-[(2-methyl-1H-indol-4-yl)oxy]-2-propanol Benzoate (Ester)
(±)-Bopindolol
rac Bopindolol
CAS号
69010-88-4
62658-63-3
PubChem SID
160969714
PubChem CID
44112

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID 价格
TRC
B675400 external link 加入购物车 请登录

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 16.797941  质子受体 3 
质子供体 2  LogD (pH = 5.5) 1.534566 
LogD (pH = 7.4) 2.7915826  Log P 4.668419 
摩尔折射率 111.0719 cm3 极化性 44.592506 Å3
极化表面积 63.35 Å2 可自由旋转的化学键 9 
里宾斯基五规则 true 
Log P 4.45  LOG S -5.38 
溶解度 1.60e-03 g/l 

分子性质

分子性质

理化性质 安全信息 产品相关信息 生物活性(PubChem)
溶解度
3.3 mg/ml [malonate salt] expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
质检报告
下载链接 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank TRC TRC
DrugBank -  DB08807 external link
Item Information
Drug Groups approved
Description Bopindolol (INN) is a beta blocker. It is an ester which acts as a prodrug for "pindolol":http://drugbank.ca/drugs/DB00960.
Indication For the management of hypertension, edema, ventricular tachycardias, and atrial fibrillation.
Pharmacology Bopindolol is a prodrug of pindolol. Pindolol is a non-selective beta-adrenergic antagonist (beta-blocker) which possesses intrinsic sympathomimetic activity (ISA) in therapeutic dosage ranges but does not possess quinidine-like membrane stabilizing activity. Pindolol impairs AV node conduction and decreases sinus rate and may also increase plasma triglycerides and decrease HDL-cholesterol levels. Pindolol is nonpolar and hydrophobic, with low to moderate lipid solubility. Pindolol has little to no intrinsic sympathomimetic activity and, unlike some other beta-adrenergic blocking agents, pindolol has little direct myocardial depressant activity and does not have an anesthetic-like membrane-stabilizing action.
Affected Organisms
• Humans and other mammals
External Links
• Wikipedia
Toronto Research Chemicals -  B675400 external link
Bopindolol is an ester prodrug of Pindolol (P468000). Bopindolol is a long acting β-adrenoceptor blocking agent. Bopindolol displays antispasmogenic activity mediated by α1-adrenoceptors and 5-HT2 receptors.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Turner, D.R. et al.: Br. J. Clin. Pharmacol., 17, 295 (1984)
  • Brodde, O.E. et al.: J. Cardio. Pharmacol., 8, S70 91986); Doggrell, S.A.: Med, Sci. Res., 17, 681 (1984)
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专利

专利

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