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34368-04-2 分子结构
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4-(2-{[4-(4-hydroxyphenyl)butan-2-yl]amino}ethyl)benzene-1,2-diol

ChemBase编号:719
分子式:C18H23NO3
平均质量:301.38012
单一同位素质量:301.1677936
SMILES和InChIs

SMILES:
Oc1cc(CCNC(CCc2ccc(O)cc2)C)ccc1O
Canonical SMILES:
CC(CCc1ccc(cc1)O)NCCc1ccc(c(c1)O)O
InChI:
InChI=1S/C18H23NO3/c1-13(2-3-14-4-7-16(20)8-5-14)19-11-10-15-6-9-17(21)18(22)12-15/h4-9,12-13,19-22H,2-3,10-11H2,1H3
InChIKey:
JRWZLRBJNMZMFE-UHFFFAOYSA-N

引用这个纪录

CBID:719 http://www.chembase.cn/molecule-719.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
4-(2-{[4-(4-hydroxyphenyl)butan-2-yl]amino}ethyl)benzene-1,2-diol
IUPAC传统名
dobutamine
商标名
Dobutamina [INN-Spanish]
Dobutamine Hcl
Dobutamine Hcl in Dextrose 5%
Dobutamine Hydrochloride
Dobutamine [Usan:Ban:Inn]
Dobutamine [Usan]
Dobutaminum [INN-Latin]
Dobutrex
Inotrex
Racemic-Dobutamine
别名
Dobutamine
CAS号
34368-04-2
PubChem SID
160964182
46505241
PubChem CID
36811

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
DrugBank DB00841 external link
PubChem 36811 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 10.141794  质子受体
质子供体 LogD (pH = 5.5) 0.55885684 
LogD (pH = 7.4) 1.1584939  Log P 2.6162553 
摩尔折射率 88.3911 cm3 极化性 34.158314 Å3
极化表面积 72.72 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P 2.97  LOG S -4.34 
溶解度 1.37e-02 g/l 

分子性质

分子性质

理化性质 生物活性(PubChem)
疏水性(logP)
3.6 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB00841 external link
Item Information
Drug Groups approved
Description A beta-2 agonist catecholamine that has cardiac stimulant action without evoking vasoconstriction or tachycardia. It is proposed as a cardiotonic after myocardial infarction or open heart surgery. [PubChem]
Indication For inotropic support in the short- term treatment of patients with cardiac decompensation due to depressed contractility resulting either from organic heart disease or from cardiac surgical procedures
Pharmacology Dobutamine is a direct-acting inotropic agent whose primary activity results from stimulation of the beta-adrenoceptors of the heart while producing comparatively mild chronotropic, hypertensive, arrhythmogenic, and vasodilative effects. Dobutamine acts primarily on beta-1 adrenergic receptors, with little effect on beta-2 or alpha receptors. It does not cause the release of endogenous norepinephrine, as does dopamine. Dobutamine is indicated when parenteral therapy is necessary for inotropic support in the short-term treatment of patients with cardiac decompensation due to depressed contractility resulting either from organic heart disease or from cardiac surgical procedures.
Affected Organisms
Humans and other mammals
Half Life 2 minutes
Elimination In human urine, the major excretion products are the conjugates of dobutamine and 3-O-methyl dobutamine.
External Links
Wikipedia
RxList
Drugs.com

参考文献

参考文献

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专利

专利

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