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23284-25-5 分子结构
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tert-butyl[3-(2-chloro-5-methylphenoxy)-2-hydroxypropyl]amine

ChemBase编号:6408
分子式:C14H22ClNO2
平均质量:271.78298
单一同位素质量:271.13390663
SMILES和InChIs

SMILES:
Clc1c(OCC(O)CNC(C)(C)C)cc(cc1)C
Canonical SMILES:
OC(COc1cc(C)ccc1Cl)CNC(C)(C)C
InChI:
InChI=1S/C14H22ClNO2/c1-10-5-6-12(15)13(7-10)18-9-11(17)8-16-14(2,3)4/h5-7,11,16-17H,8-9H2,1-4H3
InChIKey:
HQIRNZOQPUAHHV-UHFFFAOYSA-N

引用这个纪录

CBID:6408 http://www.chembase.cn/molecule-6408.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
tert-butyl[3-(2-chloro-5-methylphenoxy)-2-hydroxypropyl]amine
IUPAC传统名
bupranolol
商标名
Ophtorenin
Adomed
Betadrenol
别名
Bupranololum
Bupranol
Bupranolol
CAS号
23284-25-5
PubChem SID
160969715
PubChem CID
2475

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 DB08808 external link
PubChem 2475 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 14.087501  质子受体
质子供体 LogD (pH = 5.5) -0.20999743 
LogD (pH = 7.4) 0.6838863  Log P 2.992262 
摩尔折射率 74.8597 cm3 极化性 29.685394 Å3
极化表面积 41.49 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P 3.14  LOG S -3.28 
溶解度 1.43e-01 g/l 

分子性质

分子性质

生物活性(PubChem)

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB08808 external link
Item Information
Drug Groups approved
Description Bupranolol is a non-selective beta blocker without intrinsic sympathomimetic activity (ISA), but with strong membrane stabilizing activity. Its potency is similar to "propranolol":http://www.drugbank.ca/drugs/DB00571.
Indication Used to manage hypertension and tachycardia. Also used to treat glaucoma.
Pharmacology Bupranolol is a competitive, nonselective beta-blocker similar to propanolol without intrinsic sympathomimetic activity.
Toxicity Symptoms of overdose include bradycardia, cardiac failure, hypotension, and brochospasm.
Affected Organisms
Humans and other mammals
Biotransformation Over 90% undergo first-pass metabolism. The main metabolite is carboxybupranolol, 4-chloro-3-[3-(1,1-dimethylethylamino)-2-hydroxy-propyloxy]benzoic acid, of which 88% are eliminated renally within 24 hours.
Absorption Quickly and completely absorbed from the gut with less than 10% oral bioavailability.
Half Life 2-4 hours
Protein Binding 76%

参考文献

参考文献

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专利

专利

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