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87233-61-2 分子结构
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1-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1H-1,3-benzodiazole

ChemBase编号:955
分子式:C17H26N4O
平均质量:302.41454
单一同位素质量:302.21066147
SMILES和InChIs

SMILES:
O(CCn1c(N2CCCN(CC2)C)nc2c1cccc2)CC
Canonical SMILES:
CCOCCn1c(nc2c1cccc2)N1CCCN(CC1)C
InChI:
InChI=1S/C17H26N4O/c1-3-22-14-13-21-16-8-5-4-7-15(16)18-17(21)20-10-6-9-19(2)11-12-20/h4-5,7-8H,3,6,9-14H2,1-2H3
InChIKey:
KBUZBQVCBVDWKX-UHFFFAOYSA-N

引用这个纪录

CBID:955 http://www.chembase.cn/molecule-955.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-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)-1H-1,3-benzodiazole
IUPAC传统名
emedastine
商标名
Emadine
别名
Emedastina [INN-Spanish]
Emedastinum [INN-Latin]
Emedastine difumarate
Emedastine
1-(2-ethoxyethyl)-2-(4-methyl-1,4-diazepan-1-yl)benzimidazole
CAS号
87233-61-2
PubChem SID
160964418
46505109
PubChem CID
3219

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
苏州艾佳
AJA-O11084 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
质子受体 质子供体
LogD (pH = 5.5) -0.8740286  LogD (pH = 7.4) 1.1855345 
Log P 2.4923856  摩尔折射率 90.4747 cm3
极化性 35.620316 Å3 极化表面积 33.53 Å2
可自由旋转的化学键 里宾斯基五规则 true 
Log P 2.91  LOG S -2.32 
溶解度 1.44e+00 g/l 

分子性质

分子性质

理化性质 产品相关信息 生物活性(PubChem)
溶解度
Soluble (difumarate formulation) expand 查看数据来源
疏水性(logP)
2.6 expand 查看数据来源
纯度
97% expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB01084 external link
Item Information
Drug Groups approved
Description Emedastine is an antihistamine used in eye drops to treat allergic conjunctivitis. [Wikipedia]
Indication For the temporary relief of the signs and symptoms of allergic conjunctivitis.
Pharmacology Emedastine is a relatively selective H1-receptor antagonist.
Toxicity Somnolence and malaise have been reported following daily oral administration.
Affected Organisms
Humans and other mammals
Biotransformation Two primary metabolites, 5-hydroxyemedastine and 6-hydroxyemedastine, are excreted in the urine as both free and conjugated forms. The 5'-oxoanalogs of 5-hydroxyemedastine and 6-hydroxy-emedastine and the N-oxide are also formed as minor metabolites.
Absorption Ophthalmic use of emedastine usually does not produce measurable plasma concentrations.
Half Life The elimination half-life of oral emedastine in plasma is 3-4 hours.
Elimination Approximately 44% of the oral dose is recovered in the urine over 24 hours with only 3.6% of the dose excreted as parent drug. Two primary metabolites, 5- and 6-hydroxyemedastine, are excreted in the urine as both free and conjugated forms.
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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