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97657-92-6 分子结构
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5-(2-{2,8-dimethyl-1H,2H,3H,4H,5H-pyrido[4,3-b]indol-5-yl}ethyl)-2-methylpyridine dihydrochloride

ChemBase编号:72591
分子式:C21H27Cl2N3
平均质量:392.36518
单一同位素质量:391.15820324
SMILES和InChIs

SMILES:
n1(c2c(c3c1ccc(c3)C)CN(CC2)C)CCc1ccc(nc1)C.Cl.Cl
Canonical SMILES:
CN1CCc2c(C1)c1cc(C)ccc1n2CCc1ccc(nc1)C.Cl.Cl
InChI:
InChI=1S/C21H25N3.2ClH/c1-15-4-7-20-18(12-15)19-14-23(3)10-9-21(19)24(20)11-8-17-6-5-16(2)22-13-17;;/h4-7,12-13H,8-11,14H2,1-3H3;2*1H
InChIKey:
GTWLIQOLGOZTLF-UHFFFAOYSA-N

引用这个纪录

CBID:72591 http://www.chembase.cn/molecule-72591.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
5-(2-{2,8-dimethyl-1H,2H,3H,4H,5H-pyrido[4,3-b]indol-5-yl}ethyl)-2-methylpyridine dihydrochloride
IUPAC传统名
5-(2-{2,8-dimethyl-1H,3H,4H-pyrido[4,3-b]indol-5-yl}ethyl)-2-methylpyridine dihydrochloride
别名
Latrepirdine
Dimebolin
Dimebon
CAS号
97657-92-6
PubChem SID
162037516
PubChem CID
23729232

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
Selleck Chemicals
S1245 external link 加入购物车 请登录
数据来源 数据ID
PubChem 23729232 external link

理论计算性质

理论计算性质

JChem
质子受体 质子供体
LogD (pH = 5.5) 0.8634037  LogD (pH = 7.4) 3.081123 
Log P 3.4085224  摩尔折射率 100.7248 cm3
极化性 39.457382 Å3 极化表面积 21.06 Å2
可自由旋转的化学键 里宾斯基五规则 true 

分子性质

分子性质

安全信息 药理学性质 产品相关信息 生物活性(PubChem)
保存条件
-20°C expand 查看数据来源
作用靶点
Histamine receptors expand 查看数据来源
成盐信息
Hydrochloride expand 查看数据来源

详细说明

详细说明

Selleck Chemicals Selleck Chemicals
Selleck Chemicals -  S1245 external link
Research Area: Neurological Disease
Biological Activity:
Latrepirdine (INN, also known as dimebolin and sold as Dimebon), is an antihistamine drug. Research is continuing in both Russia and western nations into potential applications as a neuroprotective drug to combat Alzheimer’s disease and, possibly, as a nootropic as well. However, a Phase III clinical trial for Alzheimer’s disease treatment failed to show any benefit. [1]Latrepirdine operates through multiple mechanisms of action, blocking the action of neurotoxic beta-amyloid proteins, inhibiting L-type calcium channels, modulating the action of AMPA and NMDA glutamate receptors, exerting a neuroprotective effect by blocking a novel target that involves mitochondrial pores, blocking a number of other receptors including α-adrenergic, 5-HT2C, 5-HT5A, and 5-HT6. [1]

参考文献

参考文献

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  • http://en.wikipedia.org/wiki/Latrepirdine
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专利

专利

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互联网资源

互联网资源

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