您当前所在的位置:首页 > 产品中心 > 产品详细信息
98769-81-4 分子结构
点击图片或这里关闭

(2S)-2-[(S)-2-ethoxyphenoxy(phenyl)methyl]morpholine

ChemBase编号:119
分子式:C19H23NO3
平均质量:313.39082
单一同位素质量:313.1677936
SMILES和InChIs

SMILES:
O1[C@H]([C@@H](Oc2c(OCC)cccc2)c2ccccc2)CNCC1
Canonical SMILES:
CCOc1ccccc1O[C@@H](c1ccccc1)[C@H]1OCCNC1
InChI:
InChI=1S/C19H23NO3/c1-2-21-16-10-6-7-11-17(16)23-19(15-8-4-3-5-9-15)18-14-20-12-13-22-18/h3-11,18-20H,2,12-14H2,1H3/t18-,19-/m0/s1
InChIKey:
CBQGYUDMJHNJBX-OALUTQOASA-N

引用这个纪录

CBID:119 http://www.chembase.cn/molecule-119.html

Collapse All Expand All

名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
(2S)-2-[(S)-2-ethoxyphenoxy(phenyl)methyl]morpholine
IUPAC传统名
reboxetine
商标名
Edronax
Norebox
Vestra
Prolift
Solvex
Davedax
别名
Reboxetine mesylate
reboxetine
Reboxetine
CAS号
98769-81-4
PubChem SID
46504845
160963582
PubChem CID
65856

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 DB00234 external link
PubChem 65856 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
质子受体 质子供体
LogD (pH = 5.5) 0.9233303  LogD (pH = 7.4) 2.6492774 
Log P 3.2758145  摩尔折射率 89.4849 cm3
极化性 35.656822 Å3 极化表面积 39.72 Å2
可自由旋转的化学键 里宾斯基五规则 true 
Log P 3.06  LOG S -4.15 
溶解度 2.23e-02 g/l 

分子性质

分子性质

理化性质 生物活性(PubChem)
溶解度
8 mg/mL (Mesylate salt) expand 查看数据来源
疏水性(logP)
3.1 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB00234 external link
Item Information
Drug Groups approved; investigational
Description Reboxetine is an antidepressant drug used in the treatment of clinical depression, panic disorder and ADD/ADHD. Its mesylate (i.e. methanesulfonate) salt is sold under tradenames including Edronax, Norebox, Prolift, Solvex, Davedax or Vestra. Reboxetine has two chiral centers, but it only exists as two enantiomers, (R,R)-(-)- and (S,S)-(+)-reboxetine.
Indication For the treatment of clinical depression.
Pharmacology Reboxetine is a selective noradrenaline reuptake inhibitor (NaRI), the first drug of new antidepressant class. Reboxetine is an a-ariloxybenzyl derivative of morpholine. Reboxetine is primarily used to treat depression but has also been found useful in the treatment of narcolepsy and panic disorders.
Toxicity Reports of seizures (rare) have been reported
Affected Organisms
Humans and other mammals
Biotransformation Reboxetine is metabolized by dealkylation, hydroxylation and oxidation followed
by glucuronide or sulphate conjugation. It is metabolized by the cytochrome P450
CYP isoenzyme 3A4.
Absorption Reboxetine is rapidly and extensively absorbed following oral administration.
Half Life 12.5 hours
Protein Binding 98%
References
Fleishaker JC: Clinical pharmacokinetics of reboxetine, a selective norepinephrine reuptake inhibitor for the treatment of patients with depression. Clin Pharmacokinet. 2000 Dec;39(6):413-27. [Pubmed]
Edwards DM, Pellizzoni C, Breuel HP, Berardi A, Castelli MG, Frigerio E, Poggesi I, Rocchetti M, Dubini A, Strolin Benedetti M: Pharmacokinetics of reboxetine in healthy volunteers. Single oral doses, linearity and plasma protein binding. Biopharm Drug Dispos. 1995 Aug;16(6):443-60. [Pubmed]
Wienkers LC, Allievi C, Hauer MJ, Wynalda MA: Cytochrome P-450-mediated metabolism of the individual enantiomers of the antidepressant agent reboxetine in human liver microsomes. Drug Metab Dispos. 1999 Nov;27(11):1334-40. [Pubmed]
Kasper S, el Giamal N, Hilger E: Reboxetine: the first selective noradrenaline re-uptake inhibitor. Expert Opin Pharmacother. 2000 May;1(4):771-82. [Pubmed]
Fleishaker JC: Clinical pharmacokinetics of reboxetine, a selective norepinephrine reuptake inhibitor for the treatment of patients with depression. Clin Pharmacokinet. 2000 Dec;39(6):413-27. [Pubmed]
External Links
Wikipedia

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Edwards DM, Pellizzoni C, Breuel HP, Berardi A, Castelli MG, Frigerio E, Poggesi I, Rocchetti M, Dubini A, Strolin Benedetti M: Pharmacokinetics of reboxetine in healthy volunteers. Single oral doses, linearity and plasma protein binding. Biopharm Drug Dispos. 1995 Aug;16(6):443-60. Pubmed
  • Wienkers LC, Allievi C, Hauer MJ, Wynalda MA: Cytochrome P-450-mediated metabolism of the individual enantiomers of the antidepressant agent reboxetine in human liver microsomes. Drug Metab Dispos. 1999 Nov;27(11):1334-40. Pubmed
  • Kasper S, el Giamal N, Hilger E: Reboxetine: the first selective noradrenaline re-uptake inhibitor. Expert Opin Pharmacother. 2000 May;1(4):771-82. Pubmed
  • Fleishaker JC: Clinical pharmacokinetics of reboxetine, a selective norepinephrine reuptake inhibitor for the treatment of patients with depression. Clin Pharmacokinet. 2000 Dec;39(6):413-27. Pubmed
  • Fleishaker JC: Clinical pharmacokinetics of reboxetine, a selective norepinephrine reuptake inhibitor for the treatment of patients with depression. Clin Pharmacokinet. 2000 Dec;39(6):413-27. Pubmed
正在搜索,请耐心等待...(如果遇到网页错误或者长时间没有结果,请刷新页面[F5])

专利

专利

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

互联网资源

互联网资源

百度图标百度 google iconGoogle