バレニクリン

5,8,14-Triazatetracyclo[10.3.1.02,11.04,9]hexadeca-2,4,6,8,10-pentaene

HCID 170361CAS 249296-44-4

基本情報

標準SMILES
c1cnc2cc3c(cc2n1)C1CNCC3C1
InChIKey
JQSHBVHOMNKWFT-UHFFFAOYSA-N
分子式
C13H13N3
平均分子量
211.26 g/mol
単同位体質量
211.11094743

名称と識別子

優先名称
5,8,14-Triazatetracyclo[10.3.1.02,11.04,9]hexadeca-2,4,6,8,10-pentaene
IUPAC
5,8,14-triazatetracyclo[10.3.1.02,11.04,9]hexadeca-2,4,6,8,10-pentaene
現地名
バレニクリン
英語名
Varenicline
分子式
C13H13N3
分子量
211.26

名称と別名

5,8,14-triazatetracyclo[10.3.1.02,11.04,9]hexadeca-2,4,6,8,10-pentaeneAB01568242_01Varenicline (INN)5,8,14-triazatetracyclo[10.3.1.0^{2,11}.0^{4,9}]hexadeca-2(11),3,5,7,9-pentaeneNCGC00247735-01NCGC00247735-02VareniclinVarenicline?SCHEMBL225687CHEMBL556954orb1690005SCHEMBL29363551
名称をさらに表示
バレニクリン7,8,9,10-テトラヒドロ-6α,10α-メタノ-1,4,8-トリアザ-6H-シクロヘプタ[b]ナフタレン(1R,12S)-5,8,14-トリアザテトラシクロ[10.3.1.02,11.04,9]ヘキサデカ-2(11),3,5,7,9-ペンタエンChantixVarenciline10-tetrahydro-Varenicline free base7,8,9,10-tetrahydro-6H-6,10-methanoazepino[4,5-g]quinoxaline(1R,12S)-5,8,14-triazatetracyclo[10.3.1.0^{2,11}.0^{4,9}]hexadeca-2,4(9),5,7,10-pentaeneCS-861Hsdb 7591Cp 526555VARENICLINE
7,8,9,10-tetCP 526555; Champix; ChantixHMS5087H05BDBM50166908s6985T4246LAKOS005145561CS-0396

データベース識別子

CAS
249296-44-4
PubChem CID
170361
DTXSID
DTXSID70891447
Nikkaji
J2.566.151F

物性

構造計算による物性

XLogP
0.8
極性表面積
37.8 Ų
水素結合供与体数
1
水素結合受容体数
3
回転可能結合数
0
重原子数
16

物理化学的性質

融点
138.5 °C · 138.5 °C
沸点
400.6 · 400.6±40.0 °C(Predicted)
比重(密度)
1.247 · 1.247±0.06 g/cm3(Predicted)
貯蔵温度
-20 °C · Store at -20°C
溶解性
Soluble in DMSO
外見
Powder

安全と法規制

安全データ

有毒物質データの
249296-44-4(Hazardous Substances Data)

化学と産業

応用分野 · 2 件

説明Varenicline, a partial agonist of the a4b2 nicotinic receptor, is a first-in-class drug launched by Pfizer as an aid to smoking cessation treatment. Varenicline exhibits dual action by decreasing craving and withdrawal symptoms, and by decreasing the reinforcement associated with smoking. The addictive properties of nicotine are thought to be mediated in part through its action as an agonist at α4β2 neuronal nicotinic acetylcholine receptors (nAChRs). Activation of α4β2 receptors by nicotine increases the release of dopamine in the mesolimbic system, an effect that is shared by most drugs of abuse. As nicotine levels decrease, dopamine levels decline, which in turn stimulates the urge to smoke. Additionally, a reduced dopaminergic tone due to abstinence from smoking stimulates craving and the withdrawal syndrome. A partial agonist of α4β2 receptors such as varenicline is expected to elicit a moderate and sustained increase in dopamine levels to relieve craving and withdrawal symptoms. In addition, by competitively binding to a4b2 receptors and inhibiting nicotineinduced dopaminergic activation, a partial agonist could attenuate the pharmacologic reward associated with smoking.

使用Varenicline is a useful medication for smoking cessation.

上流・下流製品情報

サプライヤー50 社

北京华美互利生物化工010-56205725 · [email protected]
湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
湖北威德利化学试剂有限公司181-6332-1995 18062128043 · [email protected]
济南百隆化学有限公司[email protected] · [email protected]

補足説明

定義ChEBI: An organic heterotetracyclic compound that acts as a partial agonist for nicotinic cholinergic receptors and is used (in the form of its tartate salt) as an aid to giving up smoking.

関連反応

12 件

関連ノート

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