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タリペキソール

Talipexole

HCID 5374
ノート反応
基本情報概要名称と識別子物性化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
101626-70-4
標準SMILES
C=CCN1CCc2nc(N)sc2CC1
InChIKey
DHSSDEDRBUKTQY-UHFFFAOYSA-N
分子式
C10H15N3S
平均分子量
209.31 g/mol
単同位体質量
209.09866866

概要

6-prop-2-enyl-4,5,7,8-tetrahydrothiazolo[4,5-d]azepin-2-amine is an azepine.

名称と識別子

優先名称
Talipexole
IUPAC
6-prop-2-enyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-amine
現地名
タリペキソール
英語名
TALIPEXOLE
分子式
C10H15N3S
分子量
209.31

名称と別名

Talipexole101626-70-4TalipexolTalipexolumDTXSID80463217AM2J46Z1YBHT920DTXCID60263216-(prop-2-en-1-yl)-4H,5H,6H,7H,8H-[1,3]thiazolo[4,5-d]azepin-2-amine6-(prop-2-en-1-yl)-4H,5H,6H,7H,8H-(1,3)thiazolo(4,5-d)azepin-2-amine4H-Thiazolo(4,5-d)azepin-2-amine, 5,6,7,8-tetrahydro-6-(2-propenyl)-, dihydrochlorideRefChem:187312
名称をさらに表示
6-アリル-2-アミノ-5,6,7,8-テトラヒドロ-4H-チアゾロ[4,5-d]アゼピンタリペキソール6-アリル-5,6,7,8-テトラヒドロ-4H-チアゾロ[4,5-d]アゼピン-2-アミン5,6,7,8-テトラヒドロ-6-(2-プロペニル)-4H-チアゾロ[4,5-d]アゼピン-2-アミン2-アミノ-6-アリル-5,6,7,8-テトラヒドロ-4H-チアゾロ[4,5-d]アゼピン6-(プロパ-2-エン-1-イル)-4H,5H,6H,7H,8H-[1,3]チアゾロ[4,5-d]アゼピン-2-アミンTalipexolum [latin]Talipexol [spanish]TALIPEXOLE USP/EP/BP6-Allyl-2-amino-5,6,7,8-tetrahydro-4H-thiazolo[4,5-d]azepine6-Allyl-5,6,7,8-tetrahydro-4H-[1,3]thiazolo[4,5-d]azepin-2-amine
BHT 9202-amino-6-allyl-5,6,7,8-tetrahydro-4H-thiazolo-(5,4-d)azepin-dihydrochloride6-allyl-2-amino-5,6,7,8-tetrahydro-4H-thiazolo(4,5-d)azepin dihydrochlorideB-HT 920Talipexole [INN]6-prop-2-enyl-4,5,7,8-tetrahydro-[1,3]thiazolo[4,5-d]azepin-2-amineDomin6-allyl-5,6,7,8-tetrahydro-4H-thiazolo[4,5-d]azepin-2-amine

物性

構造計算による物性

XLogP
1.5
極性表面積
70.4 Ų
水素結合供与体数
1
水素結合受容体数
4
回転可能結合数
2
重原子数
14
形式電荷
0
複雑度
210

実験および物理化学的性質

LogP1.48

物理化学的性質

沸点
364.6 · 364.6±37.0 °C(Predicted)
比重(密度)
1.167 · 1.167±0.06 g/cm3(Predicted)
貯蔵温度
-20 °C · Store at -20°C
溶解性
Soluble in DMSO
外見
Powder
酸解離定数(Pka)
7.22 · 7.22±0.20(Predicted)

化学と産業

薬理情報

MeSH Pharmacological Classification · 3 件

Drugs that selectively bind to and activate alpha adrenergic receptors.

Mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. Several MONOAMINE OXIDASE INHIBITORS are useful as antidepressants apparently as a long-term consequence of their modulation of catecholamine levels. The tricyclic compounds useful as antidepressive agents (ANTIDEPRESSIVE AGENTS, TRICYCLIC) also appear to act through brain catecholamine systems. A third group (ANTIDEPRESSIVE AGENTS, SECOND-GENERATION) is a diverse group of drugs including some that act specifically on serotonergic systems.

Drugs that bind to and activate dopamine receptors.

応用分野 · 2 件

用途ドパミンD受容体アゴニストレボドパの長期使用による副作用を軽減する

説明Domin was launched in Japan for Parkinson's disease. The compound is readily accessible in two steps from I-allylhexahydro-4H-azepin4-one. Its antiparkinson activity resides in the fact that talipexole is a selective agonist for presynaptic dopamine D2 receptors with no D1 receptor activity. It is a clonidine-like α2-adrenoreptor agonist and has fewer GI side effects than bromocriptine the most widely used dopamine angonist. Also it is 70 times more potent than bromocriptine and has a more rapid onset of action. In addition to its anti-tremor activity there was a sedative effect but no emesis. The latter probably a result of talipexole's 5-HT3 receptor antagonistic activity. Its metabolites have no biological activity, there was no development of tolerence and its effect could be enhanced by L-dopa.

上流・下流製品情報

上流原料

チオ尿素

サプライヤー19 社

上海毕得医药科技股份有限公司400-1647117 13681763483 · [email protected]

関連反応

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化合物ノート

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このページの内容基本情報概要名称と識別子物性化学と産業関連反応化合物ノート

データベース識別子

CAS
101626-70-4
PubChem CID
5374
DTXSID
DTXSID8046321
ChEMBL
CHEMBL279085
ChEBI
CHEBI:93327
UNII
7AM2J46Z1Y
Nikkaji
J33.385I
杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]
陕西缔都化学有限公司029-029-81123119 17391733320 · [email protected]
LGM Pharma1-(800)-881-8210 · [email protected]
河南阿尔法化工有限公司0371-55013243 15324716602 · [email protected]
MedChemexpress LLC021-58955995 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
上海阿拉丁生化科技股份有限公司6206333 13167063860 · [email protected]
陕西缔都医药化工有限公司+86-29-81139210 +86-17392587031 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
上海陶术生物科技股份有限公司13564774135 · [email protected]
天津凯利奇生物科技有限公司15076683720 · [email protected]
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Musechem+1-800-259-7612 · [email protected]
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上海陶术生物科技股份有限公司+1-781-999-5354 · [email protected]
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