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104632-26-0 分子结构
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(6S)-6-N-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine

ChemBase编号:73222
分子式:C10H17N3S
平均质量:211.32708
单一同位素质量:211.11431856
SMILES和InChIs

SMILES:
[C@@H]1(CCc2c(C1)sc(n2)N)NCCC
Canonical SMILES:
CCCN[C@H]1CCc2c(C1)sc(n2)N
InChI:
InChI=1S/C10H17N3S/c1-2-5-12-7-3-4-8-9(6-7)14-10(11)13-8/h7,12H,2-6H2,1H3,(H2,11,13)/t7-/m0/s1
InChIKey:
FASDKYOPVNHBLU-ZETCQYMHSA-N

引用这个纪录

CBID:73222 http://www.chembase.cn/molecule-73222.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
(6S)-6-N-propyl-4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine
IUPAC传统名
pramipexole
别名
Mirapexin
Sifrol
Pramipexole (Mirapex)
(S)-4,5,6,7-Tetrahydro-N6-propyl-2,6-benzothiazolediamine Dihydrochloride
(S)-Pramipexole Dihydrochloride
(S)-4,5,6,7-Tetrahydro-N6-propyl-2,6-benzothiazolediamine
(S)-Pramipexole
CAS号
104632-26-0
104632-25-9
PubChem SID
162038142
PubChem CID
119570

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
PubChem 119570 external link

理论计算性质

理论计算性质

JChem
Acid pKa 17.661047  质子受体
质子供体 LogD (pH = 5.5) -1.5217185 
LogD (pH = 7.4) -0.98125774  Log P 1.7642827 
摩尔折射率 59.7672 cm3 极化性 22.761166 Å3
极化表面积 50.94 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

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
Methanol expand 查看数据来源
外观
Off-White Solid expand 查看数据来源
White Solid expand 查看数据来源
熔点
127-128°C expand 查看数据来源
288-290°C expand 查看数据来源
保存条件
-20°C expand 查看数据来源
-20°C Freezer expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
作用靶点
Dopamine receptor expand 查看数据来源
成盐信息
Free Base expand 查看数据来源
质检报告
下载链接 expand 查看数据来源

详细说明

详细说明

Selleck Chemicals Selleck Chemicals TRC TRC
Selleck Chemicals -  S2460 external link
Biological Activity:
Pramipexole (Mirapex) is a partial/full D2S, D2L, D3, D4 receptor agonist with a Ki of 3.9, 2.2, 0.5 and 5.1 nM for D2S, D2L, D3, D4 receptor, respectively. Pramipexole (Mirapex) also possesses low/insignificant affinity (500-10,000 nM) for the 5-HT1A, 5-HT1B, 5-HT1D, and α2-adrenergic receptors. Pramipexole (Mirapex) has negligible affinity (>10,000 nM) for the D1, D5, 5-HT2, α1-adrenergic, β-adrenergic, H1, and mACh receptors. Pramipexole (Mirapex) is a non-ergoline dopamine agonist revealed for treating early-stage Parkinson’s disease (PD) and restless legs syndrome (RLS). [1][2][3]References on Pramipexole (Mirapex)[1] http://en.wikipedia.org/wiki/Pramipexole, , [2] Clin Ther., 2006 Aug, 28(8):1065-78.[3] J Pharmacol Exp Ther., 2002 Nov, 303(2):805-14.
Toronto Research Chemicals -  P700755 external link
A dopamine-D2-receptor agonist. Antiparkinsonian.
Toronto Research Chemicals -  P700750 external link
(S)-Pramipexole enantiomer. A dopamine-D2-receptor agonist. Antiparkinsonian. Pramipexole (Mirapex, Mirapexin, Sifrol) is a non-ergoline dopamine agonist indicated for treating early-stage Parkinson's disease (PD) and restless legs syndrome (RLS).[1] It i

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Kvernmo T et al. Clin Ther. 2006 Aug;28(8):1065-78.
  • Schilling, J.C., et al.: Clin. Pharmacol. Ther., 51, 541 (1992)
  • Kieburtz, K., et al.: J. Am. Med. Assoc., 278, 125 (1997)
  • Mierau, J., et al.: J. Med. Chem., 30, 494 (1987)
  • Schilling, J.C., et al.: Clin. Pharmacol. Ther., 51, 541 (1987)
  • Kieburtz, K., et al.: J. Am. Med. Assoc., 278, 125 (1997)
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专利

专利

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互联网资源

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