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Merck
CN

79224

Sigma-Aldrich

1-苯基-1,3,8-三唑螺环[4.5]十烷-4-酮

≥96.0% (HPLC)

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关于此项目

经验公式(希尔记法):
C13H17N3O
化学文摘社编号:
分子量:
231.29
Beilstein:
617685
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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方案

≥96.0% (HPLC)

mp

188-191 °C

储存温度

2-8°C

SMILES字符串

O=C1NCN(c2ccccc2)C13CCNCC3

InChI

1S/C13H17N3O/c17-12-13(6-8-14-9-7-13)16(10-15-12)11-4-2-1-3-5-11/h1-5,14H,6-10H2,(H,15,17)

InChI key

HTQWGIHCFPWKAS-UHFFFAOYSA-N

基因信息

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储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A Bruinink et al.
Journal of neurochemistry, 40(5), 1227-1236 (1983-05-01)
The ontogeny of binding sites for [3H] spiperone was studied in time-pregnant rats. Binding of [3H]spiperone to fresh homogenates of pre- and postnatal rat forebrain was characterized by Scatchard analysis and competition experiments with a number of dopaminergic and serotonergic
T Araki et al.
Neuroreport, 5(1), 37-40 (1993-10-25)
Using quantitative receptor autoradiography, spirodecanone binding was evaluated in the gerbil hippocampus 1 h-1 month after cerebral ischaemia of 10 min. The spirodecanone binding was unaffected in the hippocampus up to 48 h after ischaemia. Thereafter, increased binding was found
F Murakami et al.
Pharmacology, 49(5), 286-295 (1994-11-01)
We investigated the effects of vinconate and pentobarbital against the alterations in spirodecanone binding in the gerbil striatum and hippocampus 5 h and 7 days after 10 min of cerebral ischemia, using receptor autoradiography. Vinconate and pentobarbital were given intraperitoneally
Differentiation of solubilized dopamine receptors from spirodecanone binding sites in rat striatum.
H Gorissen et al.
FEBS letters, 121(1), 133-138 (1980-11-17)
P M Laduron
Biochemical pharmacology, 37(1), 37-40 (1988-01-01)
In binding studies, stereospecificity is not a property restricted to receptor sites; indeed stereospecific binding has also been observed for acceptor sites. Therefore it does not represent a decisive criterion to make a binding site, a receptor site. However, in

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