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Merck

C8874

Sigma-Aldrich

CGP-37157

≥98% (HPLC), powder

别名:

7-氯-5-(2-氯苯基)-1,5-二氢-4,1-苯并噻唑-2-2(3H)-酮

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About This Item

经验公式(希尔记法):
C15H11Cl2NOS
CAS号:
分子量:
324.22
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.25

化驗

≥98% (HPLC)

形狀

powder

顏色

white

溶解度

DMSO: ≥20 mg/mL

儲存溫度

2-8°C

SMILES 字串

Clc1ccc2NC(=O)CSC(c3ccccc3Cl)c2c1

InChI

1S/C15H11Cl2NOS/c16-9-5-6-13-11(7-9)15(20-8-14(19)18-13)10-3-1-2-4-12(10)17/h1-7,15H,8H2,(H,18,19)

InChI 密鑰

KQEPIRKXSUIUTH-UHFFFAOYSA-N

一般說明

CGP-37157 是苯并噻氮平化合物,衍生自氯硝西泮。它可作为肌浆网/内质网 Ca2+ ATPase(SERCA)拮抗剂和兰尼碱受体通道(RyR)激动剂。CGP-37157 调节平滑肌、心脏和骨骼肌细胞以及非肌肉系统中钙的胞内信号传导。

應用

CGP-37157 作为线粒体钠钙交换剂(mNCX)抑制剂,用于研究正常线粒体钙动力学在维持树突棘生成中的作用。

生化/生理作用

线粒体 Na+/Ca2+ 交换以及肌质网钙刺激的 ATPase 和其他钙通道的特异性抑制剂。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3


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S L Colegrove et al.
The Journal of general physiology, 115(3), 351-370 (2000-02-29)
We studied how mitochondrial Ca2+ transport influences [Ca2+](i) dynamics in sympathetic neurons. Cells were treated with thapsigargin to inhibit Ca2+ accumulation by SERCA pumps and depolarized to elevate [Ca2+(i); the recovery that followed repolarization was then examined. The total Ca2+
Jake T Neumann et al.
Molecular pharmacology, 79(1), 141-147 (2010-10-07)
7-Chloro-5-(2-chlorophenyl)-1,5-dihydro-4,1-benzothiazepin-2(3H)-one [CGP-37157 (CGP)], a benzothiazepine derivative of clonazepam, is commonly used as a blocker of the mitochondrial Na+/Ca²+ exchanger. However, evidence suggests that CGP could also affect other targets, such as L-type Ca²+ channels and plasmalemma Na+/Ca²+ exchanger. Here, we
CGP-37157 inhibits the sarcoplasmic reticulum Ca2+ ATPase and activates ryanodine receptor channels in striated muscle
Neumann JT, et al.
Molecular Pharmacology, 79(1), 141-147 (2011)
Cyclophilin D regulates neuronal activity-induced filopodiagenesis by fine-tuning dendritic mitochondrial calcium dynamics
Sui S, et al.
Journal of Neurochemistry (2018)
Michael Patterson et al.
The Journal of general physiology, 129(1), 29-56 (2006-12-28)
Many models have been developed to account for stimulus-evoked [Ca(2+)] responses, but few address how responses elicited in specific cell types are defined by the Ca(2+) transport and buffering systems that operate in the same cells. In this study, we

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