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Gly-Pro-Glu_分子结构_CAS_32302-76-4)
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Gly-Pro-Glu

产品号 G3923 公司名称 Sigma Aldrich
CAS号 32302-76-4 公司网站 http://www.sigmaaldrich.com
分子式 C12H19N3O6 电 话 1-800-521-8956
分子量 301.29576 传 真
纯 度 ≥98% (HPLC) 电子邮件
保 存 Chembase数据库ID: 154297

产品价格信息

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产品别名

标题
Gly-Pro-Glu
IUPAC标准名
(2S)-2-{[(2S)-1-(2-aminoacetyl)pyrrolidin-2-yl]formamido}pentanedioic acid
IUPAC传统名
(2S)-2-{[(2S)-1-(2-aminoacetyl)pyrrolidin-2-yl]formamido}pentanedioic acid
别名
GPE
Glycyl-prolyl-glutamic acid

产品登记号

CAS号 32302-76-4
MDL号 MFCD00144405

产品性质

Empirical Formula (Hill Notation) C12H19N3O6
纯度 ≥98% (HPLC)
外观 white powder
溶解度 H2O: >5 mg/mL
MSDS下载 下载链接
保存温度 -20°C
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
Gly-Pro-Glu is a neuroprotective compound and the N-terminal tripeptide of IGF-1. Gly-Pro-Glu is neuroprotective after central administration in animal models of neurodegenerative processes, such as Huntington’s, Parkinson’s, Alzheimer’s diseases, and varies acute brain injury animal models. The neuroprotective activity is not related to its affinity to glutamate receptor. Findings indicate that GPE mimics insulin-like growth factor I effects on the somatostatin system through a mechanism independent of β-amyloid clearance that involves modulation of calcium and glycogen synthase kinase 3β signaling.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. G3923.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
详细说明 (简体中文)
Biochem/physiol Actions
Gly-Pro-Glu is a neuroprotective compound and the N-terminal tripeptide of IGF-1. Gly-Pro-Glu is neuroprotective after central administration in animal models of neurodegenerative processes, such as Huntington’s, Parkinson’s, Alzheimer’s diseases, and varies acute brain injury animal models. The neuroprotective activity is not related to its affinity to glutamate receptor. Findings indicate that GPE mimics insulin-like growth factor I effects on the somatostatin system through a mechanism independent of β-amyloid clearance that involves modulation of calcium and glycogen synthase kinase 3β signaling.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. G3923.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

参考文献