The neuroprotective activity of GPE tripeptide analogues does not correlate with glutamate receptor binding affinity-Reference-Cited by-同舟云学术

The neuroprotective activity of GPE tripeptide analogues does not correlate with glutamate receptor binding affinity

Published:2006-07 Issue:13 Volume:16 Page:3396-3400
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Alonso De Diego Sergio A.,Gutiérrez-Rodríguez Marta,Pérez de Vega M. Jesús,González-Muñiz Rosario,Herranz Rosario,Martín-Martínez Mercedes,Cenarruzabeitia Edurne,Frechilla Diana,Río Joaquín Del,Jimeno M. Luisa,García-López M. Teresa

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference34 articles.

1. Identification of Gly-Pro-Glu (GPE), the aminoterminal tripeptide of insulin-like growth factor 1 which is truncated in brain, as a novel neuroactive peptide

2. Enzymatic conversion of IGF-I to des(1–3)IGF-I in rat serum and tissues: a further potential site of growth hormone regulation of IGF-I action

3. Role of insulin-like growth factor binding proteins in limitation of IGF-I degradation into the N-methyl-d-aspartate receptor antagonist GPE: evidence from gonadotrophin-releasing hormone secretion in vitro at two developmental stages

4. The effects of the N-terminal tripeptide of insulin-like growth factor-1, glycine-proline-glutamate in different regions following hypoxic-ischemic brain injury in adult rats

5. N-terminal tripeptide of IGF-1 (GPE) prevents the loss of TH positive neurons after 6-OHDA induced nigral lesion in rats

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