Sclerotiorin and isochromophilone IV: inhibitors of Grb2-Shc interaction, isolated from Penicillium multicolor F1753

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Title
Sclerotiorin and isochromophilone IV: inhibitors of Grb2-Shc interaction, isolated from Penicillium multicolor F1753
Author(s)
Ji Youn Nam; Kwang Hee Son; Hyae Kyeong Kim; Mi Young Han; Sung Uk Kim; Jung Do Choi; Byoung-Mog Kwon
Bibliographic Citation
Journal of Microbiology and Biotechnology, vol. 10, no. 4, pp. 544-546
Publication Year
2000
Abstract
Grb2 is an important adaptor protein in the mitogenic Ras signaling pathway of receptor tyrosine kinases, and contains one SH2 domain and two SH3 domains. The SH2 domain binds to specific phosphotyrosine motifs on receptors or adaptor proteins such as Shc. The SH2 domain antagonists may lead to blocking of the oncogenic Ras signals and to developing new antitumor agents. In the course of screening SH2 antagonists from natural sources, sclerotiorin (1) and isochromophilone IV (2) were isolated from a strain, Penicillium multicolor F1753, and their structures were established by NMR spectral data. The metabolites significantly inhibited the binding between the Grb2-SH2 domain and phosphopeptide derived from the Shc protein, with IC50 values of 22 μM and 48 μM for (1) and (2), respectively. The compounds are the first non-peptidic inhibitors of the SH2 domain from a natural source.
Keyword
Grb2Shcsignal transductionantitumor
ISSN
1017-7825
Publisher
Korea Soc-Assoc-Inst
Type
Article
Appears in Collections:
Division of Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
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