Kossmehl, Gerhard; Hoppe, Frank Dirk, Zeitschrift fur Naturforschung, B: Chemical Sciences, 1993, vol. 48, # 12, p. 1807 - 1820
作者:Kossmehl, Gerhard、Hoppe, Frank Dirk
DOI:——
日期:——
Kossmehl, G.; Hoppe, F. D., Molecular Crystals and Liquid Crystals Science and Technology, Section A: Molecular Crystals and Liquid Crystals, 1994, vol. 257, p. 169 - 180
作者:Kossmehl, G.、Hoppe, F. D.
DOI:——
日期:——
Insulin and IGF-1 receptor agonists and antagonists
申请人:Pillutla Renuka
公开号:US20070004634A1
公开(公告)日:2007-01-04
Peptide sequences capable of binding to insulin and/or insulin-like growth factor receptors with either agonist or antagonist activity and identified from various peptide libraries are disclosed. This invention also identifies at least two different binding sites, which are present on insulin and insulin-like growth factor receptors, and which selectively bind the peptides of this invention. As agonists, the peptides of this invention may be useful for development as therapeutics to supplement or replace endogenous peptide hormones. The antagonist peptides may also be developed as therapeutics.
INSULIN AND IGF-1 RECEPTOR AGONISTS AND ANTAGONISTS
申请人:Pillutla Renuka
公开号:US20070265189A1
公开(公告)日:2007-11-15
Peptide sequences capable of binding to insulin and/or insulin-like growth factor receptors with either agonist or antagonist activity and identified from various peptide libraries are disclosed. This invention also identifies at least two different binding sites, which are present on insulin and insulin-like growth factor receptors, and which selectively bind the peptides of this invention. As agonists, certain of the peptides of this invention may be useful for development as therapeutics to supplement or replace endogenous peptide hormones. The antagonists may also be developed as therapeutics.
Insulin and IGF-1 Receptor Agonists and Antagonists
申请人:Pillutla Renuka
公开号:US20090053807A1
公开(公告)日:2009-02-26
Peptide sequences capable of binding to insulin and/or insulin-like growth factor receptors with either agonist or antagonist activity and identified from various peptide libraries are disclosed. This invention also identifies at least two different binding sites, which are present on insulin and insulin-like growth factor receptors, and which selectively bind the peptides of this invention. As agonists, the peptides of this invention may be useful for development as therapeutics to supplement or replace endogenous peptide hormones. The antagonist peptides may also be developed as therapeutics.