3D QSAR of novel estrogen-RGD peptide conjugates: getting insight into structural dependence of anti-osteoporosis activity and side effect of estrogen in ERT.

Abstract

To explore the structural dependence of the oral potency and side effect of estrogen-RGD peptide conjugates, here six novel conjugates were prepared via introducing RGD-tetrapeptides into both 3- and 17-positions of estradiol, and introducing RGD-octapeptides into 3-position of estrone. In an ovariectomized mouse model they exhibited higher anti-osteoporosis activity and lower side effect than estrogen. For 3D QSAR analysis the anti-osteoporosis activities of nine known conjugates estrogen-RGD tetrapeptide conjugates were also provided. Using Cerius(2) module their 3D QSAR analysis was performed, four equations with high r(2) values were established, and the structural dependence of the oral potency and side effect of them was elucidated.

• Authors: Ming Zhao, Jiangyuan Liu, Xiaoyi Zhang, Li Peng, Chunyu Li, Shiqi Peng
• Journal: Bioorganic & medicinal chemistry (Bioorg Med Chem) Vol. 17 Issue 10 Pg. 3680-9 (May 15 2009) ISSN: 1464-3391 [Electronic] England
• PMID: 19386502 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Estrogens
• Oligopeptides
• Peptides
• arginyl-glycyl-aspartic acid

Topics

• Amino Acid Sequence
• Animals
• Bone and Bones (drug effects)
• Computer Simulation
• Estrogen Replacement Therapy
• Estrogens (chemistry, pharmacology, toxicity)
• Female
• Humans
• Mice
• Models, Chemical
• Oligopeptides (chemistry, pharmacology, toxicity)
• Osteoporosis (drug therapy)
• Peptides (chemical synthesis, chemistry, pharmacology)
• Quantitative Structure-Activity Relationship