Literature DB >> 6622282

The use of a steric parameter (Y gamma) in QSAR calculations for peptide hormones.

L Nádasdi, K Medzihradszky.   

Abstract

A steric parameter (Y gamma) has been derived for alpha-amino acids to characterize the steric hindrances near to the alpha-carbon atom. This easily computable variable is suitable for quantitative structure-activity relationship (QSAR) calculations for peptide hormones. Successful multivariate analyses were performed for oxytocin and angiotensin II analogs with the help of parameters describing the lipophilic and steric properties and the measure of dispersion forces. In the case of position 4 substituted oxytocin analogs, the steric, lipophilic and H-bridge forming properties equally account for the different biological activities of the derivatives. In the case of position 5 substituted angiotensin II analogs, primarily the steric parameters account for the biological activity of the series of derivatives.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6622282     DOI: 10.1016/0196-9781(83)90103-1

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  1 in total

1.  Studies on angiotensin II and analogs: impact of substitution in position 8 on conformation and activity.

Authors:  A Aumelas; C Sakarellos; K Lintner; S Fermandjian; M C Khosla; R R Smeby; F M Bumpus
Journal:  Proc Natl Acad Sci U S A       Date:  1985-04       Impact factor: 11.205

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.