Esters of levonorgestrel (13 beta-ethyl-17 alpha-ethynyl-17 beta-hydroxygon-4-en-3-one) with a variety of aliphatic and alicyclic carboxylic acids have been prepared and characterised. In tests for the suppression of estrus in rats, esters with short-chain aliphatic acids and with cyclobutane-carboxylic acid were considerably more active than the standard, norethisterone enanthate (17 alpha-ethynyl-17 beta-hydroxyestr-4-en-3-one). Such esters show great promise for development as long-acting progestogens.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/0039-128x(83)90106-x | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!