Physiologically active derivatives of esterastin
AssigneeZaidan Hojin Biseibutsu Kagaku Kenkyu Kai
InventorsHamao Umezawa, Takaaki Aoyagi, Tomio Takeuchi
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Abstract
Three, new physiologically active derivatives of esterastin are now provided, which inhibit the activity of esterase similarly to the parent esterastin and further exhibit a higher inhibiting activity against cholesterol esterase than the parent esterastin. These three new derivatives are tetrahydroesterastin which is produced by catalytic hydrogenation of esterastin; 3,5-di-hydroxy-2-hexylhexadeca-7,10-dienoic 1,3-lactone which is produced by alkaline hydrolysis of esterastin; and 3,5-di-hydroxy-2-hexylhexadecanoic 1,3-lactone which is produced either by alkaline hydrolysis of said tetrahydroesterastin or by catalytic hydrogenation of the product of the alkaline hydrolysis of esterastin.
Claims4
The compound having the formula ##STR15## wherein R denotes a group of the formula CH.sub.3 --(CH.sub.2).sub.4 --CH.dbd.CH--CH.sub.2 --CH.dbd.CH--CH.sub.2 -- or a group of the formula CH.sub.3 --(CH.sub.2).sub.10 -- and R' denotes a hydrogen atom or a group of the formula ##STR16## provided that when R' is the group ##STR17## R is the group CH.sub.3 --(CH.sub.2).sub.10 --.
Dependencies are inferred from the claim text.