Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Lophenol, 24-methylene

Fig. 8. Formation of 24-methylene lophenol and 24-ethylidene lophenol from 24-methylene cycloartanol [9]. Fig. 8. Formation of 24-methylene lophenol and 24-ethylidene lophenol from 24-methylene cycloartanol [9].
The next question is when in the biosynthetic pathway do the two methylations take place. As already indicated, experiments with enzyme preparations demonstrate that cycloartenol is the best substrate for the first methylation. However 24-methylene lophenol (5-F) and not 24-methylene cycloartanol (2-F), is the preferred substrate for the second methylation. This is formed by the pathway indicated in Fig. 8. 24-Methylene cycloartanol (2-F) is demethylated to cycloeucalenol (8-F) which is the substrate for cycloeucalenol obtusifoliol isomerase which opens the 9,19-cyclopropane ring to form obtusifoliol (13-F) demethylation at C-14 and isomerization... [Pg.183]

A - A ) (details of these reactions are still obscure) yields 24-methylene lophenol which is then methylated to 24-ethylidene lophenol. [Pg.184]

The second methylation step has recently been demonstrated in vitro in preparations from bramble cell cultures (Fonteneau et al., 1977). The enzyme, which is microsomal, is specific for 24-methylene lophenol (5-F) and will not act on substrates with an intact cyclopropane ring such as 24-methylene cycloartanol (2-F) the product of the reaction is 24-ethylidene lophenol (2-C). A similar enzyme which uses lanosterol (1-A) as substrate was reported in the uredospores of Uromyces phaseoli (Liu and Knoche, 1974), which is one of the few fungi which synthesize C29 sterols (Liu and Knoche, 1976). [Pg.498]

VI. TRANSFORMATIONS INVOLVING 24-METHYLENE LOPHENOL AND 24-ETHYLIDENE LOPHENOL... [Pg.503]

When methylene lophenol and ethylidene lophenol are converted to sterols, the following major changes have to occur in the molecule in addition to those already indicated in Section III (1) removal of the remaining 4a-methyl group, (2) conversion of a A derivative into a A derivative, and (3) insertion of a double bond into the side chain at C-22. [Pg.501]

Tanaka and his group evaluated antihyperglycemic effects of five phytosterols named as lophenol (68), 24-methyllophenol (69), 24-ethyl-lophenol (70), cycloartanol (71) and 24-methylene-cycloartanol (72), isolated from Aloe barbadensis Miller, in type 2 diabetic db/db mice. In... [Pg.541]


See other pages where Lophenol, 24-methylene is mentioned: [Pg.311]    [Pg.312]    [Pg.185]    [Pg.496]    [Pg.311]    [Pg.312]    [Pg.181]    [Pg.185]    [Pg.496]    [Pg.219]    [Pg.116]   


SEARCH



Lophenol

© 2024 chempedia.info