Big Chemical Encyclopedia

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

Articles Figures Tables About

Aspergillus alliaceus

Papavarine H3CO Aspergillus alliaceus NRRL 315 Cunninghamella echinulata ATCC 9244 0 dealkylation [24]... [Pg.104]

Aspergillus alliaceus Aspergillus terreus Baeuveria bassiana Circinella minor Cunninghamella bertholletiae... [Pg.212]

Scheme 9. Metabolism of ellipticine by Aspergillus alliaceus NRRL 315. [Pg.360]

The microbiological transformation of ellipticine by means of Aspergillus alliaceus has been investigated 85 the principal product is 10-hydro xyellipticine, which is the same as that observed in the metabolism of ellipticine in mammalian liver, but some 11-hydroxyellipticine is also obtained. [Pg.211]

Asperlicin] (non-peptide) Aspergillus alliaceus (fungus) CCK-R antagonist [attenuates taurocholate-induced, CCK-mediated pancreatitis]... [Pg.219]

Chang, R. S., Lotti, V. J., Monaghan, R. L., et al. (1985). A potent nonpeptide cholecystokinin antagonist selective for peripheral tissues isolated from Aspergillus alliaceus. Science, 230, 177-179. [Pg.144]

FIGURE 20.87 Biotransformation of (5)-(+)-curcuphenol (282g) by Kluyveromyces marxianus and Rhizopus arrhizus and curcudiol (282n) hy Aspergillus alliaceus and Rhodotorula glutinus. [Pg.958]

See other pages where Aspergillus alliaceus is mentioned: [Pg.359]    [Pg.360]    [Pg.364]    [Pg.177]    [Pg.180]    [Pg.184]    [Pg.185]    [Pg.188]    [Pg.352]    [Pg.365]    [Pg.179]    [Pg.67]    [Pg.1474]    [Pg.1479]    [Pg.41]    [Pg.71]    [Pg.125]    [Pg.184]    [Pg.680]    [Pg.133]    [Pg.21]    [Pg.258]    [Pg.59]    [Pg.395]    [Pg.118]    [Pg.245]    [Pg.956]    [Pg.787]    [Pg.815]    [Pg.253]   
See also in sourсe #XX -- [ Pg.149 ]

See also in sourсe #XX -- [ Pg.855 ]

See also in sourсe #XX -- [ Pg.855 ]

See also in sourсe #XX -- [ Pg.125 ]

See also in sourсe #XX -- [ Pg.787 , Pg.789 ]



SEARCH



© 2024 chempedia.info