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Avermectin Ala

A final example of metabolic pathway engineering is based on polyketide and nonribosomal peptide biosynthesis. Polyketides and nonribosomal peptides are complex natural products with numerous chiral centers, which are of substantial economic benefit as pharmaceuticals. These natural products function as antibiotics [erythromycin A (65), vancomycin (66)], antifungals (rapamycin, amphotericin B), antiparasitics [avermectin Ala (67)], antitumor agents [epothiolone A (68), calicheamicin yj, and immunosuppressants [FK506 (69), cyclosporin A], Because this exponentially growing and intensely researched field has developed, the reader is directed to review articles for additional details.347-359 Also with the potential economic benefit to develop the next blockbuster pharmaceutical, a number of patents and patent applications have been published.360-366... [Pg.387]

In avermectin polyketide synthase, the last invariant Ala in the motif sequence is substituted to Thr [28]. KR domain activity is predicted to be required for the formation of avermectin aglycons. In another group of KR domains, the motif sequence corresponding region is not found, which readily accounts for their inactivity. [Pg.294]


See other pages where Avermectin Ala is mentioned: [Pg.80]    [Pg.296]    [Pg.297]    [Pg.57]    [Pg.225]    [Pg.258]    [Pg.574]    [Pg.274]    [Pg.560]    [Pg.253]    [Pg.141]    [Pg.432]    [Pg.80]    [Pg.296]    [Pg.297]    [Pg.57]    [Pg.225]    [Pg.258]    [Pg.574]    [Pg.274]    [Pg.560]    [Pg.253]    [Pg.141]    [Pg.432]    [Pg.2552]   
See also in sourсe #XX -- [ Pg.225 ]

See also in sourсe #XX -- [ Pg.390 ]




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