Publication | Closed Access
Kinamycin Biosynthesis. Synthesis, Isolation, and Incorporation of Stealthin C, an Aminobenzo[<i>b</i>]fluorene
104
Citations
13
References
1997
Year
Bioorganic ChemistryKinamycin D.Molecular BiologySecondary MetaboliteChemical BiologyPharmaceutical ChemistryKinamycin DMedicinal ChemistryBiosynthesisStealthin CNatural Product BiosynthesisNew IntermediateBiochemistryAntimicrobial CompoundNatural Product SynthesisKinamycin BiosynthesisNatural SciencesMicrobiologySynthetic Chemistry
A new intermediate in the biosynthesis of the benzo[b]fluorene antibiotic, kinamycin D, has been identified. 11-Amino-4,5,9-trihydroxy-2-methyl-10H-benzo[b]fluoren-10-one was synthesized and shown to be present in extracts of Streptomyces murayamaensisfermentations. A deuterated sample was prepared and shown to be specifically incorporated into kinamycin D. This new intermediate, now named stealthin C, is also the probable hydroxylation substrate for the biosynthesis of stealthin A by S. viridochromogenes.
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