Publication | Closed Access
Absolute Stereochemistry of Immunosuppressive Macrolide Brasilinolide A and Its New Congener Brasilinolide C
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Citations
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References
2004
Year
Chiral CentersBiosynthesisBioorganic ChemistryBiotransformationNew CongenerBiochemical TaxonomyNatural SciencesImmunologyMolecular BiologyMedicinal FungiAntigen ProcessingImmunotherapeuticsNocardia Brasiliensis Ifm0406MicrobiologyMolecular MicrobiologyAbsolute StereochemistryChemical BiologyMedicine
Brasilinolide A (2) is a 32-membered polyhydroxyl macrolide with immunosuppressive activity isolated from a pathogenic actinomycete, Nocardia brasiliensis IFM0406. The absolute configurations at 26 chiral centers of 2 and its new congener, brasilinolide C (1), were determined on the basis of the spectral data of 1 and degradation products derived from 1 and 2.
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