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Pneumocandins from Zalerion arboricola. III. Structure elucidation.
Hensens, O D; Liesch, J M; Zink, D L; Smith, J L; Wichmann, C F; Schwartz, R E.
Afiliación
  • Hensens OD; Department of Natural Products Chemistry, Merck Research Laboratories, Rahway, N.J. 07065-0900.
J Antibiot (Tokyo) ; 45(12): 1875-85, 1992 Dec.
Article en En | MEDLINE | ID: mdl-1490878
Pneumocandin B0 (6) and six related lipopeptides are antifungal and anti-Pneumocystis carinii agents from mutants of Zalerion arboricola, whose structures were determined mainly on the basis of spectroscopic analysis. They belong, along with pneumocandin A0 (L-671,329) previously isolated from these laboratories, to the echinocandin class of antifungal agents. The product from base-catalyzed ring opening involving the hemiaminal position of the dihydroxyornithine residue of B0, has been clearly defined as 6b. Modifications were limited to the 3-hydroxy-4-methylproline, 3,4-dihydroxyhomotyrosine and 4,5-dihydroxyornithine residues of pneumocandin A0.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptidos / Hongos Mitospóricos / Antibacterianos / Antifúngicos Idioma: En Revista: J Antibiot (Tokyo) Año: 1992 Tipo del documento: Article Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptidos / Hongos Mitospóricos / Antibacterianos / Antifúngicos Idioma: En Revista: J Antibiot (Tokyo) Año: 1992 Tipo del documento: Article Pais de publicación: Reino Unido