Lachnellins A, B, C, D, and Naphthalene-1,3,8-triol, Biologically Active Compounds from a Lachnellula Species (Ascomycetes)

8Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

In the course of our search for new biologically active metabolites, lachnellin A (1). a metabolite with high cytotoxic and antimicrobial activities, the structurally related lachnellins B. C and D (3, 4, 7). and naphthalene-1,3,8-triol (8), an inhibitor of malate synthase (EC 4.1.3.2), were isolated from submerged cultures of the ascomycete Lachnellula sp. A 32-89. The antimicrobial, cytotoxic and phytotoxic activities of lachnellin A depended on its reactivity and could be abolished by the addition of cysteine. The enzyme inhibiting activity of (8) was due to reactive intermediates during melanization and was no longer observed in the presence of serum albumin. In addition, rac-scytalone (9), (+)-trans-3.4-dihydro-3.4.8-trihy-droxy-l(2H)-naphthalenone (10). 2.5-dihydroxytoluene (11). and (R)-(-)-5-methylmellein (12) were obtained from the same source and biologically characterized. © 1996, Verlag der Zeitschrift für Naturforschung. All rights reserved.

Cite

CITATION STYLE

APA

Semar, M., Anke, H., Arendholzb, W. R., Velten, R., & Steglich, W. (1996). Lachnellins A, B, C, D, and Naphthalene-1,3,8-triol, Biologically Active Compounds from a Lachnellula Species (Ascomycetes). Zeitschrift Fur Naturforschung - Section C Journal of Biosciences, 51(7–8), 500–512. https://doi.org/10.1515/znc-1996-7-808

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free