Arborcandins A, B, C, D, E and F, novel 1,3-β-glucan synthase inhibitors: Physico-chemical properties and structure elucidation

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

Abstract

Arborcandins A, B, C, D, E and F, which possess potent 1,3-β-glucan synthase inhibitory activity, were isolated from the cultured broth of a filamentous fungus, strain SANK 17397. The structures of arborcandins A, B, C, D, E and F were elucidated by a combination of NMR and mass spectrometry, and established to be novel cyclic peptides containing uncommon amino acid residues.

Cite

CITATION STYLE

APA

Ohyama, T., Iwadate-Kurihara, Y., Ishikawa, T., Miyakoshi, S., Hamano, K., & Inukai, M. (2003). Arborcandins A, B, C, D, E and F, novel 1,3-β-glucan synthase inhibitors: Physico-chemical properties and structure elucidation. Journal of Antibiotics, 56(12), 1024–1032. https://doi.org/10.7164/antibiotics.56.1024

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