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Delaminomycins, novel nonpeptide extracellular matrix receptor antagonist and a new class of potent immunomodulator. I. Taxonomy, fermentation, isolation and biological activity.

作者信息

Ueno M, Amemiya M, Iijima M, Osono M, Masuda T, Kinoshita N, Ikeda T, Iinuma H, Hamada M, Ishizuka M

机构信息

Institute for Chemotherapy, Microbial Chemistry Research Foundation, Shizuoka, Japan.

出版信息

J Antibiot (Tokyo). 1993 May;46(5):719-27. doi: 10.7164/antibiotics.46.719.

DOI:10.7164/antibiotics.46.719
PMID:8390430
Abstract

In order to develop a new class of immunomodulator we have searched for a low molecular weight inhibitors of cell adhesion to components of extracellular matrix (ECM), fibronectin (FN), laminin (LM) and collagen type IV (CL), and succeeded to find a group of novel antibiotics, named delaminomycins. Delaminomycins were isolated from the mycelium and cultured broth of Streptomyces albulus MJ202-72F3. It was purified by use of centrifugal partition chromatography (CPC), preparative reverse phase HPLC and Sephadex LH-20 and was obtained as a white powder. Delaminomycins with inhibitory activity for cell adhesion to ECM components suppressed immune responses in vitro and in vivo and exhibited antimicrobial activity on Gram-positive bacteria.

摘要

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