M. Ueno et al., IC101, EXTRACELLULAR-MATRIX ANTAGONIST PRODUCED BY STREPTOMYCES SP MJ202-72F3 - PRODUCTION, ISOLATION, STRUCTURE DETERMINATION AND BIOLOGICAL-ACTIVITY, Journal of antibiotics, 46(11), 1993, pp. 1658-1665
In our search for inhibitors of cell adhesion to components of extrace
llular matrix (ECM), fibronectin, laminin and collagen type IV, we suc
ceeded in finding a novel cyclic hexadepsipeptide antibiotic, named IC
101, which was isolated from cultured mycelium of Streptomyces albulus
MJ202-72F3. It was purified by centrifugal partition chromatography,
preparative reverse phase HPLC and Sephadex LH-20 and was obtained as
a white powder. IC101 strongly inhibited cell adhesion to ECM componen
ts, suppressed immune responses in vitro and in vivo, and exhibited an
timicrobial activity on Gram-positive bacteria.