|Description||An unusual macrocyclic antibiotic from a streptomyces sp., related to kijanimicin, saccharocarcins, tetrocarcins and versipelostatin; inhibits cholesterol biosynthesis from mevalonate, and inhibits pyruvate carboxylases purified from rat liver, chicken liver and azotobacter vinelandii.|
|Purity||>99% by HPLC|
|Solubility||Soluble in ethanol, methanol, DMF or DMSO. Poor water solubility.|
Isolated from a streptomyces sp.; nanomolar cytotoxicity to murine P388 leukemia cells; shows antitumour activity in vivo against murine lewis lung carcinoma an...
An unusual aminoquinone with broad biological activity against bacteria, fungi, nematodes, viruses and tumour cells; acts as a bioreductive agent; highly depend...
A member of a potent family of macrocyclic lactones; broadly active against bacteria, fungi, insects, nematodes and protozoans; a potential agent for treating o...
A macrolide antibiotic similar in structure to erythromycin
The major analogue of a complex of C-glycoside antitumour actives isolated from a streptomyces sp.; contains a vinyl group in the 8-position; an inhibitor of th...
Prepared from maduramicin by taking advantage of the acidic carboxylic acid; the preferred formulation in animals to prevent coccidiosis and to promote growth; ...
A complex of cyclic pentopeptides isolated from streptomyces capreolus; a potent antibiotic with activity against mycobateria, and gram positive and negative or...
Belongs to a novel class of antibiotics, possessing a new terpenylated diketopiperazine structure, with antibiotic, antifungal and anthelmintic activity