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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90
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filingDate 1998-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2001-01-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20010006403-A
titleOfInvention Crambescidin Compounds
abstract Two kinds of chlorinated spermidine structures, together with known clambecidin (1-5) and propylmycaline A (6), using FABMS-induced separation from extracts of Mediterranean sponge crambe crambe Of the new hydrophobic crampesidines 834 (7), 818 (8), four new hydrophobic crampesidines 673 (9), 687 (10), 657 (11) and 13,14,15- without spermidine structures. Isorambecidin 657 (12) is obtained. Through parallel bioassays on L1210 murine leukemia cells, crampescidins 834 (7), 818 (8) and 657 (11) show five-fold cytotoxicity compared to the known cramblesidine 816 (1). Crampesidines with spermidine or spermidine derivatives exhibit antimicrobial activity against Rhodolora glutinis.
priorityDate 1997-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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