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Hyaluromycin, a new hyaluronidase inhibitor of polyketide origin from marine Streptomyces sp.


ABSTRACT: Hyaluromycin (1), a new member of the rubromycin family of antibiotics, was isolated from the culture extract of a marine-derived Streptomyces sp. as a HAase inhibitor on the basis of HAase activity screening. The structure of 1 was elucidated through the interpretation of NMR data for the compound and its 3?-O-methyl derivative in combination with an incorporation experiment with [1,2-13C2]acetate. The compound's absolute configuration was determined by the comparison of its circular dichroism (CD) spectrum with those of other rubromycins. Hyaluromycin (1) consists of a ?-rubromycin core structure possessing a 2-amino-3-hydroxycyclopent-2-enone (C5N) unit as an amide substituent of the carboxyl function; both structural units have been reported only from actinomycetes. Hyaluromycin (1) displayed approximately 25-fold more potent hyaluronidase inhibitory activity against hyaluronidase than did glycyrrhizin, a known inhibitor of plant origin.

SUBMITTER: Harunari E 

PROVIDER: S-EPMC3917283 | biostudies-literature | 2014 Jan

REPOSITORIES: biostudies-literature

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Hyaluromycin, a new hyaluronidase inhibitor of polyketide origin from marine Streptomyces sp.

Harunari Enjuro E   Imada Chiaki C   Igarashi Yasuhiro Y   Fukuda Takao T   Terahara Takeshi T   Kobayashi Takeshi T  

Marine drugs 20140121 1


Hyaluromycin (1), a new member of the rubromycin family of antibiotics, was isolated from the culture extract of a marine-derived Streptomyces sp. as a HAase inhibitor on the basis of HAase activity screening. The structure of 1 was elucidated through the interpretation of NMR data for the compound and its 3″-O-methyl derivative in combination with an incorporation experiment with [1,2-13C2]acetate. The compound's absolute configuration was determined by the comparison of its circular dichroism  ...[more]

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