1987
DOI: 10.7164/antibiotics.40.1335
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Desaminoanthracyclines from the antibotic complex ciclamycin.

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Cited by 13 publications
(9 citation statements)
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“…According to database searches, it is a new compound, which was named cinerubin K. About 500 naturally occurring Anthracycline antibiotics were reported in the literature [61,105,410] , containing at least one sugar moiety. They are characterized by their antibacterial and antitumor activities, e.g cinerubins [411] , ciclamycins [412] , musettamycin [413] , pyrromycin [398] . Antibacterial and antifungal activities of the isolated compounds (267, 269, 271~273, 275 and 276) were semi-quantitatively determined using the agar diffusion method with 9 mm paper discs and 20 µg /disk.…”
Section: Cinerubin Bmentioning
confidence: 99%
“…According to database searches, it is a new compound, which was named cinerubin K. About 500 naturally occurring Anthracycline antibiotics were reported in the literature [61,105,410] , containing at least one sugar moiety. They are characterized by their antibacterial and antitumor activities, e.g cinerubins [411] , ciclamycins [412] , musettamycin [413] , pyrromycin [398] . Antibacterial and antifungal activities of the isolated compounds (267, 269, 271~273, 275 and 276) were semi-quantitatively determined using the agar diffusion method with 9 mm paper discs and 20 µg /disk.…”
Section: Cinerubin Bmentioning
confidence: 99%
“…The strain Streptomyces capoamus is well known for the production of ciclamycin, ciclacidine, and capoamycin, an anthracyclin-class antitumor complex (Bieber et al, 1987;Gonclaves et al, 1968;Hayakawa et al, 1985;Martins and Maior, 2003) but to the best of our knowledge this strain has not been reported to produce antifungal compounds. The antifungal compound produced by this strain is fairly stable to the pH range 5-8.…”
Section: Optimization Of Production Mediummentioning
confidence: 99%
“…Further confirmation of the proposed structures was obtained by high field :H nmr spectroscopy. Detailed analysis by multiple decouplings and comparison with data from ciclamycins 4 (15) and 5 (16), which contain the same sugars in comparable positions, allowed the exact assignment of almost all peaks except those in the region between 1.5 and 2.1 ppm corresponding to the positions 2 were recorded on a Broker WM 400 spectrometer using CDC1, as solvent and TMS as an internal standard. Fabms were run in bis(2-hydroxyethyl) sulfide as the matrix on a Kratos MS 80 instrument, equipped with post-acceleration detector and high-field magnet, using a Xenon beam of 6 keV energy and a current of ca.…”
Section: Similarly the Fabms Of Retamycin E2mentioning
confidence: 99%