TY - JOUR
T1 - Colopsinol A, a novel polyhydroxyl metabolite from marine dinoflagellate Amphidinium sp.
AU - Kobayashi, Jun'ichi
AU - Kubota, Takaaki
AU - Takahashi, Miho
AU - Ishibashi, Masami
AU - Tsuda, Masashi
AU - Naoki, Hideo
PY - 1999/3/5
Y1 - 1999/3/5
N2 - Colopsinol A (1), a novel polyhydroxyl compound, has been isolated from the cultured marine dinoflagellate Amphidinium sp., from which a number of cytotoxic macrolides, amphidinolides, have been obtained to date, and the gross structure of 1 was elucidated on the basis of extensive spectroscopic analyses including recent 2D NMR techniques of CH2-selected editing HSQC as well as FABMS/MS experiments and chemical means. Colopsinol A (1), C71H119O25SNa, is the first member of a new class of polyketide natural products possessing a gentiobioside moiety and a sulfate ester. The polyketide aglycon consisted of a C56-linear aliphatic chain with one exo- methylene and two methyl branches as well as two ketones, five hydroxyl groups, and a tetrahydropyran and two epoxide rings.
AB - Colopsinol A (1), a novel polyhydroxyl compound, has been isolated from the cultured marine dinoflagellate Amphidinium sp., from which a number of cytotoxic macrolides, amphidinolides, have been obtained to date, and the gross structure of 1 was elucidated on the basis of extensive spectroscopic analyses including recent 2D NMR techniques of CH2-selected editing HSQC as well as FABMS/MS experiments and chemical means. Colopsinol A (1), C71H119O25SNa, is the first member of a new class of polyketide natural products possessing a gentiobioside moiety and a sulfate ester. The polyketide aglycon consisted of a C56-linear aliphatic chain with one exo- methylene and two methyl branches as well as two ketones, five hydroxyl groups, and a tetrahydropyran and two epoxide rings.
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U2 - 10.1021/jo981882b
DO - 10.1021/jo981882b
M3 - Article
AN - SCOPUS:0033525493
SN - 0022-3263
VL - 64
SP - 1478
EP - 1482
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
IS - 5
ER -