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Diphenyl Ethers from a Marine-Derived Aspergillus sydowii.


ABSTRACT: Six new diphenyl ethers (1?6) along with eleven known analogs were isolated from the ethyl acetate extract of a marine-derived Aspergillus sydowii guided by LC-UV-MS. Their structures were unambiguously characterized by HRESIMS, NMR, as well as chemical derivatization. Compounds 1 and 2 are rare diphenyl ether glycosides containing d-ribose. The absolute configuration of the sugar moieties in compounds 1?3 was determined by a LC-MS method. All the compounds were evaluated for their cytotoxicities against eight cancer cell lines, including 4T1, U937, PC3, HL-60, HT-29, A549, NCI-H460, and K562, and compounds 1, 5, 6, and 8?11 were found to exhibit selective cytotoxicity against different cancer cell lines.

SUBMITTER: Wang YN 

PROVIDER: S-EPMC6267227 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Diphenyl Ethers from a Marine-Derived <i>Aspergillus sydowii</i>.

Wang Ya-Nan YN   Mou Yan-Hua YH   Dong Yu Y   Wu Yan Y   Liu Bing-Yu BY   Bai Jian J   Yan Dao-Jiang DJ   Zhang Le L   Feng Dan-Qing DQ   Pei Yue-Hu YH   Hu You-Cai YC  

Marine drugs 20181116 11


Six new diphenyl ethers (<b>1</b>⁻<b>6</b>) along with eleven known analogs were isolated from the ethyl acetate extract of a marine-derived <i>Aspergillus sydowii</i> guided by LC-UV-MS. Their structures were unambiguously characterized by HRESIMS, NMR, as well as chemical derivatization. Compounds <b>1</b> and <b>2</b> are rare diphenyl ether glycosides containing d-ribose. The absolute configuration of the sugar moieties in compounds <b>1</b>⁻<b>3</b> was determined by a LC-MS method. All the  ...[more]

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