Unknown

Dataset Information

0

Bioactive Pyridone Alkaloids from a Deep-Sea-Derived Fungus Arthrinium sp. UJNMF0008.


ABSTRACT: Eight new 4-hydroxy-2-pyridone alkaloids arthpyrones D?K (1?8), along with two known analogues apiosporamide (9) and arthpyrone B (10), were isolated from a deep-sea-derived fungus Arthrinium sp. UJNMF0008. The structures of the isolated compounds were elucidated on the basis of spectroscopic methods with that of 1 being established by chemical transformation and X-ray diffraction analysis. Compounds 1 and 2 bore an ester functionality linking the pyridone and decalin moieties first reported in this class of metabolites, while 3 and 4 incorporated a rare natural hexa- or tetrahydrobenzofuro[3,2-c]pyridin-3(2H)-one motif. Compounds 3?6 and 9 exhibited moderate to significant antibacterial activity against Mycobacterium smegmatis and Staphylococcus aureus with IC50 values ranging from 1.66?42.8 ?M, while 9 displayed cytotoxicity against two human osteosarcoma cell lines (U2OS and MG63) with IC50 values of 19.3 and 11.7 ?M, respectively.

SUBMITTER: Bao J 

PROVIDER: S-EPMC5983305 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Bioactive Pyridone Alkaloids from a Deep-Sea-Derived Fungus <i>Arthrinium</i> sp. UJNMF0008.

Bao Jie J   Zhai Huijuan H   Zhu Kongkai K   Yu Jin-Hai JH   Zhang Yuying Y   Wang Yinyin Y   Jiang Cheng-Shi CS   Zhang Xiaoyong X   Zhang Yun Y   Zhang Hua H  

Marine drugs 20180522 5


Eight new 4-hydroxy-2-pyridone alkaloids arthpyrones D⁻K (<b>1</b>⁻<b>8</b>), along with two known analogues apiosporamide (<b>9</b>) and arthpyrone B (<b>10</b>), were isolated from a deep-sea-derived fungus <i>Arthrinium</i> sp. UJNMF0008. The structures of the isolated compounds were elucidated on the basis of spectroscopic methods with that of <b>1</b> being established by chemical transformation and X-ray diffraction analysis. Compounds <b>1</b> and <b>2</b> bore an ester functionality link  ...[more]

Similar Datasets

| S-EPMC6669727 | biostudies-literature
| S-EPMC6225233 | biostudies-literature
| S-EPMC7460381 | biostudies-literature
| S-EPMC6562794 | biostudies-literature
| S-EPMC4071571 | biostudies-literature
| S-EPMC5532646 | biostudies-literature
| S-EPMC8002477 | biostudies-literature
| S-EPMC6213461 | biostudies-literature
| S-EPMC7695020 | biostudies-literature
| S-EPMC8781450 | biostudies-literature