| Literature DB >> 29066796 |
Yoshihito Shiono1, Niken Istikhari Muslihah1,2, Takuma Suzuki1, Nanang Rudianto Ariefta1,3, Chairil Anwar2, Handojo Hadi Nurjanto4, Takako Aboshi1, Tetsuya Murayama1, Keitaro Tawaraya1, Takuya Koseki1, Jun Yoshida5, Narandulam Usukhbayar3, Shota Uesugi3, Ken-Ichi Kimura3.
Abstract
The novel compound, 11-O-methylpetasitol (1), was isolated from Penicillium sp. N-175-1, and two new compounds, cosmochlorins D (5) and E (6), were isolated from Phomopsis sp. N-125. In addition, three known eremophilane sesquiterpenes, sporogen-AO1 (2), petasol (3) and 6-dehydropetasol (4), were isolated from Penicillium sp. N-175-1. The structures of 1, 5 and 6 were elucidated by a combination of extensive spectroscopic analyses, including 2D NMR, high-resolution electrospray ionization time-of-flight mass spectrometry (HRESITOFMS) and chemical reactions. Compounds 2, 3, 5 and 6 exhibited cytotoxicity to HL60 and 2 and 3 to HeLa cells. Furthermore, 2 and 3 showed robust growth-restoring activity of a Saccharomyces cerevisiae (cdc2-1 rad9Δ) mutant strain, whereas 5 and 6 exhibited minor growth-restoring activity in this strain. Thus, these compounds may inhibit the growth of HL60 and HeLa cells by blocking the cell cycle, and they may be utilized as new lead compounds that act as inhibitors of survival signal transduction pathways.Entities:
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Year: 2017 PMID: 29066796 DOI: 10.1038/ja.2017.125
Source DB: PubMed Journal: J Antibiot (Tokyo) ISSN: 0021-8820 Impact factor: 2.649