Siwen Niu, Ning Wang, Chun-Lan Xie, Zuowang Fan, Zhuhua Luo, Hai-Feng Chen, Xian-Wen Yang
Index: 10.1038/s41429-018-0046-y
Full Text: HTML
Chemical investigation on the deep-sea-derived fungus Penicillium granulatum MCCC 3A00475 led to the isolation of a previously undescribed (roquefortine J, 1) and four known (2−5) roquefortine alkaloids, along with six ergosterol analogues (6−11). The planar structure of 1 was established mainly on the basis of extensive analysis of its 1D, 2D NMR, and HRESIMS spectra. The absolute configuration of 1 was determined by comparison of the calculated and experimental electronic circular dichroism spectra. Compounds 5, 6, and 7 exhibited potent anti-proliferative effects against HepG2 tumor cells with IC50 values of 7.0, 8.6, and 8.2 μM, respectively.
Reclassification of Nocardia species based on whole genome s...
2018-04-04 [10.1038/s41429-018-0043-1] |
Correction to: Halistanol sulfates I and J, new SIRT1–3 inhi...
2018-03-27 [10.1038/s41429-017-0019-6] |
Tolyprolinol, a new dipeptide from Tolypocladium sp. FKI-798...
2018-03-22 [10.1038/s41429-018-0041-3] |
Cystargamide B, a cyclic lipodepsipeptide with protease inhi...
2018-03-22 [10.1038/s41429-018-0044-0] |
Confirmation of the absolute configuration of Stachybotrin C...
2018-03-19 [10.1038/s41429-018-0042-2] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved