Shotaro Hoshino, Chin Piow Wong, Masahiro Ozeki, Huiping Zhang, Fumiaki Hayashi, Takayoshi Awakawa, Shumpei Asamizu, Hiroyasu Onaka, Ikuro Abe
Index: 10.1038/s41429-018-0040-4
Full Text: HTML
New polycyclic tetramate macrolactams, Umezawamides A (1) and B (2) were isolated from a combined-culture of Umezawaea sp. RD066910 and mycolic-acid containing bacterium Tsukamurella pulmonis TP-B0596. Their planar structures and partial stereochemistries were determined based on the spectroscopic analysis, MMFF conformational search, and ECD calculations. Umezawamides are the first secondary metabolites isolated from the genus Umezawaea and they exhibited cytotoxicities to P388 murine leukemia cells. Furthermore, umezawamide A (1) showed growth inhibitory activity against Candida albicans.
Reclassification of Nocardia species based on whole genome s...
2018-04-04 [10.1038/s41429-018-0043-1] |
Roquefortine J, a novel roquefortine alkaloid, from the deep...
2018-04-04 [10.1038/s41429-018-0046-y] |
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] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved