Ayers Sloan, Graf Tyler N, Adcock Audrey F, Kroll David J, Shen Qi, Swanson Steven M, Wani Mansukh C, Darveaux Blaise A, Pearce Cedric J, Oberlies Nicholas H
University of North Carolina at Greensboro, Department of Chemistry and Biochemistry, P.O. Box 26170, Greensboro, NC 27402.
Tetrahedron Lett. 2011 Oct 5;52(40):5128-5230. doi: 10.1016/j.tetlet.2011.07.102.
A fungal extract (MSX 63619), from the Mycosynthetix library of over 50,000 fungi, displayed promising cytotoxicity against a human tumor cell panel. Bioactivity-directed fractionation led to the isolation of an o-pyranonaphthoquinone decaketide, which we termed obionin B (1). The structure of 1 was deduced via spectroscopic and spectrometric techniques. The IC(50) value of 1 was moderate, ranging from 3 to 13 μM, depending on the cell line tested.
从拥有超过50000种真菌的Mycosynthetix文库中提取的一种真菌提取物(MSX 63619),对一组人类肿瘤细胞显示出有前景的细胞毒性。通过生物活性导向分级分离,分离出一种邻吡喃萘醌十肽,我们将其命名为obionin B(1)。通过光谱和质谱技术推导得出1的结构。1的半数抑制浓度(IC50)值适中,根据所测试的细胞系不同,范围在3至13μM之间。