Natural Products and Bioprospecting    2014, Vol. 4 Issue (4) : 207-211     DOI: 10.1007/s13659-014-0032-4
Original article |
Three New Humulane Sesquiterpenes from Cultures of the Fungus Antrodiella albocinnamomea
Zi-Ming Chen1, Qiong-Ying Fan2, Xia Yin1, Xiao-Yan Yang1, Zheng-Hui Li1, Tao Feng1, Ji-Kai Liu1
1. State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, 132#Lanhei Road, Heilongtan, Kunming 650201, Yunnan, People's Republic of China;
2. College of Life Science, Hebei Normal University, Shijiazhuang 050024, People's Republic of China;
2. College of Life Science, Hebei Normal University, Shijiazhuang 050024, People's Republic of China
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Abstract  Three new humulane-type sesquiterpenes, antrodols A-C(1-3), were isolated from cultures of the fungus Antrodiella albocinnamomea. Their structures were elucidated on the basis of extensive spectroscopic analysis. Antrodols A-C(1-3) are first examples of humulane-type sesquiterpenes isolated from cultures of higher fungi, and antrodol A(1) was the first report of humulane-type sesquiterpene with a methyl rearranged at C-3. All compounds were evaluated in the enzyme inhibition assay against two protein-tyrosine phosphatases(PTPs):MEG2 and PTP1Bc.
Keywords Antrodiella albocinnamomea      Humulane-type sesquiterpenes      Protein tyrosine phosphatase inhibitory activity     
Fund:This project was financially supported by National Natural Science Foundation of China(U1132607, 81373289, 81102346) and Youth Innovation Promotion Association of CAS(2011312D11019).
Issue Date: 11 February 2018
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Zi-Ming Chen,Qiong-Ying Fan,Xia Yin, et al. Three New Humulane Sesquiterpenes from Cultures of the Fungus Antrodiella albocinnamomea[J]. Natural Products and Bioprospecting, 2014, 4(4): 207-211.
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http://npb.kib.ac.cn/EN/10.1007/s13659-014-0032-4     OR     http://npb.kib.ac.cn/EN/Y2014/V4/I4/207
1. J.K. Liu, Drug Disc. Ther. 1, 94-103 (2007)
2. D.Z. Liu, F. Wang, T.G. Liao, J.G. Tang, W. Steglich, H.J. Zhu, J.K. Liu, Org. Lett. 8, 5749-5752 (2006)
3. X.Y. Yang, T. Feng, Z.H. Li, Y. Sheng, X. Yin, Y. Leng, J.K. Liu, Org. Lett. 14, 5382-5384 (2012)
4. L. Zhang, Y. Shen, F. Wang, Y. Leng, J.K. Liu, Phytochemistry 71, 100-103 (2010)
5. W.M. Daniewski, P.A. Grieco, J.C. Huffman, A. Rymikewicz, A. Wawrzum, Phytochemistry 20, 2733-2734 (1981)
6. W.A. Ayer, L.M. Browne, Tetrahedron 37, 2199-2248 (1981)
7. L. Hu, J.K. Liu, Z. Naturforsch. C 57, 571-574 (2002)
8. D.Q. Luo, Y. Gao, J.M. Gao, F. Wang, X.L. Yang, J.K. Liu, J. Nat. Prod. 69, 1354-1357 (2006)
9. D.Q. Luo, Y. Gao, X.L. Yang, J.G. Tang, J.K. Liu, J. Antibiot. 60, 162-165 (2007)
10. D.Q. Luo, Y. Gao, X.L. Yang, J.G. Tang, L.Y. Zhao, J.K. Liu, Helv. Chim. Acta 90, 1112-1116 (2007)
11. T. Usia, H. Iwata, A. Hiratsuka, T. Watabe, S. Kadota, Y. Tezuka, J. Nat. Prod. 67, 1079-1083 (2004)
12. M. Wei, R. Wynn, G. Hollis, B. Liao, A. Margulis, B.G. Reid, R. Klabe, P.C. Liu, M. Becker-Pasha, M. Rupar, T.C. Burn, D.E. McCall, Y. Li, J. Biomol. Screen 12, 220-228 (2007)
13. D. Imhof, A.S. Wavreille, A. May, M. Zacharias, S. Tridandapani, D. Pei, J. Biol. Chem. 281, 20271-20282 (2006)
14. X.N. Yang, J.Y. Li, Y.Y. Zhou, Q. Shen, J.W. Chen, J. Li, Biochim. Biophys. Acta 1726, 34-41 (2005)
15. W. Zhang, D. Hong, Y.Y. Zhou, Y.N. Zhang, Q. Shen, J.Y. Li, L.H. Hu, J. Li, Biochim. Biophys. Acta 1760, 1505-1512 (2006)
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