Natural Products and Bioprospecting    2011, Vol. 1 Issue (2) : 87-92     DOI: 10.1007/s13659-011-0018-4
Regular Article |
Unusual illudin-type sesquiterpenoids from cultures of Agrocybe salicacola
Liang-Yan LIUa,b, Ling ZHANGa, Tao FENGa, Zheng-Hui LIa, Ze-Jun DONGa, Xing-Yao LIa,b, Jia SUa,b, Yan LIa, Ji-Kai LIUa
a State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China;
b Graduate University of Chinese Academy of Sciences, Beijing 100039, China
Download: PDF(553 KB)   HTML ()  
Export: BibTeX | EndNote | Reference Manager | ProCite | RefWorks    
Abstract  Seven new illudin-type sesquiterpenoids, agrocybins A-G(1-7), along with three known analogues(8-10), have been isolated from the culture broth of the fungus Agrocybe salicacola. Their structures were elucidated on the basis of extensive spectroscopic data analysis and comparison with data reported in the literature. The relative stereoconfigurations of 1 and 6 were elucidated by the X-ray crystallographic diffraction analysis. Compound 1 was highly cyclized containing seven chiral carbons which arranged compactly in six rings.
Keywords Agrocybe salicacola      sesquiterpenoid      agrocybin      stereoconfiguration      X-ray     
Fund:This project was supported by the National Basic Research Program of China(973 Program, 2009CB522300), the National Natural Sciences Foundation of China(30830113), and MOST(2009ZX09501-029).
Issue Date: 24 November 2017
Service
E-mail this article
E-mail Alert
RSS
Articles by authors
Liang-Yan LIU
Ling ZHANG
Tao FENG
Zheng-Hui LI
Ze-Jun DONG
Xing-Yao LI
Jia SU
Yan LI
Ji-Kai LIU
Trendmd:   
Cite this article:   
Liang-Yan LIU,Ling ZHANG,Tao FENG, et al. Unusual illudin-type sesquiterpenoids from cultures of Agrocybe salicacola[J]. Natural Products and Bioprospecting, 2011, 1(2): 87-92.
URL:  
http://npb.kib.ac.cn/EN/10.1007/s13659-011-0018-4     OR     http://npb.kib.ac.cn/EN/Y2011/V1/I2/87
[1] Diyabalanage, T.; Mulabagal, V.; Mills, G.; DeWitt, D. L.; Nair, M. G. Food Chem. 2008, 108, 97-102.
[2] Won-Gon, K.; In-Kyoung, L.; Jong-Pyung, K.; In-Ja, R.; Hiroyuki, K.; Yoo, I. D. J. Nat. Prod. 1997, 60, 721-723.
[3] Ngai, P. H. K.; Zhao, Z.; Ng, T. B. Peptides 2005, 26, 191-196.
[4] Wang, H. X.; Ng, T. B.; Liu, Q. H. Life Sci. 2002, 70, 877-885.
[5] Tadashi, K.; Satoshi, S.; Shigoe, U. Carbohydr. Res. 1994, 251, 81-87.
[6] Yang, Z. L.; Zang, M.; Liu, X. X. Acta Bot. Yunn. 1993, 15, 18-20.
[7] Zhou, H. M.; Zhao, Y. C.; Chen, W. M.; Chai, H. M.; Li, S. H.; Zhao, J. Acta Bot. Yunn. 2010, 32, 315-322.
[8] Zhu, Y. C.; Wang, G.; Yang, X. L.; Luo, D. Q.; Zhu, Q. C.; Peng, T.; Liu, J. K. Tetrahedron Lett. 2010, 51, 3443-3445.
[9] Wang, G.; Liu, L. Y.; Zhu, Y. C.; Liu, J. K. J. Asian Nat. Prod. Res. 2011, 13, 430-433.
[10] Schobert, R.; Knauer, S.; Seibt, S.; Biersack, B. Curr. Med. Chem. 2011, 18, 790-807.
[11] Gonzalez Del Val, A.; Platas, G.; Arenal, F.; Orihuela, J. C.; Garcia, M.; Hernandez, P.; Royo, I.; De Pedro, N.; Silver, L. L.; Young, K.; Vicente, M. F.; Pelaez, F. Mycol. Res. 2003, 107, 1201-1209.
[12] Poindessous, V.; Koeppel, F.; Raymond, E.; Cvitkovic, E.; Waters, S. J.; Larsen, A. K. Int. J. Oncol. 2003, 23, 1347-1355.
[13] Serova, M.; Calvo, F.; Lokiec, F.; Koeppel, F.; Poindessous, V.; Larsen, A. K.; Van Laar, E. S.; Waters, S. J.; Cvitkovic, E.; Raymond, E. Cancer Chemoth. Pharm. 2006, 57, 491-499.
[14] Kelner, M. J.; McMorris, T. C.; Rojas, R. J.; Estes, L. A.; Suthipinjtham, P. Invest. New Drugs 2008, 26, 407-415.
[15] Pettit, G. R.; Meng, Y.; Pettit, R. K.; Herald, D. L.; Cichacz, Z. A.; Doubek, D. L.; Richert, L. J. Nat. Prod. 2010, 73, 388-392.
[16] Falk, R.; Timm, A.; Olov, S. Tetrahedron 2002, 58, 7785-7789.
[17] Alberto A.; Rosanna C.; Gianluca N.; Orso, Vajna de Pava. J. Chem. Soc., Perkin Trans. 1, 1991, 733-737.
[18] Kelner, M. J.; McMorris, T. C.; Estes, L. A.; Rutherford, M.; Montoya, M.; Goldstein, J.; Samson, K.; Starr, R.; Taetle, R. Biochem. Pharmcol. 1994, 48, 403-409.
[19] Matsuoka, A.; Hirosawa, A.; Natori, S.; Iwasaki, S.; Sofuni, T.; Ishidate, M. J. Mutat. Res. 1989, 215, 179-185;
[20] Yamada, K.; Ojika, M.; Kigoshi, H. Nat. Prod. Rep. 2007, 24, 798-813.
[21] Reed, L. J.; Muench, H. Am. J. Hyg. 1938, 27, 493-497.
[1] Miao Liu, Zheng-Xi Hu, Yuan-Qing Luo, Min Zhou, Wei-Guang Wang, Xiao-Nian Li, Xue Du, Jian-Xin Pu, Han-Dong Sun. Two New Compounds from Schisandra propinqua var. propinqua[J]. Natural Products and Bioprospecting, 2017, 7(3): 257-262.
[2] Michel Feussi Tala, Jianchun Qin, Joseph T. Ndongo, Hartmut Laatsch. New Azulene-Type Sesquiterpenoids from the Fruiting Bodies of Lactarius deliciosus[J]. Natural Products and Bioprospecting, 2017, 7(3): 269-273.
[3] Man-Si Yang, Xiao-Yue Cai, Yuan-Yuan He, Meng-Ying Lu, Shuang Liu, Wen-Xiang Wang, Zheng-Hui Li, Hong-Lian Ai, Tao Feng. Seco-sativene and Seco-longifolene Sesquiterpenoids from Cultures of Endophytic Fungus Bipolaris eleusines[J]. Natural Products and Bioprospecting, 2017, 7(1): 147-150.
[4] Mehtab Parveen, Faheem Ahmad, Ali Mohammed Malla, Shaista Azaz, Mahboob Alam, Omer A. Basudan, Manuela Ramos Silva, Pedro S. Pereira Silva. Acetylcholinesterase and Cytotoxic Activity of Chemical Constituents of Clutia lanceolata Leaves and its Molecular Docking Study[J]. Natural Products and Bioprospecting, 2016, 6(6): 267-278.
[5] Masahiko Isaka, Somporn Palasarn, Malipan Sappan, Sumalee Supothina, Thitiya Boonpratuang. Hirsutane Sesquiterpenes from Cultures of the Basidiomycete Marasmiellus sp. BCC 22389[J]. Natural Products and Bioprospecting, 2016, 6(5): 257-260.
[6] Jun-Li Yang, Ya-Min Zhao, Yan-Ping Shi. Sesquiterpenoids from the Rhizomes of Homalomena occulta[J]. Natural Products and Bioprospecting, 2016, 6(4): 211-216.
[7] Ce Kuang, Shu-Xi Jing, Yan Liu, Shi-Hong Luo, Sheng-Hong Li. Drimane Sesquiterpenoids and Isochromone Derivative from the Endophytic Fungus Pestalotiopsis sp. M-23[J]. Natural Products and Bioprospecting, 2016, 6(3): 155-160.
[8] Chang-Wei Song, Paul-Keilah Lunga, Xu-Jie Qin, Gui-Guang Cheng, Ya-Ping Liu, Xiao-Dong Luo. Chemical Constituents from the Stems of Ecdysanthera rosea[J]. Natural Products and Bioprospecting, 2014, 4(6): 319-323.
[9] Jiang-Yuan ZHAO, Tao FENG, Zheng-Hui LI, Ze-Jun DONG, Hong-Bin ZHANG, Ji-Kai LIU. Sesquiterpenoids and an ergosterol from cultures of the fungus Daedaleopsis tricolor[J]. Natural Products and Bioprospecting, 2013, 3(6): 271-276.
[10] Xiao-Yan YANG, Tao FENG, Jian-Hai DING, Zheng-Hui LI, Yan LI, Qiong-Ying FAN, Ji-Kai LIU. Two new drimane sesquiterpenoids from cultures of the basidiomycete Trichaptum biforme[J]. Natural Products and Bioprospecting, 2013, 3(4): 154-157.
[11] Wei-Wei FAN, Feng-Qing XU, Fa-Wu DONG, Xiao-Nian LI, Yan LI, Yu-Qing LIU, Jun ZHOU, Jiang-Miao HU. Dendrowardol C, a novel sesquiterpenoid from Dendrobium wardianum Warner[J]. Natural Products and Bioprospecting, 2013, 3(3): 89-92.
[12] Xiao-Yan YANG, Tao FENG, Jian-Hai DING, Xia YIN, Hua GUO, Zheng-Hui LI, Ji-Kai LIU. Five new 5, 6-seco-tremulane sesquiterpenoids from the basidiomycete Conocybe siliginea[J]. Natural Products and Bioprospecting, 2013, 3(2): 48-51.
[13] Jian-Hai DING, Tao FENG, Zheng-Hui LI, Liang LI, Ji-Kai LIU. Twelve new compounds from the basidiomycete Boreostereum vibrans[J]. Natural Products and Bioprospecting, 2012, 2(5): 200-205.
[14] Chang-Li SUN, Huan YAN, Xu-Hong LI, Xue-Fang ZHENG, Hai-Yang LIU. Terpenoids from Chloranthus elatior[J]. Natural Products and Bioprospecting, 2012, 2(4): 156-159.
[15] Chuan-Fu DONG, Lei LIU, Huai-Rong LUO, Xiao-Nian LI, Zheng-Ye GUAN, Yi-Fen WANG. Sesquilignans and sesquiterpenoid from the stem barks of Illicium simonsii and their anti-AChE activity[J]. Natural Products and Bioprospecting, 2012, 2(3): 133-137.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed