Conosilane A, an unprecedented sesquiterpene from the cultures of basidiomycete conocybe siliginea

Organic Letters

Volumn 14, Issue 20, 2012, Pages 5382-5384

  Yang, Xiao Yan ^a,b   Feng, Tao ^a   Li, Zheng Hui ^a   Sheng, Yu ^c   Yin, Xia ^a,b   Leng, Ying ^c   Liu, Ji Kai ^a  

^a KUNMING INSTITUTE OF BOTANY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

[No Author keywords available]

Indexed keywords

11BETA HYDROXYSTEROID DEHYDROGENASE; CONOSILANE A; ENZYME INHIBITOR; SESQUITERPENE;

ARTICLE; BASIDIOMYCETES; CHEMICAL STRUCTURE; CHEMISTRY; DRUG ANTAGONISM; ISOLATION AND PURIFICATION; X RAY CRYSTALLOGRAPHY;

11-BETA-HYDROXYSTEROID DEHYDROGENASES; BASIDIOMYCOTA; CRYSTALLOGRAPHY, X-RAY; ENZYME INHIBITORS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; SESQUITERPENES;

EID: 84867708279     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol302468a     Document Type: Article

References (14)

1. Koike, Y.; Wada, K.; Kusano, G.; Nozoe, S. J. Nat. Prod. 1981, 44, 362-365
2. Ohenoja, E.; Jokiranta, J.; Makinen, T.; Kaikkonen, A.; Airaksinen, M. M. J. Nat.Prod. 1987, 50, 741-744
3. Brady, L. R.; Benedict, R. G.; Tyler, V. E.; Stuntz, D. E.; Malone, M. H. Lloydia 1975, 38, 172-173
4. Pomilio, A. B.; Battista, M. E.; Vitale, A. A. Curr. Org. Chem. 2006, 10, 2075-2121
5. Strassman, R. J. Neuropsychopharmacology 1992, 7, 241-243
6. Vollenweider, F. X.; Vollenweider-Scherpenhuyzen, M. F.; Babler, A.; Vogel, H.; Hell, D. Neuroreport 1998, 9, 3897-3902
7. McCall, R. B. Neurosci. Biobehav. Rev. 1982, 6, 509-514
8. Liu, D. Z.; Wang, F.; Liu, J. K. J. Nat. Prod. 2007, 70, 1503-1506
9. Zhou, Z. Y.; Tang, J. G.; Wang, F.; Dong, Z. J.; Liu, J. K. J. Nat. Prod. 2008, 71, 1423-1426
10. Yang, X. Y.; Feng, T.; Yin, X.; Li, Z. H.; Zhang, L.; Liu, J. K. Chin. J. Chem. 2012, 30, 1231-1235
11. 2 = 0.1106. The crystal structure of compound 1 was solved by direct method SHELXS-97 and expanded using the difference Fourier techniques, refined by the program SHLXL-97 and the full-matrix least-squares calculations. Crystallographic data for the structure of compound 1 have been deposited with the Cambridge Crystallographic Data Centre (deposition no. CCDC 894182). Copies of these data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.htm (or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB21EZ, U.K.; fax (+44) 1223-336-033; or desposit@ccdc.cam.ac.uk).
12. Abraham, W. R. Curr. Med. Chem. 2001, 8, 583-606
13. Ding, J. H.; Feng, T.; Li, Z. H.; Yang, X. Y.; Guo, H.; Yin, X.; Wang, G. Q.; Liu, J. K. Org. Lett. 2012, 14, 4976-4978
14. Mosmann, T. J. Immunol. Methods 1983, 65, 55-63