Polyoxygenated diterpenoids of the eunicellin-type from the Chinese soft coral Cladiella krempfi

Tetrahedron

Volumn 69, Issue 9, 2013, Pages 2214-2219

  Cai, You Sheng ^a   Yao, Li Gong ^a   Di Pascale, Antonio ^b   Irace, Carlo ^b   Mollo, Ernesto ^c   Taglialatela Scafati, Orazio ^b   Guo, Yue Wei ^a  

^a SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

^b UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^c CNR   (Italy)

Author keywords

Bioactivity; Cladiella krempfi; Diterpenoids; Eunicellin; Structure elucidation

Indexed keywords

DITERPENOID; KREMPFENIN; LITOPHYNIN F; LITOPHYNOL A; LITOPHYNOL A ACETATE; LITOPHYNOL B; LITOPHYNOL C; OXYLITOPHYNOL; SCLEROPHYTIN A; SCLEROPHYTIN A METHYL ETHER; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTIPROLIFERATIVE ACTIVITY; ARTICLE; CHEMICAL COMPOSITION; CLADIELLA KREMPFI; CORAL; DRUG ISOLATION; DRUG TRANSFORMATION; GLIOMA CELL; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; RAT; STRUCTURE ACTIVITY RELATION; TUMOR CELL LINE;

ALCYONACEA; CLADIELLA;

EID: 84873300942     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.12.051     Document Type: Article

References (19)

1. M.J. Ortega, E. Zuba, and J. Salva J. Nat. Prod. 60 1997 485 487
2. T. Kusumi, H. Uchida, M.O. Ishitsuka, H. Yamamoto, and H. Kakisawa Chem. Lett. 1988 1077 1078
3. A.F. Ahmed, M.-H. Wu, G.-H. Wang, Y.-C. Wu, and J.-H. Sheu J. Nat. Prod. 68 2005 1051 1055
4. C.-J. Tai, J.-H. Su, M.-S. Huang, Z.-H. Wen, C.-F. Dai, and J.-H. Sheu Mar. Drugs 9 2011 2036 2045
5. T. Miyamoto, K. Yamada, N. Ikeda, T. Komori, and R. Higuchi J. Nat. Prod. 57 1994 1212 1219
6. B.-W. Chen, C.-H. Chao, J.-H. Su, C.-W. Tsai, W.-H. Wang, Z.-H. Wen, C.-Y. Huang, P.-J. Sung, Y.-C. Wu, and J.-H. Sheu Org. Biomol. Chem. 9 2011 834 844
7. D.B. Stierle, B. Carte, D.J. Faulkner, B. Tagle, and J. Clardy J. Am. Chem. Soc. 102 1980 5088 5092
8. B.H. Long, J.M. Carboni, A.J. Wasserman, L.A. Cornell, A.M. Casazza, P.R. Jensen, T. Lindel, W. Fenical, and C.R. Fairchild Cancer Res. 58 1998 1111 1115
9. O. Taglialatela-Scafati, U. Deo-Jangra, M. Campbell, M. Roberge, and R.J. Andersen Org. Lett. 4 2002 4085 4088
10. P. Sharma, and M. Alam J. Chem. Soc., Perkin Trans. 1 1988 2537 2540
11. L.A. Paquette, O.M. Moradei, P. Bernardelli, and T. Lange Org. Lett. 2 2000 1875 1878
12. M.T. Crimmins, C.S. Stauffer, and M.C. Mans Org. Lett. 13 2011 4890 4893 Some of the previous syntheses of the same compound are cited in this paper
13. M.L. Ciavatta, E. Manzo, E. Mollo, C.A. Mattia, C. Tedesco, C. Irace, Y.-W. Guo, X.-B. Li, G. Cimino, and M. Gavagnin J. Nat. Prod. 74 2011 1902 1907
14. N.S. Sarma, R. Chavakula, I.N. Rao, R. Kadirvelraj, T.N.G. Row, and I. Saito J. Nat. Prod. 56 1993 1977 1980
15. M. Ochi, K. Yamada, K. Futatsugi, H. Kotsuki, and K. Shibata Heterocycles 32 1991 29 32
16. M. Maida, A.R. Carroll, and J.C. Coll J. Chem. Ecol. 19 1993 2285 2296
17. H.M. Hassan, A.Y. Elnagar, M.A. Khanfar, A.A. Sallam, R. Mohammed, L.A. Shaala, D.T.A. Youssef, M.S. Hifnawy, and K.A. El Sayed Eur. J. Med. Chem. 46 2011 1122 1130
18. J. Denecke, K. Fiedler, U. Hacker-Klom, G. Molenkamp, H. Jurgens, and J.E.A. Wolff Anticancer Res. 17 1997 4531 4534
19. G. Mangiapia, G. D'Errico, L. Simeone, C. Irace, A. Radulescu, A. Di Pascale, A. Colonna, D. Montesarchio, and L. Paduano Biomaterials 33 2012 3770 3782