Sarcoglycosides A-C, new O-glycosylglycerol derivatives from the South China sea soft coral Sarcophyton infundibuliforme

Helvetica Chimica Acta

Volumn 92, Issue 8, 2009, Pages 1495-1502

  Li, Liang ^a   Wang, Chang Yun ^a   Shao, Chang Lun ^a   Guo, Yue Wei ^b   Li, Guo Qiang ^a   Sun, Xue Ping ^a   Han, Lei ^a   Huang, Hui ^c   Guan, Hua Shi ^a  

^a OCEAN UNIVERSITY OF CHINA   (China)

^b SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

^c SOUTH CHINA SEA INSTITUTE OF OCEANOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ARTEMIA SALINA; CHEMICAL EXAMINATION; CHEMICAL METHOD; HEXADECANOL; SOUTH CHINA SEA;

CHEMICAL COMPOUNDS;

CHIMYL ALCOHOL; GLYCEROL DERIVATIVE; GLYCOSIDE; HEXADECANOL; SARCOGLYCOSIDE A; SARCOGLYCOSIDE B; SARCOGLYCOSIDE C; UNCLASSIFIED DRUG;

ARTEMIA; ARTICLE; BIOASSAY; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CHINA; CORAL; EXTRACTION; MARINE ENVIRONMENT; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SEA; TOXICITY TESTING;

EID: 69249219113     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200900026     Document Type: Article

References (18)

1. B. F. Bowden, J. C. Coll, S. J. Mitchell, J. Mulder, G. J. Stokie, Aust. J. Chem. 1978, 31, 2049.
2. J. W. Blunt, B. R. Copp, W.-P. Hu, M. H. G. Munro, P. T. Northcote, M. P. Prinsep, Nat. Prod. Rep. 2009, 26, 170.
3. M. Zhang, K.-H. Long, Nat. Prod. Res. Dev. 1995, 7, 12.
4. C. Subrahmanyam, R. Kulatheeswaran, Indian J. Chem., Sect. B 1999, 38, 1388.
5. V. Anjaneyulu, P. V. Subba Rao, P. Radhika, H. Laatsch, L. N. Misra, Indian J. Chem., Sect. B 2000, 39, 121.
6. V. Anjaneyulu, P. V. Subba Rao, P. Radhika, H. Laatsch, R. N. Asolkar, Indian J. Chem., Sect. B 2001, 40, 405.
7. L. Li, C.-Y. Wang, H. Huang, E. Mollo, G. Cimino, Y.-W. Guo, Helv. Chim. Acta 2008, 91, 111.
8. L.-Y. Liang, S.-Z. Deng, Q. Zhang, D.-J. Xiao, H.-M. Wu, Chin. J. Mar. Drugs 2001, 6.
9. C. Subrahmanyam, C. V. R. V. Anjaneyulu, P. Satyanarayana, P. V. Subba Rao, Tetrahedron 1992, 48, 3111.
10. W. Zhang, H.-X. Lou, G.-Y. Li, H.-M. Wu, J. Asian Nat. Prod. Res. 2003, 5, 189.
11. J. Wu, L.-J. Long, Y.-S. Song, S. Zhang, Q.-X. Li, J.-S. Huang, Z.-H. Xiao, Chem. Pharm. Bull. 2005, 53, 330.
12. M. Kobayashi, K. Hayashi, K. Kawazoe, I. Kitagawa, Chem. Pharm. Bull. 1992, 40, 1404.
13. P. Baruah, N. C. Baruah, R. P. Sharma, J. N. Baruah, P. Kulanthaivel, W. Herz, Phytochemistry 1983, 22, 1741.
14. R. G. S. Ritchie, N. Cyr, B. Korsch, H. J. Koch, A. S. Perlin, Can. J. Chem. 1975, 53, 1424.
15. S. D. Stamatov, J. Stawinski, Tetrahedron Lett. 2005, 46, 1601.
16. S. H. Bhuiyan, Z. Ahmed, M. Utamura, K. Izumori, J. Ferment. Bioeng. 1998, 86, 513.
17. P. N. Solis, C.W. Wright, M. M. Anderson, M. P. Gupta, J. D. Phillipson, Planta Med. 1993, 59, 250.
18. B. N. Meyer, N. R. Ferrigni, J. E. Putnam, L. B. Jacobson, D. E. Nicols, J. L. Mclaughlin, Planta Med. 1982, 45, 31.