Isolation and structural characterisation of five new and 14 known metabolites from the commercial starfish Archaster typicus

Food Chemistry

Volumn 124, Issue 4, 2011, Pages 1634-1638

  Yang, Xian Wen ^a   Chen, Xian Qiang ^a,c   Dong, Guang ^a   Zhou, Xue Feng ^a   Chai, Xin Yun ^a   Li, Yun Qiu ^a   Yang, Bin ^a   Zhang, Wei Dong ^b   Liu, Yonghong ^a  

^a SOUTH CHINA SEA INSTITUTE OF OCEANOLOGY   (China)

^b SECOND MILITARY MEDICAL UNIVERSITY   (China)

^c CHANGCHUN UNIVERSITY OF CHINESE MEDICINE   (China)

Author keywords

Anticancer; Archaster typicus; Metabolites; Starfish; Steroids

Indexed keywords

ANTICANCER; ANTICANCER ACTIVITIES; ARCHASTER TYPICUS; CHARACTERISATION; DECANOL; SPECTROSCOPIC DATA; SPECTROSCOPIC TECHNIQUE; STARFISH; STEROIDS; SULPHATES; TUMOUR CELLS;

BIOMOLECULES; LIPIDS; METABOLISM; SODIUM;

METABOLITES;

1 O OCTADECYLGLYCERO; 15 HYDROXYEICOSA 11 ENOIC ACID; 27 NOR 5ALPHA CHOLESTANE 3BETA,4BETA,5,6ALPHA,7BETA,8,14,15ALPHA,24ALPHA NONAOL; 27 NOR 5ALPHA CHOLESTANE 3BETA,4BETA,5,6ALPHA,8,14,15ALPHA,24ALPHA, OCTAOL; 27 NOR NONAOL 6 SULPHATE; 3 O SULFOASTERONE; 5ALPHA CHOLEST 24 ENE 3BETA,4BETA,5,6ALPHA 7BETA,8,14,15ALPHA,26 NONANOL 6 SULPHATE; 5ALPHA CHOLEST 24 ENE 3BETA,4BETA,5,6ALPHA, 7BETA,8,14,15ALPHA,2226 NONAOL 6 SULPHATE; 5ALPHA CHOLEST 24 ENE 3BETA,4BETA,6ALPHA,8,14,15ALPHA,26 HEPTAOL 15 SULPHATE; 5ALPHA CHOLEST 24 ENE 3BETA,6ALPHA,8,14,15ALPHA 26 HEXAOL 15 SULPHATE; CHOLESTEROL; GLYCEROL 1 (11 EICOSENOATE); GLYCEROL 1 HEXADECENOATE; HEXADECANOIC ACID 2,3 DIHYDROXY PROPYL ESTER; SODIUM 5ALPHA CHOLESTA 9(11) 24 DIEN 3BETA,6ALPHA,20BETA TRIOL 23 ONE 3 SULPHATE; SODIUM 5ALPHA CHOLESTA 9(11) EN 3BETA,6ALPHA,20BETA TRIOL 23 ONE 3 SULPHATE; SODIUM 5ALPHA CHOLESTANE 3BETA,4BETA,6ALPHA,8,14ALPHA,15BETA,26 HEPTAOL 15 SULPHATE; SODIUM 5ALPHA CHOLESTANE 3BETA,6ALPHA,8,14ALPHA,15BETA,26 HEXAOL 15 SULPHATE; SODIUM CHOLEST 25(27) ENE 3BETA,4BETA,5ALPHA,6ALPHA,7BETA,8BETA,14ALPHA,15ALPHA,24F,26 DECANOL 6 SULPHATE; STEROID; UNCLASSIFIED DRUG; XYLOPYRANOSIDE DERIVATIVE;

ANTINEOPLASTIC ACTIVITY; ARCHASTER TYPICUS; ARTICLE; BREAST CANCER; CANCER CELL CULTURE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; EXTRACTION; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR SINGLE QUANTUM COHERENCE; HUMAN; HUMAN CELL; INFRARED SPECTROSCOPY; ISOLATION AND PURIFICATION; METABOLITE; NUCLEAR OVERHAUSER EFFECT; PROTON NUCLEAR MAGNETIC RESONANCE; STARFISH;

ARCHASTER TYPICUS; ASTEROIDEA;

EID: 77957020029     PISSN: 03088146     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.foodchem.2010.08.033     Document Type: Article

References (19)

1. Anjaneyulu V., Prasad K.H., Ravi K., Connolly J.D. Triterpenoids from Mangifera indica. Phytochemistry 1985, 24:2359-2367.
2. Finamore E., Minale L., Riccio R., Rinaldo G., Zollo F. Novel marine polyhydroxylated steroids from the starfish Myxoderma platyacanthum. Journal of Organic Chemistry 1991, 56:1146-1153.
3. Guo C.H., Cheng Y., Liu X.M., Ren H., Lin Z.H. Content determination of some nutrient compositions in gonad of Asterina pectinifera. Haiyang Kexue 2004, 28:79-81.
4. Marine species and their distributions in China's seas 1994, China Ocean Press, Beijing. Z.G. Huang (Ed.).
5. Han L., Yuang W., Cong R., Fan T. Research progress in the bioactive materials from starfish. Haiyang Huzhao Tongbao 2006, 104:110.
6. Kicha A.A., Ivanchina N.V., Kalinovskii A.L., Dmitrenok P.S., Kainara S.O., Aminin D.L., et al. Polar steroidal compounds from the Far-Eastern starfish Lethasterias nanimensis chelifera. Russian Chemical Bulletin 2004, 53:447-454.
7. Kicha A.A., Ivanchina N.V., Kalinovsky A.I., Dmitrenok P.S., Stonik V.A. Steroidal monoglycosides from the Far Eastern starfish Hippasteria kurilensis and hypothetic pathways of polyhydroxysteroid biosynthesis in starfish. Steroids 2009, 74:238-244.
8. Levina E.V., Andriyashchenko P.V., Kalinovskii A.I., Stonik V.A. Steroid compounds from the Pacific starfish Lysastrosoma anthosticta. Russian Chemical Bulletin 2001, 50:313-315.
9. Pan G.C., Guo C.H., Liu C.L., Dong X.W. Determination of nutrient constituents of Luidia quinaria von Martens. Zhongguo Haiyang Yaowu Zazhi 2006, 25:46-48.
10. Riccio R., Santaniello M., Squillace Greco O., Minale L. Structure elucidation of (22E, 24R, 25R)-24-methyl-5α-cholest-22-ene-3β, 4β, 5, 6α, 8, 14, 15α, 25, 26-nonaol and (22E, 24S)-24-methyl-5α-cholest-22-ene-3β, 4β, 5, 6α, 8, 14, 15α, 25, 28-nonaol, minor marine polyhydroxysteroids isolated from the starfish Archaster typicus. Journal of the Chemical Society, Perkin Transaction I 1989, 823-826.
11. Riccio R., Squillace Greco O., Minale L., Laurent D., Duhet D. Highly hydroxylated marine steroids from the starfish Archaster typicus. Journal of the Chemical Society, Perkin Transaction I 1986, 665-670.
12. Tang, H. F., Cheng, G., Wen, A. D., Wu, J., Yang, Z. F., & Zhao, Y. P. (2009). A steroid glycoside with anticancer activity from starfish. CN 101362790A.
13. Tang, H. F., Yi, Y. H., Cheng, G., Wen, A. D., Yang, Z. F., & Chen, X. L. (2009). The utilisation of a steroid glycoside from starfish. CN 101348515A.
14. Wang W., Jang H., Hong J., Lee C.O., Im K.S., Bae S.J., et al. Additional cytotoxic sterols and saponins from the starfish certonardoa semiregularis. Journal of Natural Products 2004, 67:1654-1660.
15. Xu, J. W., Zhang, T. M., Guo, Z. M., Ji, S. L., Zhou, S. Y., & Lu, B. H. (1997). Starfish products. CN 1164357.
16. Xu, J. W., Song, Z. L., Lu, B. H., Su, H., & Fu, X. J. (2004). Starfish biofoods. CN ncbi-p:1169462C.
17. Xu J.W., Zhang T.M., Guo Z.M., Ji S.L., Leng Z.X., Zhou S.Y., et al. Studies on comprehensive utilisation of sea star. Qilu Yuye 1995, 12:38-41.
18. Yang X.W., Zeng H.W., Liu X.H., Li S.M., Xu W., Shen Y.H., et al. Anti-inflammatory and anti-tumour effects of Abies georgei extracts. Journal of Pharmacy and Pharmacology 2008, 60:937-941.
19. Zhou P., Gu Q.Q. Survey of studies on starfish saponins and the other bioactive substances. Marine Science 2000, 24:35-37.