Antibacterial bromophenols from the marine red alga Rhodomela confervoides

Phytochemistry

Volumn 62, Issue 8, 2003, Pages 1221-1224

  Xu, Nianjun ^a,b   Fan, Xiao ^a   Yan, Xiaojun ^b   Li, Xiancui ^a   Niu, Rongli ^a   Tseng, C K ^a  

^a INSTITUTE OF OCEANOLOGY   (China)

^b NINGBO UNIVERSITY   (China)

Author keywords

Antibacterial activity; Bromophenol; Red alga; Rhodomela confervoides; Rhodomelaceae

Indexed keywords

3 BROMO 4 (2,3 DIBROMO 4,5 DIHYDROXYPHENYL)METHYL 5 (ETHOXYMETHYL) 1,3 BENZENEDIOL; 3 BROMO 4 (2,3 DIBROMO 4,5 DIHYDROXYPHENYL)METHYL 5 (HYDROXYMETHYL) 1,2 BENZENEDIOL; 3 BROMO 4 (2,3 DIBROMO 4,5 DIHYDROXYPHENYL)METHYL 5 (METHOXYMETHYL) 1,2 BENZENEDIOL; 4,4' METHYLENEBIS(5,6 DIBROMO 1,2 BENZENEDIOL); ANTIBIOTIC AGENT; BIS(2,3 DIBROMO 4,5 DIHYDROXYBENZYL)ETHER; METHANOL; PLANT EXTRACT; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; DRUG ISOLATION; DRUG STRUCTURE; ESCHERICHIA COLI; MASS SPECTROMETRY; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PSEUDOMONAS AERUGINOSA; RED ALGA; STAPHYLOCOCCUS AUREUS; STAPHYLOCOCCUS EPIDERMIDIS; STRUCTURE ANALYSIS;

ALGAE; ESCHERICHIA COLI; EUKARYOTA; PSEUDOMONAS; PSEUDOMONAS AERUGINOSA; RHODOMELA CONFERVOIDES; RHODOMELACEAE; RHODOPHYTA; STAPHYLOCOCCUS AUREUS; STAPHYLOCOCCUS EPIDERMIDIS;

EID: 0037380094     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0031-9422(03)00004-9     Document Type: Article

References (17)

1. Iliopoulou, D., Vagias, C., Harvala, C., Roussis, V., 2002. C15 acetogenins from the red alga Laurencia obtusa. Phytochemistry 59 (1), 111-116.
2. Katsui, N., Suzuki, Y., Kitamura, S., Irie, T., 1967. 5′6-Dibromoprotocatechauldehyde and 2′3-dibromo-4,5-dihydroxybenzyl methyl ether from new dibromophenols from Rhodomela larix. Tetrahedron 23, 1185-1188.
3. Kazuya, K., Takashi, A., 1977, Two new bromophoenols from the red alga, Rhodomela larix. Chem. Lett. 12, 1435-1438.
4. Kurata, K., Amiya, T., 1980. A new bromophenol from the red alga Polysiphonia urceolata. Bull. Chem. Soc. Jpn. 53, 2020-2022.
5. Kurata, K., Taniguchii, K., Takashima, K., Hayashi, I., Suzuki, M., 1997. Feeding-deterrent bromophenols from Odonthalia corymbifera. Phytochemistry 45 (3), 485-487.
6. Kurihara, H., Mitani, T., Kawabata, J., Takahashi, K., 1999. Two new bromophenols from the red alga Odonthalia corymbifera. J. Nat. Prod. 62, 882-884.
7. Lundgren, L., Olsson, K., Theander, O., 1979. Synthesis of some bromophenols present in red algae. Acta Chem. Scand. B. 33, 105-108.
8. Metzger, P., Rager, M.N., Largean, C., 2002. Botryolins A and B, two tetramethylsqualene triethers from the green microalga Botryoccus braunii. Phytochemistry 59, 839-843.
9. Minoru, S., Nobuhiko, K., Etsuro, K., 1980. Bromophenols from the red alga Rhodomela larix. Bull. Chem. Soc. Jpn. 53, 2099-2100.
10. Negi, P.S., Jayaprakasha, G.K., Jagan, M.R.L., Sakariah, K.K., 1999. Antibacterial activity of tumeric oil: a byproduct from curcumin manufacture. J. Agric. Food Chem. 47, 4297-4300.
11. Pedersen, P., Saenger, P., Fries, L., 1974. Simple brominated phenols in red algae. Phytochemistry 13 (8), 2273-2279.
12. Pederson, M., 1978. Bromochlorophenols and a brominated diphenylmethane in red algae. Phytochemistry 17, 291-293.
13. Phillips, D.W., Towers, G.H.N., 1981. Bromophenols of Rhodomela larix: chemotaxonomy of morphological forms. Biochem. Syst. Ecol. 9, 1-3.
14. Vairappan, C.S., Daitoh, M., Suzuki, M., Abe, T., Masuda, M., 2001. Antibacterial halogenated metabolites from the Malaysian Laurencia species. Phytochemistry 58, 291-297.
15. Vlachos, V., Critchley, A.T., von Holy, A., 1999. Differential antibacterial activity of extracts from selected Southern African macroalgal thalli. Bot. Mar. 42, 165-173.
16. Weinstein, B., Rold, T.L., Harrell, C.E., Burns, M.W., Waaland, J.R., 1975. Reexamination of the bromophenols in the red alga Rhodomela Larix. Phytochemistry 14, 2667-2670.
17. Xu, N.J., Fan, X., Han, L.J., Lin, W., Tseng, C.K., 2002. Study on the antibacterial activities of the ethanol extracts of seaweed. Oceanol. Limnol. Sin 33, 265-270.