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Volumn 67, Issue 19, 2006, Pages 2115-2119

Diterpenes from the Far-eastern brown alga Dictyota dichotoma

Author keywords

(+) 1,5 Cyclo 5,8,9,10 tetrahydroerogorgiaene; Cytotoxic activity; Dictyota dichotoma; Dictyotaceae; Diterpenes; Ent erogorgiaene; NMR; Sesquiterpenes; Tumor cells

Indexed keywords

DITERPENE; PLANT EXTRACT; SESQUITERPENE;

EID: 33748426461     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2006.05.041     Document Type: Article
Times cited : (19)

References (22)
  • 2
    • 0026066853 scopus 로고
    • 5-(3-Carboxymethoxyphenyl)-2-(4,5-dimethylthiazoly)-3-(4-sulfophenyl)tetrazolium, inner salt (MTS) and related analogs of 3-(4,5-dimethylthiazolyl)-2,5-diphenyltetrazolium bromide (MTT) reducing to purple water-soluble formazans as cell-viability indicators
    • Barltrop J.A., Owen T.C., Cory A.H., and Cory J.G. 5-(3-Carboxymethoxyphenyl)-2-(4,5-dimethylthiazoly)-3-(4-sulfophenyl)tetrazolium, inner salt (MTS) and related analogs of 3-(4,5-dimethylthiazolyl)-2,5-diphenyltetrazolium bromide (MTT) reducing to purple water-soluble formazans as cell-viability indicators. Bioorg. Med. Chem. Lett. 1 (1991) 611-614
    • (1991) Bioorg. Med. Chem. Lett. , vol.1 , pp. 611-614
    • Barltrop, J.A.1    Owen, T.C.2    Cory, A.H.3    Cory, J.G.4
  • 3
    • 0000475468 scopus 로고
    • Nuclear magnetic resonance spectral parameters in bicyclo[3.1.1]heptanes. α-Pinene, myrtenal, and verbenone
    • Bates R.B., and Thalacker V.P. Nuclear magnetic resonance spectral parameters in bicyclo[3.1.1]heptanes. α-Pinene, myrtenal, and verbenone. J. Org. Chem. 33 (1968) 1730-1732
    • (1968) J. Org. Chem. , vol.33 , pp. 1730-1732
    • Bates, R.B.1    Thalacker, V.P.2
  • 4
    • 29244440730 scopus 로고    scopus 로고
    • Diterpene biosynthesis by the dinoflagellate symbiont of the Caribbean gorgonian Pseudopterogorgia bipinnata
    • Boehnlein J.M., Santiago-Vazquez L.Z., and Kerr R.G. Diterpene biosynthesis by the dinoflagellate symbiont of the Caribbean gorgonian Pseudopterogorgia bipinnata. Mar. Ecol. Progr. Ser. 303 (2005) 105-111
    • (2005) Mar. Ecol. Progr. Ser. , vol.303 , pp. 105-111
    • Boehnlein, J.M.1    Santiago-Vazquez, L.Z.2    Kerr, R.G.3
  • 5
    • 0010634973 scopus 로고
    • Chemical studies of marine invertebrates. XXVIII, Diterpenes from Clavularia inflata (Coelenterata, Octocorallia, Stolonifera)
    • Braekman J.C., Daloze D., and Schulbrt R. Chemical studies of marine invertebrates. XXVIII, Diterpenes from Clavularia inflata (Coelenterata, Octocorallia, Stolonifera). Tetrahedron 34 (1978) 1551-1556
    • (1978) Tetrahedron , vol.34 , pp. 1551-1556
    • Braekman, J.C.1    Daloze, D.2    Schulbrt, R.3
  • 6
    • 0347129770 scopus 로고    scopus 로고
    • Enantioselective total synthesis of erogorgiaene: applications of asymmetric Cu-catalyzed conjugate additions of alkilzincs to acyclic enones
    • Cesati R.R., De Armas J., and Hoveyda A.H. Enantioselective total synthesis of erogorgiaene: applications of asymmetric Cu-catalyzed conjugate additions of alkilzincs to acyclic enones. J. Am. Chem. Soc. 126 (2004) 96-101
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 96-101
    • Cesati, R.R.1    De Armas, J.2    Hoveyda, A.H.3
  • 7
    • 17044429442 scopus 로고    scopus 로고
    • Direct synthesis of (+)-erogorgiaene through a kinetic enantiodifferentiating step
    • Davies H.M.L., and Walji A.M. Direct synthesis of (+)-erogorgiaene through a kinetic enantiodifferentiating step. Angew. Chem. Int. Ed. 44 (2005) 1733-1735
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 1733-1735
    • Davies, H.M.L.1    Walji, A.M.2
  • 10
    • 5644221406 scopus 로고    scopus 로고
    • Pseudopterosins P-V, new compounds from the gorgonian octocoral Pseudopterogorgia elisabethae from Providencia island, Colombian Caribbean
    • Duque C., Puyana M., Narvaez G., Osorno O., Hara N., and Fujimoto Y. Pseudopterosins P-V, new compounds from the gorgonian octocoral Pseudopterogorgia elisabethae from Providencia island, Colombian Caribbean. Tetrahedron 60 (2004) 10627-10635
    • (2004) Tetrahedron , vol.60 , pp. 10627-10635
    • Duque, C.1    Puyana, M.2    Narvaez, G.3    Osorno, O.4    Hara, N.5    Fujimoto, Y.6
  • 11
    • 0030957062 scopus 로고    scopus 로고
    • New diterpenoids from the alga Dictyota dichotoma
    • Duran R., Zubia E., Ortega M.J., and Salva J. New diterpenoids from the alga Dictyota dichotoma. Tetrahedron 53 (1997) 8675-8688
    • (1997) Tetrahedron , vol.53 , pp. 8675-8688
    • Duran, R.1    Zubia, E.2    Ortega, M.J.3    Salva, J.4
  • 12
    • 0036007872 scopus 로고    scopus 로고
    • Marine natural products
    • and previous reports in this series
    • Faulkner D.J. Marine natural products. Nat. Prod. Rep. 19 (2002) 1-48 and previous reports in this series
    • (2002) Nat. Prod. Rep. , vol.19 , pp. 1-48
    • Faulkner, D.J.1
  • 13
    • 0001631735 scopus 로고
    • Marine natural products. VIII. Pachydictyol A, an exceptional diterpene alcohol from the brown alga Pachydictyon coriaceum
    • Hirschfeld D.R., Fenical W., Lin G.H.Y., Wing R.M., Radlick P., and Sims J.J. Marine natural products. VIII. Pachydictyol A, an exceptional diterpene alcohol from the brown alga Pachydictyon coriaceum. J. Am. Chem. Soc. 95 (1973) 4049-4050
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 4049-4050
    • Hirschfeld, D.R.1    Fenical, W.2    Lin, G.H.Y.3    Wing, R.M.4    Radlick, P.5    Sims, J.J.6
  • 14
    • 0023683393 scopus 로고
    • Antitumor xenicane and norxenicane lactones from the brown alga Dictyota dichotoma
    • Ishitsuka M.O., Kusumi T., and Kakisawa H. Antitumor xenicane and norxenicane lactones from the brown alga Dictyota dichotoma. J. Org. Chem. 53 (1988) 5010-5013
    • (1988) J. Org. Chem. , vol.53 , pp. 5010-5013
    • Ishitsuka, M.O.1    Kusumi, T.2    Kakisawa, H.3
  • 15
    • 0010336443 scopus 로고
    • Studies in sesquiterpenes. XXII. Structure of mustakone and copaene
    • Kapadia V.H., Nagasampagi B.A., Naik V.G., and Dev S. Studies in sesquiterpenes. XXII. Structure of mustakone and copaene. Tetrahedron 21 (1965) 607-618
    • (1965) Tetrahedron , vol.21 , pp. 607-618
    • Kapadia, V.H.1    Nagasampagi, B.A.2    Naik, V.G.3    Dev, S.4
  • 17
    • 0022907680 scopus 로고
    • The pseodopterosins: a new class of antiinflammatory and analgesic diterpene pentosides from the marine sea whip Pseudopterogorgia elisabethae (Octocorallia)
    • Look S.A., Fenical W., Matsumoto G.K., and Clardy J. The pseodopterosins: a new class of antiinflammatory and analgesic diterpene pentosides from the marine sea whip Pseudopterogorgia elisabethae (Octocorallia). J. Org. Chem. 51 (1986) 5140-5145
    • (1986) J. Org. Chem. , vol.51 , pp. 5140-5145
    • Look, S.A.1    Fenical, W.2    Matsumoto, G.K.3    Clardy, J.4
  • 19
    • 0001276280 scopus 로고
    • Comparative study of the halogenated tyrosine derivatives from Demospongiae (Porifera)
    • Makarieva T.N., Stonik V.A., Alcolado P., and Elyakov G.B. Comparative study of the halogenated tyrosine derivatives from Demospongiae (Porifera). Comp. Biochem. Physiol. B 68 (1981) 481-484
    • (1981) Comp. Biochem. Physiol. B , vol.68 , pp. 481-484
    • Makarieva, T.N.1    Stonik, V.A.2    Alcolado, P.3    Elyakov, G.B.4
  • 20
    • 0035143674 scopus 로고    scopus 로고
    • Serrulatane diterpenes with antimycobacterial activity isolated from the West Indian sea whip Pseudopterogorgia elisabethae
    • Rodriguez A.D., and Ramirez C. Serrulatane diterpenes with antimycobacterial activity isolated from the West Indian sea whip Pseudopterogorgia elisabethae. J. Nat. Prod. 64 (2001) 100-102
    • (2001) J. Nat. Prod. , vol.64 , pp. 100-102
    • Rodriguez, A.D.1    Ramirez, C.2
  • 22
    • 0006553029 scopus 로고
    • Acetoxycrenulide, a new bicyclic cyclopropane-containing diterpenoid from the brown seaweed Dictyota crenulata
    • Sun H.H., McEnroe F.J., and Fenical W. Acetoxycrenulide, a new bicyclic cyclopropane-containing diterpenoid from the brown seaweed Dictyota crenulata. J. Org. Chem. 48 (1983) 1903-1906
    • (1983) J. Org. Chem. , vol.48 , pp. 1903-1906
    • Sun, H.H.1    McEnroe, F.J.2    Fenical, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.