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Volumn 54, Issue 3-4, 1999, Pages 246-252

Bromoisoxazoline alkaloids from the Caribbean sponge Aplysina insularis

Author keywords

Aplysina insularis; Bromoisoxazoline Alkaloids; Chemotaxonomy; Sponges; Structure Elucidation

Indexed keywords

14 OXO AEROPHOBIN 2; ALKALOID DERIVATIVE; BROMOISOXAZOLINE DERIVATIVE; CHEMOTAXONOMY; ISOLATION PROCEDURE;

EID: 0032902892     PISSN: 09395075     EISSN: None     Source Type: Journal    
DOI: 10.1515/znc-1999-3-415     Document Type: Article
Times cited : (15)

References (17)
  • 1
    • 0026772145 scopus 로고
    • 11-oxo-aerothionin:A cytotoxic antitumor bromotyrosine-derived alkaloid from the Caribbean marine sponge Aplysina lacunosa
    • Acosta A. L. and Rodriguez A. D. (1992), 11-oxo-aerothionin:a cytotoxic antitumor bromotyrosine-derived alkaloid from the Caribbean marine sponge Aplysina lacunosa. J. Nat. Prod. 55, 1007-1012.
    • (1992) J. Nat. Prod. , vol.55 , pp. 1007-1012
    • Acosta, A.L.1    Rodriguez, A.D.2
  • 2
    • 0029089519 scopus 로고
    • Biosynthesis of brominated tyrosine metabolites by Aplvsina fistularis
    • Carney J. R. and Rinehart K. L. (1995), Biosynthesis of brominated tyrosine metabolites by Aplvsina fistularis. J. Nat. Prod. 58, 971-985.
    • (1995) J. Nat. Prod. , vol.58 , pp. 971-985
    • Carney, J.R.1    Rinehart, K.L.2
  • 3
    • 0028590063 scopus 로고
    • Chemistry of verongida sponges III. Constituents of a Caribbean Verongula sp
    • Ciminiello P., Fattorusso E., Magno S. and Pansini M. (1994), Chemistry of Verongida sponges III. Constituents of a Caribbean Verongula sp. J. Nat. Prod. 57, 1564-1569.
    • (1994) J. Nat. Prod. , vol.57 , pp. 1564-1569
    • Ciminiello, P.1    Fattorusso, E.2    Magno, S.3    Pansini, M.4
  • 4
    • 0030092684 scopus 로고    scopus 로고
    • Chemistry of Verongida sponges VI. Comparison of the secondary metabolic composition of Aplysina insularis and Aplysina fulva
    • Ciminiello P., Fattorusso E., Magno S. and Pansinsi M. (1996), Chemistry of Verongida sponges VI. Comparison of the secondary metabolic composition of Aplysina insularis and Aplysina fulva. Biochem Syst. Ecol. 24, 105-113.
    • (1996) Biochem Syst. Ecol. , vol.24 , pp. 105-113
    • Ciminiello, P.1    Fattorusso, E.2    Magno, S.3    Pansinsi, M.4
  • 6
    • 0006440933 scopus 로고
    • Fast atom bombardment mass spectra of complex halogenated metabolites from Verongia sp. Sponges
    • Cimino G., Sodano G., Self R. and Fenwick R. G. (1984), Fast atom bombardment mass spectra of complex halogenated metabolites from Verongia sp. sponges. Gazz. Chim. Ital. 114, 533-538.
    • (1984) Gazz. Chim. Ital. , vol.114 , pp. 533-538
    • Cimino, G.1    Sodano, G.2    Self, R.3    Fenwick, R.G.4
  • 7
    • 0030770048 scopus 로고    scopus 로고
    • Wound activation of protoxins in marine sponge Aplysina aerophoba
    • Ebel R., Brenzinger M., Kunze A., Gross H. J. and Proksch P. (1997), Wound activation of protoxins in marine sponge Aplysina aerophoba. J. Chem. Ecol. 23, 1451-1462.
    • (1997) J. Chem. Ecol. , vol.23 , pp. 1451-1462
    • Ebel, R.1    Brenzinger, M.2    Kunze, A.3    Gross, H.J.4    Proksch, P.5
  • 9
    • 0018732148 scopus 로고
    • Marine natural products:Fistularin-1,-2 and -3 from the sponge Aplysina fistularis forma fulva
    • Gopichand Y. and Schmitz F. J. (1979), Marine natural products:fistularin-1,-2 and -3 from the sponge Aplysina fistularis forma fulva. Tetrahedron Lett.41, 3921-3924.
    • (1979) Tetrahedron Lett. , vol.41 , pp. 3921-3924
    • Gopichand, Y.1    Schmitz, F.J.2
  • 10
    • 0025108617 scopus 로고
    • Chemistry of sponges VII. 11,19-dideoxyfistularin-3 and 11-hydroxyaerothionin, bromotyrosine derivatives from Pseudoceratina durissima
    • Kernan M. R., Cambie R. C. and Bergquist P. R. (1990), Chemistry of sponges VII. 11,19-dideoxyfistularin-3 and 11-hydroxyaerothionin, bromotyrosine derivatives from Pseudoceratina durissima. J. Nat. Prod. 53, 615-622.
    • (1990) J. Nat. Prod. , vol.53 , pp. 615-622
    • Kernan, M.R.1    Cambie, R.C.2    Bergquist, P.R.3
  • 11
    • 0028913755 scopus 로고
    • Purealidins J-R, new bromotyrosine alkaloids from the Okinawan marine sponge Psamaplysilla purpurea
    • Kobayashi J., Horma K., Sasaki T. and Tsuda M. (1995), Purealidins J-R, new bromotyrosine alkaloids from the Okinawan marine sponge Psamaplysilla purpurea. Chem. Pharm. Bull. 43, 403-407.
    • (1995) Chem. Pharm. Bull. , vol.43 , pp. 403-407
    • Kobayashi, J.1    Horma, K.2    Sasaki, T.3    Tsuda, M.4
  • 14
    • 37049141803 scopus 로고
    • Aerothionin and homoaerothionin:Two tetrabromo-spirohexadienyl isoxazoles from Verongia sponges
    • Moody K., (1972), Aerothionin and homoaerothionin:two tetrabromo-spirohexadienyl isoxazoles from Verongia sponges. J. C. S. Perkin, 18-24.
    • (1972) J. C. S. Perkin , pp. 18-24
    • Moody, K.1
  • 15
    • 0002998756 scopus 로고
    • A collection of West Indian Demospongiae (Porifera). In appendix, a list of the Demospongiae hitherto recorded from the West Indies
    • Pulitzer-Finali G. (1986), A collection of West Indian Demospongiae (Porifera). In appendix, a list of the Demospongiae hitherto recorded from the West Indies. Am. Mus. civ., St. Nat. Genova. 86, 65-218.
    • (1986) Am. Mus. Civ., St. Nat. Genova. , vol.86 , pp. 65-218
    • Pulitzer-Finali, G.1
  • 16
    • 0027295091 scopus 로고
    • The structure of Aplysinamines I, II and III:New bromotyrosine-derived alkaloids from the Caribbean sponge Aplysina cauliformis
    • Rodriguez A. D. and Pina I. C. (1993), The structure of Aplysinamines I, II and III:new bromotyrosine-derived alkaloids from the Caribbean sponge Aplysina cauliformis. J. Nat. Prod. 56, 907-914.
    • (1993) J. Nat. Prod. , vol.56 , pp. 907-914
    • Rodriguez, A.D.1    Pina, I.C.2
  • 17
    • 0014110637 scopus 로고
    • Studies of antimicribial substances of sponges I
    • Sharma G. M. and Burkholder P. R. (1967), Studies of antimicribial substances of sponges I. J. Antibiotics A20, 200-203.
    • (1967) J. Antibiotics , vol.A20 , pp. 200-203
    • Sharma, G.M.1    Burkholder, P.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.