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Volumn 13, Issue 9, 2001, Pages 601-605

Absolute configuration at C14 and C85 in prymnesin-2, a potent hemolytic and ichthyotoxic glycoside isolated from the red tide alga Prymnesium parvum

Author keywords

Absolute configuration; Anisotropic NMR reagent; Fluorimetric chiral HPLC; Prymnesin 2; Red tide toxin

Indexed keywords

CARBON; GLYCOSIDE; HEMOLYTIC AGENT; PRYMNESIN 2; TOXIN; UNCLASSIFIED DRUG;

EID: 0034784209     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.1184     Document Type: Article
Times cited : (13)

References (8)
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    • Igarashi T, Satake M, Yasumoto T. Prymnesin-2: a potent ichthyotoxic and hemolytic glycoside isolated from the red tide alga Prymnesium parvum. J Am Chem Soc 1996;118:479-480.
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  • 2
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    • Structures and partial stereochemical assignments for prymnesin-1 and prymnesin-2: Potent hemolytic and ichthyotoxic glycosides isolated from the red tide alga Prymnesium parvum
    • Igarashi T, Satake M, Yasumoto T. Structures and partial stereochemical assignments for prymnesin-1 and prymnesin-2: potent hemolytic and ichthyotoxic glycosides isolated from the red tide alga Prymnesium parvum. J Am Chem Soc 1999;121:8499-8511.
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  • 3
    • 0031729479 scopus 로고    scopus 로고
    • Biological activities of prymnesin-2 isolated from a red tide alga Prymnesium parvum
    • Igarashi T, Aritake S, Yasusmoto T. Biological activities of prymnesin-2 isolated from a red tide alga Prymnesium parvum. Nat Toxins 1998;6:35-41.
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  • 4
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    • Matsumori N, Nonomura T, Sasaki M, Murata M, Tachibana K, Satake M, Yasumoto T. Long-range carbon-proton coupling constants for stereochemical assignment of acyclic structures in natural products: configuration of the C5-C9 portion of matotoxin. Tetrahedron Lett 1996;37:1269-1272.
    • (1996) Tetrahedron Lett , vol.37 , pp. 1269-1272
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  • 5
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    • New chiral anisotropic reagents, NMR tools to elucidate the absolute configurations of long-chain organic compounds
    • Kusumi T, Takahashi H, Xu P, Fukushima T, Asakawa Y, Hashimoto T, Kan Y, Inouye Y. New chiral anisotropic reagents, NMR tools to elucidate the absolute configurations of long-chain organic compounds. Tetrahedron Lett 1994;35:4397-4400.
    • (1994) Tetrahedron Lett , vol.35 , pp. 4397-4400
    • Kusumi, T.1    Takahashi, H.2    Xu, P.3    Fukushima, T.4    Asakawa, Y.5    Hashimoto, T.6    Kan, Y.7    Inouye, Y.8
  • 6
    • 0031569333 scopus 로고    scopus 로고
    • A fluorometric determination method for D,L configurations of per-O-methylated monosaccharides by anomeric 2-methyl-2-β-naphthyl-1,3-benzodioxole-4-carboxylation and high-performance liquid chromatography
    • Bai C. Ohrui H, Nishida Y, Meguro H. A fluorometric determination method for D,L configurations of per-O-methylated monosaccharides by anomeric 2-methyl-2-β-naphthyl-1,3-benzodioxole-4-carboxylation and high-performance liquid chromatography. Anal Biochem 1997;246:246-252.
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    • On the use of O-methylmandelic acid for the establishment of absolute configuration of α-chiral primary amines
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.