Alkaloid and anthraquinone derivatives produced by the marine-derived endophytic fungus Eurotium rubrum

Helvetica Chimica Acta

Volumn 95, Issue 1, 2012, Pages 163-168

  Yan, Hui Jiao ^a,b   Li, Xiao Ming ^a   Li, Chun Shun ^a   Wang, Bin Gui ^a  

^a INSTITUTE OF OCEANOLOGY   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

9 Dehydroxyeurotinone; Antibacterial activity; Antifungal activity; Cytotoxic activity; Eurotechinulin B, 12 demethyl 12 oxo ; Eurotium rubrum; Hibiscus tiliaceus

Indexed keywords

9-DEHYDROXYEUROTINONE; ANTI-BACTERIAL ACTIVITY; ANTI-FUNGAL ACTIVITY; CYTOTOXIC ACTIVITY; EUROTECHINULIN B, 12-DEMETHYL-12-OXO-; EUROTIUM; HIBISCUS TILIACEUS;

AROMATIC COMPOUNDS; CYTOTOXICITY; KETONES; METABOLITES; NITROGEN COMPOUNDS; SPECTROSCOPIC ANALYSIS; TISSUE;

FUNGI;

12 DEMETHYL 12 OXO EUROTECHINULIN; 2 O METHYL 9 DEHYDROXYEUROTINONE; 7 ISOPENTENYLCRYPTOECHINULINE D; 9 DEHYDROXYEUROTINONE; ALKALOID DERIVATIVE; ALKALOID E 7; ANTHRAQUINONE DERIVATIVE; CRYPTOECHINULINE G; EMODIC ACID; EMODIN; EUROTECHINULIN B; FUNGAL EXTRACT; ISOECHINULIN B; UNCLASSIFIED DRUG; VARIECOLORIN G; VARIECOLORIN J;

ANTIMICROBIAL ACTIVITY; ARTICLE; CANCER CELL CULTURE; CARBON NUCLEAR MAGNETIC RESONANCE; CYTOTOXICITY; DRUG ISOLATION; DRUG MECHANISM; DRUG STRUCTURE; EUROTIUM; EUROTIUM RUBRUM; FUNGAL STRAIN; FUNGUS ISOLATION; HUMAN; HUMAN CELL; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 84862909126     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201100255     Document Type: Article

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