Stephacidin B - A new stage of complexity within prenylated indole alkaloids from fungi

Angewandte Chemie - International Edition

Volumn 42, Issue 27, 2003, Pages 3068-3071

  Von Nussbaum, Franz ^a  

^a BAYER AG   (Germany)

Author keywords

Alkaloids; Amino acids; Biosynthesis; Natural products; Structure elucidation

Indexed keywords

ALKALI METAL COMPOUNDS; BIOSYNTHESIS; DIMERIZATION; MOLECULAR STRUCTURE;

PSEUDOSYMMETRIC STRUCTURE;

FUNGI;

ANTIBIOTIC AGENT; ASPERGAMIDE B; AVRAINVILLAMIDE; CJ 17665; DOPA; INDOLE ALKALOID; ISOQUINOLINE DERIVATIVE; NATURAL PRODUCT; NITRONE; STEPHACIDIN A; STEPHACIDIN B; TRYPTOPHAN; TYROSINE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ANTINEOPLASTIC ACTIVITY; ASPERGILLUS OCHRACEUS; COMBINATORIAL CHEMISTRY; CYTOTOXICITY; DRUG ISOLATION; DRUG SYNTHESIS; FERMENTATION; FUNGUS; HUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REVIEW; STEREOCHEMISTRY;

ALKALOIDS; ANIMALS; DIMERIZATION; FUNGI; INDOLES; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PROTEIN ISOPRENYLATION;

EID: 0042812136     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200301646     Document Type: Review

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