Bioxanthracenes from the insect pathogenic fungus Cordyceps pseudomilitaris BCC 1620: II. Structure elucidation

Journal of Antibiotics

Volumn 54, Issue 1, 2001, Pages 36-43

  Isaka, M ^a   Kongsaeree, P ^a   Thebtarannonth, Y ^a  

^a NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

ANTHRACENE DERIVATIVE; BIOXANTHRACENE DERIVATIVE; DIMER; MONOMER; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL PROCEDURES; CORDYCEPS PSEUDOMILITARIS; DRUG ISOLATION; DRUG STRUCTURE; FUNGUS; INSECT; NONHUMAN; PRIORITY JOURNAL; SPECTROSCOPY; STEREOCHEMISTRY; STRUCTURE ANALYSIS; X RAY CRYSTALLOGRAPHY;

CORDYCEPS PSEUDOMILITARIS;

EID: 0035130358     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.54.36     Document Type: Article

References (7)

1. Bioxanthracenes from the insect pathogenic fungus Cordyceps pseudomilitaris BCC 1620. I. Taxonomy, fermentation, isolation and antimalarial activity
2. ES-242-1, a novel compound from Verticillium sp., binds to a site on N-methyl-D-aspartate receptor that is coupled to the channel domain
3. ES-242-2, -3, -4, -5, -6, -7, and -8, novel bioxanthracenes produced by Verticillium sp., which act on the N-methyl-D-aspartate receptor
4. The first total synthesis of a bioxanthracene (-)-ES-242-4, an N-methyl-D-aspartate receptor antagonist
5. Synthesis of an N-methyl-D-aspartate receptor antagonist, ES-242-5, and its analogs
6. Absolute and atropisomeric structure of ES-242s, N-methyl-D-aspartaste receptor antagonists
7. Synthesis and biological evaluation of the analogs of bioxanthracenes ES-242s, N-methyl-D-aspartate antagonists