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illudin S

Known as: 2',3'-dihydro-2',6'-dihydroxy-2'-(hydroxymethyl)-2',4',6'-trimethylspiro(cyclo propane-1,5'-(5H)inden)-7'(6'H)-one, lampterol 
National Institutes of Health

Papers overview

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2009
2009
Acylfulvenes (AFs) are a class of antitumor agents with favorable cytotoxic selectivity profiles compared to their natural… Expand
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Highly Cited
1997
Highly Cited
1997
6-Hydroxymethylacylfulvene (HMAF; MGI 114) is a novel semisynthetic antitumor agent derived from the sesquiterpene mushroom toxin… Expand
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1994
1994
1. The urinary excretion of a metabolite of illudin S after oral administration to rat has been studied. 2. From an ethyl acetate… Expand
1992
1992
1. Enzyme systems responsible for formation of cyclopropane ring-cleavage metabolites (M1 and M2) of illudin S in rat liver were… Expand
1990
1990
1. Illudin S, a toxic principle of the basidiomycete Lampteromyces japonicus, was incubated with rat liver 9000 g supernatant and… Expand
1973
1973
The effect of the antitumor antibiotic illudin S on bacterial macromolecular synthesis was investigated. Illudin S was found to… Expand
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Highly Cited
1965
Highly Cited
1965
Abstract An antitumour factor, lampterol, C15H20O4, has been isolated from the poisonous mushroom, Lampteromyces japonicus (KAWAM… Expand
1965
1965
Abstract The structure of lampterol, an antitumor substance isolated from Lampteromyces japonicus has been established in I. 
1963
1963
AN intensive screening of about 600 mushrooms for antitumour substances1 revealed that Lampteromyces japonicus, a bioluminescent… Expand
1963
1963