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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

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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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1996
1996
1 Rats were dosed orally with illudin S, a toxic substance derived from the poisonous mushroom Lampteromyces japonicus. The… 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
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1992
1992
1. Enzyme systems responsible for formation of cyclopropane ring-cleavage metabolites (M1 and M2) of illudin S in rat liver were… Expand
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1990
1990
1. Illudin S, a toxic principle of the basidiomycete Lampteromyces japonicus, was incubated with rat liver 9000 g supernatant and… Expand
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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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1965
1965
An antitumour factor, lampterol, C15H20O4, has been isolated from the poisonous mushroom, Lampteromyces japonicus (KAWAM.) Sing… Expand
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1965
1965
Abstract The structure of lampterol, an antitumor substance isolated from Lampteromyces japonicus has been established in I. 
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1963
1963
AN intensive screening of about 600 mushrooms for antitumour substances1 revealed that Lampteromyces japonicus, a bioluminescent… Expand
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