Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,098,323 papers from all fields of science
Search
Sign In
Create Free Account
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
Create Alert
Alert
Related topics
Related topics
2 relations
Broader (2)
Antibiotics, Antineoplastic
Sesquiterpenes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Development of a method for determining illudin S in food by gas chromatography-mass spectrometry
Mieko Kanamori-Kataoka
,
Y. Seto
,
M. Kuramoto
2006
Corpus ID: 55233412
A method was developed for determining illudin S, a naturally occurring toxin in the mushroom Lampteromyces japonicus in food…
Expand
2004
2004
Activity of irofulven against human pancreatic carcinoma cell lines in vitro and in vivo.
E. V. Van Laar
,
Stephanie Roth
,
S. Weitman
,
J. Macdonald
,
S. Waters
Anticancer Research
2004
Corpus ID: 10353743
BACKGROUND Irofulven (MGI 114), a novel antitumor agent synthesized from the natural product illudin S, has a unique mechanism of…
Expand
2002
2002
Enhanced antitumor activity of irofulven in combination with thiotepa or mitomycin C
M. Kelner
,
T. Mcmorris
,
Rafael J. Rojas
,
N. Trani
,
L. Estes
Cancer Chemotherapy and Pharmacology
2002
Corpus ID: 2398491
Abstract.Purpose: Irofulven (6-hydroxymethylacylfulvene, MGI 114, NSC 683863) is a semisynthetic derivative of illudin S, a toxin…
Expand
Highly Cited
1997
Highly Cited
1997
Preclinical antitumor activity of 6-hydroxymethylacylfulvene, a semisynthetic derivative of the mushroom toxin illudin S.
J. Macdonald
,
C. Muscoplat
,
+5 authors
D. V. Von Hoff
Cancer Research
1997
Corpus ID: 1688867
6-Hydroxymethylacylfulvene (HMAF; MGI 114) is a novel semisynthetic antitumor agent derived from the sesquiterpene mushroom toxin…
Expand
1990
1990
Metabolism of illudin S, a toxic principle of Lampteromyces japonicus, by rat liver. I. Isolation and identification of cyclopropane ring-cleavage metabolites.
Koji Kariya-city Aichi-pref. Tanaka
,
T. Inoue
,
S. Kadota
,
T. Kikuchi
Xenobiotica; the fate of foreign compounds in…
1990
Corpus ID: 35892765
1. Illudin S, a toxic principle of the basidiomycete Lampteromyces japonicus, was incubated with rat liver 9000 g supernatant and…
Expand
1986
1986
[Forensic toxicological studies on Lampteromyces poisoning. Identification of illudin S (lampterol)].
M. Kawano
Igaku kenkyu. Acta medica
1986
Corpus ID: 21107118
1979
1979
Enhancement of the antitumor effect of illudin S by including it into liposomes
S. Shinozawa
,
K. Tsutsui
,
T. Oda
Experientia
1979
Corpus ID: 46097744
Entrapping illudin S in liposome markedly enhanced life prolonging effect in ddN mice bearing Ehrlich ascites tumors, presumably…
Expand
1973
1973
Mode of Action of Illudin S
J. Walser
,
P. Heinstein
Antimicrobial Agents and Chemotherapy
1973
Corpus ID: 14025736
The effect of the antitumor antibiotic illudin S on bacterial macromolecular synthesis was investigated. Illudin S was found to…
Expand
1964
1964
STEREOCHEMISTRY OF ILLUDIN-S (LAMPTEROL).
K. Nakanishi
,
M. Tada
,
Y. Yamada
Chemical and pharmaceutical bulletin
1964
Corpus ID: 37479858
1963
1963
[Isolation of lampterol from Lampteromvces japonicus (Kawam) Sing].
K. Nakanishi
,
M. Ohashi
,
N. Suzuki
,
M. Tada
,
Y. Yamada
,
S. Inagaki
Yakugaku zasshi : Journal of the Pharmaceutical…
1963
Corpus ID: 45018362
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE