| MeSH term | MeSH ID | Detail |
|---|---|---|
| Melanoma | D008545 | 69 associated lipids |
| Mushroom Poisoning | D009145 | 3 associated lipids |
Total
2
(-)-Illudin S
(-)-illudin s is a lipid of Prenol Lipids (PR) class.
Cross Reference
There are no associated biomedical information in the current reference collection.
Current reference collection contains 148 references associated with (-)-Illudin S in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.
Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.
Here are additional resources we collected from PubChem and MeSH for (-)-Illudin S
Possible diseases from mapped MeSH terms on references
We collected disease MeSH terms mapped to the references associated with (-)-Illudin S
NCBI Entrez Crosslinks
All references with (-)-Illudin S
Download all related citations| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Kornienko A et al. | Toward a Cancer Drug of Fungal Origin. | 2015 | Med Res Rev | pmid:25850821 |
| Glatt H et al. | Sulfotransferase-independent genotoxicity of illudin S and its acylfulvene derivatives in bacterial and mammalian cells. | 2014 | Arch. Toxicol. | pmid:23881331 |
| Pietsch KE et al. | Quantification of acylfulvene- and illudin S-DNA adducts in cells with variable bioactivation capacities. | 2013 | Chem. Res. Toxicol. | pmid:23227857 |
| Kasahara Y | [Clinical toxicology of mushroom poisoning. Omphalotus guepiniformis]. | 2013 | Chudoku Kenkyu | pmid:24224384 |
| Wawrzyn GT et al. | Draft genome of Omphalotus olearius provides a predictive framework for sesquiterpenoid natural product biosynthesis in Basidiomycota. | 2012 | Chem. Biol. | pmid:22726691 |
| Liu X et al. | Susceptibility of the antioxidant selenoenyzmes thioredoxin reductase and glutathione peroxidase to alkylation-mediated inhibition by anticancer acylfulvenes. | 2011 | Chem. Res. Toxicol. | pmid:21443269 |
| Pietsch KE et al. | Chemical and enzymatic reductive activation of acylfulvene to isomeric cytotoxic reactive intermediates. | 2011 | Chem. Res. Toxicol. | pmid:21939268 |
| Kasahara Y and Itou T | [Determination of illudin S in Omphalotus guepiniformis and foods that caused food poisoning by liquid chromatography with tandem mass spectrometry]. | 2009 | Shokuhin Eiseigaku Zasshi | pmid:19745584 |
| Liu X and Sturla SJ | Profiling patterns of glutathione reductase inhibition by the natural product illudin S and its acylfulvene analogues. | 2009 | Mol Biosyst | pmid:19668867 |
| Dick RA et al. | NADPH alkenal/one oxidoreductase activity determines sensitivity of cancer cells to the chemotherapeutic alkylating agent irofulven. | 2004 | Clin. Cancer Res. | pmid:14977853 |