| MeSH term | MeSH ID | Detail |
|---|---|---|
| Melanoma | D008545 | 69 associated lipids |
Total
1
(-)-Illudin M
(-)-illudin m 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 74 references associated with (-)-Illudin M 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 M
Possible diseases from mapped MeSH terms on references
We collected disease MeSH terms mapped to the references associated with (-)-Illudin M
NCBI Entrez Crosslinks
All references with (-)-Illudin M
Download all related citations| Authors | Title | Published | Journal | PubMed Link |
|---|---|---|---|---|
| Babu V and Schumacher B | A C. elegans homolog for the UV-hypersensitivity syndrome disease gene UVSSA. | 2016 | DNA Repair (Amst.) | pmid:27043179 |
| Babu V et al. | A C. elegans homolog of the Cockayne syndrome complementation group A gene. | 2014 | DNA Repair (Amst.) | pmid:25453470 |
| 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 |
| Schobert R et al. | Cancer selective metallocenedicarboxylates of the fungal cytotoxin illudin M. | 2011 | J. Med. Chem. | pmid:21848340 |
| Knauer S et al. | Melanoma-specific ferrocene esters of the fungal cytotoxin illudin M. | 2009 | Anticancer Drugs | pmid:19606019 |
| Schobert R et al. | Conjugates of the fungal cytotoxin illudin M with improved tumour specificity. | 2008 | Bioorg. Med. Chem. | pmid:18715789 |
| Bose G et al. | Synthesis, reactions and structure-activity relationships of 1-hydroxyspiro[2.5]cyclooct-4-en-3-ones: illudin analogs with in vitro cytotoxic activity. | 2006 | Bioorg. Med. Chem. | pmid:16616502 |
| 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 |
| Pirrung MC and Liu H | Modular, parallel synthesis of an illudinoid combinatorial library. | 2003 | Org. Lett. | pmid:12762702 |
| Pirrung MC and Kaliappan KP | Dipolar cycloaddition of rhodium-generated carbonyl ylides with p-quinones. | 2000 | Org. Lett. | pmid:10814321 |