Topopyrone C and its analogs are fungal isolates with anticancer activity in vitro.[2]
Names | |
---|---|
Preferred IUPAC name
5,9,11-Trihydroxy-2-methyl-4H-anthra[1,2-b]pyran-4,7,12-trione | |
Identifiers | |
3D model (JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
PubChem CID
|
|
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C18H10O7 | |
Molar mass | 338.271 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Notes
edit- ^ "KNApSAcK Metabolite Information - C00015651". www.knapsackfamily.com.
- ^ Ishiyama, D; Kanai, Y; Senda, H; Iwatani, W; Iwatani, W; Konno, H; Kanazawa, S (2000). "Novel human topoisomerase I inhibitors, topopyrones A, B, C and D. II. Structure elucidation". The Journal of Antibiotics. 53 (9): 873–8. doi:10.7164/antibiotics.53.873. PMID 11099219.