| Weight | 574.494 g/mol |
|---|---|
| Formula | C30H22O12 |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 8 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
LUTEOSKYRIN (21884-44-6)
Score:
#1827 in Biochemistry
,
#3968 in Biology
,
#4996 in Chemistry
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- Chronic toxicity and carcinogenicity in mice of the purified mycotoxins, luteoskyrin and cyclochlorotine* (Food and Cosmetics Toxicology, 1972)
- Studies on fungal metabolitesXXXI: Anthraquinonoid colouring matters of Penicillium islandicum sopp and some other fungi ()luteoskyrin, ()rubroskyrin, (+)rugulosin and their related compounds (Tetrahedron, 1973)
- Isolation of two toxic agents, luteoskyrin and chlorine-containing peptide, from the metabolites of Penicillium islandicum Sopp, with some properties thereof. (The Japanese journal of experimental medicine, 1961)
- Metabolic products of fungi. X. The structure of rubroskyrin and its relation to the structure of luteoskyrin. (Pharmaceutical bulletin, 1956)
- Inhibition of DNA synthesis and chromosome aberrations in cultured Ehrlich ascites tumor cells following treatment with luteoskyrin (Experimental Cell Research, 1969)
- Production of Luteoskyrin, a Hepatotoxic Pigment, by Penicillium islandicum Sopp (Applied and Environmental Microbiology, 1969)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC(=C2C(=C1O)C(=O)C34C5C6C(C3C(=O)C7=C(C8=C(C=C(C(=C8C(=O)C67C(C5O)C(=O)C4=C2O)O)C)O)O)O)O
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InChIKeyFAZDYVMEXQHRLI-UHFFFAOYSA-N
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