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Luteoskyrin

Catalog No. T32982 CAS 21884-44-6

Synonyms: Flavomycelin

Luteoskyrin is a hepatotoxic and hepatocarcinogenic bisdihydroanthraquinone produced by Penicillium islandicum Sopp.

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Luteoskyrin, CAS 21884-44-6

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Biological Description

Chemical Properties

Storage & Solubility Information

Description

Luteoskyrin is a hepatotoxic and hepatocarcinogenic bisdihydroanthraquinone produced by Penicillium islandicum Sopp.

Synonyms	Flavomycelin
Molecular Weight	574.494
Formula	C30H22O12
CAS No.	21884-44-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

References and Literature

1. Masuda T, Ito J, Akuzawa S, Ishii K, Takagi H, Ueno Y. Hepatic accumulation and hepatotoxicity of luteoskyrin in mice. Toxicol Lett. 1992 Jun;61(1):9-20. PubMed PMID: 1609444. 2. Tseng HH, Tseng TC. Effects of naled and dichlorvos on growth and production of Luteoskyrin byPenicillium islandicum. Mycotoxin Res. 1993 Mar;9(1):35-40. doi: 10.1007/BF03192230. PubMed PMID: 23606065. 3. Ueno Y, Ishikawa I. Production of luteoskyrin, a hepatotoxic pigment, by Penicillium islandicum Sopp. Appl Microbiol. 1969 Sep;18(3):406-9. PubMed PMID: 5373676; PubMed Central PMCID: PMC377994. 4. Ueno I, Sekijima M, Hoshino M, Ohya-Nishiguchi H, Ueno Y. Spin-trapping and direct EPR investigations on the hepatotoxic and hepatocarcinogenic actions of luteoskyrin, an anthraquinoid mycotoxin produced by Penicillium islandicum Sopp. Generations of superoxide anion and luteoskyrin semiquinone radical in the redox systems consisted of luteoskyrin and liver NADPH- or NADH-dependent reductases. Free Radic Res. 1995 Jul;23(1):41-50. PubMed PMID: 7647918.

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.

Keywords

Luteoskyrin 21884-44-6 Flavomycelin inhibitor inhibit

Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.