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CAS 10048-13-2: (3aR-cis)3a,12c-dihydro-8-hydroxy-6-methoxy-7H-furo[3',2':4,5]furo[2,3-c]xanthen-7-one
Formula:C18H12O6
InChI:InChI=1S/C18H12O6/c1-21-11-7-12-13(8-5-6-22-18(8)24-12)17-15(11)16(20)14-9(19)3-2-4-10(14)23-17/h2-8,18-19H,1H3/t8-,18+/m0/s1
InChI key:InChIKey=UTSVPXMQSFGQTM-DCXZOGHSSA-N
SMILES:O(C)C=1C2=C(C3=C(O[C@@]4([C@]3(C=CO4)[H])[H])C1)OC=5C(C2=O)=C(O)C=CC5
Synonyms:- (3aR,12cS)-3a,12c-Dihydro-8-hydroxy-6-methoxy-7H-furo[3′,2′:4,5]furo[2,3-c]xanthen-7-one
- (3aR,12cS)-8-hydroxy-6-methoxy-3a,12c-dihydro-7H-furo[3',2':4,5]furo[2,3-c]xanthen-7-one
- 3a,12c-Dihydro-8-hydroxy-6-methoxy-7H-furo(3',2':4,5)furo(2,3-c)xanthen-7-one
- 7H-Furo(3',2':4,5)furo(2,3-c)xanthen-7-one, 3a,12c-dihydro-8-hydroxy-6-methoxy-
- 7H-Furo(3',2':4,5)furo(2,3-c)xanthen-7-one, 3a,12c-dihydro-8-hydroxy-6-methoxy-, (3aR,12cS)-
- 7H-Furo(3',2':4,5)furo(2,3-c)xanthen-7-one, 3a,12c-dihydro-8-hydroxy-6-methoxy-, (3aR-cis)-
- 7H-Furo[3′,2′:4,5]furo[2,3-c]xanthen-7-one, 3a,12c-dihydro-8-hydroxy-6-methoxy-
- 7H-Furo[3′,2′:4,5]furo[2,3-c]xanthen-7-one, 3a,12c-dihydro-8-hydroxy-6-methoxy-, (3aR,12cS)-
- 7H-Furo[3′,2′:4,5]furo[2,3-c]xanthen-7-one, 3a,12c-dihydro-8-hydroxy-6-methoxy-, (3aR-cis)-
- 8-hydroxy-6-methoxy-3a,12c-dihydro-7H-furo[3',2':4,5]furo[2,3-c]xanthen-7-one
- Ccris 561
- See more synonyms
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Sterigmatocystin
CAS:SterigmatocystinFormula:C18H12O6Purity:By hplc: 99.68% (Typical Value in Batch COA)Color and Shape: light yellow powderMolecular weight:324.28g/mol7H-Furo[3',2':4,5]furo[2,3-c]xanthen-7-one, 3a,12c-dihydro-8-hydroxy-6-methoxy-, (3aR,12cS)-
CAS:Formula:C18H12O6Purity:98%Color and Shape:SolidMolecular weight:324.2842799999999Sterigmatocystin
CAS:Applications Sterigmatocystin is a carcinogenic mycotoxin that is struturally related to Aflatoxin. Sterigmatocystin has been shown to inhibit RNA synthesis in rat liver nuclei.Environmental contaminants; Food contaminants Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Nel, W. et al.: Biochem. Pharmacol., 19, 957 (1970); Purchase, I.F.H. et al.: Food Cosm. Toxicol., 8, 289 (1970);Formula:C18H12O6Color and Shape:Light YellowMolecular weight:324.28Sterigmatocystin 50 µg/mL in Acetonitrile
CAS:Controlled ProductFormula:C18H12O6Color and Shape:Single SolutionMolecular weight:324.28Sterigmatocystine
CAS:Sterigmatocystine, a G1 phase and DNA synthesis inhibitor, curbs p21 and is a mycotoxin precursor from Aspergillus versicolor.Formula:C18H12O6Purity:98%Color and Shape:Pale-Yellow Crystals Pale Yellow SolidMolecular weight:324.28Sterigmatocystin 13C18 25 µg/mL in Acetonitrile
CAS:Formula:C18H12O6Color and Shape:Single SolutionMolecular weight:342.152Sterigmatocystin 50 µg/mL in Acetonitrile
CAS:Controlled ProductFormula:C18H12O6Color and Shape:Single SolutionMolecular weight:324.28Sterigmatocystin
CAS:Sterigmatocystin is a mycotoxin, which is a secondary metabolite primarily produced by certain species of the fungi Aspergillus and Bipolaris. This compound exhibits its mode of action by interfering with DNA, RNA, and protein synthesis, ultimately disrupting cellular processes. As a precursor to the well-known aflatoxins, sterigmatocystin shares a similar structure and exhibits carcinogenic properties. In scientific research, sterigmatocystin is an important tool for studying the biochemical pathways of toxin biosynthesis and the molecular mechanisms of carcinogenesis. Researchers utilize it to investigate the cellular responses to mycotoxin exposure, specifically in liver cells, due to its hepatotoxic effects. Additionally, it serves as a model compound for understanding the detoxification pathways and resistance mechanisms in various organisms. Although not as prevalent in food supplies as aflatoxins, sterigmatocystin remains a critical focus in food safety and environmental studies due to its potential health risks.Purity:Min. 95%
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