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CAS 10048-13-2: (3aR-cis)3a,12c-diidro-8-idrossi-6-metossi-7H-furo[3',2':4,5]furo[2,3-c]xanten-7-one
Descrizione:
La sostanza chimica nota come (3aR-cis)3a,12c-diidro-8-idrossi-6-metossi-7H-furo[3',2':4,5]furo[2,3-c]xanten-7-one, con il numero CAS 10048-13-2, è un membro della famiglia delle xantone, che sono composti policiclici caratterizzati da una struttura di xantene e chetone fusa. Questo composto presenta più gruppi funzionali, tra cui un gruppo idrossile (-OH) e un gruppo metossile (-OCH3), che contribuiscono alla sua reattività chimica e potenziale attività biologica. La presenza del gruppo furo indica un sistema ad anello fuso che può influenzare la solubilità del composto e la sua interazione con obiettivi biologici. La sua stereochimica, indicata dalla designazione (3aR-cis), suggerisce disposizioni spaziali specifiche che possono influenzare le sue proprietà farmacologiche. Tali composti sono spesso studiati per le loro potenziali applicazioni in farmaceutici, coloranti e come sonde fluorescenti grazie alle loro uniche proprietà ottiche. In generale, la complessità strutturale e i gruppi funzionali presenti in questo composto lo rendono un argomento di interesse in vari campi della ricerca chimica.
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
Sinonimi:- (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
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Sterigmatocystin
CAS:SterigmatocystinFormula:C18H12O6Purezza:By hplc: 99.68% (Typical Value in Batch COA)Colore e forma: light yellow powderPeso molecolare: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:C18H12O6Purezza:98%Colore e forma:SolidPeso molecolare: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:C18H12O6Colore e forma:Light YellowPeso molecolare:324.28Ref: 4Z-S-115001
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaSterigmatocystin 50 µg/mL in Acetonitrile
CAS:Prodotto controllatoFormula:C18H12O6Colore e forma:Single SolutionPeso molecolare:324.28Sterigmatocystine
CAS:Sterigmatocystine, a G1 phase and DNA synthesis inhibitor, curbs p21 and is a mycotoxin precursor from Aspergillus versicolor.Formula:C18H12O6Purezza:98%Colore e forma:Pale-Yellow Crystals Pale Yellow SolidPeso molecolare:324.28Sterigmatocystin 13C18 25 µg/mL in Acetonitrile
CAS:Formula:C18H12O6Colore e forma:Single SolutionPeso molecolare:342.152Sterigmatocystin 50 µg/mL in Acetonitrile
CAS:Prodotto controllatoFormula:C18H12O6Colore e forma:Single SolutionPeso molecolare: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.Purezza:Min. 95%
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