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CAS 29611-03-8: (1S,6aR,9aS)-2,3,6a,9a-Tetraidro-1-idrossi-4-metossiciclopenta[c]furo[3′,2′:4,5]furo[2,3-h][1]benzopirano-11(1H)-one
Descrizione:
La sostanza chimica nota come (1S,6aR,9aS)-2,3,6a,9a-Tetraidro-1-idrossi-4-metossiciclopenta[c]furo[3′,2′:4,5]furo[2,3-h][1]benzopirano-11(1H)-one, con il numero CAS 29611-03-8, è un composto organico complesso caratterizzato dalla sua unica struttura biciclica che incorpora sia moieties di furan che di benzopirano. Questo composto presenta più stereocentri, che contribuiscono al suo specifico assetto tridimensionale e possono influenzare la sua attività biologica. La presenza di un gruppo metossile e di un gruppo idrossile suggerisce che potrebbe mostrare varie reattività chimiche, inclusi legami idrogeno e potenziali interazioni con bersagli biologici. La sua complessità strutturale indica che potrebbe possedere interessanti proprietà farmacologiche, rendendolo un candidato per ulteriori ricerche in chimica medicinale. Inoltre, la solubilità, stabilità e reattività del composto possono essere influenzate dai suoi gruppi funzionali e dalla stereochimica, che sono critici per comprendere il suo comportamento in diversi ambienti e applicazioni.
Formula:C17H14O6
InChI:InChI=1S/C17H14O6/c1-20-10-6-11-14(8-4-5-21-17(8)22-11)15-13(10)7-2-3-9(18)12(7)16(19)23-15/h4-6,8-9,17-18H,2-3H2,1H3/t8-,9-,17+/m0/s1
InChI key:InChIKey=WYIWLDSPNDMZIT-IRWWLHRVSA-N
SMILES:O(C)C=1C2=C(C=3[C@]4([C@@](OC3C1)(OC=C4)[H])[H])OC(=O)C5=C2CC[C@@H]5O
Sinonimi:- (1R,6aS,9aS)-1-hydroxy-4-methoxy-2,3,6a,9a-tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromen-11(1H)-one
- (1S,6aR,9aS)-1-hydroxy-4-methoxy-2,3,6a,9a-tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromen-11(1H)-one
- (1S,6aR,9aS)-2,3,6a,9a-Tetrahydro-1-hydroxy-4-methoxycyclopenta[c]furo[3′,2′:4,5]furo[2,3-h][1]benzopyran-11(1H)-one
- (1S-(1alpha,6abeta,9abeta))-2,3,6a,9a-Tetrahydro-1-hydroxy-4-methoxycyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-11(1H)-one
- AFL
- Aflatoxicol
- Aflatoxicol natural epimer
- Aflatoxin R<sub>0</sub>
- Aflatoxin Ro
- Ccris 11
- Cyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-11(1H)-one, 2,3,6a,9a-tetrahydro-1-hydroxy-4-methoxy-, (1S,6aR,9aS)-
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4 prodotti.
Aflatoxicol
CAS:AflatoxicolFormula:C17H14O6Purezza:By hplc: 99.6% (Typical Value in Batch COA)Colore e forma: white powderPeso molecolare:314.29g/molAflatoxicol
CAS:Aflatoxin (Aflatoxin R0) is a mutagenic and carcinogenic mycotoxin derived from aflatoxin B1 through metabolic processes facilitated by Rhizopus spp.Formula:C17H14O6Purezza:98%Colore e forma:SolidPeso molecolare:314.29Aflatoxicol
CAS:Prodotto controllatoStability Hygroscopic Applications Aflatoxicol is a reduction metabolite of Aflatoxin B1 (A357460), which is a potent environmental mutagen and carcinogen. 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 Cifford, R., et al.: Nature, 209, 312 (1966); Wogan, et al.: Food Cosmet. Toxicol., 12, 681 (1974); Sinz, M.W., et al.: J. Toxicol. Toxin Rev., 10, 87 (1991); Breinholt, V., et al.: Chem. Res. Toxicol., 8, 506 (1995); Lee, S., et al.: J. Agric. Food Chem., 49, 5171 (2001);Formula:C17H14O6Colore e forma:NeatPeso molecolare:314.29Aflatoxicol
CAS:Aflatoxicol is a derivative of aflatoxin, which is a type of mycotoxin. It is derived from the biochemical transformation of aflatoxins, predominantly by metabolic reduction, often sourced from specific fungi such as *Aspergillus flavus* and *Aspergillus parasiticus*. The mode of action of aflatoxicol involves its interaction with cellular macromolecules, causing disruption and potentially leading to toxic effects, similar to its parent compound. It is known to cause DNA adduct formation, ultimately interfering with genetic integrity. The uses and applications of aflatoxicol are primarily found in scientific research settings, particularly in toxicology and biochemistry. It serves as a critical compound in the study of carcinogenic processes and the biotransformation pathways of aflatoxins. By investigating aflatoxicol, scientists gain insights into the mechanisms of aflatoxin toxicity and its biological consequences in living organisms. This research can be pivotal in understanding human health risks and in developing strategies to mitigate exposure in agricultural and food safety contexts.Purezza:Min. 95%