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 R₀
• 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)-
• 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-
• 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)-

Aflatoxicol

CAS: 29611-03-8

Aflatoxicol

Formula: C₁₇H₁₄O₆

Purezza: By hplc: 99.6% (Typical Value in Batch COA)

Colore e forma: white powder

Peso molecolare: 314.29g/mol

Ref: 54-BIA4321

Aflatoxicol

CAS: 29611-03-8

Aflatoxin (Aflatoxin R0) is a mutagenic and carcinogenic mycotoxin derived from aflatoxin B1 through metabolic processes facilitated by Rhizopus spp.

Formula: C₁₇H₁₄O₆

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 314.29

Ref: TM-T13531

Aflatoxicol

Prodotto controllato

CAS: 29611-03-8

Stability 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: C₁₇H₁₄O₆

Colore e forma: Neat

Peso molecolare: 314.29

Ref: TR-A357543

Aflatoxicol

CAS: 29611-03-8

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.

Purezza: Min. 95%

Ref: 3D-BA162706