CAS 120-05-8: Solfuretina
Descrizione:
Solfuretina, con il numero CAS 120-05-8, è un composto chimico che appartiene alla classe dei flavonoidi, specificamente a un tipo di flavonolo. È caratterizzato dal suo aspetto cristallino giallo ed è noto per le sue potenziali attività biologiche, comprese le proprietà antiossidanti. Solfuretina è spesso studiato per i suoi effetti su vari sistemi biologici, incluso il suo ruolo nella modulazione dei processi cellulari e le sue potenziali applicazioni terapeutiche. Il composto è solubile in solventi organici ma ha una solubilità limitata in acqua. La sua struttura presenta uno scheletro di flavonoide, comune a molti composti di origine vegetale, contribuendo alla sua reattività e interazione con molecole biologiche. La ricerca su Solfuretina ha evidenziato i suoi potenziali benefici per la salute e la malattia, in particolare in relazione ai suoi effetti anti-infiammatori e neuroprotettivi. Come molti flavonoidi, Solfuretina può anche mostrare interazioni con enzimi e recettori, rendendolo un argomento di interesse negli studi farmacologici.
Formula:C15H10O5
InChI:InChI=1S/C15H10O5/c16-9-2-3-10-13(7-9)20-14(15(10)19)6-8-1-4-11(17)12(18)5-8/h1-7,16-18H/b14-6-
InChI key:InChIKey=RGNXWPVNPFAADO-NSIKDUERSA-N
SMILES:O=C\1C=2C(O/C1=C\C3=CC(O)=C(O)C=C3)=CC(O)=CC2
Sinonimi:- (2E)-2-[(3,4-dihydroxyphenyl)methylidene]-6-hydroxy-1-benzofuran-3(2H)-one
- (2Z)-2-[(3,4-Dihydroxyphenyl)methylene]-6-hydroxy-3(2H)-benzofuranone
- (2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-6-hydroxy-1-benzofuran-3(2H)-one
- 2-(3,4-Dihydroxybenzylidene)-6-hydroxy-3(2H)-benzofuranone
- 3(2H)-Benzofuranone, 2-(3,4-dihydroxybenzylidene)-6-hydroxy-
- 3(2H)-Benzofuranone, 2-[(3,4-dihydroxyphenyl)methylene]-6-hydroxy-, (2Z)-
- 3(2H)-Benzofuranone, 2-[(3,4-dihydroxyphenyl)methylene]-6-hydroxy-, (Z)-
- 3,4,6-Trihydroxyaurone
- 3′,4′,6-Trihydroxybenzalcoumaranone
- Sulfuretin
- Sulphuretin
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6 prodotti.
Sulfuretin
CAS:Sulfuretin is a naturally occurring flavonoid compound, which is found in various plants, notably in the Heartwood of *Securinega suffruticosa* and *Rhus verniciflua*. It exerts its effects through various biological pathways, including the modulation of enzyme activities, antioxidant properties, and anti-inflammatory mechanisms. The mode of action of sulfuretin involves inhibition of pro-inflammatory mediators and protection against oxidative stress, which contributes to its therapeutic potential. It has been shown to inhibit the activity of cyclooxygenase enzymes, reduce reactive oxygen species, and modulate signaling pathways involved in inflammation. Sulfuretin has been widely studied for its potential applications in medicine and pharmacology. It is investigated for its protective effects against diseases related to inflammation and oxidative damage, such as arthritis and neurodegenerative conditions. Additionally, due to its ability to modulate cellular pathways, it shows promise in cancer research, where it could serve as a chemopreventive or therapeutic agent. Its diverse biological activities continue to make sulfuretin a subject of interest in the field of natural product research.Formula:C15H10O5Purezza:Min. 95%Colore e forma:Yellow To Orange SolidPeso molecolare:270.24 g/molSulfuretin
CAS:Sulfuretin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C15H10O5Purezza:(HPLC) ≥99%Colore e forma:PowderPeso molecolare:270.253(2H)-Benzofuranone, 2-[(3,4-dihydroxyphenyl)methylene]-6-hydroxy-, (2Z)-
CAS:Formula:C15H10O5Purezza:98%Colore e forma:SolidPeso molecolare:270.2369Sulfuretin
CAS:Sulfuretin protects HepG2 cells from oxidative damage by scavenging ROS and activating HO-1 via Nrf2/ARE and JNK/ERK pathways.Formula:C15H10O5Purezza:100% - 98.91%Colore e forma:SolidPeso molecolare:270.24
![3(2H)-Benzofuranone, 2-[(3,4-dihydroxyphenyl)methylene]-6-hydroxy-, (2Z)-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb%2FDA000Q0E.jpg&w=3840&q=75)
