CAS 2009-24-7: Xantotossolo
Descrizione:
Xantotossolo, con il numero CAS 2009-24-7, è un composto che si verifica naturalmente classificato come un furanocumarina. È principalmente derivato da piante della famiglia Apiaceae, in particolare da specie come *Pastinaca sativa* (pastinaca selvatica) e specie di *Angelica*. Xantotossolo è caratterizzato dalla sua struttura complessa, che include un anello di furanò fuso a un moiety di cumarina. Questo composto presenta una gamma di attività biologiche, comprese potenziali proprietà antimicrobiche e anti-infiammatorie. È anche noto per i suoi effetti fototossici, che possono portare a reazioni cutanee all'esposizione alla luce solare. In termini di solubilità, Xantotossolo è generalmente solubile in solventi organici, ma ha una solubilità limitata in acqua. Le sue applicazioni si estendono alla medicina tradizionale e alla ricerca, dove viene studiato per il suo potenziale farmacologico. Tuttavia, si consiglia cautela a causa della sua fototossicità e dei possibili effetti avversi in individui sensibili. In generale, Xantotossolo rappresenta un argomento interessante di studio nel campo dei prodotti naturali e della chimica medicinale.
Formula:C11H6O4
InChI:InChI=1S/C11H6O4/c12-8-2-1-6-5-7-3-4-14-10(7)9(13)11(6)15-8/h1-5,13H
InChI key:InChIKey=JWVYQQGERKEAHW-UHFFFAOYSA-N
SMILES:OC=1C2=C(C=C3C1OC=C3)C=CC(=O)O2
Sinonimi:- 2-Propenoic acid, 3-(6,7-dihydroxy-5-benzofuranyl)-, δ-lactone
- 5-Benzofuranacrylic acid, 6,7-dihydroxy-, gamma-lactone (7CI)
- 5-Benzofuranacrylic acid, 6,7-dihydroxy-, δ-lactone
- 6,7-Dihydroxy-5-benzofuranacrylic acid gamma-lactone
- 7H-Furo(3,2-g)(1)benzopyran-7-one, 9-hydroxy-
- 8-Hydroxypsoralen
- 8-Hydroxypsoralene
- 9-hydroxy-7H-furo[3,2-g]chromen-7-one
- Brn 0189491
- Nsc 401269
- Psoralen, 8-hydroxy-
- Vedi altri sinonimi
Ordinare per
12 prodotti.
7H-Furo[3,2-g][1]benzopyran-7-one, 9-hydroxy-
CAS:Formula:C11H6O4Purezza:96%Colore e forma:SolidPeso molecolare:202.1629Xanthotoxol
CAS:Prodotto controllatoApplications A hydroxylated psoralen that inhibits neutrophil infiltration and brain edema induced by focal cerebral ischemia-reperfusion injury in rats. A potentially useful antiarrhythmic agent. It has been shown to be effective in the prevention of ventricular fibrillation of mice induced by chloroform, of rats induced by calcium chloride, and in treatment of rat arrhythmia induced by aconitine. Recent studies show that it may also have antioxidant and anticancer activities. References Lian, Q. et al.: Zhongcaoyao, 27, 347 (1996); He, W. et al.: Zhong. Yao. Tong., 25, 668 (2009); Prasad, K.N. et al.: Food Chem., 118, 62 (2009);Formula:C11H6O4Colore e forma:NeatPeso molecolare:202.16Xanthotoxol
CAS:Formula:C11H6O4Purezza:≥ 94.0%Colore e forma:Light beige to dark brown solidPeso molecolare:202.16Xanthotoxol
CAS:Xanthotoxol analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C11H6O4Purezza:(HPLC) ≥90%Colore e forma:PowderPeso molecolare:202.17Xanthotoxol
CAS:LactoneFormula:C11H6O4Purezza:≥ 95.0 % (HPLC)Colore e forma:PowderPeso molecolare:202.17Xanthotoxol
CAS:Xanthotoxol (Psoralen) is a bioactive furocoumarin with anti-inflammatory, antioxidant, 5-HT antagonist, and neuroprotective properties.Formula:C11H6O4Purezza:99.97%Colore e forma:SolidPeso molecolare:202.169-Hydroxy-7H-Furo[3,2-G]Chromen-7-One
CAS:9-Hydroxy-7H-Furo[3,2-G]Chromen-7-OnePeso molecolare:202.16g/molXanthotoxol
CAS:Xanthotoxol is a naturally occurring furanocoumarin, which is derived from various plant species, primarily within the Apiaceae family. This compound exhibits its biological activity through several mechanisms, including the inhibition of enzyme pathways, modulation of signaling pathways, and interaction with cellular proteins, impacting various physiological processes. Xanthotoxol is used predominantly in scientific research, exploring its potential therapeutic applications. It has been studied for its anti-inflammatory, antioxidant, and anticancer properties. In inflammation studies, Xanthotoxol has demonstrated an ability to suppress pro-inflammatory cytokines and inhibit pathways like NF-κB. As an antioxidant, it scavenges free radicals, thereby protecting cells from oxidative stress. Additionally, its anticancer effects have been observed in various cell line studies, where it induces apoptosis and inhibits cell proliferation. These properties make Xanthotoxol a compound of interest for further pharmacological research and potential drug development.Formula:C11H6O4Purezza:Min. 95%Colore e forma:Brown PowderPeso molecolare:202.16 g/mol
![7H-FURO[3,2-G][1]BENZOPYRAN-7-ONE,9-HYDROXY-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb%2FF513625.jpg&w=3840&q=75)
![7H-Furo[3,2-g][1]benzopyran-7-one, 9-hydroxy-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb%2FDA002D2L.jpg&w=3840&q=75)
![7H-Furo[3,2-g][1]benzopyran-7-one, 9-hydroxy-](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F10%2Fthumb%2FF862163.jpg&w=3840&q=75)
![9-Hydroxy-7H-Furo[3,2-G]Chromen-7-One](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F54%2Fthumb%2FOR1024999.jpg&w=3840&q=75)
