10173-01-0 Usage
Uses
Used in Pharmaceutical Development:
3,3',6-Trimethoxy-4',5,7-trihydroxyflavone is utilized as a key component in the research and development of new pharmaceutical drugs. Its anti-inflammatory and antioxidant properties make it a promising candidate for treating various inflammatory and oxidative stress-related conditions.
Used in Cancer Treatment:
In the field of oncology, 3,3',6-Trimethoxy-4',5,7-trihydroxyflavone is employed as a potential anticancer agent. Its ability to inhibit the growth of cancer cells positions it as a valuable asset in the search for novel cancer therapies.
Used in Cosmetic Products:
3,3',6-Trimethoxy-4',5,7-trihydroxyflavone is also explored for its potential use in the cosmetics industry. Its antioxidant properties may contribute to the development of products that promote skin health and protect against environmental stressors.
Used in Antioxidant Applications:
3,3',6-Trimethoxy-4',5,7-trihydroxyflavone is used as an antioxidant agent for its capacity to neutralize free radicals, thereby potentially reducing oxidative stress and associated cellular damage.
Used in Anti-Inflammatory Applications:
This flavonoid is used as an anti-inflammatory agent, leveraging its ability to reduce inflammation, which can be beneficial in managing inflammatory conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 10173-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10173-01:
(7*1)+(6*0)+(5*1)+(4*7)+(3*3)+(2*0)+(1*1)=50
50 % 10 = 0
So 10173-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O8/c1-23-11-6-8(4-5-9(11)19)16-18(25-3)15(22)13-12(26-16)7-10(20)17(24-2)14(13)21/h4-7,19-21H,1-3H3
10173-01-0Relevant academic research and scientific papers
Sepulveda-Boza, Silvia,Delhvi, Sualaheen,Cassels, Bruce K.
, p. 1301 - 1303 (1993)
The rare dihydroquercetin 3-O-β-D-xyloside, caryatin 7-O-β-D-glucoside and the previously unknown 6-methoxylated flavonoid glycoside jaceidin 5-O-β-D-glucoside were isolated from the twigs of Eucryphia glutinosa where they co-occur with the widespread reynoutrin. Key words: Eucryphia glutinosa; Eucryphiaceae; twigs; flavonoids; dihydroquercetin 3-O-β-D-xyloside; reynoutrin; jaceidin 5-O-β-D-glucoside; caryatin 7-O-β-D-glucoside.
Aritomi, Masakazu,Kawasaki, Toshio
, p. 2043 - 2048 (1984)
Droplet counter-current chromatographic separation and subsequent TLC demonstrated the existence of at least 14 phenolics in the leaves of Spinacia oleracea.Three have now been isolated and identified, respectively, as the 4'-glucuronides of 5,7,4'-trihydroxy-3,6,3'-trimethoxyflavone (jaceidin), 5,3',4'-trihydroxy-3-methoxy-6:7-methylenedioxyflavone and 5,4'-dihydroxy-3,3'-dimethoxy-6:7-methylenedioxyflavone.Key Word Index- Spinacia oleracea; Chenopodiaceae; spinach; jaceidin; 4'-glucuronide; 5,3',4'-trihydroxy-3-methoxy-6:7-methylenedioxyflavone 4'-glucuronide; 5,4'-dihydroxy-3,3'-dimethoxy-6:7-methylenedioxyflavone 4'-glucuronide; 1H NMR; 13C NMR; FABMS.
