10493-06-8 Usage
Description
2'-Hydroxy-3,4,4'-trimethoxychalcone is a yellow crystalline solid that belongs to the chalcone class of organic compounds. It is found in natural sources such as plants and has been studied for its potential biological activities, including antioxidant, anti-inflammatory, and anti-cancer properties.
Used in Pharmaceutical Industry:
2'-Hydroxy-3,4,4'-trimethoxychalcone is used as a potential therapeutic agent for various diseases due to its antioxidant, anti-inflammatory, and anti-cancer properties. It has been found to exhibit cytotoxic effects on certain cancer cell lines and has shown promise as a potential agent for the treatment of diabetes.
Used in Cosmetic Industry:
2'-Hydroxy-3,4,4'-trimethoxychalcone is used as an antioxidant in cosmetics to protect the skin from oxidative stress and prevent premature aging. Its anti-inflammatory properties can also help reduce skin inflammation and redness.
Used in Food Industry:
2'-Hydroxy-3,4,4'-trimethoxychalcone can be used as a natural food additive to enhance the antioxidant properties of food products, thereby improving their shelf life and nutritional value.
Research on 2'-hydroxy-3,4,4'-trimethoxychalcone continues to explore its potential therapeutic applications and mechanisms of action, with the aim of developing new treatments for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 10493-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,9 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10493-06:
(7*1)+(6*0)+(5*4)+(4*9)+(3*3)+(2*0)+(1*6)=78
78 % 10 = 8
So 10493-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O5/c1-21-13-6-7-14(16(20)11-13)15(19)8-4-12-5-9-17(22-2)18(10-12)23-3/h4-11,20H,1-3H3/b8-4+
10493-06-8Relevant articles and documents
Structure-activity relationship and pharmacokinetic studies of 3-O-substitutedflavonols as anti-prostate cancer agents
Li, Xiang,Zhang, Changde,Guo, Shanchun,Rajaram, Pravien,Lee, Maizie,Chen, Guanglin,Fong, Ryan,Gonzalez, Aaron,Zhang, Qiang,Zheng, Shilong,Wang, Guangdi,Chen, Qiao-Hong
, p. 978 - 993 (2018)
Thirty-eight 3-O-substituted-3′,4′-dimethoxyflavonols and twenty-five 3-O-substituted-3′,4′,7-trimethoxyflavonols have been synthesized for systematic investigation on the structure-activity relationships of 3-O-substituted-3′,4′-dimethoxyflavonols in thr
Isolation and synthesis of flavonols and comparison of their antioxidant activity
Hasan, Aurangzeb,Sadiq,Abbas,Mughal,Khan, Khalid M.,Ali, Muhammad
, p. 995 - 1003 (2010)
Phytochemical investigation of the leaves of Astragalus beckari yielded four flavonol aglycones, namely kaempferol, quercetin, 5-deoxy kaempferol and fisitin. These isolated compounds were then synthesised in the laboratory using the Algar-Flyn-Oyamad reaction. Antioxidant activity of both the isolated and synthesised flavonoids was compared using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay method. The isolated flavonoids were found to be more active.
Hydroxyaurone derivative as well as preparation method and application thereof
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Paragraph 0138; 0141, (2021/07/14)
The invention relates to a hydroxyaurone derivative as well as a preparation method and application thereof. A monomeric compound aurone separated from Kunlun chrysanthemum in Xinjiang is used as a mother nucleus compound, hydroxyl is introduced into auro
NOTCH INHIBITORS FOR USE IN THE TREATMENT OF T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA
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Page/Page column 25; 27, (2018/07/29)
Compounds of formula (I) in the capacity of compounds with anti-tumor activity for the treatment of T-cell acute lymphoblastic leukemia (T-ALL).
