3151-82-4 Usage
Description
5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one, commonly known as aesculetin, is a naturally occurring compound found in plants such as horse chestnut, aloe, and fig. It is a member of the coumarin class of chemical compounds, which are recognized for their antioxidant, anti-inflammatory, and anti-cancer properties. Aesculetin possesses potential therapeutic effects on various health conditions, including diabetes, inflammation, and cancer, due to its ability to reduce pain and swelling, protect cells from free radical damage, and inhibit cancer cell growth and induce apoptosis.
Uses
Used in Pharmaceutical Industry:
5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one is used as a therapeutic agent for its anti-inflammatory properties, helping to reduce pain and swelling in various conditions. Its antioxidant effects also contribute to cell protection against damage caused by free radicals.
Used in Anticancer Applications:
In the field of oncology, 5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one is utilized as an anti-cancer agent, showing potential in inhibiting the growth of cancer cells and inducing apoptosis, which could be beneficial in the treatment of various types of cancer.
Used in Nutraceutical Industry:
5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one is used as a dietary supplement for its health-promoting properties, including its potential to alleviate symptoms of diabetes and inflammation, and to support overall cellular health through its antioxidant mechanisms.
Used in Cosmetic Industry:
In cosmetics, 5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one may be employed for its anti-inflammatory and antioxidant properties, potentially beneficial in skincare products for reducing inflammation and protecting the skin from oxidative stress.
Used in Research and Development:
5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one is used as a subject of scientific research to further explore its potential health benefits and therapeutic applications, with ongoing studies aiming to understand its mechanisms of action and optimize its use in medicine and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 3151-82-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3151-82:
(6*3)+(5*1)+(4*5)+(3*1)+(2*8)+(1*2)=64
64 % 10 = 4
So 3151-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O6/c1-21-16-14(20)13-11(19)9-12(10-7-5-4-6-8-10)24-15(13)17(22-2)18(16)23-3/h4-9,20H,1-3H3
3151-82-4Relevant articles and documents
STRUCTURES OF TWO NEW FLAVONOIDS FROM Scutellaria ramosissima
Yuldashev, M.P.,Batirov, E.Kh.,Nigmatullaev, A.,Malikov, V.M.
, p. 324 - 327 (1994)
The new 2(S)-2',5-dihydroxy-7-β-D-glucopyranosyloxyflavanone has been isolated from the epigeal part of Scutellaria ramosissima M.Pop.Oroxylin A, woganin, 2',6'-trihydroxy-6,7,8-trimethoxyflavone, and vanillic and syringic acids, and also the new substance 5,6-dihydroxy-7,8-dimethoxyflavone, have been isolated from the roots of this plant for the first time.The structures of the flavonoids isolated have been established on the basis of chemical transformations and spectral characteristics.
