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3-(4-hydroxyphenyl)-7-methoxy-2H-chromen-2-one, also known as apigenin 7-O-methyl ether or acacetin, is a naturally occurring flavonoid compound found in various plants, including chamomile and passionflower. This chemical is characterized by its unique structure, featuring a 2H-chromen-2-one core with a 4-hydroxyphenyl group at position 3 and a methoxy group at position 7. Apigenin 7-O-methyl ether exhibits a range of biological activities, such as antioxidant, anti-inflammatory, and anticancer properties, making it a subject of interest in pharmaceutical and nutraceutical research. Its potential health benefits and therapeutic applications are being actively explored, with ongoing studies aiming to better understand its mechanisms of action and optimize its use in various health-related contexts.

6468-37-7

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6468-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6468-37-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6468-37:
(6*6)+(5*4)+(4*6)+(3*8)+(2*3)+(1*7)=117
117 % 10 = 7
So 6468-37-7 is a valid CAS Registry Number.

6468-37-7Downstream Products

6468-37-7Relevant academic research and scientific papers

Synthesis and biological evaluation of 3-arylcoumarin derivatives as potential anti-diabetic agents

Hu, Yuheng,Wang, Bing,Yang, Jie,Liu, Teng,Sun, Jie,Wang, Xiaojing

, p. 15 - 30 (2018/10/31)

A variety of substituted 3-arylcoumarin derivatives were synthesised through microwave radiation heating. The method has characteristics of environmental friendliness, economy, simple separation, and purification process, less by-products and high reaction yield. Those 3-arylcoumarin derivatives were screened for antioxidant, α-glucosidase inhibitory and advanced glycation end-products (AGEs) formation inhibitory. Most compounds exhibited significant antioxidant and AGEs formation inhibitory activities. Anti-diabetic activity studies showed that compounds 11 and 17 were equipotent to the standard drug glibenclamide in vivo. According to the experimental results, the target compound 35 can be used as a lead compound for the development of new anti-diabetic drugs. The whole experiment showed that anti-diabetic activity is prevalent in 3-arylcoumarins, which added a new natural skeleton to the development of anti-diabetic active drugs.

Synthesis and biological evaluation of 3-arylcoumarins as potential anti-Alzheimer's disease agents

Yang, Jie,Zhang, Pingping,Hu, Yuheng,Liu, Teng,Sun, Jie,Wang, Xiaojing

, p. 651 - 656 (2019/02/19)

Alzheimer's disease, a neurodegenerative illness, has the extremely complex pathogenesis. Accumulating evidence indicates there is a close relationship between several enzymes and Alzheimer's disease. Various substituted 3-arylcoumarin derivatives were synthesised, and their in vitro activity, including cholinesterase inhibitory activity, monoamine oxidase inhibitory activity, and antioxidant activity were investigated. Most of the compounds exhibited high activity; therefore 3-arylcoumarin compounds have the potential as drug candidates for the treatment of Alzheimer's disease.

Decarboxylation of α,β-unsaturated aromatic lactones: Synthesis of: E-ortho -hydroxystilbenes from 3-arylcoumarins or isoaurones

Huang, Xihua,Liu, Jie,Sheng, Jianfei,Song, Xianheng,Du, Zhibo,Li, Mingkang,Zhang, Xuejing,Zou, Yong

supporting information, p. 804 - 808 (2018/03/06)

A simple and environmentally friendly strategy for the synthesis of E-ortho-hydroxystilbenes has been established. Two kinds of α,β-unsaturated aromatic lactones, i.e. the 3-arylcoumarins and the isoaurones, could both readily undergo a cascade hydrolyzation/decarboxylation reaction in the presence of KOH in ethylene glycol to afford the desired E-ortho-hydroxystilbenes in moderate to high yields.

Novel coumarin compound and application thereof

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Paragraph 0062; 0062; 0063; 0064, (2017/08/29)

The invention relates to the technical field of novel materials and organic chemicals, in particular to a novel compound, a process technology for chemically preparing the novel compound, application of the novel compound and a radiation curing formula pr

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