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(R)-3,4-Dihydro-8-methoxy-3,5-dimethylisocoumarin is a naturally occurring organic compound belonging to the isocoumarin family. It is characterized by a unique structure, featuring a 3,4-dihydro-isocoumarin core with a methyl group at the 3-position, another methyl group at the 5-position, and a methoxy group at the 8-position. This chiral molecule exhibits a specific (R)-configuration, which is crucial for its biological activity and potential applications. It is known for its presence in various plants and has been studied for its potential pharmacological properties, such as antioxidant and anti-inflammatory effects. The compound's structure and stereochemistry play a significant role in determining its interactions with biological targets, making it a subject of interest in the field of natural product chemistry and drug discovery.

7736-76-7

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7736-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7736-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,3 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7736-76:
(6*7)+(5*7)+(4*3)+(3*6)+(2*7)+(1*6)=127
127 % 10 = 7
So 7736-76-7 is a valid CAS Registry Number.

7736-76-7Relevant academic research and scientific papers

Isocoumarin derivative as well as preparation method and medical application thereof

-

, (2020/03/17)

The invention belongs to the technical field of chemical medicines, and relates to an isocoumarin compound of general formula (I) and a preparation method and medical application, of the isocoumarin compound in preparation of medicines for treating and mo

Discovery, synthesis, biological evaluation and molecular docking study of (R)-5-methylmellein and its analogs as selective monoamine oxidase A inhibitors

Huang, Chao,Xiong, Juan,Guan, Hui-Da,Wang, Chang-Hong,Lei, Xinsheng,Hu, Jin-Feng

, p. 2027 - 2040 (2019/04/10)

(R)-5-Methylmellein (5-MM), the major ingredient in the fermented mycelia of the medicinal fungus Xylaria nigripes (called Wuling Shen in Chinese)? was found to be a selective inhibitor against monoamine oxidase A (MAO-A) and might play an important role in the clinical usage of this edible fungus as an anti-depressive traditional Chinese medicine (TCM). Based on the discovery and hypothesis, a variety of (R)-5-MM analogs were synthesized and evaluated in vitro against two monoamine oxidase isoforms (MAO-A and MAO-B). Most synthetic analogs showed selective inhibition of MAO-A with IC50 values ranging from 0.06 to 29 μM, and compound 13aR is the most potent analog with high selectivity (IC50, MAO-A: 0.06 μM; MAO-B: >50 μM). Interestingly, the enzyme kinetics study of 13aR indicated that this ligand seemed to bind in the MAO-A active site according to so-called “tight-binding inhibition” mode. The molecular docking study of 13aR was thereafter performed in order to rationalize the obtained biological results.

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