487-71-8 Usage
Description
2-Methoxy-benzene-1,3,5-triol, also known as gentisic acid, is a phenolic compound found in plants such as gentian root and fruits like strawberries. It possesses antioxidant properties, which help protect cells and tissues from damage caused by free radicals. Additionally, it has been studied for its potential anti-inflammatory and anti-cancer properties.
Used in Pharmaceutical Industry:
2-Methoxy-benzene-1,3,5-triol is used as a pharmaceutical ingredient for its antioxidant, anti-inflammatory, and anti-cancer properties. It can be incorporated into medications to help protect cells and tissues from damage and potentially treat inflammatory and cancerous conditions.
Used in Food Industry:
2-Methoxy-benzene-1,3,5-triol is used as a flavoring agent in the food industry. Its natural presence in fruits like strawberries makes it a suitable candidate for enhancing the flavor of various food products.
Used in Skincare Products:
2-Methoxy-benzene-1,3,5-triol is used as an ingredient in skincare products due to its antioxidant and anti-inflammatory properties. It can help protect the skin from damage caused by free radicals and potentially reduce inflammation and signs of aging.
Check Digit Verification of cas no
The CAS Registry Mumber 487-71-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 487-71:
(5*4)+(4*8)+(3*7)+(2*7)+(1*1)=88
88 % 10 = 8
So 487-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O4/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3,8-10H,1H3
487-71-8Relevant articles and documents
Total Synthesis of Hispidulin and the Structural Basis for Its Inhibition of Proto-oncogene Kinase Pim-1
Chao, Shi-Wei,Su, Ming-Yuan,Chiou, Lih-Chu,Chen, Liang-Chieh,Chang, Chung-I,Huang, Wei-Jan
, p. 1969 - 1976 (2015/09/08)
(Figure Presented). A new method is applied to synthesize hispidulin, a natural flavone with a broad spectrum of biological activities. Hispidulin exhibits inhibitory activity against the oncogenic protein kinase Pim-1. Crystallographic analysis of Pim-1 bound to hispidulin reveals a binding mode distinct from that of quercetin, suggesting that the binding potency of flavonoids is determined by their hydrogen-bonding interactions with the hinge region of the kinase. Overall, this work may facilitate construction of a library of hispidulin-derived compounds for investigating the structure-activity relationship of flavone-based Pim-1 inhibitors.
Synthesis of isoflavones. V. Irigenin and tectorigenin.
Baker,Downing,Floyd,Gilbert,Ollis
, p. 1219 - 1223 (2007/10/08)
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