31524-62-6 Usage
Description
Isobavachin is a naturally occurring compound that belongs to the flavonoid family. It is derived from various plant sources and has been found to exhibit a range of biological activities, making it a promising candidate for pharmaceutical and industrial applications.
Uses
Used in Pharmaceutical Industry:
Isobavachin is used as a bioactive compound for its ant-idiabetic activity. It has shown remarkable in vitro activity, making it a potential candidate for the development of new drugs to treat diabetes.
Used in Chemical Industry:
Isobavachin is used as a parent compound for the synthesis of other flavonoid derivatives, such as I315240. These derivatives can be further explored for their potential applications in various fields, including pharmaceuticals, cosmetics, and agriculture.
Used in Cosmetics Industry:
Isobavachin can be used as an active ingredient in the development of skincare products due to its potential antioxidant and anti-inflammatory properties. These properties may contribute to the improvement of skin health and the treatment of various skin conditions.
Used in Agricultural Industry:
Isobavachin can be utilized as a natural pesticide or fungicide due to its bioactive properties. It may help in the development of eco-friendly and sustainable solutions for pest and disease control in agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 31524-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,2 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31524-62:
(7*3)+(6*1)+(5*5)+(4*2)+(3*4)+(2*6)+(1*2)=86
86 % 10 = 6
So 31524-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H20O4/c1-12(2)3-8-15-17(22)10-9-16-18(23)11-19(24-20(15)16)13-4-6-14(21)7-5-13/h3-7,9-10,19,21-22H,8,11H2,1-2H3/t19-/m0/s1
31524-62-6Relevant articles and documents
Regio- and stereospecific prenylation of flavonoids by Sophora flavescens prenyltransferase
Chen, Ridao,Liu, Xiao,Zou, Jianhua,Yin, Yunze,Ou, Bin,Li, Jianhua,Wang, Ruishan,Xie, Dan,Zhang, Peicheng,Dai, Jungui
, p. 1817 - 1828 (2013/07/19)
Prenylflavonoids are valuable natural products that are widely distributed in plants. They often possess divergent biological properties, including phytoestrogenic, anti-bacterial, anti-tumor, and anti-diabetic activities. The reaction catalyzed by prenyltransferases represents a Friedel-Crafts alkylation of the flavonoid skeleton in the biosynthesis of natural prenylflavonoids and often contributes to the structural diversity and biological activity of these compounds. However, only a few plant flavonoid prenyltransferases have been identified thus far, and these prenyltransferases exhibit strict substrate specificity and low catalytic efficiency. In this article, a flavonoid prenyltransferase from Sophora flavescens, SfFPT, has been identified that displays high catalytic efficiency with high regiospecificity acting on C-8 of structurally different types of flavonoid (i.e., flavanone, flavone, flavanonol, and dihydrochalcone, etc.). Furthermore, SfPFT exhibits strict stereospecificity for levorotatory flavanones to produce (2S)-prenylflavanones. This study is the first to demonstrate the substrate promiscuity and stereospecificity of a plant flavonoid prenyltransferase in vitro. Given its substrate promiscuity and high catalytic efficiency, SfFPT can be used as an environmentally friendly and efficient biological catalyst for the regio- and stereospecific prenylation of flavonoids to produce bioactive compounds for potential therapeutic applications. Copyright
