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3-O-[(E)-4-(4-(tert-butyl)phenyl)-2-oxobut-3-en-1-yl]kaempferol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1338577-22-2

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1338577-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338577-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,5,7 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1338577-22:
(9*1)+(8*3)+(7*3)+(6*8)+(5*5)+(4*7)+(3*7)+(2*2)+(1*2)=182
182 % 10 = 2
So 1338577-22-2 is a valid CAS Registry Number.

1338577-22-2Downstream Products

1338577-22-2Relevant academic research and scientific papers

FLAVONE DERIVATIVES AND THEIR PREPARATIVE METHOD AND MEDICAL USE

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Paragraph 0030; 0039, (2013/09/12)

Flavone derivatives, preparative method of the derivatives and use thereof as medicaments for treating diabetes. The structure of the derivatives is presented by formula 1: In the structure, R1 and R2, which are identical or not, represent hydrogen atom, halogen, cyano, hydroxyl, trifluoromethyl, thio-methyl, benzyloxy, C1-C8 linear chain or branch chain alkyl, C1-C8 linear chain or branch chain alkoxy. The pharmacological test indicates that the flavone derivatives can significantly increase the glucose consumption of Hep-G2 cell with insulin resistance activity, promote translocation of glucose transporter 4 of skeletal muscle cells (L6GLUT4myc) at different level, and significantly increase glucose intake and utilization by cells. The test proves the fact for the first time that the flavone derivatives can significantly promote translocation of glucose transporter 4 of skeletal muscle cells, and one of the mechanisms for treating diabetes is activating the cell AMPK phosphorylation and phosphorylating the downstream ACC.

Synthesis and biological activity of novel tiliroside derivants

Qin, Nan,Li, Chun-Bao,Jin, Mei-Na,Shi, Li-Huan,Duan, Hong-Quan,Niu, Wen-Yan

, p. 5189 - 5195 (2011/11/14)

A series of new tiliroside derivatives were synthesized and characterized by analytical 1H NMR, 13C NMR and mass spectrometry. All of the compounds were evaluated for anti-diabetic properties in vitro using HepG2 cells. Compounds 3c, 3d, and 3i-l caused significant enhancements in glucose consumption by insulin-resistant HepG2 cells compared with control cells and cells that were exposed to metformin (an anti-diabetic drug). Moreover, compound 3l significantly activated adenosine 5′-monophosphate-activated protein kinase activity and reduced acetyl-CoA carboxylase activity. Thus, the tiliroside derivative 3l offers potential to be developed as a new approach for treating type II diabetes.

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