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acetic acid 4-{2-[2-(1H-indol-3-yl)-ethylcarbamoyl]-vinyl}-2-methoxy-phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1027893-20-4

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1027893-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027893-20-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,8,9 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1027893-20:
(9*1)+(8*0)+(7*2)+(6*7)+(5*8)+(4*9)+(3*3)+(2*2)+(1*0)=154
154 % 10 = 4
So 1027893-20-4 is a valid CAS Registry Number.

1027893-20-4Relevant academic research and scientific papers

Design, synthesis, and evaluation of pharmacological properties of cinnamic derivatives as antiatherogenic agents

Lapeyre, Caroline,Delomenède, Mélanie,Bedos-Belval, Florence,Duran, Hubert,Nègre-Salvayre, Anne,Baltas, Michel

, p. 8115 - 8124 (2005)

A series of cinnamic and phosphonocinnamic derivatives have been synthesized and their ability to inhibit cell-mediated LDL oxidation and oxidized LDL-induced cytotoxicity was investigated. Electron-donating substituents surrounding the necessary 4-OH gro

Induction of adiponectin by natural and synthetic phenolamides in mouse and human preadipocytes and its enhancement by docosahexaenoic acid

Yamazaki, Yoshimitsu,Kawano, Yasuhiro,Uebayasi, Masami

, p. 290 - 300 (2008/09/16)

Adiponectin, the adipose-derived cytokine, plays an important role in preventing metabolic syndromes. To develop new adiponectin inducers, eight species of ferulic esters and amides, and five related compounds were synthesized and tested on the stimulation of adiponectin production in mouse 3T3-L1 and normal human preadipocytes. The ferulamides with an aromatic ring in the N-substituent are very active in inducing adiponectin as compared with the known active compounds, curcumin, [6]-gingerol, and capsaicin, and furthermore the activities of these ferulamides are remarkably stronger than those of the corresponding esters or the straight chain octylamide. The most active compound, N-(2-phenylethyl)ferulamide (7), was found to activate the PPAR (peroxisome proliferator-activated receptor) γ-RXR (retinoid X receptor) α heterodimeric complex in the PPRE (PPAR-responsive element)-driven luciferase reporter assay. The adiponectin production by 7 is synergistically enhanced by coaddition of a PPARγ-specific agonist, pioglitazone (PGZ), or another PPARγ agonist, docosahexaenoic acid (DHA), in cultured preadipocytes. The compound 7 alone did not show a statistically significant effect on the plasma adiponectin level in KK-Ay/Ta mice, while 1% 7 in the diets significantly lowered the blood glucose and triglyceride levels and 0.3% 7 mixed with DHA oil in the diets significantly increased the adiponectin level as compared with the control. These results suggest that the present ferulamides would be useful lead compounds in developing more potent agents for treatment of metabolic syndromes through promoting the endogenous adiponectin production, and that such an activity is possibly enhanced by the coadministration with DHA.

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