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2-(3-{3-[(2,2-diphenylethyl)({[3-(trifluoromethoxy)phenyl]methyl})amino]propoxy}phenyl)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1106977-63-2

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1106977-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1106977-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,6,9,7 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1106977-63:
(9*1)+(8*1)+(7*0)+(6*6)+(5*9)+(4*7)+(3*7)+(2*6)+(1*3)=162
162 % 10 = 2
So 1106977-63-2 is a valid CAS Registry Number.

1106977-63-2Downstream Products

1106977-63-2Relevant academic research and scientific papers

LXR AGONISTS AND USES THEREOF

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Paragraph 0529; 0530, (2017/03/28)

This invention features compounds that modulate the activity of liver X receptors, pharmaceutical compositions including the compounds of the invention, and methods of utilizing those compositions for modulating the activity of liver X receptors in the treatment of cancer.

LXR AGONISTS AND USES THEREOF

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Page/Page column 101, (2015/07/23)

This invention features compounds that modulate the activity of liver X receptors, pharmaceutical compositions including the compounds of the invention, and methods of utilizing those compositions for modulating the activity of liver X receptors in the treatment of cancer.

SYNTHETIC LIGANDS SELECTIVE FOR LXRbeta OVER LXRalpha, IDENTIFICATION AND METHODS OF USE THEREOF

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Page/Page column 9, (2009/02/11)

LXR nuclear receptor agonists have been previously shown to increase cholesterol efflux, raise plasma HDL cholesterol, stimulate cholesterol excretion, and reduce atherosclerotic lesions. However, these agonists have also been associated with the unwanted side effect of hypertriglyeridemia. This hypertriglyeridemia appears to be mediated by the LXRalpha subtype rather than LXRbeta, which suggests that LXRbeta-selective agonists are attractive candidates for modulation of human lipid metabolism. The present application provides novel LXRbeta-selective ligands that preferably modulate LXRbeta over LXRalpha. These ligands may be used to treat a variety of diseases associated with LXR, such as for example lipid metabolism disorders, atherosclerosis, Alzheimer disease, and inflammation.

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