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4-nitro-N-(3-(trifluoromethyl)phenyl)-benzo[c][1,2,5]oxadiazol-5-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

413612-30-3

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413612-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 413612-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,3,6,1 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 413612-30:
(8*4)+(7*1)+(6*3)+(5*6)+(4*1)+(3*2)+(2*3)+(1*0)=103
103 % 10 = 3
So 413612-30-3 is a valid CAS Registry Number.

413612-30-3Downstream Products

413612-30-3Relevant academic research and scientific papers

INHIBITION OF HIF-2α HETERODIMERIZATION WITH HIF1β (ARNT)

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Paragraph 093; 095, (2014/06/11)

Provided is a method of inhibiting heterodimerization of HIF-2α to HIF1β (ARNT) comprising binding certain small molecules to the HIF-2α PAS-B domain cavity but not to HIF1α and inhibiting HIF-2α heterodimerization to HIF1β (ARNT) but not inhibiting HIF1α

Development of inhibitors of the PAS-B domain of the HIF-2α transcription factor

Rogers, Jamie L.,Bayeh, Liela,Scheuermann, Thomas H.,Longgood, Jamie,Key, Jason,Naidoo, Jacinth,Melito, Lisa,Shokri, Cameron,Frantz, Doug E.,Bruick, Richard K.,Gardner, Kevin H.,MacMillan, John B.,Tambar, Uttam K.

supporting information, p. 1739 - 1747 (2013/03/29)

Hypoxia inducible factors (HIFs) are heterodimeric transcription factors induced in a variety of pathophysiological settings, including cancer. We describe the first detailed structure-activity relationship study of small molecules designed to inhibit HIF-2α-ARNT heterodimerization by binding an internal cavity of the HIF-2α PAS-B domain. Through a series of biophysical characterizations of inhibitor-protein interactions (NMR and X-ray crystallography), we have established the structural requirements for artificial inhibitors of the HIF-2α-ARNT PAS-B interaction. These results may serve as a foundation for discovering therapeutic agents that function by a novel mode of action.

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