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N-phenethyl-2-(pyridin-2-yl)quinazolin-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

586984-06-7

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586984-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 586984-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,6,9,8 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 586984-06:
(8*5)+(7*8)+(6*6)+(5*9)+(4*8)+(3*4)+(2*0)+(1*6)=227
227 % 10 = 7
So 586984-06-7 is a valid CAS Registry Number.

586984-06-7Downstream Products

586984-06-7Relevant academic research and scientific papers

Pyridinylquinazolines selectively inhibit human methionine aminopeptidase-1 in cells

Zhang, Feiran,Bhat, Shridhar,Gabelli, Sandra B.,Chen, Xiaochun,Miller, Michelle S.,Nacev, Benjamin A.,Cheng, Yim Ling,Meyers, David J.,Tenney, Karen,Shim, Joong Sup,Crews, Phillip,Amzel, L. Mario,Ma, Dawei,Liu, Jun O.

, p. 3996 - 4016 (2013/07/19)

Methionine aminopeptidases (MetAPs), which remove the initiator methionine from nascent peptides, are essential in all organisms. While MetAP2 has been demonstrated to be a therapeutic target for inhibiting angiogenesis in mammals, MetAP1 seems to be vital for cell proliferation. Our earlier efforts identified two structural classes of human MetAP1 (HsMetAP1)-selective inhibitors (1-4), but all of them failed to inhibit cellular HsMetAP1. Using Mn(II) or Zn(II) to activate HsMetAP1, we found that 1-4 could only effectively inhibit purified HsMetAP1 in the presence of physiologically unachievable concentrations of Co(II). In an effort to seek Co(II)-independent inhibitors, a novel structural class containing a 2-(pyridin-2-yl)quinazoline core has been discovered. Many compounds in this class potently and selectively inhibited HsMetAP1 without Co(II). Subsequently, we demonstrated that 11j, an auxiliary metal-dependent inhibitor, effectively inhibited HsMetAP1 in primary cells. This is the first report that an HsMetAP1-selective inhibitor is effective against its target in cells.

INHIBITORS OF HUMAN METHIONINE AMINOPEPTIDASE 1 AND METHODS OF TREATING DISORDERS

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Page/Page column 52, (2009/06/27)

Described herein are novel pyrimidine-pyridine compounds, methods of inhibiting methionine aminopeptidase and treating disorders (or symptoms thereof) associated with methionine aminopeptidase, wherein a compound of the invention is administered to a subject.

QUINAZOLINE DERIVATIVES FOR THE TREATMENT AND PREVENTION OF DIABETES AND OBESITY

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Page/Page column 27, (2008/12/08)

The present invention relates to novel quinazoline derivatives effective in lowering blood glucose level and body weight, and a medicine for treatment and/or prevention of diabetes and/or obesity, which comprises the compound as an active ingredient.

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