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1223396-64-2

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1223396-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1223396-64-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,3,3,9 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1223396-64:
(9*1)+(8*2)+(7*2)+(6*3)+(5*3)+(4*9)+(3*6)+(2*6)+(1*4)=142
142 % 10 = 2
So 1223396-64-2 is a valid CAS Registry Number.

1223396-64-2Downstream Products

1223396-64-2Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR GLUCOSE TRANSPORT INHIBITION

-

, (2011/10/13)

Glucose deprivation is an attractive strategy in cancer research and treatment. Cancer cells upregulate glucose uptake and metabolism for maintaining accelerated growth and proliferation rates. Specifically blocking these processes is likely to provide new insights to the role of glucose transport and metabolism in tumorigenesis, as well as in apoptosis. As solid tumors outgrow the surrounding vasculature, they encounter microenvironments with a limited supply of nutrients leading to a glucose deprived environment in some regions of the tumor. Cancer cells living in the glucose deprived environment undergo changes to prevent glucose deprivation-induced apoptosis. Knowing how cancer cells evade apoptosis induction is also likely to yield valuable information and knowledge of how to overcome the resistance to apoptosis induction in cancer cells. Disclosed herein are novel anticancer compounds that inhibit basal glucose transport, resulting in tumor suppression and new methods for the study of glucose deprivation in animal cancer research.

Novel inhibitors of basal glucose transport as potential anticancer agents

Zhang, Weihe,Liu, Yi,Chen, Xiaozhuo,Bergmeier, Stephen C.

scheme or table, p. 2191 - 2194 (2010/06/15)

Cancer cells commonly show increased levels of glucose uptake and dependence. A potential strategy for the treatment of cancer may be the inhibition of basal glucose transport. We report here the synthesis of a small library of polyphenolic esters that inhibit basal glucose transport in H1299 lung and other cancer cells. These basal glucose transport inhibitors also inhibit cancer cell growth in H1299 cells, and these two activities appear to be correlated.

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