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4-(3-(4-(cyclopentyl(amino)(phenyl)methyl)piperidin-1-yl)propoxy)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1560968-53-7

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1560968-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1560968-53-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,0,9,6 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1560968-53:
(9*1)+(8*5)+(7*6)+(6*0)+(5*9)+(4*6)+(3*8)+(2*5)+(1*3)=197
197 % 10 = 7
So 1560968-53-7 is a valid CAS Registry Number.

1560968-53-7Downstream Products

1560968-53-7Relevant academic research and scientific papers

High-affinity small-molecule inhibitors of the menin-mixed lineage leukemia (MLL) interaction closely mimic a natural protein-protein interaction

He, Shihan,Senter, Timothy J.,Pollock, Jonathan,Han, Changho,Upadhyay, Sunil Kumar,Purohit, Trupta,Gogliotti, Rocco D.,Lindsley, Craig W.,Cierpicki, Tomasz,Stauffer, Shaun R.,Grembecka, Jolanta

, p. 1543 - 1556 (2014/03/21)

The protein-protein interaction (PPI) between menin and mixed lineage leukemia (MLL) plays a critical role in acute leukemias, and inhibition of this interaction represents a new potential therapeutic strategy for MLL leukemias. We report development of a novel class of small-molecule inhibitors of the menin-MLL interaction, the hydroxy- and aminomethylpiperidine compounds, which originated from HTS of ~288000 small molecules. We determined menin-inhibitor co-crystal structures and found that these compounds closely mimic all key interactions of MLL with menin. Extensive crystallography studies combined with structure-based design were applied for optimization of these compounds, resulting in MIV-6R, which inhibits the menin-MLL interaction with IC50 = 56 nM. Treatment with MIV-6 demonstrated strong and selective effects in MLL leukemia cells, validating specific mechanism of action. Our studies provide novel and attractive scaffold as a new potential therapeutic approach for MLL leukemias and demonstrate an example of PPI amenable to inhibition by small molecules.

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