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1-(4-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl}piperazin-1-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1206594-13-9

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1206594-13-9 Usage

Chemical structure

Contains a piperazine ring and a boron-containing group.

Usage

Used as a building block in organic synthesis and pharmaceutical research.

Applications

Potential applications in medicinal chemistry, development of new drugs, and biologically active molecules.

Unique structure

Its unique structure and reactivity make it a valuable tool for the synthesis of complex organic molecules.

Boron-containing group

The boron-containing group in the compound confers specific properties that can be exploited in biological and chemical applications.

Versatility

A versatile and useful chemical compound.

Fields of application

Potential applications in various fields of science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 1206594-13-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,5,9 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1206594-13:
(9*1)+(8*2)+(7*0)+(6*6)+(5*5)+(4*9)+(3*4)+(2*1)+(1*3)=139
139 % 10 = 9
So 1206594-13-9 is a valid CAS Registry Number.

1206594-13-9Relevant academic research and scientific papers

Structure-based design, synthesis, and evaluation of inhibitors with high selectivity for PARP-1 over PARP-2

Yu, Jiang,Luo, Lingling,Hu, Tong,Cui, Yating,Sun, Xiao,Gou, Wenfeng,Hou, Wenbin,Li, Yiliang,Sun, Tiemin

, (2021/10/20)

The poly (ADP-ribose) polymerase (PARP) inhibitors play a crucial role in cancer therapy. However, most approved PARP inhibitors have lower selectivity to PARP-1 than to PARP-2, so they will inevitably have side effects. Based on the different catalytic domains of PARP-1 and PARP-2, we developed a strategy to design and synthesize highly selective PARP-1 inhibitors. Compounds Y17, Y29, Y31 and Y49 showed excellent PARP-1 inhibition, and their IC50 values were 0.61, 0.66, 0.41 and 0.96 nM, respectively. Then, Y49 (PARP-1 IC50 = 0.96 nM, PARP-2 IC50 = 61.90 nM, selectivity PARP-2/PARP-1 = 64.5) was proved to be the most selective inhibitor of PARP-1. Compounds Y29 and Y49 showed stronger inhibitory effect on proliferation in BRCA1 mutant MX-1 cells than in other cancer cells. In the MDA-MB-436 xenotransplantation model, Y49 was well tolerated and showed remarkable single dose activity. The design strategy proposed in this paper is of far-reaching significance for the further construction of the next generation of selective PARP-1 inhibitors.

BICYCLIC HETEROARYL KINASE INHIBITORS AND METHODS OF USE

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Page/Page column 113-114, (2011/12/14)

Provided are compounds having an inhibitory effect on kinases including Mixed Lineage Kinases. Also provided are pharmaceutical compositions, methods of preparing the compounds, synthetic intermediates, and methods of using the compounds, independently or in combination with other therapeutic agents, for treating diseases and conditions that are affected by Mixed Lineage Kinase inhibition. Also provided are methods of treatment of neuropsychiatric disorders that comprise the inhibition of Mixed Lineage Kinases.

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