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2-(2-fluorophenoxy)-N-(3-pyridyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

406928-41-4

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406928-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406928-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,9,2 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 406928-41:
(8*4)+(7*0)+(6*6)+(5*9)+(4*2)+(3*8)+(2*4)+(1*1)=154
154 % 10 = 4
So 406928-41-4 is a valid CAS Registry Number.

406928-41-4Relevant academic research and scientific papers

Discovery of 2-phenoxyacetamides as inhibitors of the Wnt-depalmitoleating enzyme NOTUM from an X-ray fragment screen

Atkinson, Benjamin N.,Steadman, David,Zhao, Yuguang,Sipthorp, James,Vecchia, Luca,Ruza, Reinis R.,Jeganathan, Fiona,Lines, Georgie,Frew, Sarah,Monaghan, Amy,Kj?r, Svend,Bictash, Magda,Jones, E. Yvonne,Fish, Paul V.

supporting information, p. 1361 - 1369 (2019/08/21)

NOTUM is a carboxylesterase that has been shown to act by mediating the O-depalmitoleoylation of Wnt proteins resulting in suppression of Wnt signaling. Here, we describe the development of NOTUM inhibitors that restore Wnt signaling for use in in vitro disease models where NOTUM over activity is an underlying cause. A crystallographic fragment screen with NOTUM identified 2-phenoxyacetamide 3 as binding in the palmitoleate pocket with modest inhibition activity (IC50 33 μM). Optimization of hit 3 by SAR studies guided by SBDD identified indazole 38 (IC50 0.032 μM) and isoquinoline 45 (IC50 0.085 μM) as potent inhibitors of NOTUM. The binding of 45 to NOTUM was rationalized through an X-ray co-crystal structure determination which showed a flipped binding orientation compared to 3. However, it was not possible to combine NOTUM inhibition activity with metabolic stability as the majority of the compounds tested were rapidly metabolized in an NADPH-independent manner.

Synthesis of N-Azaaryl anilines: An efficient protocol via smiles rearrangement

Xia, Shuai,Wang, Li-Ying,Sun, Heng-Zhi,Yue, Huan,Wang, Xiu-Hua,Tan, Jia-Lian,Wang, Yin,Hou, Di,He, Xiao-Yan,Mun, Ki-Cheol,Kumar, B. Prem,Zuo, Hua,Shin, Dong-Soo

supporting information, p. 394 - 398 (2013/08/25)

An efficient process for the synthesis of N-azaaryl anilines via Smiles rearrangement as a tool. A variety of Nazaaryl anilines were generated by the reaction of substituted phenols, substituted anilines, aminopyridines and chloroacetyl chloride or pyrido

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