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3-methyl-N-(6-(4-(3-methylbutanamido)phenyl)pyridin-3-yl)butanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1597448-39-9

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1597448-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1597448-39-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,7,4,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1597448-39:
(9*1)+(8*5)+(7*9)+(6*7)+(5*4)+(4*4)+(3*8)+(2*3)+(1*9)=229
229 % 10 = 9
So 1597448-39-9 is a valid CAS Registry Number.

1597448-39-9Downstream Products

1597448-39-9Relevant academic research and scientific papers

A kind of benzene ring - aromatic ring series compound, its preparation method and medical use

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Paragraph 0125; 0131; 0133, (2017/12/05)

The invention relates to a phenyl ring-aromatic ring cascaded micro-molecular organic compound which can be used as a protein-tyrosine-phosphatase subtype inhibitor and is shown in a general formula I as described in the specification. The compound can be used as a tool compound for research on the biological functions of a variety of subtypes of a protein-tyrosine-phosphatase family in cell signal transduction, so novel means is provided for prevention and treatment of cancers, metabolism and immunological diseases, cardiovascular diseases and nervous diseases. The invention also relates to a preparation method and medicinal application of the compound.

Synthesis and biological evaluation of novel bis-aromatic amides as novel PTP1B inhibitors

Wang, Wen-Long,Huang, Chao,Gao, Li-Xin,Tang, Chun-Lan,Wang, Jun-Qing,Wu, Min-Chen,Sheng, Li,Chen, Hai-Jun,Nan, Fa-Jun,Li, Jing-Ya,Li, Jia,Feng, Bainian

supporting information, p. 1889 - 1894 (2014/04/17)

A series of bis-aromatic amides was designed, synthesized, and evaluated as a new class of inhibitors with IC50 values in the micromolar range against protein tyrosine phosphatase 1B (PTP1B). Among them, compound 15 displayed an IC50 value of 2.34 ± 0.08 μM with 5-fold preference over TCPTP. More importantly, the treatment of CHO/HIR cells with compound 15 resulted in increased phosphorylation of insulin receptor (IR), which suggested extensive cellular activity of compound 15. These results provided novel lead compounds for the design of inhibitors of PTP1B as well as other PTPs.

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