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6-chloro-2-methyl-N-phenylpyrimidin-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

700810-97-5

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700810-97-5 Usage

Family

Pyrimidine

Applications

Used in the development of pharmaceuticals and agrochemicals

Potential Applications

Treatment of various diseases, including cancer and parasitic infections

Unique Structure

Valuable tool in drug discovery and development, as well as in agricultural research

Safety

Proper handling and safety precautions must be taken when working with CMPPA

Check Digit Verification of cas no

The CAS Registry Mumber 700810-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,0,8,1 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 700810-97:
(8*7)+(7*0)+(6*0)+(5*8)+(4*1)+(3*0)+(2*9)+(1*7)=125
125 % 10 = 5
So 700810-97-5 is a valid CAS Registry Number.

700810-97-5Relevant academic research and scientific papers

PHOSPHOROUS DERIVATIVES AS KINASE INHIBITORS

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Paragraph 0606, (2015/09/22)

The invention features compounds of the general formula: in which the variable groups are as defined herein, and to their preparation and use.

Synthesis and structure-activity relationship study of triazine-based inhibitors of the DNA binding of NF-κB

Fujii, Shinya,Kobayashi, Takanobu,Nakatsu, Aki,Miyazawa, Hiroshi,Kagechika, Hiroyuki

, p. 700 - 708 (2014/08/05)

Nuclear transcription factor nuclear factor-kappa B (NF-κB) has diverse pathophysiological functions, and NF-κ B inhibitors are considered to be candidates for multiple therapeutic applications. We previously reported a novel triazine-based NF-κB inhibitor, 2-anilino-4,6-dichloro-1,3,5- triazine (NI241), that directly inhibits DNA binding of NF-κB. Here, we report synthesis of a series of triazine derivatives and evaluation of their structure-activity relationships for NF-κB inhibition. We found that 2-amino-4,6-dichloro-1,3,5-triazine substructure is essential for the inhibitory activity of the lead compound NI241, and modification of NI241 by introduction of an m-methoxy substituent on the phenyl ring afforded the more potent derivative 28. The structure-activity relationships identified in this study suggested a possible mechanism of irreversible NF-κB inhibition by NI241, and should be helpful in the design of other NF-κB inhibitors.

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