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Pyrido[2,3-d]pyrimidin-7(1H)-one, 2,4-diamino-5-methyl-6-(phenylmethyl)- is a complex organic compound with the molecular formula C14H15N5O. It is a derivative of pyrido[2,3-d]pyrimidin-7(1H)-one, characterized by the presence of two amino groups at the 2nd and 4th positions, a methyl group at the 5th position, and a phenylmethyl group at the 6th position. Pyrido[2,3-d]pyrimidin-7(1H)-one, 2,4-diamino-5-methyl-6-(phenylmethyl)- is of interest in medicinal chemistry due to its potential as a scaffold for the development of new drugs, particularly in the area of antiviral and anticancer therapies. Its structure allows for various modifications, which can lead to the synthesis of a range of bioactive molecules with different properties and activities.

4871-67-4

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4871-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4871-67-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4871-67:
(6*4)+(5*8)+(4*7)+(3*1)+(2*6)+(1*7)=114
114 % 10 = 4
So 4871-67-4 is a valid CAS Registry Number.

4871-67-4Relevant academic research and scientific papers

NAD+-dependent DNA ligase inhibitors

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Page/Page column 9; 10, (2008/06/13)

Disclosed herein are pyrido[2,3-d]pyrimidines having the structure wherein R1, and R2 are independently selected from nitro and amino; wherein R3 is selected from alkyl (C1-C10) and cycloalkyl (C3-C8); wherein R4 is selected from hydrogen, benzyl, alkyl (C1-C10), cycloalkyl (C3-C8), arylalkyl (C4-C8), and aryl (C3-C8); wherein R5 and R6 are independently selected from hydrogen, benzyl, alkyl (C1-C10), cycloalkyl (C3-C8), arylalkyl (C4-C14), and aryl (C3-C8); wherein R3 and R4 may form a ring; wherein R5 and R6 may form a ring or a heterocyclic structure; and wherein R5 and R6 are independently unsubstituted or substituted, wherein each substituent is independently selected from halogen, amino, alkyl (C1-C6), haloalkyl (C1-C6), alkoxy(C1-C6), alkylenedioxy, aryl, heteroaryl, and cycloalkyl (C3-C8). Also disclosed are methods for the preparation of compounds of Formula I and various intermediates. These compounds are useful as NAD+-dependent DNA ligase inhibitors.

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