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2,4(1H,3H)-Pyrimidinedione, 6-amino-3-cyclohexyl-1-phenylis a pyrimidinedione derivative with the molecular formula C14H16N2O2. It features a cyclohexyl and phenyl substituent at the 3 and 1 position, respectively, and an amino group at the 6 position. 2,4(1H,3H)-Pyrimidinedione, 6-amino-3-cyclohexyl-1-phenylhas potential applications in pharmaceutical research and development, particularly in medicinal chemistry. Its unique structure and properties make it a promising candidate for the development of novel drugs targeting specific biological pathways or receptors.

658061-43-9

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658061-43-9 Usage

Uses

Used in Pharmaceutical Research and Development:
2,4(1H,3H)-Pyrimidinedione, 6-amino-3-cyclohexyl-1-phenylis used as a compound in pharmaceutical research and development for its potential to target specific biological pathways or receptors. Its unique structure and properties make it a candidate for the development of novel drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,4(1H,3H)-Pyrimidinedione, 6-amino-3-cyclohexyl-1-phenylis used as a compound for the synthesis of new drugs. Its structure and properties may exhibit certain biological activities that could be of interest for further investigation, making it a valuable asset in the search for new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 658061-43-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,8,0,6 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 658061-43:
(8*6)+(7*5)+(6*8)+(5*0)+(4*6)+(3*1)+(2*4)+(1*3)=169
169 % 10 = 9
So 658061-43-9 is a valid CAS Registry Number.

658061-43-9Upstream product

658061-43-9Relevant academic research and scientific papers

Structure and activity relationships of novel uracil derivatives as topical anti-inflammatory agents

Isobe, Yoshiaki,Tobe, Masanori,Inoue, Yoshifumi,Isobe, Masakazu,Tsuchiya, Masami,Hayashi, Hideya

, p. 4933 - 4940 (2007/10/03)

In order to create novel, topical anti-inflammatory compounds exhibiting more potent activities than lead compound CX-659S (1), we designed and synthesized various derivatives of 1 focusing on the uracil N(1)- and N(3)-substituents, and evaluated their an

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