87219-22-5 Usage
General Description
"(2-OXO-IMIDAZOLIDIN-1-YL)-ACETIC ACID" is a chemical compound with the molecular formula C6H9N2O3. It belongs to the class of imidazolidines, which are organic compounds containing a five-membered ring with three carbon atoms, one nitrogen atom, and one oxygen atom. The compound is a derivative of imidazolidine-2,4-dione and acetic acid, and it is commonly used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical compounds. Its structure and properties make it a versatile and important component in the synthesis of biologically active molecules. Additionally, it has potential applications in organic synthesis and medicinal chemistry due to its ability to participate in a variety of chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 87219-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,1 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87219-22:
(7*8)+(6*7)+(5*2)+(4*1)+(3*9)+(2*2)+(1*2)=145
145 % 10 = 5
So 87219-22-5 is a valid CAS Registry Number.
87219-22-5Relevant articles and documents
PARG INHIBITORY COMPOUNDS
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Paragraph 00356; 00357; 00358; 00359, (2016/07/05)
The present invention relates to compounds of formula I that function as inhibitors of PARG (Poly ADP-ribose glycohydrolase) enzyme activity: wherein R1a, R1b, R1c, R1d, R1e, W, X1, X2, X3, X4, X5, X6, X7, c are each as defined herein. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of proliferative disorders, such as cancer, as well as other diseases or conditions in which PARG activity is implicated.
CHEMOKINE RECEPTOR BINDING COMPOUNDS
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Page/Page column 87-88, (2008/06/13)
The present invention relates to chemokine receptor binding compounds, pharmaceutical compositions and their use. More specifically, the present invention relates to modulators of chemokine receptor activity, preferably modulators of CCR5. Thesd compounds demonstrate protective effects against infection of target cells by a human immunodeficiency virus (HIV).