106732-52-9 Usage
Uses
Used in Pharmaceutical Development:
3-(N-prolylamine)-2-oxo-1-pyrrolidineacetamide is used as a precursor in the synthesis of pharmaceutical compounds for [application reason]. Its role in neurotransmitter release and antinociceptive effects make it a promising candidate for the development of drugs targeting neurological and pain-related conditions.
Used in Peptide Synthesis:
In the field of organic chemistry, 3-(N-prolylamine)-2-oxo-1-pyrrolidineacetamide is used as a building block for peptide synthesis, contributing to the creation of complex peptide structures with specific biological functions.
Used in Research and Development:
3-(N-prolylamine)-2-oxo-1-pyrrolidineacetamide is utilized as a research compound in the study of its biological activity and pharmacological properties, aiding in the advancement of medical knowledge and the discovery of new therapeutic agents.
Used in Organic Chemistry:
As a key component in the formation of certain natural products, 3-(N-prolylamine)-2-oxo-1-pyrrolidineacetamide is used in organic chemistry to explore its role in the synthesis of bioactive natural compounds and to understand the underlying mechanisms of their formation.
Check Digit Verification of cas no
The CAS Registry Mumber 106732-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,3 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106732-52:
(8*1)+(7*0)+(6*6)+(5*7)+(4*3)+(3*2)+(2*5)+(1*2)=109
109 % 10 = 9
So 106732-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N4O3/c12-9(16)6-15-5-3-8(11(15)18)14-10(17)7-2-1-4-13-7/h7-8,13H,1-6H2,(H2,12,16)(H,14,17)/t7-,8-/m0/s1
106732-52-9Relevant academic research and scientific papers
Dopamine Receptor Modulation by Conformationally Constrained Analogues of Pro-Leu-Gly-NH2
Yu, Kuo-Long,Rajakumar, G.,Srivastava, Lalit K.,Mishra, Ram K.,Johnson, Rodney L.
, p. 1430 - 1436 (2007/10/02)
Two series of conformationally constrained analogues of Pro-Leu-Gly-NH2 (PLG) have been synthesized.In one series of analogues, the Leu-Gly-NH2 dipeptide segment of PLG was replaced with the γ-lactam residues 3(S)- and 3(R)-amino-2-oxopyrrolidineacetamide
