19953-58-3 Usage
Uses
Used in Pharmaceutical Industry:
2-Methyl-6-phenyl-3,7-dihydroimidazo[1,2-a]pyrazin-3-one is used as a pharmaceutical agent for its antiviral, antifungal, and anticancer properties. Its diverse biological activities make it a promising candidate for the development of novel therapeutic agents to combat various diseases.
Used in Central Nervous System Depressant Applications:
In the pharmaceutical industry, 2-Methyl-6-phenyl-3,7-dihydroimidazo[1,2-a]pyrazin-3-one is also being studied for its potential use as a central nervous system depressant. Its ability to modulate the central nervous system makes it a candidate for the treatment of conditions that require sedation or anxiety reduction.
Used in Anxiolytic Applications:
Furthermore, 2-Methyl-6-phenyl-3,7-dihydroimidazo[1,2-a]pyrazin-3-one is being explored for its potential as an anxiolytic agent. Its capacity to alleviate anxiety could be beneficial in the management of stress-related disorders and conditions.
Used in Medicinal Chemistry Research:
2-Methyl-6-phenyl-3,7-dihydroimidazo[1,2-a]pyrazin-3-one's unique structure also makes it an interesting target for medicinal chemistry research. Researchers are investigating its properties to develop new therapeutic agents that can address unmet medical needs and improve patient outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 19953-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,5 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19953-58:
(7*1)+(6*9)+(5*9)+(4*5)+(3*3)+(2*5)+(1*8)=153
153 % 10 = 3
So 19953-58-3 is a valid CAS Registry Number.
19953-58-3Relevant academic research and scientific papers
Influence of electron-donating and electron-withdrawing substituents on the Chemiluminescence behavior of Coelenterazine analogs
Saito, Ryota,Hirano, Takashi,Maki, Shojiro,Niwa, Haruki,Ohashi, Mamoru
scheme or table, p. 90 - 99 (2011/04/12)
Coelenterazine analogs 3a3e possessing various substituents at the para-position of the 6-phenyl group (R = CF3, F, H, OMe, and NMe 2) were synthesized, and the chemiluminescent properties of 3a3e in dimethyl sulfoxide (DMSO) were investigated quantitatively. Chemiluminescence maxima observed in the range of 454478nm showed a bathochromic shift as the electron-donating ability of R increased. Chemiluminescence quantum yields (φCL) were obtained in the range of 0.00060.0018. The analog 3a possessing the electron-withdrawing CF3 group showed a slight decrease in its φCL value. The fluorescence quantum yields (φF) of the light emitter, 2-acetamidopyrazine anions 4a --4e- , were observed in the range of 0.0050.21 and showed substituent dependency in that the increment in the electronwithdrawing ability of R decreases the φF value. The efficiency of generation of the singlet-excited 4a--4e- (φS) showed a small change in the range of 0.0080.015. From these quantitative analyses of the quantum efficiencies, we found that an electron-donating substituent R is not required for the efficient generation of a singlet-excited light emitter, but is required for the high φF of the emitter.
