777935-07-6 Usage
Chemical class
2(1H)-Quinolinone belongs to the quinolone class of compounds.
Molecular weight
The molecular weight of 2(1H)-Quinolinone is 389.49 g/mol.
Structure
2(1H)-Quinolinone has a 3,4-dihydroquinoline core structure with a 1-(3-methoxypropyl) group and a 7-(phenylmethoxy) group.
Therapeutic potential
2(1H)-Quinolinone has potential therapeutic applications due to its ability to inhibit the activity of certain enzymes and proteins.
Mechanism of action
The exact mechanism of action of 2(1H)-Quinolinone is still being studied, but it is believed to involve the inhibition of certain enzymes and proteins.
Pharmacological properties
The specific pharmacological properties of 2(1H)-Quinolinone are still being researched and have not been fully elucidated.
Further research needed
Additional studies are needed to fully understand the potential uses and properties of 2(1H)-Quinolinone.
Check Digit Verification of cas no
The CAS Registry Mumber 777935-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,7,9,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 777935-07:
(8*7)+(7*7)+(6*7)+(5*9)+(4*3)+(3*5)+(2*0)+(1*7)=226
226 % 10 = 6
So 777935-07-6 is a valid CAS Registry Number.
777935-07-6Relevant articles and documents
Equipotent activity in both enantiomers of a series of ketopiperazine-based renin inhibitors
Powell, Noel A.,Clay, Emma H.,Holsworth, Daniel D.,Bryant, John W.,Ryan, Michael J.,Jalaie, Mehran,Zhang, Erli,Edmunds, Jeremy J.
, p. 2371 - 2374 (2007/10/03)
We have found that both enantiomeric configurations of the 6-alkoxymethyl-1-aryl-2-piperazinone scaffold display equipotent renin inhibition activity and similar SAR patterns. This enantiomeric flexibility is in contrast to a previously reported 3-alkoxym
