Chemical Research Letters, May 2021. The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. Name: 2-(9-Oxoacridin-10(9H)-yl)acetic acid,38609-97-1, Name is 2-(9-Oxoacridin-10(9H)-yl)acetic acid, SMILES is O=C(O)CN(C1=C2C=CC=C1)C3=CC=CC=C3C2=O, belongs to pyrrolines compound. In a document, author is Nagao, Y, introduce the new discover.
Synthesis of a new class of cathepsin B inhibitors exploiting a unique reaction cascade
Chiral 5-substituted 3-pyrrolin-2-ones bearing L-Ile-L-Pro-OH or L-Phe-NHCH2Ph were successfully synthesized by utilizing a characteristic reaction cascade based on alkaline hydrolysis of the corresponding diethyl alpha-hydroxy-alpha-(beta-propiolamide)malonates. Among the synthesized chiral pyrrolinones, compound 5S-9 proved to be the most potent inhibitor against cathepsin B, (C) 2000 Elsevier Science Ltd. All rights reserved.
I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 38609-97-1 help many people in the next few years. Name: 2-(9-Oxoacridin-10(9H)-yl)acetic acid.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem