51135-39-8Relevant articles and documents
Umbelliferone-oxindole hybrids as novel apoptosis inducing agents
Nagarsenkar, Atulya,Guntuku, Lalita,Prajapti, Santosh Kumar,Guggilapu, Sravanthi Devi,Sonar, Rajkiran,Vegi, Ganga Modi Naidu,Babu, Bathini Nagendra
, p. 12604 - 12610 (2017/11/06)
In furtherance of our endeavour towards the synthesis of novel bioactive agents, a panel of (E)-3-((7-hydroxy-4-methyl-2-oxo-2H-chromen-8-yl)methylene)indolin-2-one derivatives were synthesized using diverse 5-substituted oxindoles and 7-hydroxy-4-methyl-
Cycloalkyl - containing 5-acylindolinones, the preparation thereof and their use as medicaments
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Page/Page column 9, (2008/06/13)
The present invention relates to cycloalkyl-containing 5-acylindolinones of general formula wherein R1 to R3 are defined as in claims 1 to 6, the tautomers, the enantiomers, the diastereomers, the mixtures thereof and the salts thereof, which have valuable pharmacological properties, particularly an inhibiting effect on protein kinases, particularly an inhibiting effect on the activity of glycogen synthase kinase (GSK-3).
Alkyl-containing 5-acylindolinones, the preparation thereof and their use as medicaments
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Page/Page column 8, (2008/06/13)
The present invention relates to alkyl-containing 5-acylindolinones of general formula wherein R1 to R3 are defined herein, the tautomers, the enantiomers, the diastereomers, the mixtures thereof and the salts thereof, which have val