Evolution of 3-(4-hydroxyphenyl)indoline-2-one as a scaffold for potent and selective anticancer activity.
Matthew W BoudreauPaul J HergenrotherPublished in: RSC medicinal chemistry (2022)
Development of targeted anticancer modalities has prompted a new era in cancer treatment that is notably different from the age of radical surgery and highly toxic chemotherapy. Behind each effective compound is a rich and complex history from first identification of chemical matter, detailed optimization, and mechanistic investigations, ultimately leading to exciting molecules for drug development. Herein we review the history and on-going journey of one such anticancer scaffold, the 3-(4-hydroxyphenyl)indoline-2-ones. With humble beginnings in 19th century Bavaria, we review this scaffold's synthetic history and anticancer optimization, including its recent demonstration of tumor eradication of drug-resistant, estrogen receptor-positive breast cancer. Compounds containing the 3-(4-hydroxyphenyl)indoline-2-one pharmacophore are emerging as intriguing candidates for the treatment of cancer.
Keyphrases
- drug resistant
- estrogen receptor
- positive breast cancer
- multidrug resistant
- tissue engineering
- acinetobacter baumannii
- minimally invasive
- papillary thyroid
- coronary artery bypass
- molecular dynamics
- cancer therapy
- locally advanced
- helicobacter pylori infection
- coronary artery disease
- atrial fibrillation
- bioinformatics analysis
- cystic fibrosis
- rectal cancer
- childhood cancer