| Literature DB >> 34207360 |
Ahmed Elkamhawy1,2, Qili Lu1, Hossam Nada1, Jiyu Woo1, Guofeng Quan1, Kyeong Lee1.
Abstract
Discoidin domain receptor (DDR) is a collagen-activated receptor tyrosine kinase that plays critical roles in regulating essential cellular processes such as morphogenesis, differentiation, proliferation, adhesion, migration, invasion, and matrix remodeling. As a result, DDR dysregulation has been attributed to a variety of human cancer disorders, for instance, non-small-cell lung carcinoma (NSCLC), ovarian cancer, glioblastoma, and breast cancer, in addition to some inflammatory and neurodegenerative disorders. Since the target identification in the early 1990s to date, a lot of efforts have been devoted to the development of DDR inhibitors. From a medicinal chemistry perspective, we attempted to reveal the progress in the development of the most promising DDR1 and DDR2 small molecule inhibitors covering their design approaches, structure-activity relationship (SAR), biological activity, and selectivity.Entities:
Keywords: DDR1 and DDR2; cancer; discoidin domain receptor (DDR); kinase inhibitors; structure-activity relationship (SAR)
Year: 2021 PMID: 34207360 DOI: 10.3390/ijms22126535
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923