Study of PARP inhibitors for breast cancer based on enhanced multiple kernel function SVR with PSO

PARP1 is one of six enzymes required for the highly error-prone DNA repair pathway microhomology-mediated end joining (MMEJ) and needs to be inhibited when over-expressed. In order to study the PARP1 inhibitory effect of fused tetracyclic or pentacyclic dihydrodiazepinoindolone derivatives (FTPDDs)...

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Bibliographic Details
Main Authors: Haohan Xue, Ruixuan Zhang, Xudong Yan, Ruihan Wang, Peijian Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-02-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2024.1257253/full