This work identified dual PARP/GPX4 inhibitors via a structure-based hybridization strategy and explored the dual-target antitumor effect in blocking the progression of TNBC, finding that compound 12 exhibited potent biochemical inhibitory activities against both PARP and GPX4.
Zi-An Wang, Rong-Ke Li, Jia-Dai Liu et al.· Journal of Medicinal Chemist...· 0 citations
Compound 43 exhibited potent molecular and cellular IRAK4 inhibitory activities as well as in vivo anti-inflammatory activities in both LPS-induced acute inflammation and collagen-induced arthritis models alongside favorable pharmacokinetic properties, indicating that compound 43 is a valuable lead compound for further...
Zhen-Wei Zhang, Xue Wang, Xuan Luo et al.· Journal of Medicinal Chemist...· 0 citations
Hydrogen sulfide (H2S) is an endogenous gasotransmitter with therapeutic potential for stroke. Our previous work identified that ADT-OH, an H2S donor with mitochondrial uncoupling activity, protects against stroke by activating the SQR-UCP2-AMPK pathway. Here, we launched a medicinal chemistry campaign based on hit com...
Peng Song, Yuan Li, Xiaohan Song et al.· Journal of Medicinal Chemist...· 0 citations
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