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Bioorganic Chemistry|April 4, 2022
Discovery of a highly potent CECR2 bromodomain inhibitor with 7H-pyrrolo[2,3-d] pyrimidine scaffoldHaibo Lu, Tian Lu, Shijia Zu, et al.
The Journal of Biological Chemistry|October 12, 2018
2-Hydroxy-oleic acid does not activate sphingomyelin synthase activityBin Lou, Qi Liu, Jiahui Hou, et al.
Bioorganic & Medicinal Chemistry|June 16, 2012
Antitumor agents 294. Novel E-ring-modified camptothecin-4β-anilino-4'-O-demethyl-epipodophyllotoxin conjugates as DNA topoisomerase I inhibitors and cytotoxic agentsDeyong Ye, Qian Shi, Chung-Hang Leung, et al.
Acta Pharmaceutica Sinica. B|March 5, 2025
Discovery of a novel thiophene carboxamide analogue as a highly potent and selective sphingomyelin synthase 2 inhibitor for dry eye disease therapyJintong Yang, Yiteng Lu, Kexin Hu, et al.
ACS Chemical Biology|February 19, 2020
Site-Selective Phosphoglycerate Mutase 1 Acetylation by a Small MoleculeXiaodan Zhang, Lulu Jiang, Ke Huang, et al.
European Journal of Medicinal Chemistry|December 24, 2018
Discovery, synthesis and anti-atherosclerotic activities of a novel selective sphingomyelin synthase 2 inhibitorYali Li, Taomin Huang, Bin Lou, et al.
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