New structural scaffold discovery via fragment-based drug design: Hydroxymethyl indazole derivatives as XOR/URAT1 dual inhibitors
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DOI: https://doi.org/10.1007/s00044-025-03505-2
文献链接: https://link.springer.com/10.1007/s00044-025-03505-2
其他信息:
出版社: Springer Science and Business Media LLC
作者: Haiqing Ma; Hongming Chen; Lei Zhang; Jing Li
全文下载地址: https://link.springer.com/content/pdf/10.1007/s00044-025-03505-2.pdf
