Furo[2,3- f ]quinazolin-7(6 H )-one Derivatives as Potent, Selective, and Orally Bioavailable MAT2A Inhibitors for MTAP-Deficient Cancer Therapy
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DOI: https://doi.org/10.1021/acs.jmedchem.5c02062
文献链接: https://pubs.acs.org/doi/10.1021/acs.jmedchem.5c02062
其他信息:
出版社: American Chemical Society (ACS)
作者: Zihan Shi; Kexin Lin; Lijie Lin; Zhiyi Chen; Zhiyin Xie; Yaoliang Sun; Rongrong Cui; Sulin Zhang; Mingyue Zheng; Shilin Xu
全文下载地址: https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.5c02062
