Lv4
560 积分 2022-04-28 加入
Discovery of SMD-6346: A Potent, Selective, and Orally Active SMARCA2 Degrader for Targeting SMARCA4-Deficient Human Cancers
17天前
已完结
Synthesis and biological evaluation of 4,7,9-trisubstituted benzoxazepines as antileishmanial agents
26天前
已完结
Diazo‐Based Construction of Heterocyclic Systems Via a X−H Insertion/Cyclization Cascade
1个月前
已完结
Manufacturing Process for 6-Bromo-N,N-bis(4-methoxybenzyl)-4-methyl-5-(trifluoromethyl)pyridin-2-amine, a Key Intermediate in the Synthesis of KRAS G12C Inhibitor Divarasib
7个月前
已完结
Process Development and Kilogram-Scale Manufacture of Key Intermediates toward Single-Enantiomer CELMoDs: Synthesis of Iberdomide·BSA, Part 1
10个月前
已完结
An Expedient Approach for the Synthesis of TAM and MET Receptor Kinase Inhibitor’s Core (R)-2-((4-(4-Amino-2-fluorophenoxy)-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)amino)propan-1-ol
11个月前
已完结
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