结合
产量(工程)
有效载荷(计算)
药品
化学
组合化学
序列(生物学)
药理学
肽
医学
数学
计算机科学
材料科学
生物化学
数学分析
冶金
网络数据包
计算机网络
作者
Jeremy S. Parker,Marc McCormick,David W. Anderson,Beatrice A. Maltman,Lakshmaiah Gingipalli,Dorin Toader
标识
DOI:10.1021/acs.oprd.7b00232
摘要
Significant development and scale-up work was completed on the synthesis of an antibody drug conjugate payload based on the tubulysin natural products. This work included the development of new routes to the tubuvaline and tubuphenylaniline portions of the molecules, as well as extensive optimization of the solid phase peptide synthesis used to assemble the molecule. The initial route (21 steps longest linear sequence, 0.01% overall yield) was improved to a new, more robust route (19 steps longest linear sequence, 2.4% overall yield) affording a 240-fold increase in overall yield and allowing delivery of over 86 g of the required molecule.
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