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A Comparison of Physicochemical Property Profiles of Marketed Oral Drugs and Orally Bioavailable Anti-Cancer Protein Kinase Inhibitors in Clinical Development

机译:市售口服药物和口服生物利用抗癌蛋白激酶抑制剂的理化性质比较

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摘要

This manuscript describes a comparison of the physicochemical properties of marketed oral drugs with those of 45 structurally confirmed orally bioavailable anti-cancer protein kinase inhibitors currently in different phases of clinical development. It is evident from the data presented that these kinase inhibitors are on average larger (over 110Da), more lipophilic (over 1.5 log units) and more complex (approximately two more rotatable bonds) than those of marketed oral drugs. In contrast, hydrogen bond donor (HBD) and hydrogen bond acceptor (HBA) counts are not significantly different.
机译:该手稿描述了市售口服药物与目前临床开发不同阶段中的45种经结构确认的口服可生物利用的抗癌蛋白激酶抑制剂的理化性质的比较。从提供的数据中可以明显看出,与市售口服药物相比,这些激酶抑制剂平均更大(大于110Da),亲脂性更大(超过1.5 log单位)和更复杂(大约两个更大的可旋转键)。相反,氢键供体(HBD)和氢键受体(HBA)的计数没有显着差异。

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