Department of Chemistry, Auckland Bioengineering Institute, The University of Auckland, Auckland 1142, New Zealand.
Eur J Med Chem. 2010 Dec;45(12):5646-52. doi: 10.1016/j.ejmech.2010.09.018. Epub 2010 Sep 17.
Known drug space (KDS) was analysed for the occurrence of natural products and their derivatives. A database of 1000 marketed drugs was compiled. It was found that 10% of the drugs on the market are unaltered natural products, 29% are their derivatives (semi-synthetics) and the rest (61%) have a synthetic origin. Of the natural products, and their derivatives, polycyclic drugs were the most abundant at 21% followed by simple drugs (16%) and steroids (15%). In regard to the molecular descriptors the natural products had larger statistical means and standard deviations than their synthetic counterparts. It was found that KDS occupies a larger volume in chemical space with respect to drug-like chemicals, i.e., KDS fully encompasses drug-like chemical space with the parameters of molecular weight≤800 g mol(-1), log P≤6.5, hydrogen bond acceptors≤15, hydrogen bond donors≤7, polar surface area≤180 Å2, and rotatable bonds≤17. Only 13% of the drugs analysed are outside one or more of these parameters. The definition of KDS gives drug designers a larger volume to work in compared to drug-like chemical space. However, the bulk of known drugs are found within the volume of drug-like chemical space.
已知药物空间(KDS)被分析是否存在天然产物及其衍生物。编译了一个包含 1000 种上市药物的数据库。结果发现,市场上有 10%的药物是未经修饰的天然产物,29%是它们的衍生物(半合成物),其余 61%则具有合成来源。在天然产物及其衍生物中,多环药物最为丰富,占 21%,其次是简单药物(16%)和类固醇(15%)。在分子描述符方面,天然产物的统计均值和标准差均大于其合成对应物。研究发现,KDS 在化学空间中相对于类药性化学物质占据更大的体积,即 KDS 完全包含类药性化学物质空间,这些参数包括分子量≤800 g mol(-1)、log P≤6.5、氢键受体≤15、氢键供体≤7、极性表面积≤180 Å2和可旋转键≤17。分析的药物中只有 13%超出一个或多个这些参数。KDS 的定义为药物设计师提供了一个比类药性化学物质空间更大的工作体积。然而,大部分已知药物都存在于类药性化学物质空间的体积内。