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具有生物学相关性的化合物成为药物的机会更大吗?

Do biologically relevant compounds have more chance to be drugs?

作者信息

Kong De-Xin, Ren Wei, Lü Wei, Zhang Hong-Yu

机构信息

College of Life Science and Technology, Huazhong Agricultural University, Wuhan 430070, China.

出版信息

J Chem Inf Model. 2009 Oct;49(10):2376-81. doi: 10.1021/ci900229c.

Abstract

To prove the innate advantages of endogenous compounds/fragments for drug discovery and development, a novel index termed biological relevance (BR) is proposed. The results clearly indicate its ability to distinguish between synthetic chemicals, bioactive compounds, drug candidates, and launched drugs. Primarily, the average BR of the databases investigated decreases in the order DNP > CMC > ACD-3D > MDDR. Second, for compounds with the same bioactivity, drugs (CMC) possess higher average BR than their candidates (MDDR). These results suggest that compounds with higher BR have more chance to survive the drug development pipeline. Third, the above conclusion is supported by the fact that compounds in the later development phases possess higher BR than those in the earlier phases. Comparisons were made between BR and other indices, including toxicity, druglikeness, and natural productlikeness.

摘要

为证明内源性化合物/片段在药物发现与开发方面的固有优势,提出了一种名为生物相关性(BR)的新指标。结果清楚地表明了其区分合成化学品、生物活性化合物、候选药物和上市药物的能力。首先,所研究数据库的平均BR按以下顺序降低:DNP>CMC>ACD - 3D>MDDR。其次,对于具有相同生物活性的化合物,药物(CMC)的平均BR高于其候选药物(MDDR)。这些结果表明,具有较高BR的化合物更有可能在药物开发流程中留存下来。第三,后期开发阶段的化合物比早期阶段的化合物具有更高的BR,这一事实支持了上述结论。还对BR与其他指标进行了比较,包括毒性、类药性质和类天然产物性质。

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