Oral Druggable Space beyond the Rule of 5: Insights from Drugs and Clinical Candidates

被引:533
作者
Doak, Bradley Croy [1 ]
Over, Bjorn [2 ]
Giordanetto, Fabrizio [3 ]
Kihlberg, Jan [1 ]
机构
[1] Uppsala Univ, Dept Chem, BMC, S-75123 Uppsala, Sweden
[2] AstraZeneca R&D, CVMD iMed, S-43183 Molndal, Sweden
[3] Taros Chem GmbH & Co KG, Med Chem, D-44227 Dortmund, Germany
来源
CHEMISTRY & BIOLOGY | 2014年 / 21卷 / 09期
关键词
NS3 PROTEASE INHIBITOR; PASSIVE MEMBRANE-PERMEABILITY; REDUCED PLASMA-CONCENTRATIONS; INTRAMOLECULAR HYDROGEN-BOND; P-GLYCOPROTEIN TRANSPORT; CACO-2 CELL MONOLAYERS; ESTER TRANSFER PROTEIN; IN-SILICO PREDICTION; HCV NS5A INHIBITOR; X-RAY-ANALYSIS;
D O I
10.1016/j.chembiol.2014.08.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The rule of 5 (Ro5) is a set of in silico guidelines applied to drug discovery to prioritize compounds with an increased likelihood of high oral absorption. It has been influential in reducing attrition due to poor pharmacokinetics over the last 15 years. However, strict reliance on the Ro5 may have resulted in lost opportunities, particularly for difficult targets. To identify opportunities for oral drug discovery beyond the Ro5 (bRo5), we have comprehensively analyzed drugs and clinical candidates with molecular weight (MW) > 500 Da. We conclude that oral drugs are found far bRo5 and properties such as intramolecular hydrogen bonding, macrocyclization, dosage, and formulations can be used to improve bRo5 bioavailability. Natural products and structure-based design, often from peptidic leads, are key sources for oral bRo5 drugs. These insights should help guide the design of oral drugs in bRo5 space, which is of particular interest for difficult targets.
引用
收藏
页码:1115 / 1142
页数:28
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