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• W2000246385 abstract "The importance of striving for and maintaining drug-like physicochemical properties during the hit and lead optimization process is now well documented, and many published studies have suggested optimal ranges and/or limits for key molecule descriptors such as size, lipophilicity, H-bonding characteristics, rotatable bond and aromatic ring counts, particularly with regard to the design of orally administered drugs. The aim of this article is to review various approaches that have been used to represent molecule properties graphically in the context of oral 'drug likeness', with the goal of improving the decision making of medicinal chemists during the drug discovery process." @default.
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• W2000246385 date "2011-01-01" @default.
• W2000246385 modified "2023-10-14" @default.
• W2000246385 title "The graphical representation of ADME-related molecule properties for medicinal chemists" @default.
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• W2000246385 doi "https://doi.org/10.1016/j.drudis.2010.11.002" @default.
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