Analysis of physicochemical properties of protein–protein interaction modulators suggests stronger alignment with the "rule of five". Issue 10 (2nd September 2021)
- Record Type:
- Journal Article
- Title:
- Analysis of physicochemical properties of protein–protein interaction modulators suggests stronger alignment with the "rule of five". Issue 10 (2nd September 2021)
- Main Title:
- Analysis of physicochemical properties of protein–protein interaction modulators suggests stronger alignment with the "rule of five"
- Authors:
- Truong, Jia
George, Ashwin
Holien, Jessica K. - Abstract:
- Abstract : The physicochemical properties of protein–protein interaction (PPI) modulators vary between those on the market, those in clinical trials, and those in the early drug discovery pipeline. Abstract : Despite the important roles played by protein–protein interactions (PPIs) in disease, they have been long considered as 'undruggable'. However, recent advances have suggested that PPIs are druggable but may not follow conventional rules of 'drug ability'. Here we explore which physicochemical parameters are essential for a PPI modulator to be a clinical drug by analysing the physicochemical properties of small-molecule PPI modulators in the market, in clinical trials, and published. Our analysis reveals that those compounds currently on the market have a larger range of values for most of the physicochemical parameters, whereas those in clinical trials fit much more stringently to standard drug-like parameters. This observation was particularly true for molecular weight, clog P and topological polar surface area, where aside from a few outliers, most of the compounds in clinical trials fit within standard drug-like parameters. This implies that the newer PPI modulators are more drug-like than those currently on the market, suggesting that designing new PPI-specific screening libraries should remain within standard drug-like parameters in order to obtain a clinical candidate. Taken together, our analysis has important implications for designing future drug discoveryAbstract : The physicochemical properties of protein–protein interaction (PPI) modulators vary between those on the market, those in clinical trials, and those in the early drug discovery pipeline. Abstract : Despite the important roles played by protein–protein interactions (PPIs) in disease, they have been long considered as 'undruggable'. However, recent advances have suggested that PPIs are druggable but may not follow conventional rules of 'drug ability'. Here we explore which physicochemical parameters are essential for a PPI modulator to be a clinical drug by analysing the physicochemical properties of small-molecule PPI modulators in the market, in clinical trials, and published. Our analysis reveals that those compounds currently on the market have a larger range of values for most of the physicochemical parameters, whereas those in clinical trials fit much more stringently to standard drug-like parameters. This observation was particularly true for molecular weight, clog P and topological polar surface area, where aside from a few outliers, most of the compounds in clinical trials fit within standard drug-like parameters. This implies that the newer PPI modulators are more drug-like than those currently on the market, suggesting that designing new PPI-specific screening libraries should remain within standard drug-like parameters in order to obtain a clinical candidate. Taken together, our analysis has important implications for designing future drug discovery campaigns aimed at targeting PPIs. … (more)
- Is Part Of:
- RSC medicinal chemistry. Volume 12:Issue 10(2021)
- Journal:
- RSC medicinal chemistry
- Issue:
- Volume 12:Issue 10(2021)
- Issue Display:
- Volume 12, Issue 10 (2021)
- Year:
- 2021
- Volume:
- 12
- Issue:
- 10
- Issue Sort Value:
- 2021-0012-0010-0000
- Page Start:
- 1731
- Page End:
- 1749
- Publication Date:
- 2021-09-02
- Subjects:
- Pharmaceutical chemistry -- Periodicals
615.19005 - Journal URLs:
- http://www.rsc.org/ ↗
https://www.rsc.org/journals-books-databases/about-journals/rsc-medicinal-chemistry ↗ - DOI:
- 10.1039/d1md00213a ↗
- Languages:
- English
- ISSNs:
- 2632-8682
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.751550
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19733.xml