RASA: A Rapid Retrosynthesis-Based Scoring Method for the Assessment of Synthetic Accessibility of Drug-like Molecules

In this account, a rapid retrosynthesis-based scoring method for the assessment of synthetic accessibility of drug-like molecules, called RASA (Retrosynthesis-based Assessment of Synthetic Accessibility) is devised. RASA first constructs a synthesis tree for the target molecule based on retrosynthetic analysis; in this process a series of strategies are suggested for limiting combinatorial explosion of the synthesis tree. A scoring function (RASA-score) for the assessment of synthetic accessibility is then proposed based on the optional effective synthetic routes, the complexity of reaction, and the difficulty of separation/purification associated with the most favorable synthetic route. The contributions of individual components are calibrated by linear regression analysis based on the synthetic accessibility estimates of a training set (100 compounds) given by a group of medicinal chemists (G1). Two external test sets (TS1 and TS2), whose synthetic accessibility estimates were given by the group G1 medicinal chemists and another group (G2) of medicinal chemists (from literature), respectively, were adopted for the evaluation of RASA. The correlation coefficient between the calculated RASA-score values and the estimated scores by medicinal chemists for TS1 is 0.807 and that for TS2 is 0.792, which demonstrate the validity and reliability of RASA. The validity and reliability as well as the high speed of RASA and its capability of suggesting synthetic routes enable it a useful tool in drug discovery.

[1]  Gisbert Schneider,et al.  Computer-based de novo design of drug-like molecules , 2005, Nature Reviews Drug Discovery.

[2]  A. Ghose,et al.  Atomic Physicochemical Parameters for Three‐Dimensional Structure‐Directed Quantitative Structure‐Activity Relationships I. Partition Coefficients as a Measure of Hydrophobicity , 1986 .

[3]  Tudor I. Oprea,et al.  Rapid Evaluation of Synthetic and Molecular Complexity for in Silico Chemistry , 2005, J. Chem. Inf. Model..

[4]  René Barone,et al.  A New and Simple Approach to Chemical Complexity. Application to the Synthesis of Natural Products , 2001, J. Chem. Inf. Comput. Sci..

[5]  A. Pierce,et al.  Docking study yields four novel inhibitors of the protooncogene Pim-1 kinase. , 2008, Journal of medicinal chemistry.

[6]  William L. Jorgensen,et al.  Computer-assisted synthetic analysis. Synthetic strategies based on appendages and the use of reconnective transforms , 1976 .

[7]  Weihua Li,et al.  Discovery of potent ligands for estrogen receptor beta by structure-based virtual screening. , 2010, Journal of medicinal chemistry.

[8]  J C Baber,et al.  Predicting synthetic accessibility: application in drug discovery and development. , 2004, Mini reviews in medicinal chemistry.

[9]  Brian K. Shoichet,et al.  Virtual screening of chemical libraries , 2004, Nature.

[10]  Matthew H Todd,et al.  Computer-aided organic synthesis. , 2005, Chemical Society reviews.

[11]  Yu-Quan Wei,et al.  Pharmacophore modeling study based on known spleen tyrosine kinase inhibitors together with virtual screening for identifying novel inhibitors. , 2009, Bioorganic & medicinal chemistry letters.

[12]  Philip N. Judson,et al.  Starting material oriented retrosynthetic analysis in the LHASA program. 1. General description , 1992, J. Chem. Inf. Comput. Sci..

[13]  Ji-Xia Ren,et al.  Pharmacophore modeling and virtual screening for the discovery of new transforming growth factor-beta type I receptor (ALK5) inhibitors. , 2009, European journal of medicinal chemistry.

[14]  Johann Gasteiger,et al.  Structure and reaction based evaluation of synthetic accessibility , 2007, J. Comput. Aided Mol. Des..

[15]  H. Choo,et al.  Novel GSK-3β inhibitors from sequential virtual screening , 2008 .

[16]  Peter Ertl,et al.  Estimation of synthetic accessibility score of drug-like molecules based on molecular complexity and fragment contributions , 2009, J. Cheminformatics.

[17]  Johann Gasteiger,et al.  Computer‐Assisted Planning of Organic Syntheses: The Second Generation of Programs , 1996 .

[18]  E. Corey General methods for the construction of complex molecules , 1967 .

[19]  Yang Liu,et al.  Route Designer: A Retrosynthetic Analysis Tool Utilizing Automated Retrosynthetic Rule Generation , 2009, J. Chem. Inf. Model..

[20]  A. Schuffenhauer,et al.  Complex molecules: do they add value? , 2005, Current opinion in chemical biology.

[21]  Sheng-Yong Yang,et al.  PhDD: a new pharmacophore-based de novo design method of drug-like molecules combined with assessment of synthetic accessibility. , 2010, Journal of molecular graphics & modelling.

[22]  S. Krishnan,et al.  Simulation and Evaluation of Chemical Synthesis - SECS: An Application of Artificial Intelligence Techniques , 1978, Artif. Intell..

[23]  Gilman D. Veith,et al.  A rapid method for estimating log P for organic chemicals , 1979 .