Background
The goal of accessing ADME properties is to understand how a potential drug candidate interacts with the human body, including absorption, distribution, metabolism, and excretion. This knowledge is crucial for evaluating efficacy, safety, and clinical potential, guiding drug development for optimal therapeutic outcomes. Fang et al. 2023 has disclosed DMPK datasets collected over 20 months across six ADME in vitro endpoints, which are human and rat liver microsomal stability, MDR1-MDCK efflux ratio, solubility, and human and rat plasma protein binding. The dataset contains 885 to 3087 measures for the corresponding endpoints. The compounds show the chemical diversity across all ranges of the endpoints which are microsomal stability, plasma protein binding, permeability, and solubility.
Benchmarking
The goal* of this benchmark is to perform a single task, which is to the best predictive model for rat liver microsomal stability.
Description of readout
- Readouts:
LOG RLM_CLint (mL/min/kg)
- Bioassay readout: Intrinsic clearance
- Optimization objective: Higher value
Molecule data resource
Reference: https://doi.org/10.1021/acs.jcim.3c00160
Train/test split
In this benchmark set, the same train/test sets in the fang2023 paper were used for the 6 endpoints human and rat liver microsomal stability, MDR1-MDCK efflux ratio, solubility, and human and rat plasma protein binding, respectively.
See more details at https://github.com/molecularinformatics/Computational-ADME/tree/main/MPNN.
Distribution of the train/test in the chemical space
Related links
The full curation and creation process is documented here.
