chemprop 1.2.0

Molecular Property Prediction with Message Passing Neural Networks

Molecular Property Prediction

This repository contains message passing neural networks for molecular property prediction as described in the paper Analyzing Learned Molecular Representations for Property Prediction and as used in the paper A Deep Learning Approach to Antibiotic Discovery.

Documentation: Full documentation of Chemprop is available at https://chemprop.readthedocs.io/en/latest/.

Website: A web prediction interface with some trained Chemprop models is available at chemprop.csail.mit.edu.

Tutorial: These slides provide a Chemprop tutorial and highlight recent additions as of April 28th, 2020.

COVID-19 Update

Please see aicures.mit.edu and the associated data GitHub repo for information about our recent efforts to use Chemprop to identify drug candidates for treating COVID-19.

Table of Contents

• Requirements
• Installation
  • Option 1: Installing from PyPi
  • Option 2: Installing from source
  • Docker
• Web Interface
• Data
• Training
  • Train/Validation/Test Splits
  • Cross validation
  • Ensembling
  • Hyperparameter Optimization
  • Aggregation
  • Additional Features
    • RDKit 2D Features
    • Custom Features
    • Atomic Features
• Predicting
• Interpreting Model Prediction
• TensorBoard
• Results

Requirements

For small datasets (~1000 molecules), it is possible to train models within a few minutes on a standard laptop with CPUs only. However, for larger datasets and larger Chemprop models, we recommend using a GPU for significantly faster training.

To use chemprop with GPUs, you will need:

• cuda >= 8.0
• cuDNN

Installation

Chemprop can either be installed from PyPi via pip or from source (i.e., directly from this git repo). The PyPi version includes a vast majority of Chemprop functionality, but some functionality is only accessible when installed from source.

Both options require conda, so first install Miniconda from https://conda.io/miniconda.html.

Then proceed to either option below to complete the installation. Note that on machines with GPUs, you may need to manually install a GPU-enabled version of PyTorch by following the instructions here.

Option 1: Installing from PyPi

1. conda create -n chemprop python=3.8
2. conda activate chemprop
3. conda install -c conda-forge rdkit
4. pip install git+https://github.com/bp-kelley/descriptastorus
5. pip install chemprop

Option 2: Installing from source

1. git clone https://github.com/chemprop/chemprop.git
2. cd chemprop
3. conda env create -f environment.yml
4. conda activate chemprop
5. pip install -e .

Docker

Chemprop can also be installed with Docker. Docker makes it possible to isolate the Chemprop code and environment. To install and run our code in a Docker container, follow these steps:

1. git clone https://github.com/chemprop/chemprop.git
2. cd chemprop
3. Install Docker from https://docs.docker.com/install/
4. docker build -t chemprop .
5. docker run -it chemprop:latest

Note that you will need to run the latter command with nvidia-docker if you are on a GPU machine in order to be able to access the GPUs. Alternatively, with Docker 19.03+, you can specify the --gpus command line option instead.

In addition, you will also need to ensure that the CUDA toolkit version in the Docker image is compatible with the CUDA driver on your host machine. Newer CUDA driver versions are backward-compatible with older CUDA toolkit versions. To set a specific CUDA toolkit version, add cudatoolkit=X.Y to environment.yml before building the Docker image.

Web Interface

For those less familiar with the command line, Chemprop also includes a web interface which allows for basic training and predicting. An example of the website (in demo mode with training disabled) is available here: chemprop.csail.mit.edu.

You can start the web interface on your local machine in two ways. Flask is used for development mode while gunicorn is used for production mode.

Flask

Run chemprop_web (or optionally python web.py if installed from source) and then navigate to localhost:5000 in a web browser.

Gunicorn

Gunicorn is only available for a UNIX environment, meaning it will not work on Windows. It is not installed by default with the rest of Chemprop, so first run:

pip install gunicorn

Next, navigate to chemprop/web and run gunicorn --bind {host}:{port} 'wsgi:build_app()'. This will start the site in production mode.

• To run this server in the background, add the --daemon flag.
• Arguments including init_db and demo can be passed with this pattern: 'wsgi:build_app(init_db=True, demo=True)'
• Gunicorn documentation can be found here.

Data

In order to train a model, you must provide training data containing molecules (as SMILES strings) and known target values. Targets can either be real numbers, if performing regression, or binary (i.e. 0s and 1s), if performing classification. Target values which are unknown can be left as blanks.

Our model can either train on a single target ("single tasking") or on multiple targets simultaneously ("multi-tasking").

The data file must be be a CSV file with a header row. For example:

smiles,NR-AR,NR-AR-LBD,NR-AhR,NR-Aromatase,NR-ER,NR-ER-LBD,NR-PPAR-gamma,SR-ARE,SR-ATAD5,SR-HSE,SR-MMP,SR-p53
CCOc1ccc2nc(S(N)(=O)=O)sc2c1,0,0,1,,,0,0,1,0,0,0,0
CCN1C(=O)NC(c2ccccc2)C1=O,0,0,0,0,0,0,0,,0,,0,0
...

By default, it is assumed that the SMILES are in the first column (can be changed using --number-of-molecules) and the targets are in the remaining columns. However, the specific columns containing the SMILES and targets can be specified using the --smiles_columns <column_1> ... and --target_columns <column_1> <column_2> ... flags, respectively.

Datasets from MoleculeNet and a 450K subset of ChEMBL from http://www.bioinf.jku.at/research/lsc/index.html have been preprocessed and are available in data.tar.gz. To uncompress them, run tar xvzf data.tar.gz.

Training

To train a model, run:

chemprop_train --data_path <path> --dataset_type <type> --save_dir <dir>

where <path> is the path to a CSV file containing a dataset, <type> is either "classification" or "regression" depending on the type of the dataset, and <dir> is the directory where model checkpoints will be saved.

For example:

chemprop_train --data_path data/tox21.csv --dataset_type classification --save_dir tox21_checkpoints

A full list of available command-line arguments can be found in chemprop/args.py.

If installed from source, chemprop_train can be replaced with python train.py.

Notes:

• The default metric for classification is AUC and the default metric for regression is RMSE. Other metrics may be specified with --metric <metric>.
• --save_dir may be left out if you don't want to save model checkpoints.
• --quiet can be added to reduce the amount of debugging information printed to the console. Both a quiet and verbose version of the logs are saved in the save_dir.

Train/Validation/Test Splits

Our code supports several methods of splitting data into train, validation, and test sets.

Random: By default, the data will be split randomly into train, validation, and test sets.

Scaffold: Alternatively, the data can be split by molecular scaffold so that the same scaffold never appears in more than one split. This can be specified by adding --split_type scaffold_balanced.

Separate val/test: If you have separate data files you would like to use as the validation or test set, you can specify them with --separate_val_path <val_path> and/or --separate_test_path <test_path>.

Note: By default, both random and scaffold split the data into 80% train, 10% validation, and 10% test. This can be changed with --split_sizes <train_frac> <val_frac> <test_frac>. For example, the default setting is --split_sizes 0.8 0.1 0.1. Both also involve a random component and can be seeded with --seed <seed>. The default setting is --seed 0.

Cross validation

k-fold cross-validation can be run by specifying --num_folds <k>. The default is --num_folds 1.

Ensembling

To train an ensemble, specify the number of models in the ensemble with --ensemble_size <n>. The default is --ensemble_size 1.

Hyperparameter Optimization

Although the default message passing architecture works quite well on a variety of datasets, optimizing the hyperparameters for a particular dataset often leads to marked improvement in predictive performance. We have automated hyperparameter optimization via Bayesian optimization (using the hyperopt package), which will find the optimal hidden size, depth, dropout, and number of feed-forward layers for our model. Optimization can be run as follows:

chemprop_hyperopt --data_path <data_path> --dataset_type <type> --num_iters <n> --config_save_path <config_path>

where <n> is the number of hyperparameter settings to try and <config_path> is the path to a .json file where the optimal hyperparameters will be saved.

If installed from source, chemprop_hyperopt can be replaced with python hyperparameter_optimization.py.

Once hyperparameter optimization is complete, the optimal hyperparameters can be applied during training by specifying the config path as follows:

chemprop_train --data_path <data_path> --dataset_type <type> --config_path <config_path>

Note that the hyperparameter optimization script sees all the data given to it. The intended use is to run the hyperparameter optimization script on a dataset with the eventual test set held out. If you need to optimize hyperparameters separately for several different cross validation splits, you should e.g. set up a bash script to run hyperparameter_optimization.py separately on each split's training and validation data with test held out.

Aggregation

By default, the atom-level representations from the message passing network are averaged over all atoms of a molecule to yield a molecule-level representation. Alternatively, the atomic vectors can be summed up (by specifying --aggregration sum) or summed up and divided by a constant number N (by specifying --aggregration norm --aggregation_norm <N>). A reasonable value for N is usually the average number of atoms per molecule in the dataset of interest. The default is --aggregation_norm 100.

Additional Features

While the model works very well on its own, especially after hyperparameter optimization, we have seen that adding computed molecule-level features can further improve performance on certain datasets. Features can be added to the model using the --features_generator <generator> flag for molecule-level features, or --atom_descriptors <mode> for atom-level features, or both.

RDKit 2D Features

As a starting point, we recommend using pre-normalized RDKit features by using the --features_generator rdkit_2d_normalized --no_features_scaling flags. In general, we recommend NOT using the --no_features_scaling flag (i.e. allow the code to automatically perform feature scaling), but in the case of rdkit_2d_normalized, those features have been pre-normalized and don't require further scaling.

The full list of available features for --features_generator is as follows.

morgan is binary Morgan fingerprints, radius 2 and 2048 bits. morgan_count is count-based Morgan, radius 2 and 2048 bits. rdkit_2d is an unnormalized version of 200 assorted rdkit descriptors. Full list can be found at the bottom of our paper: https://arxiv.org/pdf/1904.01561.pdf rdkit_2d_normalized is the CDF-normalized version of the 200 rdkit descriptors.

Custom Features

If you install from source, you can modify the code to load custom features as follows:

1. Generate features: If you want to generate features in code, you can write a custom features generator function in chemprop/features/features_generators.py. Scroll down to the bottom of that file to see a features generator code template.
2. Load features: If you have features saved as a numpy .npy file or as a .csv file, you can load the features by using --features_path /path/to/features. Note that the features must be in the same order as the SMILES strings in your data file. Also note that .csv files must have a header row and the features should be comma-separated with one line per molecule.

Atomic Features

Similar to the additional molecular features described above, you can also provide additional atomic features via --atom_descriptors_path /path/to/features with valid file formats:

• .npz file, where descriptors are saved as 2D array for each molecule in the exact same order as the SMILES strings in your data file.
• .pkl / .pckl / .pickle containing a pandas dataframe with smiles as index and a numpy array of descriptors as columns.
• .sdf containing all mol blocks with descriptors as entries.

The order of the descriptors for each atom per molecule must match the ordering of atoms in the RDKit molecule object. Further information on supplying atomic descriptors can be found here. Users must select in which way atom descriptors are used, where the command line option --atom_descriptors descriptor concatenates the new features to the embedded atomic features after the D-MPNN, or the option --atom_descriptors feature concatenates the features to each atomic feature vector before the D-MPNN, so that they are used during message-passing.

Predicting

To load a trained model and make predictions, run predict.py and specify:

• --test_path <path> Path to the data to predict on.
• A checkpoint by using either:
  • --checkpoint_dir <dir> Directory where the model checkpoint(s) are saved (i.e. --save_dir during training). This will walk the directory, load all .pt files it finds, and treat the models as an ensemble.
  • --checkpoint_path <path> Path to a model checkpoint file (.pt file).
• --preds_path Path where a CSV file containing the predictions will be saved.

For example:

chemprop_predict --test_path data/tox21.csv --checkpoint_dir tox21_checkpoints --preds_path tox21_preds.csv

or

chemprop_predict --test_path data/tox21.csv --checkpoint_path tox21_checkpoints/fold_0/model_0/model.pt --preds_path tox21_preds.csv

If installed from source, chemprop_predict can be replaced with python predict.py.

Interpreting

It is often helpful to provide explanation of model prediction (i.e., this molecule is toxic because of this substructure). Given a trained model, you can interpret the model prediction using the following command:

chemprop_interpret --data_path data/tox21.csv --checkpoint_dir tox21_checkpoints/fold_0/ --property_id 1

If installed from source, chemprop_interpret can be replaced with python interpret.py.

The output will be like the following:

• The first column is a molecule and second column is its predicted property (in this case NR-AR toxicity).
• The third column is the smallest substructure that made this molecule classified as toxic (which we call rationale).
• The fourth column is the predicted toxicity of that substructure.

As shown in the first row, when a molecule is predicted to be non-toxic, we will not provide any rationale for its prediction.

smiles	NR-AR	rationale	rationale_score
O=[N+]([O-])c1cc(C(F)(F)F)cc([N+](=O)[O-])c1Cl	0.014
CC1(C)O[C@@H]2C[C@H]3[C@@H]4C[C@H](F)C5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1	0.896	C[C@]12C=CC(=O)C=C1[CH2:1]C[CH2:1][CH2:1]2	0.769
C[C@]12CC[C@H]3[C@@H](CC[C@@]45O[C@@H]4C(O)=C(C#N)C[C@]35C)[C@@H]1CC[C@@H]2O	0.941	C[C@]12C[CH:1]=[CH:1][C@H]3O[C@]31CC[C@@H]1[C@@H]2CC[C:1][CH2:1]1	0.808
C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@]2(O)C(=O)COP(=O)([O-])[O-]	0.957	C1C[CH2:1][C:1][C@@H]2[C@@H]1[C@@H]1CC[C:1][C:1]1C[CH2:1]2	0.532

Chemprop's interpretation script explains model prediction one property at a time. --property_id 1 tells the script to provide explanation for the first property in the dataset (which is NR-AR). In a multi-task training setting, you will need to change --property_id to provide explanation for each property in the dataset.

For computational efficiency, we currently restricted the rationale to have maximum 20 atoms and minimum 8 atoms. You can adjust these constraints through --max_atoms and --min_atoms argument.

Please note that the interpreting framework is currently only available for models trained on properties of single molecules, that is, multi-molecule models generated via the --number_of_molecules command are not supported.

TensorBoard

During training, TensorBoard logs are automatically saved to the same directory as the model checkpoints. To view TensorBoard logs, first install TensorFlow with pip install tensorflow. Then run tensorboard --logdir=<dir> where <dir> is the path to the checkpoint directory. Then navigate to http://localhost:6006.

Results

We compared our model against MolNet by Wu et al. on all of the MolNet datasets for which we could reproduce their splits (all but Bace, Toxcast, and qm7). When there was only one fold provided (scaffold split for BBBP and HIV), we ran our model multiple times and reported average performance. In each case we optimize hyperparameters on separate folds, use rdkit_2d_normalized features when useful, and compare to the best-performing model in MolNet as reported by Wu et al. We did not ensemble our model in these results.

Results on regression datasets (lower is better)

Dataset	Size	Metric	Ours	MolNet Best Model
QM8	21,786	MAE	0.011 ± 0.000	0.0143 ± 0.0011
QM9	133,885	MAE	2.666 ± 0.006	2.4 ± 1.1
ESOL	1,128	RMSE	0.555 ± 0.047	0.58 ± 0.03
FreeSolv	642	RMSE	1.075 ± 0.054	1.15 ± 0.12
Lipophilicity	4,200	RMSE	0.555 ± 0.023	0.655 ± 0.036
PDBbind (full)	9,880	RMSE	1.391 ± 0.012	1.25 ± 0
PDBbind (core)	168	RMSE	2.173 ± 0.090	1.92 ± 0.07
PDBbind (refined)	3,040	RMSE	1.486 ± 0.026	1.38 ± 0

Results on classification datasets (higher is better)

Dataset	Size	Metric	Ours	MolNet Best Model
PCBA	437,928	PRC-AUC	0.335 ± 0.001	0.136 ± 0.004
MUV	93,087	PRC-AUC	0.041 ± 0.007	0.184 ± 0.02
HIV	41,127	ROC-AUC	0.776 ± 0.007	0.792 ± 0
BBBP	2,039	ROC-AUC	0.737 ± 0.001	0.729 ± 0
Tox21	7,831	ROC-AUC	0.851 ± 0.002	0.829 ± 0.006
SIDER	1,427	ROC-AUC	0.676 ± 0.014	0.648 ± 0.009
ClinTox	1,478	ROC-AUC	0.864 ± 0.017	0.832 ± 0.037

Lastly, you can find the code to our original repo at https://github.com/wengong-jin/chemprop and for the Mayr et al. baseline at https://github.com/yangkevin2/lsc_experiments .