Pith. sign in

REVIEW 3 cited by

Chemception: A Deep Neural Network with Minimal Chemistry Knowledge Matches the Performance of Expert-developed QSAR/QSPR Models

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 1706.06689 v1 pith:BP7CTE75 submitted 2017-06-20 stat.ML cs.AIcs.CEcs.CVcs.LG

classification stat.MLcs.AIcs.CEcs.CVcs.LG
keywords deepchemceptionneuralchemistrylearningnetworkpredictionactivity
verification ladder T0 review T1 audit T2 compute T3 formal
0 comments
read the original abstract

In the last few years, we have seen the transformative impact of deep learning in many applications, particularly in speech recognition and computer vision. Inspired by Google's Inception-ResNet deep convolutional neural network (CNN) for image classification, we have developed "Chemception", a deep CNN for the prediction of chemical properties, using just the images of 2D drawings of molecules. We develop Chemception without providing any additional explicit chemistry knowledge, such as basic concepts like periodicity, or advanced features like molecular descriptors and fingerprints. We then show how Chemception can serve as a general-purpose neural network architecture for predicting toxicity, activity, and solvation properties when trained on a modest database of 600 to 40,000 compounds. When compared to multi-layer perceptron (MLP) deep neural networks trained with ECFP fingerprints, Chemception slightly outperforms in activity and solvation prediction and slightly underperforms in toxicity prediction. Having matched the performance of expert-developed QSAR/QSPR deep learning models, our work demonstrates the plausibility of using deep neural networks to assist in computational chemistry research, where the feature engineering process is performed primarily by a deep learning algorithm.

Discussion (0). Continue with ORCID to comment.

Forward citations

Cited by 3 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. ChemMLLM: Chemical Multimodal Large Language Model

    cs.LG 2025-05 reject novelty 6.0 of 10

    A chemical multimodal LLM is trained to understand and generate molecule images alongside SMILES and text, with claims of state-of-the-art results on five new tasks.

  2. Generic Vision and Cross-Attention for Reaction Yield Prediction

    cs.LG 2026-08 conditional novelty 5.0 of 10

    A frozen ImageNet vision model reading 2D molecular drawings outperforms a quantum-descriptor tabular model for C-N coupling yield prediction, and cross-attention fusion gives 5.27% RMSE.

  3. CROP: Integrating Topological and Spatial Structures via Cross-View Prefixes for Molecular LLMs

    q-bio.QM 2025-08 conditional novelty 5.0 of 10

    Cross-view prefix resampling, guided by the LLM's SMILES encoding, lets a Galactica-based model exploit molecular graphs and images at low context cost, improving captioning, IUPAC naming, and property prediction.

Pith tools