# CheMixNet: Mixed DNN Architectures for Predicting Chemical Properties using Multiple Molecular Representations

arXiv: https://arxiv.org/abs/1811.08283 · HTML: https://mlsanity.com/paper/1811.08283/

## Key facts

- Cited by 8 papers in the map (data through 14 Oct 2026).
- First posted on arXiv 14 Nov 2018.

## Built on by (most cited first, 8 of 8)

- [Large-Scale Chemical Language Representations Capture Molecular Structure and Properties](https://mlsanity.com/paper/2106.09553/) (2021)
- [Deep Learning Methods for Small Molecule Drug Discovery: A Survey](https://mlsanity.com/paper/2303.00313/) (2023)
- [Molecular Joint Representation Learning via Multi-modal Information](https://mlsanity.com/paper/2211.14042/) (2022)
- [End-to-End Attention-based Image Captioning](https://mlsanity.com/paper/2104.14721/) (2021)
- [Large language models, physics-based modeling, experimental measurements: the trinity of data-scarce learning of polymer properties](https://mlsanity.com/paper/2407.02770/) (2024)
- [Artificial Intelligence in Material Engineering: A review on applications of AI in Material Engineering](https://mlsanity.com/paper/2209.11234/) (2022)
- [A Gaussian process model for chemoinformatics with application to the hazard classification of organic solvents](https://mlsanity.com/paper/2405.09989/) (2024)
- [Random Copolymer inverse design system orienting on Accurate discovering of Antimicrobial peptide-mimetic copolymers](https://mlsanity.com/paper/2212.00023/) (2022)

## Abstract (arXiv)

SMILES is a linear representation of chemical structures which encodes the connection table, and the stereochemistry of a molecule as a line of text with a grammar structure denoting atoms, bonds, rings and chains, and this information can be used to predict chemical properties. Molecular fingerprints are representations of chemical structures, successfully used in similarity search, clustering, classification, drug discovery, and virtual screening and are a standard and computationally efficient abstract representation where structural features are represented as a bit string. Both SMILES and molecular fingerprints are different representations for describing the structure of a molecule. There exist several predictive models for learning chemical properties based on either SMILES or molecular fingerprints. Here, our goal is to build predictive models that can leverage both these molecular representations. In this work, we present CheMixNet -- a set of neural networks for predicting chemical properties from a mixture of features learned from the two molecular representations -- SMILES as sequences and molecular fingerprints as vector inputs. We demonstrate the efficacy of CheMixNet architectures by evaluating on six different datasets. The proposed CheMixNet models not only outperforms the candidate neural architectures such as contemporary fully connected networks that uses molecular fingerprints and 1-D CNN and RNN models trained SMILES sequences, but also other state-of-the-art architectures such as Chemception and Molecular Graph Convolutions.