Open Access Article

This Open Access Article is licensed under a Creative Commons Attribution-Non Commercial 3.0 Unported Licence

J. S.
Smith
^{a},
O.
Isayev
*^{b} and
A. E.
Roitberg
*^{a}
^{a}University of Florida, Department of Chemistry, PO Box 117200, Gainesville, FL, USA 32611-7200. E-mail: roitberg@ufl.edu
^{b}University of North Carolina at Chapel Hill, Division of Chemical Biology and Medicinal Chemistry, UNC Eshelman School of Pharmacy, Chapel Hill, NC, USA 27599. E-mail: olexandr@olexandrisayev.com

Received
31st December 2016
, Accepted 7th February 2017

First published on 8th February 2017

Deep learning is revolutionizing many areas of science and technology, especially image, text, and speech recognition. In this paper, we demonstrate how a deep neural network (NN) trained on quantum mechanical (QM) DFT calculations can learn an accurate and transferable potential for organic molecules. We introduce ANAKIN-ME (Accurate NeurAl networK engINe for Molecular Energies) or ANI for short. ANI is a new method designed with the intent of developing transferable neural network potentials that utilize a highly-modified version of the Behler and Parrinello symmetry functions to build single-atom atomic environment vectors (AEV) as a molecular representation. AEVs provide the ability to train neural networks to data that spans both configurational and conformational space, a feat not previously accomplished on this scale. We utilized ANI to build a potential called ANI-1, which was trained on a subset of the GDB databases with up to 8 heavy atoms in order to predict total energies for organic molecules containing four atom types: H, C, N, and O. To obtain an accelerated but physically relevant sampling of molecular potential surfaces, we also proposed a Normal Mode Sampling (NMS) method for generating molecular conformations. Through a series of case studies, we show that ANI-1 is chemically accurate compared to reference DFT calculations on much larger molecular systems (up to 54 atoms) than those included in the training data set.

In SE methods, some of the computationally expensive integrals are replaced with empirically determined parameters. This results in a very large speed up. However, the accuracy is also substantially degraded compared to high level ab initio methods due to the imposed approximations.^{7} Also, the computational cost of SE methods is still very high compared to classical force fields (FFs), potentially limiting the system size that can be studied.

Classical force fields or empirical interatomic potentials (EPs) simplify the description of interatomic interactions even further by summing components of the bonded, angular, dihedral, and non-bonded contributions fitted to a simple analytical form. EPs can be used in large-scale atomistic simulations with significantly reduced computational cost. More accurate EPs have been long sought after to improve statistical sampling and accuracy of molecular dynamics (MD) and Monte-Carlo (MC) simulations. However, EPs are generally reliable only near equilibrium. These, typically nonreactive empirical potentials, are widely used for drug design, condensed matter and polymer research.^{8–11} Thus, such potentials are usually not applicable for investigations of chemical reactions and transition states. One exception to this is the ReaxFF force field,^{12} which is capable of studying chemical reactions and transition states. However, ReaxFF, like most reactive force fields, must generally be reparameterized from system to system and therefore lacks an “out-of-the-box” level of transferability. Furthermore, each application of FF and EP needs to be carefully pondered, as their accuracy varies among different systems. In fact, performing benchmarks to determine the optimal FF combination for the problem at hand is usually unavoidable. Unfortunately, there are no systematic ways for improving or estimating the transferability of EPs.

Machine learning (ML) is emerging as a powerful approach to construct various forms of transferable^{13–15} and non-transferable^{16,17} atomistic potentials utilizing regression algorithms. ML methods have been successfully applied in a variety of applications in chemistry, including the prediction of reaction pathways,^{18} QM excited state energies,^{19} formation energies,^{20} atomic forces, nuclear magnetic resonance chemical shifts,^{21} and assisting in the search of novel materials.^{22} ML potentials have shown promise in predicting molecular energies with QM accuracy with a speed up of as much as 5 orders of magnitude. The key to transferable methods is finding a correct molecular representation that allows and improves learning in the chosen ML method. As discussed by Behler,^{23} there are three criteria that such representations must adhere to in order to ensure energy conservation and be useful for ML models: they must be rotationally and translationally invariant, the exchange of two identical atoms must yield the same result, and given a set of atomic positions and types the representation must describe a molecule's conformation in a unique way. Several such representations have been developed,^{24–27} but true transferability and extensibility to complex chemical environments, i.e. all degrees of freedom for arbitrary organic molecules, with chemical accuracy has yet to be accomplished.

In 2007, Behler and Parrinello (BP) developed an approximate molecular representation, called symmetry functions (SFs), that take advantage of chemical locality in order to make neural network potentials^{25} (NNPs) transferable. These SFs have been successfully applied to chemical reaction studies for a single chemical system or the study of bulk systems such as water. Bartók et al. also suggested an alternative representation called smooth overlap of atomic positions (SOAP), where the similarity between two neighborhood environments is directly defined.^{28} Very recent work, that introduced a new method known as deep tensor neural networks (DTNNs),^{15} provides further evidence that NNPs can model a general QM molecular potential when trained to a diverse set of molecular energies. So far, the DTNN model was only trained to small test data sets to show the model could predict molecular energies in specific cases, i.e. equilibrium geometries of organic molecules or the energy along the path of short QM molecular dynamics trajectories. In our experience, training to trajectories can bias the fitness of a model to the specific trajectory used for training, especially along short trajectories. Also, DTNN potentials were not shown to predict energies for larger systems than those included in the training set.

Since the introduction of BP SFs, they have been employed in numerous studies where neural network potentials (NNPs) are trained to molecular total energies sampled from MD data to produce a function that can predict total energies of molecular conformations outside of the training set. In general, the NNPs developed in these studies are non-transferable, aside from bulk materials^{25,29} and water cases.^{30} None of the studies that utilize the SFs of Behler and Parrinello have presented a NNP that is truly transferable between complex chemical environments, such as those found in organic molecules, aside from one limited case of all trans-alkanes^{31} where non-equilibrium structures and potential surface smoothness are not considered. We suggest two reasons for the lack of transferability of the SFs. Firstly, as originally defined, SFs lack the functional form to create recognizable features (spatial arrangements of atoms found in common organic molecules, e.g. a benzene ring, alkenes, functional groups) in the molecular representation, a problem that can prevent a neural network from learning interactions in one molecule and then transferring its knowledge to another molecule upon prediction. Secondly, the SFs have limited atomic number differentiation, which empirically hinders training in complex chemical environments. In general, the combination of these reasons limits the original SFs to studies of either chemically symmetric systems with one or two atom types or very small single molecule data sets.

In this work, we present a transferable deep learning^{32,33} potential that is applicable to complex and diverse molecular systems well beyond the training data set. We introduce ANAKIN-ME (Accurate NeurAl networK engINe for Molecular Energies) or ANI for short. ANI is a new method for developing NNPs that utilizes a modified version of the original SFs to build single-atom atomic environment vectors (AEVs) as a molecular representation. AEVs solve the transferability problems that hindered the original Behler and Parrinello SFs in complex chemical environments. With AEVs, the next goal of ANI becomes to sample a statistically diverse set of molecular interactions, within a domain of interest, during the training of an ANI class “potential” to produce a transferable NNP. This requires a very large data set that spans molecular conformational and configurational space, simultaneously. An ANI potential trained in this way is well suited to predict energies for molecules within the desired training set domain (organic molecules in this paper), which is shown to be extensible to larger molecules than those included in the training set.

ANI uses an inherently parallel computational algorithm. It is implemented in an in-house software package, called NeuroChem, which takes advantage of the computational power of graphics processing units (GPU) to accelerate the training, testing, and prediction of molecular total energies via an ANI potential. Finally, we show the accuracy of ANI-1 compared to its reference DFT level of theory and, for context, three popular semi-empirical QM methods, AM1, PM6, and DFTB, through four case studies. All case studies only consider larger organic molecules than ANI-1 was trained to predict energies for, providing strong evidence of the transferability of ANI-1.

(1) |

In this way, E_{T} has the form of a sum over all i “atomic contributions” to the total energy. Aside from transferability, an added advantage of this simple summation is that it allows for a near linear scaling in computational complexity with added cores or GPUs, up to the number of atoms in the system of interest.

The _{i}^{X} vectors are key to allowing this functional form of the total energy to be utilized. For an atom i, _{i}^{X} is designed to give a numerical representation, accounting for both radial and angular features, of i's local chemical environment. The local atomic environment approximation is achieved with a piece-wise cutoff function:

(2) |

To probe the local radial environment for an atom i, the following radial symmetry function, introduced by Behler and Parrinello, produces radial elements, G^{R}_{m} of _{i}^{X},

(3) |

The index m is over a set of η and R_{s} parameters. The parameter η is used to change the width of the Gaussian distribution while the purpose of R_{s} is to shift the center of the peak. In an ANI potential, only a single η is used to produce thin Gaussian peaks and multiple R_{s} are used to probe outward from the atomic center. The reasoning behind this specific use of parameters is two-fold: firstly, when probing with many small η parameters, vector elements can grow to very large values, which are detrimental to the training of NNPs. Secondly, using R_{s} in this manner allows the probing of very specific regions of the radial environment, which helps with transferability. G^{R}_{m}, for a set of M = {m_{1}, m_{2}, m_{3},…} = {(η_{1}, R_{s1}), (η_{2}, R_{s2}), (η_{3}, R_{s3}),…} parameters, is plotted in Fig. 2A. M consist of a constant η for all m and multiple R_{s} parameters to show a visualization of how each vector element probes its own distinct region of an atom's radial environment.

We made two modifications to the original version of Behler and Parrinello's angular symmetry function to produce one better suited to probing the local angular environment of complex chemical systems. The first addition is θ_{s}, which allows an arbitrary number of shifts in the angular environment, and the second is a modified exponential factor that allows an R_{s} parameter to be added. The R_{s} addition allows the angular environment to be considered within radial shells based on the average of the distance from the neighboring atoms. The effect of these two changes is that AEV elements are generally smaller because they overlap atoms in different angular regions less and they provide a distinctive image of various molecular features, a property that assists neural networks in learning the energetics of specific bonding patterns, ring patterns, functional groups, or other molecular features.

Given atoms i, j, and k, an angle θ_{ijk}, centered on atom i, is computed along with two distances R_{ij} and R_{ik}. A single element, of _{i}^{X}, to probe the angular environment of atom i, takes the form of a sum over all j and k neighboring atom pairs, of the product of a radial and an angular factor,

(4) |

The Gaussian factor combined with the cutoff functions, like the radial symmetry functions, allows chemical locality to be exploited in the angular symmetry functions. In this case, the index m is over four separate parameters: ζ, θ_{s}, η, and R_{s}. η and R_{s} serve a similar purpose as in eqn (3). Applying a θ_{s} parameter allows probing of specific regions of the angular environment in a similar way as is accomplished with R_{s} in the radial part. Also, ζ changes the width of the peaks in the angular environment. for several m are plotted in Fig. 2B while the original angular function is plotted in Fig. 2C. With the original Behler and Parrinello angular function, only two shifting values were possible in the angular environment, 0 and π. The modified angular function allows an arbitrary number to be chosen, allowing for better resolution of the angular environment. As with its radial analog, this helps to keep the elements of _{i}^{X} small for better NNP performance and allows probing of specific regions of the angular chemical environment.

2.2.1 Atomic number differentiated atomic environment vector.
In this work, we differentiate between atomic numbers in the AEV by supplying a radial part for each atomic number and an angular part for each atomic number pair in the local chemical environment. The original BPSFs treat all atoms identically in the summation over all atoms, and thus individual atomic number specific NNPs are unable to distinguish between a carbon, hydrogen, or any other atom type at some distance. Through empirical evidence, provided in Table S4 of the ESI,† we have found that discriminating between atomic numbers allows for training to much lower error on diverse multi-molecule training sets and permits better transferability.

For AEVs built from N atom types, this leads to N radial sub-AEVs and N(N + 1)/2 angular sub-AEVs. ESI Fig. S1† gives an example of an atomic number differentiated AEV for the carbon atom in formic acid with only 8 radial symmetry functions and 8 angular symmetry functions. The figure shows an overlay of two AEVs each representing a different C–O–H angle with the rest of the structure frozen. From this figure, it is easy to identify the different features which represent formic acid and it also provides clear information on the conformation of the molecule. It is this clearly defined “fingerprint” that allows the modified symmetry functions to perform well in such diverse chemical environments.

To carry out normal mode sampling on an energy minimized molecule of N_{a} atoms, first a set of N_{f} normal mode coordinates, Q = {q_{1}, q_{2}, q_{3},…q_{Nf}}, is computed at the desired ab initio level of theory, where N_{f} = 3N_{a} − 5 for linear molecules and N_{f} = 3N_{a} − 6 for all others. The corresponding force constants, K = {K_{1}, K_{2}, K_{3},…,K_{Nf}}, are obtained alongside Q. Then a set of N_{f} uniformly distributed pseudo-random numbers, c_{i}, are generated such that is in the range [0, 1]. Next, a displacement, R_{i}, for each normal mode coordinate is computed by setting a harmonic potential equal to the c_{i} scaled average energy of the system of particles at some temperature, T. Solving for the displacement gives:

(5) |

The choice of temperature is dependent on the intended use of the ANI potential being trained. However, it should be noted that this method of sampling the potential surface of a molecule is simply an approximation for generating structures. In practice, NMS works best when generating windows of the potential surface of many molecules to be used in the training of the same ANI potential. The reasoning behind this is as follows: if any interactions are missed or not sampled well by NMS, it is possible that other molecules in the data set contain the same or similar interactions. Therefore, the accuracy of using such a sampling method is dependent on not only the number of points per window but also the number of distinct molecules included in the data set.

The ANI-1 data set employed in this work, was generated from a subset of the GDB-11 database containing molecules without the fluorine atom. This leaves only molecules with H, C, N, and O after hydrogens are added with RDKit. Also, given the sheer number of molecules (40.3 million) in the GDB-11 database, as of the time of this article, only reference data for molecules up to 8 atoms of C, N, and O have been computed. In total, 57951 molecules are included in our current data set, the ANI-1 data set. A breakdown of how many molecules are included from each GDB-11 subset is given in ESI Table S1.† All energies are computed with neutral molecules in the singlet spin state.

In this work, we propose a Normal Mode Sampling (NMS) method that works by calculating the normal modes of a molecule, then randomly perturbing the equilibrium structure along these normal modes out to a maximum energy (see Section 2.3 for details on NMS). The ANI-1 data set was generated by applying NMS to every molecule with 8 or less heavy atoms in the GDB-11 database. Using the wB97X^{39} DFT functional with the 6-31G(d) basis set in the Gaussian 09 electronic structure package,^{46} the following steps are followed to generate the data set:

(1) Convert SMILES strings to 3D structures and add hydrogens to fill valence orbitals.

(2) Optimize each molecule in the database using tight convergence criteria.

(3) Generate normal modes for each optimized molecule with an ultra-fine DFT grid.

(4) Use the NMS method to generate K structures for each molecule in the database. The exact number of structures per molecule is determined using K = S(3N − 6). S is an empirically determined value dependent on the number of heavy atoms in the molecule and N is the total number of atoms in the molecule, including hydrogens.

(5) Calculate single point energies for each of the generated structures.

Using this procedure to generate the ANI-1 data set results in molecular energies for a total of ∼17.2 million conformations generated from ∼58k small molecules. For each molecule's individual set of random conformations, 80% is used for training, while 10% is used for each validation and testing of the ANI-1 model.

For practical considerations, the value S from step 3 is large (about 500) for very small molecules and is gradually reduced as the number of heavy atoms, and molecule diversity, grows. Table S1 in the ESI† shows the parameters used in the production of the ANI-1 data set, including the S values used for each GDB-11 database subset as well as the per atom test set RMSE of an ANI potential vs. DFT for each subset.

Finding a good set of atomic environment vector () parameters to compute molecular representations plays a major role in how well the ANI-1 potential trains and performs. Too many parameters will lead to networks that are very large, and thus hard to train. Too few parameters result in low resolution of the local chemical environment, which is detrimental to transferability and training in general. For the ANI-1 potential, 32 evenly spaced radial shifting parameters are used for the radial part of and a total of 8 radial and 8 angular shifting parameters are used for the angular part. The specific AEV parameters were chosen with a few goals in mind: to minimize the size of the AEV, to maximize the resolution of the local atomic environments, and to cover all space within the cutoff radius provided. Keeping these goals in mind the choice of parameters can be automated to simply chose multiple R_{s} and θ_{s} parameters equally spaced and setting the η and ζ parameters such that one function overlaps with its neighboring function slightly, as shown in Fig. 2A and B. With four atom types, this leads to a total of 768 elements in . The cutoff radii of 4.6 Å for the radial and 3.1 Å for the angular symmetry functions were chosen based on the distribution of atomic distances and an assumption that angular environments are less sampled in the ANI-1 data set, empirical testing verified this to be the case.

The choice of network architecture also plays a major role in how well a potential performs. Too small of a network reduces the flexibility of the function which can hinder performance and too large can lead to bad generalization across structures due to overtraining, especially on small data sets. With larger data sets, a bigger and more flexible network can be used to yield better results. We empirically tested many network architectures. Generally, 3 to 4 hidden layer networks with between 32 and 128 nodes per layer performed the best. The best ANI potential (ANI-1), employed in this work, was trained to 80% of the 17 + M data points, and has the following pyramidal architecture: 768:128:128:64:1. That is, 768 input values followed by a 128-node hidden layer followed by another hidden layer with 128 nodes, a 64-node hidden layer, and finally a single output node for a total of 124033 optimizable parameters per each individual atomic number neural network potential. All hidden layer nodes use a Gaussian activation function^{48} while the output node uses a linear activation function. The weights are randomly initialized from a normal distribution in the range (−1/d, 1/d), where d is the number of inputs into the node. The neural network bias parameters are all initialized to zero.

To train the weights, the program randomly samples structures from the training set in a mini-batch of 1024 molecules. Next a cost derivative w.r.t. each weight is calculated through back-propagation from the exponential cost function:^{49}

(6) |

We performed extensive benchmark and case studies to estimate the accuracy of the ANI-1 potential compared to DFT reference calculations. As baselines, in the first test case we compare ANI-1 to a sorted coulomb matrix^{13} (CM) molecular representation with a multilayer perceptron (MLP) neural network model, baseline 1, and to an ANI type neural network model trained where the AEVs are not type differentiated, baseline 2. MLP's were chosen in baseline 1 because of their ability to train to very large data sets via batched learning. Table S4 in the ESI† provides details of these baselines for comparison to the ANI method.

To highlight the true transferability of the ANI-1 potential, all molecules considered in the following test cases contain greater than eight heavy atoms. The atom counts for these test systems range from 10 to 24 heavy atoms up to a total of 53 atoms. Firstly, we analyzed ANI-1's overall performance, goodness of fit, and transferability to non-minimized structures with a total of 8245 conformations generated using NMS on 134 randomly selected molecules from GDB-11, each with 10 heavy atoms. In the second case study, we look at the accuracy of ANI-1 in predicting the relative energies of DFT energy minimized C_{10}H_{20} isomers with respect to the lowest energy isomer. Thirdly, energy differences are compared for energy minimized conformers of the drug molecule retinol. And finally, four rigid scans, a bond stretch, an angle bend, and two dihedral rotations on relatively large drug molecules are carried out on ANI-1 and compared with reference DFT results. For comparison, we also show the performance of popular DFTB, PM6, and AM1 semi-empirical methods in all the test cases presented.

Fig. 4A is a correlation plot of the computed ANI-1 energies, E_{cmp}, vs. the DFT reference energies, E_{ref}. The ANI-1 potential achieves an RMSE of only 1.8 kcal mol^{−1} over the entire random sampling. Fig. 4B–D provides the same comparison but for popular semi-empirical methods to the DFT reference energies. If only relative energies within 30.0 kcal mol^{−1} of the minimum energy are considered, the ANI-1, DFTB, PM6, and AM1 methods obtain an RMSE of 0.6, 2.4, 3.6, and 4.2 kcal mol^{−1}, respectively. ESI Table S3† lists the total energy and relative energy error of the ANI-1 potential as an energy cap, E^{cap}, is lowered until finally only minimum energy structures are considered.

Fig. 4E shows how the RMSE of an ANI potential to reference DFT decreases as the number of distinct molecules grows in the training set. From this plot, it is clear that the addition of more data leads to better fits, with the largest and most diverse data set achieving an RMSE of just 1.8 kcal mol^{−1}. Inclusion of molecules with 7 heavy atoms, mostly mono-substituted aromatic compounds, yields a dramatic reduction of the RMSE. This figure, along with Fig. 3, stands as evidence that increasing the size and diversity of an ANI training set leads to better fitness and transferability, meaning future parameterization will yield even better results.

The total energies produced by ANI-1, baseline 1, and baseline 2 for the GDB-10 test set are also compared. ANI-1, when trained on the full ANI-1 training set, achieves a total energy RMSE of 1.9 kcal mol^{−1} while baseline 1 and baseline 2 achieve a RMSE of 493.7 kcal mol^{−1} and 6.6 kcal mol^{−1}, respectively. While the baselines perform better on the ANI-1 test set, as seen in ESI Fig. S4,† their performance on the GDB-10 test set shows that both suffer from an inability to extend their learned interactions to larger molecules. For baseline 1, this is caused by the coulomb matrix having elements which remain a constant zero throughout training, yet when a larger molecule is tested on it, those elements have non-zero values. These non-zero values are then fed into untrained network parameters, which yields arbitrary results. For baseline 2, the problem comes from the fact that the AEVs have an inability to differentiate between atom types, creating confusion during the learning process.

Fig. 5 shows that the ANI-1 potential properly predicts the minimum energy structure and continues to match the energies of the ring containing structures, indices 1–4 on the x-axis, with a very low error and with proper ordering. Also, when moving from the ringed structures to the linear alkenes, index 4 to 5, the ANI-1 potential approximates the DFT energy difference between these two classes of molecules very well. The linear alkanes, indices 5–13, fit very well to the DFT energies. Overall the ANI-1 potential achieves an RMSE of 0.2 kcal mol^{−1}. In contrast, both DFTB and PM6 methods incorrectly predict the relative stability of ring containing structures. Energies of isomers 5–13 are systematically underestimated by about 6–7 kcal mol^{−1}.

Fig. 6A shows ΔE between each retinol conformer for DFT while B shows the same for ANI-1 and C for DFTB. Aside from some minor shading differences, the comparison of A and B clearly shows how well the ANI-1 energy differences match that of the DFT calculations. Fig. 6D and E contain |ΔΔE| plots corresponding to A vs. B and A vs. C, respectively, and shows that the ANI-1 potential can predict DFT energy differences of these large structural changes to a very low error. In total, ANI-1 and DFTB achieve a RMSE to the DFT ΔE of 0.6 kcal mol^{−1} and 1.2 kcal mol^{−1}, respectively. However, DFTB severely over estimates energies of conformers 2 and 7.

Fig. 7A shows a bond stretch, from 1.2 Å to 1.8 Å, of the N–C bond (labeled 1 and 2) in the analgesic drug molecule fentanyl.^{52} The bond equilibrium distance was calculated separately for each method and was found to be 1.3 Å for DFT, 1.4 Å for ANI-1, 1.4 Å for DFTB, and 1.4 Å for PM6. Fig. 7B presents an angle bend, from 90.0° to 135.0°, for the C–C–C angle labeled 1–2–3 in the structure of fentanyl included within the plot. As with the bond stretch, the ANI-1 potential produces an angle bend potential surface with a very low RMSE of only 0.4 kcal mol^{−1} while maintaining a very smooth curvature for accurate force calculations. ANI-1 produces an angle bend potential with an equilibrium angle ∼1.0° from the DFT equilibrium. PM6 and DFTB produce equilibrium structures at ∼1.1° and ∼0.8°, respectively, from the DFT calculation.

Finally, Fig. 7C and D depict rotations of the dihedral angles labeled in the two figures. Fig. 7C shows a C–C–C–C dihedral rotation potential in the molecule 4-cyclohexyl-1-butanol, while Fig. 7D is for an N–C–C–C dihedral angle in the drug molecule called lisdexamfetamine.^{53} The ANI-1 potential manages to capture all minima to within 3.0° of the DFT potentials for both plots, which is better or comparable to the semi-empirical methods. As expected both semi-empirical methods severely underestimate dihedral rotation barriers, and in the case of lisdexamfetamine give an unrealistic shape of potential surface.

Again, both figures not only fit well to the potential surface but model it very well by reproducing the shape and smoothness of the surface. This fact shows that the ANI-1 potential does produce a smooth potential, one that could provide forces, for use in molecular dynamics simulations or optimization problems.

As the results clearly show, the ANI method is a potential game-changer for molecular simulation. Even the current version, ANI-1, is more accurate vs. the reference DFT level of theory in the provided test cases than DFTB, and PM6, two of the most widely used semi-empirical QM methods. Besides being accurate, a single point energy, and eventually forces, can be calculated as many as six orders of magnitude faster than through DFT. Empirical evidence shows the computational scaling per atom of the method is roughly equivalent to a classical force field for very large molecules.

The accuracy of the ANI method is heavily dependent on the data used during training. Thus, continuing to augment the ANI-1 data set with new molecules and including more atomic numbers will improve the accuracy of the trained ANI potential further as well as extend the method to new chemical environments.

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## Footnote |

† Electronic supplementary information (ESI) available. See DOI: 10.1039/c6sc05720a |

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