Applying molecular similarity used for evaluating the accuracy of retention index predictions in gas chromatography using deep learning

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When predicting retention indices using deep learning, there is usually no way to assess the reliability of the prediction for a particular molecule. In this work, using stationary phases based on polyethylene glycol and the NIST 17 database as an example, it is shown that, on average, the closer the molecule in the training data set is to the compound being predicted, the more accurate the prediction. Tanimoto similarity of “molecular fingerprints” ECFP is the most appropriate molecular similarity calculation algorithm for this problem among the four considered. It is shown that for a number of transformation products of unsymmetrical dimethylhydrazine, whose structure was established using this prediction, it could be very unreliable.

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作者简介

D. Matyushin

A. N. Frumkin Institute of Physical Chemistry and Electrochemistry of the Russian Academy of Sciences

Email: shonastya@yandex.ru
俄罗斯联邦, Moscow, 119071

A. Sholokhova

A. N. Frumkin Institute of Physical Chemistry and Electrochemistry of the Russian Academy of Sciences

编辑信件的主要联系方式.
Email: shonastya@yandex.ru
俄罗斯联邦, Moscow, 119071

M. Khrisanfov

A. N. Frumkin Institute of Physical Chemistry and Electrochemistry of the Russian Academy of Sciences; M. V. Lomonosov Moscow State University

Email: shonastya@yandex.ru
俄罗斯联邦, Moscow, 119071; Moscow, 119991

S. Borovikova

A. N. Frumkin Institute of Physical Chemistry and Electrochemistry of the Russian Academy of Sciences

Email: shonastya@yandex.ru
俄罗斯联邦, Moscow, 119071

参考

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2. Fig. 1. Distribution of the number of molecules N in the NIST 17 retention index database (polar stationary phases) according to Smax values (maximum molecular similarity value for all pairs including the molecule in question and molecules from the training set) for the four molecular similarity calculation methods. Dark gray indicates “poorly predicted molecules” (absolute prediction error greater than 100), light gray indicates the remaining molecules.

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3. Fig. 2. Dependence of the total number of molecules N (solid circles and lines) and the fraction of “poorly predicted molecules” (absolute prediction error greater than 100) F (rectangles) on the value of Smax (maximum molecular similarity value for all pairs including the considered molecule and molecules from the training set).

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4. Fig. 3. Distribution of the number of molecules N over the absolute prediction error for different values of Smax (maximum molecular similarity value for all pairs including the molecule under consideration and molecules from the training set) for the two molecular similarity calculation methods.

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5. Fig. 4. ROC curves (specificity-sensitivity curves) for predicting whether a molecule is “poorly predicted” (absolute prediction error greater than 100) using different molecular similarity calculation algorithms. Curves for algorithms for which the area under the curve differs by no more than 0.02 are labeled with a single line type for readability.

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6. Fig. 5. Structures of the transformation products of unsymmetrical dimethylhydrazine proposed in [9] and Smax values (molecular similarity value between the molecule under consideration and the closest molecule from the training set) for each of them. ECFP molecular similarity calculation method.

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