ChemRxiv
These are preliminary reports that have not been peer-reviewed. They should not be regarded as conclusive, guide clinical practice/health-related behavior, or be reported in news media as established information. For more information, please see our FAQs.
FragVectorsPreprint.pdf (5.86 MB)

Distributed Representation of Chemical Fragments

preprint
submitted on 19.10.2017, 20:30 and posted on 20.10.2017, 16:01 by Suman Chakravarti

1. Approximately 3.7 million (3,700,103) PubChem compounds were used in training the fragment vectors. Five million compounds (from CID 1 to 5,000,000) were downloaded in SMILES format from PubChem Download Service1 for this purpose. Inorganic part of salts, charges on certain atoms were neutralized, components of mixtures were split and only one chemical from sets of duplicates were kept. Approximately 100,000 chemicals were held out for future needs.

2. Hansen2 and Bursi3 Ames mutagenicity benchmark datasets were used. The data was preprocessed in the same way as the PubChem chemicals, except in the case of duplicates, the compound with the highest mutagenicity value was retained, leaving 6771 compounds (3639 mutagenic and 3132 non-mutagenic).

3. A dataset of 575 compounds was taken from the publication of Ghose et al4 to compute molar refractivity of the fragments.

An in-house dataset5 of 7000 chemicals (Zhu Hao et al) with their experimentally observed LogP was also used to help in computing LogP contribution of the fragments.

1. PubChem Download Service, URL: https://pubchem.ncbi.nlm.nih.gov/pc_fetch/pc_fetch.cgi.

2. Hansen, K., Mika, S., Schroeter, T., Sutter, A., Laak, A. T., Steger-Hartmann, T., Heinrich, N. and Müller, K. R. (2009) Benchmark Data Set for in Silico Prediction of Ames Mutagenicity. J. Chem. Inf. Model. 49, 2077-2081.

3. Kazius, J., McGuire, R., Bursi, R. (2005) Derivation and validation of toxicophores for mutagenicity prediction. J. Med. Chem. 48, 312-320.

4. Ghose, A. K., Crippen, G. M. (1987) Atomic physicochemical parameters for three-dimensional-structure-directed quantitative structure-activity relationships. 2. Modeling dispersive and hydrophobic interactions. J. Chem. Inf. Comput. Sci. 27(1), 21-35.

Zhu, H., Sedykh, A., Chakravarti, S. K., Klopman, G. (2005) A new group contribution approach to the calculation of LogP. Current Computer-Aided Drug Design 1, 3-9.

Funding

No grants

History

Topic

  • Computational chemistry and modeling

Email Address of Submitting Author

chakravarti@multicase.com

Institution

MultiCASE Inc

Country

United States of America

ORCID For Submitting Author

0000-0001-7745-8747

Declaration of Conflict of Interest

The author is employed by MultiCASE Inc.

Exports