Application of the PharmPrint Methodology to Two Protein Kinases-Reference-Cited by-同舟云学术

Application of the PharmPrint Methodology to Two Protein Kinases

Published:2004-06-24 Issue:5 Volume:44 Page:1803-1809
ISSN:0095-2338
Container-title:Journal of Chemical Information and Computer Sciences
language:en
Short-container-title:J. Chem. Inf. Comput. Sci.

Author:

Deanda Felix¹,Stewart Eugene L.¹

Affiliation:

1. Computational, Analytical, and Structural Sciences, GlaxoSmithKline, Five Moore Drive, Research Triangle Park, North Carolina 27709

Publisher

American Chemical Society (ACS)

Subject

Computational Theory and Mathematics,Computer Science Applications,Information Systems,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ci0498968

Reference10 articles.

1. Pharmacophore Fingerprinting. 1. Application to QSAR and Focused Library Design

2. Pharmacophore Fingerprinting. 2. Application to Primary Library Design

3. MDL Drug Data Report (MDDR); MDL Information Systems, Inc. San Leandro, CA, 2000.

4. Evaluation of Quantitative Structure−Activity Relationship Methods for Large-Scale Prediction of Chemicals Binding to the Estrogen Receptor

5. Martin, Y. C. 3D QSAR: Current State, Scope, and Limitations. InPerspectives in Drug Discovery and Design; Kubinyi, H., Folkers, G., Martin, Y. C., Eds.; Kluwer Academic Publishers: London, Great Britain, 1998; Vols. 12/13/14, pp 3−23.

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