KEGG is a database resource for understanding high-level functions and utilities of the biological system, such as the cell, the organism and the ecosystem, from molecular-level information, especially large-scale molecular datasets generated by genome sequencing and other high-throughput experimental technologies. A recent paper is: Molecular network analysis of diseases and drugs in KEGG. Kanehisa M. Methods Mol Biol. 2013;939:263-75. doi: 10.1007/978-1-62703-107-3_17. We are grateful to the authors for creating and curating KEGG and thank them for making the structures available via PubChem for incorporation into ZINC.
We assess the chemical diversity of a subset by clustering the molecules. First, we sort ligands by increasing molecular weight. Then, we use the SUBSET 1.0 algorithm ( Voigt JH, Bienfait B, Wang S, Nicklaus MC. JCICS, 2001, 41, 702-12) to progressively select compounds that differ from those previously selected by at least the Tanimoto cutoff, using ChemAxon default fingerprints. The resulting representatives have two interesting properties:
|Tanimoto Cutoff Level||60%||70%||80%||90%||100%|
|Number of Representatives||1,733||2,964||4,755||7,316||17,116|
We compute the physical properties of each molecule in the subset, and graph them below.
Download Calculated Physical Properties
|Format||Reference(pH 7)||Mid(pH 6-8)||High(pH 8-9.5)||Low(pH 4.5-6)||Download
|MOL2||All||All||All||All||Single Usual Metals All||Single Usual Metals All|
|SDF||All||All||All||All||Single Usual Metals All||Single Usual Metals All|
|Flexibase||0 1 2 3 4 5 6 7 8 9 10 11 12 13 14||0 1 2||0 1 2||0 1||Single Usual Metals All||Single Usual Metals All|