All nature-inspired (biogenic-like) compounds; see wiki
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 | 100% |
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Number of Representatives | Not Available |
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 Unix | Download Windows |
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SMILES | Not Available | Not Available | Not Available | Not Available | ||
MOL2 | Not Available | Not Available | Not Available | Not Available | ||
SDF | Not Available | Not Available | Not Available | Not Available | ||
Flexibase | Not Available | Not Available | Not Available | Not Available |