This node implements a fast descriptor based 3D similarity measure described by Ballester et al ([Bellester, P.J. and Richards, W.G. , Ultrafast shape recognition to search compound databases for similar molecular shapes, Journal of Computational Chemistry, 2007, 28:1711-1723]). The approach calculates the distances of each atom to four specific points: the centroid of the molecule, the atom that is closest to the centroid, the atom that is farthest from the centroid and the atom that is farthest from the previous atom. Thus we get 4 sets of distance distributions. The final descriptor set is generated by evaluating the first three moments of each distance distribution.
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- 3D D-Similarity21 %
- 3D Coordinates11 %
- Molecule to CDK11 %
- RDKit Canon SMILES8 %
- 3D WHIM5 %
Column Appender5 %- SDF Reader5 %
- OpenBabel5 %
- MolConverter3 %
- RDKit Add Conformers3 %
- RDKit Open 3D Alignment3 %
- Load SD-Files (SDF)3 %
- Mol2 Reader3 %
- XLogP3 %
- Structure Sketcher3 %
- RDKit Generate Coords3 %
- RDKit Optimize Geometry3 %
- Molecular Properties3 %
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