Fingerprints

Input Ports

Table containing molecular structure based on which the fingerprints should be calculated.

Output Ports

As input but with an additional column.

Popular Predecessors

• SDF Reader10 %
• Molecule to CDK5 %
• Rule Engine3 %
• Molecule Type Cast3 %
• Reference Row Filter2 %
• Java Snippet (simple)2 %
• Row Filter (deprecated)2 %
• CDK to Molecule2 %
• RDKit Canon SMILES1 %
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• String to Molecule1 %
• Table Reader1 %
• Smiles Directory Reader1 %
• Fingerprints1 %
• Substructure Search1 %
• 2D Coordinates1 %
• 3D Coordinates1 %
• Canvas Molecular Descriptors1 %
• Canonical SMILES1 %
• Table Creator1 %
• Missing Value1 %
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• Concatenate< 1 %
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• Partitioning< 1 %
• Column Rename< 1 %
• RowID< 1 %
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• Connectivity< 1 %
• Molecular Properties< 1 %
• Fingerprint Similarity< 1 %
• Structure Sketcher< 1 %
• RDKit Descriptor Calculation< 1 %
• RDKit Find Murcko Scaffolds< 1 %
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• Molecule Converter (Naomi)< 1 %
• CSV Reader< 1 %
• Duplicate Row Filter< 1 %
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• Constant Value Column Filter< 1 %
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• k-Means< 1 %
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• String Manipulation< 1 %
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• Maestro Molecular Properties< 1 %
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• RDKit To InChI< 1 %
• File Reader< 1 %
• Murcko Scaffold< 1 %
• Valence Checker< 1 %
• MAE-to-Smiles< 1 %
• Fingerprints Expander< 1 %
• Statistics< 1 %
• Counter Generation< 1 %
• Excel Reader (XLS)< 1 %
• Python Script (2⇒1)< 1 %
• Mass Calculator< 1 %
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• Molecule-to-MAE< 1 %
• Smiles Reader< 1 %
• PDB Describe Heterogens< 1 %
• PDB Connector< 1 %
• MolImporter< 1 %
• Standardizer< 1 %
• Fingerprint Similarity< 1 %
• CSV Reader< 1 %
• Java Snippet< 1 %
• Recursive Loop End< 1 %
• Category to Number< 1 %
• Column Merger< 1 %
• Correlation Filter< 1 %
• Joiner< 1 %
• Normalizer (Apply)< 1 %
• Table Transposer< 1 %
• Merge Variables< 1 %
• SDF Inserter< 1 %
• Excel Reader (XLS)< 1 %
• Single Selection (legacy)< 1 %
• Element Filter< 1 %
• Symmetry< 1 %
• CIR< 1 %
• Get Molecule From Clipboard< 1 %
• Read MDB< 1 %
• Molecule Properties< 1 %
• Read ASCII< 1 %
• Organic Splitter< 1 %
• MCS Scaffold Finder< 1 %
• PDB Reader< 1 %
• String-to-Type< 1 %
• Speedy SMILES Remove Dummy Atoms Filter< 1 %
• Speedy SMILES Organic Subset Molecules Filter< 1 %
• Speedy SMILES De-salt< 1 %
• Speedy SMILES Enumerate Stereoisomers< 1 %
• Speedy SMILES Strip Stereochemistry< 1 %
• Load Local Mol2 Files< 1 %
• Load SD-Files (SDF)< 1 %
• Benchmark Start< 1 %
• Chemical Fingerprint< 1 %
• Interaction Fingerprint Retriever< 1 %
• ChemSpider< 1 %
• Chemical Sketcher< 1 %
• Chemical Structures File Reader< 1 %
• Strings to Binary Objects< 1 %
• Try (Data Ports)< 1 %
• Variable to Table Row< 1 %
• Database Reader< 1 %
• MDS (DistMatrix)< 1 %
• Perl Scripting< 1 %
• Auto-Binner< 1 %
• Binner (Dictionary)< 1 %
• Reference Row Splitter< 1 %
• Normalizer< 1 %
• SDF Extractor< 1 %
• SDF Stripper< 1 %
• Molfile Reader< 1 %
• Fingerprint Bayesian Learner< 1 %
• DB Reader< 1 %
• DB Query Reader< 1 %
• Call Local Workflow (Row Based)< 1 %
• MoSS MCSS Molecule Similarity< 1 %
• Column Filter (legacy)< 1 %
• Table View (JavaScript)< 1 %
• Structure Converter< 1 %
• Ceres Draw< 1 %
• Atom Signatures< 1 %
• Depiction< 1 %
• 3D D-Similarity< 1 %
• Sum Formula< 1 %
• RDKit Calculate Charges< 1 %
• RDKit Diversity Picker< 1 %
• RDKit Fingerprint Reader< 1 %
• RDKit Count-Based Fingerprint< 1 %
• RDKit Remove Hs< 1 %
• CIR< 1 %
• ChEMBLdb Connector< 1 %
• Speedy SMILES Heavy Atom Count (HAC)< 1 %
• Fingerprint From String< 1 %
• Fast Tanimoto< 1 %
• Regex Substring< 1 %
• Loop End< 1 %
• PCA< 1 %
• String to Number< 1 %
• Table Validator< 1 %
• Double to Integer< 1 %
• Missing Value Column Filter< 1 %
• Row Sampling< 1 %
• Shuffle< 1 %
• Column Splitter< 1 %
• Table Difference Finder< 1 %
• Data Generator< 1 %
• Color Manager< 1 %
• Fingerprint Bayesian Predictor< 1 %
• 3D WHIM< 1 %
• RDKit Molecule Highlighting< 1 %
• RDKit Kekulizer< 1 %

Popular Successors

• Fingerprint Similarity13 %
• Expand Bit Vector4 %
• Fingerprints Expander4 %
• Number To String3 %
• Atom Signatures2 %
• Show all 238 recommendations