Scientific & technical presentation Standardizer January 2008.

28
Scientific & technical presentation Standardizer January 2008

Transcript of Scientific & technical presentation Standardizer January 2008.

Page 1: Scientific & technical presentation Standardizer January 2008.

Scientific & technical presentation

Standardizer

January 2008

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Why standardize structures?

To recognize the same compound represented with different chemical forms

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Custom transformations

Custom transformationsBuilt-in functions

Availability

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Mesomers

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Tautomersoxo-enol, enamine-imine

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Tautomerspyridone-pyridol

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Solvent removal

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Specific counterion removal

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Built-in functions

Custom transformations

Built-in functionsAvailability

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Fragment removal

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Aromatization

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Dearomatization

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Hydrogen conversionsconverting implicit hydrogens to explicit

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Hydrogen conversionsconverting explicit hydrogens to implicit

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2D Cleaning

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Template-based Cleaning2D-coordinate calculation of macrocycles or bridged systems

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query

Template-based Cleaningaligning search results to the query

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Stereo manipulations removing absolute R/S and E/Z stereo configurations

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Stereo manipulations setting the absolute stereo (chiral) flag for stereo molecules

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Stoichiometry expansionexpanding reaction stoichiometry

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Stoichiometry expansionexpanding salt stoichiometry

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Group manipulation

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Availability

Custom transformations

Built-in functions

Availability

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API and command line interface

Standardizer st = new Standardizer(new File("standardize.xml"));st.standardize(mol);

standardize input.sdf -c config.xml -o output.smiles

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Graphical User Interface

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Features

General– aromatize/dearomatize– add/remove explicit

hydrogens

Transforms– mesomers

– tautomers

– functional groups

Removals– solvents– counterions by list– remove smallest fragment– keep largest fragment– R-groups

Stereo– remove stereo features– set the absolute stereo flag

Sgroups– expand/contract/ungroup– clear/set the absolute stereo

flag– expand stoichiometry of

attached data

Cleaning– partial– full– template based

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Features

Compatible– MOL, SDF, RXN, RDF (V2000/V3000)– SMILES, SMARTS/SMIRKS (recursive too)– MRV, CML, PDB

Flexible– customizable parameters– customizable conversions

Available– full API– command line interface– integration with JChem Base and Cartridge– documentation and examples– free for the Academic community

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