Identifier Index

[ A B C D E F G H I J K L M N O P Q R S T U V W X Y Z _ ]

_

__add__() (in DiscreteValueVect)	__instance_size__ (in SmilesParserParams)	__sub__() (in UIntSparseIntVect)
__add__() (in ExplicitBitVect)	__instance_size__ (in TDTMolSupplier)	__sub__() (in ULongSparseIntVect)
__add__() (in IntSparseIntVect)	__instance_size__ (in AdjustQueryParameters)	__sub__() (in Point2D)
__add__() (in LongSparseIntVect)	__instance_size__ (in DiscreteValueVect)	__sub__() (in Point3D)
__add__() (in UIntSparseIntVect)	__instance_size__ (in ExplicitBitVect)	__sub__() (in PointND)
__add__() (in ULongSparseIntVect)	__instance_size__ (in FPBReader)	__tablename__ (in Compound)
__add__() (in Point2D)	__instance_size__ (in IntSparseIntVect)	__test__ (in rdkit.Dbase.StorageUtils)
__add__() (in Point3D)	__instance_size__ (in LongSparseIntVect)	__test__ (in rdkit.VLib.NodeLib.SmartsRemover)
__add__() (in PointND)	__instance_size__ (in MultiFPBReader)	__version_info (in rdkit.Chem.fmcs.fmcs')
__and__() (in DiscreteValueVect)	__instance_size__ (in SparseBitVect)	__VERSION_STRING (in rdkit.ML.AnalyzeComposite)
__and__() (in ExplicitBitVect)	__instance_size__ (in UIntSparseIntVect)	__VERSION_STRING (in rdkit.ML.BuildComposite)
__and__() (in IntSparseIntVect)	__instance_size__ (in ULongSparseIntVect)	__VERSION_STRING (in rdkit.ML.EnrichPlot)
__and__() (in LongSparseIntVect)	__instance_size__ (in Point2D)	__VERSION_STRING (in rdkit.ML.GrowComposite)
__and__() (in SparseBitVect)	__instance_size__ (in Point3D)	__VERSION_STRING (in rdkit.ML.ScreenComposite)
__and__() (in UIntSparseIntVect)	__instance_size__ (in PointND)	__warningregistry__ (in rdkit.Chem.FastSDMolSupplier)
__and__() (in ULongSparseIntVect)	__instance_size__ (in UniformGrid3D_)	__xor__() (in ExplicitBitVect)
__bool__() (in EnumerateLibraryBase)	__instance_size__ (in BitCorrMatGenerator)	__xor__() (in SparseBitVect)
__bool__() (in EnumerationStrategyBase)	__instance_size__ (in InfoBitRanker)	_addCanvasText1() (in Canvas)
__call__() (in PropertyFunctor)	__instance_size__ (in HierarchicalClusterPicker)	_addCanvasText2() (in Canvas)
__call__() (in SaltRemover)	__instance_size__ (in MaxMinPicker)	_addCoarseAndMediumGrids() (in SubshapeAligner)
__call__() (in SubshapeAligner)	__instance_size__ (in _listSt6vectorIiSaIiEE)	_AddDataToDb() (in rdkit.Dbase.DbUtils)
__call__() (in SubshapeBuilder)	__instance_size__ (in _listi)	_AdjustColHeadings() (in rdkit.Dbase.DbUtils)
__call__() (in PropertyFunctor)	__instance_size__ (in _vectSs)	_ApplyNodeScales() (in rdkit.ML.DecTree.TreeVis)
__call__() (in PythonPropertyFunctor)	__instance_size__ (in _vectSt6vectorIdSaIdEE)	_asdict() (in InchiResult)
__call__() (in CDXImageTransformer)	__instance_size__ (in _vectSt6vectorIiSaIiEE)	_asdict() (in MolKeyResult)
__call__() (in CactvsImageTransformer)	__instance_size__ (in _vectSt6vectorIjSaIjEE)	_asdict() (in ADSparameter)
__call__() (in RDImageTransformer)	__instance_size__ (in _vectd)	_asdict() (in QEDproperties)
__call__() (in ReportLabImageTransformer)	__instance_size__ (in _vecti)	_asdict() (in Atom)
__call__() (in ActFunc)	__instance_size__ (in _vectj)	_asdict() (in Bond)
__cmp__() (in Cluster)	__invert__() (in ExplicitBitVect)	_asdict() (in DirectedEdge)
__cmp__() (in QuantTreeNode)	__invert__() (in SparseBitVect)	_asdict() (in EnumerationMolecule)
__cmp__() (in TreeNode)	__ior__() (in UniformGrid3D_)	_asdict() (in OutgoingEdge)
__contains__() (in IntStringMap)	__isub__() (in DiscreteValueVect)	_asdict() (in Subgraph)
__contains__() (in starting_from)	__isub__() (in IntSparseIntVect)	_AssignClusterLocations() (in ClusterRenderer)
__contains__() (in ROMolList)	__isub__() (in LongSparseIntVect)	_AssignPointLocations() (in ClusterRenderer)
__contains__() (in VectMolVect)	__isub__() (in UIntSparseIntVect)	_AssignSymmetryClasses() (in rdkit.Chem.GraphDescriptors)
__contains__() (in VectSizeT)	__isub__() (in ULongSparseIntVect)	_atom_class_dict (in rdkit.Chem.fmcs.fmcs')
__contains__() (in VectorOfStringVectors)	__isub__() (in Point2D)	_atom_smarts_no_aromaticity (in rdkit.Chem.fmcs.fmcs')
__contains__() (in MOL_SPTR_VECT)	__isub__() (in Point3D)	_AtomFlipper (in rdkit.Chem.EnumerateStereoisomers)
__contains__() (in _listPN5RDKit4AtomE)	__isub__() (in PointND)	_available_closures (in rdkit.Chem.fmcs.fmcs')
__contains__() (in _listPN5RDKit4BondE)	__isub__() (in UniformGrid3D_)	_availTransforms (in rdkit.ML.Data.Transforms)
__contains__() (in FilterCatalogEntryList)	__iter__() (in IntStringMap)	_BondFlipper (in rdkit.Chem.EnumerateStereoisomers)
__contains__() (in MatchTypeVect)	__iter__() (in _RangeBitsGenerator)	_BreadthFirstSplit() (in rdkit.ML.Cluster.ClusterUtils)
__contains__() (in MolList)	__iter__() (in _UniqueRandomBitsGenerator)	_buildCanonArrowhead() (in rdkit.Chem.Features.ShowFeats)
__contains__() (in VectFilterMatch)	__iter__() (in ThresholdScreener)	_BuildFp() (in DbFpSupplier)
__copy__() (in CartesianProductStrategy)	__iter__() (in TopNScreener)	_BuildMol() (in DbMolSupplier)
__copy__() (in EnumerationStrategyBase)	__iter__() (in MolSupplier)	_bulkConvert (in rdkit.Chem.Lipinski)
__copy__() (in EvenSamplePairsStrategy)	__iter__() (in EnumerateLibraryBase)	_CalcAsphericity_version (in rdkit.Chem.rdMolDescriptors)
__copy__() (in RandomSampleAllBBsStrategy)	__iter__() (in ROMolList)	_CalcAUTOCORR2D_version (in rdkit.Chem.rdMolDescriptors)
__copy__() (in RandomSampleStrategy)	__iter__() (in VectMolVect)	_CalcAUTOCORR3D_version (in rdkit.Chem.rdMolDescriptors)
__copy__() (in Mol)	__iter__() (in VectSizeT)	_CalcChi0n_version (in rdkit.Chem.rdMolDescriptors)
__copy__() (in RWMol)	__iter__() (in VectorOfStringVectors)	_CalcChi0v_version (in rdkit.Chem.rdMolDescriptors)
__copyAll() (in rdkit.Chem.FeatMaps.FeatMapUtils)	__iter__() (in MOL_SPTR_VECT)	_CalcChi1n_version (in rdkit.Chem.rdMolDescriptors)
__DEBUG (in rdkit.ML.Descriptors.Parser)	__iter__() (in ResonanceMolSupplier)	_CalcChi1v_version (in rdkit.Chem.rdMolDescriptors)
__deepcopy__() (in Mol)	__iter__() (in _ROAtomSeq)	_CalcChi2n_version (in rdkit.Chem.rdMolDescriptors)
__deepcopy__() (in RWMol)	__iter__() (in _ROQAtomSeq)	_CalcChi2v_version (in rdkit.Chem.rdMolDescriptors)
__del__() (in Displayable)	__iter__() (in _listPN5RDKit4AtomE)	_CalcChi3n_version (in rdkit.Chem.rdMolDescriptors)
__del__() (in RecapHierarchyNode)	__iter__() (in _listPN5RDKit4BondE)	_CalcChi3v_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in IntStringMap)	__iter__() (in FilterCatalogEntryList)	_CalcChi4n_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in ROMolList)	__iter__() (in MatchTypeVect)	_CalcChi4v_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in VectMolVect)	__iter__() (in MolList)	_CalcChiNn_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in VectSizeT)	__iter__() (in VectFilterMatch)	_CalcChiNv_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in VectorOfStringVectors)	__iter__() (in ForwardSDMolSupplier)	_CalcCrippenContribs() (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in MOL_SPTR_VECT)	__iter__() (in SDMolSupplier)	_CalcCrippenDescriptors_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in _listPN5RDKit4AtomE)	__iter__() (in SmilesMolSupplier)	_CalcEccentricity_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in _listPN5RDKit4BondE)	__iter__() (in TDTMolSupplier)	_CalcExactMolWt_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in FilterCatalogEntryList)	__iter__() (in DbResultBase)	_CalcFractionCSP3_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in MatchTypeVect)	__iter__() (in VLibNode)	_CalcGETAWAY_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in MolList)	__iter__() (in _lazyDataSeq)	_CalcHallKierAlpha_version (in rdkit.Chem.rdMolDescriptors)
__delitem__() (in VectFilterMatch)	__len__() (in IntStringMap)	_CalcInertialShapeFactor_version (in rdkit.Chem.rdMolDescriptors)
__div__() (in Point2D)	__len__() (in RandomAccessDbFpSupplier)	_CalcKappa1_version (in rdkit.Chem.rdMolDescriptors)
__div__() (in Point3D)	__len__() (in TopNScreener)	_CalcKappa2_version (in rdkit.Chem.rdMolDescriptors)
__div__() (in PointND)	__len__() (in FGHierarchyNode)	_CalcKappa3_version (in rdkit.Chem.rdMolDescriptors)
__doc__ (in rdkit.DataStructs)	__len__() (in Generator)	_CalcLabuteASA_version (in rdkit.Chem.rdMolDescriptors)
__eq__() (in ExplicitBitVect)	__len__() (in RandomAccessDbMolSupplier)	_CalcLabuteASAContribs() (in rdkit.Chem.rdMolDescriptors)
__eq__() (in IntSparseIntVect)	__len__() (in ROMolList)	_CalcMolFormula_version (in rdkit.Chem.rdMolDescriptors)
__eq__() (in LongSparseIntVect)	__len__() (in VectMolVect)	_CalcMolWt() (in rdkit.Chem.rdMolDescriptors)
__eq__() (in SparseBitVect)	__len__() (in VectSizeT)	_CalcMolWt_version (in rdkit.Chem.rdMolDescriptors)
__eq__() (in UIntSparseIntVect)	__len__() (in VectorOfStringVectors)	_CalcMORSE_version (in rdkit.Chem.rdMolDescriptors)
__eq__() (in ULongSparseIntVect)	__len__() (in MOL_SPTR_VECT)	_CalcNPossible() (in MLDataSet)
__eq__() (in QuantTreeNode)	__len__() (in MolHolderBase)	_CalcNPossible() (in MLQuantDataSet)
__eq__() (in TreeNode)	__len__() (in SubstructLibrary)	_CalcNPR1_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in ChemicalReaction)	__len__() (in MolBundle)	_CalcNPR2_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in FreeChemicalFeature)	__len__() (in ResonanceMolSupplier)	_CalcNumAliphaticCarbocycles_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in MolCatalog)	__len__() (in _ROAtomSeq)	_CalcNumAliphaticHeterocycles_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in MolCatalogEntry)	__len__() (in _ROBondSeq)	_CalcNumAliphaticRings_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in Mol)	__len__() (in _ROQAtomSeq)	_CalcNumAmideBonds_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in FilterCatalog)	__len__() (in _listPN5RDKit4AtomE)	_CalcNumAromaticCarbocycles_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in FragCatalog)	__len__() (in _listPN5RDKit4BondE)	_CalcNumAromaticHeterocycles_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in DiscreteValueVect)	__len__() (in FilterCatalogEntryList)	_CalcNumAromaticRings_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in ExplicitBitVect)	__len__() (in MatchTypeVect)	_CalcNumAtomStereoCenters_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in IntSparseIntVect)	__len__() (in MolList)	_CalcNumBridgeheadAtoms_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in LongSparseIntVect)	__len__() (in VectFilterMatch)	_CalcNumHBA_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in SparseBitVect)	__len__() (in SDMolSupplier)	_CalcNumHBD_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in UIntSparseIntVect)	__len__() (in SmilesMolSupplier)	_CalcNumHeteroatoms_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in ULongSparseIntVect)	__len__() (in TDTMolSupplier)	_CalcNumHeterocycles_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in Point2D)	__len__() (in LazySig)	_CalcNumLipinskiHBA_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in Point3D)	__len__() (in TopNContainer)	_CalcNumLipinskiHBD_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in PointND)	__len__() (in VectCollection)	_CalcNumRings_version (in rdkit.Chem.rdMolDescriptors)
__getinitargs__() (in UniformGrid3D_)	__len__() (in DiscreteValueVect)	_CalcNumRotatableBonds_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in IntStringMap)	__len__() (in ExplicitBitVect)	_CalcNumSaturatedCarbocycles_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in RandomAccessDbFpSupplier)	__len__() (in FPBReader)	_CalcNumSaturatedHeterocycles_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in TopNScreener)	__len__() (in MultiFPBReader)	_CalcNumSaturatedRings_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in Generator)	__len__() (in SparseBitVect)	_CalcNumSpiroAtoms_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in RandomAccessDbMolSupplier)	__len__() (in RandomAccessDbResultSet)	_CalcNumUnspecifiedAtomStereoCenters_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in VerboseCachingTargetsMatcher)	__len__() (in Point2D)	_CalcPBF_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in ROMolList)	__len__() (in Point3D)	_CalcPMI1_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in VectMolVect)	__len__() (in PointND)	_CalcPMI2_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in VectSizeT)	__len__() (in Cluster)	_CalcPMI3_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in VectorOfStringVectors)	__len__() (in Composite)	_CalcRadiusOfGyration_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in MOL_SPTR_VECT)	__len__() (in Forest)	_CalcRDF_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in MolBundle)	__len__() (in GenericPicker)	_CalcSpherocityIndex_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in ResonanceMolSupplier)	__lt__() (in QuantTreeNode)	_CalcTPSA_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in _ROAtomSeq)	__lt__() (in TreeNode)	_CalcTPSAContribs() (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in _ROBondSeq)	__missing__() (in AtomSmartsNoAromaticity)	_calculateBeta() (in rdkit.Chem.TorsionFingerprints)
__getitem__() (in _ROQAtomSeq)	__missing__() (in CachingTargetsMatcher)	_CalculateEntropies() (in rdkit.Chem.GraphDescriptors)
__getitem__() (in _listPN5RDKit4AtomE)	__missing__() (in Uniquer)	_CalcWHIM_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in _listPN5RDKit4BondE)	__mul__() (in Point2D)	_canonArrowhead (in rdkit.Chem.Features.ShowFeats)
__getitem__() (in FilterCatalogEntryList)	__mul__() (in Point3D)	_canUse3D (in rdkit.Chem.Draw.IPythonConsole)
__getitem__() (in IntPair)	__mul__() (in PointND)	_CenterTForm() (in rdkit.ML.Data.Transforms)
__getitem__() (in MatchTypeVect)	__ne__() (in ExplicitBitVect)	_cgoArrowhead() (in rdkit.Chem.Features.ShowFeats)
__getitem__() (in MolList)	__ne__() (in IntSparseIntVect)	_ChargeDescriptors() (in rdkit.Chem.Descriptors)
__getitem__() (in VectFilterMatch)	__ne__() (in LongSparseIntVect)	_check_atom_classes() (in rdkit.Chem.fmcs.fmcs')
__getitem__() (in SDMolSupplier)	__ne__() (in SparseBitVect)	_checkBounds() (in Pharmacophore)
__getitem__() (in SmilesMolSupplier)	__ne__() (in UIntSparseIntVect)	_checkMatch() (in rdkit.Chem.Pharm3D.EmbedLib)
__getitem__() (in TDTMolSupplier)	__ne__() (in ULongSparseIntVect)	_checkMatchDirections() (in SubshapeAligner)
__getitem__() (in LazySig)	__new__() (in InchiResult)	_checkMatchFeatures() (in SubshapeAligner)
__getitem__() (in TopNContainer)	__new__() (in MolKeyResult)	_checkMatchShape() (in SubshapeAligner)
__getitem__() (in VectCollection)	__new__() (in ADSparameter)	_checkPlanarity() (in rdkit.Chem.Features.FeatDirUtilsRD)
__getitem__() (in DiscreteValueVect)	__new__() (in QEDproperties)	_clusterInit() (in FingerprinterDetails)
__getitem__() (in ExplicitBitVect)	__new__() (in Atom)	_computeQuantBounds() (in NaiveBayesClassifier)
__getitem__() (in FPBReader)	__new__() (in Bond)	_ConnectivityInvariants_version (in rdkit.Chem.rdMolDescriptors)
__getitem__() (in IntSparseIntVect)	__new__() (in DirectedEdge)	_ConnectToSchema() (in rdkit.Chem.MolDb.Loader_sa)
__getitem__() (in LongSparseIntVect)	__new__() (in EnumerationMolecule)	_ConstructSQL() (in rdkit.Chem.Fingerprints.MolSimilarity)
__getitem__() (in SparseBitVect)	__new__() (in OutgoingEdge)	_ConvertModelPerformance() (in rdkit.ML.ModelPackage.PackageUtils)
__getitem__() (in UIntSparseIntVect)	__new__() (in Subgraph)	_copy_sd_tags() (in rdkit.Chem.fmcs.fmcs')
__getitem__() (in ULongSparseIntVect)	__next__() (in EnumerateLibraryBase)	_countCache (in rdkit.Chem.Pharm2D.Utils)
__getitem__() (in RandomAccessDbResultSet)	__next__() (in EnumerationStrategyBase)	_Counter() (in rdkit.Chem.fmcs.fmcs')
__getitem__() (in Point2D)	__nonzero__() (in MCSResult)	_CountMatches() (in rdkit.Chem.Fragments)
__getitem__() (in Point3D)	__nonzero__() (in MCSResult)	_CreateBondDictEtc() (in rdkit.Chem.GraphDescriptors)
__getitem__() (in PointND)	__nonzero__() (in EnumerateLibraryBase)	_createCanvas() (in rdkit.Chem.Draw)
__getitem__() (in Composite)	__nonzero__() (in EnumerationStrategyBase)	_CreateTable() (in CompositeRun)
__getitem__() (in MLDataSet)	__or__() (in DiscreteValueVect)	_ctab_has_atoms() (in rdkit.Chem.MolKey.MolKey)
__getitem__() (in Forest)	__or__() (in ExplicitBitVect)	_ctab_remove_chiral_flag() (in rdkit.Chem.MolKey.MolKey)
__getitem__() (in GenericPicker)	__or__() (in IntSparseIntVect)	_dataSeq (in rdkit.Chem.Fingerprints.MolSimilarity)
__getnewargs__() (in InchiResult)	__or__() (in LongSparseIntVect)	_dataSeq (in rdkit.VLib.NodeLib.DbPickleSupplier)
__getnewargs__() (in MolKeyResult)	__or__() (in SparseBitVect)	_descList (in rdkit.Chem.Descriptors)
__getnewargs__() (in ADSparameter)	__or__() (in UIntSparseIntVect)	_descriptor_EState_VSA() (in rdkit.Chem.EState.EState_VSA)
__getnewargs__() (in QEDproperties)	__or__() (in ULongSparseIntVect)	_descriptor_VSA_EState() (in rdkit.Chem.EState.EState_VSA)
__getnewargs__() (in Atom)	__package__ (in RDConfig)	_descriptorDocstring() (in rdkit.Chem.EState.EState_VSA)
__getnewargs__() (in Bond)	__package__ (in RDRandom)	_details (in rdkit.ML.ScreenComposite)
__getnewargs__() (in DirectedEdge)	__package__ (in rdkit.Avalon)	_displaySubshapeSkelPt() (in rdkit.Chem.Subshape.SubshapeObjects)
__getnewargs__() (in EnumerationMolecule)	__package__ (in rdkit.Avalon.pyAvalonTools)	_doLine() (in Canvas)
__getnewargs__() (in OutgoingEdge)	__package__ (in rdkit.Chem.AllChem)	_doLine() (in Canvas)
__getnewargs__() (in Subgraph)	__package__ (in rdkit.Chem.AtomPairs.Pairs)	_doMatch() (in rdkit.Chem.TorsionFingerprints)
__getstate__() (in InchiResult)	__package__ (in rdkit.Chem.AtomPairs.Sheridan)	_doMatchExcept1() (in rdkit.Chem.TorsionFingerprints)
__getstate__() (in MolKeyResult)	__package__ (in rdkit.Chem.AtomPairs.Torsions)	_doNotMatch() (in rdkit.Chem.TorsionFingerprints)
__getstate__() (in PropertyMol)	__package__ (in rdkit.Chem.AtomPairs.Utils)	_drawBond() (in MolDrawing)
__getstate__() (in ADSparameter)	__package__ (in rdkit.Chem.AtomPairs)	_DrawClusterTree() (in rdkit.ML.Cluster.ClusterVis)
__getstate__() (in QEDproperties)	__package__ (in rdkit.Chem.BRICS)	_drawerToImage() (in rdkit.Chem.Draw)
__getstate__() (in Atom)	__package__ (in rdkit.Chem.BuildFragmentCatalog)	_drawLabel() (in MolDrawing)
__getstate__() (in Bond)	__package__ (in rdkit.Chem.ChemUtils.AlignDepict)	_DrawToLimit() (in ClusterRenderer)
__getstate__() (in DirectedEdge)	__package__ (in rdkit.Chem.ChemUtils.BulkTester)	_drawWedgedBond() (in MolDrawing)
__getstate__() (in EnumerationMolecule)	__package__ (in rdkit.Chem.ChemUtils.DescriptorUtilities)	_exampleCode() (in rdkit.Chem.EState.EState)
__getstate__() (in OutgoingEdge)	__package__ (in rdkit.Chem.ChemUtils.SDFToCSV)	_exampleCode() (in rdkit.Chem.EState.Fingerprinter)
__getstate__() (in Subgraph)	__package__ (in rdkit.Chem.ChemUtils.TemplateExpand)	_exampleCode() (in rdkit.Chem.Pharm2D.Matcher)
__getstate__() (in VectCollection)	__package__ (in rdkit.Chem.ChemUtils)	_exampleCode() (in rdkit.DataStructs.TopNContainer)
__getstate__() (in PointND)	__package__ (in rdkit.Chem.ChemicalFeatures)	_exampleCode() (in rdkit.ML.DecTree.Tree)
__getstate_manages_dict__ (in PropertyMol)	__package__ (in rdkit.Chem.ChemicalForceFields)	_exampleCode() (in rdkit.ML.Descriptors.CompoundDescriptors)
__iadd__() (in DiscreteValueVect)	__package__ (in rdkit.Chem.Crippen)	_exampleCode() (in rdkit.ML.Descriptors.Parser)
__iadd__() (in ExplicitBitVect)	__package__ (in rdkit.Chem.Descriptors)	_ExampleCounter() (in rdkit.ML.DecTree.TreeVis)
__iadd__() (in IntSparseIntVect)	__package__ (in rdkit.Chem.Descriptors3D)	_exploder() (in rdkit.Chem.ChemUtils.TemplateExpand)
__iadd__() (in LongSparseIntVect)	__package__ (in rdkit.Chem.Draw.IPythonConsole)	_fact() (in rdkit.Chem.Pharm2D.Utils)
__iadd__() (in UIntSparseIntVect)	__package__ (in rdkit.Chem.Draw.MolDrawing')	_featColors (in rdkit.Chem.Features.ShowFeats)
__iadd__() (in ULongSparseIntVect)	__package__ (in rdkit.Chem.Draw.SimilarityMaps)	_FeatureInvariants_version (in rdkit.Chem.rdMolDescriptors)
__iadd__() (in Point2D)	__package__ (in rdkit.Chem.Draw)	_fields (in InchiResult)
__iadd__() (in Point3D)	__package__ (in rdkit.Chem.Draw.cairoCanvas)	_fields (in MolKeyResult)
__iadd__() (in PointND)	__package__ (in rdkit.Chem.Draw.canvasbase)	_fields (in ADSparameter)
__iadd__() (in UniformGrid3D_)	__package__ (in rdkit.Chem.Draw.mplCanvas)	_fields (in QEDproperties)
__iand__() (in UniformGrid3D_)	__package__ (in rdkit.Chem.Draw.qtCanvas)	_fields (in Atom)
__idiv__() (in IntSparseIntVect)	__package__ (in rdkit.Chem.Draw.rdMolDraw2D)	_fields (in Bond)
__idiv__() (in LongSparseIntVect)	__package__ (in rdkit.Chem.Draw.spingCanvas)	_fields (in DirectedEdge)
__idiv__() (in UIntSparseIntVect)	__package__ (in rdkit.Chem.EState.AtomTypes)	_fields (in EnumerationMolecule)
__idiv__() (in ULongSparseIntVect)	__package__ (in rdkit.Chem.EState.EState)	_fields (in OutgoingEdge)
__idiv__() (in Point2D)	__package__ (in rdkit.Chem.EState.EState_VSA)	_fields (in Subgraph)
__idiv__() (in Point3D)	__package__ (in rdkit.Chem.EState.Fingerprinter)	_findAvgVec() (in rdkit.Chem.Features.FeatDirUtilsRD)
__idiv__() (in PointND)	__package__ (in rdkit.Chem.EState)	_findBinIdx() (in SigFactory)
__imul__() (in IntSparseIntVect)	__package__ (in rdkit.Chem.EnumerateStereoisomers)	_findCentralBond() (in rdkit.Chem.TorsionFingerprints)
__imul__() (in LongSparseIntVect)	__package__ (in rdkit.Chem.FastSDMolSupplier)	_findHydAtoms() (in rdkit.Chem.Features.FeatDirUtilsRD)
__imul__() (in UIntSparseIntVect)	__package__ (in rdkit.Chem.FeatFinderCLI)	_FindStartPoints() (in rdkit.ML.Data.cQuantize)
__imul__() (in ULongSparseIntVect)	__package__ (in rdkit.Chem.FeatMaps.FeatMapParser)	_findVersions() (in MolecularDescriptorCalculator)
__imul__() (in Point2D)	__package__ (in rdkit.Chem.FeatMaps.FeatMapPoint)	_FingerprintDensity() (in rdkit.Chem.Descriptors)
__imul__() (in Point3D)	__package__ (in rdkit.Chem.FeatMaps.FeatMapUtils)	_fingerprinter() (in rdkit.Chem.PandasTools)
__imul__() (in PointND)	__package__ (in rdkit.Chem.FeatMaps.FeatMaps)	_fingerprinterInit() (in FingerprinterDetails)
__init__() (in Displayable)	__package__ (in rdkit.Chem.FeatMaps)	_finish() (in RandomAccessDbResultSet)
__init__() (in MolViewer)	__package__ (in rdkit.Chem.Features.FeatDirUtilsRD)	_fix_all() (in rdkit.Chem.MolKey.MolKey)
__init__() (in PropertyFunctor)	__package__ (in rdkit.Chem.Features.ShowFeats)	_fix_chemdraw_header() (in rdkit.Chem.MolKey.MolKey)
__init__() (in Font)	__package__ (in rdkit.Chem.Features)	_fix_line_ends() (in rdkit.Chem.MolKey.MolKey)
__init__() (in MolDrawing)	__package__ (in rdkit.Chem.FilterCatalog)	_float_tol (in rdkit.ML.Data.Quantize)
__init__() (in Canvas)	__package__ (in rdkit.Chem.Fingerprints.ClusterMols)	_fn() (in rdkit.Chem.Lipinski)
__init__() (in Canvas)	__package__ (in rdkit.Chem.Fingerprints.DbFpSupplier)	_gacRecurse() (in RecapHierarchyNode)
__init__() (in Canvas)	__package__ (in rdkit.Chem.Fingerprints.FingerprintMols)	_GenerateRandomEnsemble() (in rdkit.ML.DecTree.BuildSigTree)
__init__() (in Canvas)	__package__ (in rdkit.Chem.Fingerprints.MolSimilarity)	_GenPoints() (in Cluster)
__init__() (in IntStringMap)	__package__ (in rdkit.Chem.Fingerprints.SimilarityScreener)	_GenVarTable() (in rdkit.ML.Data.Quantize)
__init__() (in MolDraw2D)	__package__ (in rdkit.Chem.Fingerprints)	_get_bad_mol_identification_string() (in rdkit.Chem.MolKey.MolKey)
__init__() (in MolDraw2DSVG)	__package__ (in rdkit.Chem.Fraggle.FraggleSim)	_get_chiral_identification_string() (in rdkit.Chem.MolKey.MolKey)
__init__() (in MolDrawOptions)	__package__ (in rdkit.Chem.Fraggle)	_get_identification_string() (in rdkit.Chem.MolKey.MolKey)
__init__() (in map_indexing_suite_IntStringMap_entry)	__package__ (in rdkit.Chem.FragmentCatalog)	_get_image() (in rdkit.Chem.PandasTools)
__init__() (in Canvas)	__package__ (in rdkit.Chem.FragmentMatcher)	_get_match_bond_indices() (in rdkit.Chem.fmcs.fmcs')
__init__() (in StereoEnumerationOptions)	__package__ (in rdkit.Chem.Fragments)	_get_nth_prime() (in rdkit.Chem.fmcs.fmcs')
__init__() (in _AtomFlipper)	__package__ (in rdkit.Chem.FunctionalGroups)	_get_null_mol_identification_string() (in rdkit.Chem.MolKey.MolKey)
__init__() (in _BondFlipper)	__package__ (in rdkit.Chem.GraphDescriptors)	_get_svg_image() (in rdkit.Chem.PandasTools)
__init__() (in _RangeBitsGenerator)	__package__ (in rdkit.Chem.Graphs)	_get_threshold_count() (in rdkit.Chem.fmcs.fmcs')
__init__() (in _UniqueRandomBitsGenerator)	__package__ (in rdkit.Chem.Lipinski)	_getAllTriangles() (in rdkit.Chem.Subshape.SubshapeAligner)
__init__() (in FeatMapParser)	__package__ (in rdkit.Chem.MACCSkeys)	_getAtomInvariantsWithRadius() (in rdkit.Chem.TorsionFingerprints)
__init__() (in FeatMapPoint)	__package__ (in rdkit.Chem.MCS)	_getBinId() (in rdkit.ML.NaiveBayes.ClassificationModel)
__init__() (in FeatMap)	__package__ (in rdkit.Chem.MolCatalog)	_GetBitSummaryData() (in SigFactory)
__init__() (in FilterMatcher)	__package__ (in rdkit.Chem.MolDb.FingerprintUtils)	_getBondAttachmentCoordinates() (in MolDrawing)
__init__() (in DbFpSupplier)	__package__ (in rdkit.Chem.MolDb.Loader)	_getBondOffset() (in MolDrawing)
__init__() (in ForwardDbFpSupplier)	__package__ (in rdkit.Chem.MolDb.Loader_orig)	_getBondsForTorsions() (in rdkit.Chem.TorsionFingerprints)
__init__() (in RandomAccessDbFpSupplier)	__package__ (in rdkit.Chem.MolDb)	_getCanvas() (in rdkit.Chem.Draw)
__init__() (in FingerprinterDetails)	__package__ (in rdkit.Chem.MolKey.InchiInfo)	_GetCountDict() (in rdkit.Chem.GraphDescriptors)
__init__() (in SimilarityScreener)	__package__ (in rdkit.Chem.MolKey.MolKey)	_getFeatDict() (in rdkit.Chem.Pharm3D.EmbedLib)
__init__() (in ThresholdScreener)	__package__ (in rdkit.Chem.MolKey)	_getFlippers() (in rdkit.Chem.EnumerateStereoisomers)
__init__() (in TopNScreener)	__package__ (in rdkit.Chem.MolSurf)	_getHeavyAtomNeighbors() (in rdkit.Chem.TorsionFingerprints)
__init__() (in FragmentMatcher)	__package__ (in rdkit.Chem.PandasTools)	_getImplicitPropertiesFlag() (in ChemicalReaction)
__init__() (in FGHierarchyNode)	__package__ (in rdkit.Chem.PeriodicTable')	_getIndexforTorsion() (in rdkit.Chem.TorsionFingerprints)
__init__() (in MCSResult)	__package__ (in rdkit.Chem.Pharm2D.Generate)	_getLinePoints() (in CanvasBase)
__init__() (in InchiInfo)	__package__ (in rdkit.Chem.Pharm2D.Gobbi_Pharm2D)	_GetLocalError() (in rdkit.ML.DecTree.PruneTree)
__init__() (in Generator)	__package__ (in rdkit.Chem.Pharm2D.Matcher)	_getOffsetBondPts() (in MolDrawing)
__init__() (in SigFactory)	__package__ (in rdkit.Chem.Pharm2D.SigFactory)	_getPandasVersion() (in rdkit.Chem.PandasTools)
__init__() (in ExcludedVolume)	__package__ (in rdkit.Chem.Pharm2D.Utils)	_getSameAtomOrder() (in rdkit.Chem.TorsionFingerprints)
__init__() (in ExplicitPharmacophore)	__package__ (in rdkit.Chem.Pharm2D)	_getSmartsSaltsFromFile() (in rdkit.Chem.SaltRemover)
__init__() (in Pharmacophore)	__package__ (in rdkit.Chem.Pharm3D.EmbedLib)	_getSmartsSaltsFromStream() (in rdkit.Chem.SaltRemover)
__init__() (in PropertyMol)	__package__ (in rdkit.Chem.Pharm3D.ExcludedVolume)	_GetSubstructMatch() (in rdkit.Chem.Draw.IPythonConsole)
__init__() (in MolViewer)	__package__ (in rdkit.Chem.Pharm3D.Pharmacophore)	_GetSubstructMatches() (in rdkit.Chem.Draw.IPythonConsole)
__init__() (in RecapHierarchyNode)	__package__ (in rdkit.Chem.Pharm3D)	_GetTetrahedralFeatVect() (in rdkit.Chem.Features.FeatDirUtilsRD)
__init__() (in SaltRemover)	__package__ (in rdkit.Chem.PropertyMol)	_getTorsionAtomPositions() (in rdkit.Chem.TorsionFingerprints)
__init__() (in ShapeWithSkeleton)	__package__ (in rdkit.Chem.PyMol)	_getVectNormal() (in rdkit.Chem.Features.ShowFeats)
__init__() (in SkeletonPoint)	__package__ (in rdkit.Chem.QED)	_globalArrowCGO (in rdkit.Chem.Features.ShowFeats)
__init__() (in SubshapeShape)	__package__ (in rdkit.Chem.Randomize)	_globalSphereCGO (in rdkit.Chem.Features.ShowFeats)
__init__() (in DbMolSupplier)	__package__ (in rdkit.Chem.Recap)	_greet (in rdkit.Chem.ChemUtils.TemplateExpand)
__init__() (in ForwardDbMolSupplier)	__package__ (in rdkit.Chem.ReducedGraphs)	_HAcceptors() (in rdkit.Chem.Lipinski)
__init__() (in RandomAccessDbMolSupplier)	__package__ (in rdkit.Chem.SATIS)	_HasSubstructMatchStr() (in rdkit.Chem.rdchem)
__init__() (in MolSupplier)	__package__ (in rdkit.Chem.SaltRemover)	_HDonors() (in rdkit.Chem.Lipinski)
__init__() (in CachingTargetsMatcher)	__package__ (in rdkit.Chem.Scaffolds.MurckoScaffold)	_HeightFirstSplit() (in rdkit.ML.Cluster.ClusterUtils)
__init__() (in CangenNode)	__package__ (in rdkit.Chem.Scaffolds.ScaffoldTree)	_Heteroatoms() (in rdkit.Chem.Lipinski)
__init__() (in FragmentedTypedMolecule)	__package__ (in rdkit.Chem.Scaffolds)	_hkDeltas() (in rdkit.Chem.GraphDescriptors)
__init__() (in MCSResult)	__package__ (in rdkit.Chem.ShowMols)	_identify() (in rdkit.Chem.MolKey.MolKey)
__init__() (in Timer)	__package__ (in rdkit.Chem.SimpleEnum.Enumerator)	_indexCombinations (in rdkit.Chem.Pharm2D.Utils)
__init__() (in TypedFragment)	__package__ (in rdkit.Chem.SimpleEnum)	_Init() (in rdkit.Chem.Crippen)
__init__() (in TypedMolecule)	__package__ (in rdkit.Chem.Subshape.BuilderUtils)	_init() (in rdkit.Chem.Pharm2D.Gobbi_Pharm2D)
__init__() (in Uniquer)	__package__ (in rdkit.Chem.Subshape.SubshapeAligner)	_initColumnNamesAndTypes() (in DbResultBase)
__init__() (in VerboseCachingTargetsMatcher)	__package__ (in rdkit.Chem.Subshape.SubshapeBuilder)	_initializeFeats() (in FeatMap)
__init__() (in VerboseHeapOps)	__package__ (in rdkit.Chem.Subshape.SubshapeObjects)	_initializeFeats() (in ExplicitPharmacophore)
__init__() (in _SingleBest)	__package__ (in rdkit.Chem.Subshape)	_initializeFeats() (in Pharmacophore)
__init__() (in starting_from)	__package__ (in rdkit.Chem.Suppliers.DbMolSupplier)	_initializeMatrices() (in Pharmacophore)
__init__() (in CartesianProductStrategy)	__package__ (in rdkit.Chem.Suppliers.MolSupplier)	_InitKeys() (in rdkit.Chem.MACCSkeys)
__init__() (in ChemicalReaction)	__package__ (in rdkit.Chem.Suppliers)	_initMemberData() (in ShapeWithSkeleton)
__init__() (in EnumerateLibrary)	__package__ (in rdkit.Chem.TemplateAlign)	_initMemberData() (in SkeletonPoint)
__init__() (in EnumerateLibraryBase)	__package__ (in rdkit.Chem.TorsionFingerprints)	_initMemberData() (in SubshapeShape)
__init__() (in EnumerationParams)	__package__ (in rdkit.Chem)	_initPatterns() (in SaltRemover)
__init__() (in EnumerationStrategyBase)	__package__ (in rdkit.Chem.fmcs)	_initPatterns() (in SmartsFilter)
__init__() (in EvenSamplePairsStrategy)	__package__ (in rdkit.Chem.fmcs.fmcs')	_initPatterns() (in SmartsRemover)
__init__() (in ROMolList)	__package__ (in rdkit.Chem.inchi)	_InitScoreTable() (in rdkit.DataStructs.BitEnsembleDb)
__init__() (in RandomSampleAllBBsStrategy)	__package__ (in rdkit.Chem.rdChemReactions)	_initTopN() (in TopNScreener)
__init__() (in RandomSampleStrategy)	__package__ (in rdkit.Chem.rdChemicalFeatures)	_insertBlock() (in rdkit.Dbase.DbUtils)
__init__() (in ReactionFingerprintParams)	__package__ (in rdkit.Chem.rdDepictor)	_InstallDescriptors() (in rdkit.Chem.EState.EState_VSA)
__init__() (in VectMolVect)	__package__ (in rdkit.Chem.rdDistGeom)	_InstallDescriptors() (in rdkit.Chem.MolSurf)
__init__() (in VectSizeT)	__package__ (in rdkit.Chem.rdFMCS)	_is_achiral_by_symmetry() (in rdkit.Chem.MolKey.InchiInfo)
__init__() (in VectorOfStringVectors)	__package__ (in rdkit.Chem.rdForceFieldHelpers)	_isCallable() (in rdkit.Chem.Descriptors)
__init__() (in FreeChemicalFeature)	__package__ (in rdkit.Chem.rdMMPA)	_isotope_dict (in rdkit.Chem.fmcs.fmcs')
__init__() (in EmbedParameters)	__package__ (in rdkit.Chem.rdMolAlign)	_LabuteHelper() (in rdkit.Chem.MolSurf)
__init__() (in MCSAtomCompareParameters)	__package__ (in rdkit.Chem.rdMolCatalog)	_LayeredFingerprint_version (in rdkit.Chem.rdmolops)
__init__() (in MCSBondCompareParameters)	__package__ (in rdkit.Chem.rdMolChemicalFeatures)	_lazyDataSeq (in rdkit.VLib.NodeLib.DbPickleSupplier)
__init__() (in MCSParameters)	__package__ (in rdkit.Chem.rdMolDescriptors)	_legacyReactionToImage() (in rdkit.Chem.Draw)
__init__() (in MCSResult)	__package__ (in rdkit.Chem.rdMolHash)	_listi
__init__() (in O3A)	__package__ (in rdkit.Chem.rdMolTransforms)	_listPN5RDKit4AtomE (in rdkit.Chem.rdchem)
__init__() (in MolCatalog)	__package__ (in rdkit.Chem.rdPartialCharges)	_listPN5RDKit4BondE (in rdkit.Chem.rdchem)
__init__() (in MolCatalogEntry)	__package__ (in rdkit.Chem.rdRGroupDecomposition)	_listSt6vectorIiSaIiEE
__init__() (in MolChemicalFeature)	__package__ (in rdkit.Chem.rdReducedGraphs)	_LoadPatterns() (in rdkit.Chem.Fragments)
__init__() (in MolChemicalFeatureFactory)	__package__ (in rdkit.Chem.rdSLNParse)	_log2 (in rdkit.ML.InfoTheory.entropy)
__init__() (in AtomPairsParameters)	__package__ (in rdkit.Chem.rdShapeHelpers)	_log2val (in rdkit.Chem.GraphDescriptors)
__init__() (in Properties)	__package__ (in rdkit.Chem.rdStructChecker)	_LookUpBondOrder() (in rdkit.Chem.GraphDescriptors)
__init__() (in PropertyFunctor)	__package__ (in rdkit.Chem.rdSubstructLibrary)	_LookupDist() (in rdkit.ML.Cluster.Murtagh)
__init__() (in PropertyRangeQuery)	__package__ (in rdkit.Chem.rdchem)	_loopOverMatchingFeats() (in FeatMap)
__init__() (in PythonPropertyFunctor)	__package__ (in rdkit.Chem.rdfiltercatalog)	_make() (in InchiResult)
__init__() (in MOL_SPTR_VECT)	__package__ (in rdkit.Chem.rdfragcatalog)	_make() (in MolKeyResult)
__init__() (in RGroupDecomposition)	__package__ (in rdkit.Chem.rdinchi)	_make() (in ADSparameter)
__init__() (in RGroupDecompositionParameters)	__package__ (in rdkit.Chem.rdmolfiles)	_make() (in QEDproperties)
__init__() (in StructChecker)	__package__ (in rdkit.Chem.rdmolops)	_make() (in Atom)
__init__() (in StructCheckerOptions)	__package__ (in rdkit.Chem.rdqueries)	_make() (in Bond)
__init__() (in CachedMolHolder)	__package__ (in rdkit.Chem.rdtrajectory)	_make() (in DirectedEdge)
__init__() (in CachedSmilesMolHolder)	__package__ (in rdkit.DataManip.Metric)	_make() (in EnumerationMolecule)
__init__() (in CachedTrustedSmilesMolHolder)	__package__ (in rdkit.DataManip.Metric.rdMetricMatrixCalc)	_make() (in OutgoingEdge)
__init__() (in FPHolderBase)	__package__ (in rdkit.DataManip)	_make() (in Subgraph)
__init__() (in MolHolder)	__package__ (in rdkit.DataStructs.BitEnsemble)	_make_racemate_inchi() (in rdkit.Chem.MolKey.MolKey)
__init__() (in MolHolderBase)	__package__ (in rdkit.DataStructs.BitEnsembleDb)	_maximize_options (in rdkit.Chem.fmcs.fmcs')
__init__() (in PatternHolder)	__package__ (in rdkit.DataStructs.BitUtils)	_maxPathLen (in rdkit.Chem.AtomPairs.Pairs)
__init__() (in SubstructLibrary)	__package__ (in rdkit.DataStructs.HierarchyVis)	_maxPathLen (in rdkit.Chem.AtomPairs.Sheridan)
__init__() (in Atom)	__package__ (in rdkit.DataStructs.LazySignature)	_molge() (in rdkit.Chem.PandasTools)
__init__() (in AtomMonomerInfo)	__package__ (in rdkit.DataStructs.TopNContainer)	_MolPlusFingerprint() (in rdkit.Chem.PandasTools)
__init__() (in AtomPDBResidueInfo)	__package__ (in rdkit.DataStructs.VectCollection)	_MolsToGridImage() (in rdkit.Chem.Draw)
__init__() (in Bond)	__package__ (in rdkit.DataStructs)	_MolsToGridSVG() (in rdkit.Chem.Draw)
__init__() (in Conformer)	__package__ (in rdkit.DataStructs.cDataStructs)	_moltoimg() (in rdkit.Chem.Draw)
__init__() (in EditableMol)	__package__ (in rdkit.Dbase.DbConnection)	_MolToSDBlock() (in rdkit.Chem.fmcs.fmcs')
__init__() (in Mol)	__package__ (in rdkit.Dbase.DbInfo)	_moltoSVG() (in rdkit.Chem.Draw)
__init__() (in MolBundle)	__package__ (in rdkit.Dbase.DbModule)	_MorganFingerprint_version (in rdkit.Chem.rdMolDescriptors)
__init__() (in PeriodicTable)	__package__ (in rdkit.Dbase.DbReport)	_new_best() (in _SingleBest)
__init__() (in QueryAtom)	__package__ (in rdkit.Dbase.DbResultSet)	_NewPyFindStartPoints() (in rdkit.ML.Data.Quantize)
__init__() (in RWMol)	__package__ (in rdkit.Dbase.DbUtils)	_NewPyRecurseOnBounds() (in rdkit.ML.Data.Quantize)
__init__() (in ResonanceMolSupplier)	__package__ (in rdkit.Dbase.StorageUtils)	_NewPyRecurseOnBounds() (in rdkit.ML.Data.Quantize)
__init__() (in RingInfo)	__package__ (in rdkit.Dbase)	_nextDisplayId (in rdkit.Chem.DSViewer)
__init__() (in _ROAtomSeq)	__package__ (in rdkit.DistanceGeometry.DistGeom)	_NextLine() (in FeatMapParser)
__init__() (in _ROBondSeq)	__package__ (in rdkit.DistanceGeometry)	_nextMatch() (in ThresholdScreener)
__init__() (in _ROQAtomSeq)	__package__ (in rdkit.ForceField)	_NormalizeTForm() (in rdkit.ML.Data.Transforms)
__init__() (in _listPN5RDKit4AtomE)	__package__ (in rdkit.ForceField.rdForceField)	_NumAdjacencies() (in rdkit.Chem.GraphDescriptors)
__init__() (in _listPN5RDKit4BondE)	__package__ (in rdkit.Geometry)	_numCombDict (in rdkit.Chem.Pharm2D.Utils)
__init__() (in ExclusionList)	__package__ (in rdkit.Geometry.rdGeometry)	_nVal() (in rdkit.Chem.GraphDescriptors)
__init__() (in FilterCatalog)	__package__ (in rdkit.ML.AnalyzeComposite)	_offsetDblBond() (in MolDrawing)
__init__() (in FilterCatalogEntry)	__package__ (in rdkit.ML.BuildComposite)	_okToKekulizeMol() (in rdkit.Chem.Draw)
__init__() (in FilterCatalogEntryList)	__package__ (in rdkit.ML.Cluster.Butina)	_originalSettings (in rdkit.Chem.PandasTools)
__init__() (in FilterCatalogParams)	__package__ (in rdkit.ML.Cluster.ClusterUtils)	_parsePoint() (in FeatMapParser)
__init__() (in FilterHierarchyMatcher)	__package__ (in rdkit.ML.Cluster.ClusterVis)	_patternOrder (in rdkit.Chem.Crippen)
__init__() (in FilterMatch)	__package__ (in rdkit.ML.Cluster.Clustering)	_pattyDefs (in rdkit.Chem.AtomPairs.Sheridan)
__init__() (in FilterMatcherBase)	__package__ (in rdkit.ML.Cluster.Clusters)	_picks (in GenericPicker)
__init__() (in IntPair)	__package__ (in rdkit.ML.Cluster.Murtagh)	_prime_stream (in rdkit.Chem.fmcs.fmcs')
__init__() (in MatchTypeVect)	__package__ (in rdkit.ML.Cluster.Resemblance)	_primes (in rdkit.Chem.fmcs.fmcs')
__init__() (in MolList)	__package__ (in rdkit.ML.Cluster.Standardize)	_processVoteList() (in rdkit.ML.ScreenComposite)
__init__() (in PythonFilterMatcher)	__package__ (in rdkit.ML.Cluster)	_Pruner() (in rdkit.ML.DecTree.PruneTree)
__init__() (in SmartsMatcher)	__package__ (in rdkit.ML.Composite.AdjustComposite)	_pyChi0n() (in rdkit.Chem.GraphDescriptors)
__init__() (in VectFilterMatch)	__package__ (in rdkit.ML.Composite.BayesComposite)	_pyChi0v() (in rdkit.Chem.GraphDescriptors)
__init__() (in FragCatGenerator)	__package__ (in rdkit.ML.Composite.Composite)	_pyChi1n() (in rdkit.Chem.GraphDescriptors)
__init__() (in FragCatParams)	__package__ (in rdkit.ML.Composite)	_pyChi1v() (in rdkit.Chem.GraphDescriptors)
__init__() (in FragCatalog)	__package__ (in rdkit.ML.CompositeRun)	_pyChi2n() (in rdkit.Chem.GraphDescriptors)
__init__() (in FragFPGenerator)	__package__ (in rdkit.ML.Data.DataUtils)	_pyChi2v() (in rdkit.Chem.GraphDescriptors)
__init__() (in ForwardSDMolSupplier)	__package__ (in rdkit.ML.Data.FindQuantBounds)	_pyChi3n() (in rdkit.Chem.GraphDescriptors)
__init__() (in PDBWriter)	__package__ (in rdkit.ML.Data.MLData)	_pyChi3v() (in rdkit.Chem.GraphDescriptors)
__init__() (in SDMolSupplier)	__package__ (in rdkit.ML.Data.Quantize)	_pyChi4n() (in rdkit.Chem.GraphDescriptors)
__init__() (in SDWriter)	__package__ (in rdkit.ML.Data.SplitData)	_pyChi4v() (in rdkit.Chem.GraphDescriptors)
__init__() (in SmilesMolSupplier)	__package__ (in rdkit.ML.Data.Stats)	_pyChiNn_() (in rdkit.Chem.GraphDescriptors)
__init__() (in SmilesParserParams)	__package__ (in rdkit.ML.Data.Transforms)	_pyChiNv_() (in rdkit.Chem.GraphDescriptors)
__init__() (in SmilesWriter)	__package__ (in rdkit.ML.Data)	_pyGenMACCSKeys() (in rdkit.Chem.MACCSkeys)
__init__() (in TDTMolSupplier)	__package__ (in rdkit.ML.Data.cQuantize)	_pyGetAtomContribs() (in rdkit.Chem.Crippen)
__init__() (in TDTWriter)	__package__ (in rdkit.ML.DecTree.BuildQuantTree)	_pyGetScaffoldForMol() (in rdkit.Chem.Scaffolds.MurckoScaffold)
__init__() (in AdjustQueryParameters)	__package__ (in rdkit.ML.DecTree.BuildSigTree)	_pyHallKierAlpha() (in rdkit.Chem.GraphDescriptors)
__init__() (in BitEnsemble)	__package__ (in rdkit.ML.DecTree.CrossValidate)	_pyKappa1() (in rdkit.Chem.GraphDescriptors)
__init__() (in LazySig)	__package__ (in rdkit.ML.DecTree.DecTree)	_pyKappa2() (in rdkit.Chem.GraphDescriptors)
__init__() (in TopNContainer)	__package__ (in rdkit.ML.DecTree.Forest)	_pyKappa3() (in rdkit.Chem.GraphDescriptors)
__init__() (in VectCollection)	__package__ (in rdkit.ML.DecTree.ID3)	_pyLabuteHelper() (in rdkit.Chem.MolSurf)
__init__() (in DiscreteValueVect)	__package__ (in rdkit.ML.DecTree.PruneTree)	_pyMolLogP() (in rdkit.Chem.Crippen)
__init__() (in ExplicitBitVect)	__package__ (in rdkit.ML.DecTree.QuantTree)	_pyMolMR() (in rdkit.Chem.Crippen)
__init__() (in FPBReader)	__package__ (in rdkit.ML.DecTree.SigTree)	_PyRecurseOnBounds() (in rdkit.ML.Data.Quantize)
__init__() (in IntSparseIntVect)	__package__ (in rdkit.ML.DecTree.Tree)	_pyTPSA() (in rdkit.Chem.MolSurf)
__init__() (in LongSparseIntVect)	__package__ (in rdkit.ML.DecTree.TreeUtils)	_pyTPSAContribs() (in rdkit.Chem.MolSurf)
__init__() (in MultiFPBReader)	__package__ (in rdkit.ML.DecTree.TreeVis)	_RangeBitsGenerator (in rdkit.Chem.EnumerateStereoisomers)
__init__() (in SparseBitVect)	__package__ (in rdkit.ML.DecTree)	_rawD (in rdkit.Chem.EState.AtomTypes)
__init__() (in UIntSparseIntVect)	__package__ (in rdkit.ML.Descriptors.CompoundDescriptors)	_RDKFingerprint_version (in rdkit.Chem.rdmolops)
__init__() (in ULongSparseIntVect)	__package__ (in rdkit.ML.Descriptors.Descriptors)	_ReadPatts() (in rdkit.Chem.Crippen)
__init__() (in DbConnect)	__package__ (in rdkit.ML.Descriptors.MoleculeDescriptors)	_readPattyDefs() (in rdkit.Chem.AtomPairs.Sheridan)
__init__() (in CDXImageTransformer)	__package__ (in rdkit.ML.Descriptors.Parser)	_RemapInput() (in Composite)
__init__() (in CactvsImageTransformer)	__package__ (in rdkit.ML.Descriptors)	_replace() (in InchiResult)
__init__() (in RDImageTransformer)	__package__ (in rdkit.ML.EnrichPlot)	_replace() (in MolKeyResult)
__init__() (in ReportLabImageTransformer)	__package__ (in rdkit.ML.GrowComposite)	_replace() (in ADSparameter)
__init__() (in DbResultBase)	__package__ (in rdkit.ML.InfoTheory.BitClusterer)	_replace() (in QEDproperties)
__init__() (in DbResultSet)	__package__ (in rdkit.ML.InfoTheory.BitRank)	_replace() (in Atom)
__init__() (in RandomAccessDbResultSet)	__package__ (in rdkit.ML.InfoTheory)	_replace() (in Bond)
__init__() (in ForceField)	__package__ (in rdkit.ML.InfoTheory.entropy)	_replace() (in DirectedEdge)
__init__() (in MMFFMolProperties)	__package__ (in rdkit.ML.InfoTheory.rdInfoTheory)	_replace() (in EnumerationMolecule)
__init__() (in Point2D)	__package__ (in rdkit.ML.KNN.CrossValidate)	_replace() (in OutgoingEdge)
__init__() (in Point3D)	__package__ (in rdkit.ML.KNN.DistFunctions)	_replace() (in Subgraph)
__init__() (in PointND)	__package__ (in rdkit.ML.KNN.KNNClassificationModel)	_RIEHelper() (in rdkit.ML.Scoring.Scoring)
__init__() (in UniformGrid3D_)	__package__ (in rdkit.ML.KNN.KNNModel)	_ROAtomSeq (in rdkit.Chem.rdchem)
__init__() (in ClusterRenderer)	__package__ (in rdkit.ML.KNN.KNNRegressionModel)	_ROBondSeq (in rdkit.Chem.rdchem)
__init__() (in Cluster)	__package__ (in rdkit.ML.KNN)	_ROQAtomSeq (in rdkit.Chem.rdchem)
__init__() (in BayesComposite)	__package__ (in rdkit.ML.MLUtils.VoteImg)	_RotatableBonds() (in rdkit.Chem.Lipinski)
__init__() (in Composite)	__package__ (in rdkit.ML.MLUtils)	_roundtripTests (in rdkit.Dbase.StorageUtils)
__init__() (in MLDataSet)	__package__ (in rdkit.ML.MatOps)	_runDetails (in rdkit.ML.BuildComposite)
__init__() (in MLQuantDataSet)	__package__ (in rdkit.ML.ModelPackage.PackageUtils)	_runDetails (in rdkit.ML.GrowComposite)
__init__() (in DecTreeNode)	__package__ (in rdkit.ML.ModelPackage.Packager)	_runDoctests() (in rdkit.Chem.AllChem)
__init__() (in Forest)	__package__ (in rdkit.ML.ModelPackage)	_runDoctests() (in rdkit.Chem.AtomPairs.Pairs)
__init__() (in QuantTreeNode)	__package__ (in rdkit.ML.NaiveBayes.ClassificationModel)	_runDoctests() (in rdkit.Chem.AtomPairs.Sheridan)
__init__() (in SigTreeNode)	__package__ (in rdkit.ML.NaiveBayes.CrossValidate)	_runDoctests() (in rdkit.Chem.AtomPairs.Torsions)
__init__() (in TreeNode)	__package__ (in rdkit.ML.NaiveBayes)	_runDoctests() (in rdkit.Chem.AtomPairs.Utils)
__init__() (in CompoundDescriptorCalculator)	__package__ (in rdkit.ML.Neural.ActFuncs)	_runDoctests() (in rdkit.Chem.Descriptors)
__init__() (in DescriptorCalculator)	__package__ (in rdkit.ML.Neural.CrossValidate)	_runDoctests() (in rdkit.Chem.FeatMaps.FeatMapPoint)
__init__() (in MolecularDescriptorCalculator)	__package__ (in rdkit.ML.Neural.NetNode)	_runDoctests() (in rdkit.Chem.Fingerprints.DbFpSupplier)
__init__() (in BitClusterer)	__package__ (in rdkit.ML.Neural.Network)	_runDoctests() (in rdkit.Chem.Fraggle.FraggleSim)
__init__() (in BitCorrMatGenerator)	__package__ (in rdkit.ML.Neural.Trainers)	_runDoctests() (in rdkit.Chem.MolKey.MolKey)
__init__() (in InfoBitRanker)	__package__ (in rdkit.ML.Neural)	_runDoctests() (in rdkit.Chem.PandasTools)
__init__() (in KNNClassificationModel)	__package__ (in rdkit.ML.SLT.Risk)	_runDoctests() (in rdkit.Chem.Pharm2D.Utils)
__init__() (in KNNModel)	__package__ (in rdkit.ML.SLT)	_runDoctests() (in rdkit.Chem.Pharm3D.EmbedLib)
__init__() (in KNNRegressionModel)	__package__ (in rdkit.ML.Scoring.Scoring)	_runDoctests() (in rdkit.Chem.QED)
__init__() (in ModelPackage)	__package__ (in rdkit.ML.Scoring)	_runDoctests() (in rdkit.Chem.SaltRemover)
__init__() (in NaiveBayesClassifier)	__package__ (in rdkit.ML.ScreenComposite)	_runDoctests() (in rdkit.Chem.Scaffolds.MurckoScaffold)
__init__() (in Sigmoid)	__package__ (in rdkit.ML)	_runDoctests() (in rdkit.Chem.SimpleEnum.Enumerator)
__init__() (in TanH)	__package__ (in rdkit.ML.files)	_runDoctests() (in rdkit.DataStructs.BitUtils)
__init__() (in NetNode)	__package__ (in rdkit.Numerics)	_runDoctests() (in rdkit.DataStructs.LazySignature)
__init__() (in Network)	__package__ (in rdkit.Numerics.rdAlignment)	_runDoctests() (in rdkit.DataStructs.VectCollection)
__init__() (in BackProp)	__package__ (in rdkit.SimDivFilters.SimilarityPickers)	_runDoctests() (in rdkit.ML.Data.DataUtils)
__init__() (in ReFile)	__package__ (in rdkit.SimDivFilters)	_runDoctests() (in rdkit.ML.Data.SplitData)
__init__() (in SpreadPicker)	__package__ (in rdkit.SimDivFilters.rdSimDivPickers)	_runDoctests() (in rdkit.ML.KNN.DistFunctions)
__init__() (in TopNOverallPicker)	__package__ (in rdkit.VLib.Filter)	_runDoctests() (in rdkit.SimDivFilters.SimilarityPickers)
__init__() (in HierarchicalClusterPicker)	__package__ (in rdkit.VLib.Node)	_runDoctests() (in rdkit.VLib.Filter)
__init__() (in MaxMinPicker)	__package__ (in rdkit.VLib.NodeLib.DbMolSupply)	_runDoctests() (in rdkit.VLib.Node)
__init__() (in FilterNode)	__package__ (in rdkit.VLib.NodeLib.DbPickleSupplier)	_runDoctests() (in rdkit.VLib.NodeLib.SDSupply)
__init__() (in VLibNode)	__package__ (in rdkit.VLib.NodeLib.SDSupply)	_runDoctests() (in rdkit.VLib.NodeLib.SmartsMolFilter)
__init__() (in DbMolSupplyNode)	__package__ (in rdkit.VLib.NodeLib.SmartsMolFilter)	_runDoctests() (in rdkit.VLib.NodeLib.SmartsRemover)
__init__() (in DbPickleSupplyNode)	__package__ (in rdkit.VLib.NodeLib.SmartsRemover)	_runDoctests() (in rdkit.VLib.NodeLib.SmilesDupeFilter)
__init__() (in _lazyDataSeq)	__package__ (in rdkit.VLib.NodeLib.SmilesDupeFilter)	_runDoctests() (in rdkit.VLib.NodeLib.SmilesOutput)
__init__() (in SDSupplyNode)	__package__ (in rdkit.VLib.NodeLib.SmilesOutput)	_runDoctests() (in rdkit.VLib.NodeLib.SmilesSupply)
__init__() (in SmartsFilter)	__package__ (in rdkit.VLib.NodeLib.SmilesSupply)	_runDoctests() (in rdkit.VLib.Output)
__init__() (in SmartsRemover)	__package__ (in rdkit.VLib.NodeLib)	_runDoctests() (in rdkit.VLib.Supply)
__init__() (in DupeFilter)	__package__ (in rdkit.VLib.NodeLib.demo)	_runDoctests() (in rdkit.VLib.Transform)
__init__() (in OutputNode)	__package__ (in rdkit.VLib.Output)	_saltRemover (in rdkit.Chem.PandasTools)
__init__() (in SmilesSupplyNode)	__package__ (in rdkit.VLib.Supply)	_save_other_tags() (in rdkit.Chem.fmcs.fmcs')
__init__() (in OutputNode)	__package__ (in rdkit.VLib.Transform)	_scaleMetric() (in rdkit.ML.Cluster.ClusterVis)
__init__() (in SupplyNode)	__package__ (in rdkit.VLib)	_ScoreToDb() (in rdkit.DataStructs.BitEnsembleDb)
__init__() (in TransformNode)	__package__ (in rdkit.rdBase')	_screenerInit() (in FingerprinterDetails)
__initCalled (in rdkit.Chem.MolKey.MolKey)	__reduce__() (in FreeChemicalFeature)	_server (in rdkit.Chem.PyMol)
__instance_size__ (in IntStringMap)	__repr__() (in map_indexing_suite_IntStringMap_entry)	_setImplicitPropertiesFlag() (in ChemicalReaction)
__instance_size__ (in MolDraw2DSVG)	__repr__() (in MCSResult)	_SetNodeBits() (in rdkit.Chem.FunctionalGroups)
__instance_size__ (in MolDrawOptions)	__repr__() (in InchiResult)	_SetStreamIndices() (in SDMolSupplier)
__instance_size__ (in map_indexing_suite_IntStringMap_entry)	__repr__() (in MolKeyResult)	_setup() (in KNNModel)
__instance_size__ (in CartesianProductStrategy)	__repr__() (in ADSparameter)	_setupDescriptors() (in rdkit.Chem.Descriptors)
__instance_size__ (in ChemicalReaction)	__repr__() (in QEDproperties)	_ShortestPathsMatch() (in rdkit.Chem.Pharm2D.Generate)
__instance_size__ (in EnumerateLibrary)	__repr__() (in Atom)	_simpleTest() (in rdkit.ML.DecTree.TreeVis)
__instance_size__ (in EnumerationParams)	__repr__() (in Bond)	_SingleBest (in rdkit.Chem.fmcs.fmcs')
__instance_size__ (in EvenSamplePairsStrategy)	__repr__() (in DirectedEdge)	_smartsFromSmartsLine() (in rdkit.Chem.SaltRemover)
__instance_size__ (in ROMolList)	__repr__() (in EnumerationMolecule)	_smartsPatterns (in rdkit.Chem.Crippen)
__instance_size__ (in RandomSampleAllBBsStrategy)	__repr__() (in OutgoingEdge)	_splashMessage (in rdkit.Chem.FeatFinderCLI)
__instance_size__ (in RandomSampleStrategy)	__repr__() (in Subgraph)	_StandardTForm() (in rdkit.ML.Data.Transforms)
__instance_size__ (in ReactionFingerprintParams)	__safe_for_unpickling__ (in ChemicalReaction)	_StripMol() (in SaltRemover)
__instance_size__ (in VectMolVect)	__safe_for_unpickling__ (in FreeChemicalFeature)	_SubForAtomicVars() (in rdkit.ML.Descriptors.Parser)
__instance_size__ (in VectSizeT)	__safe_for_unpickling__ (in MolCatalog)	_SubForCompoundDescriptors() (in rdkit.ML.Descriptors.Parser)
__instance_size__ (in VectorOfStringVectors)	__safe_for_unpickling__ (in MolCatalogEntry)	_SubMethodArgs() (in rdkit.ML.Descriptors.Parser)
__instance_size__ (in FreeChemicalFeature)	__safe_for_unpickling__ (in Mol)	_take() (in rdkit.Dbase.DbUtils)
__instance_size__ (in EmbedParameters)	__safe_for_unpickling__ (in FilterCatalog)	_test() (in rdkit.Chem.BRICS)
__instance_size__ (in MCSAtomCompareParameters)	__safe_for_unpickling__ (in FragCatalog)	_test() (in rdkit.Chem.FragmentMatcher)
__instance_size__ (in MCSBondCompareParameters)	__safe_for_unpickling__ (in DiscreteValueVect)	_test() (in rdkit.Chem.MACCSkeys)
__instance_size__ (in MCSParameters)	__safe_for_unpickling__ (in ExplicitBitVect)	_test() (in rdkit.Chem.MCS)
__instance_size__ (in MolCatalog)	__safe_for_unpickling__ (in IntSparseIntVect)	_test() (in rdkit.Chem.PropertyMol)
__instance_size__ (in MolCatalogEntry)	__safe_for_unpickling__ (in LongSparseIntVect)	_test() (in rdkit.Chem.TemplateAlign)
__instance_size__ (in AtomPairsParameters)	__safe_for_unpickling__ (in SparseBitVect)	_test() (in rdkit.Chem)
__instance_size__ (in Properties)	__safe_for_unpickling__ (in UIntSparseIntVect)	_test() (in rdkit.Dbase.StorageUtils)
__instance_size__ (in PythonPropertyFunctor)	__safe_for_unpickling__ (in ULongSparseIntVect)	_test() (in rdkit.VLib.NodeLib.DbMolSupply)
__instance_size__ (in MOL_SPTR_VECT)	__safe_for_unpickling__ (in Point2D)	_test() (in rdkit.VLib.NodeLib.DbPickleSupplier)
__instance_size__ (in RGroupDecomposition)	__safe_for_unpickling__ (in Point3D)	_testChain() (in rdkit.ML.DecTree.PruneTree)
__instance_size__ (in RGroupDecompositionParameters)	__safe_for_unpickling__ (in PointND)	_testRandom() (in rdkit.ML.DecTree.PruneTree)
__instance_size__ (in StructChecker)	__safe_for_unpickling__ (in UniformGrid3D_)	_testSpecific() (in rdkit.ML.DecTree.PruneTree)
__instance_size__ (in StructCheckerOptions)	__setitem__() (in IntStringMap)	_times (in rdkit.Chem.Pharm3D.EmbedLib)
__instance_size__ (in CachedMolHolder)	__setitem__() (in ROMolList)	_ToClusters() (in rdkit.ML.Cluster.Murtagh)
__instance_size__ (in CachedSmilesMolHolder)	__setitem__() (in VectMolVect)	_toJSON() (in rdkit.Chem.Draw.IPythonConsole)
__instance_size__ (in CachedTrustedSmilesMolHolder)	__setitem__() (in VectSizeT)	_toPNG() (in rdkit.Chem.Draw.IPythonConsole)
__instance_size__ (in MolHolder)	__setitem__() (in VectorOfStringVectors)	_toReactionPNG() (in rdkit.Chem.Draw.IPythonConsole)
__instance_size__ (in PatternHolder)	__setitem__() (in MOL_SPTR_VECT)	_toReactionSVG() (in rdkit.Chem.Draw.IPythonConsole)
__instance_size__ (in SubstructLibrary)	__setitem__() (in _listPN5RDKit4AtomE)	_toSVG() (in rdkit.Chem.Draw.IPythonConsole)
__instance_size__ (in Atom)	__setitem__() (in _listPN5RDKit4BondE)	_trianglesInPharmacophore (in rdkit.Chem.Pharm2D.Utils)
__instance_size__ (in AtomMonomerInfo)	__setitem__() (in FilterCatalogEntryList)	_UniqueRandomBitsGenerator (in rdkit.Chem.EnumerateStereoisomers)
__instance_size__ (in AtomPDBResidueInfo)	__setitem__() (in MatchTypeVect)	_update_times() (in rdkit.Chem.fmcs.fmcs')
__instance_size__ (in Conformer)	__setitem__() (in MolList)	_UpdateLength() (in Cluster)
__instance_size__ (in EditableMol)	__setitem__() (in VectFilterMatch)	_usage (in rdkit.Chem.ChemUtils.TemplateExpand)
__instance_size__ (in Mol)	__setitem__() (in DiscreteValueVect)	_usage (in rdkit.Chem.Features.ShowFeats)
__instance_size__ (in MolBundle)	__setitem__() (in ExplicitBitVect)	_usageDoc (in rdkit.Chem.Fingerprints.ClusterMols)
__instance_size__ (in RWMol)	__setitem__() (in IntSparseIntVect)	_usageDoc (in rdkit.Chem.Fingerprints.FingerprintMols)
__instance_size__ (in ResonanceMolSupplier)	__setitem__() (in LongSparseIntVect)	_usageDoc (in rdkit.Chem.Fingerprints.MolSimilarity)
__instance_size__ (in _listPN5RDKit4AtomE)	__setitem__() (in SparseBitVect)	_validate() (in _lazyDataSeq)
__instance_size__ (in _listPN5RDKit4BondE)	__setitem__() (in UIntSparseIntVect)	_vectd
__instance_size__ (in ExclusionList)	__setitem__() (in ULongSparseIntVect)	_vecti
__instance_size__ (in FilterCatalog)	__setitem__() (in PointND)	_vectj
__instance_size__ (in FilterCatalogEntry)	__setitem__() (in MLDataSet)	_vectSs
__instance_size__ (in FilterCatalogEntryList)	__setstate__() (in PropertyMol)	_vectSt6vectorIdSaIdEE
__instance_size__ (in FilterCatalogParams)	__setstate__() (in VectCollection)	_vectSt6vectorIiSaIiEE
__instance_size__ (in FilterHierarchyMatcher)	__setstate__() (in PointND)	_vectSt6vectorIjSaIjEE
__instance_size__ (in FilterMatch)	__str__() (in FeatMap)	_verbose (in rdkit.Chem.Pharm2D.Generate)
__instance_size__ (in IntPair)	__str__() (in MCSResult)	_verbose (in rdkit.Chem.Pharm2D.Matcher)
__instance_size__ (in MatchTypeVect)	__str__() (in ExplicitPharmacophore)	_verbose (in rdkit.Chem.Pharm2D.SigFactory)
__instance_size__ (in MolList)	__str__() (in Pharmacophore)	_verbose (in rdkit.Chem.Pharm2D.Utils)
__instance_size__ (in PythonFilterMatcher)	__str__() (in FilterMatcherBase)	_verbose (in rdkit.ML.BuildComposite)
__instance_size__ (in SmartsMatcher)	__str__() (in Composite)	_verbose (in rdkit.ML.DecTree.PruneTree)
__instance_size__ (in VectFilterMatch)	__str__() (in Forest)	_verbose (in rdkit.ML.GrowComposite)
__instance_size__ (in FragCatGenerator)	__str__() (in QuantTreeNode)	_version (in rdkit.Chem.ChemUtils.TemplateExpand)
__instance_size__ (in FragCatParams)	__str__() (in TreeNode)	_version (in rdkit.Chem.Features.ShowFeats)
__instance_size__ (in FragCatalog)	__str__() (in Network)	_version() (in rdkit.rdBase')
__instance_size__ (in FragFPGenerator)	__sub__() (in DiscreteValueVect)	_VertexDegrees() (in rdkit.Chem.GraphDescriptors)
__instance_size__ (in SDMolSupplier)	__sub__() (in IntSparseIntVect)	_welcomeMessage (in rdkit.Chem.Features.ShowFeats)
__instance_size__ (in SmilesMolSupplier)	__sub__() (in LongSparseIntVect)