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 _ ]

I

i (in rdkit.Chem.BRICS)	Init() (in MultiFPBReader)	ipython_3d (in rdkit.Chem.Draw.IPythonConsole)
i (in rdkit.VLib.NodeLib.demo)	Init() (in ModelPackage)	ipython_useSVG (in rdkit.Chem.Draw.IPythonConsole)
i1 (in rdkit.Chem.BRICS)	InitFromDaylightString() (in rdkit.DataStructs.cDataStructs)	IPythonConsole (in rdkit.Chem.Draw)
i2 (in rdkit.Chem.BRICS)	initFromFeat() (in FeatMapPoint)	Is3D() (in Conformer)
id (in BitGainsInfo)	initFromFile() (in ExplicitPharmacophore)	is_in_ring (in Atom)
ID3 (in rdkit.ML.DecTree)	initFromLines() (in ExplicitPharmacophore)	is_in_ring (in Bond)
ID3() (in rdkit.ML.DecTree.ID3)	initFromString() (in ExplicitPharmacophore)	IsAliphaticQueryAtom() (in rdkit.Chem.rdqueries)
ID3Boot() (in rdkit.ML.DecTree.ID3)	InitFromString() (in EnumerateLibraryBase)	IsAromaticQueryAtom() (in rdkit.Chem.rdqueries)
Ignore (in FeatDirScoreMode)	Initialize() (in ChemicalReaction)	IsAtomInRingOfSize() (in RingInfo)
ignoreSmoothingFailures (in EmbedParameters)	Initialize() (in EnumerationStrategyBase)	IsBondInRingOfSize() (in RingInfo)
inchi (in InchiResult)	Initialize() (in ForceField)	IsInitialized() (in ChemicalReaction)
inchi (in MolKeyResult)	InitializeCheckMol() (in rdkit.Avalon.pyAvalonTools)	IsInRing() (in Atom)
inchi (in rdkit.Chem)	InitializePyMol() (in MolViewer)	IsInRing() (in Bond)
INCHI_AVAILABLE (in rdkit.Chem.inchi)	InitialSeed (in MCSParameters)	IsInRingQueryAtom() (in rdkit.Chem.rdqueries)
INCHI_COMPUTATION_ERROR (in rdkit.Chem.MolKey.MolKey)	initParser() (in rdkit.Chem.ChemUtils.AlignDepict)	IsInRingSize() (in Atom)
INCHI_READWRITE_ERROR (in rdkit.Chem.MolKey.MolKey)	initParser() (in rdkit.Chem.ChemUtils.SDFToCSV)	IsInRingSize() (in Bond)
InchiInfo (in rdkit.Chem.MolKey)	initParser() (in rdkit.Chem.FeatFinderCLI)	IsMoleculeAgent() (in ChemicalReaction)
InchiInfo (in rdkit.Chem.MolKey.InchiInfo)	InitRandomNumbers() (in rdkit.ML.Data.DataUtils)	IsMoleculeProduct() (in ChemicalReaction)
InchiReadWriteError (in rdkit.Chem.inchi)	initStruchk() (in rdkit.Chem.MolKey.MolKey)	IsMoleculeReactant() (in ChemicalReaction)
InchiResult (in rdkit.Chem.MolKey.MolKey)	InNRingsEqualsQueryAtom() (in rdkit.Chem.rdqueries)	isNaN() (in rdkit.Chem.Pharm3D.EmbedLib)
InchiToInchiKey() (in rdkit.Chem.inchi)	InNRingsGreaterQueryAtom() (in rdkit.Chem.rdqueries)	Isotope (in rdkit.Chem.rdRGroupDecomposition)
InchiToInchiKey() (in rdkit.Chem.rdinchi)	InNRingsLessQueryAtom() (in rdkit.Chem.rdqueries)	Isotope (in RGroupLabelling)
InchiToMol() (in rdkit.Chem.rdinchi)	InputFormat (in rdkit.Chem.SaltRemover)	isotope_re (in rdkit.Chem.MolKey.InchiInfo)
includeAgents (in ReactionFingerprintParams)	Insert() (in TopNContainer)	IsotopeEqualsQueryAtom() (in rdkit.Chem.rdqueries)
includeAtomNumbers (in DrawingOptions)	InsertColumnData() (in DbConnect)	IsotopeGreaterQueryAtom() (in rdkit.Chem.rdqueries)
includeAtomTags (in MolDrawOptions)	InsertData() (in DbConnect)	IsotopeLabels (in rdkit.Chem.rdRGroupDecomposition)
index (in CangenNode)	InstallIPythonRenderer() (in rdkit.Chem.Draw.IPythonConsole)	IsotopeLabels (in RGroupLabels)
IndexToRDId() (in rdkit.Dbase.StorageUtils)	InstallPandasTools() (in rdkit.Chem.PandasTools)	IsotopeLessQueryAtom() (in rdkit.Chem.rdqueries)
InertialShapeFactor() (in rdkit.Chem.Descriptors3D)	INTERSECT (in SubshapeCombineOperations)	IsReactionTemplateMoleculeAgent() (in rdkit.Chem.rdChemReactions)
inFileName (in RunDetails)	intersect_counts() (in rdkit.Chem.fmcs.fmcs')	IsTerminal() (in Cluster)
InfoBitRanker (in rdkit.ML.InfoTheory.rdInfoTheory)	IntPair (in rdkit.Chem.rdfiltercatalog)	IsUnsaturatedQueryAtom() (in rdkit.Chem.rdqueries)
InfoGain() (in rdkit.ML.InfoTheory.rdInfoTheory)	IntSparseIntVect (in rdkit.DataStructs.cDataStructs)	IsValid() (in FilterMatcher)
InfoTheory (in rdkit.ML)	IntStringMap (in rdkit.Chem.Draw.rdMolDraw2D)	IsValid() (in FilterCatalogEntry)
InfoType (in rdkit.ML.InfoTheory.rdInfoTheory)	InvertChirality() (in Atom)	IsValid() (in FilterMatcherBase)
Init() (in FragmentMatcher)	io (in rdkit.VLib.NodeLib.demo)	IsValid() (in SmartsMatcher)
Init() (in SigFactory)	IONIC (in BondType)	isValidRingCut() (in rdkit.Chem.Fraggle.FraggleSim)
Init() (in FPBReader)	Ipc() (in rdkit.Chem.GraphDescriptors)