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Identifier Index
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I
i
(in
rdkit.Chem.BRICS
)
init()
(in
FastSDMolSupplier
)
Int32
(in
rdkit.PySVD.SVDPack
)
i
(in
rdkit.VLib.NodeLib.demo
)
Init()
(in
FragmentMatcher
)
Int32
(in
rdkit.PySVD.SVDSimilarity
)
id
(in
BitGainsInfo
)
Init()
(in
SigFactory
)
Int8
(in
rdkit.Chem.Features.FeatDirUtils
)
ID3
(in
rdkit.ML.DecTree
)
Init()
(in
Pharm2DSig
)
Int8
(in
rdkit.PySVD.SVDPack
)
ID3()
(in
rdkit.ML.DecTree.ID3
)
Init()
(in
ModelPackage
)
Int8
(in
rdkit.PySVD.SVDSimilarity
)
ID3Boot()
(in
rdkit.ML.DecTree.ID3
)
InitFromDaylightString()
(in
rdkit.DataStructs
)
INTERSECT
(in
SubshapeCombineOperations
)
idx1
(in
rdkit.Chem.BuildFragmentCatalog
)
initFromFeat()
(in
FeatMapPoint
)
IntSparseIntVect
(in
rdkit.DataStructs.cDataStructs
)
idx1
(in
rdkit.Chem.Fingerprints.ClusterMols
)
initFromFile()
(in
ExplicitPharmacophore
)
invert
(in
rdkit.Chem.Features.FeatDirUtils
)
idx1
(in
rdkit.Chem.Fingerprints.FingerprintMols
)
initFromLines()
(in
ExplicitPharmacophore
)
invert
(in
rdkit.PySVD.SVDPack
)
idx1
(in
rdkit.Chem.Fingerprints.MolSimilarity
)
InitFromSequence()
(in
pySparseIntVect
)
invert
(in
rdkit.PySVD.SVDSimilarity
)
idx2
(in
rdkit.Chem.BuildFragmentCatalog
)
initFromString()
(in
ExplicitPharmacophore
)
InvertChirality()
(in
Atom
)
idx2
(in
rdkit.Chem.Fingerprints.ClusterMols
)
Initialize()
(in
ChemicalReaction
)
io
(in
rdkit.VLib.NodeLib.demo
)
idx2
(in
rdkit.Chem.Fingerprints.FingerprintMols
)
Initialize()
(in
ForceField
)
IONIC
(in
BondType
)
idx2
(in
rdkit.Chem.Fingerprints.MolSimilarity
)
InitializePyMol()
(in
MolViewer
)
Ipc()
(in
rdkit.Chem.GraphDescriptors
)
Ignore
(in
FeatDirScoreMode
)
InitRandomNumbers()
(in
rdkit.ML.Data.DataUtils
)
Is3D()
(in
Conformer
)
includeAtomNumbers
(in
MolDrawing
)
Insert()
(in
TopNContainer
)
IsAtomInRingOfSize()
(in
RingInfo
)
IndexToRDId()
(in
rdkit.Dbase.StorageUtils
)
InsertColumnData()
(in
DbConnect
)
IsBondInRingOfSize()
(in
RingInfo
)
inFileName
(in
RunDetails
)
InsertData()
(in
DbConnect
)
IsInitialized()
(in
ChemicalReaction
)
INFO
(in
RDLogger
)
Int0
(in
rdkit.Chem.Features.FeatDirUtils
)
IsInRing()
(in
Atom
)
info()
(in
logger
)
Int0
(in
rdkit.PySVD.SVDPack
)
IsInRing()
(in
Bond
)
InfoBitRanker
(in
rdkit.ML.InfoTheory.rdInfoTheory
)
Int0
(in
rdkit.PySVD.SVDSimilarity
)
IsInRingSize()
(in
Atom
)
InfoGain()
(in
rdkit.ML.InfoTheory.rdInfoTheory
)
Int16
(in
rdkit.Chem.Features.FeatDirUtils
)
IsInRingSize()
(in
Bond
)
InfoTheory
(in
rdkit.ML
)
Int16
(in
rdkit.PySVD.SVDPack
)
isNaN()
(in
rdkit.Chem.Pharm3D.EmbedLib
)
InfoType
(in
rdkit.ML.InfoTheory.rdInfoTheory
)
Int16
(in
rdkit.PySVD.SVDSimilarity
)
isPresent()
(in
rdkit.Logger.Logger
)
Init()
(in
rdkit.Chem.Draw.DrawUtils
)
Int32
(in
rdkit.Chem.Features.FeatDirUtils
)
IsTerminal()
(in
Cluster
)
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