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]
N
nActs
(in
RunDetails
)
next()
(in
DbResultSet
)
not_equal
(in
rdkit.PySVD.SVDPack
)
NaiveBayes
(in
rdkit.ML
)
next()
(in
RandomAccessDbResultSet
)
not_equal
(in
rdkit.PySVD.SVDSimilarity
)
NaiveBayesClassifier
(in
rdkit.ML.NaiveBayes.ClassificationModel
)
next()
(in
FilterNode
)
nPerClass
(in
BitGainsInfo
)
name
(in
rdkit.Chem.AvailDescriptors
)
next()
(in
VLibNode
)
nPointDistDict
(in
rdkit.Chem.Pharm2D.Utils
)
name
(in
Font
)
next()
(in
DbMolSupplyNode
)
numAtomPairFingerprintBits
(in
AtomPairsParameters
)
name
(in
rdkit.Chem.Fragments
)
next()
(in
DbPickleSupplyNode
)
NumAtomRings()
(in
RingInfo
)
nameCol
(in
RunDetails
)
next()
(in
_lazyDataSeq
)
NumBitsInCommon()
(in
rdkit.DataStructs.cDataStructs
)
NameModel()
(in
SigTreeNode
)
next()
(in
SDSupplyNode
)
NumBondRings()
(in
RingInfo
)
NameModel()
(in
KNNClassificationModel
)
next()
(in
SmilesSupplyNode
)
numBranchBits
(in
AtomPairsParameters
)
NameModel()
(in
KNNRegressionModel
)
next()
(in
OutputNode
)
NumChildren()
(in
VectCollection
)
NameModel()
(in
NaiveBayesClassifier
)
next()
(in
SupplyNode
)
NumCombinations()
(in
rdkit.Chem.Pharm2D.Utils
)
nameTable
(in
rdkit.Chem.PeriodicTable'
)
next()
(in
TransformNode
)
Numerics
(in rdkit)
NameTree()
(in
TreeNode
)
NextItem()
(in
ForwardDbFpSupplier
)
numericTypes
(in
rdkit.ML.Data.MLData
)
nBits
(in
RunDetails
)
NextItem()
(in
RandomAccessDbFpSupplier
)
numFeatThresh
(in
SubshapeAligner
)
nbrCount
(in
SubshapeBuilder
)
NextMol()
(in
ForwardDbMolSupplier
)
numFpBits
(in
rdkit.Chem.AtomPairs.Pairs
)
nDistPointDict
(in
rdkit.Chem.Pharm2D.Utils
)
NextMol()
(in
RandomAccessDbMolSupplier
)
NumHAcceptors()
(in
rdkit.Chem.Lipinski
)
nDumped
(in
rdkit.Chem.ChemUtils.TemplateExpand
)
NextMol()
(in
MolSupplier
)
NumHDonors()
(in
rdkit.Chem.Lipinski
)
Negate()
(in
FilterNode
)
NHOHCount()
(in
rdkit.Chem.Lipinski
)
NumHeteroatoms()
(in
rdkit.Chem.Lipinski
)
negative
(in
rdkit.Chem.Features.FeatDirUtils
)
NHOHSmarts
(in
rdkit.Chem.Lipinski
)
numMols
(in
RunDetails
)
negative
(in
rdkit.PySVD.SVDPack
)
noCarbonSymbols
(in
MolDrawing
)
NumMols()
(in
SDWriter
)
negative
(in
rdkit.PySVD.SVDSimilarity
)
NOCount()
(in
rdkit.Chem.Lipinski
)
NumMols()
(in
SmilesWriter
)
NetNode
(in
rdkit.ML.Neural
)
NOCountSmarts
(in
rdkit.Chem.Lipinski
)
NumMols()
(in
TDTWriter
)
NetNode
(in
rdkit.ML.Neural.NetNode
)
Node
(in
rdkit.VLib
)
NumOnBits()
(in
BitVect
)
Network
(in
rdkit.ML.Neural
)
nodeColor
(in
VisOpts
)
NumOnBits()
(in
SparseBitVect
)
Network
(in
rdkit.ML.Neural.Network
)
NodeLib
(in
rdkit.VLib
)
numPathBits
(in
rdkit.Chem.AtomPairs.Pairs
)
Neural
(in
rdkit.ML
)
nodeRad
(in
VisOpts
)
numPathBits
(in
AtomPairsParameters
)
next()
(in
FastSDMolSupplier
)
NoMerge
(in
DirMergeMode
)
numPiBits
(in
AtomPairsParameters
)
next()
(in
DbFpSupplier
)
NoMerge
(in
MergeMetric
)
NumPiElectrons()
(in
rdkit.Chem.AtomPairs.Utils
)
next()
(in
ThresholdScreener
)
NONE
(in
BondDir
)
NumRings()
(in
RingInfo
)
next()
(in
TopNScreener
)
NORMAL
(in
rdkit.Chem.Features.ShowFeats
)
NumRotatableBonds()
(in
rdkit.Chem.Lipinski
)
next()
(in
MolSupplier
)
Normalize()
(in
Point2D
)
numTable
(in
rdkit.Chem.PeriodicTable'
)
next()
(in
SDMolSupplier
)
Normalize()
(in
Point3D
)
numTypeBits
(in
AtomPairsParameters
)
next()
(in
SmilesMolSupplier
)
Normalize()
(in
PointND
)
NumValenceElectrons()
(in
rdkit.Chem.Descriptors
)
next()
(in
TDTMolSupplier
)
not_equal
(in
rdkit.Chem.Features.FeatDirUtils
)
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