molecular descriptor calculator.
[Original repository](https://github.com/mordred-descriptor/mordred) is currently unmaintained. This maintained fork is brought to you by folks at [ProteinQure](https://www.proteinqure.com/).
>>> from mordred import Calculator, descriptors
>>> n_all = len(Calculator(descriptors, ignore_3D=False).descriptors)
>>> n_2D = len(Calculator(descriptors, ignore_3D=True).descriptors)
>>> print("2D: {:5}\n3D: {:5}\n------------\ntotal: {:5}".format(n_2D, n_all - n_2D, n_all))
2D: 1613
3D: 213
------------
total: 1826install conda
install mordred
$ conda install -c rdkit -c mordred-descriptor mordred
install rdkit python package
install mordred
$ pip install 'mordred[full]' # install with extra requires # or $ pip install mordred
$ python -m mordred.tests
calculate all descriptors
$ python -m mordred example.smi
name,ECIndex,WPath,WPol,Zagreb1, (snip)
benzene,36,27,3,24.0, (snip)
chrolobenzene,45,42,5,30.0, (snip)save to file (display progress bar)
$ python -m mordred example.smi -o example.csv
50%|███████████████████████████████████████▌ | 1/2 [00:00<00:00, 7.66it/s]stream read (low memory, no number of molecules information)
$ python -m mordred example.smi -s -o example.csv
0it [00:00, ?it/s]only ABCIndex
$ python -m mordred example.smi -d ABCIndex
name,ABC,ABCGG
benzene,4.242640687119286,3.9999999999999996
chlorobenzene,5.059137268047012,4.785854275382693ABCIndex and AcidBase
$ python -m mordred example.smi -d ABCIndex -d AcidBase
name,ABC,ABCGG,nAcid,nBase
benzene,4.242640687119286,3.9999999999999996,0,0
chlorobenzene,5.059137268047012,4.785854275382693,0,0multiple input
$ python -m mordred example.smi example2.smi -d ABCIndex
name,ABC,ABCGG
benzene,4.242640687119286,3.9999999999999996
chlorobenzene,5.059137268047012,4.785854275382693
pentane,2.8284271247461903,3.1462643699419726show help
$ python -m mordred --help
usage: python -m mordred [-h] [--version] [-t {auto,sdf,mol,smi}] [-o OUTPUT]
[-p PROCESSES] [-q] [-s] [-d DESC] [-3] [-v]
INPUT [INPUT ...]
positional arguments:
INPUT
optional arguments:
-h, --help show this help message and exit
--version input molecular file
-t {auto,sdf,mol,smi}, --type {auto,sdf,mol,smi}
input filetype (default: auto)
-o OUTPUT, --output OUTPUT
output file path (default: stdout)
-p PROCESSES, --processes PROCESSES
number of processes (default: number of logical
processors)
-q, --quiet hide progress bar
-s, --stream stream read
-d DESC, --descriptor DESC
descriptors to calculate (default: all)
-3, --3D use 3D descriptors (require sdf or mol file)
-v, --verbosity verbosity
descriptors: ABCIndex AcidBase AdjacencyMatrix Aromatic AtomCount
Autocorrelation BalabanJ BaryszMatrix BCUT BertzCT BondCount CarbonTypes Chi
Constitutional CPSA DetourMatrix DistanceMatrix EccentricConnectivityIndex
EState ExtendedTopochemicalAtom FragmentComplexity Framework GeometricalIndex
GravitationalIndex HydrogenBond InformationContent KappaShapeIndex Lipinski
McGowanVolume MoeType MolecularDistanceEdge MolecularId MomentOfInertia MoRSE
PathCount Polarizability RingCount RotatableBond SLogP TopologicalCharge
TopologicalIndex TopoPSA VdwVolumeABC VertexAdjacencyInformation WalkCount
Weight WienerIndex ZagrebIndex>>> from rdkit import Chem
>>> from mordred import Calculator, descriptors
# create descriptor calculator with all descriptors
>>> calc = Calculator(descriptors, ignore_3D=True)
>>> len(calc.descriptors)
1613
>>> len(Calculator(descriptors, ignore_3D=True, version="1.0.0"))
1612
# calculate single molecule
>>> mol = Chem.MolFromSmiles('c1ccccc1')
>>> calc(mol)[:3]
[4.242640687119286, 3.9999999999999996, 0]
# calculate multiple molecule
>>> mols = [Chem.MolFromSmiles(smi) for smi in ['c1ccccc1Cl', 'c1ccccc1O', 'c1ccccc1N']]
# as pandas
>>> df = calc.pandas(mols)
>>> df['SLogP']
0 2.3400
1 1.3922
2 1.2688
Name: SLogP, dtype: float64see examples
Moriwaki H, Tian Y-S, Kawashita N, Takagi T (2018) Mordred: a molecular descriptor calculator. Journal of Cheminformatics 10:4 . doi: 10.1186/s13321-018-0258-y