datamol.convert

from_df(df, smiles_column='smiles', mol_column=None, conserve_smiles=False, sanitize=True)

Convert a dataframe to a list of mols.

For the reverse operation, you might to check dm.to_df().

Note

If smiles_column is used to build the molecules, this property is removed from the molecules' properties. You can decide to conserve the SMILES column by setting conserve_smiles to True.

Parameters:

Name	Type	Description	Default
df	pd.DataFrame	a dataframe.	required
smiles_column	Optional[str]	Column name to extract the molecule.	'smiles'
mol_column	Optional[str]	Column name to extract the molecule. It takes precedence over smiles_column.	None
conserve_smiles	bool	Whether to conserve the SMILES in the mols' props.	False
sanitize	bool	Whether to sanitize if smiles_column is not None.	True

Source code in datamol/convert.py

def from_df(
    df: pd.DataFrame,
    smiles_column: Optional[str] = "smiles",
    mol_column: Optional[str] = None,
    conserve_smiles: bool = False,
    sanitize: bool = True,
) -> List[Mol]:
    """Convert a dataframe to a list of mols.

    For the reverse operation, you might to check `dm.to_df()`.

    Note:
        If `smiles_column` is used to build the molecules, this property
        is removed from the molecules' properties. You can decide to conserve
        the SMILES column by setting `conserve_smiles` to True.

    Args:
        df: a dataframe.
        smiles_column: Column name to extract the molecule.
        mol_column: Column name to extract the molecule. It takes
            precedence over `smiles_column`.
        conserve_smiles: Whether to conserve the SMILES in the mols' props.
        sanitize: Whether to sanitize if `smiles_column` is not None.
    """

    if smiles_column is None and mol_column is None:
        raise ValueError("Either `smiles_column` or `mol_column` must be not None.")

    if len(df) == 0:
        return []

    # Try to detect the mol column if `mol_column` is None.
    if mol_column is None:
        for col in df.columns:
            if isinstance(df[col].iloc[0], Mol):
                mol_column = col

    def _row_to_mol(row):

        props = row.to_dict()

        if mol_column is not None:
            mol = props.pop(mol_column)
        else:

            if conserve_smiles:
                smiles = props[smiles_column]
            else:
                # If a SMILES column is used to create the molecule then it is removed from the
                # properties.
                smiles = props.pop(smiles_column)

            mol = dm.to_mol(smiles, sanitize=sanitize)

        if mol is None:
            return None

        dm.set_mol_props(mol, props)
        return mol

    return df.apply(_row_to_mol, axis=1).tolist()

from_inchi(inchi, sanitize=True, remove_hs=True)

Convert an InChi to a mol.

Parameters:

Name	Type	Description	Default
inchi	Optional[str]	an inchi string.	required
sanitize	bool	do sanitize.	True
remove_hs	bool	do remove hs.	True

Returns:

Type	Description
Optional[Mol]	mol

Source code in datamol/convert.py

def from_inchi(
    inchi: Optional[str],
    sanitize: bool = True,
    remove_hs: bool = True,
) -> Optional[Mol]:
    """Convert an InChi to a mol.

    Args:
        inchi: an inchi string.
        sanitize: do sanitize.
        remove_hs: do remove hs.

    Returns:
        mol
    """
    if inchi is None:
        return None

    return Chem.MolFromInchi(inchi, sanitize=sanitize, removeHs=remove_hs)

from_selfies(selfies, as_mol=False)

Convert a SEFLIES to a smiles or a mol.

Parameters:

Name	Type	Description	Default
selfies	str	a selfies.	required
as_mol	str	whether to return a mol or a smiles.	False

Returns:

Type	Description
Optional[Union[str, Mol]]	smiles or mol.

Source code in datamol/convert.py

def from_selfies(selfies: str, as_mol: bool = False) -> Optional[Union[str, Mol]]:
    """Convert a SEFLIES to a smiles or a mol.

    Args:
        selfies: a selfies.
        as_mol (str, optional): whether to return a mol or a smiles.

    Returns:
        smiles or mol.
    """
    if selfies is None:
        return None

    smiles = sf.decoder(selfies)

    if as_mol and smiles is not None:
        return dm.to_mol(smiles)

    return smiles

from_smarts(smarts)

Convert a SMARTS string to a molecule

Parameters:

Name	Type	Description	Default
smarts	Optional[str]	a smarts string	required

Source code in datamol/convert.py

def from_smarts(smarts: Optional[str]) -> Optional[Mol]:
    """Convert a SMARTS string to a molecule

    Args:
        smarts: a smarts string
    """

    if smarts is None:
        return None
    return Chem.MolFromSmarts(smarts)  # type: ignore

render_mol_df(df)

Render the molecules column in a dataframe. The rendering is performed in-place only. So nothing is returned.

Parameters:

Name	Type	Description	Default
df	pd.DataFrame	a dataframe.	required

Source code in datamol/convert.py

def render_mol_df(df: pd.DataFrame):
    """Render the molecules column in a dataframe. The rendering is performed
    in-place only. So nothing is returned.

    Args:
        df: a dataframe.
    """
    # NOTE(hadim): replace by `PandaTools.ChangeMoleculeRendering` once
    # https://github.com/rdkit/rdkit/issues/3563 is fixed.
    _ChangeMoleculeRendering(df)

smiles_as_smarts(mol, keep_hs=True)

Convert a smiles to a smarts if possible

Parameters:

Name	Type	Description	Default
mol	Union[str, Mol]	a molecule.	required
keep_hs	bool	Whether to keep hydrogen. This will increase the count of H atoms for atoms with attached hydrogens to create a valid smarts without further substitution allowed e.g. [H]-[CH]-[] -> [H]-[CH2]-[]	True

Returns:

Type	Description
Optional[str]	smarts of the molecule

Source code in datamol/convert.py

def smiles_as_smarts(mol: Union[str, Mol], keep_hs: bool = True) -> Optional[str]:
    """Convert a smiles to a smarts if possible

    Args:
        mol: a molecule.
        keep_hs: Whether to keep hydrogen. This will increase the count of H atoms
            for atoms with attached hydrogens to create a valid smarts without further substitution allowed
            e.g. [H]-[CH]-[*] -> [H]-[CH2]-[*]

    Returns:
        smarts of the molecule
    """

    if isinstance(mol, str):
        mol = dm.to_mol(mol)

    if mol is None:
        return None

    # Change the isotope to 99
    for atom in mol.GetAtoms():  # type: ignore
        if keep_hs:
            s = sum(na.GetAtomicNum() == 1 for na in atom.GetNeighbors())
            if s:
                atom.SetNumExplicitHs(atom.GetTotalNumHs() + s)
        atom.SetIsotope(99)

    # Print out the smiles, all the atom attributes will be fully specified
    smarts = to_smiles(mol, isomeric=True, explicit_bonds=True)

    if smarts is None:
        return None

    # Remove the 99 isotope labels
    smarts = re.sub(r"\[99", "[", smarts)
    return smarts

to_df(mols, smiles_column='smiles', mol_column=None, include_private=False, include_computed=False, render_df_mol=True, render_all_df_mol=False)

Convert a list of mols to a dataframe using each mol properties as a column.

For the reverse operation, you might to check dm.from_df().

Parameters:

Name	Type	Description	Default
mols	List[Mol]	a molecule.	required
smiles_column	Optional[str]	name of the SMILES column.	'smiles'
mol_column	Optional[str]	Name of the column. If not None, rdkit.Chem.PandaTools is used to add a molecule column.	None
include_private	bool	Include private properties in the columns.	False
include_computed	bool	Include computed properties in the columns.	False
render_df_mol	bool	whether to render the molecule in the dataframe to images. If called once, it will be applied for the newly created dataframe with mol in it.	True
render_all_df_mol	bool	Whether to render all pandas dataframe mol column as images.	False

Source code in datamol/convert.py

def to_df(
    mols: List[Mol],
    smiles_column: Optional[str] = "smiles",
    mol_column: Optional[str] = None,
    include_private: bool = False,
    include_computed: bool = False,
    render_df_mol: bool = True,
    render_all_df_mol: bool = False,
) -> Optional[pd.DataFrame]:
    """Convert a list of mols to a dataframe using each mol properties
    as a column.

    For the reverse operation, you might to check `dm.from_df()`.

    Args:
        mols: a molecule.
        smiles_column: name of the SMILES column.
        mol_column: Name of the column. If not None, rdkit.Chem.PandaTools
            is used to add a molecule column.
        include_private: Include private properties in the columns.
        include_computed: Include computed properties in the columns.
        render_df_mol: whether to render the molecule in the dataframe to images.
            If called once, it will be applied for the newly created dataframe with
            mol in it.
        render_all_df_mol: Whether to render all pandas dataframe mol column as images.
    """

    # Init a dataframe
    df = pd.DataFrame()

    # Feed it with smiles
    if smiles_column is not None:
        smiles = [to_smiles(mol) for mol in mols]
        df[smiles_column] = smiles

    # Add a mol column
    if mol_column is not None:
        df[mol_column] = mols

    # Add any other properties present in the molecule
    props = [
        mol.GetPropsAsDict(
            includePrivate=include_private,
            includeComputed=include_computed,
        )
        for mol in mols
    ]
    props_df = pd.DataFrame(props)

    if smiles_column is not None and smiles_column in props_df.columns:
        logger.warning(
            f"The SMILES column name provided ('{smiles_column}') is already present in the properties"
            " of the molecules. THe returned dataframe will two columns with the same name."
        )

    # Concat the df with the properties df
    df = pd.concat([df, props_df], axis=1)

    # Render mol column to images
    if render_df_mol is True and mol_column is not None:

        render_mol_df(df)

        if render_all_df_mol:
            PandasTools.RenderImagesInAllDataFrames()

    return df

to_inchi(mol)

Convert a mol to a standard Inchi.

Parameters:

Name	Type	Description	Default
mol	Union[str, Mol]	a molecule.	required

Source code in datamol/convert.py

def to_inchi(mol: Union[str, Mol]) -> Optional[str]:
    """Convert a mol to a standard Inchi.

    Args:
        mol: a molecule.
    """

    if isinstance(mol, str):
        mol = dm.to_mol(mol)

    if mol is None:
        return None

    inchi_val = Chem.MolToInchi(mol)
    if not inchi_val:
        return None
    return inchi_val

to_inchi_non_standard(mol, fixed_hydrogen_layer=True, undefined_stereocenter=True, reconnected_metal_layer=True, tautomerism_keto_enol=True, tautomerism_15=True, options=None)

Convert a mol to a non-standard Inchi.

Note that turning all the flags to False will result in the standard Inchi.

Warning: this function will return a non-standard Inchi. See https://www.inchi-trust.org/technical-faq-2 for details.

It's important to not mix standard and non-standard InChi. If you don't know much about non-standard InChi, we highly recommend you to use the standard InChi with dm.to_inchi().

Parameters:

Name	Type	Description	Default
mol	Union[str, Mol]	a molecule.	required
fixed_hydrogen_layer	bool	whether to include a fixed hydrogen layer (/FixedH).	True
undefined_stereocenter	bool	whether to include an undefined stereocenter layer (/SUU).	True
reconnected_metal_layer	bool	whether to include reconnected metals (/RecMet).	True
tautomerism_keto_enol	bool	whether to account tautomerism keto-enol (/KET).	True
tautomerism_15	bool	whether to account 1,5-tautomerism (/15T).	True
options	Optional[List[str]]	More InchI options in a form of a list of string. Example: ["/SRel", "/AuxNone"].	None

Source code in datamol/convert.py

def to_inchi_non_standard(
    mol: Union[str, Mol],
    fixed_hydrogen_layer: bool = True,
    undefined_stereocenter: bool = True,
    reconnected_metal_layer: bool = True,
    tautomerism_keto_enol: bool = True,
    tautomerism_15: bool = True,
    options: Optional[List[str]] = None,
) -> Optional[str]:
    """Convert a mol to a non-standard Inchi.

    Note that turning all the flags to `False` will result in the standard Inchi.

    **Warning**: this function will return a **non-standard** Inchi. See
    https://www.inchi-trust.org/technical-faq-2 for details.

    It's important to not mix standard and non-standard InChi. If you don't know
    much about non-standard InChi, we highly recommend you to use the
    standard InChi with `dm.to_inchi()`.

    Args:
        mol: a molecule.
        fixed_hydrogen_layer: whether to include a fixed hydrogen layer (`/FixedH`).
        undefined_stereocenter: whether to include an undefined stereocenter layer (`/SUU`).
        reconnected_metal_layer: whether to include reconnected metals (`/RecMet`).
        tautomerism_keto_enol: whether to account tautomerism keto-enol (`/KET`).
        tautomerism_15: whether to account 1,5-tautomerism (`/15T`).
        options: More InchI options in a form of a list of string. Example:
            `["/SRel", "/AuxNone"]`.
    """

    if isinstance(mol, str):
        mol = dm.to_mol(mol)

    if mol is None:
        return None

    inchi_options = _process_inchi_options(
        fixed_hydrogen_layer=fixed_hydrogen_layer,
        undefined_stereocenter=undefined_stereocenter,
        reconnected_metal_layer=reconnected_metal_layer,
        tautomerism_keto_enol=tautomerism_keto_enol,
        tautomerism_15=tautomerism_15,
        options=options,
    )

    inchi_val = Chem.MolToInchi(mol, options=inchi_options)
    if not inchi_val:
        return None
    return inchi_val

to_inchikey(mol)

Convert a mol to a standard InchiKey.

Parameters:

Name	Type	Description	Default
mol	Union[str, Mol]	a molecule	required

Source code in datamol/convert.py

def to_inchikey(mol: Union[str, Mol]) -> Optional[str]:
    """Convert a mol to a standard InchiKey.

    Args:
        mol: a molecule
    """
    if isinstance(mol, str):
        mol = dm.to_mol(mol)

    if mol is None:
        return None

    inchikey = Chem.MolToInchiKey(mol)
    if not inchikey:
        return None
    return inchikey

to_inchikey_non_standard(mol, fixed_hydrogen_layer=True, undefined_stereocenter=True, reconnected_metal_layer=True, tautomerism_keto_enol=True, tautomerism_15=True, options=None)

Convert a mol to a non-standard InchiKey.

Note that turning all the flags to False will result in the standard InchiKey.

Warning: this function will return a non-standard InchiKey. See https://www.inchi-trust.org/technical-faq-2 for details.

It's important to not mix standard and non-standard InChiKey. If you don't know much about non-standard InchiKey, we highly recommend you to use the standard InchiKey with dm.to_inchikey().

Parameters:

Name	Type	Description	Default
mol	Union[str, Mol]	a molecule	required
fixed_hydrogen_layer	bool	whether to include a fixed hydrogen layer (/FixedH).	True
undefined_stereocenter	bool	whether to include an undefined stereocenter layer (/SUU).	True
reconnected_metal_layer	bool	whether to include reconnected metals (/RecMet).	True
tautomerism_keto_enol	bool	whether to account tautomerism keto-enol (/KET).	True
tautomerism_15	bool	whether to account 1,5-tautomerism (/15T).	True
options	Optional[List[str]]	More InchI options in a form of a list of string. Example: ["/SRel", "/AuxNone"].	None

Source code in datamol/convert.py

def to_inchikey_non_standard(
    mol: Union[str, Mol],
    fixed_hydrogen_layer: bool = True,
    undefined_stereocenter: bool = True,
    reconnected_metal_layer: bool = True,
    tautomerism_keto_enol: bool = True,
    tautomerism_15: bool = True,
    options: Optional[List[str]] = None,
) -> Optional[str]:
    """Convert a mol to a non-standard InchiKey.

    Note that turning all the flags to `False` will result in the standard InchiKey.

    **Warning**: this function will return a **non-standard** InchiKey. See
    https://www.inchi-trust.org/technical-faq-2 for details.

    It's important to not mix standard and non-standard InChiKey. If you don't know
    much about non-standard InchiKey, we highly recommend you to use the
    standard InchiKey with `dm.to_inchikey()`.

    Args:
        mol: a molecule
        fixed_hydrogen_layer: whether to include a fixed hydrogen layer (`/FixedH`).
        undefined_stereocenter: whether to include an undefined stereocenter layer (`/SUU`).
        reconnected_metal_layer: whether to include reconnected metals (`/RecMet`).
        tautomerism_keto_enol: whether to account tautomerism keto-enol (`/KET`).
        tautomerism_15: whether to account 1,5-tautomerism (`/15T`).
        options: More InchI options in a form of a list of string. Example:
            `["/SRel", "/AuxNone"]`.
    """

    if isinstance(mol, str):
        mol = dm.to_mol(mol)

    if mol is None:
        return None

    inchi_options = _process_inchi_options(
        fixed_hydrogen_layer=fixed_hydrogen_layer,
        undefined_stereocenter=undefined_stereocenter,
        reconnected_metal_layer=reconnected_metal_layer,
        tautomerism_keto_enol=tautomerism_keto_enol,
        tautomerism_15=tautomerism_15,
        options=options,
    )

    inchikey = Chem.MolToInchiKey(mol, options=inchi_options)
    if not inchikey:
        return None
    return inchikey

to_selfies(mol)

Convert a mol to SELFIES.

Parameters:

Name	Type	Description	Default
mol	Union[str, Mol]	a molecule or a SMILES.	required

Returns:

Name	Type	Description
selfies	Optional[str]	SELFIES string.

Source code in datamol/convert.py

def to_selfies(mol: Union[str, Mol]) -> Optional[str]:
    """Convert a mol to SELFIES.

    Args:
        mol: a molecule or a SMILES.

    Returns:
        selfies: SELFIES string.
    """

    if isinstance(mol, Mol):
        mol = to_smiles(mol)

    if mol is None:
        return None
    selfies = sf.encoder(mol)

    if selfies == -1:
        return None

    return selfies

to_smarts(mol)

Convert a mol to SMARTS format

Parameters:

Name	Type	Description	Default
mol	Mol	a molecule.	required

Source code in datamol/convert.py

def to_smarts(mol: Mol) -> Optional[str]:
    """Convert a mol to SMARTS format

    Args:
        mol: a molecule.
    """

    if mol is None:
        return None

    return Chem.MolToSmarts(mol)  # type: ignore

to_smiles(mol, canonical=True, isomeric=True, kekulize=False, ordered=False, explicit_bonds=False, explicit_hs=False, randomize=False, cxsmiles=False, allow_to_fail=False, with_atom_indices=False)

Convert a mol to a SMILES.

Parameters:

Name	Type	Description	Default
mol	Mol	a molecule.	required
canonical	bool	if false no attempt will be made to canonicalize the molecule.	True
isomeric	bool	whether to include information about stereochemistry in the SMILES.	True
kekulize	bool	whether to return the kekule version of the SMILES.	False
ordered	bool	whether to force reordering of the atoms first.	False
explicit_bonds	bool	if true, all bond orders will be explicitly indicated in the output SMILES.	False
explicit_hs	bool	if true, all H counts will be explicitly indicated in the output SMILES.	False
randomize	bool	whether to randomize the generated smiles. Override canonical.	False
cxsmiles	bool	Whether to return a CXSMILES instead of a SMILES.	False
allow_to_fail	bool	Raise an error if the conversion to SMILES fails. Return None otherwise.	False
with_atom_indices	bool	Whether to add atom indices to the SMILES.	False

Source code in datamol/convert.py

def to_smiles(
    mol: Mol,
    canonical: bool = True,
    isomeric: bool = True,
    kekulize: bool = False,
    ordered: bool = False,
    explicit_bonds: bool = False,
    explicit_hs: bool = False,
    randomize: bool = False,
    cxsmiles: bool = False,
    allow_to_fail: bool = False,
    with_atom_indices: bool = False,
) -> Optional[str]:
    """Convert a mol to a SMILES.

    Args:
        mol: a molecule.
        canonical: if false no attempt will be made to canonicalize the molecule.
        isomeric: whether to include information about stereochemistry in the SMILES.
        kekulize: whether to return the kekule version of the SMILES.
        ordered: whether to force reordering of the atoms first.
        explicit_bonds: if true, all bond orders will be explicitly indicated in the output SMILES.
        explicit_hs: if true, all H counts will be explicitly indicated in the output SMILES.
        randomize: whether to randomize the generated smiles. Override `canonical`.
        cxsmiles: Whether to return a CXSMILES instead of a SMILES.
        allow_to_fail: Raise an error if the conversion to SMILES fails. Return None otherwise.
        with_atom_indices: Whether to add atom indices to the SMILES.
    """

    if ordered and canonical is False:
        mol = dm.reorder_atoms(mol)

    if randomize:
        mol = dm.randomize_atoms(mol)
        canonical = False

    if with_atom_indices:
        mol = dm.atom_indices_to_mol(mol, copy=True)

    smiles = None
    try:

        if cxsmiles:
            smiles = rdmolfiles.MolToCXSmiles(
                mol,
                isomericSmiles=isomeric,
                canonical=canonical,
                allBondsExplicit=explicit_bonds,
                allHsExplicit=explicit_hs,
                kekuleSmiles=kekulize,
            )

        else:
            smiles = rdmolfiles.MolToSmiles(
                mol,
                isomericSmiles=isomeric,
                canonical=canonical,
                allBondsExplicit=explicit_bonds,
                allHsExplicit=explicit_hs,
                kekuleSmiles=kekulize,
            )

    except Exception as e:

        if allow_to_fail:
            raise e

        return None

    return smiles