Draw molecules with Plotly.
Make molecules look the way you want it!
The package provides global control of aesthetics with config
, and allows for local control by specifying details
for every atom, bond, and ring.
(Development still in progress. So there are some bugs. But its working pretty well so far!)
Pip installable package available.
pip install chemdraw
- numpy (1.23.1)
- Used for math
- plotly (5.9.0)
- Plots molecules
- kaleido (0.1.0post1)
- Converts plotly graphs to images (png, svg, etc.)
- I am not using the most recent version of kaleido as it does not play nice with my computer. Try the newest version, but if you are having issues install this specific version.
- rdkit (2022.3.4)
- Convert SMILES to position coordinates.
- Pillow (9.2.0)
- Used for image manipulation.
- scikit-learn (1.1.1)
- Used to reorient molecules.
(Image may be distorted from viewer, but real image is not.)
import chemdraw
mol = "O=C(C)Oc1ccccc1C(=O)O"
drawer = chemdraw.Drawer(mol, title=mol)
fig = drawer.draw()
fig.show()
import chemdraw
molecules = [
"CCCCCCCCCC",
"CC(CC(CCC)C)CC",
"CCC1CC1",
"C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O)O)O)O)O",
"O=C(C)Oc1ccccc1C(=O)O",
"C1(CCC2)=C3C2=CC4=C5C3=C(CCC5CCC4)C=C1",
"CC(C)(C)N(C)C(=O)C14C3C2C1C5C2C3C45C(=O)C69C8C7C6C%10C7C8C9%10",
"CC3C(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C(CC(=O)O3)(C(C)C)O)(C(C)C)O",
"N#CCC1(CC(O1)C2=CC(=NC2=O)OC)O"
]
drawer = chemdraw.GridDrawer(molecules)
drawer.draw_png("example_2.png")
Atom Numbers (black text)
Bond Numbers (gray text)
Ring Numbers (maroon text)
import chemdraw
mol = "C1(CCC2)=C3C2=CC4=C5C3=C(CCC5CCC4)C=C1"
config = chemdraw.Config()
config.atom_numbers.show = True
config.bond_numbers.show = True
config.ring_numbers.show = True
drawer = chemdraw.Drawer(mol, title=mol, config=config)
fig = drawer.draw()
fig.show()
import chemdraw
mol = "C1(CCC2)=C3C2=CC4=C5C3=C(CCC5CCC4)C=C1"
molecule = chemdraw.Molecule(mol)
for ring in molecule.rings:
ring.highlight.show = True # all rings are highlighted (with default highlight_color)
if ring.aromatic: # highlighted aromatic green
ring.highlight.color = "rgba(0,255,0,0.5)"
drawer = chemdraw.Drawer(molecule, title=mol)
fig = drawer.draw()
fig.show()
import chemdraw
mol = "C1(CCC2)=C3C2=CC4=C5C3=C(CCC5CCC4)C=C1"
molecule = chemdraw.Molecule(mol)
# highlight outer ring bonds and atoms
bond_ids = [0, 1, 2, 19, 5, 6, 21, 15, 14, 13, 12, 11, 10, 16, 17, 18]
for id_ in bond_ids:
molecule.bonds[id_].highlight.show = True
for atom in molecule.atoms:
atom.highlight.show = True
# highlight inner bonds and atoms
accent_color = "rgb(252,186,63)"
molecule.bonds[8].highlight.show = True
molecule.bonds[8].highlight.color = accent_color
molecule.bonds[20].highlight.show = True
molecule.bonds[20].highlight.color = accent_color
atoms_ids = [4, 8, 9]
for id_ in atoms_ids:
molecule.atoms[id_].highlight.color = accent_color
drawer = chemdraw.Drawer(molecule, title=mol)
fig = drawer.draw()
fig.show()
From mole file
import chemdraw
mole_file_name = "ketcher_mol_file.txt"
mol = chemdraw.Molecule(mole_file=mole_file_name)
drawer = chemdraw.Drawer(mol)
fig = drawer.draw()
fig.show()
Add parenthesis to a SMILES
import chemdraw
mol = chemdraw.Molecule("OC(=O)CCCCC(=O)NCCCCCCN")
mol.add_parenthesis([0, 15], sub_script="n")
drawer = chemdraw.Drawer(mol)
fig = drawer.draw()
fig.show()
You can also pass a file path to mole files into 'Molecule'. Support for V2000 only.
import chemdraw
mole_file_name = "examples/mol_files/poly_diblock.txt"
mol = chemdraw.Molecule(mole_file=mole_file_name)
molecule_drawer = chemdraw.Drawer(mol)
fig = molecule_drawer.draw()
fig.show()
For more information on how the code works see: chemdraw.README.md