def calc_properties(smiles_list):
logp_vals, mw_vals = [], []
for smiles in smiles_list:
mol = Chem.MolFromSmiles(smiles)
logp_vals.append(MolLogP(mol, True))
mw_vals.append(ExactMolWt(mol))
return pd.DataFrame({'logp': logp_vals, 'mw': mw_vals})
def score(self, smiles):
mol = Chem.MolFromSmiles(smiles)
try:
logp = MolLogP(mol)
except:
logp = -1000
sa_score = -sascorer.calculateScore(mol)
cycle_list = nx.cycle_basis(nx.Graph(rdmolops.GetAdjacencyMatrix(mol)))
if len(cycle_list) == 0:
cycle_length = 0
else:
cycle_length = max([len(j) for j in cycle_list])
if cycle_length <= 6:
cycle_length = 0
else:
cycle_length = cycle_length - 6
cycle_score = -cycle_length
sa_score_norm = (sa_score - self._sa_mean) / self._sa_std
logp_norm = (logp - self._logp_mean) / self._logp_std
cycle_score_norm = (cycle_score - self._cycle_mean) / self._cycle_std
return sa_score_norm + logp_norm + cycle_score_norm
def eval_function(text):
generated = ''.join(text)
try:
decoded = DeepSMILESLanguageModelUtils.decode(generated,
start='<s>',
end='</s>')
DeepSMILESLanguageModelUtils.sanitize(decoded)
except Exception:
return 0
# extracted = DeepSMILESLanguageModelUtils.extract(generated)
# tokenized = DeepSMILESTokenizer(extracted)
# len_score = len(tokenized.get_tokens()) / (text_length - 1) # provide more reward for longer text sequences
decoded = DeepSMILESLanguageModelUtils.decode(generated,
start='<s>',
end='</s>')
smiles = DeepSMILESLanguageModelUtils.sanitize(decoded)
mol = Chem.MolFromSmiles(smiles)
logp = factor * MolLogP(mol)
logp_score = (logp - logp_min) / (logp_max - logp_min
) # normalize logP between 0 and 1
score = logp_score # (logp_score * 0.5) + (len_score * 0.5)
logger.info("%s, %s" % (generated, str(score)))
return score
def save(self,
force_insert=False,
force_update=False,
using=None,
update_fields=None,
*args,
**kwargs):
smiles = self.smiles
if smiles:
try:
self.mol = Chem.MolFromSmiles(smiles)
self.mol_block = Chem.MolToMolBlock(self.mol)
self.mol_weight = Descriptors.ExactMolWt(self.mol)
self.alogp = MolLogP(self.mol)
self.hba = NumHAcceptors(self.mol)
self.hbd = NumHDonors(self.mol)
self.psa = Chem.MolSurf.TPSA(self.mol)
self.rtb = NumRotatableBonds(self.mol)
super(Compound, self).save(*args, **kwargs)
self.formula = Chem.rdMolDescriptors.CalcMolFormula(self.mol)
self.bfp = MORGANBV_FP(Value(smiles))
except (ValueError, TypeError):
print "Error when storing mol object"
pass
super(Compound, self).save(*args, **kwargs)
def save(self,
force_insert=False,
force_update=False,
using=None,
update_fields=None):
self.molecule_chembl_id_url = 'https://www.ebi.ac.uk/chembl/compound/inspect/{}'.format(
self.molecule_chembl_id)
super(ChEMBL_small_molecule, self).save()
smiles = self.molecule_smile
if smiles:
try:
self.mol = Chem.MolFromSmiles(smiles)
self.mol_block = Chem.MolToMolBlock(self.mol)
self.mol_weight = Descriptors.ExactMolWt(self.mol)
self.alogp = MolLogP(self.mol)
self.hba = NumHAcceptors(self.mol)
self.hbd = NumHDonors(self.mol)
self.psa = Chem.MolSurf.TPSA(self.mol)
self.rtb = NumRotatableBonds(self.mol)
super(ChEMBL_small_molecule, self).save()
self.formula = Chem.rdMolDescriptors.CalcMolFormula(self.mol)
self.bfp = MORGANBV_FP(Value(smiles))
except (ValueError, TypeError):
print('Error when storing mol object')
pass
super(ChEMBL_small_molecule, self).save()
def get_logP(smi_list):
logP_list = []
for smi in smi_list:
m = Chem.MolFromSmiles(smi)
logP_list.append(MolLogP(m))
return logP_list
def preprocess(dataset, dir_input):
train_smiles = list(dataset['SMILES'])
train_adducts = dataset['Adducts']
train_ccs = list(dataset['CCS'])
adducts_encoder = AdductToOneHotEncoder()
adducts_encoder.fit(train_adducts)
adducts = adducts_encoder.transform(train_adducts)
Smiles, molecules, adjacencies, properties, descriptors = '', [], [], [], []
for i, smi in enumerate(train_smiles):
if '.' in smi:
continue
smi = Chem.MolToSmiles(Chem.MolFromSmiles(smi))
mol = Chem.MolFromSmiles(smi)
mol = Chem.AddHs(mol)
atoms = create_atoms(mol)
i_jbond_dict = create_ijbonddict(mol)
fingerprints = extract_fingerprints(atoms, i_jbond_dict, radius)
adjacency = create_adjacency(mol)
Smiles += smi + '\n'
molecules.append(fingerprints)
adjacencies.append(adjacency)
properties.append([[train_ccs[i]]])
descriptors.append([
ExactMolWt(mol),
MolLogP(mol),
GetFormalCharge(mol),
CalcNumRings(mol),
CalcNumRotatableBonds(mol),
CalcLogS(mol),
AcidCount(mol),
BaseCount(mol),
APolar(mol),
BPolar(mol)
])
properties = np.array(properties)
mean, std = np.mean(properties), np.std(properties)
properties = np.array((properties - mean) / std)
os.makedirs(dir_input, exist_ok=True)
with open(dir_input + 'Smiles.txt', 'w') as f:
f.write(Smiles)
np.save(dir_input + 'molecules', molecules)
np.save(dir_input + 'adducts', adducts)
np.save(dir_input + 'adjacencies', adjacencies)
np.save(dir_input + 'properties', properties)
np.save(dir_input + 'descriptors', descriptors)
np.save(dir_input + 'mean', mean)
np.save(dir_input + 'std', std)
dump_dictionary(fingerprint_dict,
dir_input + 'fingerprint_dict.pickle')
def calc_properties(smi):
# returns logP, TPSA, MW, MR
m = Chem.MolFromSmiles(smi.numpy())
logP = MolLogP(m)
tpsa = CalcTPSA(m)
# sas = calculateScore(m)
mw = ExactMolWt(m)
mr = MolMR(m)
return np.asarray(logP), np.asarray(tpsa), np.asarray(mw), np.asarray(mr)
def analyze(self, smiles: List[str], only_drugs=True) -> pd.DataFrame:
features = self.preprocessor.transform(smiles)
# RDKit molecular properties
inchikey = []
weight = []
logp = []
hdonors = []
hacceptors = []
for example in smiles:
mol = MolFromSmiles(example)
if not mol:
raise ValueError("Malformed molecule passed in to analyze")
inchikey.append(MolToInchiKey(mol))
weight.append(ExactMolWt(mol))
logp.append(MolLogP(mol))
hdonors.append(NumHDonors(mol))
hacceptors.append(NumHAcceptors(mol))
# Scores
safety = self.safety.predict(features)
feasibility = self.feasibility.predict(features)
bbbp = self.bbbp.predict_proba(features)
dataframe = pd.DataFrame(
{
"key": inchikey,
"smiles": smiles,
"weight": weight,
"logp": logp,
"hdonors": hdonors,
"hacceptors": hacceptors,
"safety": safety,
"feasibility": feasibility,
"bbbp": (i[1] for i in bbbp),
}
)
if only_drugs:
# Lipinsky's rules
dataframe = dataframe[dataframe.weight < 500]
dataframe = dataframe[dataframe.hdonors <= 5]
dataframe = dataframe[dataframe.hacceptors <= 10]
dataframe = dataframe[dataframe.logp <= 5]
# Filter too toxic and infeasible compounds
dataframe = dataframe[dataframe.safety > 0.75]
dataframe = dataframe[dataframe.feasibility > 0.75]
dataframe = dataframe.reset_index(drop=True)
return dataframe
def process_smile(row):
"""Return molecular properties """
try:
smi = row.strip()
m = Chem.MolFromSmiles(smi)
logP = MolLogP(m)
length = len(list(smi))
del m
return smi, logP, length
except:
return None, None, None
def check_lipinski(mol):
fgs = load_functional_groups()
h_donors = Lipinski.NumHDonors(mol.rdmol)
h_acceptors = Lipinski.NumHAcceptors(mol.rdmol)
log_p = MolLogP(mol.rdmol)
wt = MolWt(mol.rdmol)
if h_donors <= 5 and h_acceptors <= 5 and log_p < 5:
if wt >= 450:
mol.join(fgs['terminal_fg'].get_random())
return True, False
else:
return True, False
else:
return False, False
def read_ZINC_smiles(file_name, num_mol):
f = open(file_name, 'r')
contents = f.readlines()
smi_list = []
logP_list = []
for i in tqdm_notebook(range(num_mol), desc='Reading Data'):
smi = contents[i].strip()
m = Chem.MolFromSmiles(smi)
smi_list.append(smi)
logP_list.append(MolLogP(m))
logP_list = np.asarray(logP_list).astype(float)
return smi_list, logP_list
def read_ZINC_smiles(num_mol):
f = open('ZINC.smiles', 'r')
contents = f.readlines()
smi_list = []
logP_list = []
tpsa_list = []
for i in range(num_mol):
smi = contents[i].strip()
m = Chem.MolFromSmiles(smi)
smi_list.append(smi)
logP_list.append(MolLogP(m))
tpsa_list.append(CalcTPSA(m))
logP_list = np.asarray(logP_list).astype(float)
tpsa_list = np.asarray(tpsa_list).astype(float)
return smi_list, logP_list, tpsa_list
def get_global_features(mol):
"""Computes global-level features for a molecule.
Parameters
----------
mol : rdkit mol
Returns
-------
[np.ndarray]
Global-level features
"""
# MW, TPSA, logP, n.hdonors
mw = MolWt(mol)
tpsa = CalcTPSA(mol)
logp = MolLogP(mol)
n_hdonors = NumHDonors(mol)
desc = np.array([mw, tpsa, logp, n_hdonors], dtype=np.float32)
return desc
def calc_properties(smi):
# returns logP, TPSA, MW, MR
# normalize quantities
m = Chem.MolFromSmiles(smi.numpy())
logP = np.asarray(MolLogP(m))
logP = (logP - LOGP_MEAN) / LOGP_STD
tpsa = np.asarray(CalcTPSA(m))
tpsa = np.log10(tpsa + 1)
tpsa = (tpsa - TPSA_MEAN) / TPSA_STD
# sas = calculateScore(m)
mw = np.asarray(ExactMolWt(m))
mw = np.log10(mw + 1)
mw = (mw - MW_MEAN) / MW_STD
mr = np.asarray(MolMR(m))
mr = np.log10(mr + 1)
mr = (mr - MR_MEAN) / MR_STD
return logP, tpsa, mw, mr
def read_ZINC(num_mol):
f = open('ZINC.smiles', 'r')
contents = f.readlines()
smi = []
fps = []
logP = []
tpsa = []
for i in range(num_mol):
smi = contents[i].strip()
m = Chem.MolFromSmiles(smi)
fp = AllChem.GetMorganFingerprintAsBitVect(m, 2)
arr = np.zeros((1, ))
DataStructs.ConvertToNumpyArray(fp, arr)
fps.append(arr)
logP.append(MolLogP(m))
tpsa.append(CalcTPSA(m))
fps = np.asarray(fps)
logP = np.asarray(logP)
tpsa = np.asarray(tpsa)
return fps, logP, tpsa
def calc_properties(smi):
"""
:param smi:
:return: logP, TPSA, MR, MW
"""
m = Chem.MolFromSmiles(smi.numpy())
logP = np.asarray(MolLogP(m))
logP = (logP - LOGP_MEAN) / LOGP_STD
tpsa = np.asarray(CalcTPSA(m))
tpsa = np.log10(tpsa + 1)
tpsa = (tpsa - TPSA_MEAN) / TPSA_STD
# sas = calculateScore(m)
mw = np.asarray(ExactMolWt(m))
mw = np.log10(mw + 1)
mw = (mw - MW_MEAN) / MW_STD
mr = np.asarray(MolMR(m))
mr = np.log10(mr + 1)
mr = (mr - MR_MEAN) / MR_STD
return logP, tpsa, mr, mw
def read_ZINC(num_mol):
f = open('../Data/logP/ZINC.smiles', 'r')
contents = f.readlines()
list_smi = []
fps = []
logP = []
tpsa = []
for i in tqdm_notebook(range(num_mol)):
smi = contents[i].strip()
list_smi.append(smi)
m = Chem.MolFromSmiles(smi)
fp = AllChem.GetMorganFingerprintAsBitVect(m, 2)
arr = np.zeros((1, ))
DataStructs.ConvertToNumpyArray(fp, arr)
fps.append(arr)
logP.append(MolLogP(m))
tpsa.append(CalcTPSA(m))
fps = np.asarray(fps).astype(float)
logP = np.asarray(logP).astype(float)
tpsa = np.asarray(tpsa).astype(float)
return list_smi, logP, tpsa
logps = []
nhdonors = []
values = []
dataset = []
for data in list(LABEL_GUIDE.keys()) + ["cyp"]:
with open(os.path.join(DATA_PATH, data, f"data_{data}.pt"),
"rb") as handle:
inchis, v = pickle.load(handle)
values.extend(v)
for inchi in tqdm(inchis):
mol = MolFromInchi(inchi)
mws.append(MolWt(mol))
logps.append(MolLogP(mol))
nhdonors.append(NumHDonors(mol))
dataset.append(DATASET_GUIDE[data])
df = pd.DataFrame({
"Molecular weight (gr./mol)": mws,
r"aLog$P$": logps,
"No. hydrogen donors": nhdonors,
"values": values,
"dataset": dataset,
})
f, axs = plt.subplots(1, 3, figsize=(18, 6))
axs[0].grid(alpha=0.5)
axs[1].grid(alpha=0.5)
import numpy as np
from utils import *
from rdkit import Chem
from rdkit.Chem.Crippen import MolLogP
molecules = np.load("./inputs/molecules.npy")
char = np.load("./inputs/char.npy")
N = 200000
logP_list = []
for i in range(N):
smi = convert_to_smiles(molecules[i], char)
mol = Chem.MolFromSmiles(smi)
logP = MolLogP(mol)
logP_list.append(logP)
np.save("./inputs/logP.npy", np.asarray(logP_list))
def cal_prop(s):
m = Chem.MolFromSmiles(s)
if m is None : return None
return Chem.MolToSmiles(m), ExactMolWt(m), MolLogP(m), CalcNumHBD(m), CalcNumHBA(m), CalcTPSA(m)
def convert_to_clogp(SMILES):
mol = MS(SMILES)
logp = MolLogP(mol)
return logp
def logP_benchmark(smi):
m = Chem.MolFromSmiles(smi.numpy())
logP = MolLogP(m)
return np.asarray(logP)
_, _, char, vocab, _, _ = load_data(args.prop_file, args.seq_length)
vocab_size = len(char)
model = GNMTP(vocab_size,
args
)
model.restore(args.save_file)
target_prop = np.array([[float(p) for p in args.target_prop.split()] for _ in range(args.batch_size)])
start_codon = np.array([np.array(list(map(vocab.get, 'X')))for _ in range(args.batch_size)])
smiles = []
for _ in range(args.num_iteration):
latent_vector = s = np.random.normal(args.mean, args.stddev, (args.batch_size, args.latent_size))
generated = model.sample(latent_vector, target_prop, start_codon, args.seq_length)
smiles += [convert_to_smiles(generated[i], char) for i in range(len(generated))]
print ('number of trial : ', len(smiles))
smiles = list(set([s.split('E')[0] for s in smiles] ))
print ('number of generated smiles : ', len(smiles))
ms = [Chem.MolFromSmiles(s) for s in smiles]
ms = [m for m in ms if m is not None]
print ('number of valid smiles : ', len(ms))
with open(args.result_filename, 'w') as w:
w.write('smiles\t MW\t LogP\t TPSA\n')
for m in ms:
try:
w.write('%s\t%.3f\t%.3f\t%.3f\n' %(Chem.MolToSmiles(m), ExactMolWt(m), MolLogP(m), CalcTPSA(m)))
except:
continue
def lipinski_filter(smiles):
mol = MolFromSmiles(smiles)
return MolLogP(mol) <= 5 and NumHAcceptors(mol) <= 10 and NumHDonors(mol) <= 5 and 100 <= ExactMolWt(mol) <= 500
def get_logP(mol):
''' clogP 或 LogP '''
return MolLogP(mol)
s for s in smiles[:20000] if Chem.MolFromSmiles(s).GetNumAtoms() < 50
]
print('Number of smiles:', len(smiles))
Y = []
num_data = 20000
st = time.time()
for s in smiles[:num_data]:
m = Chem.MolFromSmiles(s)
logp = MolLogP(m)
Y.append(logp)
end = time.time()
print(f'Time:{(end-st):.3f}')
#Dataset
from torch.utils.data import Dataset, DataLoader
from rdkit.Chem.rdmolops import GetAdjacencyMatrix
class MolDataset(Dataset):
score = logp_score # (logp_score * 0.5) + (len_score * 0.5)
logger.info("%s, %s" % (generated, str(score)))
return score
# mcts = LanguageModelMCTSWithUCB1(lm, width, text_length, eval_function)
mcts = LanguageModelMCTSWithPUCT(lm,
width,
text_length,
eval_function,
cpuct=5)
state = start_state
logger.info("beginning search...")
mcts.search(state, num_simulations)
best = mcts.get_best_sequence()
generated_text = ''.join(best[0])
logger.info("generated text: %s (score: %s, perplexity: %s)" %
(generated_text, str(best[1]), lm.perplexity(generated_text)))
decoded = DeepSMILESLanguageModelUtils.decode(generated_text,
start='<s>',
end='</s>')
smiles = DeepSMILESLanguageModelUtils.sanitize(decoded)
mol = Chem.MolFromSmiles(smiles)
logp = MolLogP(mol)
logger.info("SMILES: %s, logP: %s" % (smiles, logp))
lm = EmptyDeepSMILESLanguageModel(vocab, n=6)
current_best_score = None
current_best_smiles = None
beats_current = lambda score: score < current_best_score
for i in range(1000):
generated = lm.generate(num_chars=25, text_seed="<s>")
try:
decoded = DeepSMILESLanguageModelUtils.decode(generated,
start='<s>',
end='</s>')
sanitized = DeepSMILESLanguageModelUtils.sanitize(decoded)
mol = Chem.MolFromSmiles(sanitized)
logp_score = MolLogP(mol)
logger.info("successful: %s , score: %s" %
(sanitized, str(logp_score)))
if current_best_score is None or beats_current(logp_score):
current_best_score = logp_score
current_best_smiles = sanitized
except Exception as e:
pass
logger.info("best: %s , score: %s" %
(current_best_smiles, str(current_best_score)))
from rdkit import Chem
from rdkit.Chem.Crippen import MolLogP
with open('../id_smiles.txt') as f, open('data.txt', 'w') as w:
for l in f:
m_id, s1, s2 = l.split()
m1, m2 = Chem.MolFromSmiles(s1), Chem.MolFromSmiles(s2)
if m1 is None or m2 is None: continue
c1, c2 = MolLogP(m1), MolLogP(m2)
w.write(m_id + '\t' + str(c1) + '\t' + str(c2) + '\n')
