def testImpliedValence(self):
# Given Rule 3, an open parenthesis implies at least two
# nbrs.
self.assertRaises(ValenceError, ParseSmiles, "C1CN1(", True)
mol = ParseSmiles("C1CN1(", True, 4)
self.assertRaises(ValenceError, ParseSmiles, "CN(=", True)
mol = ParseSmiles("CN(=", True, 4)
def testBasic(self):
mol = ParseSmiles("c1ccccc1", False) # Will be kekulized
bondorders = [bond.order for bond in mol.bonds]
self.assertEqual(sum(x == 1 for x in bondorders), 3)
self.assertEqual(sum(x == 2 for x in bondorders), 3)
mol = ParseSmiles("c1ccccc1 ", False) # Will be kekulized
bondorders = [bond.order for bond in mol.bonds]
self.assertEqual(sum(x == 1 for x in bondorders), 3)
self.assertEqual(sum(x == 2 for x in bondorders), 3)
mol = ParseSmiles("c1ccccc1.", partial=True) # Will be kekulized
bondorders = [bond.order for bond in mol.bonds]
self.assertEqual(sum(x == 1 for x in bondorders), 3)
self.assertEqual(sum(x == 2 for x in bondorders), 3)
mol = ParseSmiles("c1ccccc1", True) # Won't be kekulized
bondorders = [bond.order for bond in mol.bonds]
self.assertEqual(sum(x == 1 for x in bondorders), 6)
self.assertEqual(sum(bond.arom for bond in mol.bonds), 6)
mol = ParseSmiles("c1ccccc1C", True) # Will be kekulized
bondorders = [bond.order for bond in mol.bonds]
self.assertEqual(sum(x == 1 for x in bondorders), 4)
self.assertEqual(sum(x == 2 for x in bondorders), 3)
def testAsterisk(self):
mol = ParseSmiles("*", True)
self.assertEqual(mol.atoms[0].element, 0)
self.assertEqual(mol.atoms[0].implh, 0)
mol = ParseSmiles("[*H]", True)
self.assertEqual(mol.atoms[0].element, 0)
self.assertEqual(mol.atoms[0].implh, 1)
def testEffectOfOpenRing(self):
# If there's a ring opening, there must be an additional
# valence (if at the outermost branching level).
ParseSmiles("C1C=N", True)
self.assertRaises(ValenceError, ParseSmiles, "C1C=N2", True)
ParseSmiles("C1C=NC", True)
ParseSmiles("c1(=O", True)
ParseSmiles("c1(=O)", True)
def testIsotope(self):
good = ["[12CH4]"]
bad = [
"[0CH4]", "[1", "[12", "[123", "[v", "[C@", "[C@@", "[CH", "[CH4",
"[C+", "[C+2", "[C++", "[C++ "
]
self.check(good, bad)
self.assertEqual(ParseSmiles("[12CH4]").atoms[0].isotope, 12)
self.assertEqual(ParseSmiles("[123CH4]").atoms[0].isotope, 123)
def testRuleThree(self):
"""Whether to require that the final branch be unparenthesised"""
smis = ["C(O(C))", "C(O).C"]
for smi in smis:
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, False)
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, True)
ParseSmiles(smi, False, 4)
smis = ["C(O)"] # these are fine as partial but not otherwise
for smi in smis:
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, False)
ParseSmiles(smi, True)
ParseSmiles(smi, False, 4)
def testBasic(self):
good = ["C>O>N", "C>>N"]
empty = ["C>>", ">>N", ">O>", "C.>>.N"]
bad = ["C>O>N>S"]
for smi in good:
mol = ParseSmiles(smi, partial=False)
for smi in bad + empty:
self.assertRaises(SMILESSyntaxError,
ParseSmiles,
smi,
partial=False)
for smi in empty:
mol = ParseSmiles(smi, partial=False, rulesToIgnore=1)
def testRuleSix(self):
"""Whether to require ring closure symbols immediately after atoms"""
smis = ["C(1)CCC1", "C(CCC1)1"]
for smi in smis:
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, False)
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, True)
ParseSmiles(smi, False, 32)
def testRuleFive(self):
"""Whether to allow bond closures across disconnected components"""
smis = ["C1.C1"]
for smi in smis:
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, False)
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, True)
ParseSmiles(smi, False, 16)
def testRuleFour(self):
"""Whether to allow a dot within parentheses"""
smis = ["C(C.C)C"]
for smi in smis:
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, False)
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, True)
ParseSmiles(smi, False, 8)
def check(self, good, bad):
for smi in good:
ParseSmiles(smi, partial=False)
for smi in bad:
self.assertRaises(SMILESSyntaxError,
ParseSmiles,
smi,
partial=False)
def testHardCases(self):
smis = [
"c12c3c4c5c1c6c7c8c9c6c%10c5c%11c%12c4c%13c%14c%15c-%16c%17c%13c%12c%18c%19c%17c%20c%16c%21c%22=c%23c%24c(c8c%25C%24%26C%27(C%26)c%22c%20c%28c%19c%29c%30c(c%27%28)-c%25c9c%30c%10c%11c%29%18)c%31c7c2c%32-c%31c%23C%21%33C%15(c%32c%143)C%33",
"c12c3c4c5c6c1c-7c8c9c2c%10c3c%11c%12c%13c%14c%15c%16c%17c%13c%11c4c%18c%17c-%19c%20C%21%22c%23c%24-c%25c%26C%21(C%22)c(c%19%16)c-%27c%15C%28%29c%14c-%30c%12c%10c%31c9c%32c-%33c(c%31%30)C%28(C%29)c(c%26%27)c%33c%25C%34(C%328C%34)c%24c7c6c%23c%20c5%18",
"c12c3c4c5c6c7c4c8c9c%10c%11c8c%12c7c%13c-%14c6c%15c%16c%14c%17c%18c%19c%20c%21=c%22c%23c%24c(c1c(c93)c%25c%24c%26c%22c%27c%21c%18c%28C%17%29C%13(c%12c%30-c%28c%27c(c%11%30)c%26c%10%25)C%31C%29C(=N)CCC%31)c%32c-%33c2c5c%15c%33c(c%19%16)C%20C%32%23",
"c12c3c4c5c6c7c8c5c9c%10c4c1c%11c%12c%13c2c%14c%15c3c6c%16c%15c%17c%18c%19c%16c7c%20c%19c%21c%22c%18c%23c%17c%14c%13c%24c%23c%25c%22c%26c%27c%28c%29c(c%12c%24c%28%25)-c%11c%10C%30%31C%29(c%27c-%32c(c%26%21)c%20c8c%32c%309)CC(=N)CC%31"
]
for smi in smis:
mol = ParseSmiles(smi, False)
def testCharge(self):
data = [
("[NH4+]", 1),
("[CH3-]", -1),
("[CH2--]", -2),
]
for smi, charge in data:
mol = ParseSmiles(smi, False)
self.assertTrue(mol.atoms[0].charge, charge)
def testRuleSeven(self):
"""Whether to reject aromatic bond symbols"""
# Aromatic bond symbols are not needed in a SMILES string
# - an aromatic bond connecting two lowercase atoms is implicit
# - the meaning of an aromatic bond attached to an uppercase atom
# is a matter of intense debate
smi = "c1:c:c:c:c:c1"
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, False)
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, True)
ParseSmiles(smi, False, 64)
def testCoverage(self):
smis = [
"Cs1(=O)ccccn1", # S-oxides
"c1c#cccc1", # benzyne
"n1cnc[n-]1", # from SMILES benchmark
"[nH]1cnnn1", # ditto
"n1cnco1", # ditto
"n1(cno[cH+]1)C", # ditto
"O[p+]1(O)cccc1", # invented molecule
"[s-]1(O)cccc1" # invented molecule
]
for smi in smis:
mol = ParseSmiles(smi, partial=False)
def testBugs(self):
# Don't raise valence errors for the following
good = ["c1O", "c1cc(sc1="]
for smi in good:
mol = ParseSmiles(smi, partial=True)
self.assertRaises(ValenceError, ParseSmiles, "CN(C)=", True)
# The following is 5-valent at least, and we only allow 3-valent
# nitrogens.
self.assertRaises(ValenceError, ParseSmiles, "CCN(=O)(", True)
# The second bond closure was not contributing to the
# adjusted valence due to a 'break' statement
self.assertRaises(ValenceError, ParseSmiles, "C=C3=1", True)
def testBonds(self):
mol = ParseSmiles("CCO", False)
self.assertTrue(mol.getBond(mol.atoms[0], mol.atoms[1]))
self.assertTrue(mol.getBond(mol.atoms[1], mol.atoms[2]))
self.assertFalse(mol.getBond(mol.atoms[0], mol.atoms[2]))
def testRuleOne(self):
"""Whether to allow empty molecules, like C..C"""
smi = "C..C"
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, False)
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, True)
ParseSmiles(smi, False, 1)
def testCoverage(self):
for smi in ["[Eu]C", "[N](=C)(C)(C)C"]:
self.assertRaises(ValenceError, ParseSmiles, smi, True)
# TEMPO
mol = ParseSmiles("C1(C)(C)N([O])C(C)(C)CCC1", partial=False)
mol = ParseSmiles("FC[CH2]", partial=True)
def testInvalid(self):
mol = ParseSmiles("[CH3]C", True)
self.assertRaises(ValenceError, ParseSmiles, "[CH2]C", True)
self.assertRaises(ValenceError, ParseSmiles, "[CH3]1C", True)
self.assertRaises(ValenceError, ParseSmiles, "[CH2]=1C", True)
def testRuleTwo(self):
"Whether to allow an empty branch like C()C"
smi = "C()C"
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, False)
self.assertRaises(SMILESSyntaxError, ParseSmiles, smi, True)
ParseSmiles(smi, False, 2)
def testRingClosures(self):
smis = ["c1.c1", "c1.c:1", "C1.C:1"]
for smi in smis:
mol = ParseSmiles(smi, rulesToIgnore=16 | 64)
self.assertEqual(2, mol.bonds[0].order)
self.assertTrue(mol.bonds[0].arom)
def testBasic(self):
smis = ["cc", "c:c", "C:C"] # What about c=c? Is this [C]=[C]?
for smi in smis:
mol = ParseSmiles(smi, rulesToIgnore=64)
self.assertEqual(2, mol.bonds[0].order)
self.assertTrue(mol.bonds[0].arom)
