@Test
public void methyleneCyclopropeneTest() {
IAtomContainer mol = builder.newInstance(IAtomContainer.class);
AbstractSignatureTest.addCarbons(mol, 4);
AbstractSignatureTest.addHydrogens(mol, 1, 2);
AbstractSignatureTest.addHydrogens(mol, 2, 1);
AbstractSignatureTest.addHydrogens(mol, 3, 1);
mol.addBond(0, 1, IBond.Order.DOUBLE);
mol.addBond(0, 2, IBond.Order.SINGLE);
mol.addBond(0, 3, IBond.Order.SINGLE);
mol.addBond(2, 3, IBond.Order.DOUBLE);
MoleculeSignature molSig = new MoleculeSignature(mol);
String sigFor2Height1 = molSig.signatureStringForVertex(2, 1);
String sigFor3Height1 = molSig.signatureStringForVertex(3, 1);
Assert.assertTrue(
"Height 1 signatures for atoms 2 and 3" + " should be the same",
sigFor2Height1.equals(sigFor3Height1));
String sigFor2Height2 = molSig.signatureStringForVertex(2, 1);
String sigFor3Height2 = molSig.signatureStringForVertex(3, 1);
Assert.assertTrue(
"Height 2 signatures for atoms 2 and 3" + " should be the same",
sigFor2Height2.equals(sigFor3Height2));
}
/** A unit test for JUnit */
@Test
public void testBug791091() {
String smiles = "";
IAtomContainer molecule = new AtomContainer();
SmilesGenerator sg = new SmilesGenerator();
molecule.addAtom(new Atom("C"));
molecule.addAtom(new Atom("C"));
molecule.addAtom(new Atom("C"));
molecule.addAtom(new Atom("C"));
molecule.addAtom(new Atom("N"));
molecule.addBond(0, 1, IBond.Order.SINGLE);
molecule.addBond(1, 2, IBond.Order.SINGLE);
molecule.addBond(2, 4, IBond.Order.SINGLE);
molecule.addBond(4, 0, IBond.Order.SINGLE);
molecule.addBond(4, 3, IBond.Order.SINGLE);
fixCarbonHCount(molecule);
try {
smiles = sg.createSMILES(molecule);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
if (standAlone) {
System.err.println("SMILES: " + smiles);
}
Assert.assertEquals("N1(C)CCC1", smiles);
}
/** A bug reported for JChemPaint. */
@Test
public void testSFBug956923() throws Exception {
String smiles = "";
IAtomContainer molecule = new AtomContainer();
SmilesGenerator sg = new SmilesGenerator();
Atom sp2CarbonWithOneHydrogen = new Atom("C");
sp2CarbonWithOneHydrogen.setHybridization(Hybridization.SP2);
sp2CarbonWithOneHydrogen.setImplicitHydrogenCount(1);
molecule.addAtom(sp2CarbonWithOneHydrogen);
molecule.addAtom((Atom) sp2CarbonWithOneHydrogen.clone());
molecule.addAtom((Atom) sp2CarbonWithOneHydrogen.clone());
molecule.addAtom((Atom) sp2CarbonWithOneHydrogen.clone());
molecule.addAtom((Atom) sp2CarbonWithOneHydrogen.clone());
molecule.addAtom((Atom) sp2CarbonWithOneHydrogen.clone());
molecule.addBond(0, 1, IBond.Order.SINGLE);
molecule.addBond(1, 2, IBond.Order.SINGLE);
molecule.addBond(2, 3, IBond.Order.SINGLE);
molecule.addBond(3, 4, IBond.Order.SINGLE);
molecule.addBond(4, 5, IBond.Order.SINGLE);
molecule.addBond(5, 0, IBond.Order.SINGLE);
try {
smiles = sg.createSMILES(molecule);
} catch (Exception exc) {
Assert.fail(exc.getMessage());
}
Assert.assertEquals("c1ccccc1", smiles);
}
/**
* (2S)-butan-2-ol
*
* @cdk.inchi InChI=1/C4H10O/c1-3-4(2)5/h4-5H,3H2,1-2H3/t4-/s2
*/
@Test
public void _2S_butan_2_ol() throws Exception {
IAtomContainer ac = new AtomContainer();
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("O"));
ac.addAtom(new Atom("H"));
ac.addBond(0, 1, SINGLE);
ac.addBond(1, 2, SINGLE);
ac.addBond(2, 3, SINGLE);
ac.addBond(2, 4, SINGLE);
ac.addBond(2, 5, SINGLE);
ac.addStereoElement(
new TetrahedralChirality(
ac.getAtom(2),
new IAtom[] {
ac.getAtom(1), // C-C
ac.getAtom(3), // C
ac.getAtom(4), // O
ac.getAtom(5), // H
},
ANTI_CLOCKWISE));
Graph g = convert(ac);
assertThat(g.toSmiles(), is("CC[C@](C)(O)[H]"));
}
/**
* Get the expected set of molecules.
*
* @return The IAtomContainerSet
*/
private IAtomContainerSet getExpectedProducts() {
IAtomContainerSet setOfProducts = builder.newInstance(IAtomContainerSet.class);
IAtomContainer molecule = builder.newInstance(IAtomContainer.class);
molecule.addAtom(builder.newInstance(IAtom.class, "C"));
molecule.getAtom(0).setFormalCharge(1);
molecule.addAtom(builder.newInstance(IAtom.class, "C"));
molecule.addBond(0, 1, IBond.Order.SINGLE);
molecule.addAtom(builder.newInstance(IAtom.class, "C"));
molecule.addBond(1, 2, IBond.Order.SINGLE);
molecule.addAtom(builder.newInstance(IAtom.class, "C"));
molecule.addBond(2, 3, IBond.Order.SINGLE);
molecule.addAtom(builder.newInstance(IAtom.class, "C"));
molecule.addBond(3, 4, IBond.Order.SINGLE);
molecule.addAtom(builder.newInstance(IAtom.class, "C"));
molecule.addBond(4, 5, IBond.Order.SINGLE);
try {
addExplicitHydrogens(molecule);
} catch (Exception e) {
e.printStackTrace();
}
molecule.getAtom(0).setFormalCharge(0);
molecule.addSingleElectron(new SingleElectron(molecule.getAtom(0)));
try {
AtomContainerManipulator.percieveAtomTypesAndConfigureAtoms(molecule);
makeSureAtomTypesAreRecognized(molecule);
} catch (CDKException e) {
e.printStackTrace();
}
setOfProducts.addAtomContainer(molecule);
return setOfProducts;
}
@Test
public void s_penta_2_3_diene_expl_h() throws Exception {
IAtomContainer m = new AtomContainer(5, 4, 0, 0);
m.addAtom(new Atom("C"));
m.addAtom(new Atom("C"));
m.addAtom(new Atom("C"));
m.addAtom(new Atom("C"));
m.addAtom(new Atom("C"));
m.addAtom(new Atom("H"));
m.addAtom(new Atom("H"));
m.addBond(0, 1, IBond.Order.SINGLE);
m.addBond(1, 2, IBond.Order.DOUBLE);
m.addBond(2, 3, IBond.Order.DOUBLE);
m.addBond(3, 4, IBond.Order.SINGLE);
m.addBond(1, 5, IBond.Order.SINGLE);
m.addBond(3, 6, IBond.Order.SINGLE);
int[][] atoms =
new int[][] {
{0, 5, 6, 4},
{5, 0, 6, 4},
{5, 0, 4, 6},
{0, 5, 4, 6},
{4, 6, 5, 0},
{4, 6, 0, 5},
{6, 4, 0, 5},
{6, 4, 5, 0},
};
Stereo[] stereos =
new Stereo[] {
Stereo.CLOCKWISE,
Stereo.ANTI_CLOCKWISE,
Stereo.CLOCKWISE,
Stereo.ANTI_CLOCKWISE,
Stereo.CLOCKWISE,
Stereo.ANTI_CLOCKWISE,
Stereo.CLOCKWISE,
Stereo.ANTI_CLOCKWISE
};
for (int i = 0; i < atoms.length; i++) {
IStereoElement element =
new ExtendedTetrahedral(
m.getAtom(2),
new IAtom[] {
m.getAtom(atoms[i][0]),
m.getAtom(atoms[i][1]),
m.getAtom(atoms[i][2]),
m.getAtom(atoms[i][3])
},
stereos[i]);
m.setStereoElements(Collections.singletonList(element));
assertThat(convert(m).toSmiles(), is("CC(=[C@]=C(C)[H])[H]"));
}
}
/** @cdk.inchi InChI=1/C4H5N/c1-2-4-5-3-1/h1-5H */
@Test
public void xtestPyrrole() throws Exception {
IAtomContainer enol = new AtomContainer();
// atom block
IAtom atom1 = new Atom(Elements.CARBON);
atom1.setHybridization(Hybridization.SP2);
IAtom atom2 = new Atom(Elements.CARBON);
atom2.setHybridization(Hybridization.SP2);
IAtom atom3 = new Atom(Elements.CARBON);
atom3.setHybridization(Hybridization.SP2);
IAtom atom4 = new Atom(Elements.CARBON);
atom4.setHybridization(Hybridization.SP2);
IAtom atom5 = new Atom(Elements.NITROGEN);
atom5.setHybridization(Hybridization.SP2);
atom5.setImplicitHydrogenCount(1);
// bond block
IBond bond1 = new Bond(atom1, atom2);
IBond bond2 = new Bond(atom2, atom3);
IBond bond3 = new Bond(atom3, atom4);
IBond bond4 = new Bond(atom4, atom5);
IBond bond5 = new Bond(atom5, atom1);
enol.addAtom(atom1);
enol.addAtom(atom2);
enol.addAtom(atom3);
enol.addAtom(atom4);
enol.addAtom(atom5);
enol.addBond(bond1);
enol.addBond(bond2);
enol.addBond(bond3);
enol.addBond(bond4);
enol.addBond(bond5);
// perceive atom types
AtomContainerManipulator.percieveAtomTypesAndConfigureAtoms(enol);
// now have the algorithm have a go at it
enol = fbot.kekuliseAromaticRings(enol);
Assert.assertNotNull(enol);
// Assert.assertTrue(fbot.isOK(enol));
// now check whether it did the right thing
Assert.assertEquals(CDKConstants.BONDORDER_DOUBLE, enol.getBond(0).getOrder());
;
Assert.assertEquals(CDKConstants.BONDORDER_SINGLE, enol.getBond(1).getOrder());
;
Assert.assertEquals(CDKConstants.BONDORDER_DOUBLE, enol.getBond(2).getOrder());
;
Assert.assertEquals(CDKConstants.BONDORDER_SINGLE, enol.getBond(3).getOrder());
;
Assert.assertEquals(CDKConstants.BONDORDER_SINGLE, enol.getBond(4).getOrder());
;
}
@Test
public void cyclobuteneTest() {
String expectedA = "[C]([C]([C,0])=[C]([C,0]))";
String expectedB = "[C]([C]([C,0])[C](=[C,0]))";
IAtomContainer cyclobutene = builder.newInstance(IAtomContainer.class);
AbstractSignatureTest.addCarbons(cyclobutene, 4);
cyclobutene.addBond(0, 1, IBond.Order.SINGLE);
cyclobutene.addBond(0, 2, IBond.Order.SINGLE);
cyclobutene.addBond(1, 3, IBond.Order.DOUBLE);
cyclobutene.addBond(2, 3, IBond.Order.SINGLE);
Assert.assertEquals(expectedA, canonicalStringFromMolecule(cyclobutene));
String expectedFullString = "2" + expectedA + " + 2" + expectedB;
String actualFullString = fullStringFromMolecule(cyclobutene);
Assert.assertEquals(expectedFullString, actualFullString);
}
/**
* Selects an optimum edge for elimination in structures without N2 nodes.
*
* <p>This might be severely broken! Would have helped if there was an explanation of how this
* algorithm worked.
*
* @param ring
* @param molecule
*/
private IBond checkEdges(IRing ring, IAtomContainer molecule) {
IRing r1, r2;
IRingSet ringSet = ring.getBuilder().newInstance(IRingSet.class);
IBond bond;
int minMaxSize = Integer.MAX_VALUE;
int minMax = 0;
logger.debug("Molecule: " + molecule);
Iterator<IBond> bonds = ring.bonds().iterator();
while (bonds.hasNext()) {
bond = (IBond) bonds.next();
molecule.removeElectronContainer(bond);
r1 = getRing(bond.getAtom(0), molecule);
r2 = getRing(bond.getAtom(1), molecule);
logger.debug("checkEdges: " + bond);
if (r1.getAtomCount() > r2.getAtomCount()) {
ringSet.addAtomContainer(r1);
} else {
ringSet.addAtomContainer(r2);
}
molecule.addBond(bond);
}
for (int i = 0; i < ringSet.getAtomContainerCount(); i++) {
if (((IRing) ringSet.getAtomContainer(i)).getBondCount() < minMaxSize) {
minMaxSize = ((IRing) ringSet.getAtomContainer(i)).getBondCount();
minMax = i;
}
}
return (IBond) ring.getElectronContainer(minMax);
}
public void addHydrogens(IAtomContainer mol, IAtom atom, int n) {
for (int i = 0; i < n; i++) {
IAtom h = builder.newInstance(IAtom.class, "H");
mol.addAtom(h);
mol.addBond(builder.newInstance(IBond.class, atom, h));
}
}
/**
* Procedure required by the CDOInterface. This function is only supposed to be called by the JCFL
* library
*/
public void endObject(String objectType) {
logger.debug("END: " + objectType);
if (objectType.equals("Molecule")) {
eventReader.fireFrameRead();
clearData();
} else if (objectType.equals("Atom")) {
currentMolecule.addAtom(currentAtom);
} else if (objectType.equals("Bond")) {
logger.debug("Bond(" + bond_id + "): " + bond_a1 + ", " + bond_a2 + ", " + bond_order);
if (bond_a1 > currentMolecule.getAtomCount() || bond_a2 > currentMolecule.getAtomCount()) {
logger.error(
"Cannot add bond between at least one non-existant atom: "
+ bond_a1
+ " and "
+ bond_a2);
} else {
IAtom a1 = currentMolecule.getAtom(bond_a1);
IAtom a2 = currentMolecule.getAtom(bond_a2);
IBond b = builder.newBond(a1, a2, bond_order);
if (bond_id != null) b.setID(bond_id);
if (bond_stereo != -99) {
b.setStereo(bond_stereo);
}
currentMolecule.addBond(b);
}
}
}
public static IAtomContainer makeFragment4() {
IAtomContainer mol = DefaultChemObjectBuilder.getInstance().newInstance(IAtomContainer.class);
mol.addAtom(new Atom("C")); // 0
mol.addAtom(new Atom("C")); // 1
mol.addBond(0, 1, IBond.Order.SINGLE); // 1
return mol;
}
@BeforeClass
public static void setup() throws Exception {
molecule = new AtomContainer();
molecule.addAtom(new Atom("Cl"));
molecule.addAtom(new Atom("C"));
molecule.addAtom(new Atom("Br"));
molecule.addAtom(new Atom("I"));
molecule.addAtom(new Atom("H"));
molecule.addBond(0, 1, Order.SINGLE);
molecule.addBond(1, 2, Order.SINGLE);
molecule.addBond(1, 3, Order.SINGLE);
molecule.addBond(1, 4, Order.SINGLE);
ligands =
new IAtom[] {
molecule.getAtom(4), molecule.getAtom(3), molecule.getAtom(2), molecule.getAtom(0)
};
}
@Test
public void fusedSquareMultipleBondTest() {
IAtomContainer mol = builder.newInstance(IAtomContainer.class);
String expected = "[C]([C]([C,1])[C]([C,0])[C](=[C,1])[C](=[C,0]))";
AbstractSignatureTest.addCarbons(mol, 7);
mol.addBond(0, 1, IBond.Order.SINGLE);
mol.addBond(0, 2, IBond.Order.SINGLE);
mol.addBond(0, 3, IBond.Order.SINGLE);
mol.addBond(0, 4, IBond.Order.SINGLE);
mol.addBond(1, 5, IBond.Order.DOUBLE);
mol.addBond(2, 5, IBond.Order.SINGLE);
mol.addBond(3, 6, IBond.Order.SINGLE);
mol.addBond(4, 6, IBond.Order.DOUBLE);
MoleculeSignature molSig = new MoleculeSignature(mol);
String sigFor0 = molSig.signatureStringForVertex(0);
Assert.assertEquals(expected, sigFor0);
}
@Test
public void testNotCharged() throws Exception {
IAtomContainer mol = builder.newInstance(IAtomContainer.class);
mol.addAtom(builder.newInstance(IAtom.class, "C"));
mol.getAtom(0).setFormalCharge(-1);
mol.addAtom(builder.newInstance(IAtom.class, "C"));
mol.addBond(0, 1, Order.DOUBLE);
mol.addAtom(builder.newInstance(IAtom.class, "F"));
mol.addBond(1, 2, Order.SINGLE);
addExplicitHydrogens(mol);
lpcheck.saturate(mol);
DoubleResult result = ((DoubleResult) descriptor.calculate(mol.getAtom(0), mol).getValue());
Assert.assertEquals(0.0, result.doubleValue(), 0.00001);
}
public static IAtomContainer makeFragment3() {
IAtomContainer mol = DefaultChemObjectBuilder.getInstance().newInstance(IAtomContainer.class);
mol.addAtom(new Atom("C")); // 0
mol.addAtom(new Atom("C")); // 1
mol.addAtom(new Atom("C")); // 2
mol.addAtom(new Atom("C")); // 3
mol.addAtom(new Atom("C")); // 4
mol.addAtom(new Atom("C")); // 5
mol.addAtom(new Atom("C")); // 6
mol.addBond(0, 1, IBond.Order.SINGLE); // 1
mol.addBond(0, 2, IBond.Order.SINGLE); // 2
mol.addBond(0, 3, IBond.Order.SINGLE); // 3
mol.addBond(0, 4, IBond.Order.SINGLE); // 4
mol.addBond(3, 5, IBond.Order.DOUBLE); // 5
mol.addBond(5, 6, IBond.Order.SINGLE); // 6
return mol;
}
/**
* (Z)-1,2-difluoroethene
*
* @cdk.inchi InChI=1/C2H2F2/c3-1-2-4/h1-2H/b2-1-
*/
@Test
public void z_1_2_difluoroethene() throws Exception {
IAtomContainer ac = new AtomContainer();
ac.addAtom(new Atom("F"));
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("F"));
ac.addBond(0, 1, SINGLE);
ac.addBond(1, 2, DOUBLE);
ac.addBond(2, 3, SINGLE);
ac.addStereoElement(
new DoubleBondStereochemistry(
ac.getBond(1), new IBond[] {ac.getBond(0), ac.getBond(2)}, TOGETHER));
Graph g = convert(ac);
assertThat(g.toSmiles(), is("F/C=C\\F"));
}
@Before
public void setUp() {
this.parser = new SmilesParser(DefaultChemObjectBuilder.getInstance());
this.builder = DefaultChemObjectBuilder.getInstance();
mol = builder.newInstance(IAtomContainer.class);
mol.addAtom(builder.newInstance(IAtom.class, "C"));
mol.addAtom(builder.newInstance(IAtom.class, "C"));
mol.addBond(0, 1, IBond.Order.SINGLE);
molSig = new MoleculeSignature(mol);
}
/**
* This is a mock test where we don't want aromatic bonds to have a configuration.
* (Z)-1,2-difluoroethene is not aromatic but a 'real' example would be porphyrins.
*
* @cdk.inchi InChI=1/C2H2F2/c3-1-2-4/h1-2H/b2-1-
*/
@Test
public void z_1_2_difluoroethene_aromatic() throws Exception {
IAtomContainer ac = new AtomContainer();
ac.addAtom(new Atom("F"));
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("F"));
ac.addBond(0, 1, SINGLE);
ac.addBond(1, 2, DOUBLE);
ac.addBond(2, 3, SINGLE);
ac.getBond(1).setFlag(CDKConstants.ISAROMATIC, true);
ac.addStereoElement(
new DoubleBondStereochemistry(
ac.getBond(1), new IBond[] {ac.getBond(0), ac.getBond(2)}, TOGETHER));
Graph g = convert(ac);
assertThat(g.toSmiles(), is("F[CH]:[CH]F"));
}
/** Tests the method saturate(). */
@Test
public void testSaturate_NumberingProblem() throws Exception {
IAtomContainer mol = new AtomContainer();
Atom a1 = new Atom("C");
mol.addAtom(a1);
Atom a2 = new Atom("C");
mol.addAtom(a2);
Atom a3 = new Atom("C");
mol.addAtom(a3);
Atom a4 = new Atom("H");
mol.addAtom(a4);
Atom a5 = new Atom("C");
mol.addAtom(a5);
Atom a6 = new Atom("H");
mol.addAtom(a6);
Atom a7 = new Atom("S");
mol.addAtom(a7);
Atom a8 = new Atom("H");
mol.addAtom(a8);
Atom a9 = new Atom("H");
mol.addAtom(a9);
Bond b1 = new Bond(a1, a2, IBond.Order.SINGLE);
mol.addBond(b1);
Bond b2 = new Bond(a1, a3, IBond.Order.SINGLE);
mol.addBond(b2);
Bond b3 = new Bond(a1, a4, IBond.Order.SINGLE);
mol.addBond(b3);
Bond b4 = new Bond(a5, a2, IBond.Order.SINGLE);
mol.addBond(b4);
Bond b5 = new Bond(a2, a6, IBond.Order.SINGLE);
mol.addBond(b5);
Bond b6 = new Bond(a3, a7, IBond.Order.SINGLE);
mol.addBond(b6);
Bond b7 = new Bond(a3, a8, IBond.Order.SINGLE);
mol.addBond(b7);
Bond b8 = new Bond(a7, a5, IBond.Order.SINGLE);
mol.addBond(b8);
Bond b9 = new Bond(a5, a9, IBond.Order.SINGLE);
mol.addBond(b9);
satcheck.saturate(mol);
Assert.assertEquals(IBond.Order.SINGLE, b1.getOrder());
Assert.assertEquals(IBond.Order.DOUBLE, b2.getOrder());
Assert.assertEquals(IBond.Order.SINGLE, b6.getOrder());
Assert.assertEquals(IBond.Order.SINGLE, b8.getOrder());
Assert.assertEquals(IBond.Order.DOUBLE, b4.getOrder());
}
@Test
public void testBenzeneWithDoubleBonds() {
IAtomContainer benzene = builder.newInstance(IAtomContainer.class);
AbstractSignatureTest.addCarbons(benzene, 6);
for (int i = 0; i < 6; i++) {
AbstractSignatureTest.addHydrogens(benzene, i, 1);
}
benzene.addBond(0, 1, IBond.Order.SINGLE);
benzene.addBond(1, 2, IBond.Order.DOUBLE);
benzene.addBond(2, 3, IBond.Order.SINGLE);
benzene.addBond(3, 4, IBond.Order.DOUBLE);
benzene.addBond(4, 5, IBond.Order.SINGLE);
benzene.addBond(5, 0, IBond.Order.DOUBLE);
MoleculeSignature signature = new MoleculeSignature(benzene);
String carbonSignature = signature.signatureStringForVertex(0);
for (int i = 1; i < 6; i++) {
String carbonSignatureI = signature.signatureStringForVertex(i);
Assert.assertEquals(carbonSignature, carbonSignatureI);
}
}
@Test
public void napthaleneSkeletonHeightTest() {
IAtomContainer napthalene = builder.newInstance(IAtomContainer.class);
for (int i = 0; i < 10; i++) {
napthalene.addAtom(builder.newInstance(IAtom.class, "C"));
}
napthalene.addBond(0, 1, IBond.Order.SINGLE);
napthalene.addBond(0, 5, IBond.Order.SINGLE);
napthalene.addBond(1, 2, IBond.Order.SINGLE);
napthalene.addBond(1, 6, IBond.Order.SINGLE);
napthalene.addBond(2, 3, IBond.Order.SINGLE);
napthalene.addBond(2, 9, IBond.Order.SINGLE);
napthalene.addBond(3, 4, IBond.Order.SINGLE);
napthalene.addBond(4, 5, IBond.Order.SINGLE);
napthalene.addBond(6, 7, IBond.Order.SINGLE);
napthalene.addBond(7, 8, IBond.Order.SINGLE);
napthalene.addBond(8, 9, IBond.Order.SINGLE);
MoleculeSignature molSig = new MoleculeSignature(napthalene);
int height = 2;
Map<String, Orbit> orbits = new HashMap<String, Orbit>();
for (int i = 0; i < napthalene.getAtomCount(); i++) {
String signatureString = molSig.signatureStringForVertex(i, height);
Orbit orbit;
if (orbits.containsKey(signatureString)) {
orbit = orbits.get(signatureString);
} else {
orbit = new Orbit(signatureString, height);
orbits.put(signatureString, orbit);
}
orbit.addAtom(i);
}
Assert.assertEquals(3, orbits.size());
}
@Test
public void writeAtomClass() throws Exception {
IAtomContainer ac = new AtomContainer();
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("C"));
ac.addAtom(new Atom("O"));
ac.addBond(0, 1, SINGLE);
ac.addBond(1, 2, SINGLE);
ac.getAtom(0).setProperty(CDKConstants.ATOM_ATOM_MAPPING, 3);
ac.getAtom(1).setProperty(CDKConstants.ATOM_ATOM_MAPPING, 1);
ac.getAtom(2).setProperty(CDKConstants.ATOM_ATOM_MAPPING, 2);
assertThat(convert(ac).toSmiles(), is("[CH3:3][CH2:1][OH:2]"));
}
@Test
public void s_penta_2_3_diene_impl_h() throws Exception {
IAtomContainer m = new AtomContainer(5, 4, 0, 0);
m.addAtom(new Atom("C"));
m.addAtom(new Atom("C"));
m.addAtom(new Atom("C"));
m.addAtom(new Atom("C"));
m.addAtom(new Atom("C"));
m.addBond(0, 1, IBond.Order.SINGLE);
m.addBond(1, 2, IBond.Order.DOUBLE);
m.addBond(2, 3, IBond.Order.DOUBLE);
m.addBond(3, 4, IBond.Order.SINGLE);
IStereoElement element =
new ExtendedTetrahedral(
m.getAtom(2),
new IAtom[] {m.getAtom(0), m.getAtom(1), m.getAtom(3), m.getAtom(4)},
CLOCKWISE);
m.setStereoElements(Collections.singletonList(element));
assertThat(convert(m).toSmiles(), is("CC=[C@@]=CC"));
}
private void processBondsBlock(int lineCount, IAtomContainer container) throws IOException {
for (int i = 0; i < lineCount; i++) {
String line = input.readLine();
int atom1 = Integer.parseInt(line.substring(10, 13).trim()) - 1;
int atom2 = Integer.parseInt(line.substring(16, 19).trim()) - 1;
if (container.getBond(container.getAtom(atom1), container.getAtom(atom2)) == null) {
IBond bond =
container.getBuilder().newBond(container.getAtom(atom1), container.getAtom(atom2));
int order = Integer.parseInt(line.substring(23).trim());
bond.setOrder(BondManipulator.createBondOrder((double) order));
container.addBond(bond);
} // else: bond already present; CTX store the bonds twice
}
}
@Test
public void testNNMolecule_IAtomContainer() {
IAtomContainer acetone = new org.openscience.cdk.AtomContainer();
IAtom c1 = acetone.getBuilder().newAtom("C");
IAtom c2 = acetone.getBuilder().newAtom("C");
IAtom o = acetone.getBuilder().newAtom("O");
IAtom c3 = acetone.getBuilder().newAtom("C");
acetone.addAtom(c1);
acetone.addAtom(c2);
acetone.addAtom(c3);
acetone.addAtom(o);
IBond b1 = acetone.getBuilder().newBond(c1, c2, IBond.Order.SINGLE);
IBond b2 = acetone.getBuilder().newBond(c1, o, IBond.Order.DOUBLE);
IBond b3 = acetone.getBuilder().newBond(c1, c3, IBond.Order.SINGLE);
acetone.addBond(b1);
acetone.addBond(b2);
acetone.addBond(b3);
IMolecule m = new NNMolecule(acetone);
Assert.assertNotNull(m);
Assert.assertEquals(4, m.getAtomCount());
Assert.assertEquals(3, m.getBondCount());
}
public static IAtomContainer makePropylAmine() {
IAtomContainer mol = DefaultChemObjectBuilder.getInstance().newInstance(IAtomContainer.class);
Atom atom = new Atom("C");
atom.setID("0");
mol.addAtom(atom); // 0
atom = new Atom("C");
atom.setID("1");
mol.addAtom(atom); // 1
atom = new Atom("C");
atom.setID("2");
mol.addAtom(atom); // 2
atom = new Atom("N");
atom.setID("3");
mol.addAtom(atom); // 3
mol.addBond(0, 1, IBond.Order.SINGLE); // 1
mol.addBond(1, 2, IBond.Order.SINGLE); // 2
mol.addBond(2, 3, IBond.Order.SINGLE); // 3
return mol;
}
/** A unit test for JUnit */
@Test
public void testBondPermutation() {
IAtomContainer mol = new AtomContainer();
mol.addAtom(new Atom("S"));
mol.addAtom(new Atom("O"));
mol.addAtom(new Atom("O"));
mol.addAtom(new Atom("O"));
mol.addAtom(new Atom("O"));
mol.addBond(0, 1, IBond.Order.DOUBLE);
mol.addBond(0, 2, IBond.Order.DOUBLE);
mol.addBond(0, 3, IBond.Order.SINGLE);
mol.addBond(0, 4, IBond.Order.SINGLE);
mol.getAtom(3).setImplicitHydrogenCount(1);
mol.getAtom(4).setImplicitHydrogenCount(1);
AtomContainerBondPermutor acbp = new AtomContainerBondPermutor(mol);
SmilesGenerator sg = new SmilesGenerator();
String smiles = "";
String oldSmiles = sg.createSMILES(mol);
while (acbp.hasNext()) {
smiles = sg.createSMILES(new AtomContainer((AtomContainer) acbp.next()));
// logger.debug(smiles);
Assert.assertEquals(oldSmiles, smiles);
}
}
/** A unit test for JUnit */
@Test
public void testAlanin() throws Exception {
HydrogenPlacer hydrogenPlacer = new HydrogenPlacer();
IAtomContainer mol1 = new AtomContainer();
SmilesGenerator sg = new SmilesGenerator();
mol1.addAtom(new Atom("N", new Point2d(1, 0)));
// 1
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 2
mol1.addAtom(new Atom("F", new Point2d(1, 2)));
// 3
mol1.addAtom(new Atom("C", new Point2d(0, 0)));
// 4
mol1.addAtom(new Atom("C", new Point2d(1, 4)));
// 5
mol1.addAtom(new Atom("O", new Point2d(1, 5)));
// 6
mol1.addAtom(new Atom("O", new Point2d(1, 6)));
// 7
mol1.addBond(0, 1, IBond.Order.SINGLE);
// 1
mol1.addBond(1, 2, IBond.Order.SINGLE, IBond.Stereo.UP);
// 2
mol1.addBond(1, 3, IBond.Order.SINGLE, IBond.Stereo.DOWN);
// 3
mol1.addBond(1, 4, IBond.Order.SINGLE);
// 4
mol1.addBond(4, 5, IBond.Order.SINGLE);
// 5
mol1.addBond(4, 6, IBond.Order.DOUBLE);
// 6
addExplicitHydrogens(mol1);
hydrogenPlacer.placeHydrogens2D(mol1, 1.0);
IsotopeFactory ifac = IsotopeFactory.getInstance(mol1.getBuilder());
ifac.configureAtoms(mol1);
String smiles1 = null;
if (standAlone) {
display(mol1);
}
smiles1 = sg.createSMILES(mol1, true, new boolean[mol1.getBondCount()]);
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals("[H]OC(=O)[C@](F)(N([H])[H])C([H])([H])[H]", smiles1);
mol1.getBond(1).setStereo(IBond.Stereo.DOWN);
mol1.getBond(2).setStereo(IBond.Stereo.UP);
smiles1 = sg.createSMILES(mol1, true, new boolean[mol1.getBondCount()]);
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals("[H]OC(=O)[C@](F)(C([H])([H])[H])N([H])[H]", smiles1);
}
/**
* A unit test for JUnit
*
* @throws Exception
*/
@Test
public void testStabilizationComparative() throws Exception {
IAtomContainer mol1 = builder.newInstance(IAtomContainer.class);
mol1.addAtom(builder.newInstance(IAtom.class, "C"));
mol1.addAtom(builder.newInstance(IAtom.class, "C"));
mol1.getAtom(1).setFormalCharge(1);
mol1.addBond(0, 1, Order.SINGLE);
mol1.addAtom(builder.newInstance(IAtom.class, "C"));
mol1.addBond(1, 2, Order.SINGLE);
mol1.addAtom(builder.newInstance(IAtom.class, "O"));
mol1.addBond(1, 3, Order.SINGLE);
addExplicitHydrogens(mol1);
lpcheck.saturate(mol1);
DoubleResult result1 = ((DoubleResult) descriptor.calculate(mol1.getAtom(1), mol1).getValue());
IAtomContainer mol2 = builder.newInstance(IAtomContainer.class);
mol2.addAtom(builder.newInstance(IAtom.class, "C"));
mol2.addAtom(builder.newInstance(IAtom.class, "C"));
mol2.getAtom(1).setFormalCharge(1);
mol2.addBond(0, 1, Order.SINGLE);
mol2.addAtom(builder.newInstance(IAtom.class, "O"));
mol2.addBond(1, 2, Order.SINGLE);
addExplicitHydrogens(mol2);
lpcheck.saturate(mol2);
DoubleResult result2 = ((DoubleResult) descriptor.calculate(mol2.getAtom(1), mol2).getValue());
IAtomContainer mol3 = builder.newInstance(IAtomContainer.class);
mol3.addAtom(builder.newInstance(IAtom.class, "C"));
mol3.addAtom(builder.newInstance(IAtom.class, "C"));
mol3.getAtom(1).setFormalCharge(1);
mol3.addBond(0, 1, Order.SINGLE);
mol3.addAtom(builder.newInstance(IAtom.class, "C"));
mol3.addBond(1, 2, Order.SINGLE);
addExplicitHydrogens(mol3);
lpcheck.saturate(mol3);
DoubleResult result3 = ((DoubleResult) descriptor.calculate(mol3.getAtom(1), mol3).getValue());
Assert.assertTrue(result3.doubleValue() < result2.doubleValue());
Assert.assertTrue(result2.doubleValue() < result1.doubleValue());
}