/// <summary> Calculate the number of missing hydrogens by substracting the number of
/// bonds for the atom from the expected number of bonds. Charges are included
/// in the calculation. The number of expected bonds is defined by the AtomType
/// generated with the AtomTypeFactory.
///
/// </summary>
/// <param name="atom"> Description of the Parameter
/// </param>
/// <param name="throwExceptionForUnknowAtom"> Should an exception be thrown if an unknown atomtype is found or 0 returned ?
/// </param>
/// <returns> Description of the Return Value
/// </returns>
/// <seealso cref="AtomTypeFactory">
/// </seealso>
public virtual int calculateNumberOfImplicitHydrogens(IAtom atom, double bondOrderSum, IBond[] connectedBonds, bool throwExceptionForUnknowAtom)
{
int missingHydrogen = 0;
if (atom is IPseudoAtom)
{
// don't figure it out... it simply does not lack H's
}
else if (atom.AtomicNumber == 1 || atom.Symbol.Equals("H"))
{
//UPGRADE_WARNING: Data types in Visual C# might be different. Verify the accuracy of narrowing conversions. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1042'"
missingHydrogen = (int)(1 - bondOrderSum - atom.getFormalCharge());
}
else
{
//logger.info("Calculating number of missing hydrogen atoms");
// get default atom
IAtomType[] atomTypes = getAtomTypeFactory(atom.Builder).getAtomTypes(atom.Symbol);
if (atomTypes.Length == 0 && throwExceptionForUnknowAtom)
{
return(0);
}
//logger.debug("Found atomtypes: " + atomTypes.Length);
if (atomTypes.Length > 0)
{
IAtomType defaultAtom = atomTypes[0];
//logger.debug("DefAtom: ", defaultAtom);
//UPGRADE_WARNING: Data types in Visual C# might be different. Verify the accuracy of narrowing conversions. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1042'"
missingHydrogen = (int)(defaultAtom.BondOrderSum - bondOrderSum + atom.getFormalCharge());
if (atom.getFlag(CDKConstants.ISAROMATIC))
{
bool subtractOne = true;
for (int i = 0; i < connectedBonds.Length; i++)
{
if (connectedBonds[i].Order == 2 || connectedBonds[i].Order == CDKConstants.BONDORDER_AROMATIC)
{
subtractOne = false;
}
}
if (subtractOne)
{
missingHydrogen--;
}
}
//logger.debug("Atom: ", atom.Symbol);
//logger.debug(" max bond order: " + defaultAtom.BondOrderSum);
//logger.debug(" bond order sum: " + bondOrderSum);
//logger.debug(" charge : " + atom.getFormalCharge());
}
else
{
//logger.warn("Could not find atom type for ", atom.Symbol);
}
}
return(missingHydrogen);
}
/// <summary> Generates the SMILES string for the atom
///
/// </summary>
/// <param name="a"> the atom to generate the SMILES for.
/// </param>
/// <param name="buffer"> the string buffer that the atom is to be
/// apended to.
/// </param>
/// <param name="container"> the AtomContainer to analyze.
/// </param>
/// <param name="chiral"> is a chiral smiles wished?
/// </param>
/// <param name="parent"> the atom we came from.
/// </param>
/// <param name="atomsInOrderOfSmiles"> a vector containing the atoms in the order
/// they are in the smiles.
/// </param>
/// <param name="currentChain"> The chain we currently deal with.
/// </param>
/// <param name="doubleBondConfiguration"> Description of Parameter
/// </param>
private void parseAtom(IAtom a, System.Text.StringBuilder buffer, IAtomContainer container, bool chiral, bool[] doubleBondConfiguration, IAtom parent, System.Collections.ArrayList atomsInOrderOfSmiles, System.Collections.ArrayList currentChain)
{
System.String symbol = a.Symbol;
bool stereo = BondTools.isStereo(container, a);
bool brackets = symbol.Equals("B") || symbol.Equals("C") || symbol.Equals("N") || symbol.Equals("O") || symbol.Equals("P") || symbol.Equals("S") || symbol.Equals("F") || symbol.Equals("Br") || symbol.Equals("I") || symbol.Equals("Cl");
brackets = !brackets;
//System.out.println("in parseAtom()");
//Deal with the start of a double bond configuration
if (isStartOfDoubleBond(container, a, parent, doubleBondConfiguration))
{
buffer.Append('/');
}
if (a is IPseudoAtom)
{
buffer.Append("[*]");
}
else
{
System.String mass = generateMassString(a);
brackets = brackets | !mass.Equals("");
System.String charge = generateChargeString(a);
brackets = brackets | !charge.Equals("");
if (chiral && stereo)
{
brackets = true;
}
if (brackets)
{
buffer.Append('[');
}
buffer.Append(mass);
if (a.getFlag(CDKConstants.ISAROMATIC))
{
// Strictly speaking, this is wrong. Lower case is only used for sp2 atoms!
buffer.Append(a.Symbol.ToLower());
}
else if (a.Hybridization == CDKConstants.HYBRIDIZATION_SP2)
{
buffer.Append(a.Symbol.ToLower());
}
else
{
buffer.Append(symbol);
}
if (a.getProperty(RING_CONFIG) != null && a.getProperty(RING_CONFIG).Equals(UP))
{
buffer.Append('/');
}
if (a.getProperty(RING_CONFIG) != null && a.getProperty(RING_CONFIG).Equals(DOWN))
{
buffer.Append('\\');
}
if (chiral && stereo && (BondTools.isTrigonalBipyramidalOrOctahedral(container, a) != 0 || BondTools.isSquarePlanar(container, a) || BondTools.isTetrahedral(container, a, false) != 0))
{
buffer.Append('@');
}
if (chiral && stereo && BondTools.isSquarePlanar(container, a))
{
buffer.Append("SP1");
}
//chiral
//hcount
buffer.Append(charge);
if (brackets)
{
buffer.Append(']');
}
}
//System.out.println("in parseAtom() after dealing with Pseudoatom or not");
//Deal with the end of a double bond configuration
if (isEndOfDoubleBond(container, a, parent, doubleBondConfiguration))
{
IAtom viewFrom = null;
for (int i = 0; i < currentChain.Count; i++)
{
if (currentChain[i] == parent)
{
int k = i - 1;
while (k > -1)
{
if (currentChain[k] is IAtom)
{
viewFrom = (IAtom)currentChain[k];
break;
}
k--;
}
}
}
if (viewFrom == null)
{
for (int i = 0; i < atomsInOrderOfSmiles.Count; i++)
{
if (atomsInOrderOfSmiles[i] == parent)
{
viewFrom = (IAtom)atomsInOrderOfSmiles[i - 1];
}
}
}
bool afterThisAtom = false;
IAtom viewTo = null;
for (int i = 0; i < currentChain.Count; i++)
{
if (afterThisAtom && currentChain[i] is IAtom)
{
viewTo = (IAtom)currentChain[i];
break;
}
if (afterThisAtom && currentChain[i] is System.Collections.ArrayList)
{
viewTo = (IAtom)((System.Collections.ArrayList)currentChain[i])[0];
break;
}
if (a == currentChain[i])
{
afterThisAtom = true;
}
}
try
{
if (BondTools.isCisTrans(viewFrom, a, parent, viewTo, container))
{
buffer.Append('\\');
}
else
{
buffer.Append('/');
}
}
catch (CDKException ex)
{
//If the user wants a double bond configuration, where there is none, we ignore this.
}
}
System.Collections.ArrayList v = System.Collections.ArrayList.Synchronized(new System.Collections.ArrayList(10));
System.Collections.IEnumerator it = getRingOpenings(a, v).GetEnumerator();
System.Collections.IEnumerator it2 = v.GetEnumerator();
//System.out.println("in parseAtom() after checking for Ring openings");
//UPGRADE_TODO: Method 'java.util.Iterator.hasNext' was converted to 'System.Collections.IEnumerator.MoveNext' which has a different behavior. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1073_javautilIteratorhasNext'"
while (it.MoveNext())
{
//UPGRADE_TODO: Method 'java.util.Iterator.next' was converted to 'System.Collections.IEnumerator.Current' which has a different behavior. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1073_javautilIteratornext'"
System.Int32 integer = (System.Int32)it.Current;
//UPGRADE_TODO: Method 'java.util.Iterator.next' was converted to 'System.Collections.IEnumerator.Current' which has a different behavior. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1073_javautilIteratornext'"
IBond b = container.getBond((IAtom)it2.Current, a);
//UPGRADE_WARNING: Data types in Visual C# might be different. Verify the accuracy of narrowing conversions. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1042'"
int type = (int)b.Order;
if (type == 2 && !b.getFlag(CDKConstants.ISAROMATIC))
{
buffer.Append("=");
}
else if (type == 3 && !b.getFlag(CDKConstants.ISAROMATIC))
{
buffer.Append("#");
}
buffer.Append(integer);
}
atomsInOrderOfSmiles.Add(a);
//System.out.println("End of parseAtom()");
}
/// <summary> Append the symbol for the bond order between <code>a1</code> and <code>a2</code>
/// to the <code>line</code>.
///
/// </summary>
/// <param name="line"> the StringBuffer that the bond symbol is appended to.
/// </param>
/// <param name="a1"> Atom participating in the bond.
/// </param>
/// <param name="a2"> Atom participating in the bond.
/// </param>
/// <param name="atomContainer"> the AtomContainer that the SMILES string is generated
/// for.
/// </param>
private void parseBond(System.Text.StringBuilder line, IAtom a1, IAtom a2, IAtomContainer atomContainer)
{
//System.out.println("in parseBond()");
if (a1.getFlag(CDKConstants.ISAROMATIC) && a1.getFlag(CDKConstants.ISAROMATIC))
{
return;
}
if (atomContainer.getBond(a1, a2) == null)
{
return;
}
int type = 0;
//UPGRADE_WARNING: Data types in Visual C# might be different. Verify the accuracy of narrowing conversions. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1042'"
type = (int)atomContainer.getBond(a1, a2).Order;
if (type == 1)
{
}
else if (type == 2)
{
line.Append("=");
}
else if (type == 3)
{
line.Append("#");
}
else
{
// //System.out.println("Unknown bond type");
}
}
/// <summary> Tests the <code>ring</code> in the <code>molecule</code> for aromaticity. Uses the
/// Hückle rule (4n + 2) pie electrons. sp<sup>2</sup> hybridized C contibute 1 electron non
/// sp<sup>2</sup> hybridized heteroatoms contribute 2 electrons (N and O should never be sp in
/// or anything else in a ring and d electron elements get to complicated)
/// sp<sup>2</sup> hybridized heteroatoms contribute 1 electron hybridization is worked out by
/// counting the number of bonds with order 2. Therefore sp<sup>2</sup> hybridization is assumed
/// if there is one bond of order 2. Otherwise sp<sup>3</sup> hybridization is assumed.
///
/// </summary>
/// <param name="ring"> the ring to test
/// </param>
/// <param name="atomContainer"> the AtomContainer the ring is in
/// </param>
/// <returns> true if the ring is aromatic false otherwise.
/// </returns>
protected internal static bool isAromatic(IRing ring, IAtomContainer atomContainer)
{
IAtom[] ringAtoms = ring.Atoms;
int eCount = 0;
IBond[] conectedBonds;
int numDoubleBond = 0;
bool allConnectedBondsSingle;
for (int i = 0; i < ringAtoms.Length; i++)
{
IAtom atom = ringAtoms[i];
numDoubleBond = 0;
allConnectedBondsSingle = true;
conectedBonds = atomContainer.getConnectedBonds(atom);
for (int j = 0; j < conectedBonds.Length; j++)
{
IBond bond = conectedBonds[j];
if (bond.Order == 2 && ring.contains(bond))
{
numDoubleBond++;
}
// Count the Electron if bond order = 1.5
else if (bond.Order == 1.5 && ring.contains(bond))
{
numDoubleBond = 1;
}
if (bond.Order != 1)
{
allConnectedBondsSingle = false;
}
}
if (numDoubleBond == 1)
{
//C or heteroatoms both contibute 1 electron in sp2 hybridized form
eCount++;
}
else if (!atom.Symbol.Equals("C"))
{
//Heteroatom probably in sp3 hybrid therefore 2 electrons contributed.
eCount = eCount + 2;
}
else if (atom.getFlag(CDKConstants.ISAROMATIC))
{
eCount++;
}
else if (allConnectedBondsSingle && atom.Symbol.Equals("C") && atom.getFormalCharge() == 1.0)
{
// This is for tropylium and kinds.
// Dependence on hybridisation would be better:
// empty p-orbital is needed
continue;
}
else
{
return(false);
}
}
if (eCount - 2 != 0 && (eCount - 2) % 4 == 0)
{
return(true);
}
return(false);
}
/// <summary> Calculate the number of missing hydrogens by substracting the number of
/// bonds for the atom from the expected number of bonds. Charges are included
/// in the calculation. The number of expected bonds is defined by the AtomType
/// generated with the AtomTypeFactory.
///
/// </summary>
/// <param name="atom"> Description of the Parameter
/// </param>
/// <param name="throwExceptionForUnknowAtom"> Should an exception be thrown if an unknown atomtype is found or 0 returned ?
/// </param>
/// <returns> Description of the Return Value
/// </returns>
/// <seealso cref="AtomTypeFactory">
/// </seealso>
public virtual int calculateNumberOfImplicitHydrogens(IAtom atom, double bondOrderSum, IBond[] connectedBonds, bool throwExceptionForUnknowAtom)
{
int missingHydrogen = 0;
if (atom is IPseudoAtom)
{
// don't figure it out... it simply does not lack H's
}
else if (atom.AtomicNumber == 1 || atom.Symbol.Equals("H"))
{
//UPGRADE_WARNING: Data types in Visual C# might be different. Verify the accuracy of narrowing conversions. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1042'"
missingHydrogen = (int) (1 - bondOrderSum - atom.getFormalCharge());
}
else
{
//logger.info("Calculating number of missing hydrogen atoms");
// get default atom
IAtomType[] atomTypes = getAtomTypeFactory(atom.Builder).getAtomTypes(atom.Symbol);
if (atomTypes.Length == 0 && throwExceptionForUnknowAtom)
return 0;
//logger.debug("Found atomtypes: " + atomTypes.Length);
if (atomTypes.Length > 0)
{
IAtomType defaultAtom = atomTypes[0];
//logger.debug("DefAtom: ", defaultAtom);
//UPGRADE_WARNING: Data types in Visual C# might be different. Verify the accuracy of narrowing conversions. "ms-help://MS.VSCC.v80/dv_commoner/local/redirect.htm?index='!DefaultContextWindowIndex'&keyword='jlca1042'"
missingHydrogen = (int) (defaultAtom.BondOrderSum - bondOrderSum + atom.getFormalCharge());
if (atom.getFlag(CDKConstants.ISAROMATIC))
{
bool subtractOne = true;
for (int i = 0; i < connectedBonds.Length; i++)
{
if (connectedBonds[i].Order == 2 || connectedBonds[i].Order == CDKConstants.BONDORDER_AROMATIC)
subtractOne = false;
}
if (subtractOne)
missingHydrogen--;
}
//logger.debug("Atom: ", atom.Symbol);
//logger.debug(" max bond order: " + defaultAtom.BondOrderSum);
//logger.debug(" bond order sum: " + bondOrderSum);
//logger.debug(" charge : " + atom.getFormalCharge());
}
else
{
//logger.warn("Could not find atom type for ", atom.Symbol);
}
}
return missingHydrogen;
}
/// <summary> The method is known to fail for certain compounds. For more information, see
/// cdk.test.limitations package.
///
/// </summary>
public virtual void saturate(IAtomContainer atomContainer)
{
/* newSaturate(atomContainer);
* }
* public void oldSaturate(AtomContainer atomContainer) throws CDKException { */
IAtom partner = null;
IAtom atom = null;
IAtom[] partners = null;
IAtomType[] atomTypes1 = null;
IAtomType[] atomTypes2 = null;
IBond bond = null;
for (int i = 1; i < 4; i++)
{
// handle atoms with degree 1 first and then proceed to higher order
for (int f = 0; f < atomContainer.AtomCount; f++)
{
atom = atomContainer.getAtomAt(f);
//logger.debug("symbol: ", atom.Symbol);
atomTypes1 = getAtomTypeFactory(atom.Builder).getAtomTypes(atom.Symbol);
if (atomTypes1.Length > 0)
{
//logger.debug("first atom type: ", atomTypes1[0]);
if (atomContainer.getBondCount(atom) == i)
{
if (atom.getFlag(CDKConstants.ISAROMATIC) && atomContainer.getBondOrderSum(atom) < atomTypes1[0].BondOrderSum - atom.getHydrogenCount())
{
partners = atomContainer.getConnectedAtoms(atom);
for (int g = 0; g < partners.Length; g++)
{
partner = partners[g];
//logger.debug("Atom has " + partners.Length + " partners");
atomTypes2 = getAtomTypeFactory(atom.Builder).getAtomTypes(partner.Symbol);
if (atomTypes2.Length == 0)
{
return;
}
if (atomContainer.getBond(partner, atom).getFlag(CDKConstants.ISAROMATIC) && atomContainer.getBondOrderSum(partner) < atomTypes2[0].BondOrderSum - partner.getHydrogenCount())
{
//logger.debug("Partner has " + atomContainer.getBondOrderSum(partner) + ", may have: " + atomTypes2[0].BondOrderSum);
bond = atomContainer.getBond(atom, partner);
//logger.debug("Bond order was " + bond.Order);
bond.Order = bond.Order + 1;
//logger.debug("Bond order now " + bond.Order);
break;
}
}
}
if (atomContainer.getBondOrderSum(atom) < atomTypes1[0].BondOrderSum - atom.getHydrogenCount())
{
//logger.debug("Atom has " + atomContainer.getBondOrderSum(atom) + ", may have: " + atomTypes1[0].BondOrderSum);
partners = atomContainer.getConnectedAtoms(atom);
for (int g = 0; g < partners.Length; g++)
{
partner = partners[g];
//logger.debug("Atom has " + partners.Length + " partners");
atomTypes2 = getAtomTypeFactory(atom.Builder).getAtomTypes(partner.Symbol);
if (atomTypes2.Length == 0)
{
return;
}
if (atomContainer.getBondOrderSum(partner) < atomTypes2[0].BondOrderSum - partner.getHydrogenCount())
{
//logger.debug("Partner has " + atomContainer.getBondOrderSum(partner) + ", may have: " + atomTypes2[0].BondOrderSum);
bond = atomContainer.getBond(atom, partner);
//logger.debug("Bond order was " + bond.Order);
bond.Order = bond.Order + 1;
//logger.debug("Bond order now " + bond.Order);
break;
}
}
}
}
}
}
}
}
