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//
//  Copyright (C) 2002-2012 Greg Landrum and Rational Discovery LLC
//
//   @@ All Rights Reserved @@
//  This file is part of the RDKit.
//  The contents are covered by the terms of the BSD license
//  which is included in the file license.txt, found at the root
//  of the RDKit source tree.
//
#ifndef _RD_SMILESWRITE_H
#define _RD_SMILESWRITE_H

#include <string>
#include <vector>

namespace RDKit {
class Atom;
class Bond;
class ROMol;
namespace SmilesWrite {
//! \brief returns true if the atom number is in the SMILES organic subset
bool inOrganicSubset(int atomicNumber);

//! \brief returns the SMILES for an atom
/*!
  \param atom : the atom to work with
  \param doKekule : we're doing kekulized smiles (e.g. don't use
    lower case for the atom label)
  \param bondIn : the bond we came into the atom on (used for
    chirality calculation
  \param allHsExplicit : if true, hydrogen counts will be provided for every
  atom.
*/
std::string GetAtomSmiles(const Atom *atom, bool doKekule = false,
                          const Bond *bondIn = 0, bool allHsExplicit = false);

//! \brief returns the SMILES for a bond
/*!
  \param bond : the bond to work with
  \param atomToLeftIdx : the index of the atom preceding \c bond
    in the SMILES
  \param doKekule : we're doing kekulized smiles (e.g. write out
    bond orders for aromatic bonds)
  \param allBondsExplicit : if true, symbols will be included for all bonds.
*/
std::string GetBondSmiles(const Bond *bond, int atomToLeftIdx = -1,
                          bool doKekule = false, bool allBondsExplicit = false);
}

//! \brief returns canonical SMILES for a molecule
/*!
  \param mol : the molecule in question.
  \param doIsomericSmiles : include stereochemistry and isotope information
      in the SMILES
  \param doKekule : do Kekule smiles (i.e. don't use aromatic bonds)
  \param rootedAtAtom : make sure the SMILES starts at the specified atom.
      The resulting SMILES is not, of course, canonical.
  \param canonical : if false, no attempt will be made to canonicalize the
  SMILES
  \param allBondsExplicit : if true, symbols will be included for all bonds.
  \param allHsExplicit : if true, hydrogen counts will be provided for every
  atom.
 */
std::string MolToSmiles(const ROMol &mol, bool doIsomericSmiles = false,
                        bool doKekule = false, int rootedAtAtom = -1,
                        bool canonical = true, bool allBondsExplicit = false,
                        bool allHsExplicit = false);

//! \brief returns canonical SMILES for part of a molecule
/*!
  \param mol : the molecule in question.
  \param atomsToUse : indices of the atoms in the fragment
  \param bondsToUse : indices of the bonds in the fragment. If this is not
  provided,
                      all bonds between the atoms in atomsToUse will be included
  \param atomSymbols : symbols to use for the atoms in the output SMILES
  \param bondSymbols : sybmols to use for the bonds in the output SMILES
  \param doIsomericSmiles : include stereochemistry and isotope information
      in the SMILES
  \param doKekule : do Kekule smiles (i.e. don't use aromatic bonds)
  \param rootedAtAtom : make sure the SMILES starts at the specified atom.
      The resulting SMILES is not, of course, canonical.
  \param canonical : if false, no attempt will be made to canonicalize the
  SMILES
  \param allBondsExplicit : if true, symbols will be included for all bonds.
  \param allHsExplicit : if true, hydrogen counts will be provided for every
  atom.

  \b NOTE: the bondSymbols are *not* currently used in the canonicalization.

 */
std::string MolFragmentToSmiles(const ROMol &mol,
                                const std::vector<int> &atomsToUse,
                                const std::vector<int> *bondsToUse = 0,
                                const std::vector<std::string> *atomSymbols = 0,
                                const std::vector<std::string> *bondSymbols = 0,
                                bool doIsomericSmiles = false,
                                bool doKekule = false, int rootedAtAtom = -1,
                                bool canonical = true,
                                bool allBondsExplicit = false,
                                bool allHsExplicit = false);
}
#endif