// $Id: Functional_Group_Hierarchy.txt 10346 2013-07-04 14:53:03Z landrgr1 $ // Created by Greg Landrum, October 2006 // Format: Name\tSmarts\tLabel\tRemovalReaction (optional) // // NOTES: // 1) be sure to make the distinguishing feature of the functional group // the first atom in the pattern // 2) the RemovalReaction (if present) is used to remove the functional // group from the molecule. This is necessary for cases like boronic // ethers where the full functional group cannot be specified in SMARTS. // AcidChloride C(=O)Cl Acid Chloride AcidChloride.Aromatic [$(C-!@[a])](=O)(Cl) Aromatic AcidChloride.Aliphatic [$(C-!@[A;!Cl])](=O)(Cl) Aliphatic CarboxylicAcid C(=O)[O;H,-] Carboxylic acid CarboxylicAcid.Aromatic [$(C-!@[a])](=O)([O;H,-]) Aromatic CarboxylicAcid.Aliphatic [$(C-!@[A;!O])](=O)([O;H,-]) Aliphatic CarboxylicAcid.AlphaAmino [$(C-[C;!$(C=[!#6])]-[N;!H0;!$(N-[!#6;!#1]);!$(N-C=[O,N,S])])](=O)([O;H,-]) alpha Amino Acid SulfonylChloride [$(S-!@[#6])](=O)(=O)(Cl) Sulfonyl Chloride SulfonylChloride.Aromatic [$(S-!@c)](=O)(=O)(Cl) Aromatic SulfonylChloride.Aliphatic [$(S-!@C)](=O)(=O)(Cl) Aliphatic Amine [N;$(N-[#6]);!$(N-[!#6;!#1]);!$(N-C=[O,N,S])] Amine Amine.Primary [N;H2;D1;$(N-!@[#6]);!$(N-C=[O,N,S])] Primary Amine.Primary.Aromatic [N;H2;D1;$(N-!@c);!$(N-C=[O,N,S])] Primary aromatic Amine.Primary.Aliphatic [N;H2;D1;$(N-!@C);!$(N-C=[O,N,S])] Primary aliphatic Amine.Secondary [N;H1;D2;$(N(-[#6])-[#6]);!$(N-C=[O,N,S])] Secondary Amine.Secondary.Aromatic [N;H1;D2;$(N(-[c])-[#6]);!$(N-C=[O,N,S])] Secondary aromatic Amine.Secondary.Aliphatic [N;H1;D2;$(N(-C)-C);!$(N-C=[O,N,S])] Secondary aliphatic Amine.Tertiary [N;H0;D3;$(N(-[#6])(-[#6])-[#6]);!$(N-C=[O,N,S])] Tertiary Amine.Tertiary.Aromatic [N;H0;D3;$(N(-[c])(-[#6])-[#6]);$(N-C=[O,N,S])] Tertiary aromatic Amine.Tertiary.Aliphatic [N;H0;D3;$(N(-C)(-C)-C);!$(N-C=[O,N,S])] Tertiary aliphatic Amine.Aromatic [N;$(N-c);!$(N-[!#6;!#1]);!$(N-C=[O,N,S])] Aromatic Amine.Aliphatic [N;!$(N-c);$(N-C);!$(N-[!#6;!#1]);!$(N-C=[O,N,S])] Aliphatic Amine.Cyclic [N;R;$(N-[#6]);!$(N-[!#6;!#1]);!$(N-C=[O,N,S])] Cyclic BoronicAcid [$(B-!@[#6])](O)(O) Boronic Acid [#6:1]-!@[B:2]([O:3])[O:4]>>[#6:1][X].[B:2]([O:3])[O:4] BoronicAcid.Aromatic [$(B-!@c)](O)(O) Aromatic [c:1]-!@[B:2]([O:3])[O:4]>>[c:1][X].[B:2]([O:3])[O:4] BoronicAcid.Aliphatic [$(B-!@C)](O)(O) Aliphatic [C:1]-!@[B:2]([O:3])[O:4]>>[C:1][X].[B:2]([O:3])[O:4] Isocyanate [$(N-!@[#6])](=!@C=!@O) Isocyanate Isocyanate.Aromatic [$(N-!@c)](=!@C=!@O) Aromatic Isocyanate.Aliphatic [$(N-!@C)](=!@C=!@O) Aliphatic Alcohol [O;H1;$(O-!@[#6;!$(C=!@[O,N,S])])] Alcohol Alcohol.Aromatic [O;H1;$(O-!@c)] Aromatic Alcohol.Aliphatic [O;H1;$(O-!@[C;!$(C=!@[O,N,S])])] Aliphatic Aldehyde [CH;D2;!$(C-[!#6;!#1])]=O Aldehyde Aldehyde.Aromatic [CH;D2;$(C-!@[a])](=O) Aromatic Aldehyde.Aliphatic [CH;D2;$(C-!@C)](=O) Aliphatic Halogen [$([F,Cl,Br,I]-!@[#6]);!$([F,Cl,Br,I]-!@C-!@[F,Cl,Br,I]);!$([F,Cl,Br,I]-[C,S](=[O,S,N]))] Halogen Halogen.Aromatic [F,Cl,Br,I;$(*-!@c)] Aromatic Halogen.Aliphatic [$([F,Cl,Br,I]-!@C);!$([F,Cl,Br,I]-!@C-!@[F,Cl,Br,I])] Aliphatic Halogen.NotFluorine [$([Cl,Br,I]-!@[#6]);!$([Cl,Br,I]-!@C-!@[F,Cl,Br,I]);!$([Cl,Br,I]-[C,S](=[O,S,N]))] Not Fluorine Halogen.NotFluorine.Aliphatic [$([Cl,Br,I]-!@C);!$([Cl,Br,I]-!@C-!@[F,Cl,Br,I]);!$([Cl,Br,I]-[C,S](=[O,S,N]))] Aliphatic Not Fluorine Halogen.NotFluorine.Aromatic [$([Cl,Br,I]-!@c)] Aromatic Not Fluorine Halogen.Bromine [Br;$([Br]-!@[#6]);!$([Br]-!@C-!@[F,Cl,Br,I]);!$([Br]-[C,S](=[O,S,N]))] Bromine Halogen.Bromine.Aliphatic [Br;$(Br-!@C);!$(Br-!@C-!@[F,Cl,Br,I]);!$(Br-[C,S](=[O,S,N]))] Aliphatic Bromine Halogen.Bromine.Aromatic [Br;$(Br-!@c)] Aromatic Bromine Halogen.Bromine.BromoKetone [Br;$(Br-[CH2]-C(=O)-[#6])] Bromoketone Azide [N;H0;$(N-[#6]);D2]=[N;D2]=[N;D1] Azide Azide.Aromatic [N;H0;$(N-c);D2]=[N;D2]=[N;D1] Aromatic Azide Azide.Aliphatic [N;H0;$(N-C);D2]=[N;D2]=[N;D1] Aliphatic Azide Nitro [N;H0;$(N-[#6]);D3](=[O;D1])~[O;D1] Nitro Nitro.Aromatic [N;H0;$(N-c);D3](=[O;D1])~[O;D1] Aromatic Nitro Nitro.Aliphatic [N;H0;$(N-C);D3](=[O;D1])~[O;D1] Aliphatic Nitro TerminalAlkyne [C;$(C#[CH])] Terminal Alkyne // Copyright (c) 2010, Novartis Institutes for BioMedical Research Inc. // All rights reserved. // // Redistribution and use in source and binary forms, with or without // modification, are permitted provided that the following conditions are // met: // // * Redistributions of source code must retain the above copyright // notice, this list of conditions and the following disclaimer. // * Redistributions in binary form must reproduce the above // copyright notice, this list of conditions and the following // disclaimer in the documentation and/or other materials provided // with the distribution. // * Neither the name of Novartis Institutes for BioMedical Research Inc. // nor the names of its contributors may be used to endorse or promote // products derived from this software without specific prior written permission. // // THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS // "AS IS" AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT // LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR // A PARTICULAR PURPOSE ARE DISCLAIMED. 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