Break Down in Order To Build Up: Decomposing Small Molecules for Fragment-Based Drug Design with eMolFrag

Constructing high-quality libraries of molecular building blocks is essential for successful fragment-based drug discovery. In this communication, we describe eMolFrag, a new open-source software to decompose organic compounds into nonredundant fragments retaining molecular connectivity information....

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Vydané v:Journal of chemical information and modeling Ročník 57; číslo 4; s. 627
Hlavní autori: Liu, Tairan, Naderi, Misagh, Alvin, Chris, Mukhopadhyay, Supratik, Brylinski, Michal
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 24.04.2017
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Abstract Constructing high-quality libraries of molecular building blocks is essential for successful fragment-based drug discovery. In this communication, we describe eMolFrag, a new open-source software to decompose organic compounds into nonredundant fragments retaining molecular connectivity information. Given a collection of molecules, eMolFrag generates a set of unique fragments comprising larger moieties, bricks, and smaller linkers connecting bricks. These building blocks can subsequently be used to construct virtual screening libraries for targeted drug discovery. The robustness and computational performance of eMolFrag is assessed against the Directory of Useful Decoys, Enhanced database conducted in serial and parallel modes with up to 16 computing cores. Further, the application of eMolFrag in de novo drug design is illustrated using the adenosine receptor. eMolFrag is implemented in Python, and it is available as stand-alone software and a web server at www.brylinski.org/emolfrag and https://github.com/liutairan/eMolFrag .
AbstractList Constructing high-quality libraries of molecular building blocks is essential for successful fragment-based drug discovery. In this communication, we describe eMolFrag, a new open-source software to decompose organic compounds into nonredundant fragments retaining molecular connectivity information. Given a collection of molecules, eMolFrag generates a set of unique fragments comprising larger moieties, bricks, and smaller linkers connecting bricks. These building blocks can subsequently be used to construct virtual screening libraries for targeted drug discovery. The robustness and computational performance of eMolFrag is assessed against the Directory of Useful Decoys, Enhanced database conducted in serial and parallel modes with up to 16 computing cores. Further, the application of eMolFrag in de novo drug design is illustrated using the adenosine receptor. eMolFrag is implemented in Python, and it is available as stand-alone software and a web server at www.brylinski.org/emolfrag and https://github.com/liutairan/eMolFrag .
Constructing high-quality libraries of molecular building blocks is essential for successful fragment-based drug discovery. In this communication, we describe eMolFrag, a new open-source software to decompose organic compounds into nonredundant fragments retaining molecular connectivity information. Given a collection of molecules, eMolFrag generates a set of unique fragments comprising larger moieties, bricks, and smaller linkers connecting bricks. These building blocks can subsequently be used to construct virtual screening libraries for targeted drug discovery. The robustness and computational performance of eMolFrag is assessed against the Directory of Useful Decoys, Enhanced database conducted in serial and parallel modes with up to 16 computing cores. Further, the application of eMolFrag in de novo drug design is illustrated using the adenosine receptor. eMolFrag is implemented in Python, and it is available as stand-alone software and a web server at www.brylinski.org/emolfrag and https://github.com/liutairan/eMolFrag .Constructing high-quality libraries of molecular building blocks is essential for successful fragment-based drug discovery. In this communication, we describe eMolFrag, a new open-source software to decompose organic compounds into nonredundant fragments retaining molecular connectivity information. Given a collection of molecules, eMolFrag generates a set of unique fragments comprising larger moieties, bricks, and smaller linkers connecting bricks. These building blocks can subsequently be used to construct virtual screening libraries for targeted drug discovery. The robustness and computational performance of eMolFrag is assessed against the Directory of Useful Decoys, Enhanced database conducted in serial and parallel modes with up to 16 computing cores. Further, the application of eMolFrag in de novo drug design is illustrated using the adenosine receptor. eMolFrag is implemented in Python, and it is available as stand-alone software and a web server at www.brylinski.org/emolfrag and https://github.com/liutairan/eMolFrag .
Author Naderi, Misagh
Alvin, Chris
Liu, Tairan
Mukhopadhyay, Supratik
Brylinski, Michal
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References 17238248 - J Chem Inf Model. 2007 Jan-Feb;47(1):47-58
9611787 - J Chem Inf Comput Sci. 1998 May-Jun;38(3):511-22
18792903 - ChemMedChem. 2008 Oct;3(10):1503-7
21982300 - J Cheminform. 2011 Oct 07;3:33
17139284 - Nat Rev Drug Discov. 2006 Dec;5(12):993-6
8320553 - J Comput Aided Mol Des. 1993 Apr;7(2):127-53
15801836 - J Med Chem. 2005 Apr 7;48(7):2457-68
9667972 - J Med Chem. 1998 Jul 16;41(15):2835-45
22716043 - J Med Chem. 2012 Jul 26;55(14):6582-94
19207419 - Chem Biol Drug Des. 2009 Feb;73(2):168-78
17315990 - J Chem Inf Model. 2007 Mar-Apr;47(2):656-67
11259830 - Adv Drug Deliv Rev. 2001 Mar 1;46(1-3):3-26
1583540 - J Comput Aided Mol Des. 1992 Feb;6(1):61-78
24681908 - Bioinformatics. 2014 Jul 15;30(14):2081-3
11123985 - J Med Chem. 2000 Dec 14;43(25):4768-80
15154776 - J Chem Inf Comput Sci. 2004 May-Jun;44(3):1079-87
15602551 - Nature. 2004 Dec 16;432(7019):855-61
21736325 - J Chem Inf Model. 2011 Aug 22;51(8):1775-87
18612831 - J Comput Aided Mol Des. 2008 Oct;22(10):761-72
28144341 - Beilstein J Org Chem. 2016 Dec 12;12 :2694-2718
21513346 - J Chem Inf Model. 2011 May 23;51(5):1083-91
12196200 - Biochem Soc Trans. 2002 Aug;30(4):797-9
26981157 - J Cheminform. 2016 Mar 15;8:14
References_xml – reference: 1583540 - J Comput Aided Mol Des. 1992 Feb;6(1):61-78
– reference: 11259830 - Adv Drug Deliv Rev. 2001 Mar 1;46(1-3):3-26
– reference: 28144341 - Beilstein J Org Chem. 2016 Dec 12;12 :2694-2718
– reference: 11123985 - J Med Chem. 2000 Dec 14;43(25):4768-80
– reference: 17238248 - J Chem Inf Model. 2007 Jan-Feb;47(1):47-58
– reference: 21736325 - J Chem Inf Model. 2011 Aug 22;51(8):1775-87
– reference: 18612831 - J Comput Aided Mol Des. 2008 Oct;22(10):761-72
– reference: 15154776 - J Chem Inf Comput Sci. 2004 May-Jun;44(3):1079-87
– reference: 17315990 - J Chem Inf Model. 2007 Mar-Apr;47(2):656-67
– reference: 21513346 - J Chem Inf Model. 2011 May 23;51(5):1083-91
– reference: 26981157 - J Cheminform. 2016 Mar 15;8:14
– reference: 15801836 - J Med Chem. 2005 Apr 7;48(7):2457-68
– reference: 24681908 - Bioinformatics. 2014 Jul 15;30(14):2081-3
– reference: 9611787 - J Chem Inf Comput Sci. 1998 May-Jun;38(3):511-22
– reference: 8320553 - J Comput Aided Mol Des. 1993 Apr;7(2):127-53
– reference: 22716043 - J Med Chem. 2012 Jul 26;55(14):6582-94
– reference: 9667972 - J Med Chem. 1998 Jul 16;41(15):2835-45
– reference: 12196200 - Biochem Soc Trans. 2002 Aug;30(4):797-9
– reference: 17139284 - Nat Rev Drug Discov. 2006 Dec;5(12):993-6
– reference: 18792903 - ChemMedChem. 2008 Oct;3(10):1503-7
– reference: 21982300 - J Cheminform. 2011 Oct 07;3:33
– reference: 19207419 - Chem Biol Drug Des. 2009 Feb;73(2):168-78
– reference: 15602551 - Nature. 2004 Dec 16;432(7019):855-61
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Snippet Constructing high-quality libraries of molecular building blocks is essential for successful fragment-based drug discovery. In this communication, we describe...
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SubjectTerms Databases, Factual
Drug Design
Models, Molecular
Molecular Conformation
Purinergic P1 Receptor Antagonists - chemistry
Purinergic P1 Receptor Antagonists - pharmacology
Receptors, Purinergic P1 - metabolism
Software
Title Break Down in Order To Build Up: Decomposing Small Molecules for Fragment-Based Drug Design with eMolFrag
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