-
1
-
-
80052002666
-
Lessons Learned from Molecular Scaffold Analysis
-
Hu, Y.; Stumpfe, D.; Bajorath, J. Lessons Learned from Molecular Scaffold Analysis J. Chem. Inf. Model. 2011, 51, 1742-1753
-
(2011)
J. Chem. Inf. Model.
, vol.51
, pp. 1742-1753
-
-
Hu, Y.1
Stumpfe, D.2
Bajorath, J.3
-
2
-
-
0029894013
-
The Properties of Known Drugs. 1. Molecular Frameworks
-
Bemis, G. W.; Murcko, M. A. The Properties of Known Drugs. 1. Molecular Frameworks J. Med. Chem. 1996, 39, 2887-2893
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2887-2893
-
-
Bemis, G.W.1
Murcko, M.A.2
-
3
-
-
0001867008
-
Definition of Templates within Combinatorial Libraries
-
Katritzky, A. R.; Kiely, J. S.; Hebert, N.; Chassaing, C. Definition of Templates within Combinatorial Libraries J. Comb. Chem. 2000, 2, 2-5
-
(2000)
J. Comb. Chem.
, vol.2
, pp. 2-5
-
-
Katritzky, A.R.1
Kiely, J.S.2
Hebert, N.3
Chassaing, C.4
-
4
-
-
0038042482
-
Chemical Substructures in Drug Discovery
-
Merlot, C.; Domine, D.; Cleva, C.; Church, D. J. Chemical Substructures in Drug Discovery Drug Discovery Today 2003, 8, 594-602
-
(2003)
Drug Discovery Today
, vol.8
, pp. 594-602
-
-
Merlot, C.1
Domine, D.2
Cleva, C.3
Church, D.J.4
-
5
-
-
33750701141
-
On Scaffolds and Hopping in Medicinal Chemistry
-
Brown, N.; Jacoby, E. On Scaffolds and Hopping in Medicinal Chemistry Mini-Rev. Med. Chem. 2006, 6, 1217-1229
-
(2006)
Mini-Rev. Med. Chem.
, vol.6
, pp. 1217-1229
-
-
Brown, N.1
Jacoby, E.2
-
6
-
-
0033523672
-
Scaffold-Hopping" by Topological Pharmacophore Search: A Contribution to Virtual Screening
-
Schneider, G.; Neidhart, W.; Giller, T.; Schmid, G. Scaffold- Hopping" by Topological Pharmacophore Search: A Contribution to Virtual Screening Angew. Chem., Int. Ed. 1999, 19, 2894-2896
-
(1999)
Angew. Chem., Int. Ed.
, vol.19
, pp. 2894-2896
-
-
Schneider, G.1
Neidhart, W.2
Giller, T.3
Schmid, G.4
-
7
-
-
18244365837
-
HierS: Hierarchical Scaffold Clustering Using Topological Chemical Graphs
-
Wilkens, S. J.; Janes, J.; Su, A. I. HierS: Hierarchical Scaffold Clustering Using Topological Chemical Graphs J. Med. Chem. 2005, 48, 182-193
-
(2005)
J. Med. Chem.
, vol.48
, pp. 182-193
-
-
Wilkens, S.J.1
Janes, J.2
Su, A.I.3
-
8
-
-
33846871027
-
The Scaffold Tree - Visualization of the Scaffold Universe by Hierarchical Scaffold Classification
-
Schuffenhauer, A.; Ertl, P.; Roggo, S.; Wetzel, S.; Koch, M. A.; Waldmann, H. The Scaffold Tree - Visualization of the Scaffold Universe by Hierarchical Scaffold Classification J. Chem. Inf. Model. 2007, 47, 47-58
-
(2007)
J. Chem. Inf. Model.
, vol.47
, pp. 47-58
-
-
Schuffenhauer, A.1
Ertl, P.2
Roggo, S.3
Wetzel, S.4
Koch, M.A.5
Waldmann, H.6
-
9
-
-
33746740077
-
Quest for the Rings. in Silico Exploration of Ring Universe to Identify Novel Bioactive Heteroaromatic Scaffolds
-
Ertl, P.; Jelfs, S.; Mühlbacher, J.; Schuffenhauer, A.; Selzer, P. Quest for the Rings. In Silico Exploration of Ring Universe To Identify Novel Bioactive Heteroaromatic Scaffolds J. Med. Chem. 2006, 49, 4568-4573
-
(2006)
J. Med. Chem.
, vol.49
, pp. 4568-4573
-
-
Ertl, P.1
Jelfs, S.2
Mühlbacher, J.3
Schuffenhauer, A.4
Selzer, P.5
-
10
-
-
49449097923
-
Scaffold Topologies 1. Exhaustive Enumeration up to Eight Rings
-
Pollock, S. N.; Coutsias, E. A.; Wester, M. J.; Oprea, T. I. Scaffold Topologies 1. Exhaustive Enumeration up to Eight Rings J. Chem. Inf. Model. 2008, 48, 1304-1310
-
(2008)
J. Chem. Inf. Model.
, vol.48
, pp. 1304-1310
-
-
Pollock, S.N.1
Coutsias, E.A.2
Wester, M.J.3
Oprea, T.I.4
-
11
-
-
65649142070
-
Heteroaromatic Rings of the Future
-
Pitt, W. R.; Parry, D. M.; Perry, B. G.; Groom, C. R. Heteroaromatic Rings of the Future J. Med. Chem. 2009, 52, 2952-2963
-
(2009)
J. Med. Chem.
, vol.52
, pp. 2952-2963
-
-
Pitt, W.R.1
Parry, D.M.2
Perry, B.G.3
Groom, C.R.4
-
12
-
-
0037020329
-
Drug Design Strategies for Targeting G-Protein-Coupled Receptors
-
Klabunde, T.; Hessler, G. Drug Design Strategies for Targeting G-Protein-Coupled Receptors ChemBioChem 2002, 3, 928-944
-
(2002)
ChemBioChem
, vol.3
, pp. 928-944
-
-
Klabunde, T.1
Hessler, G.2
-
13
-
-
33644872086
-
Privileged Substructures as Leads in Medicinal Chemistry
-
Constantino, L.; Barlocco, D. Privileged Substructures as Leads in Medicinal Chemistry Curr. Med. Chem. 2006, 13, 65-85
-
(2006)
Curr. Med. Chem.
, vol.13
, pp. 65-85
-
-
Constantino, L.1
Barlocco, D.2
-
14
-
-
41649105837
-
Kinase-likeness and Kinase-privileged Fragments: Toward Virtual Polypharmacology
-
Aronov, A. M.; McClain, B.; Moody, C. S.; Murcko, M. A. Kinase-likeness and Kinase-privileged Fragments: Toward Virtual Polypharmacology J. Med. Chem. 2008, 51, 1214-1222
-
(2008)
J. Med. Chem.
, vol.51
, pp. 1214-1222
-
-
Aronov, A.M.1
McClain, B.2
Moody, C.S.3
Murcko, M.A.4
-
15
-
-
77249139237
-
Systematic Analysis of Public Domain Compound Potency Data Identifies Selective Molecular Scaffolds across Druggable Target Families
-
Hu, Y.; Wassermann, A. M.; Lounkine, E.; Bajorath, J. Systematic Analysis of Public Domain Compound Potency Data Identifies Selective Molecular Scaffolds across Druggable Target Families J. Med. Chem. 2010, 53, 752-758
-
(2010)
J. Med. Chem.
, vol.53
, pp. 752-758
-
-
Hu, Y.1
Wassermann, A.M.2
Lounkine, E.3
Bajorath, J.4
-
16
-
-
78650715341
-
Polypharmacology Directed Data Mining: Identification of Promiscuous Chemotypes with different Activity Profiles and Comparison to Approved Drugs
-
Hu, Y.; Bajorath, J. Polypharmacology Directed Data Mining: Identification of Promiscuous Chemotypes with different Activity Profiles and Comparison to Approved Drugs J. Chem. Inf. Model. 2010, 50, 2112-2118
-
(2010)
J. Chem. Inf. Model.
, vol.50
, pp. 2112-2118
-
-
Hu, Y.1
Bajorath, J.2
-
17
-
-
79955027927
-
Global Assessment of Scaffold Hopping Potential for Current Pharmaceutical Target
-
Hu, Y.; Bajorath, J. Global Assessment of Scaffold Hopping Potential for Current Pharmaceutical Target Med. Chem. Commun. 2010, 1, 339-344
-
(2010)
Med. Chem. Commun.
, vol.1
, pp. 339-344
-
-
Hu, Y.1
Bajorath, J.2
-
18
-
-
77957665087
-
Structural and Potency Relationships between Scaffolds of Compounds Active against Human Targets
-
Hu, Y.; Bajorath, J. Structural and Potency Relationships between Scaffolds of Compounds Active against Human Targets ChemMedChem 2010, 5, 1681-1685
-
(2010)
ChemMedChem
, vol.5
, pp. 1681-1685
-
-
Hu, Y.1
Bajorath, J.2
-
19
-
-
77952000491
-
Molecular Scaffolds with High Propensity to Form Multi-Target Activity Cliffs
-
Hu, Y.; Bajorath, J. Molecular Scaffolds with High Propensity to Form Multi-Target Activity Cliffs J. Chem. Inf. Model. 2010, 50, 500-510
-
(2010)
J. Chem. Inf. Model.
, vol.50
, pp. 500-510
-
-
Hu, Y.1
Bajorath, J.2
-
20
-
-
68049094985
-
Bioactivity-guided Mapping and Navigation of Chemical Space
-
Renner, S.; van Otterlo, W. A. L.; Seoane, M. D.; Möcklinghoff, S.; Hofmann, B.; Wetzel, S.; Schuffenhauer, A.; Ertl, P.; Oprea, T. I.; Steinhilber, D.; Brunsveld, L.; Rauh, D.; Waldmann, H. Bioactivity-guided Mapping and Navigation of Chemical Space Nat. Chem. Biol. 2009, 5, 585-592
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 585-592
-
-
Renner, S.1
Van Otterlo, W.A.L.2
Seoane, M.D.3
Möcklinghoff, S.4
Hofmann, B.5
Wetzel, S.6
Schuffenhauer, A.7
Ertl, P.8
Oprea, T.I.9
Steinhilber, D.10
Brunsveld, L.11
Rauh, D.12
Waldmann, H.13
-
21
-
-
79952176565
-
A Scaffold-Tree-Merging Strategy for Prospective Bioactivity Annotation of γ-Pyrones
-
Wetzel, S.; Wilk, W.; Chammaa, S.; Sperl, B.; Roth, A. G.; Yektaoglu, A.; Renner, S.; Berg, T.; Arenz, A.; Giannis, A.; Oprea, T. I.; Rauh, D.; Kaiser, M.; Waldmann, H. A Scaffold-Tree-Merging Strategy for Prospective Bioactivity Annotation of γ-Pyrones Angew. Chem. 2010, 122, 3748-3752
-
(2010)
Angew. Chem.
, vol.122
, pp. 3748-3752
-
-
Wetzel, S.1
Wilk, W.2
Chammaa, S.3
Sperl, B.4
Roth, A.G.5
Yektaoglu, A.6
Renner, S.7
Berg, T.8
Arenz, A.9
Giannis, A.10
Oprea, T.I.11
Rauh, D.12
Kaiser, M.13
Waldmann, H.14
-
22
-
-
84855739333
-
-
European Bioinformatics Institute (EBI): Cambridge, (accessed September 1, 2011)
-
ChEMBL; European Bioinformatics Institute (EBI): Cambridge, 2011. http://www.ebi.ac.uk/chembl/ (accessed September 1, 2011).
-
(2011)
ChEMBL
-
-
-
23
-
-
0036662353
-
Using Molecular Equivalence Numbers to Visually Explore Structural Features that Distinguish Chemical Libraries
-
Xu, Y.-J.; Johnson, M. Using Molecular Equivalence Numbers to Visually Explore Structural Features that Distinguish Chemical Libraries J. Med. Chem. 2002, 42, 912-926
-
(2002)
J. Med. Chem.
, vol.42
, pp. 912-926
-
-
Xu, Y.-J.1
Johnson, M.2
-
24
-
-
0242490780
-
Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks
-
Shannon, P.; Markiel, A.; Ozier, O.; Baliga, N. S.; Wang, J. T.; Ramage, D.; Amin, N.; Schwikowski, B.; Ideker, T. Cytoscape: a Software Environment for Integrated Models of Biomolecular Interaction Networks Genome Res. 2003, 13, 2498-2504
-
(2003)
Genome Res.
, vol.13
, pp. 2498-2504
-
-
Shannon, P.1
Markiel, A.2
Ozier, O.3
Baliga, N.S.4
Wang, J.T.5
Ramage, D.6
Amin, N.7
Schwikowski, B.8
Ideker, T.9
|