-
1
-
-
0000353230
-
The characterization of chemical structures using molecular properties. A survey
-
Livingstone, D.J. The characterization of chemical structures using molecular properties. A survey. J. Chem. Inf. Comput. Sci. 2000, 40, 195-209.
-
(2000)
J. Chem. Inf. Comput. Sci.
, vol.40
, pp. 195-209
-
-
Livingstone, D.J.1
-
2
-
-
0033779243
-
Molecular descriptors in chemoinformatics, computational combinatorial chemistry, and virtual screening
-
Xue, L.; Bajorath, J. Molecular descriptors in chemoinformatics, computational combinatorial chemistry, and virtual screening. Combin. Chem. High Throughput Screen. 2000, 3, 363-372.
-
(2000)
Combin. Chem. High Throughput Screen
, vol.3
, pp. 363-372
-
-
Xue, L.1
Bajorath, J.2
-
3
-
-
0035292795
-
Selected concepts and investigations in compound classification, molecular descriptor analysis, and virtual screening
-
Bajorath, J. Selected concepts and investigations in compound classification, molecular descriptor analysis, and virtual screening. J. Chem. Inf. Comput. Sci. 2001, 41, 233-245.
-
(2001)
J. Chem. Inf. Comput. Sci.
, vol.41
, pp. 233-245
-
-
Bajorath, J.1
-
5
-
-
0000228805
-
Variability of molecular descriptors in compound databases revealed by Shannon entropy calculations
-
Godden, J.W.; Stahura, F.L.; Bajorath, J. Variability of molecular descriptors in compound databases revealed by Shannon entropy calculations. J. Chem. Inf. Comput. Sci. 2000, 40, 796-800.
-
(2000)
J. Chem. Inf. Comput. Sci.
, vol.40
, pp. 796-800
-
-
Godden, J.W.1
Stahura, F.L.2
Bajorath, J.3
-
6
-
-
0035412802
-
Differential Shannon entropy as a sensitive measure of differences in database variability of molecular descriptors
-
Godden, J.W.; Bajorath, J. Differential Shannon entropy as a sensitive measure of differences in database variability of molecular descriptors. J. Chem. Inf. Comput. Sci. 2001, 41, 1060-1066.
-
(2001)
J. Chem. Inf. Comput. Sci.
, vol.41
, pp. 1060-1066
-
-
Godden, J.W.1
Bajorath, J.2
-
7
-
-
0036432427
-
Chemical descriptors with distinct levels of information content and varying sensitivity to differences between selected compound databases identified by SE-DSE analysis
-
Godden, J.W.; Bajorath, J. Chemical descriptors with distinct levels of information content and varying sensitivity to differences between selected compound databases identified by SE-DSE analysis. J. Chem. Inf. Comput. Sci. 2002, 42, 87-93.
-
(2002)
J. Chem. Inf. Comput. Sci.
, vol.42
, pp. 87-93
-
-
Godden, J.W.1
Bajorath, J.2
-
8
-
-
0034268411
-
Distinguishing between natural products and synthetic molecules by Shannon descriptor entropy analysis and binary QSAR calculations
-
Stahura, F.L.; Godden, J.W.; Xue, L.; Bajorath, J. Distinguishing between natural products and synthetic molecules by Shannon descriptor entropy analysis and binary QSAR calculations. J. Chem. Inf. Comput. Sci. 2000, 40, 1245-1252.
-
(2000)
J. Chem. Inf. Comput. Sci.
, vol.40
, pp. 1245-1252
-
-
Stahura, F.L.1
Godden, J.W.2
Xue, L.3
Bajorath, J.4
-
9
-
-
0033104653
-
Statistical investigation into the structural complementarity of natural products and synthetic compounds
-
Henkel, T.; Brunne, R.M.; Muller, H.; Reichel, F. Statistical investigation into the structural complementarity of natural products and synthetic compounds. Angew. Chem., Intl. Ed. Engl. 1999, 38, 643-647.
-
(1999)
Angew. Chem., Intl. Ed. Engl.
, vol.38
, pp. 643-647
-
-
Henkel, T.1
Brunne, R.M.2
Muller, H.3
Reichel, F.4
-
10
-
-
0002510887
-
Avoiding investments in doomed drugs
-
Lipinski, C.A. Avoiding investments in doomed drugs. Current Drug Discovery 2001, 1(2), 17-19.
-
(2001)
Current Drug Discovery
, vol.1
, Issue.2
, pp. 17-19
-
-
Lipinski, C.A.1
-
11
-
-
0033955479
-
Prediction of aqueous solubility in drug design
-
Taskinen, J. Prediction of aqueous solubility in drug design. Curr. Opin. Drug Discov. Dev. 2000, 3, 102-107.
-
(2000)
Curr. Opin. Drug Discov. Dev.
, vol.3
, pp. 102-107
-
-
Taskinen, J.1
-
12
-
-
0034608316
-
Prediction of drug solubility from Monte Carlo simulations
-
Jorgensen, W.L.; Duffy, E.M. Prediction of drug solubility from Monte Carlo simulations. Bioorg. Med. Chem. Lett. 2000, 10, 1155-1158.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1155-1158
-
-
Jorgensen, W.L.1
Duffy, E.M.2
-
13
-
-
0002615508
-
Prediction of aqueous solubility for a diverse set of heteroatom-containing organic compounds using a quantitative structure-property relationship
-
Sutter, J.M.; Jurs, P.C. Prediction of aqueous solubility for a diverse set of heteroatom-containing organic compounds using a quantitative structure-property relationship. J. Chem. Inf. Comput. Sci. 1996, 36, 100-107.
-
(1996)
J. Chem. Inf. Comput. Sci.
, vol.36
, pp. 100-107
-
-
Sutter, J.M.1
Jurs, P.C.2
-
14
-
-
0000445633
-
Prediction of aqueous solubility of organic compounds from molecular structure
-
Mitchell, B.E.; Jurs, P.C. Prediction of aqueous solubility of organic compounds from molecular structure. J. Chem. Inf. Comput. Sci. 1998, 38, 489-496.
-
(1998)
J. Chem. Inf. Comput. Sci.
, vol.38
, pp. 489-496
-
-
Mitchell, B.E.1
Jurs, P.C.2
-
15
-
-
0035470268
-
Prediction of aqueous solubility of heteroatom-containing organic compounds from molecular structure
-
McElroy, N.R.; Jurs, P.C. Prediction of aqueous solubility of heteroatom-containing organic compounds from molecular structure. J. Chem. Inf. Comput. Sci. 2001, 41, 1237-1247.
-
(2001)
J. Chem. Inf. Comput. Sci.
, vol.41
, pp. 1237-1247
-
-
McElroy, N.R.1
Jurs, P.C.2
-
16
-
-
0032061266
-
Aqueous solubility prediction of drugs based on molecular topology and neural network modeling
-
Huuskonen, J.; Salo, M.; Taskinen, J. Aqueous solubility prediction of drugs based on molecular topology and neural network modeling. J. Chem. Inf. Comput. Sci. 1998, 38, 450-456.
-
(1998)
J. Chem. Inf. Comput. Sci.
, vol.38
, pp. 450-456
-
-
Huuskonen, J.1
Salo, M.2
Taskinen, J.3
-
17
-
-
0035526162
-
Estimation of aqueous solubility of chemical compounds using E-state indices
-
Tetko, I.V.; Tanchuk, V.Y.; Kasheva, T.N.; Villa, A.E.P. Estimation of aqueous solubility of chemical compounds using E-state indices. J. Chem. Inf. Comput. Sci. 2001, 41, 1488-1493.
-
(2001)
J. Chem. Inf. Comput. Sci.
, vol.41
, pp. 1488-1493
-
-
Tetko, I.V.1
Tanchuk, V.Y.2
Kasheva, T.N.3
Villa, A.E.P.4
-
18
-
-
0001645890
-
Estimation of aqueous solubility for a diverse set of organic compounds based on molecular topology
-
Huuskonen, J. Estimation of aqueous solubility for a diverse set of organic compounds based on molecular topology. J. Chem. Inf. Comput. Sci. 2000, 40, 773-777.
-
(2000)
J. Chem. Inf. Comput. Sci.
, vol.40
, pp. 773-777
-
-
Huuskonen, J.1
-
19
-
-
0026914713
-
Estimation of aqueous solubility of organic molecules by the group contribution approach. Application to the study of biodegradation
-
Klopman, G.; Wang, S.; Balthasar, D.M. Estimation of aqueous solubility of organic molecules by the group contribution approach. Application to the study of biodegradation. J. Chem. Inf. Comput. Sci. 1992, 32, 474-482.
-
(1992)
J. Chem. Inf. Comput. Sci.
, vol.32
, pp. 474-482
-
-
Klopman, G.1
Wang, S.2
Balthasar, D.M.3
-
20
-
-
0035273557
-
Estimation of aqueous solubility of organic molecules by the group contribution approach
-
Klopman, G.; Zhao, H. Estimation of aqueous solubility of organic molecules by the group contribution approach. J. Chem. Inf. Comput. Sci. 2001, 41, 439-445.
-
(2001)
J. Chem. Inf. Comput. Sci.
, vol.41
, pp. 439-445
-
-
Klopman, G.1
Zhao, H.2
-
21
-
-
0000120618
-
The E-state as the basis for molecular structure space definition and structure similarity
-
Hall, L.H.; Kier, L.B. The E-state as the basis for molecular structure space definition and structure similarity. J. Chem. Inf. Comput. Sci. 2000, 40, 784-791.
-
(2000)
J. Chem. Inf. Comput. Sci.
, vol.40
, pp. 784-791
-
-
Hall, L.H.1
Kier, L.B.2
-
22
-
-
0032605748
-
Binary QSAR: A new method for the determination of quantitative structure activity relationships
-
Labute, P. Binary QSAR: a new method for the determination of quantitative structure activity relationships. Pac. Symp. Biocomput. 1999, 7, 444-455.
-
(1999)
Pac. Symp. Biocomput.
, vol.7
, pp. 444-455
-
-
Labute, P.1
-
23
-
-
0003856787
-
-
Syracuse Research Corporation, SRC Environment Science Center: Syracuse, NY
-
Physical/Chemical Property database (PHYSPROP); Syracuse Research Corporation, SRC Environment Science Center: Syracuse, NY, 1994.
-
(1994)
Physical/Chemical Property database (PHYSPROP)
-
-
-
24
-
-
0034351504
-
Widely applicable set of descriptors
-
Labute, P.A. widely applicable set of descriptors. J. Mol. Graph. Model. 2000, 18, 464-477.
-
(2000)
J. Mol. Graph. Model
, vol.18
, pp. 464-477
-
-
Labute, P.A.1
-
25
-
-
0032619434
-
Binary quantitative structure-activity relationship (QSAR) analysis of estrogen receptor ligands
-
Gao, H.; Williams, C.; Labute, P.; Bajorath, J. Binary quantitative structure-activity relationship (QSAR) analysis of estrogen receptor ligands. J. Chem. Inf. Comput. Sci. 1999, 39, 164-168.
-
(1999)
J. Chem. Inf. Comput. Sci.
, vol.39
, pp. 164-168
-
-
Gao, H.1
Williams, C.2
Labute, P.3
Bajorath, J.4
-
26
-
-
0032233660
-
Comparison of binary and 2D QSAR analyses using inhibitors of human carbonic anhydrase II as a test case
-
Gao, H.; Bajorath, J. Comparison of binary and 2D QSAR analyses using inhibitors of human carbonic anhydrase II as a test case. Mol. Divers. 1999, 4, 115-30.
-
(1999)
Mol. Divers.
, vol.4
, pp. 115-130
-
-
Gao, H.1
Bajorath, J.2
-
27
-
-
0035263417
-
Application of BCUT metrics and genetic algorithm in binary QSAR analysis
-
Gao, H. Application of BCUT metrics and genetic algorithm in binary QSAR analysis. J. Chem. Inf. Comput. Sci. 2001, 41, 402-407.
-
(2001)
J. Chem. Inf. Comput. Sci.
, vol.41
, pp. 402-407
-
-
Gao, H.1
-
29
-
-
45249127902
-
Principal component analysis and partial least squares regression
-
Glen, W.G.; Dunn, W.J.; Scott, D.R. Principal component analysis and partial least squares regression. Tetrahedron Comput. Methodol. 1989, 2, 349-376.
-
(1989)
Tetrahedron Comput. Methodol.
, vol.2
, pp. 349-376
-
-
Glen, W.G.1
Dunn, W.J.2
Scott, D.R.3
-
30
-
-
0004313704
-
-
Chemical Computing Group Inc.: 1255 University Street, Montreal, Quebec, Canada, H3B 3X3
-
MOE (Molecular Operating Environment), version 2001.01; Chemical Computing Group Inc.: 1255 University Street, Montreal, Quebec, Canada, H3B 3X3.
-
MOE (Molecular Operating Environment), version 2001.01
-
-
-
31
-
-
0017933162
-
Criteria for choosing subsets to obtain maximum relative entropy
-
Williams, P.W. Criteria for choosing subsets to obtain maximum relative entropy. Computer J. 1978, 21, 57-62.
-
(1978)
Computer J.
, vol.21
, pp. 57-62
-
-
Williams, P.W.1
-
32
-
-
0011514228
-
Selection of screens for three-dimensional substructure searching
-
Cringean, J.K.; Pepperrell, C.A.; Poirrette, A.R.; Willett, P. Selection of screens for three-dimensional substructure searching. Tetrahedron Comput. Methodol. 1990, 3, 37-46.
-
(1990)
Tetrahedron Comput. Methodol.
, vol.3
, pp. 37-46
-
-
Cringean, J.K.1
Pepperrell, C.A.2
Poirrette, A.R.3
Willett, P.4
-
33
-
-
0026327618
-
Pharmacophoric pattern matching in files of three-dimensional structures: Characterization and use of generalized valence angle screens
-
Poirrette, A.R.; Willett, P.; Allen, F.H. Pharmacophoric pattern matching in files of three-dimensional structures: characterization and use of generalized valence angle screens. J. Mol. Graph. 1991, 9, 203-217.
-
(1991)
J. Mol. Graph.
, vol.9
, pp. 203-217
-
-
Poirrette, A.R.1
Willett, P.2
Allen, F.H.3
|