-
1
-
-
0007250271
-
Application of combinatorial technology to drug discovery
-
Moos, W.H., Pavia, M.R., Ellington, A.D. and Kay, B.K. (Eds.), ESCOM, Leiden
-
a. Patel, D.V., Application of combinatorial technology to drug discovery, In Moos, W.H., Pavia, M.R., Ellington, A.D. and Kay, B.K. (Eds.), Annual Reports in Combinatorial Chemistry and Molecular Diversity, Vol. 1, ESCOM, Leiden, 1997, pp. 78-79.
-
(1997)
Annual Reports in Combinatorial Chemistry and Molecular Diversity
, vol.1
, pp. 78-79
-
-
Patel, D.V.1
-
2
-
-
0010371404
-
Techniques for single-compound synthesis
-
Moos, W.H., Pavia, M.R., Ellington, A.D. and Kay, B.K. (Eds.), ESCOM, Leiden
-
b. Sarshar, S. and Mjalli, A.M.M., Techniques for single-compound synthesis, In Moos, W.H., Pavia, M.R., Ellington, A.D. and Kay, B.K. (Eds.), Annual Reports in Combinatorial Chemistry and Molecular Diversity, Vol. 1, ESCOM, Leiden 1997, pp. 19-29.
-
(1997)
Annual Reports in Combinatorial Chemistry and Molecular Diversity
, vol.1
, pp. 19-29
-
-
Sarshar, S.1
Mjalli, A.M.M.2
-
3
-
-
0030477258
-
Combinatorial synthesis of small organic molecules
-
c. Balkenhohl, F., Bussche-Hunnefeld, C., Lansky, A. and Zechel, C., Combinatorial synthesis of small organic molecules, Angew. Chem., Int. Ed. Engl., 35 (1996) 2288-2337.
-
(1996)
Angew. Chem., Int. Ed. Engl.
, vol.35
, pp. 2288-2337
-
-
Balkenhohl, F.1
Bussche-Hunnefeld, C.2
Lansky, A.3
Zechel, C.4
-
4
-
-
0028318863
-
Applications of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies, and future directions
-
d. Gordon, E.M., Barrett, R.W., Dower, W.J., Fodor, S.P.A. and Gallop, M.A., Applications of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies, and future directions, J. Med. Chem., 37 (1994) 1385-401.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1385-1401
-
-
Gordon, E.M.1
Barrett, R.W.2
Dower, W.J.3
Fodor, S.P.A.4
Gallop, M.A.5
-
5
-
-
0000577984
-
The 'one-bead-one-compound' combinatorial library method
-
a. Lam, K.S., Lebl, M. and Krchnak, V., The 'one-bead-one-compound' combinatorial library method, Chem. Rev., 97 (1997) 411-448.
-
(1997)
Chem. Rev.
, vol.97
, pp. 411-448
-
-
Lam, K.S.1
Lebl, M.2
Krchnak, V.3
-
6
-
-
0031151959
-
Encoding methods for combinatorial chemistry
-
b. Czarnik, A.W., Encoding methods for combinatorial chemistry, Curr. Opin. Chem. Biol., 1 (1997) 60-66.
-
(1997)
Curr. Opin. Chem. Biol.
, vol.1
, pp. 60-66
-
-
Czarnik, A.W.1
-
7
-
-
0030252582
-
Design, synthesis and use of binary encoded synthetic chemical libraries
-
c. Baldwin, J.J., Design, synthesis and use of binary encoded synthetic chemical libraries, Mol. Diversity, 2 (1996) 81-88.
-
(1996)
Mol. Diversity
, vol.2
, pp. 81-88
-
-
Baldwin, J.J.1
-
8
-
-
0029895291
-
Encoded combinatorial chemistry: Binary coding using chemically robust secondary amine tags
-
d. Ni, Z.-J., Maclean, D., Holmes, C.P. and Gallop, M.A., Encoded combinatorial chemistry: binary coding using chemically robust secondary amine tags, Methods Enzymol., 267 (1996) 261-272.
-
(1996)
Methods Enzymol.
, vol.267
, pp. 261-272
-
-
Ni, Z.-J.1
Maclean, D.2
Holmes, C.P.3
Gallop, M.A.4
-
9
-
-
0002760030
-
Approaches and technologies for screening large combinatorial libraries
-
Gordon, E.M. and Kerwin, J.F. (Eds.), Wiley-Liss, New York, NY
-
a. Sigal, N.H. and Chelsky, D., Approaches and technologies for screening large combinatorial libraries, In Gordon, E.M. and Kerwin, J.F. (Eds.), Combinatorial Chemistry and Molecular Diversity in Drug Discovery, Wiley-Liss, New York, NY, 1998, pp. 433-443.
-
(1998)
Combinatorial Chemistry and Molecular Diversity in Drug Discovery
, pp. 433-443
-
-
Sigal, N.H.1
Chelsky, D.2
-
10
-
-
0002837758
-
Strategies for screening combinatorial libraries
-
Gordon, E.M. and Kerwin, J.F. (Eds.), Wiley-Liss, New York, NY
-
b. Beutel, B.A., Strategies for screening combinatorial libraries, In Gordon, E.M. and Kerwin, J.F. (Eds.), Combinatorial Chemistry and Molecular Diversity in Drug Discovery, Wiley-Liss, New York, NY, 1998, pp. 421-432.
-
(1998)
Combinatorial Chemistry and Molecular Diversity in Drug Discovery
, pp. 421-432
-
-
Beutel, B.A.1
-
11
-
-
33748243831
-
Radiofrequency encoded combinatorial chemistry
-
a. Nicolaou, K.C., Xiao, X.-Y, Parandoosh, Z., Senyei, A. and Nova, M.P., Radiofrequency encoded combinatorial chemistry, Angew. Chem., Int. Ed. Engl., 34 (1995) 2289-2291.
-
(1995)
Angew. Chem., Int. Ed. Engl.
, vol.34
, pp. 2289-2291
-
-
Nicolaou, K.C.1
Xiao, X.-Y.2
Parandoosh, Z.3
Senyei, A.4
Nova, M.P.5
-
12
-
-
0002602282
-
Radiofrequency encoding and additional techniques for the structure elucidation of synthetic combinatorial libraries
-
Wilson, S.R. and Czarnik, A.W. (Eds.), John Wiley & Sons, New York, NY
-
b. Xiao, X.-Y and Nova, M.P., Radiofrequency encoding and additional techniques for the structure elucidation of synthetic combinatorial libraries, In Wilson, S.R. and Czarnik, A.W. (Eds.), Combinatorial Chemistry Synthesis and Application, John Wiley & Sons, New York, NY, 1997, pp. 135-152.
-
(1997)
Combinatorial Chemistry Synthesis and Application
, pp. 135-152
-
-
Xiao, X.-Y.1
Nova, M.P.2
-
13
-
-
0028222149
-
L-735,524: An orally bioavailable human immunodeficiency virus type 1 protease inhibitor
-
a. Vacca, J.P., Dorsey, B.D., Schleif, W.A., Levin, R.B., McDaniel, S.L., Darke, P.L., Zugay, J., Quintero, J.C. and Blahy, O.M., L-735,524: an orally bioavailable human immunodeficiency virus type 1 protease inhibitor, Proc. Natl. Acad. Sci. USA, 91 (1994) 4096-4100.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 4096-4100
-
-
Vacca, J.P.1
Dorsey, B.D.2
Schleif, W.A.3
Levin, R.B.4
McDaniel, S.L.5
Darke, P.L.6
Zugay, J.7
Quintero, J.C.8
Blahy, O.M.9
-
14
-
-
0030040462
-
Formation of phenylpiperazines by a novel alumina supported bis-alkylation
-
b. Mishani, Eyal, Dence, C.S., McCarthy, T.J. and Welch, M.J., Formation of phenylpiperazines by a novel alumina supported bis-alkylation, Tetrahedron Lett., 37 (1996) 319-322.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 319-322
-
-
Mishani1
Eyal2
Dence, C.S.3
McCarthy, T.J.4
Welch, M.J.5
-
15
-
-
0027230174
-
(S)-N-tert-butyl-3-(4-(2-methoxyphenyl)piperazin-1-yl)-2- phenylpropanamide [(S)-WAY-100135]: A selective antagonist at presynaptic and postsynaptic 5-HT1A receptors
-
c. Cliffe, I.A., Brightwell, C.I., Fletcher, A., Forster, E.A., Mansell, H.L., Reilly, Y., Routledge, C. and White, A.C., (S)-N-tert-butyl-3-(4-(2-methoxyphenyl)piperazin-1-yl)-2-phenylpropanamide [(S)-WAY-100135]: a selective antagonist at presynaptic and postsynaptic 5-HT1A receptors, J. Med. Chem., 36 (1993) 1509-1510.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 1509-1510
-
-
Cliffe, I.A.1
Brightwell, C.I.2
Fletcher, A.3
Forster, E.A.4
Mansell, H.L.5
Reilly, Y.6
Routledge, C.7
White, A.C.8
-
16
-
-
0028788888
-
Cycloalkylpiperazines as HIV-1 protease inhibitors: Enhanced oral absorption
-
d. Kim, B.M., Evans, B.E., Gilbert, K.F., Hanifin, C.M., Vacca, J.P., Michelson, S.R., Darke, P.L., Zugay, J.A., Emini, E.A., Schleif, W., Lin, J.H., Chen, I.-W., Vastag, K., Anderson, P.S. and Huff, J.R., Cycloalkylpiperazines as HIV-1 protease inhibitors: enhanced oral absorption, Bioorg. Med. Chem. Lett., 5 (1995) 2707-2712.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2707-2712
-
-
Kim, B.M.1
Evans, B.E.2
Gilbert, K.F.3
Hanifin, C.M.4
Vacca, J.P.5
Michelson, S.R.6
Darke, P.L.7
Zugay, J.A.8
Emini, E.A.9
Schleif, W.10
Lin, J.H.11
Chen, I.-W.12
Vastag, K.13
Anderson, P.S.14
Huff, J.R.15
-
17
-
-
0027507763
-
Synthesis and structure-activity relationships of a novel series of non-peptide AT2-selective angiotensin II receptor antagonists
-
a. Wu, M.T., Ikeler, T.J., Ashton, W.T., Chang, R.S.L., Lotti, V.J. and Greenlee, W.J., Synthesis and structure-activity relationships of a novel series of non-peptide AT2-selective angiotensin II receptor antagonists, Bioorg. Med. Chem. Lett., 3 (1993) 2023.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 2023
-
-
Wu, M.T.1
Ikeler, T.J.2
Ashton, W.T.3
Chang, R.S.L.4
Lotti, V.J.5
Greenlee, W.J.6
-
18
-
-
6744268389
-
-
N,N-diacylpiperazines, PCT Int. Appl WO 9220661
-
b. Ashton, W.T., Greenlee, W.J., Wu, M.T., Dorn, C.P., MacCoss, M. and Mills, S.G., N,N-diacylpiperazines, PCT Int. Appl WO 9220661.
-
-
-
Ashton, W.T.1
Greenlee, W.J.2
Wu, M.T.3
Dorn, C.P.4
MacCoss, M.5
Mills, S.G.6
-
19
-
-
6744272342
-
-
Preparation of N,N-diacylpiperazinecarboxylates as tachykinin antagonists, PCT Int. Appl. WO 9413646
-
Mills, Sa.G., Budhu, R.J., Dorn, C.P., Greenlee, W.J., Maccoss, M. and Wu, M.T., Preparation of N,N-diacylpiperazinecarboxylates as tachykinin antagonists, PCT Int. Appl. WO 9413646.
-
-
-
Mills, Sa.G.1
Budhu, R.J.2
Dorn, C.P.3
Greenlee, W.J.4
Maccoss, M.5
Wu, M.T.6
-
20
-
-
0029118635
-
Asymmetric hydrogenation of tetrahydropyrazines: Synthesis of (S)-piperazine-2-tert-butylcarboxamide, an intermediate in the preparation of the HIV protease inhibitor indinavir
-
a. Rossen, K., Weissman, S.A., Sager, J., Reamer, R.A., Askin, D., Volante, R.P. and Reider, P.J., Asymmetric hydrogenation of tetrahydropyrazines: synthesis of (S)-piperazine-2-tert-butylcarboxamide, an intermediate in the preparation of the HIV protease inhibitor indinavir, Tetrahedron Lett., 36 (1995) 6419-6422.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 6419-6422
-
-
Rossen, K.1
Weissman, S.A.2
Sager, J.3
Reamer, R.A.4
Askin, D.5
Volante, R.P.6
Reider, P.J.7
-
21
-
-
0029872589
-
A 24-week open-label phase I/II evaluation of the HIV protease inhibitor MK-639 (indinavir)
-
b. Stein, D.S., Fish, D.G., Bilello, J.A., Preston, S.L., Martineau, G.L. and Drusano, G.L., A 24-week open-label phase I/II evaluation of the HIV protease inhibitor MK-639 (indinavir), AIDS, 10 (1996) 485-492.
-
(1996)
AIDS
, vol.10
, pp. 485-492
-
-
Stein, D.S.1
Fish, D.G.2
Bilello, J.A.3
Preston, S.L.4
Martineau, G.L.5
Drusano, G.L.6
-
22
-
-
0032510277
-
Generation of a piperazine-2-carboxamide library: A practical application of the phenol-sulfide react and release linker
-
Breitenbucher, J.G., Johnson, C.R., Haight, M. and Phelan, J.C., Generation of a piperazine-2-carboxamide library: a practical application of the phenol-sulfide react and release linker, Tetrahedron Lett., 39 (1998) 1295-1298.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 1295-1298
-
-
Breitenbucher, J.G.1
Johnson, C.R.2
Haight, M.3
Phelan, J.C.4
-
23
-
-
0032542040
-
Evaluation of a structure-based statine cyclic diamino amide encoded combinatorial library against plasmepsin II and cathepsin D
-
DiIanni Carroll, C., Johnson, T.O., Tao, S., Lauri, G., Orlowski, M., Gluzman, I.Y., Goldberg, D.E. and Dolle, R.E., Evaluation of a structure-based statine cyclic diamino amide encoded combinatorial library against plasmepsin II and cathepsin D, Bioorg. Med. Chem. Lett., 8 (1998) 3203-3206.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 3203-3206
-
-
DiIanni Carroll, C.1
Johnson, T.O.2
Tao, S.3
Lauri, G.4
Orlowski, M.5
Gluzman, I.Y.6
Goldberg, D.E.7
Dolle, R.E.8
-
24
-
-
0024435682
-
New preparations of the N-methyl-D-aspartate receptor antagonist, 4-(3-phosphonopropyl)-2-piperazinecarboxylic acid (CPP)
-
Bigge, C.F., Hays, S.J., Novak, P.M., Drummond, J.T., Johnson, G. and Bobovski, T.P., New preparations of the N-methyl-D-aspartate receptor antagonist, 4-(3-phosphonopropyl)-2-piperazinecarboxylic acid (CPP), Tetrahedron Lett., 39 (1989) 5193-5196.
-
(1989)
Tetrahedron Lett.
, vol.39
, pp. 5193-5196
-
-
Bigge, C.F.1
Hays, S.J.2
Novak, P.M.3
Drummond, J.T.4
Johnson, G.5
Bobovski, T.P.6
-
25
-
-
0032503569
-
Backbone amide linker strategy for solidphase synthesis of C-terminal-modified and cyclic peptides
-
Jensen, K.J., Alsina, J., Songster, M.F., Vagner, J., Albericio, F. and Barany, G., Backbone amide linker strategy for solidphase synthesis of C-terminal-modified and cyclic peptides, J. Am. Chem. Soc., 120 (1998) 5441-5452.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 5441-5452
-
-
Jensen, K.J.1
Alsina, J.2
Songster, M.F.3
Vagner, J.4
Albericio, F.5
Barany, G.6
-
26
-
-
0030932342
-
Solid-phase synthesis of 1,4-benzodiazepine-2,5-diones. Library preparation and demonstration of synthesis generality
-
Boojamra, C.G., Burow, K., Thompson, L.A. and Ellman, J.A., Solid-phase synthesis of 1,4-benzodiazepine-2,5-diones. Library preparation and demonstration of synthesis generality, J. Org. Chem., 62 (1997) 1240-1256.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1240-1256
-
-
Boojamra, C.G.1
Burow, K.2
Thompson, L.A.3
Ellman, J.A.4
-
27
-
-
45949119318
-
An improved method for anchoring of 9-fluorenylmethoxycarbonyl amino acids to 4-alkoxybenzyl alcohol resins
-
Sieber, P., An improved method for anchoring of 9-fluorenylmethoxycarbonyl amino acids to 4-alkoxybenzyl alcohol resins, Tetrahedron Lett., 28 (1987) 6147-6150.
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 6147-6150
-
-
Sieber, P.1
-
28
-
-
0001923937
-
Design and diversity analysis of large combinatorial libraries using cell-based methods
-
a. Schnur, D.J., Design and diversity analysis of large combinatorial libraries using cell-based methods, Chem. Inf. Comput. Sci., 39 (1999) 36-45.
-
(1999)
Chem. Inf. Comput. Sci.
, vol.39
, pp. 36-45
-
-
Schnur, D.J.1
-
29
-
-
15844383852
-
Selecting combinatorial libraries to optimize diversity and physical properties
-
b. Gillet, V.J., Willett, P., Bradshaw, J. and Green, D.V.S., Selecting combinatorial libraries to optimize diversity and physical properties, J. Chem. Inf. Comput. Sci., 39 (1999) 169-177.
-
(1999)
J. Chem. Inf. Comput. Sci.
, vol.39
, pp. 169-177
-
-
Gillet, V.J.1
Willett, P.2
Bradshaw, J.3
Green, D.V.S.4
-
30
-
-
0031024171
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
Lipinski, C.A., Lombardo, F., Dominy, B.W. and Feeney, P.J., Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings, Adv. Drug Delivery Rev., 23 (1997) 3-25.
-
(1997)
Adv. Drug Delivery Rev.
, vol.23
, pp. 3-25
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
31
-
-
6744249288
-
-
Daylight Chemical Information Systems, Inc., Mission Viejo, CA
-
Daylight Chemical Information Systems, Inc., Mission Viejo, CA.
-
-
-
-
32
-
-
0005686498
-
-
Oxford Molecular, Oxford
-
Chem-X software, Oxford Molecular, Oxford.
-
Chem-X Software
-
-
-
33
-
-
0041406392
-
Experiences with searching for molecular similarity in conformationally flexible 3D databases
-
Dean, P.M. (Ed.), Blackie Academic and Professional, Glasgow
-
a. Mason, J.S., Experiences with searching for molecular similarity in conformationally flexible 3D databases, In Dean, P.M. (Ed.), Molecular Similarity in Drug Design, Blackie Academic and Professional, Glasgow, 1995, pp. 138-162.
-
(1995)
Molecular Similarity in Drug Design
, pp. 138-162
-
-
Mason, J.S.1
-
34
-
-
0002556215
-
Partition-based selection
-
Willett, P. (Ed.), Kluwer, Dordrecht
-
b. Mason, J.S. and Pickett, S.D., Partition-based selection, In Willett, P. (Ed.), Perspectives in Drug Discovery and Design (PD3) - Special Issue on Computational Methods for the Analysis of Molecular Diversity, Kluwer, Dordrecht, 1997, pp. 85-114.
-
(1997)
Perspectives in Drug Discovery and Design (PD3) - Special Issue on Computational Methods for the Analysis of Molecular Diversity
, pp. 85-114
-
-
Mason, J.S.1
Pickett, S.D.2
-
35
-
-
0000465937
-
Diversity pro-filing and design using 3D pharmacophores: Pharmacophore-derived queries (PDQ)
-
c. Pickett, S.D., Mason, J.S. and McLay, I.M., Diversity pro-filing and design using 3D pharmacophores: pharmacophore-derived queries (PDQ), J. Chem. Inf. Comput. Sci., 36 (1996) 1214-1223.
-
(1996)
J. Chem. Inf. Comput. Sci.
, vol.36
, pp. 1214-1223
-
-
Pickett, S.D.1
Mason, J.S.2
McLay, I.M.3
-
36
-
-
0033606988
-
New 4-point pharmacophore method for molecular similarity and diversity applications: Overview of the method and applications, including a novel approach to the design of combinatorial libraries containing privileged substructures
-
d. Mason, J.S., Morize, I., Menard, P.R., Cheney, D.L., Hulme, C. and Labaudiniere, R.F., New 4-point pharmacophore method for molecular similarity and diversity applications: Overview of the method and applications, including a novel approach to the design of combinatorial libraries containing privileged substructures, J. Med. Chem., 42 (1999) 3251-3264.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3251-3264
-
-
Mason, J.S.1
Morize, I.2
Menard, P.R.3
Cheney, D.L.4
Hulme, C.5
Labaudiniere, R.F.6
-
37
-
-
0346601301
-
Kinetics of acid-catalyzed cyclization of substituted hydantoinamides to substituted hydantoins
-
Kavalek, J., Machacek, V., Svobodova, G. and Sterba, V., Kinetics of acid-catalyzed cyclization of substituted hydantoinamides to substituted hydantoins, Collect. Czech. Chem. Commun., 8 (1987) 1999-2004.
-
(1987)
Collect. Czech. Chem. Commun.
, vol.8
, pp. 1999-2004
-
-
Kavalek, J.1
Machacek, V.2
Svobodova, G.3
Sterba, V.4
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