-
1
-
-
0032600590
-
Parallel personal comments on 'classical' papers in combinatorial chemistry
-
Lebl, M., Parallel personal comments on 'classical' papers in combinatorial chemistry, J. Comb. Chem., 1 (1999) 3-24.
-
(1999)
J. Comb. Chem.
, vol.1
, pp. 3-24
-
-
Lebl, M.1
-
2
-
-
0032873699
-
High throughput screening for drug discovery: Continually transitioning into new technology
-
Fox, S., Farr-Jones, S. and Yund, M. A., High throughput screening for drug discovery: Continually transitioning into new technology, J. Biomol. Screening, 4 (1999) 183-186.
-
(1999)
J. Biomol. Screening
, vol.4
, pp. 183-186
-
-
Fox, S.1
Farr-Jones, S.2
Yund, M.A.3
-
3
-
-
0037092610
-
How to escape the bottleneck of medicinal chemistry
-
(a) Wess, G., How to escape the bottleneck of medicinal chemistry, Drug Discov. Today, 7 (2002) 533-535.
-
(2002)
Drug Discov. Today
, vol.7
, pp. 533-535
-
-
Wess, G.1
-
4
-
-
0035426577
-
Industrial-scale genomics-based drug design and discovery
-
(b) Dean, P. M., Zanders, E. D. and Bailey, D. S., Industrial-scale, genomics-based drug design and discovery, Trends Biotechnol., 19 (2001) 856-864.
-
(2001)
Trends Biotechnol.
, vol.19
, pp. 856-864
-
-
Dean, P.M.1
Zanders, E.D.2
Bailey, D.S.3
-
5
-
-
0034256065
-
The in silico world of virtual libraries
-
(c) Leach, A. R. and Hann, M. M., The in silico world of virtual libraries, Drug Discov. Today, 5 (2000) 326-336.
-
(2000)
Drug Discov. Today
, vol.5
, pp. 326-336
-
-
Leach, A.R.1
Hann, M.M.2
-
6
-
-
0035358567
-
Lead compounds discovered from libraries
-
(a) Golebiowski, A., Klopfenstein, S. R. and Portlock, D. E., Lead compounds discovered from libraries, Curr. Opin. Chem. Biol., 5 (2001) 273-284.
-
(2001)
Curr. Opin. Chem. Biol.
, vol.5
, pp. 273-284
-
-
Golebiowski, A.1
Klopfenstein, S.R.2
Portlock, D.E.3
-
7
-
-
0036937606
-
Recent advances in molecular diversity
-
(b) Waller, C. L., Recent advances in molecular diversity, Mol. Div., 5 (2000) 174-174.
-
(2000)
Mol. Div.
, vol.5
, pp. 174-174
-
-
Waller, C.L.1
-
8
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
(a) 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., 46 (2001) 3-26.
-
(2001)
Adv. Drug. Delivery Rev.
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
9
-
-
0033179183
-
Recognizing molecules with drug-like properties
-
(b) Walters, W. P., Murcko, A. and Murcko, M. A., Recognizing molecules with drug-like properties, Curr. Opin. Chem. Biol., 3 (1999) 384-387.
-
(1999)
Curr. Opin. Chem. Biol.
, vol.3
, pp. 384-387
-
-
Walters, W.P.1
Murcko, A.2
Murcko, M.A.3
-
10
-
-
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
-
11
-
-
0035324944
-
Molecular complexity and its impact on the probability of finding leads for drug discovery
-
(a) Hann, M. M., Leach, A. R. and Harper, G., Molecular complexity and its impact on the probability of finding leads for drug discovery, Chem. Inf. Com., Sci., 41 (2001) 856-864.
-
(2001)
Chem. Inf. Com., Sci.
, vol.41
, pp. 856-864
-
-
Hann, M.M.1
Leach, A.R.2
Harper, G.3
-
12
-
-
0032600672
-
Beyond mere diversity: Tailoring combinatorial libraries for drug discovery
-
(b) Martin, E. J. and Critchlow, R. E., Beyond mere diversity: Tailoring combinatorial libraries for drug discovery, J. Comb. Chem., 1 (1999) 32-45.
-
(1999)
J. Comb. Chem.
, vol.1
, pp. 32-45
-
-
Martin, E.J.1
Critchlow, R.E.2
-
13
-
-
0035903506
-
Medicinal chemistry: Challenges and opportunities
-
Wess, G., Urmann, M. and Sickenberger, B., Medicinal chemistry: Challenges and opportunities, Angew. Chem. Int. Ed., 40 (2001) 3341-3350.
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 3341-3350
-
-
Wess, G.1
Urmann, M.2
Sickenberger, B.3
-
14
-
-
0035313896
-
Screening for human ADME/Tox drug properties in drug discovery
-
(a) Li, A. P., Screening for human ADME/Tox drug properties in drug discovery, Drug Discov. Today, 6 (2001) 357-366.
-
(2001)
Drug Discov. Today
, vol.6
, pp. 357-366
-
-
Li, A.P.1
-
15
-
-
0034283752
-
ADME/PK as part of a rational approach to drug discovery
-
(b) Eddershaw, P. J., Beresford, A. P. and Bayliss, M. K., ADME/PK as part of a rational approach to drug discovery, Drug Discov. Today, 5 (2000) 409-414.
-
(2000)
Drug Discov. Today
, vol.5
, pp. 409-414
-
-
Eddershaw, P.J.1
Beresford, A.P.2
Bayliss, M.K.3
-
16
-
-
0037119336
-
From protein domains to drug candidates - Natural products as guiding principles in the design and synthesis of compound libraries
-
Breinbauer, R., Vetter, I. R. and Waldmann, H., From protein domains to drug candidates - Natural products as guiding principles in the design and synthesis of compound libraries, Angew. Chem. Int. Ed., 41 (2002) 2878-2890.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 2878-2890
-
-
Breinbauer, R.1
Vetter, I.R.2
Waldmann, H.3
-
17
-
-
0004106191
-
-
(eds.) Cold Spring Harbor Laboratory Press, New York
-
Varki, A., Cummings, R., Esko, J., Freeze, H., Hart, G. and Marth, J., Essential of Glycobiology, (eds.) Cold Spring Harbor Laboratory Press, New York, 1999.
-
(1999)
Essential of Glycobiology
-
-
Varki, A.1
Cummings, R.2
Esko, J.3
Freeze, H.4
Hart, G.5
Marth, J.6
-
18
-
-
0027318961
-
Biological roles of oligosaccharides: All of the theories are correct
-
(b) Varki, A., Biological roles of oligosaccharides: all of the theories are correct, Glycobiology, 3 (1993) 97-130.
-
(1993)
Glycobiology
, vol.3
, pp. 97-130
-
-
Varki, A.1
-
19
-
-
0035793331
-
Combinatorial chemistry toward understanding the function(s) of carbohydrates and carbohydrate conjugates
-
(a) Barkley, A. and Arya, P., Combinatorial chemistry toward understanding the function(s) of carbohydrates and carbohydrate conjugates, Chem. Eur. J., 7 (2001) 555-563.
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 555-563
-
-
Barkley, A.1
Arya, P.2
-
20
-
-
0034599659
-
Glycopeptide and oligosaccharide libraries
-
(b) St Hilaire, P. M. and Meldal, M., Glycopeptide and oligosaccharide libraries, Angew. Chem. Int. Ed., 39 (2000) 1162-1179.
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 1162-1179
-
-
St. Hilaire, P.M.1
Meldal, M.2
-
21
-
-
0032914765
-
Mimics of complex carbohydrates recognized by receptors
-
(a) Wong, C.-H., Mimics of complex carbohydrates recognized by receptors, Acc. Chem. Res., 32 (1999) 376-385.
-
(1999)
Acc. Chem. Res.
, vol.32
, pp. 376-385
-
-
Wong, C.-H.1
-
22
-
-
0033549740
-
Carbohydrate mimetics: A new strategy for tackling the problem of carbohydrate-mediated biological recognition
-
(b) Sears, P. and Wong, C. H., Carbohydrate mimetics: A new strategy for tackling the problem of carbohydrate-mediated biological recognition, Angew. Chem. Int. Ed., 38 (1999) 2301-2324.
-
(1999)
Angew. Chem. Int. Ed.
, vol.38
, pp. 2301-2324
-
-
Sears, P.1
Wong, C.H.2
-
23
-
-
0024239320
-
Methods for drug discovery: Development of potent, selective, orally effective cholecystokinin antagonists
-
Evans, B. E., Rittle, K. E., Bock, M. G., DiPardo, R. M., Freidinger, R. M., Whitter, W. L., Lundell, G. F., Veber, D. F., Anderson, P. S. and Chang, R. S., Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists, J. Med. Chem., 31 (1988) 2235-2246.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 2235-2246
-
-
Evans, B.E.1
Rittle, K.E.2
Bock, M.G.3
DiPardo, R.M.4
Freidinger, R.M.5
Whitter, W.L.6
Lundell, G.F.7
Veber, D.F.8
Anderson, P.S.9
Chang, R.S.10
-
24
-
-
0000669419
-
Comprehensive survey of combinatorial library synthesis: 2001
-
(a) Dolle, R. E., Comprehensive survey of combinatorial library synthesis: 2001, J. Comb. Chem., 4 (2002) 369-418.
-
(2002)
J. Comb. Chem.
, vol.4
, pp. 369-418
-
-
Dolle, R.E.1
-
25
-
-
0035513630
-
Comprehensive survey of combinatorial library synthesis: 2000
-
(b) Dolle, R. E., Comprehensive survey of combinatorial library synthesis: 2000, J. Comb. Chem., 3 (2001) 477-517.
-
(2001)
J. Comb. Chem.
, vol.3
, pp. 477-517
-
-
Dolle, R.E.1
-
26
-
-
0035977234
-
Synthesis of novel guanidinoglycoside: 2-glycosylamino 4,5-dihydro-6-pyrimidinone
-
Lin, P. S., Lee, C. L. and Sim, M. M., Synthesis of novel guanidinoglycoside: 2-glycosylamino 4,5-dihydro-6-pyrimidinone, J. Org. Chem., 66 (2001) 8243-8247.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 8243-8247
-
-
Lin, P.S.1
Lee, C.L.2
Sim, M.M.3
-
27
-
-
0036420223
-
Dihydropyridine C-glycoconjugates by Hantzsch cyclocondensation. Synthesis of a C(6)-glycosylated nifedipine analogue
-
(a) Dondoni, A., Massi, A., Minghini, E. and Bertolasi, V., Dihydropyridine C-glycoconjugates by Hantzsch cyclocondensation. Synthesis of a C(6)-glycosylated nifedipine analogue, Helv. Chim. Acta, 85 (2002) 3331-3348.
-
(2002)
Helv. Chim. Acta
, vol.85
, pp. 3331-3348
-
-
Dondoni, A.1
Massi, A.2
Minghini, E.3
Bertolasi, V.4
-
28
-
-
0037019968
-
Three-component Biginelli cyclocondensation reaction using C-glycosylated substrates. Preparation of a collection of dihydropyrimidinone glycoconjugates and the synthexis of C-glycosylated monastrol analogues
-
(b) Dondoni, A., Massi, A., Sabbatini, S. and Bertolasi, V., Three-component Biginelli cyclocondensation reaction using C-glycosylated substrates. Preparation of a collection of dihydropyrimidinone glycoconjugates and the synthexis of C-glycosylated monastrol analogues, J. Org. Chem., 67 (2002) 6979-6994.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 6979-6994
-
-
Dondoni, A.1
Massi, A.2
Sabbatini, S.3
Bertolasi, V.4
-
29
-
-
0036140454
-
Two-and three-component Hantzsch reaction using C-glycosylated reagents. Approach to the asymmetric synthesis of 1,4-diyhydropyridines
-
(c) Dondoni, A., Massi, A. and Minghini, E., Two-and three-component Hantzsch reaction using C-glycosylated reagents. Approach to the asymmetric synthesis of 1,4-diyhydropyridines, Synlett, 1 (2002) 89-92.
-
(2002)
Synlett
, vol.1
, pp. 89-92
-
-
Dondoni, A.1
Massi, A.2
Minghini, E.3
-
30
-
-
0035796960
-
Towards the synthesis of C-glycosylated dihydropyrimidine libraries via the three-component Biginelli reaction. A novel approach to artificial nucleosides
-
(d) Dondoni, A., Massi, A. and Sabbatini, S., Towards the synthesis of C-glycosylated dihydropyrimidine libraries via the three-component Biginelli reaction. A novel approach to artificial nucleosides, Tetrahedron Lett., 42 (2001) 4495-4497.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 4495-4497
-
-
Dondoni, A.1
Massi, A.2
Sabbatini, S.3
-
31
-
-
0034665244
-
Maximizing synthetic efficiency: Multi-component transformations lead the way
-
(a) Bienayme, H., Hulme, C., Oddon, G. and Schmitt, P., Maximizing synthetic efficiency: Multi-component transformations lead the way, Chem. Eur. J., 6 (2000) 3321-3329.
-
(2000)
Chem. Eur. J.
, vol.6
, pp. 3321-3329
-
-
Bienayme, H.1
Hulme, C.2
Oddon, G.3
Schmitt, P.4
-
32
-
-
0033929179
-
Since 1995 the new chemistry of multicomponent reactions and their libraries, including their heterocyclic chemistry
-
(b) Ugi, I., Domling, A. and Wemer, B., Since 1995 the new chemistry of multicomponent reactions and their libraries, including their heterocyclic chemistry, J. Heterocyclic Chem., 37 (2000) 647-658.
-
(2000)
J. Heterocyclic Chem.
, vol.37
, pp. 647-658
-
-
Ugi, I.1
Domling, A.2
Wemer, B.3
-
33
-
-
0036012737
-
Recent developments in the chemistry of dihydropyridines
-
(a) Lavilla, R., Recent developments in the chemistry of dihydropyridines, J. Chem. Soc., Perkin Trans. 1, 9 (2002) 1141-1156.
-
(2002)
J. Chem. Soc., Perkin Trans. 1
, vol.9
, pp. 1141-1156
-
-
Lavilla, R.1
-
35
-
-
0034518876
-
Recent advances in the Biginelli dihydropyrimidine synthesis. New tricks from an old dog
-
For reviews see: (a) Kappe, C. O., Recent advances in the Biginelli dihydropyrimidine synthesis. New tricks from an old dog, Acc. Chem. Res., 33 (2000) 879-888.
-
(2000)
Acc. Chem. Res.
, vol.33
, pp. 879-888
-
-
Kappe, C.O.1
-
36
-
-
0027205552
-
100 Years of the Biginelli dihydropyrimidine synthesis
-
(b) Kappe, C. O., 100 Years of the Biginelli dihydropyrimidine synthesis, Tetrahedron, 49 (1993) 6937-6963.
-
(1993)
Tetrahedron
, vol.49
, pp. 6937-6963
-
-
Kappe, C.O.1
-
38
-
-
34250472293
-
Dihydropyridines a new group of strongly effective coronary therapeutic agents
-
(b) Bossert, F. and Vater, W., Dihydropyridines, a new group of strongly effective coronary therapeutic agents, Naturwissenschaften, 58 (1971) 578.
-
(1971)
Naturwissenschaften
, vol.58
, pp. 578
-
-
Bossert, F.1
Vater, W.2
-
39
-
-
0034519777
-
Biologically active dihydropyrimidinones of the Biginelli-type: A literature survey
-
For a survey on this topic with leading references, see: Kappe, C. O., Biologically active dihydropyrimidinones of the Biginelli-type: a literature survey, Eur. J. Med. Chem., 35 (2000) 1043-1052.
-
(2000)
Eur. J. Med. Chem.
, vol.35
, pp. 1043-1052
-
-
Kappe, C.O.1
-
40
-
-
0347994341
-
Cerebrocrast (1OS-1212) normalizes disturbances of learning, attention, emotional behavior and brain biogenic amine levels in prenatally hypoxized rats
-
Klusa, V., Semenova, T. D., Medvinskaya, N. I. and Fast, A. E., Cerebrocrast (1OS-1212) normalizes disturbances of learning, attention, emotional behavior and brain biogenic amine levels in prenatally hypoxized rats, Latvijas Zinatnu Akademijas Vestis, 11/12 (1995) 156-161.
-
(1995)
Latvijas Zinatnu Akademijas Vestis
, vol.11-12
, pp. 156-161
-
-
Klusa, V.1
Semenova, T.D.2
Medvinskaya, N.I.3
Fast, A.E.4
-
41
-
-
0033615357
-
Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen
-
Mayer, T. U., Kapoor, T. M., Haggarty, S. J., King, R. W., Schreiber, S. L. and Mitchison, T. J., Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen, Science 286 (1999) 971-974.
-
(1999)
Science
, vol.286
, pp. 971-974
-
-
Mayer, T.U.1
Kapoor, T.M.2
Haggarty, S.J.3
King, R.W.4
Schreiber, S.L.5
Mitchison, T.J.6
-
42
-
-
0026342780
-
1,4-Dihydropyridines - Effects of chirality and conformation on the calcium-antagonist and calcium agonist activities
-
Goldmann, S. and Stoltefuss, J., 1,4-dihydropyridines - effects of chirality and conformation on the calcium-antagonist and calcium agonist activities, Angew. Chem. Int. Ed., 30 (1991) 1559-1578.
-
(1991)
Angew. Chem. Int. Ed.
, vol.30
, pp. 1559-1578
-
-
Goldmann, S.1
Stoltefuss, J.2
-
43
-
-
0034583249
-
Formylation of carbohydrates and the evolution of synthetic routes to artificial oligosaccharides and glycoconjugates
-
(a) Dondoni, A., Formylation of carbohydrates and the evolution of synthetic routes to artificial oligosaccharides and glycoconjugates, Pure App. Chem., 72 (2000) 1577-1588.
-
(2000)
Pure App. Chem.
, vol.72
, pp. 1577-1588
-
-
Dondoni, A.1
-
44
-
-
0028076365
-
Thiazole-based synthesis of formyl C-glycosides
-
(b) Dondoni, A. and Schemnann, M. C., Thiazole-based synthesis of formyl C-glycosides, J. Org. Chem., 59 (1994) 6404-6412.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 6404-6412
-
-
Dondoni, A.1
Schemnann, M.C.2
-
47
-
-
0032524801
-
Unprecedented catalytic three component one-pot condensation reaction: An efficient synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones
-
Hu, E. H., Sidler, D. R. and Dolling, U. H., Unprecedented catalytic three component one-pot condensation reaction: An efficient synthesis of 5-alkoxycarbonyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones, J. Org. Chem., 63 (1998) 3454-3457.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 3454-3457
-
-
Hu, E.H.1
Sidler, D.R.2
Dolling, U.H.3
-
48
-
-
0034674776
-
Lanthanide triflate catalyzed Biginelli reaction. One-pot synthesis of dihydropyrimidinones under solvent-free conditions
-
Ma, Y., Qian, C. T., Wang, L. M. and Yang, M., Lanthanide triflate catalyzed Biginelli reaction. One-pot synthesis of dihydropyrimidinones under solvent-free conditions, J. Org. Chem., 65 (2000) 3864-3868.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 3864-3868
-
-
Ma, Y.1
Qian, C.T.2
Wang, L.M.3
Yang, M.4
-
49
-
-
0035812731
-
Absolute configuration in 4-alkyl- and 4-aryl-3,4-dihydro-2(1H)-pyrimidones: A combined theoretical and experimental investigation
-
Uray, G., Verdino, P., Belaj, F., Kappe, C. O. and Fabian, W. M. F., Absolute configuration in 4-alkyl- and 4-aryl-3,4-dihydro-2(1H)-pyrimidones: A combined theoretical and experimental investigation, J. Org. Chem., 66 (2001) 6685-6694.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 6685-6694
-
-
Uray, G.1
Verdino, P.2
Belaj, F.3
Kappe, C.O.4
Fabian, W.M.F.5
-
50
-
-
0034708729
-
Synthesis and reactions of Biginelli compounds, part 19 - X-ray structure, conformational analysis, enantioseparation, and determination of absolute configuration of the mitotic kinesin Eg5 inhibitor monastrol
-
Kappe, C. O., Shishkin, O. V., Uray, G. and Verdino, P., Synthesis and reactions of Biginelli compounds, part 19 - X-ray structure, conformational analysis, enantioseparation, and determination of absolute configuration of the mitotic kinesin Eg5 inhibitor monastrol, Tetrahedron, 56 (2000) 1859-1862.
-
(2000)
Tetrahedron
, vol.56
, pp. 1859-1862
-
-
Kappe, C.O.1
Shishkin, O.V.2
Uray, G.3
Verdino, P.4
-
51
-
-
0031662778
-
In vitro antifungal activities of a series of dication-substituted carbazoles, furans, and benzimidazoles
-
Del Poeta, M., Schell, W. A., Dykstra, C. C., Jones, S. K., Tidwell, R. R., Kumar, A., Boykin, D. W. and Perfect, J. R., In vitro antifungal activities of a series of dication-substituted carbazoles, furans, and benzimidazoles, Antimicrob. Agents Chemother., 42 (1998) 2503-2510.
-
(1998)
Antimicrob. Agents Chemother.
, vol.42
, pp. 2503-2510
-
-
Del Poeta, M.1
Schell, W.A.2
Dykstra, C.C.3
Jones, S.K.4
Tidwell, R.R.5
Kumar, A.6
Boykin, D.W.7
Perfect, J.R.8
-
52
-
-
0027516081
-
Synthesis of 2-imidazolidinylidenepropanedinitrile derivatives as stimulators of gastrointestinal motility 1
-
Sasho, S., Obase, H., Ichikawa, S., Kitazawa, T., Nonaka, H., Yoshizaki, R., Ishii, A. and Shuto, K., Synthesis of 2-imidazolidinylidenepropanedinitrile derivatives as stimulators of gastrointestinal motility 1, J. Med. Chem., 36 (1993) 572-579.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 572-579
-
-
Sasho, S.1
Obase, H.2
Ichikawa, S.3
Kitazawa, T.4
Nonaka, H.5
Yoshizaki, R.6
Ishii, A.7
Shuto, K.8
|