-
1
-
-
11144298973
-
Exploring biology with small organic molecules
-
Stockwell, B. R. Exploring biology with small organic molecules. Nature, 2004, 432, 846-854.
-
(2004)
Nature
, vol.432
, pp. 846-854
-
-
Stockwell, B.R.1
-
2
-
-
33845903833
-
Drugs for bad bugs: Confronting the challenges of antibacterial discovery
-
Payne, D. J.; Gwynn, M. N.; Holmes, D. J.; Pomplinano, D. L. Drugs for bad bugs: confronting the challenges of antibacterial discovery. Nat. Rev. Drug. Discov., 2007, 6, 29-40.
-
(2007)
Nat. Rev. Drug. Discov.
, vol.6
, pp. 29-40
-
-
Payne, D.J.1
Gwynn, M.N.2
Holmes, D.J.3
Pomplinano, D.L.4
-
3
-
-
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.; Whiter, W. L.; Lundell, G. F; Veber, D. F.; Anderson, P. S.; Chang, R. S. L.; Lottie, V. J.; Cerino, D. J.; Chen, T. B.; Kling, P. J.; Kunkel, K. A.; Springer, J. P.; Hirshfield, J. Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists. J. Med. Chem., 1988, 31, 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
Whiter, W.L.6
Lundell, G.F.7
Veber, D.F.8
Anderson, P.S.9
Chang, R.S.L.10
Lottie, V.J.11
Cerino, D.J.12
Chen, T.B.13
Kling, P.J.14
Kunkel, K.A.15
Springer, J.P.16
Hirshfield, J.17
-
4
-
-
0027191479
-
Protein β-turn mimetics I. Design, synthesis, and evaluation in model cyclic peptides
-
Ripka, W. C.; De Lucca, G. V.; Bach, A. C.; Pottorf, R. S.; Blaney, J. M. Protein β-turn mimetics I. Design, synthesis, and evaluation in model cyclic peptides. Tetrahedron, 1993, 49, 3593-3608.
-
(1993)
Tetrahedron
, vol.49
, pp. 3593-3608
-
-
Ripka, W.C.1
De Lucca, G.V.2
Bach, A.C.3
Pottorf, R.S.4
Blaney, J.M.5
-
5
-
-
4243159924
-
Privileged structures: Applications in drug discovery
-
De Simone, R. W.; Currie, K. S.; Mitchell, S. A.; Darrow, J. W.; Pippin, D. A. Privileged structures: applications in drug discovery. Comb. Chem. High Throughput Screen., 2004, 7, 473-494.
-
(2004)
Comb. Chem. High Throughput Screen.
, vol.7
, pp. 473-494
-
-
De Simone, R.W.1
Currie, K.S.2
Mitchell, S.A.3
Darrow, J.W.4
Pippin, D.A.5
-
6
-
-
77952477596
-
Privileged scaffolds for library design and drug discovery
-
Matthew, E. W.; Scott, A. S.; Brent, R. S. Privileged scaffolds for library design and drug discovery. Curr. Opin. Chem. Biol., 2010, 14, 347-361.
-
(2010)
Curr. Opin. Chem. Biol.
, vol.14
, pp. 347-361
-
-
Matthew, E.W.1
Scott, A.S.2
Brent, R.S.3
-
7
-
-
0001874067
-
The pharmacon-receptor-effector concept: A basis for understanding the transmission of information in biological systems
-
O'Brien, R.D. (Ed.), Plenum Press, New York
-
Ariens, E. J.; Beld, A. J.; Rodrigues de Miranda, J. F.; Simonis, A. M. The pharmacon-receptor-effector concept: a basis for understanding the transmission of information in biological systems. In O'Brien, R.D. (Ed.), The Receptors, A Comprehensive Treatise, Plenum Press, New York. 1979, 1, pp 33-91.
-
(1979)
The Receptors, a Comprehensive Treatise
, vol.1
, pp. 33-91
-
-
Ariens, E.J.1
Beld, A.J.2
Rodrigues De Miranda, J.F.3
Simonis, A.M.4
-
8
-
-
0020442579
-
Molecular conformation and biological activity of central nervous system active drugs
-
Andrews, P. R.; Lloyd, E. J. Molecular conformation and biological activity of central nervous system active drugs. Med. Res. Rev., 1982, 2, 355-393.
-
(1982)
Med. Res. Rev.
, vol.2
, pp. 355-393
-
-
Andrews, P.R.1
Lloyd, E.J.2
-
9
-
-
0029894013
-
The properties of known drugs, 1. Molecular frameworks
-
Bemis, G.; Murko, M. M. 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.1
Murko, M.M.2
-
10
-
-
4344569207
-
The different strategies for designing GPCR and kinase targeted libraries
-
Lowrie, J. F.; Delisle, R. K.; Hobbs, D. W.; Diller, D. J. The Different Strategies for Designing GPCR and Kinase Targeted Libraries. Comb. Chem. High. Through. Screen., 2004, 7, 495-510.
-
(2004)
Comb. Chem. High. Through. Screen.
, vol.7
, pp. 495-510
-
-
Lowrie, J.F.1
Delisle, R.K.2
Hobbs, D.W.3
Diller, D.J.4
-
11
-
-
0037366605
-
The combinatorial synthesis of bicyclic privileged structures or privileged substructures
-
Horton, D. A.; Bourne, G. T.; Smythe, M. L. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures. Chem. Rev., 2003, 103, 893-930.
-
(2003)
Chem. Rev.
, vol.103
, pp. 893-930
-
-
Horton, D.A.1
Bourne, G.T.2
Smythe, M.L.3
-
13
-
-
0042121318
-
Medicinal chemistry of target family-directed masterkeys
-
Muller, G. Medicinal chemistry of target family-directed masterkeys. Drug Discovery Today, 2003, 8, 681-691.
-
(2003)
Drug Discovery Today
, vol.8
, pp. 681-691
-
-
Muller, G.1
-
14
-
-
15444374352
-
2(3H)-benzoxazolone and bioisosters as privileged scaffold in the design of pharmacological probes
-
Poupaert, J.; Carato, P.; Colacillo, E. 2(3H)-benzoxazolone and bioisosters as "privileged scaffold" in the design of pharmacological probes. Curr. Med. Chem., 2005, 12, 877-885.
-
(2005)
Curr. Med. Chem.
, vol.12
, pp. 877-885
-
-
Poupaert, J.1
Carato, P.2
Colacillo, E.3
-
15
-
-
33644872086
-
Privileged structures as leads in medicinal chemistry
-
Luca, C.; Daniela, B. Privileged structures as leads in medicinal chemistry. Curr. Med. Chem., 2006, 13, 65-85.
-
(2006)
Curr. Med. Chem.
, vol.13
, pp. 65-85
-
-
Luca, C.1
Daniela, B.2
-
16
-
-
0037030653
-
Molecular properties that influence the oral bioavailability of drug candidates
-
Veber, D. F.; Johnson, S. R.; Cheng, H-Y; Smith, B. R., Ward, K. W.; Kopple, K. D. Molecular Properties That Influence the Oral Bioavailability of Drug Candidates. J. Med. Chem., 2002, 45, 2615- 2623.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 2615-2623
-
-
Veber, D.F.1
Johnson, S.R.2
Cheng, H.-Y.3
Smith, B.R.4
Ward, K.W.5
Kopple, K.D.6
-
17
-
-
0032058905
-
RECAP-retro synthetic combinatorial analysis procedure: A powerful new technique for identifying privileged molecular fragments with useful applications in combinatorial chemistry
-
Lewell, X. Q.; Judd, D. B.; Watson, S. P.; Hann, M. M. RECAP-retrosynthetic combinatorial analysis procedure: a powerful new technique for identifying privileged molecular fragments with useful applications in combinatorial chemistry. J. Chem. Inf. Comput. Sci., 1998, 38, 511-522.
-
(1998)
J. Chem. Inf. Comput. Sci.
, vol.38
, pp. 511-522
-
-
Lewell, X.Q.1
Judd, D.B.2
Watson, S.P.3
Hann, M.M.4
-
18
-
-
0034618541
-
Privileged molecules for protein binding identified from NMR-based screening
-
Hajduk, P. J.; Bures, M.; Praestgaard, J.; Fesik, S. W. Privileged Molecules for Protein Binding Identified from NMR-Based Screening. J. Med. Chem., 2000, 43, 3443-3447.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3443-3447
-
-
Hajduk, P.J.1
Bures, M.2
Praestgaard, J.3
Fesik, S.W.4
-
19
-
-
0842304428
-
Recognition of privileged structures by G-protein coupled receptors
-
Bondensgaart, K.; Ankerson, M.; Thogersen, H.; Hansen, B. S.; Wulff, B. S.; Bywater, R. P. Recognition of Privileged Structures by G-Protein Coupled Receptors. J. Med. Chem., 2004, 47, 888- 899.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 888-899
-
-
Bondensgaart, K.1
Ankerson, M.2
Thogersen, H.3
Hansen, B.S.4
Wulff, B.S.5
Bywater, R.P.6
-
20
-
-
17244370796
-
Over one hundred peptide-activated G protein-coupled receptors recognize ligands with turn structure
-
Tyndall, J. D. A.; Pfeiffer, B.; Abbenante, G.; Fairlie, D. P Over one hundred peptide-activated G protein-coupled receptors recognize ligands with turn structure. Chem. Rev., 2005, 105, 793- 826.
-
(2005)
Chem. Rev.
, vol.105
, pp. 793-826
-
-
Tyndall, J.D.A.1
Pfeiffer, B.2
Abbenante, G.3
Fairlie, D.P.4
-
21
-
-
0027068161
-
Larger and more weakly coordinating anions: NB(OTeF5)6- and Ti(OTeF5)62
-
Bunin, B. A.; Ellman, J. A. Larger and more weakly coordinating anions: Nb(OTeF5)6- and Ti(OTeF5)62. J. Am. Chem. Soc., 1992, 114, 10997-10998.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 10997-10998
-
-
Bunin, B.A.1
Ellman, J.A.2
-
22
-
-
0027202613
-
Diversomers: An approach to nonpeptide, nonoligomeric chemical diversity
-
De Witt, S. H.; Kiely, J. S.; Stankovic, C. J.; Schroeder, M. C.; Cody, D. M. R.; Pavia, M. R.. "Diversomers": An approach to nonpeptide, nonoligomeric chemical diversity. Proc. Natl. Acad. Sci. U. S. A., 1993, 90, 6909-6913.
-
(1993)
Proc. Natl. Acad. Sci. U. S. A
, vol.90
, pp. 6909-6913
-
-
De Witt, S.H.1
Kiely, J.S.2
Stankovic, C.J.3
Schroeder, M.C.4
Cody, D.M.R.5
Pavia, M.R.6
-
23
-
-
0029146716
-
Solid-phase synthesis of defined 1, 4- benzodiazepine-2, 5-dione mixtures
-
Goff, D. A.; Zuckermann, R. N. Solid-phase synthesis of defined 1, 4- benzodiazepine-2, 5-dione mixtures. J. Org. Chem., 1995, 60, 5744-5745.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 5744-5745
-
-
Goff, D.A.1
Zuckermann, R.N.2
-
24
-
-
0030569368
-
Solid phase synthesis of 1, 4-benzodiazepine-2, 5-diones
-
Mayer, J. P.; Zhang, J. W.; Bjergarde, K.; Lenz, D. M.;Gaudino, J. J. Solid phase synthesis of 1, 4-benzodiazepine-2, 5-diones. Tetrahedron Lett., 1996, 37, 8081-8084.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 8081-8084
-
-
Mayer, J.P.1
Zhang, J.W.2
Bjergarde, K.3
Lenz, D.M.4
Gaudino, J.J.5
-
25
-
-
0028304203
-
A general method for the solid phase synthesis of ureas
-
Hutchins, S. M.; Chapman, K. T. A general method for the solid phase synthesis of ureas. Tetrahedron Lett., 1994, 35, 4055-4058.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 4055-4058
-
-
Hutchins, S.M.1
Chapman, K.T.2
-
26
-
-
0027104788
-
Research article polymersupported synthesis of 2, 5-disubstituted tetrahydrofurans
-
Beebe, X.; Schore, N. E.; Kurth, M. J. Research Article Polymersupported synthesis of 2, 5-disubstituted tetrahydrofurans. J. Am. Chem. Soc., 1992, 114, 10061-10062.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 10061-10062
-
-
Beebe, X.1
Schore, N.E.2
Kurth, M.J.3
-
27
-
-
0028021332
-
Post-modification of peptoid side chains: [3+2] cycloaddition of nitrile oxides with alkenes and alkynes on the solidphase
-
Pei, Y. H.; Moos, W. H. Post-modification of peptoid side chains: [3+2] cycloaddition of nitrile oxides with alkenes and alkynes on the solidphase. Tetrahedron Lett., 1994, 35, 5825-5828.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 5825-5828
-
-
Pei, Y.H.1
Moos, W.H.2
-
28
-
-
0028053596
-
Heck reactions in solid phase synthesis
-
Yu, K.-L.; Deshpande, M. S.; Vyas, D. M. Heck reactions in solid phase synthesis. Tetrahedron Lett., 1994, 35, 8919-8922.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 8919-8922
-
-
Yu, K.-L.1
Deshpande, M.S.2
Vyas, D.M.3
-
29
-
-
0028031367
-
Formation of carbon-carbon bond on solid support: Application of the stille reaction
-
Deshpande, M. S. Formation of carbon-carbon bond on solid support: Application of the stille reaction. Tetrahedron Lett., 1994, 35, 5613- 5614.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 5613-5614
-
-
Deshpande, M.S.1
-
30
-
-
0028088788
-
Biaryl synthesis via suzuki coupling on a solid support
-
Frenette, R.; Friesen, R. W. Biaryl synthesis via suzuki coupling on a solid support. Tetrahedron Lett., 1994, 35, 9177-9180.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 9177-9180
-
-
Frenette, R.1
Friesen, R.W.2
-
31
-
-
0029011229
-
Solid phase synthesis of aryl ethers via the mitsunobu reaction
-
Rano, T. A.; Chapman, K. T. Solid phase synthesis of aryl ethers via the mitsunobu reaction. Tetrahedron Lett., 1995, 36, 3789-3792.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 3789-3792
-
-
Rano, T.A.1
Chapman, K.T.2
-
32
-
-
17744405184
-
Synthesis of epothilones A and B in solid and solution phase
-
Nicolaou, K. C.; Winssinger, N.; Pastor, J.; Ninkovic, S.; Sarabia, F.; He, Y.; Vourloumis, D.; Yang, Z.; Li, T.; Giannakakou, P.; Hamel, E. Synthesis of epothilones A and B in solid and solution phase. Nature, 1997, 387, 268-272.
-
(1997)
Nature
, vol.387
, pp. 268-272
-
-
Nicolaou, K.C.1
Winssinger, N.2
Pastor, J.3
Ninkovic, S.4
Sarabia, F.5
He, Y.6
Vourloumis, D.7
Yang, Z.8
Li, T.9
Giannakakou, P.10
Hamel, E.11
-
33
-
-
0032576190
-
Solid and solution phase synthesis and biological evaluation of combinatorial sarcodictyin libraries
-
Nicolaou, K. C.; Winssinger, N.; Vourloumis, D.; Ohshima, T.; Kim, S.; Pfefferkorn, J.; Xu, J.-Y.; Li, T. Solid and Solution Phase Synthesis and Biological Evaluation of Combinatorial Sarcodictyin Libraries. J. Am. Chem. Soc., 1998, 120, 10814-10826.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 10814-10826
-
-
Nicolaou, K.C.1
Winssinger, N.2
Vourloumis, D.3
Ohshima, T.4
Kim, S.5
Pfefferkorn, J.6
Xu, J.-Y.7
Li, T.8
-
34
-
-
0033549539
-
Polymer-supported synthesis of non-oligomeric natural products
-
Watson, C. Polymer-Supported Synthesis of Non-Oligomeric Natural Products. Angew. Chem., Int. Ed., 1999, 38, 1903-1908.
-
(1999)
Angew. Chem., Int. Ed.
, vol.38
, pp. 1903-1908
-
-
Watson, C.1
-
35
-
-
0035293182
-
Solution- and solid-phase strategies for the design, synthesis, and screening of libraries based on natural product templates: A comprehensive survey
-
Hall, D. G.; Manku, S.; Wang, F. Solution- and Solid-Phase Strategies for the Design, Synthesis, and Screening of Libraries Based on Natural Product Templates: A Comprehensive Survey. J. Comb. Chem., 2001, 3, 125-150.
-
(2001)
J. Comb. Chem.
, vol.3
, pp. 125-150
-
-
Hall, D.G.1
Manku, S.2
Wang, F.3
-
36
-
-
0035688790
-
Solid phase synthesis of complex natural products and libraries thereof
-
Nicolaou, K. C.; Pfefferkorn, J. A. Solid phase synthesis of complex natural products and libraries thereof. Biopolymers, 2001, 60, 171-193.
-
(2001)
Biopolymers
, vol.60
, pp. 171-193
-
-
Nicolaou, K.C.1
Pfefferkorn, J.A.2
-
37
-
-
23644433348
-
Stereoselective synthesis of constrained azacyclic hydroxyethylene isosteres as aspartic protease inhibitors: Dipolar cycloaddition and related methodologies toward branched pyrrolidine and pyrrolidinone carboxylic acids
-
Hanessian, S.; Yun, H.; Hou, Y.; Tintelnot-Blomley, M. Stereoselective Synthesis of Constrained Azacyclic Hydroxyethylene Isosteres as Aspartic Protease Inhibitors: Dipolar Cycloaddition and Related Methodologies toward Branched Pyrrolidine and Pyrrolidinone Carboxylic Acids. J. Org. Chem., 2005, 70, 6746-6756.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 6746-6756
-
-
Hanessian, S.1
Yun, H.2
Hou, Y.3
Tintelnot-Blomley, M.4
-
38
-
-
37549069915
-
Discovery of an orally efficaceous 4- phenoxypyrrolidine-based BACE-1 inhibitor
-
Iserloh, U.; Pan, J.; Stamford, A. W.; Kennedy, M. E.; Zhang, Q.; Zhang, L.; Parker, E. M.; McHugh, N. A.; Favreau, L.;Strickland, C.; Voit, J. Discovery of an orally efficaceous 4- phenoxypyrrolidine-based BACE-1 inhibitor. Bioorg. Med. Chem. Lett., 2008, 18, 418-422.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 418-422
-
-
Iserloh, U.1
Pan, J.2
Stamford, A.W.3
Kennedy, M.E.4
Zhang, Q.5
Zhang, L.6
Parker, E.M.7
McHugh, N.A.8
Favreau, L.9
Strickland, C.10
Voit, J.11
-
39
-
-
67651124983
-
-
Washburn, D. G.; Hoang, T. H.; Frazee, J. S.; Johnson, L.; Hammond, M.; Manns, S.; Madauss, K. P.; Williams, S. P.; Duraiswami, C.; Tran, T. B.; Stewart, E. L.; Grygielko, E. T.; Glace, L. E.; Trizna, W.; Nagilla, R.; Bray, J. D.; Thompson, S. K. Bioorg. Med. Chem. Lett., 2009, 19, 4664-4668.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 4664-4668
-
-
Washburn, D.G.1
Hoang, T.H.2
Frazee, J.S.3
Johnson, L.4
Hammond, M.5
Manns, S.6
Madauss, K.P.7
Williams, S.P.8
Duraiswami, C.9
Tran, T.B.10
Stewart, E.L.11
Grygielko, E.T.12
Glace, L.E.13
Trizna, W.14
Nagilla, R.15
Bray, J.D.16
Thompson, S.K.17
-
40
-
-
34548563715
-
Pyrrolidinones as potent functional antagonists of the human melanocortin-4 receptor
-
Jiang, W.; Tucci, F. C.; Tran, J. A.; Fleck, B. A.; Wen, J.; Markison, S.; Marinkovic, D.; Chen, C. W.; Arellano, M.; Hoare, S. R.; Johns, M.; Foster, A. C.; Saunders, J.; Chen, C. Pyrrolidinones as potent functional antagonists of the human melanocortin-4 receptor. Bioorg. Med. Chem. Lett., 2007, 17, 5610- 5613.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 5610-5613
-
-
Jiang, W.1
Tucci, F.C.2
Tran, J.A.3
Fleck, B.A.4
Wen, J.5
Markison, S.6
Marinkovic, D.7
Chen, C.W.8
Arellano, M.9
Hoare, S.R.10
Johns, M.11
Foster, A.C.12
Saunders, J.13
Chen, C.14
-
41
-
-
0034658164
-
Solid-phase parallel synthesis of azarene pyrrolidinones as factor Xa inhibitors
-
Gong, Y.; Becker, M.; Choi-Sledeski, Y. M.; Davis, R. S.; Salvono, J. M.; Chu, V.; Brown, K. D.; Pauls, H. W. Solid-phase parallel synthesis of azarene pyrrolidinones as factor Xa inhibitors. Bioorg. Med. Chem. Lett., 2000, 10, 1033-1036.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 1033-1036
-
-
Gong, Y.1
Becker, M.2
Choi-Sledeski, Y.M.3
Davis, R.S.4
Salvono, J.M.5
Chu, V.6
Brown, K.D.7
Pauls, H.W.8
-
42
-
-
0033539030
-
Sulfonamidopyrrolidinone factor Xa Inhibitors: Potency and selectivity enhancements via P-1 and P-4 optimization
-
Choi-Sledeski, Y. M.; Mcgarry, D. G.; Green, D. M.; Mason, H. J.; Becker, M. R.; Davis, R. S.; Ewing, W. R.; Dankulich, W. P.; manetta, V. E.; Morris, R. L.; Spada, A. P.; Cheney, D. L.; Brown, K. D.; Colussi, D. J.; Chu, V.; Heran, C. L.; Morgan, S. R.; Bentley, R. G.; Leadley, R. J.; Maigan, S.; Guilloteau, J. P.; Dunwiddie, C. T.; Pauls, H. W. Sulfonamidopyrrolidinone Factor Xa Inhibitors: Potency and Selectivity Enhancements via P-1 and P-4 Optimization. J. Med. Chem., 1999, 42, 3572-3587.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3572-3587
-
-
Choi-Sledeski, Y.M.1
Mcgarry, D.G.2
Green, D.M.3
Mason, H.J.4
Becker, M.R.5
Davis, R.S.6
Ewing, W.R.7
Dankulich, W.P.8
Manetta, V.E.9
Morris, R.L.10
Spada, A.P.11
Cheney, D.L.12
Brown, K.D.13
Colussi, D.J.14
Chu, V.15
Heran, C.L.16
Morgan, S.R.17
Bentley, R.G.18
Leadley, R.J.19
Maigan, S.20
Guilloteau, J.P.21
Dunwiddie, C.T.22
Pauls, H.W.23
more..
-
43
-
-
52049086004
-
Synthesis of 5-(1-H or 1-alkyl-5-oxopyrrolidin-3-yl)-8- hydroxy- [1, 6]-naphthyridine-7-carboxamide inhibitors of HIV-1 integrase
-
Melamed, J. Y.; Egbertson, M. S.; Varga, S.; Vacca, J. P.; Moyer, G.; Gabryelski, L.; Felock, P. J.; Stillmock, K. A.; Witmer, M. V.; Schleif, W.; Hazuda, D. J.; Leonard, Y.; Jin, L.; Ellis, J. D.; young, S. D. Synthesis of 5-(1-H or 1-alkyl-5-oxopyrrolidin-3-yl)-8- hydroxy- [1, 6]-naphthyridine-7- carboxamide inhibitors of HIV-1 integrase. Bioorg. Med. Chem. Lett., 2008, 18, 5307-5310.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 5307-5310
-
-
Melamed, J.Y.1
Egbertson, M.S.2
Varga, S.3
Vacca, J.P.4
Moyer, G.5
Gabryelski, L.6
Felock, P.J.7
Stillmock, K.A.8
Witmer, M.V.9
Schleif, W.10
Hazuda, D.J.11
Leonard, Y.12
Jin, L.13
Ellis, J.D.14
Young, S.D.15
-
44
-
-
0021337327
-
Assessment of selective inhibition of rat cerebral cortical calcium-independent and calcium-dependent phosphodiesterases in crude extracts using deoxycyclic AMP and potassium ions
-
Davis, C. W. Assessment of selective inhibition of rat cerebral cortical calcium-independent and calcium-dependent phosphodiesterases in crude extracts using deoxycyclic AMP and potassium ions. Biochim. Biophy. Acta., 1984, 797, 354-362.
-
(1984)
Biochim. Biophy. Acta.
, vol.797
, pp. 354-362
-
-
Davis, C.W.1
-
45
-
-
0017120229
-
4-(3- Cyclopentyloxy-4-methoxyphenyl)-2-pyrrolidone (ZK 62711): A potent inhibitor of adenosine cyclic 3', 5'-monophosphate phosphodiesterases in homogenates and tissue slices from rat brain
-
Schwabe, U.; Miyake, M.; Ohga, Y.; Daly, J. W. 4-(3- Cyclopentyloxy-4- methoxyphenyl)-2-pyrrolidone (ZK 62711): a Potent Inhibitor of Adenosine Cyclic 3', 5'-Monophosphate Phosphodiesterases in Homogenates and Tissue Slices from Rat Brain. Mol. Pharmacol., 1976, 12, 900-910.
-
(1976)
Mol. Pharmacol.
, vol.12
, pp. 900-910
-
-
Schwabe, U.1
Miyake, M.2
Ohga, Y.3
Daly, J.W.4
-
46
-
-
0024419684
-
Isolation of similar rolipram-inhibitable cyclic-AMP-specific phosphor distresses from rat brain and heart
-
Nemoz, G.; Moueqqit, M.; Prigent, A.-F.; Pacheco, H. Isolation of similar rolipram-inhibitable cyclic-AMP-specific phosphodiesterases from rat brain and heart. Eur. J. Biochem., 1989, 184, 511-545.
-
(1989)
Eur. J. Biochem.
, vol.184
, pp. 511-545
-
-
Nemoz, G.1
Moueqqit, M.2
Prigent, A.-F.3
Pacheco, H.4
-
47
-
-
0023088944
-
The identification of a new cyclic nucleotide phosphor dies erase activity in human and guinea-pig cardiac ventricle, Implications for the mechanism of action of selective phosphor dies erase inhibitors
-
Reeves, M. L.; Leigh, B. K.; England, P. J. The identification of a new cyclic nucleotide phosphodiesterase activity in human and guinea-pig cardiac ventricle. Implications for the mechanism of action of selective phosphodiesterase inhibitors. Biochem. J., 1987, 241, 535-541.
-
(1987)
Biochem. J.
, vol.241
, pp. 535-541
-
-
Reeves, M.L.1
Leigh, B.K.2
England, P.J.3
-
48
-
-
0025215525
-
Primary sequence of cyclic nucleotide phosphodiesterase isozymes and the design of selective inhibitors
-
Beavo, J. A.; Reifmyder, D. H. Primary sequence of cyclic nucleotide phosphodiesterase isozymes and the design of selective inhibitors. Trends Pharm. Sci., 1990, 11, 150-155.
-
(1990)
Trends Pharm. Sci.
, vol.11
, pp. 150-155
-
-
Beavo, J.A.1
Reifmyder, D.H.2
-
49
-
-
0022459284
-
Stereo specific binding of the antidepressant rolipram to brain protein structures
-
Schneider, H. H.; Schmiechen, R.; Brezinaki, M.; Seidler, J. Stereospecific binding of the antidepressant rolipram to brain protein structures. Eur. J. Pharmacol., 1986, 127, 105-115.
-
(1986)
Eur. J. Pharmacol.
, vol.127
, pp. 105-115
-
-
Schneider, H.H.1
Schmiechen, R.2
Brezinaki, M.3
Seidler, J.4
-
50
-
-
0027314171
-
Stereo specificity of rolipram actions on eosinophil cyclic AMP-specific phosphodiesterase
-
Souness, J. E.; Scott, L. C. Stereospecificity of rolipram actions on eosinophil cyclic AMP-specific phosphodiesterase. Biochem. J., 1993, 291, 389-395.
-
(1993)
Biochem. J.
, vol.291
, pp. 389-395
-
-
Souness, J.E.1
Scott, L.C.2
-
51
-
-
0024317918
-
Auto radiographic mapping of a selective cyclic adenosine monophosphate phosphodiesterase in rat brain with the antidepressant [3H]rolipram
-
Kaulen, P.; Brbing, G.; Schneider, H. H.; Sarter, M.; Baumgarten, H. G. Autoradiographic mapping of a selective cyclic adenosine monophosphate phosphodiesterase in rat brain with the antidepressant [3H]rolipram. Brain. Res., 1989, 503, 229-245.
-
(1989)
Brain. Res.
, vol.503
, pp. 229-245
-
-
Kaulen, P.1
Brbing, G.2
Schneider, H.H.3
Sarter, M.4
Baumgarten, H.G.5
-
52
-
-
0026528829
-
Coexpression of human cAMP-specific phosphodiesterase activity and high affinity rolipram binding in yeast
-
Torphy, T. J.; Stadel, J. M.; Burman, M.; Cieelineki, L. B.; McLaughlin, M. M.; White, J. R.; Livi, G. P. Coexpression of human cAMP-specific phosphodiesterase activity and high affinity rolipram binding in yeast. J. Biol. Chem., 1992, 267, 1798-1804.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 1798-1804
-
-
Torphy, T.J.1
Stadel, J.M.2
Burman, M.3
Cieelineki, L.B.4
McLaughlin, M.M.5
White, J.R.6
Livi, G.P.7
-
53
-
-
0020560845
-
Neurotropic effects of the optical isomers of the selective adenosine cyclic 3', 5'-monophosphate phosphodiesterase inhibitor rolipram in rats in-vivo
-
Wachtel, H. J. Neurotropic effects of the optical isomers of the selective adenosine cyclic 3', 5'-monophosphate phosphodiesterase inhibitor rolipram in rats in-vivo. Pharm. Pharmacol., 1983, 35, 440-444.
-
(1983)
Pharm. Pharmacol.
, vol.35
, pp. 440-444
-
-
Wachtel, H.J.1
-
54
-
-
0022531996
-
Rolipram, a stereospecific inhibitor of calmodulin-independent phosphodiesterase, causes betaadrenoceptor sub sensitivity in rat cerebral cortex
-
Schultz, J. E.; Schmidt, B. H. Rolipram, a stereospecific inhibitor of calmodulin-independent phosphodiesterase, causes betaadrenoceptor subsensitivity in rat cerebral cortex. Naunyn- Schmiedeberg's Arch Pharmacol., 1986, 333, 23-30.
-
(1986)
Naunyn- Schmiedeberg's Arch Pharmacol.
, vol.333
, pp. 23-30
-
-
Schultz, J.E.1
Schmidt, B.H.2
-
55
-
-
77954559548
-
Solid-phase synthesis of n-substituted pyrrolidinone tethered N-substituted piperidines via ugi reaction
-
Liu, Z.; Nefzi, A. Solid-Phase Synthesis of N-Substituted Pyrrolidinone Tethered N-substituted Piperidines via Ugi Reaction. J. Comb. Chem., 2010, 12, 566-570.
-
(2010)
J. Comb. Chem.
, vol.12
, pp. 566-570
-
-
Liu, Z.1
Nefzi, A.2
-
56
-
-
74049137864
-
Solid phase synthesis of novel pyrrolidinedione analogs as potent HIV-1 integrase inhibitors
-
Pendri, A.; Troyer, T. L.; Sofia, M. J.; Walker, M. A.; Naidu, B. N.; Banville, J.; Meanwell, N. A.; Dicker, I.; Lin, Z.; Krystal, M.; Gerritz, S. W. Solid Phase Synthesis of Novel Pyrrolidinedione Analogs as Potent HIV-1 Integrase Inhibitors. J. Comb. Chem., 2010, 12, 84-90.
-
(2010)
J. Comb. Chem.
, vol.12
, pp. 84-90
-
-
Pendri, A.1
Troyer, T.L.2
Sofia, M.J.3
Walker, M.A.4
Naidu, B.N.5
Banville, J.6
Meanwell, N.A.7
Dicker, I.8
Lin, Z.9
Krystal, M.10
Gerritz, S.W.11
-
57
-
-
0002407606
-
Synthesis of 1, 4-dihydropyridines by cyclocondensation reactions
-
Sausins, A.; Duburs, G. Synthesis of 1, 4-dihydropyridines by cyclocondensation reactions. Heterocycles, 1988, 27, 269-289.
-
(1988)
Heterocycles
, vol.27
, pp. 269-289
-
-
Sausins, A.1
Duburs, G.2
-
58
-
-
0031693885
-
Combinatorial synthesis and screening of a chemical library of 1, 4-dihydropyridine calcium channel blockers
-
Gordecv, M. F.; Patel, D. V.; England, B. P.; Jonnalagadda, S.; Combs, J. D.; Gordon, E. M. Combinatorial synthesis and screening of a chemical library of 1, 4-dihydropyridine calcium channel blockers. Bioorg. Med. Chem., 1998, 6, 883-889.
-
(1998)
Bioorg. Med. Chem.
, vol.6
, pp. 883-889
-
-
Gordecv, M.F.1
Patel, D.V.2
England, B.P.3
Jonnalagadda, S.4
Combs, J.D.5
Gordon, E.M.6
-
59
-
-
0030038838
-
Approaches to combinatorial synthesis of heterocyclic: A solid-phase synthesis of 1, 4-dihydropyridines
-
Gordecv, M. F.; Patel, D. V.; Gordon, E. M. Approaches to combinatorial synthesis of heterocycles: A solid-phase synthesis of 1, 4-dihydropyridines. J. Org. Chem., 1996, 61, 924-928.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 924-928
-
-
Gordecv, M.F.1
Patel, D.V.2
Gordon, E.M.3
-
60
-
-
0020579260
-
Novel dihydropyridines with positive inotropic action through activation of Ca2+ channels
-
Schramm, M.; Thomas, G.; Towart, R.; Franckowiak, G. Novel dihydropyridines with positive inotropic action through activation of Ca2+ channels. Nature, 1983, 303, 535-537.
-
(1983)
Nature
, vol.303
, pp. 535-537
-
-
Schramm, M.1
Thomas, G.2
Towart, R.3
Franckowiak, G.4
-
61
-
-
0030200397
-
Approaches to combinatorial synthesis of heterocyclic: Solid phase synthesis of pyridines and pyrido [2, 3-d]pyrimidines
-
Gordecv, M. F.; Patel, D. V.; Wu, J.; Gordon, E. M. Approaches to combinatorial synthesis of heterocycles: Solid phase synthesis of pyridines and pyrido [2, 3-d]pyrimidines. Tetrahedron Lett., 1996, 37, 4643-4646.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4643-4646
-
-
Gordecv, M.F.1
Patel, D.V.2
Wu, J.3
Gordon, E.M.4
-
62
-
-
15444346896
-
Potent tetra cyclic guanine inhibitors of PDE1 and PDE5 cyclic guano sine monophosphate phosphodiesterases with oral antihypertensive activity
-
Ahn, H.-S.; Bercovici, A.; Boykow, G.; Bronnenkant, A.; Chackalamannil, S.; Chow, J.; Cleven, R.; Cook, J.; Czarniecki, M.; Domalski, C.; Fawzi, A.; Green, M.; Gundes, A.; Ho, G.; Laudicina, M.; Lindo, N.; Ma, K.; Manna, M.; McKittrick, B.; Mirzai, B.; Nechuta, T.; Neustadt, B.; Puchalski, C.; Pula, K.; Silverman, L.; Smith, E.; Stamford, A.; Tedesco, R. P.; Tsai, H.; Tulshian, D.; Vaccaro, H.; Watkins, R. W.; Weng, X.; Witkowski, J. T.; Xia, Y.; Zhang, H. Potent tetracyclic guanine inhibitors of PDE1 and PDE5 cyclic guanosine monophosphate phosphodiesterases with oral antihypertensive activity. J. Med. Chem., 1997, 40, 2196-2210.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2196-2210
-
-
Ahn, H.-S.1
Bercovici, A.2
Boykow, G.3
Bronnenkant, A.4
Chackalamannil, S.5
Chow, J.6
Cleven, R.7
Cook, J.8
Czarniecki, M.9
Domalski, C.10
Fawzi, A.11
Green, M.12
Gundes, A.13
Ho, G.14
Laudicina, M.15
Lindo, N.16
Ma, K.17
Manna, M.18
McKittrick, B.19
Mirzai, B.20
Nechuta, T.21
Neustadt, B.22
Puchalski, C.23
Pula, K.24
Silverman, L.25
Smith, E.26
Stamford, A.27
Tedesco, R.P.28
Tsai, H.29
Tulshian, D.30
Vaccaro, H.31
Watkins, R.W.32
Weng, X.33
Witkowski, J.T.34
Xia, Y.35
Zhang, H.36
more..
-
63
-
-
6844260514
-
Synthesis and evaluation of polycyclic pyrazolo [3, 4-d]pyrimidines as PDE1 and PDE5 cGMP phosphodiesterase inhibitors
-
Xia, Y.; Chackalamannil, S.; Czarniecki, M.; Tsai, H.; Vaccaro, H.; Cleven, R.; Cook, J.; Ahamad, F.; Watkins, R.; Zhang, H. Synthesis and evaluation of polycyclic pyrazolo [3, 4-d]pyrimidines as PDE1 and PDE5 cGMP phosphodiesterase inhibitors. J. Med. Chem., 1997, 40, 4372-4377.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 4372-4377
-
-
Xia, Y.1
Chackalamannil, S.2
Czarniecki, M.3
Tsai, H.4
Vaccaro, H.5
Cleven, R.6
Cook, J.7
Ahamad, F.8
Watkins, R.9
Zhang, H.10
-
64
-
-
20544450535
-
Synthesis of 2, 4, 6-trisubstituted pyrimidines as ant malarial agents
-
Agarwal, A.; Srivastava, K.; Puri, S. K.; Chauhan, P. M. S. Synthesis of 2, 4, 6-trisubstituted pyrimidines as antimalarial agents. Bioorg. Med. Chem., 2005, 13 4645-4650.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 4645-4650
-
-
Agarwal, A.1
Srivastava, K.2
Puri, S.K.3
Chauhan, P.M.S.4
-
65
-
-
0037038320
-
Novel short chain chloroquine analogues retain activity against chloroquine resistant k1 plasmodium falciparum
-
Stocks, P. A.; Raynes, K. J.; Bray, P. G.; Park, B. K.; Neill, P. M.; Ward, S. A. Novel short chain chloroquine analogues retain activity against chloroquine resistant k1 plasmodium falciparum. J. Med. Chem., 2002, 45, 4975-4983.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 4975-4983
-
-
Stocks, P.A.1
Raynes, K.J.2
Bray, P.G.3
Park, B.K.4
Neill, P.M.5
Ward, S.A.6
-
66
-
-
9644287864
-
Syntheses of 2, 4, 6-trisubstituted pyrimidine derivatives as a new class of antifilarial topoisomerase II inhibitors
-
Katiyar, S. B.; Bansal, I.; Saxena, J. K.; Chauhan, P. M. S. Syntheses of 2, 4, 6-trisubstituted pyrimidine derivatives as a new class of antifilarial topoisomerase II inhibitors. Bioorg. Med. Chem. Lett., 2005, 15, 47-50.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 47-50
-
-
Katiyar, S.B.1
Bansal, I.2
Saxena, J.K.3
Chauhan, P.M.S.4
-
67
-
-
34948859041
-
A facile synthesis and fungicidal activities of novel fluorine-containing pyrido [4, 3- d]pyrimidin-4(3H)-ones
-
Ren, Q.; Cui, Z.; He, H.; Gu, Y. A facile synthesis and fungicidal activities of novel fluorine-containing pyrido [4, 3- d]pyrimidin-4(3H)-ones. J. Fluorine Chemistry, 2007, 128, 1369- 1375.
-
(2007)
J. Fluorine Chemistry
, vol.128
, pp. 1369-1375
-
-
Ren, Q.1
Cui, Z.2
He, H.3
Gu, Y.4
-
68
-
-
84891725538
-
Fungicidal 5-substituted pyrimidine derivatives, compositions, and method of use there for
-
Eckhardt, W.; Huxdey, P. Fungicidal 5-substituted pyrimidine derivatives, compositions, and method of use therefor. Biotechnology Advances, 1988, 6, 339.
-
(1988)
Biotechnology Advances
, vol.6
, pp. 339
-
-
Eckhardt, W.1
Huxdey, P.2
-
69
-
-
0037740664
-
Novel pyrazolo [3, 4-d]pyrimidine-based inhibitors of staphylococcus aureus DNA polymerase III: Design, synthesis, and biological evaluation
-
Ali, A.; Taylor, G. E.; Ellsworth, K.; Harris, G.; Painter, R.; Silver, L. L.; Young, K. Novel pyrazolo [3, 4-d]pyrimidine-based inhibitors of Staphylococcus aureus DNA polymerase III: design, synthesis, and biological evaluation. J. Med. Chem., 2003, 46, 1824-1830.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 1824-1830
-
-
Ali, A.1
Taylor, G.E.2
Ellsworth, K.3
Harris, G.4
Painter, R.5
Silver, L.L.6
Young, K.7
-
70
-
-
0030610833
-
Effect of N9-methylation and bridge atom variation on the activity of 5- substituted 2, 4-diaminopyrrolo [2, 3-d]pyrimidines against dihydrofolate reductases from pneumocystis carinii and Toxoplasma gondii
-
Gangjee, A.; Mavandadi, F.; Sherry, F.; Queener, S. F. Effect of N9-methylation and bridge atom variation on the activity of 5- substituted 2, 4-diaminopyrrolo [2, 3-d]pyrimidines against dihydrofolate reductases from Pneumocystis carinii and Toxoplasma gondii. J. Med. Chem., 1997, 40, 1173-1177.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1173-1177
-
-
Gangjee, A.1
Mavandadi, F.2
Sherry, F.3
Queener, S.F.4
-
71
-
-
33750090397
-
Synthesis of 2, 4, 6-trisubstituted pyrimidine and triazine heterocycles as antileishmanial agents
-
Sunduru, N.; Agarwal, A.; Katiyar, S. B.; Goyal, N.; Gupta, S.; Chauhan, P. M. S. Synthesis of 2, 4, 6-trisubstituted pyrimidine and triazine heterocycles as antileishmanial agents. Bioorg. Med. Chem., 2006, 14, 7706-7715.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 7706-7715
-
-
Sunduru, N.1
Agarwal, A.2
Katiyar, S.B.3
Goyal, N.4
Gupta, S.5
Chauhan, P.M.S.6
-
72
-
-
33747336783
-
Structurally diverse 5- substituted pyrimidine nucleosides as inhibitors of leishmania donovani promastigotes in vitro
-
Torrence, P. F.; Xuesen, Fan-X.; Zhang, X.; Philippe, M.; Loiseau, P. M. Structurally diverse 5- substituted pyrimidine nucleosides as inhibitors of Leishmania donovani promastigotes in vitro. Bioorg. Med. Chem. Lett., 2006, 16, 5047-5051.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 5047-5051
-
-
Torrence, P.F.1
Xuesen, F.-X.2
Zhang, X.3
Philippe, M.4
Loiseau, P.M.5
-
73
-
-
0026096182
-
Chemotherapeutic agents, XXI: Synthesis of Pi-deficient pyrimidines as leishmanicides
-
Ram, V. J. Chemotherapeutic agents, XXI: Synthesis of Pi-deficient pyrimidines as leishmanicides. Arch Pharm(Weinheim), 1991, 324, 837-839.
-
(1991)
Arch Pharm(Weinheim)
, vol.324
, pp. 837-839
-
-
Ram, V.J.1
-
74
-
-
0025875711
-
Highly potent and selective inhibition of human immunodeficiency virus type 1 by a novel series of 6-substituted acyclouridine derivatives
-
Baba, M.; De Clercq, E.; Tanaka, H.; Ubasawa, M.; Takashima, H.; Sekiya, K.; Nitta, I.; Umezu, K.; Walter, R. T.; Mori, S. Highly potent and selective inhibition of human immunodeficiency virus type 1 by a novel series of 6-substituted acyclouridine derivatives. Mol. Pharmacol., 1991, 39, 805-810.
-
(1991)
Mol. Pharmacol.
, vol.39
, pp. 805-810
-
-
Baba, M.1
De Clercq, E.2
Tanaka, H.3
Ubasawa, M.4
Takashima, H.5
Sekiya, K.6
Nitta, I.7
Umezu, K.8
Walter, R.T.9
Mori, S.10
-
75
-
-
0027094782
-
Synthesis and antiviral activity of deoxy analogs of 1- [(2-hydroxyethoxy)methyl]-6- (phenylthio)thymine (HEPT) as potent and selective anti-HIV-1 agents
-
Tanaka, H.; Takashima, H.; Ubasawa, M.; Sekiya, K.; Nitta, I.; Baba, M.; Shigetak, S.; Walker, R. T.; De Clercq, E.; Miyasaka, T. Synthesis and antiviral activity of deoxy analogs of 1- [(2-hydroxyethoxy)methyl]-6- (phenylthio)thymine (HEPT) as potent and selective anti-HIV-1 agents. J. Med. Chem., 1992, 35, 4713-4719.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4713-4719
-
-
Tanaka, H.1
Takashima, H.2
Ubasawa, M.3
Sekiya, K.4
Nitta, I.5
Baba, M.6
Shigetak, S.7
Walker, R.T.8
De Clercq, E.9
Miyasaka, T.10
-
76
-
-
15444340492
-
Dihydro(alkylthio)(naphthylmethyl)oxopyrimidines: Novel non- nucleoside reverse transcriptase inhibitors of the S-DABO series
-
Mai, A.; Artico, M.; Sbardella, G.; Quartarone, S.; Massa, S.; Loi, A. G.; De Montis, A.; Scintu, F.; Putzolu, M.; La Colla, P. Dihydro(alkylthio) (naphthylmethyl)oxopyrimidines: Novel Non- Nucleoside Reverse Transcriptase Inhibitors of the S-DABO Series. J. Med. Chem., 1997, 40, 1447-1454.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1447-1454
-
-
Mai, A.1
Artico, M.2
Sbardella, G.3
Quartarone, S.4
Massa, S.5
Loi, A.G.6
De Montis, A.7
Scintu, F.8
Putzolu, M.9
La Colla, P.10
-
77
-
-
0028209910
-
Structure-activity relationships and conformational features of antiherpetic pyrimidine and purine nucleoside analogues, A review
-
Kulikowski, T. Structure-activity relationships and conformational features of antiherpetic pyrimidine and purine nucleoside analogues. A review. Pharm World Sci., 1994, 16, 127-138.
-
(1994)
Pharm World Sci.
, vol.16
, pp. 127-138
-
-
Kulikowski, T.1
-
78
-
-
17944391700
-
Highly potent and selective αVβ3-receptor antagonists: Solid-phase synthesis and SAR of 1-substituted 4- amino-1H-pyrimidin-2-ones
-
Zechel, C.; Backfisch, G.; Delzer, J.; Geneste, H.; Graef, C.; Hornberger, W.; Kling, A.; Lange, U. E. W.; Lauterbach, A.; Seitz, W.; Subkowski, T. J. Highly potent and selective αVβ3-receptor antagonists: solid-phase synthesis and SAR of 1-substituted 4- amino-1H-pyrimidin-2-ones. Biorg. Med. Chem. Lett., 2003, 13, 165-169.
-
(2003)
Biorg. Med. Chem. Lett.
, vol.13
, pp. 165-169
-
-
Zechel, C.1
Backfisch, G.2
Delzer, J.3
Geneste, H.4
Graef, C.5
Hornberger, W.6
Kling, A.7
Lange, U.E.W.8
Lauterbach, A.9
Seitz, W.10
Subkowski, T.J.11
-
79
-
-
66149119702
-
Parallel Solid-Phase Synthesis and High-Throughput 1H NMR Evaluation of a 96-Member 1, 2, 4-Trisubstituted-pyrimidin-6-one-5-carboxylic acid library
-
Hamper, B. C.; Kesselring, A. S.; Chott, R. C.; Yang, S. Parallel Solid-Phase Synthesis and High-Throughput 1H NMR Evaluation of a 96-Member 1, 2, 4-Trisubstituted-pyrimidin-6-one-5-carboxylic Acid Library. J. Comb. Chem., 2009, 11, 469-480.
-
(2009)
J. Comb. Chem.
, vol.11
, pp. 469-480
-
-
Hamper, B.C.1
Kesselring, A.S.2
Chott, R.C.3
Yang, S.4
-
80
-
-
33747881275
-
Solid-phase synthesis of 4- biaryl-piperidine-4-carboxamides
-
Zhu, J.; Pottorf, R. S.; Player, M. R. Solid-phase synthesis of 4- biaryl-piperidine-4-carboxamides. Tetrahedron Lett., 2006, 47, 7267-7270.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 7267-7270
-
-
Zhu, J.1
Pottorf, R.S.2
Player, M.R.3
-
81
-
-
85047674714
-
Solid phase synthesis of aryl and benzylpiperazines and their application in combinatorial chemistry
-
Dankwardt, S. M.; Newman, S. R.; Krstenansky, J. L. Solid phase synthesis of aryl and benzylpiperazines and their application in combinatorial chemistry. Tetrahedron Lett., 1995, 36, 4923-4926.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 4923-4926
-
-
Dankwardt, S.M.1
Newman, S.R.2
Krstenansky, J.L.3
-
82
-
-
20544440614
-
Inhibitors of metallo-beta-lactamase generated from beta-lactam antibiotics
-
Badarau, A.; Llinás, A.; Laws, A. P.; Damblon, C.; Page, M. I. Inhibitors of metallo-beta-lactamase generated from beta-lactam antibiotics. Biochemistry, 2005, 44, 8578-8589.
-
(2005)
Biochemistry
, vol.44
, pp. 8578-8589
-
-
Badarau, A.1
Llinás, A.2
Laws, A.P.3
Damblon, C.4
Page, M.I.5
-
83
-
-
14944385165
-
Force field design and molecular dynamics simulations of the carbapenem and cephamycin-resistant dinuclear zinc metallo-β-lactamase from bacteroides fragilis and its complex with a biphenyl tetrazole inhibitor
-
Park, H.; Merz, K. M. Force Field Design and Molecular Dynamics Simulations of the Carbapenem and Cephamycin-Resistant Dinuclear Zinc Metallo-β-lactamase from Bacteroides fragilis and Its Complex with a Biphenyl Tetrazole Inhibitor. J. Med. Chem., 2005, 48, 1630-1637.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1630-1637
-
-
Park, H.1
Merz, K.M.2
-
84
-
-
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
-
Mason, J. S.; Morize, I.; Menard, P. R.; Cheney, D. L.; Hulme, C.; Labaudinière, 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., 1999, 42, 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
Labaudinière, R.F.6
-
85
-
-
0031575632
-
Solid phase synthesis of biphenyltetrazole derivatives
-
Yoo, S.-E.; Seo, J.-S.; Yi, K.-Y.; Gong, Y.-D. Solid phase synthesis of biphenyltetrazole derivatives. Tetrahedron Lett., 1997, 38, 1203- 1206.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 1203-1206
-
-
Yoo, S.-E.1
Seo, J.-S.2
Yi, K.-Y.3
Gong, Y.-D.4
-
86
-
-
2342519911
-
Solid- phase synthesis of 5-biphenyl-2-yl-1h-tetrazoles
-
Kivrakidou, O.; Brase, S.; Hulshorst, F.; Griebenow, N. Solid- Phase Synthesis of 5-Biphenyl-2-yl-1H-tetrazoles. Org. Lett., 2004, 6, 1143-1146.
-
(2004)
Org. Lett.
, vol.6
, pp. 1143-1146
-
-
Kivrakidou, O.1
Brase, S.2
Hulshorst, F.3
Griebenow, N.4
-
87
-
-
0742286908
-
A general synthesis of substituted indoles from cyclic enol ethers and enol lactones
-
Campos, K. R.; Woo, J. C. S.; Lee, S.; Tillyer R. D. A General Synthesis of Substituted Indoles from Cyclic Enol Ethers and Enol Lactones. Org. Lett., 2004, 6, 79-82.
-
(2004)
Org. Lett.
, vol.6
, pp. 79-82
-
-
Campos, K.R.1
Woo, J.C.S.2
Lee, S.3
Tillyer, R.D.4
-
88
-
-
0035931468
-
Solid-phase optimisation of achiral amidinobenzyl indoles as potent and selective factor Xa inhibitors
-
Heinelt, U.; Herok, S.; Matter, H.; Wildgoose, P. Solid-phase optimisation of achiral amidinobenzyl indoles as potent and selective factor Xa inhibitors. Bioorg. Med. Chem. Lett., 2001, 11, 227-230.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 227-230
-
-
Heinelt, U.1
Herok, S.2
Matter, H.3
Wildgoose, P.4
-
89
-
-
0030607199
-
Heck reaction on solid support: Synthesis of indole analogs
-
Yun, W.; Mohan, R. Heck reaction on solid support: synthesis of indole analogs. Tetrahedron Lett., 1996, 37, 7189-7192.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 7189-7192
-
-
Yun, W.1
Mohan, R.2
-
90
-
-
0031592570
-
Solid-phase synthesis of indoles using the palladium-catalysed coupling of alkynes with iodoaniline derivatives
-
Fagnola, M. C.; Candiani, I.; Visentin, G.; Cabri, W.; Zarini, F.; Mongelli, N.; Bedeschi, A. Solid-phase synthesis of indoles using the palladium-catalysed coupling of alkynes with iodoaniline derivatives. Tetrahedron Lett., 1997, 38, 2307-2310.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 2307-2310
-
-
Fagnola, M.C.1
Candiani, I.2
Visentin, G.3
Cabri, W.4
Zarini, F.5
Mongelli, N.6
Bedeschi, A.7
-
91
-
-
0033618318
-
Solid-phase synthesis of nhydroxyindoles and benzo [c]isoxazoles by C-arylation of substituted acetonitriles and 1, 3-dicarbonyl compounds with polystyrene-bound aryl fluorides
-
Stephensen, H.; Zaragoza, F. Solid-phase synthesis of Nhydroxyindoles and benzo [c]isoxazoles by C-arylation of substituted acetonitriles and 1, 3-dicarbonyl compounds with polystyrene-bound aryl fluorides. Tetrahedron Lett., 1999, 40, 5799-5802.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 5799-5802
-
-
Stephensen, H.1
Zaragoza, F.2
-
92
-
-
0030784858
-
The solid phase synthesis of tri-substituted indoles
-
Collini, M. D.; Ellingboe, J. W. The Solid Phase Synthesis of Tri- Substituted Indoles. Tetrahedron Lett., 1997, 38, 7963-7966.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 7963-7966
-
-
Collini, M.D.1
Ellingboe, J.W.2
-
93
-
-
0034641492
-
The solid-phase nenitzescu indole synthesis
-
Ketcha, D. M.; Wilsonb, L. J.; Portlockb, D. E. The solid-phase Nenitzescu indole synthesis. Tetrahedron Lett., 2000, 41, 6253- 6257.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 6253-6257
-
-
Ketcha, D.M.1
Wilsonb, L.J.2
Portlockb, D.E.3
-
94
-
-
0031550841
-
Solid phase synthesis of spiroindoline
-
Cheng, Y.; Chapman, K. T. Solid phase synthesis of spiroindoline. Tetrahedron Lett., 1997, 38, 1497-1500.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 1497-1500
-
-
Cheng, Y.1
Chapman, K.T.2
-
95
-
-
0012961594
-
-
Ullmann's Encyclopedia of Industrial Chemistry, 15 Jun
-
Collin, G.; Höke, H. Quinoline and Isoquinoline. Ullmann's Encyclopedia of Industrial Chemistry; 15 Jun 2000.
-
(2000)
Quinoline and Isoquinoline
-
-
Collin, G.1
Höke, H.2
-
96
-
-
0030235033
-
Isolation, characterization, and substrate utilization of a quinoline-degrading bacterium
-
O'Loughlin, E. J.; Kehrmeyer, S. R.; Sims, G. K. Isolation, characterization, and substrate utilization of a quinoline-degrading bacterium. International Biodeterioration and Biodegradation, 1996, 38, 107-118.
-
(1996)
International Biodeterioration and Biodegradation
, vol.38
, pp. 107-118
-
-
O'Loughlin, E.J.1
Kehrmeyer, S.R.2
Sims, G.K.3
-
97
-
-
0032505240
-
Solid-phase synthesis of benzimidazoles
-
Mayer, J. P.; Lewis, G. S.; McGee, C.; Danute, B.-D. Solid-phase synthesis of benzimidazoles. Tetrahedron Lett., 1998, 39, 6655- 6658.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 6655-6658
-
-
Mayer, J.P.1
Lewis, G.S.2
McGee, C.3
Danute, B.-D.4
-
98
-
-
0032497665
-
Solid-phase synthesis of substituted 1-phenyl-2-aminomethyl- benzimidazoles and 1- phenyl-2-thiomethyl-benzimidazoles
-
Tumelty, D.; Schwarz, M. K.; Needels, M. C. Solid-phase synthesis of substituted 1-phenyl-2-aminomethyl-benzimidazoles and 1- phenyl-2-thiomethyl- benzimidazoles. Tetrahedron Lett., 1998, 39, 7467-7470.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 7467-7470
-
-
Tumelty, D.1
Schwarz, M.K.2
Needels, M.C.3
-
99
-
-
0033515847
-
A new traceless solid-phase synthesis strategy: Synthesis of a benzimidazole library
-
Huang, W.; Searborough, R. M. A new "traceless" solid-phase synthesis strategy: Synthesis of a benzimidazole library. Tetrahedron Lett., 1999, 40, 2665-2668.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 2665-2668
-
-
Huang, W.1
Searborough, R.M.2
-
100
-
-
0023947251
-
Structure of the novel antibiotics boxazomycins A, B, and C
-
Kusumi, T.; Ooi, T.; Walchi, M. R.; Kakisawa, H. Structure of the novel antibiotics boxazomycins A, B, and C. J. Am. Chem. Soc., 1988, 110, 2954-2958.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 2954-2958
-
-
Kusumi, T.1
Ooi, T.2
Walchi, M.R.3
Kakisawa, H.4
-
101
-
-
0029082133
-
Synthesis of boxazomycin B and related analogs
-
Suto, M. J.; Turner, W. R. Synthesis of Boxazomycin B and related analogs. Tetrahedron Lett., 1995, 36, 7213-7216.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 7213-7216
-
-
Suto, M.J.1
Turner, W.R.2
-
102
-
-
0016397947
-
Structure of A23187, a divalent cation ionophore
-
Chaney, M. O.; Demarco, P. V.; Jones, N. D.; Occolowitz, J. L. Structure of A23187, a divalent cation ionophore. J. Am. Chem. Soc., 1974, 96, 1932-1933.
-
(1974)
J. Am. Chem. Soc.
, vol.96
, pp. 1932-1933
-
-
Chaney, M.O.1
Demarco, P.V.2
Jones, N.D.3
Occolowitz, J.L.4
-
103
-
-
0020362680
-
Production by controlled biosynthesis of a novel ionophore antibiotic, cezomycin (demethylamino A23187)
-
David, L.; Dergomard, A. Production by controlled biosynthesis of a novel ionophore antibiotic, cezomycin (demethylamino A23187). J. Antibiot., 1982, 35, 1409-1411.
-
(1982)
J. Antibiot.
, vol.35
, pp. 1409-1411
-
-
David, L.1
Dergomard, A.2
-
104
-
-
0021077941
-
Isolation and characterization of a novel polyether antibiotic of the pyrrolether class, antibiotic X- 14885A
-
Westly, J. W.; Liu, J. W.; Blount, J. F.; Sello, L. H.; Troupe, N.; Miller, P. A. Isolation and characterization of a novel polyether antibiotic of the pyrrolether class, antibiotic X- 14885A. J. Antibiot., 1983, 36, 1275-1278.
-
(1983)
J. Antibiot.
, vol.36
, pp. 1275-1278
-
-
Westly, J.W.1
Liu, J.W.2
Blount, J.F.3
Sello, L.H.4
Troupe, N.5
Miller, P.A.6
-
105
-
-
0018727026
-
Antiparasitic agents. 3. Synthesis and anthelmintic activities of novel 2-pyridinyl-5- isothiocyanatobenzimidazoles
-
Haugwitz, R. D.; Maurer, B. V.; Jacobs, G. A.; Narayanan, V. L.; Cruthers, L. R.; Szanto, J. Antiparasitic agents. 3. Synthesis and anthelmintic activities of novel 2-pyridinyl-5- isothiocyanatobenzimidazoles. J. Med. Chem., 1979, 22, 1113- 1118.
-
(1979)
J. Med. Chem.
, vol.22
, pp. 1113-1118
-
-
Haugwitz, R.D.1
Maurer, B.V.2
Jacobs, G.A.3
Narayanan, V.L.4
Cruthers, L.R.5
Szanto, J.6
-
106
-
-
0020401705
-
Antiparasitic agents, 5. Synthesis and anthelmintic activities of novel 2- heteroaromatic-substituted isothiocyanatobenzoxazoles and -benzothiazoles
-
Haugwitz, R. D.; Angel, R. G.; Jacobs, G. A.; Maurer, B. V.; Narayanan, V. L.; Cruthers, L. R.; Szanto, J. Antiparasitic agents. 5. Synthesis and anthelmintic activities of novel 2- heteroaromatic-substituted isothiocyanatobenzoxazoles and -benzothiazoles. J. Med. Chem., 1982, 25, 969-974.
-
(1982)
J. Med. Chem.
, vol.25
, pp. 969-974
-
-
Haugwitz, R.D.1
Angel, R.G.2
Jacobs, G.A.3
Maurer, B.V.4
Narayanan, V.L.5
Cruthers, L.R.6
Szanto, J.7
-
107
-
-
0016422882
-
2-aryl-5-benzoxazolealkanoic acid derivatives with notable anti-inflammatory activity
-
Dunwell, D. W.; Evans, D.; Hicks, T. A.; Cashin, C. H.; Kitchen, A. 2-Aryl-5-benzoxazolealkanoic acid derivatives with notable antiinflammatory activity. J. Med. Chem., 1975, 18, 53-58.
-
(1975)
J. Med. Chem.
, vol.18
, pp. 53-58
-
-
Dunwell, D.W.1
Evans, D.2
Hicks, T.A.3
Cashin, C.H.4
Kitchen, A.5
-
108
-
-
0016818043
-
Synthesis and anti-inflammatory activity of some 2-heteroaryl-alpha- methyl-5- benzoxazoleacetic acids
-
Dunwell, D. W.; Evans, D.; Hicks, T. A. Synthesis and antiinflammatory activity of some 2-heteroaryl-alpha-methyl-5- benzoxazoleacetic acids. J. Med. Chem., 1975, 18, 1158-1159.
-
(1975)
J. Med. Chem.
, vol.18
, pp. 1158-1159
-
-
Dunwell, D.W.1
Evans, D.2
Hicks, T.A.3
-
109
-
-
0017619144
-
Synthesis and anti-inflammatory activity of some 2-substituted 4- and 7- benzoxazoleacetic and alpha-methylacetic acids
-
Evans, D.; Smith, C. E.; Williamson, W. R. N. Synthesis and antiinflammatory activity of some 2-substituted 4- and 7- benzoxazoleacetic and alpha-methylacetic acids. J. Med. Chem., 1977, 20, 169-171.
-
(1977)
J. Med. Chem.
, vol.20
, pp. 169-171
-
-
Evans, D.1
Smith, C.E.2
Williamson, W.R.N.3
-
110
-
-
0017390043
-
Synthesis and anti-inflammatory activity of some 2-aryl-6- benzoxazoleacetic acid derivatives
-
Dunwell, D. W.; Evans, D. Synthesis and antiinflammatory activity of some 2-aryl-6-benzoxazoleacetic acid derivatives. J. Med. Chem., 1977, 20, 797-801.
-
(1977)
J. Med. Chem.
, vol.20
, pp. 797-801
-
-
Dunwell, D.W.1
Evans, D.2
-
111
-
-
0026546559
-
Design, synthesis, and kinetic evaluation of a unique class of elastase inhibitors, the peptidyl alpha-ketobenzoxazoles, and the x-ray crystal structure of the covalent complex between porcine pancreatic elastase and Ac- Ala-Pro-Val-2-benzoxazole
-
Edwards, P. D.; Meyer, E. F.; Vijahalakshmi, J.; Tuthill, P. A.; Andisik, D. A.; Gomes, B.; Strimpler, A. Design, synthesis, and kinetic evaluation of a unique class of elastase inhibitors, the peptidyl alpha-ketobenzoxazoles, and the x-ray crystal structure of the covalent complex between porcine pancreatic elastase and Ac- Ala-Pro-Val-2-benzoxazole. J. Am. Chem. Soc., 1992, 114, 1854- 1863.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 1854-1863
-
-
Edwards, P.D.1
Meyer, E.F.2
Vijahalakshmi, J.3
Tuthill, P.A.4
Andisik, D.A.5
Gomes, B.6
Strimpler, A.7
-
112
-
-
0029025244
-
Peptidyl alpha-ketoheterocyclic inhibitors of human neutrophil elastase, 2 Effect of varying the heterocyclic ring on in vitro potency
-
Edwards, P. D.; Wolanin, D. J.; Andisik, D. W.; Davis, M. W. Peptidyl alpha-ketoheterocyclic inhibitors of human neutrophil elastase. 2. Effect of varying the heterocyclic ring on in vitro potency. J. Med. Chem., 1995, 38, 76-85.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 76-85
-
-
Edwards, P.D.1
Wolanin, D.J.2
Andisik, D.W.3
Davis, M.W.4
-
113
-
-
0028818054
-
Peptidyl alpha-ketoheterocyclic inhibitors of human neutrophil elastase, 3 In vitro and in vivo potency of a series of peptidyl alpha- ketobenzoxazoles
-
Edwards, P. D.; Zottola, M. A.; Davis, M.; Williams, J.; Tuthill, P. A. Peptidyl alpha-ketoheterocyclic inhibitors of human neutrophil elastase. 3 In vitro and in vivo potency of a series of peptidyl alpha- ketobenzoxazoles. J. Med. Chem., 1995, 38, 3972-3982.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3972-3982
-
-
Edwards, P.D.1
Zottola, M.A.2
Davis, M.3
Williams, J.4
Tuthill, P.A.5
-
114
-
-
0026560204
-
Studies on antiulcer drugs. II. Synthesis and antiulcer activities of imidazo [1, 2-alpha]pyridinyl-2-alkylaminobenzoxazoles and 5, 6, 7, 8-tetrahydroimidazo [1, 2-alpha]pyridinyl derivatives
-
Katsura, Y.; Nishino, S.; Inoue, Y.; Tomoi, M.; Takasugi, H. Studies on antiulcer drugs. II. Synthesis and antiulcer activities of imidazo [1, 2-alpha]pyridinyl-2-alkylaminobenzoxazoles and 5, 6, 7, 8-tetrahydroimidazo [1, 2-alpha]pyridinyl derivatives. Chem Pharm Bull., 1992, 40, 371-380.
-
(1992)
Chem Pharm Bull.
, vol.40
, pp. 371-380
-
-
Katsura, Y.1
Nishino, S.2
Inoue, Y.3
Tomoi, M.4
Takasugi, H.5
-
115
-
-
0026704324
-
Studies on antiulcer drugs. III. Synthesis and antiulcer activities of imidazo [1, 2-a]pyridinylethylbenzoxazoles and related compounds, A novel class of histamine H2-receptor antagonists
-
Katsura, Y.; Nishino, S.; Inoue, Y.; Tomoi, M.; Itoh, H.; Takasugi, H. Studies on antiulcer drugs. III. Synthesis and antiulcer activities of imidazo [1, 2- A]pyridinylethylbenzoxazoles and related compounds. A novel class of histamine H2-receptor antagonists. Chem Pharm Bull., 1992, 40, 1424-1438.
-
(1992)
Chem Pharm Bull.
, vol.40
, pp. 1424-1438
-
-
Katsura, Y.1
Nishino, S.2
Inoue, Y.3
Tomoi, M.4
Itoh, H.5
Takasugi, H.6
-
116
-
-
27444446821
-
3 receptor partial agonist for treatment of diarrhea- predominant irritable bowel syndrome
-
3 Receptor Partial Agonist for Treatment of Diarrhea- Predominant Irritable Bowel Syndrome. J. Med. Chem., 2005, 48, 7075-7079.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 7075-7079
-
-
Yoshida, S.1
Shiokawa, S.2
Kawano, K.-I.3
Ito, T.4
Murakami, H.5
Suzuki, H.6
Sato, Y.7
-
117
-
-
39049159714
-
Synthesis, metal ion binding, and biological evaluation of new anticancer 2-(2'- hydroxyphenyl)benzoxazole analogs of UK-1
-
McKee, L. M.; Kerwin, S. M. Synthesis, metal ion binding, and biological evaluation of new anticancer 2-(2'- hydroxyphenyl)benzoxazole analogs of UK-1. Bioorg. Med. Chem., 2008, 16, 1775-1783.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 1775-1783
-
-
McKee, L.M.1
Kerwin, S.M.2
-
118
-
-
0030865756
-
Solid-phase synthesis of benzoxazoles via mitsunobu reaction
-
Fengjiang, W.; James, R. H. Solid-phase synthesis of benzoxazoles via mitsunobu reaction. Tetrahedron Lett., 1997, 38, 6529-6532.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 6529-6532
-
-
Fengjiang, W.1
James, R.H.2
-
119
-
-
0035408970
-
Solid-phase synthesis of benzoxazoles from 3-nitrotyrosine
-
Beebe, X.; Wodka, D.; Sowin, T. J. Solid-Phase Synthesis of Benzoxazoles from 3-Nitrotyrosine. J. Comb. Chem., 2001, 3, 360- 366.
-
(2001)
J. Comb. Chem.
, vol.3
, pp. 360-366
-
-
Beebe, X.1
Wodka, D.2
Sowin, T.J.3
-
120
-
-
33744504493
-
Solid-phase synthesis of the 2- aminobenzoxazole library using thioether linkage as the safety- catch linker
-
Hwang, J. Y., Gong, Y. D. Solid-Phase Synthesis of the 2- Aminobenzoxazole Library Using Thioether Linkage as the Safety- Catch Linker. J. Comb. Chem., 2006, 8, 297-303.
-
(2006)
J. Comb. Chem.
, vol.8
, pp. 297-303
-
-
Hwang, J.Y.1
Gong, Y.D.2
-
121
-
-
33746367448
-
Combinatorial synthesis of benzothiazoles and benzimidazoles using a traceless aniline linker
-
Hioki, H.; Matsushita, K.; Kubo, M.; Kodama, M. Combinatorial Synthesis of Benzothiazoles and Benzimidazoles Using a Traceless Aniline Linker. J. Comb. Chem., 2006, 8, 462-463.
-
(2006)
J. Comb. Chem.
, vol.8
, pp. 462-463
-
-
Hioki, H.1
Matsushita, K.2
Kubo, M.3
Kodama, M.4
-
122
-
-
44749087580
-
A one-pot, two-step microwave assisted synthesis of highly functionalized benzoxazoles using solid-supported reagents (SSRs)
-
Macro, R.; Sara, S.; Maurizio, B. A one-pot, two-step microwaveassisted synthesis of highly functionalized benzoxazoles using solid-supported reagents (SSRs). Tetrahedron Lett., 2008, 49, 4464-4466.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 4464-4466
-
-
Macro, R.1
Sara, S.2
Maurizio, B.3
-
123
-
-
0028093182
-
Inhibition of cyclin-dependent kinases by purine analogues
-
Veseley, J,; Havlicek, L.; Strnad, M.; Blow, J. J.; Donella- Deana, A.; Pinna, L.; Letham, D. S.; Kato, J.-Y.; Detivaud, L.; Leclerc, S.; Meijer, L. Inhibition of cyclin-dependent kinases by purine analogues. Eur. J. Biochem., 1994, 224, 771-786.
-
(1994)
Eur. J. Biochem.
, vol.224
, pp. 771-786
-
-
Veseley, J.1
Havlicek, L.2
Strnad, M.3
Blow, J.J.4
Donella- Deana, A.5
Pinna, L.6
Letham, D.S.7
Kato, J.-Y.8
Detivaud, L.9
Leclerc, S.10
Meijer, L.11
-
124
-
-
0031028163
-
Inhibition of cyclin-dependent kinases by purine analogues: Crystal structure of human cdk2 complexes with roscovitine
-
De Azevedo, W. F.; Leclerc, S.; Meijer, L., Havlicek, L.; Strnad, M.; Kim, S. H. Inhibition of cyclin-dependent kinases by purine analogues: crystal structure of human cdk2 complexed with roscovitine. Eur. J. Biochem., 1997, 243, 518-524.
-
(1997)
Eur. J. Biochem.
, vol.243
, pp. 518-524
-
-
De Azevedo, W.F.1
Leclerc, S.2
Meijer, L.3
Havlicek, L.4
Strnad, M.5
Kim, S.H.6
-
125
-
-
0033041709
-
Synthesis and in vitro evaluation of novel 2, 6, 9-trisubstituted purines acting as cyclin-dependent kinase inhibitors
-
Legraverend, M.; Ludwig, O.; Bisagni, E.; Leclerc, S.; Meijer, L.; Giocanti, N.; Sadri, R, Favaudon, V. Synthesis and in vitro evaluation of novel 2, 6, 9-trisubstituted purines acting as cyclin-dependent kinase inhibitors. Bioorg. Med. Chem., 1999, 7, 1281-1293.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 1281-1293
-
-
Legraverend, M.1
Ludwig, O.2
Bisagni, E.3
Leclerc, S.4
Meijer, L.5
Giocanti, N.6
Sadri, R.7
Favaudon, V.8
-
126
-
-
0034642532
-
Cyclin dependent kinase inhibitors: Useful targets in cell cycle regulation
-
Sielecki, T. M.; Boylan, J. F.; Benfield, P. A., Trainor, G. L. Cyclindependent kinase inhibitors: useful targets in cell cycle regulation. J. Med. Chem., 2000, 43, 1-18.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1-18
-
-
Sielecki, T.M.1
Boylan, J.F.2
Benfield, P.A.3
Trainor, G.L.4
-
127
-
-
0029839205
-
New purines and purine analogs as modulators of multidrug resistance
-
Dhainaut, A.; Regnier, G,; Tizot, A.; Pierre, A.; Leonce, S.; Guilbaud, N.; Kraus-Berthier, L.; Atassi, G. New Purines and Purine Analogs as Modulators of Multidrug Resistance. J. Med. Chem., 1996, 39, 4099-4108.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 4099-4108
-
-
Dhainaut, A.1
Regnier, G.2
Tizot, A.3
Pierre, A.4
Leonce, S.5
Guilbaud, N.6
Kraus-Berthier, L.7
Atassi, G.8
-
128
-
-
0034183890
-
Solid phase synthesis of purines from pyrimidines
-
Raffaella, D. L.; Ian, H. G.; Christopher, D. F. Solid Phase Synthesis of Purines from Pyrimidines. J. Comb. Chem., 2000, 2, 249-253.
-
(2000)
J. Comb. Chem.
, vol.2
, pp. 249-253
-
-
Raffaella, D.L.1
Ian, H.G.2
Christopher, D.F.3
-
129
-
-
78149339341
-
Solid-phase synthesis of highly diverse purine-hydroxyquinolinone bisheterocycles
-
Vankova, B.; Hlavac, J.; Soural, M. Solid-Phase Synthesis of Highly Diverse Purine-Hydroxyquinolinone Bisheterocycles. J. Comb. Chem., 2010, 12, 890-894.
-
(2010)
J. Comb. Chem.
, vol.12
, pp. 890-894
-
-
Vankova, B.1
Hlavac, J.2
Soural, M.3
-
130
-
-
0030762381
-
Solid support synthesis of tetrahydroquinolines via the grieco three component condensation
-
Kiselyov, A. S.; Armstrong, R. W. Solid Support Synthesis of Tetrahydroquinolines via the Grieco Three Component Condensation. Tetrahedron Lett., 1997, 38, 6163-6166.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 6163-6166
-
-
Kiselyov, A.S.1
Armstrong, R.W.2
-
132
-
-
0032499988
-
Immobilized aldehydes and olefins in the solid support synthesis of tetrahydroquinolines via a three component condensation
-
Kiselyov, A. S.; Smith, L.; Virgilio, A.; Armstrong, R. W. Immobilized aldehydes and olefins in the solid support synthesis of tetrahydroquinolines via a three component condensation. Tetrahedron, 1998, 54, 7987-7996.
-
(1998)
Tetrahedron
, vol.54
, pp. 7987-7996
-
-
Kiselyov, A.S.1
Smith, L.2
Virgilio, A.3
Armstrong, R.W.4
-
133
-
-
0034929896
-
A solid-phase approach to tetrahydrochromano [4, 3-b]quinolines
-
Zhang, D. W.; Kiselyov, A. S. A Solid-Phase Approach to Tetrahydrochromano [4, 3-b]quinolines. Synlett, 2001, 1173-1175.
-
(2001)
Synlett
, pp. 1173-1175
-
-
Zhang, D.W.1
Kiselyov, A.S.2
-
134
-
-
0032564639
-
Solid-phase synthesis of heterocycles via palladium-catalyzed annulations
-
Wang, Y.; Huang, T. N. Solid-phase synthesis of heterocycles via palladium-catalyzed annulations. Tetrahedron Lett., 1998, 39, 9605-9608.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 9605-9608
-
-
Wang, Y.1
Huang, T.N.2
-
135
-
-
0028033520
-
Quinapril: A reappraisal of its pharmacology and therapeutic efficacy in cardiovascular Disorders
-
Plosker, G. L.; Sorkin, E. M. Quinapril: A Reappraisal of its Pharmacology and Therapeutic Efficacy in Cardiovascular Disorders. Drugs, 1994, 48, 227-252.
-
(1994)
Drugs
, vol.48
, pp. 227-252
-
-
Plosker, G.L.1
Sorkin, E.M.2
-
136
-
-
0018765159
-
Nomifensine: A review of its pharmacological properties and therapeutic efficacy in Depressive illness
-
Brogden, R. N.; Heel, R. C.; Speight, T. M.; Avery, G. S. Nomifensine: A Review of its Pharmacological Properties and Therapeutic Efficacy in Depressive Illness. Drugs, 1979, 18, 1-24.
-
(1979)
Drugs
, vol.18
, pp. 1-24
-
-
Brogden, R.N.1
Heel, R.C.2
Speight, T.M.3
Avery, G.S.4
-
137
-
-
33646201531
-
Antitumor activity of tetrahydroisoquinoline analogues 3-epi-jorumycin and 3-epi-renieramycin
-
Lane, J. W.; Estevezc, A.; Mortarac, K.; Callanc, O.; Spencerc, J. R.; Williams, R. M. Antitumor activity of tetrahydroisoquinoline analogues 3-epi-jorumycin and 3-epi-renieramycin G. Bioorg. Med. Chem. Lett., 2006, 16, 3180-3183.
-
(2006)
G. Bioorg. Med. Chem. Lett.
, vol.16
, pp. 3180-3183
-
-
Lane, J.W.1
Estevezc, A.2
Mortarac, K.3
Callanc, O.4
Spencerc, J.R.5
Williams, R.M.6
-
138
-
-
0028784613
-
The solid phase synthesis of dihydro- and tetrahydroisoquinolines
-
Meutermans, W. D. F.; Alewood, P. F. The solid phase synthesis of dihydro- and tetrahydroisoquinolines. Tetrahedron Lett., 1995, 36, 7709-7712.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 7709-7712
-
-
Meutermans, W.D.F.1
Alewood, P.F.2
-
139
-
-
0342371152
-
1, 2, 6-trisubstituted tetrahydroisoquinoline derivatives by solid-phase synthesis
-
Rolfing, K.; Thiel, M.; Kunzer, H. 1, 2, 6-Trisubstituted Tetrahydroisoquinoline Derivatives by Solid-Phase Synthesis. Synlett, 1996, 1036-1038.
-
(1996)
Synlett
, pp. 1036-1038
-
-
Rolfing, K.1
Thiel, M.2
Kunzer, H.3
-
140
-
-
0030575349
-
Solid phase synthesis of tetrahydroisoquinolines and tetrahydroimidazopyridines
-
Hutchins, S. M.; Chapman, K. T. Solid phase synthesis of tetrahydroisoquinolines & tetrahydroimidazopyridines. Tetrahedron Lett., 1996, 37, 4865-4868.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4865-4868
-
-
Hutchins, S.M.1
Chapman, K.T.2
-
141
-
-
0034599948
-
The solid phase synthesis of tetrahydroisoquinolines having cdc25B inhibitory activity
-
Fritzen, E. L.; Brightwell, A. S.; Erickson, L. A.; Romero, D. L. The solid phase synthesis of tetrahydroisoquinolines having cdc25B inhibitory activity. Bioorg. Med. Chem. Lett., 2000, 10, 649-652.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 649-652
-
-
Fritzen, E.L.1
Brightwell, A.S.2
Erickson, L.A.3
Romero, D.L.4
-
142
-
-
4143121319
-
Solid-phase synthesis of 1, 2, 3, 4-tetrahydroisoquinoline derivatives employing support-bound tyrosine esters in the pictet-spengler reaction
-
Kane, T. R.; Ly, C. Q.; Kelly, D. E.; Dener, J. M. Solid-Phase Synthesis of 1, 2, 3, 4-Tetrahydroisoquinoline Derivatives Employing Support-Bound Tyrosine Esters in the Pictet-Spengler Reaction. J. Comb. Chem., 2004, 6, 564-572.
-
(2004)
J. Comb. Chem.
, vol.6
, pp. 564-572
-
-
Kane, T.R.1
Ly, C.Q.2
Kelly, D.E.3
Dener, J.M.4
-
143
-
-
0003869167
-
-
Academic Press, New York, Chapter 14
-
Brown, H. C.; in Baude, E. A. and Nachod, F. C., Determination of Organic Structures by Physical Methods. Academic Press, New York, 1955, Chapter 14.
-
(1955)
Determination of Organic Structures by Physical Methods
-
-
Brown, H.C.1
In Baude, E.A.2
Nachod, F.C.3
-
144
-
-
0030235033
-
Isolation, characterization, and substrate utilization of a quinoline-degrading bacterium
-
O'Loughlin, E. J.; Kehrmeyer, S. R.; Sims, G. K. Isolation, characterization, and substrate utilization of a quinoline-degrading bacterium. International Biodeterioration and Biodegradation, 1996, 38, 107-118.
-
(1996)
International Biodeterioration and Biodegradation
, vol.38
, pp. 107-118
-
-
O'Loughlin, E.J.1
Kehrmeyer, S.R.2
Sims, G.K.3
-
145
-
-
3242702692
-
Structurally diverse 2, 6-disubstituted quinoline derivatives by solid-phase synthesis
-
Ruhland, I. T.; Kiinzer, H. Structurally diverse 2, 6-disubstituted quinoline derivatives by solid-phase synthesis. Tetrahedron Lett., 1996, 37, 2757-2760.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 2757-2760
-
-
Ruhland, I.T.1
Kiinzer, H.2
-
146
-
-
0031562030
-
Combinatorial synthesis of heterocycles: Solid phase synthesis of 2-arylquinoline-4-carboxylic acid derivatives
-
Gopalsamy, A.; Pallai, P. V. Combinatorial synthesis of heterocycles: Solid phase synthesis of 2-arylquinoline-4-carboxylic acid derivatives. Tetrahedron Lett., 1997, 38, 907-910.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 907-910
-
-
Gopalsamy, A.1
Pallai, P.V.2
-
147
-
-
0002147258
-
Novel functionalized titanium(IV) benzylidenes for the traceless solid-phase synthesis of indoles
-
Calum, M.; Richard, C. H.; Dieter, W. H. Novel Functionalized Titanium(IV) Benzylidenes for the Traceless Solid-Phase Synthesis of Indoles. Org. Lett., 2002, 4, 75-78.
-
(2002)
Org. Lett.
, vol.4
, pp. 75-78
-
-
Calum, M.1
Richard, C.H.2
Dieter, W.H.3
-
148
-
-
0033757346
-
Epidermal growth factor receptor tyrosine kinase inhibitors as anticancer agents
-
Ciardiello, F. Epidermal growth factor receptor tyrosine kinase inhibitors as anticancer agents. Drugs, 2000, 60, 25-32.
-
(2000)
Drugs
, vol.60
, pp. 25-32
-
-
Ciardiello, F.1
-
149
-
-
0035899182
-
6- substituted-4-(3-bromophenylamino)quinazolines as putative irreversible inhibitors of the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases with enhanced antitumor activity
-
Tsou, H. R.; Mamuya, N.; Johnson, B. D.; Reich, M. F.; Gruber, B. C.; Ye, F.; Nilakantan, R.; Shen, R.; Discafani, C.; DeBlanc, R.; Davis, R.; Koehn, F. E.; Greenberger, L. M.; Wang, Y. F.; Wissner, A. 6- Substituted-4-(3- bromophenylamino)quinazolines as Putative Irreversible Inhibitors of the Epidermal Growth Factor Receptor (EGFR) and Human Epidermal Growth Factor Receptor (HER-2) Tyrosine Kinases with Enhanced Antitumor Activity. J. Med. Chem., 2001, 44, 2719-2734.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 2719-2734
-
-
Tsou, H.R.1
Mamuya, N.2
Johnson, B.D.3
Reich, M.F.4
Gruber, B.C.5
Ye, F.6
Nilakantan, R.7
Shen, R.8
Discafani, C.9
DeBlanc, R.10
Davis, R.11
Koehn, F.E.12
Greenberger, L.M.13
Wang, Y.F.14
Wissner, A.15
-
150
-
-
0034611617
-
Tyrosine kinase inhibitors, 17, irreversible inhibitors of the epidermal growth factor receptor: 4-(Phenylamino)quinazolineand 4-(Phenylamino)pyrido [3, 2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions
-
Smaill, J. B.; Rewcastle, G. W.; Loo, J. A.; Greis, K. D.; Chan, O. H.; Reyner, E. L.; Lipka, E.; Showalter, H. D.; Vincent, P. W.; Elliott, W. L.; Denny, W. A. Tyrosine Kinase Inhibitors. 17. Irreversible Inhibitors of the Epidermal Growth Factor Receptor: 4-(Phenylamino)quinazolineand 4-(Phenylamino)pyrido [3, 2-d]pyrimidine-6-acrylamides Bearing Additional Solubilizing Functions. J. Med. Chem., 2000, 43, 1380-1397.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1380-1397
-
-
Smaill, J.B.1
Rewcastle, G.W.2
Loo, J.A.3
Greis, K.D.4
Chan, O.H.5
Reyner, E.L.6
Lipka, E.7
Showalter, H.D.8
Vincent, P.W.9
Elliott, W.L.10
Denny, W.A.11
-
151
-
-
0034128898
-
Inhibition of clinically relevant mutant variants of HIV-1 by quinazolinone non-nucleoside reverse transcriptase inhibitors
-
Corbett, J. W.; Ko, S. S.; Rodgers, J. D.; Gearhart, L. A.; Magnus, N. A.; Bacheler, L. T.; Diamond, S.; Je.rey, S.; Klabe, R. M.; Cordova, B. C.; Garber, S.; Logue, K.; Trainor, G. L.; Anderson, P. S.; Erickson-Viitanen, S. K. Inhibition of Clinically Relevant Mutant Variants of HIV-1 by Quinazolinone Non-Nucleoside Reverse Transcriptase Inhibitors. J. Med. Chem., 2000, 43, 2019- 2030.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2019-2030
-
-
Corbett, J.W.1
Ko, S.S.2
Rodgers, J.D.3
Gearhart, L.A.4
Magnus, N.A.5
Bacheler, L.T.6
Diamond, S.7
Jerey, S.8
Klabe, R.M.9
Cordova, B.C.10
Garber, S.11
Logue, K.12
Trainor, G.L.13
Anderson, P.S.14
Erickson-Viitanen, S.K.15
-
152
-
-
0033523896
-
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents
-
Kung, P. P.; Casper, M. D.; Cook, K. L.; Wilson-Lingardo, L.; Risen, L. M.; Vickers, T. A.; Ranken, R.; Blyn, L. B.; Wyatt, J. R.; Cook, P. D.; Ecker, D. J. Structure-Activity Relationships of Novel 2-Substituted Quinazoline Antibacterial Agents. J. Med. Chem., 1999, 42, 4705-4713.
-
(1999)
J. Med. Chem
, vol.42
, pp. 4705-4713
-
-
Kung, P.P.1
Casper, M.D.2
Cook, K.L.3
Wilson-Lingardo, L.4
Risen, L.M.5
Vickers, T.A.6
Ranken, R.7
Blyn, L.B.8
Wyatt, J.R.9
Cook, P.D.10
Ecker, D.J.11
-
153
-
-
0034727872
-
Optimization of substituted n-3- benzylimidazoquinazolinone sulfonamides as potent and selective PDE5 inhibitors
-
Rotella, D. P.; Sun, Z.; Zhu, Y.; Krupinski, J.; Pongrac, R.; Seliger, L.; Normandin, D.; Macor, J. E. Optimization of Substituted N-3- Benzylimidazoquinazolinone Sulfonamides as Potent and Selective PDE5 Inhibitors. J. Med. Chem., 2000, 43, 5037-5043.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 5037-5043
-
-
Rotella, D.P.1
Sun, Z.2
Zhu, Y.3
Krupinski, J.4
Pongrac, R.5
Seliger, L.6
Normandin, D.7
Macor, J.E.8
-
154
-
-
0034213365
-
3 receptor
-
3 Receptor. J. Med. Chem., 2000, 43, 2227-2238.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2227-2238
-
-
Van Muijlwijk-Koezen, J.E.1
Timmerman, H.2
Van Der Goot, H.3
Menge, W.M.4
Frijtag Von Drabbe Kunzel, J.5
De Groote, M.6
Ijzerman, A.P.7
-
155
-
-
0028970173
-
Trimetrexate: A review of its pharmacodynamic and pharmacokinetic properties and therapeutic potential in the treatment of pneumocystis carinii pneumonia
-
Fulton, B.; Wagsta., A. J.; McTavish, D. Trimetrexate: A Review of its Pharmacodynamic and Pharmacokinetic Properties and Therapeutic Potential in the Treatment of Pneumocystis carinii Pneumonia. Drugs, 1995, 49, 563-576.
-
(1995)
Drugs
, vol.49
, pp. 563-576
-
-
Fulton, B.1
Wagsta, A.J.2
McTavish, D.3
-
156
-
-
0028357051
-
Anagrelide: A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in the treatment of thrombocythaemia
-
Spencer, C. M.; Brogden, R. N. Anagrelide: A Review of its Pharmacodynamic and Pharmacokinetic Properties, and Therapeutic Potential in the Treatment of Thrombocythaemia. Drugs, 1994, 47, 809-822.
-
(1994)
Drugs
, vol.47
, pp. 809-822
-
-
Spencer, C.M.1
Brogden, R.N.2
-
158
-
-
0032548074
-
Design, synthesis, and biological activity of prazosin-related antagonists, role of the piperazine and furan units of prazosin on the selectivity for α1-adrenoreceptor subtypes
-
Bolognesi, M. L.; Budriesi, R.; Chiarini, A.; Poggesi, E.; Leonardi, A.; Melchiorre, C. Design, Synthesis, and Biological Activity of Prazosin-Related Antagonists. Role of the Piperazine and Furan Units of Prazosin on the Selectivity for α1-Adrenoreceptor Subtypes. J. Med. Chem., 1998, 41, 4844-4853.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 4844-4853
-
-
Bolognesi, M.L.1
Budriesi, R.2
Chiarini, A.3
Poggesi, E.4
Leonardi, A.5
Melchiorre, C.6
-
159
-
-
0025679332
-
Ketanserin, A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in hypertension and peripheral vascular disease
-
Brogden, R. N.; Sorkin, E. M. Ketanserin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in hypertension and peripheral vascular disease. Drugs, 1990, 40, 903-949.
-
(1990)
Drugs
, vol.40
, pp. 903-949
-
-
Brogden, R.N.1
Sorkin, E.M.2
-
160
-
-
0030784701
-
Solid-phase synthesis of 3, 4- dihydroquinazoline
-
Wang, F.; Hauske, J. R. Solid-phase synthesis of 3, 4- dihydroquinazoline. Tetrahedron Lett., 1997, 38, 8651-8654.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 8651-8654
-
-
Wang, F.1
Hauske, J.R.2
-
161
-
-
0033613705
-
A decarboxylative traceless linker approach for the solid phase synthesis of quinazolines
-
Cobb, J. M.; Fiorini, M. T.; Goddard, C. R.; Theoclitou, M. E.; Abell, C. A decarboxylative traceless linker approach for the solid phase synthesis of quinazolines. Tetrahedron Lett., 1999, 40, 1045- 1048.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 1045-1048
-
-
Cobb, J.M.1
Fiorini, M.T.2
Goddard, C.R.3
Theoclitou, M.E.4
Abell, C.5
-
162
-
-
0035955835
-
Solid-phase synthesis of 3, 4-dihydroquinazoline derivatives
-
Zhang, J.; Barker, J.; Boliang, L.; Saneii, H. Solid-phase synthesis of 3, 4-dihydroquinazoline derivatives. Tetrahedron Lett., 2001, 42, 8405-8408.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 8405-8408
-
-
Zhang, J.1
Barker, J.2
Boliang, L.3
Saneii, H.4
-
163
-
-
0034699864
-
Efficient solidphase synthesis of quinazoline-2-thioxo-4-ones with SynPhase™ lanterns
-
Makino, S.; Suzuki, N.; Nakanishi, E.; Tsuji, T. Efficient solidphase synthesis of quinazoline-2-thioxo-4-ones with SynPhase™ lanterns. Tetrahedron Lett., 2000, 41, 8333-8337.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 8333-8337
-
-
Makino, S.1
Suzuki, N.2
Nakanishi, E.3
Tsuji, T.4
-
164
-
-
0035099866
-
Solid-phase synthesis of quinazoline-2, 4-diones using SNAR reaction
-
Makino, S.; Suzuki, N.; Nakanishi, E.; Tsuji, T. Solid-phase Synthesis of Quinazoline-2, 4-diones Using SNAr Reaction. Synlett, 2001, 333-336.
-
(2001)
Synlett
, pp. 333-336
-
-
Makino, S.1
Suzuki, N.2
Nakanishi, E.3
Tsuji, T.4
-
165
-
-
0035951944
-
Solid-phase synthesis of 1, 3- disubstituted 2-thioxoquinazoline-4-ones using SNAR reaction
-
Makino, S.; Nakanishi, E.; Tsuji, T. Solid-phase synthesis of 1, 3- disubstituted 2-thioxoquinazoline-4-ones using SNAr reaction. Tetrahedron Lett., 2001, 42, 1749-1752.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 1749-1752
-
-
Makino, S.1
Nakanishi, E.2
Tsuji, T.3
-
166
-
-
0345119100
-
Solid phase synthesis of 2-aminoquinazoline- based compounds
-
Srivastava, G. K.; Kesarwani, A. P.; Grover, R. K.; Srinivasan, T.; Roy, R.; Kundu, B. Solid Phase Synthesis of 2-Aminoquinazoline- Based Compounds. J. Comb. Chem., 2003, 5, 769-774.
-
(2003)
J. Comb. Chem.
, vol.5
, pp. 769-774
-
-
Srivastava, G.K.1
Kesarwani, A.P.2
Grover, R.K.3
Srinivasan, T.4
Roy, R.5
Kundu, B.6
-
167
-
-
18144386189
-
Base catalyzed intramolecular transamidation of 2- aminoquinazoline derivatives on solid phase
-
Grover, R.; Kesarwani, A. P.; Srivastava, G. K.; Kundu, B.; Roy, R. Base catalyzed intramolecular transamidation of 2- aminoquinazoline derivatives on solid phase. Tetrahedron, 2005, 61, 5011-5018.
-
(2005)
Tetrahedron
, vol.61
, pp. 5011-5018
-
-
Grover, R.1
Kesarwani, A.P.2
Srivastava, G.K.3
Kundu, B.4
Roy, R.5
-
168
-
-
0033519706
-
1, 2, 5-oxadiazole N-oxide derivatives and related compounds as potential antitrypanosomal drugs: Structure-activity relationships
-
Cerecetto, H.; Di Maio, R.; Gonzalez, M.; Risso, M.; Saenz, P.; Seoane, G.; Denicola, A.; Peluffo, G.; Quijano, C.; Olea-Azar, C. 1, 2, 5-Oxadiazole N-Oxide Derivatives and Related Compounds as Potential Antitrypanosomal Drugs: Structure-Activity Relationships. J. Med. Chem., 1999, 42, 1941-1950.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 1941-1950
-
-
Cerecetto, H.1
Di Maio, R.2
Gonzalez, M.3
Risso, M.4
Saenz, P.5
Seoane, G.6
Denicola, A.7
Peluffo, G.8
Quijano, C.9
Olea-Azar, C.10
-
169
-
-
0033535524
-
Piperazine imidazo [1, 5-a]quinoxaline ureas as high-affinity GABAA Ligands of dual functionality
-
Jacobsen, E. J.; Stelzer, L. S.; TenBrink, R. E.; Belonga, K. L.; Carter, D. B.; Im, H. K.; Im, W. B.; Sethy, V. H.; Tang, A. H.; Von Voigtlander, P. F.; Petke, J. D.; Zhong, W. Z.; Mickelson, J. W. Piperazine Imidazo [1, 5-a]quinoxaline Ureas as High-Affinity GABAA Ligands of Dual Functionality. J. Med. Chem., 1999, 42, 1123-1144.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 1123-1144
-
-
Jacobsen, E.J.1
Stelzer, L.S.2
TenBrink, R.E.3
Belonga, K.L.4
Carter, D.B.5
Im, H.K.6
Im, W.B.7
Sethy, V.H.8
Tang, A.H.9
Von Voigtlander, P.F.10
Petke, J.D.11
Zhong, W.Z.12
Mickelson, J.W.13
-
170
-
-
0027249930
-
Quinoxaline N-oxide containing potent angiotensin II receptor antagonists: Synthesis, biological properties, and structure activity relationships
-
Kim, K. S.; Qian, L.; Bird, J. E.; Dickinson, K. E.; Moreland, S.; Schaeffer, T. R.; Waldron, T. L.; Delaney, C. L.; Weller, H. N.; Miller, A. V. Quinoxaline N-oxide containing potent angiotensin II receptor antagonists: synthesis, biological properties, and structureactivity relationships. J. Med. Chem., 1993, 36, 2335-2342.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2335-2342
-
-
Kim, K.S.1
Qian, L.2
Bird, J.E.3
Dickinson, K.E.4
Moreland, S.5
Schaeffer, T.R.6
Waldron, T.L.7
Delaney, C.L.8
Weller, H.N.9
Miller, A.V.10
-
171
-
-
0025306964
-
4-Amino [1, 2, 4]triazolo [4, 3-a]quinoxalines, A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants
-
Sarges, R.; Howard, H. R.; Browne, R. G.; Lebel, L. A.; Seymour, P. A.; Koe, B. K. 4-Amino [1, 2, 4]triazolo [4, 3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants. J. Med. Chem., 1990, 33, 2240-2254.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2240-2254
-
-
Sarges, R.1
Howard, H.R.2
Browne, R.G.3
Lebel, L.A.4
Seymour, P.A.5
Koe, B.K.6
-
172
-
-
0035942520
-
Design, synthesis, and biological evaluation of analogues of the antitumor agent, 2-{4- [(7-chloro-2-quinoxalinyl)oxy]phenoxy} propionic acid (XK469)
-
Hazeldine, S. T.; Polin, L.; Kushner, J.; Paluch, J.; White, K.; Edelstein, M.; Palomino, E.; Corbett, T. H.; Horwitz, J. P. Design, Synthesis, and Biological Evaluation of Analogues of the Antitumor Agent, 2-{4- [(7-Chloro-2-quinoxalinyl)oxy]phenoxy} propionic Acid (XK469). J. Med. Chem., 2001, 44, 1758-1776.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 1758-1776
-
-
Hazeldine, S.T.1
Polin, L.2
Kushner, J.3
Paluch, J.4
White, K.5
Edelstein, M.6
Palomino, E.7
Corbett, T.H.8
Horwitz, J.P.9
-
173
-
-
0030789783
-
Solid phase synthesis of 3, 4- disubstituted-7-carbamoyl-1, 2, 3, 4-tetrahydroquinoxalin-2-ones
-
Lee, J.; Murray, W. V.; Rivero, R. A. Solid Phase Synthesis of 3, 4- Disubstituted-7-carbamoyl-1, 2, 3, 4-tetrahydroquinoxalin-2-ones. J. Org. Chem., 1997, 62, 3874-3879.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 3874-3879
-
-
Lee, J.1
Murray, W.V.2
Rivero, R.A.3
-
174
-
-
0032548880
-
Solid-phase synthesis of benzopiperazinones
-
Morales, G. A.; Corbett, J. W.; Degrado, W. F. Solid-Phase Synthesis of Benzopiperazinones. J. Org. Chem., 1998, 63, 1172- 1177.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 1172-1177
-
-
Morales, G.A.1
Corbett, J.W.2
Degrado, W.F.3
-
175
-
-
0033515570
-
Solid-Phase Synthesis of Substituted 4-Acyl-1, 2, 3, 4- tetrahydroquinoxalin-2-ones
-
Zaragoza, F.; Stephensen, H. Solid-Phase Synthesis of Substituted 4-Acyl-1, 2, 3, 4-tetrahydroquinoxalin-2-ones. J. Org. Chem., 1999, 64, 2555-2557.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 2555-2557
-
-
Zaragoza, F.1
Stephensen, H.2
-
176
-
-
0346465017
-
Revolutionizing resin handling for combinatorial synthesis
-
Atrash, B.; Bradley, M.; Kobylecki, R.; Cowell, D.; Reader, J. Revolutionizing Resin Handling for Combinatorial Synthesis. Angew. Chem., Int. Ed. Engl., 2001, 113, 964-967.
-
(2001)
Angew. Chem., Int. Ed. Engl.
, vol.113
, pp. 964-967
-
-
Atrash, B.1
Bradley, M.2
Kobylecki, R.3
Cowell, D.4
Reader, J.5
-
177
-
-
0034175574
-
Solid-phase synthesis of branched thiohydantoin benzimidazolinethiones and branched thiohydantoin tetrahydroquinoxalinediones
-
Nefzi, A.; Giulianotti, M. A.; Houghten, R. A. Solid-phase synthesis of branched thiohydantoin benzimidazolinethiones and branched thiohydantoin tetrahydroquinoxalinediones. Tetrahedron Lett., 2000, 41, 2283-2287.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 2283-2287
-
-
Nefzi, A.1
Giulianotti, M.A.2
Houghten, R.A.3
-
178
-
-
0033992005
-
Solid phase synthesis of 5, 6, 7, 8-tetrahydro-1himidazo [4, 5-g]quinoxalin-6-ones
-
Mazurov, A. Solid phase synthesis of 5, 6, 7, 8-tetrahydro-1Himidazo [ 4, 5-g]quinoxalin-6-ones. Tetrahedron Lett., 2000, 41, 7- 10.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 7-10
-
-
Mazurov, A.1
-
179
-
-
0342657817
-
A solid phase traceless synthesis of quinoxalinones
-
Krchnak, V.; Szabo, L.; Vagner, J. A solid phase traceless synthesis of quinoxalinones. Tetrahedron Lett., 2000, 41, 2835-2838.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 2835-2838
-
-
Krchnak, V.1
Szabo, L.2
Vagner, J.3
-
180
-
-
0035953011
-
A solid-phase traceless synthesis of tetrahydroquinoxalines
-
Krchnak, V.; Smith, J.; Vagner, J. A solid-phase traceless synthesis of tetrahydroquinoxalines. Tetrahedron Lett., 2001, 42, 2443-2446.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 2443-2446
-
-
Krchnak, V.1
Smith, J.2
Vagner, J.3
-
181
-
-
0035813415
-
Solid-phase synthesis of quinoxalines on synphase™ lanterns
-
Wu, Z.; Ede, N. J. Solid-phase synthesis of quinoxalines on SynPhase™ Lanterns. Tetrahedron Lett., 2001, 42, 8115-8118.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 8115-8118
-
-
Wu, Z.1
Ede, N.J.2
-
182
-
-
25444436218
-
Solid-phase synthesis of quinoxaline, thiazine, and oxazine analogs through a benzyne intermediate
-
Seth, D.; Xiaobing, W.; Kit, S. L.; Mark J. K. Solid-phase synthesis of quinoxaline, thiazine, and oxazine analogs through a benzyne intermediate. Tetrahedron Lett., 2005, 46, 7443-7446.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 7443-7446
-
-
Seth, D.1
Xiaobing, W.2
Kit, S.L.3
Mark, J.K.4
-
183
-
-
84863758389
-
Piperazine amide linker for cyclative cleavage from solid support: Traceless synthesis of dihydroquinoxalin-2-ones
-
Neagoie, C.; Krchnak, V. Piperazine Amide Linker for Cyclative Cleavage from Solid Support: Traceless Synthesis of Dihydroquinoxalin-2-ones. Comb. Sci., 2012, 14, 399-402.
-
(2012)
Comb. Sci.
, vol.14
, pp. 399-402
-
-
Neagoie, C.1
Krchnak, V.2
-
184
-
-
7744242263
-
Quinoline, quinazoline and acridone alkaloids
-
Michael, J. P. Quinoline, quinazoline and acridone alkaloids. Nat. Prod. Rep., 2004, 21, 650-668.
-
(2004)
Nat. Prod. Rep.
, vol.21
, pp. 650-668
-
-
Michael, J.P.1
-
185
-
-
0000155296
-
-
Ansell, M. F. Ed. Supplements to the 2nd ed. Elsevier: Amsterdam
-
Johne, S. In Rodd's Chemistry of Carbon Compounds; Ansell, M. F., Ed.; Supplements to the 2nd ed.; Elsevier: Amsterdam, 1995; IV 1/2, 223.
-
(1995)
Rodd's Chemistry of Carbon Compounds
, vol.4
, Issue.1-2
, pp. 223
-
-
Johne, S.1
-
187
-
-
33847356832
-
Molecular- docking-guided design, synthesis, and biologic evaluation of radioiodinated quinazolinone prodrugs
-
Chen, K.; Aowad, A. F.; Adelstein, S. J.; Kassis, A. I. Molecular- Docking-Guided Design, Synthesis, and Biologic Evaluation of Radioiodinated Quinazolinone Prodrugs. J. Med. Chem., 2007, 50, 663-673.
-
(2007)
J. Med. Chem.
, vol.50
, pp. 663-673
-
-
Chen, K.1
Aowad, A.F.2
Adelstein, S.J.3
Kassis, A.I.4
-
188
-
-
0023679901
-
Synthesis and histamine H2-antagonist activity of 4- quinazolinone derivatives
-
Ogawa, N.; Yoshida, T.; Aratani, T.; Koshinaka, E.; Kato, H.; Ito, Y. Synthesis and histamine H2-antagonist activity of 4- quinazolinone derivatives. Chem. Pharm. Bull., 1988, 36, 2955- 2967.
-
(1988)
Chem. Pharm. Bull.
, vol.36
, pp. 2955-2967
-
-
Ogawa, N.1
Yoshida, T.2
Aratani, T.3
Koshinaka, E.4
Kato, H.5
Ito, Y.6
-
189
-
-
0025365265
-
Potent inhibition of thymidylate synthase by two series of nonclassical quinazolines
-
McNamara, D. J.; Berman, E. M.; Fry, D. W.; Werbel, L. M. Potent inhibition of thymidylate synthase by two series of nonclassical quinazolines. J. Med. Chem., 1998, 33, 2045-2051.
-
(1998)
J. Med. Chem.
, vol.33
, pp. 2045-2051
-
-
McNamara, D.J.1
Berman, E.M.2
Fry, D.W.3
Werbel, L.M.4
-
190
-
-
0026699588
-
Synthesis and activity in cognition-related tests of novel 2-benzoylamino-4-oxoquinazolines
-
Levin, J. I.; Fanshawe, W. J.; Epstein, J. W.; Beer, B.; Bartus, R. T.; Dean, R. L. Synthesis and activity in cognition-related tests of novel 2-benzoylamino-4-oxoquinazolines. Bioorg. Med. Chem. Lett., 1992, 2, 349-352.
-
(1992)
Bioorg. Med. Chem. Lett.
, vol.2
, pp. 349-352
-
-
Levin, J.I.1
Fanshawe, W.J.2
Epstein, J.W.3
Beer, B.4
Bartus, R.T.5
Dean, R.L.6
-
191
-
-
0033598323
-
Substituted isoquinolines and quinazolines as potential antiinflammatory agents, Synthesis and biological evaluation of inhibitors of tumor necrosis factor α
-
Chao, Q.; Deng, L.; Shih, H.; Leoni, L. M.; Genini, D.; Carson, D. A.; Cottam, H. B. Substituted Isoquinolines and Quinazolines as Potential Antiinflammatory Agents. Synthesis and Biological Evaluation of Inhibitors of Tumor Necrosis Factor α. J. Med. Chem., 1999, 42, 3860-3873.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3860-3873
-
-
Chao, Q.1
Deng, L.2
Shih, H.3
Leoni, L.M.4
Genini, D.5
Carson, D.A.6
Cottam, H.B.7
-
192
-
-
0030723851
-
Solid phase synthesis of quinazolinones
-
Mayer, J. M.; Lewis, G. S.; Curtis, M. J. Solid phase synthesis of quinazolinones. Tetrahedron Lett., 1997, 38, 8445-8448.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 8445-8448
-
-
Mayer, J.M.1
Lewis, G.S.2
Curtis, M.J.3
-
193
-
-
0001003013
-
Solid-phase synthesis of 3H-quinazolin-4-ones based on an aza wittig-mediated annulation strategy
-
Villalgordo, J. M.; Orbrencht, D.; Chucholowsky, A. Solid-Phase Synthesis of 3H-Quinazolin-4-ones Based on an Aza Wittig- Mediated annulation Strategy. Synlett, 1998, 1405-1407.
-
(1998)
Synlett
, pp. 1405-1407
-
-
Villalgordo, J.M.1
Orbrencht, D.2
Chucholowsky, A.3
-
194
-
-
0037047538
-
A traceless approach for the parallel solid-phase synthesis of 2-(Arylamino)quinazolinones
-
Yu, Y.; Ostresh, J. M.; Houghten, R. A. A Traceless Approach for the Parallel Solid-Phase Synthesis of 2-(Arylamino)quinazolinones. J. Org. Chem., 2002, 67, 5831-5834.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 5831-5834
-
-
Yu, Y.1
Ostresh, J.M.2
Houghten, R.A.3
-
195
-
-
0037025731
-
Solid-phase synthesis of quinazolin-4(3H)-ones with three-point diversity
-
Kesarwarni, A. P.; Srivastava, G. K.; Rastogi, S. K.; Kundu, B. Solid-phase synthesis of quinazolin-4(3H)-ones with three-point diversity. Tetrahedron Lett., 2002, 43, 5579-5581.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 5579-5581
-
-
Kesarwarni, A.P.1
Srivastava, G.K.2
Rastogi, S.K.3
Kundu, B.4
-
196
-
-
0034220357
-
Combinatorial synthesis of heterocycles: Solid-phase synthesis of 2-amino-4(1h)-quinazolinone derivatives
-
Gopalsamy, A.; Yang, H. Combinatorial Synthesis of Heterocycles: Solid-Phase Synthesis of 2-Amino-4(1H)-quinazolinone Derivatives. J. Comb. Chem., 2000, 2, 378-381.
-
(2000)
J. Comb. Chem.
, vol.2
, pp. 378-381
-
-
Gopalsamy, A.1
Yang, H.2
-
197
-
-
0034596426
-
A concise and efficient solid-phase synthesis of 2-amino-4(3H)- quinazolinones
-
Yang, R.-Y.; Kaplan, A. A concise and efficient solid-phase synthesis of 2-amino-4(3H)-quinazolinones. Tetrahedron Lett., 2000, 41, 7005-7008.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 7005-7008
-
-
Yang, R.-Y.1
Kaplan, A.2
-
198
-
-
0035344876
-
A polymer- bound iminophosphorane approach for the synthesis of quinazolines
-
Zhang, W.; Mayer, J. P.; Hall, S. E.; Weigel, J. A. A Polymer- Bound Iminophosphorane Approach for the Synthesis of Quinazolines. J. Comb. Chem., 2001, 3, 255-256.
-
(2001)
J. Comb. Chem.
, vol.3
, pp. 255-256
-
-
Zhang, W.1
Mayer, J.P.2
Hall, S.E.3
Weigel, J.A.4
-
199
-
-
28244479033
-
Solid-phase synthesis of 2-aminoquinazolinone derivatives with two- and three-point diversity
-
Kundu, B.; Partani, P.; Duggineni, S.; Sawant, D. Solid-Phase Synthesis of 2-Aminoquinazolinone Derivatives with Two- and Three-Point Diversity. J. Comb. Chem., 2005, 7, 909-915.
-
(2005)
J. Comb. Chem.
, vol.7
, pp. 909-915
-
-
Kundu, B.1
Partani, P.2
Duggineni, S.3
Sawant, D.4
-
200
-
-
0034970413
-
Pharmacotherapy of generalized anxiety disorder
-
Jonathan, R. T.; Davidson, M. D. Pharmacotherapy of generalized anxiety disorder. J. Clin. Psychiatry, 2001, 62, 46-50.
-
(2001)
J. Clin. Psychiatry
, vol.62
, pp. 46-50
-
-
Jonathan, R.T.1
Davidson, M.D.2
-
201
-
-
0035017542
-
A psychiatric perspective on insomnia
-
McCall, W. V. A psychiatric perspective on insomnia. J. Clin. Psychiatry, 2001, 62, 27-32.
-
(2001)
J. Clin. Psychiatry
, vol.62
, pp. 27-32
-
-
McCall, W.V.1
-
202
-
-
0033967522
-
Treatment of status epilepticus with midazolam in the critical care setting
-
Hanley, D. F.; Pozo, M. Treatment of status epilepticus with midazolam in the critical care setting. Int. J. Clin. Pract., 2000, 54, 30-35.
-
(2000)
Int. J. Clin. Pract.
, vol.54
, pp. 30-35
-
-
Hanley, D.F.1
Pozo, M.2
-
203
-
-
13044263877
-
Preparation and biological activity of novel tricyclic GPIIB/IIIa antagonists
-
Robarge, K. D.; Dina, M. S.; Somers, T. C.; Lee, A.; Rawson, T. E.; Olivero, A. G.; Tischler, M. H.; Webb, R. R.; Weese, K. J.; Aliagas, I.; Blackburn, B. K. Preparation and biological activity of novel tricyclic GPIIb/IIIa antagonists. Bioorg. Med. Chem., 1998, 6, 2345-2381.
-
(1998)
Bioorg. Med. Chem.
, vol.6
, pp. 2345-2381
-
-
Robarge, K.D.1
Dina, M.S.2
Somers, T.C.3
Lee, A.4
Rawson, T.E.5
Olivero, A.G.6
Tischler, M.H.7
Webb, R.R.8
Weese, K.J.9
Aliagas, I.10
Blackburn, B.K.11
-
204
-
-
0033602275
-
Conformational preferences in a benzodiazepine series of potent nonpeptide fibrinogen receptor antagonists
-
Keenan, R. M.; Callahan, J. F.; Samanen, J. M.; Bondinell, W. E.; Calvo, R. R.; Chen, L.; DeBrosse, C.; Eggleston, D. S.; Haltiwanger, R. C.; Hwang, S. M.; Jakas, D. R.; Ku, T. W.; Miller, W. H.; Newlander, K. A.; Nichols, A.; Parker, M. F.; Southhall, L. S.; Uzinskas, I.; Vasko-Moser, J. A.; Venslavsky, J. W.; Wong, A. S.; Huffman, W. F. Conformational Preferences in a Benzodiazepine Series of Potent Nonpeptide Fibrinogen Receptor Antagonists. J. Med. Chem., 1999, 42, 545-559.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 545-559
-
-
Keenan, R.M.1
Callahan, J.F.2
Samanen, J.M.3
Bondinell, W.E.4
Calvo, R.R.5
Chen, L.6
DeBrosse, C.7
Eggleston, D.S.8
Haltiwanger, R.C.9
Hwang, S.M.10
Jakas, D.R.11
Ku, T.W.12
Miller, W.H.13
Newlander, K.A.14
Nichols, A.15
Parker, M.F.16
Southhall, L.S.17
Uzinskas, I.18
Vasko-Moser, J.A.19
Venslavsky, J.W.20
Wong, A.S.21
Huffman, W.F.22
more..
-
205
-
-
0023042881
-
A selective imidazobenzodiazepine antagonist of ethanol in the rat
-
Suzdak, P. D.; Glowa, J. R.; Crawley, J. N.; Schwartz, R. D.; Skolnick, P.; Paul, S. M. A selective imidazobenzodiazepine antagonist of ethanol in the rat. Science, 1986, 234, 1243-1247.
-
(1986)
Science
, vol.234
, pp. 1243-1247
-
-
Suzdak, P.D.1
Glowa, J.R.2
Crawley, J.N.3
Schwartz, R.D.4
Skolnick, P.5
Paul, S.M.6
-
206
-
-
15144345474
-
Class III antiarrhythmic activity in vivo by selective blockade of the slowly activating cardiac delayed rectifier potassium current IKS by (R)-2-(2, 4- Trifluoromethyl)-N- [2-oxo-5-phenyl- 1-(2, 2, 2- trifluoroethyl)-2, 3-dihydro- 1H-benzo [e] [1, 4]diazepin-3- yl]acetamide
-
Selnick, H. G.; Liverton, N. J.; Baldwin, J. J.; Butcher, J. W.; Claremon, D. A.; Elliott, J. M.; Freidinger, R. M.; King, S. A.; Libby, B. E.; McIntyre, C. J.; Pribush, D. A.; Remy, D. C.; Smith, G. R.; Tebben, A. J.; Jurkiewicz, N. K.; Lynch, J. J.; Salata, J. J.; Sanguinetti, M. C.; Siegl, P. K.; Slaughter, D. E.; Vyas, K. Class III Antiarrhythmic Activity in vivo by Selective Blockade of the Slowly Activating Cardiac Delayed Rectifier Potassium Current IKs by (R)-2-(2, 4- Trifluoromethyl)-N- [2-oxo-5-phenyl- 1-(2, 2, 2- trifluoroethyl)-2, 3-dihydro- 1H-benzo [e] [1, 4]diazepin-3- yl]acetamide. J. Med. Chem., 1997, 40, 3865-3868.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 3865-3868
-
-
Selnick, H.G.1
Liverton, N.J.2
Baldwin, J.J.3
Butcher, J.W.4
Claremon, D.A.5
Elliott, J.M.6
Freidinger, R.M.7
King, S.A.8
Libby, B.E.9
McIntyre, C.J.10
Pribush, D.A.11
Remy, D.C.12
Smith, G.R.13
Tebben, A.J.14
Jurkiewicz, N.K.15
Lynch, J.J.16
Salata, J.J.17
Sanguinetti, M.C.18
Siegl, P.K.19
Slaughter, D.E.20
Vyas, K.21
more..
-
207
-
-
14444285742
-
5-Fluoro-2-methyl-N- [4-(5Hpyrrolo [ 2, 1-c]- [1, 4]benzodiazepin-10(11H) -ylcarbonyl)-3- chlorophenyl]benzamide (VPA-985): An orally active arginine vasopressin antagonist with selectivity for V2 receptors
-
Albright, J. D.; Reich, M. F.; De los Santos, E. G.; Dusza, J. P.; Sum, F. W.; Venkatesan, A. M.; Coupet, J.; Chan, P. S.; Ru, X.; Mazandarani, H.; Bailey, T. 5-Fluoro-2-methyl-N- [4-(5Hpyrrolo [ 2, 1-c]- [1, 4]benzodiazepin-10(11H)-ylcarbonyl)-3- chlorophenyl]benzamide (VPA-985): An Orally Active Arginine Vasopressin Antagonist with Selectivity for V2 Receptors. J. Med. Chem., 1998, 41, 2442-2444.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2442-2444
-
-
Albright, J.D.1
Reich, M.F.2
De Los Santos, E.G.3
Dusza, J.P.4
Sum, F.W.5
Venkatesan, A.M.6
Coupet, J.7
Chan, P.S.8
Ru, X.9
Mazandarani, H.10
Bailey, T.11
-
208
-
-
0028968716
-
Synthesis and anti-HIV-1 Activity of 4, 5, 6, 7-tetrahydro-5- methylimidazo [4, 5, 1-jk] [1, 4] benzodiazepin-2(1H)-one (TlBO) derivatives
-
Ho, W.; Kukla, M. J.; Breslin, H. J.; Ludovici, D. W.; Grous, P. P.; Diamond, C. J.; Miranda, M.; Rodgers, J. D.; Ho, C. Y.; De Clercq, E.; Pauwels, R.; Andries, K.; Janssen, M. A. C.; Janssen, P. A. Synthesis and Anti-HIV-1 Activity of 4, 5, 6, 7-Tetrahydro-5- methylimidazo [4, 5, 1-jk] [1, 4]benzodiazepin-2(1H)-one (TlBO) Derivatives. J. Med. Chem., 1995, 38, 794-802.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 794-802
-
-
Ho, W.1
Kukla, M.J.2
Breslin, H.J.3
Ludovici, D.W.4
Grous, P.P.5
Diamond, C.J.6
Miranda, M.7
Rodgers, J.D.8
Ho, C.Y.9
De Clercq, E.10
Pauwels, R.11
Andries, K.12
Janssen, M.A.C.13
Janssen, P.A.14
-
209
-
-
15444358348
-
5-(Piperidin-2-yl)- and 5- (Homopiperidin-2-yl)-1, 4-benzodiazepines: High-affinity, basic ligands for the cholecystokinin-B receptor
-
Castro, J. L.; Broughton, H. B.; Russell, M. G.; Rathbone, D.; Watt, A. P.; Ball, R. G.; Chapman, K. L.; Patel, S.; Smith, A. J.; Marshall, G. R.; Matassa, V. G. 5-(Piperidin-2-yl)- and 5- (Homopiperidin-2-yl)-1, 4-benzodiazepines: High-Affinity, Basic Ligands for the Cholecystokinin-B Receptor. J. Med. Chem., 1997, 40, 2491-2501.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2491-2501
-
-
Castro, J.L.1
Broughton, H.B.2
Russell, M.G.3
Rathbone, D.4
Watt, A.P.5
Ball, R.G.6
Chapman, K.L.7
Patel, S.8
Smith, A.J.9
Marshall, G.R.10
Matassa, V.G.11
-
210
-
-
0033053885
-
Circumdatins D, E, and F: Further fungal benzodiazepine analogues from aspergillus ochraceus
-
Rahbaek, L.; Breinholt, J. Circumdatins D, E, and F: Further Fungal Benzodiazepine Analogues from Aspergillus ochraceus. J. Nat. Prod., 1999, 62, 904-905.
-
(1999)
J. Nat. Prod.
, vol.62
, pp. 904-905
-
-
Rahbaek, L.1
Breinholt, J.2
-
211
-
-
0032948888
-
Sclerotigenin: A new antiinsectan benzodiazepine from the sclerotia of penicillium sclerotigenum
-
Joshi, B. K.; Gloer, J. B.; Wicklow, D. T.; Dowd, P. F. Sclerotigenin: A New Antiinsectan Benzodiazepine from the Sclerotia of Penicillium sclerotigenum. J. Nat. Prod., 1999, 62, 650-652.
-
(1999)
J. Nat. Prod.
, vol.62
, pp. 650-652
-
-
Joshi, B.K.1
Gloer, J.B.2
Wicklow, D.T.3
Dowd, P.F.4
-
212
-
-
0000303445
-
Organic syntheses with functionalized polymers: IV, Synthesis of 1, 3-dihydro-5-phenyl- 2H-1, 4-benzodiazepin-2-ones
-
Camps, F.; Castells, J.; Font, J.; Pi, J. Organic syntheses with functionalized polymers: IV. Synthesis of 1, 3-dihydro-5-phenyl- 2H-1, 4-benzodiazepin-2-ones. Anales de Química., 1974, 70, 848- 849.
-
(1974)
Anales de Química
, vol.70
, pp. 848-849
-
-
Camps, F.1
Castells, J.2
Font, J.3
Pi, J.4
-
213
-
-
0035935132
-
Solidphase friedel-crafts acylation on polystyrene resins-synthesis of antiepiletic 1-aryl-3, 5-dihydro-4H-2, 3-benzodiazepin-4-ones
-
Bevacqua, F.; Basso, A.; Gitto, R.; Bradley, M.; Chimirri, A. Solidphase Friedel-Crafts acylation on polystyrene resins-synthesis of antiepiletic 1-aryl-3, 5-dihydro-4H-2, 3-benzodiazepin-4-ones. Tetrahedron Lett., 2001, 42, 7683-7685.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 7683-7685
-
-
Bevacqua, F.1
Basso, A.2
Gitto, R.3
Bradley, M.4
Chimirri, A.5
-
214
-
-
0035974391
-
Parallel synthesis of 4, 5- dihydro-1H-1, 4-benzodiazepine-2, 3-diones
-
Nefzi, A.; Ong, N. A.; Houghten, R. A. Parallel synthesis of 4, 5- dihydro-1H-1, 4-benzodiazepine-2, 3-diones. Tetrahedron Lett., 2001, 42, 5141-5143.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 5141-5143
-
-
Nefzi, A.1
Ong, N.A.2
Houghten, R.A.3
-
215
-
-
0034609167
-
Solid-phase synthesis of DNA-interactive pyrrolo [2, 1-c] [1, 4] benzodiazepines
-
Berry, J. M.; Howard, P. W.; Thurston, D. E. Solid-phase synthesis of DNA-interactive pyrrolo [2, 1-c] [1, 4]benzodiazepines. Tetrahedron Lett., 2000, 41, 6171-6174.
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 6171-6174
-
-
Berry, J.M.1
Howard, P.W.2
Thurston, D.E.3
-
216
-
-
0033617212
-
Solid-phase synthesis of 3, 4, 5- substituted 1, 5-benzodiazepin-2-ones
-
Lee, J.; Gauthier, D.; Rivero, R. A. Solid-Phase Synthesis of 3, 4, 5- Substituted 1, 5-Benzodiazepin-2-ones. J. Org. Chem., 1999, 64, 3060-3065.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 3060-3065
-
-
Lee, J.1
Gauthier, D.2
Rivero, R.A.3
-
217
-
-
0028928237
-
Solid-phase synthesis of structurally diverse 1, 4-benzodiazepine derivatives using the stille coupling reaction
-
Plunkett, M. J.; Ellman, J. A. Solid-Phase Synthesis of Structurally Diverse 1, 4-Benzodiazepine Derivatives Using the Stille Coupling Reaction. J. Am. Chem. Soc., 1995, 117, 3306-3307.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 3306-3307
-
-
Plunkett, M.J.1
Ellman, J.A.2
-
218
-
-
0001339949
-
Germanium and silicon linking strategies for traceless solid-phase synthesis
-
Plunkett, M. J.; Ellman, J. A. Germanium and Silicon Linking Strategies for Traceless Solid-Phase Synthesis. J. Org. Chem., 1997, 62, 2885-2893.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 2885-2893
-
-
Plunkett, M.J.1
Ellman, J.A.2
-
219
-
-
0032511925
-
Solid-phase synthesis of 1, 5-benzodiazepin-2-ones
-
Schwarz, M. K.; Tumelty, D.; Gallop, M. A. Solid-phase synthesis of 1, 5-benzodiazepin-2-ones. Tetrahedron Lett., 1998, 39, 8397- 8400.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 8397-8400
-
-
Schwarz, M.K.1
Tumelty, D.2
Gallop, M.A.3
-
220
-
-
0035847664
-
Solid-phase synthesis of pyrrolo [2, 1-c] and benzodiazepine-5, 11-diones
-
Kamal, A.; Reddy, G. S. K.; Raghavan, S. Solid-phase synthesis of pyrrolo [2, 1-c] and benzodiazepine-5, 11-diones. Bioorg. Med. Chem. Lett., 2001, 11, 387-389.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 387-389
-
-
Kamal, A.1
Reddy, G.S.K.2
Raghavan, S.3
-
221
-
-
0035944194
-
Efficient reduction of aromatic nitro/azido groups on solid support employing indium: Synthesis of pyrrolo [2, 1-c] [1, 4] benzodiazepine-5, 11-diones
-
Kamal, A.; Reddy, G. S. K.; Reddy, K. L. Efficient reduction of aromatic nitro/azido groups on solid support employing indium: synthesis of pyrrolo [2, 1-c] [1, 4]benzodiazepine-5, 11-diones. Tetrahedron Lett., 2001, 42, 6969-6971.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 6969-6971
-
-
Kamal, A.1
Reddy, G.S.K.2
Reddy, K.L.3
-
222
-
-
0030694340
-
Solid-phase synthesis of diverse tetrahydro-1, 4-benzodiazepine-2-ones
-
Bhalay, G.; Blaney, P.; Palmer, V. H.; Baxter, A. D. Solid-phase synthesis of diverse tetrahydro-1, 4-benzodiazepine-2-ones. Tetrahedron Lett., 1997, 38, 8375-8378.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 8375-8378
-
-
Bhalay, G.1
Blaney, P.2
Palmer, V.H.3
Baxter, A.D.4
-
223
-
-
0030932342
-
Solid-phase synthesis of 1, 4-benzodiazepine-2, 5-diones, Library preparation and demonstration of synthesis generality
-
Boojamra, C. G.; Burow, K. M.; Thompson, L. A.; Ellman, J. A. Solid-Phase Synthesis of 1, 4-Benzodiazepine-2, 5-diones. Library Preparation and Demonstration of Synthesis Generality. J. Org. Chem., 1997, 62, 1240-1256.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1240-1256
-
-
Boojamra, C.G.1
Burow, K.M.2
Thompson, L.A.3
Ellman, J.A.4
-
224
-
-
0020163940
-
Conformation and biological activity of cyclic peptides
-
Kessler, H. Conformation and Biological Activity of Cyclic Peptides. Angew. Chem., Int. Ed. Engl., 1982, 21, 512-523.
-
(1982)
Angew. Chem., Int. Ed. Engl.
, vol.21
, pp. 512-523
-
-
Kessler, H.1
-
225
-
-
0000314051
-
Synthetic studies of biologically active marine cyclopeptides
-
Wipf, P. Synthetic Studies of Biologically Active Marine Cyclopeptides. Chem. Rev., 1995, 95, 2115-2134.
-
(1995)
Chem. Rev.
, vol.95
, pp. 2115-2134
-
-
Wipf, P.1
-
226
-
-
0028318863
-
Applications of combinatorial technologies to drug discovery, 2. Combinatorial organic synthesis, library screening strategies, and future directions
-
Gordon, E. M.; Barrett, R. W.; Dower, W. J.; Fodor, S. P.; Gallop, M. A. Applications of Combinatorial Technologies to Drug Discovery. 2. Combinatorial Organic Synthesis, Library Screening Strategies, and Future Directions. J. Med. Chem., 1994, 37, 1385-1401.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1385-1401
-
-
Gordon, E.M.1
Barrett, R.W.2
Dower, W.J.3
Fodor, S.P.4
Gallop, M.A.5
-
227
-
-
0035820171
-
The synthesis of cyclic peptides
-
Lambert, J. N.; Mitchell, J. P.; Roberts, K. D. The synthesis of cyclic peptides. J. Chem. Soc. Perkin Trans. 1, 2001, 471-484.
-
(2001)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 471-484
-
-
Lambert, J.N.1
Mitchell, J.P.2
Roberts, K.D.3
-
228
-
-
0001241742
-
Stereoisomere peptid- bibliotheken und peptidmimetika zum design von selektiven Inhibitoren des αv β3-Integrins für eine neuartige Krebstherapie
-
Haubner, R.; Finsinger, D.; Kessler, H. Stereoisomere Peptid- Bibliotheken und Peptidmimetika zum Design von selektiven Inhibitoren des αv β3-Integrins für eine neuartige Krebstherapie. Angew Chem, 1997, 109, 1440-1456.
-
(1997)
Angew Chem
, vol.109
, pp. 1440-1456
-
-
Haubner, R.1
Finsinger, D.2
Kessler, H.3
-
229
-
-
0030768536
-
Stereoisomeric peptide libraries and peptidomimetics for designing selective inhibitors of the αvβ3 integrin for a new cancer therapy
-
Haubner, R.; Finsinger, D.; Kessler, H. Stereoisomeric Peptide Libraries and Peptidomimetics for Designing Selective Inhibitors of the αvβ3 Integrin for a New Cancer Therapy. Angew. Chem. Int. Ed. Engl. 1997, 36, 1374-1389.
-
(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 1374-1389
-
-
Haubner, R.1
Finsinger, D.2
Kessler, H.3
-
230
-
-
0030689868
-
Chemistry and molecular biology in the search for new LHRH antagonists
-
Kutscher, B.; Bernd, M.; Beckers, T.; Polymeropoulos, E. E.; Engel, J. Chemistry and Molecular Biology in the Search for New LHRH Antagonists. Angew. Chem. Int. Ed. Engl., 1997, 36, 2148-2161.
-
(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 2148-2161
-
-
Kutscher, B.1
Bernd, M.2
Beckers, T.3
Polymeropoulos, E.E.4
Engel, J.5
-
231
-
-
84877957673
-
-
Eds.
-
Kates, S. A.; Solé, N. A.; Albericio, F.; Barany, G., Basava, C.; Anantharamaiah, G. M., Eds., Boston, Birkhauser: 1994, 39-58.
-
(1994)
Boston, Birkhauser
, pp. 39-58
-
-
Kates, S.A.1
Solé, N.A.2
Albericio, F.3
Barany, G.4
Basava, C.5
Anantharamaiah, G.M.6
-
232
-
-
0000078888
-
Chemistry and molecular biology in the search for new LHRH antagonists
-
Solid phase synthesis of cyclic peptides, Peptides: Design, Synthesis and Biological Activity
-
Solid phase synthesis of cyclic peptides, Peptides: Design, Synthesis and Biological Activity., Kutscher, B.; Bernd, M.; Beckers, T.; Polymeropoulos, E. E.; Engel, J Chemistry and Molecular Biology in the Search for New LHRH Antagonists. Angew. Chem., 1997, 109, 2240-2254.
-
(1997)
Angew. Chem.
, vol.109
, pp. 2240-2254
-
-
Kutscher, B.1
Bernd, M.2
Beckers, T.3
Polymeropoulos, E.E.4
Engel, J.5
-
233
-
-
0026320903
-
Solid phase synthesis of a cyclic peptide using FMOC chemistry
-
McMurray, J. Solid phase synthesis of a cyclic peptide using fmoc chemistry. Tetrahedron Lett., 1991, 32, 7679-7682.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 7679-7682
-
-
McMurray, J.1
-
234
-
-
85047674165
-
Efficient preparation of cyclic peptide mixtures by solid phase synthesis and cyclization cleavage with oxime resin
-
Mihara, H.; Yamabe, S.; Nildome, T.; Aoyagi, H.; Kumagai, H. Efficient preparation of cyclic peptide mixtures by solid phase synthesis and cyclization cleavage with oxime resin. Tetrahedron Lett., 1995, 36, 4837-4840.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 4837-4840
-
-
Mihara, H.1
Yamabe, S.2
Nildome, T.3
Aoyagi, H.4
Kumagai, H.5
-
235
-
-
0028108821
-
Peptide-cyclizations on solid support: A fast and efficient route to small cyclopeptides
-
Richter, L. S.; Tom, J. Y. K.; Brunier, J. P. Peptide-Cyclizations on solid support: A fast and efficient route to small cyclopeptides. Tetrahedron Lett., 1994, 35, 5547-5550.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 5547-5550
-
-
Richter, L.S.1
Tom, J.Y.K.2
Brunier, J.P.3
-
236
-
-
0033584984
-
Solid phase synthesis of head-to-tail cyclic peptides using a sulfonamide safety-catch linker: The cleavage by cyclization approach
-
Yang, L.; Moriello, G. Solid phase synthesis of 'head-to-tail' cyclic peptides using a sulfonamide 'safety-catch' linker: the cleavage by cyclization approach. Tetrahedron Lett., 1999, 40, 8197-8200.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 8197-8200
-
-
Yang, L.1
Moriello, G.2
-
237
-
-
0035855309
-
Solid phase synthesis of cyclic peptides by oxidative cyclative cleavage of an aryl hydrazide linker-synthesis of stylostatin 1
-
Rosenbaum, C.; Waldmann, H. Solid phase synthesis of cyclic peptides by oxidative cyclative cleavage of an aryl hydrazide linker-synthesis of stylostatin 1. Tetrahedron Lett., 2001, 42, 5677-5680.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 5677-5680
-
-
Rosenbaum, C.1
Waldmann, H.2
-
238
-
-
0014911848
-
Subsequent activation of carboxylic derivatives by oxidation or elimination of water, Application for cyclizing peptides
-
Wieland, T.; Lewalter, J.; Birr, C. Subsequent activation of carboxylic derivatives by oxidation or elimination of water; application for cyclizing peptides. Liebigs Ann. Chem., 1970, 740, 31-47.
-
(1970)
Liebigs Ann. Chem.
, vol.740
, pp. 31-47
-
-
Wieland, T.1
Lewalter, J.2
Birr, C.3
-
239
-
-
77953224486
-
Onresin peptide macrocyclization using thiol-ene click chemistry
-
Aimetti, A. A.; Shoemaker, R. K.; Linc, C.-C.; Anseth, K. S. Onresin peptide macrocyclization using thiol-ene click chemistry. Chem. Commun., 2010, 46, 4061-4063.
-
(2010)
Chem. Commun.
, vol.46
, pp. 4061-4063
-
-
Aimetti, A.A.1
Shoemaker, R.K.2
Linc, C.-C.3
Anseth, K.S.4
-
240
-
-
79957814016
-
On resin side-chain cyclization of complex peptides using CUAAC
-
Ingale, S.; Dawson, P. E. On Resin Side-Chain Cyclization of Complex Peptides Using CuAAC. Org. Lett., 2011, 13, 2822-2825.
-
(2011)
Org. Lett.
, vol.13
, pp. 2822-2825
-
-
Ingale, S.1
Dawson, P.E.2
-
241
-
-
80054752348
-
Design and facile solid-phase synthesis of conformation ally constrained bicyclic peptoids
-
Lee, J. H.; Kim, H.-S.; Lim, H.-S. Design and Facile Solid-Phase Synthesis of Conformationally Constrained Bicyclic Peptoids. Org. Lett., 2011, 13, 5012-5015.
-
(2011)
Org. Lett.
, vol.13
, pp. 5012-5015
-
-
Lee, J.H.1
Kim, H.-S.2
Lim, H.-S.3
|