-
2
-
-
0032948663
-
Hodges JC. Solid-supported reagent strategies for rapid purification of combinatorial synthesis products
-
Booth RJ, Hodges JC. Solid-supported reagent strategies for rapid purification of combinatorial synthesis products. Ace Chem Research (1999) 32:18-26.
-
Ace Chem Research (1999) 32:18-26.
-
-
Booth, R.J.1
-
4
-
-
0032534853
-
Salituro FG, Court JJ, Deininger DD, Kim EE, LJ B, Novak PM, Rao BG, Pazhanisamy S, Schairer WC, Tung RD. Design, synthesis and conformational analysis of a novel series of HIV protease inhibitors
-
Baker CT, Salituro FG, Court JJ, Deininger DD, Kim EE, LJ B, Novak PM, Rao BG, Pazhanisamy S, Schairer WC, Tung RD. Design, synthesis and conformational analysis of a novel series of HIV protease inhibitors. Bioorg Med Chem Lett (1998) 8:3631-3636.
-
Bioorg Med Chem Lett (1998) 8:3631-3636.
-
-
Baker, C.T.1
-
7
-
-
0028968619
-
Expedient method for the solid-phase synthesis of aspartic acid protease inhibitors directed toward the generation of libraries
-
Kick EK, Ellman JA. Expedient method for the solid-phase synthesis of aspartic acid protease inhibitors directed toward the generation of libraries. J Med Chem (1995) 38:1427-1430.
-
J Med Chem (1995) 38:1427-1430.
-
-
Kick, E.K.1
Ellman, J.A.2
-
8
-
-
0032555095
-
Solid-phase synthesis of N-substituted amidinophenoxy pyridines as factor Xa inhibitors
-
Mohan R, Yun W, Buckman BO, Liang A, Trinh L, Morrissey MM. Solid-phase synthesis of N-substituted amidinophenoxy pyridines as factor Xa inhibitors. Bioorg Med Chem Lett (1998) 8:1877-1882.
-
Bioorg Med Chem Lett (1998) 8:1877-1882.
-
-
Mohan, R.1
Yun, W.2
Buckman, B.O.3
Liang, A.4
Trinh, L.5
Morrissey, M.M.6
-
9
-
-
0032492707
-
Lee K, Lee EJ, Koh JS. Solid phase synthesis of benzyiamine-derived sulfonamide library
-
Kim SW, Hong CY, Lee K, Lee EJ, Koh JS. Solid phase synthesis of benzyiamine-derived sulfonamide library. Bioorg Med Chem Lett (1998) 8:735-738.
-
Bioorg Med Chem Lett (1998) 8:735-738.
-
-
Kim, S.W.1
Hong, C.Y.2
-
10
-
-
15444357766
-
Witherup KM, Tucker TJ, Brady SF, Sisko JT, Naylor-Olsen AM, Lewis SD, Lucas BJ, Vacca JP: Design of novel, potent, noncovalent inhibitors of thrombin with nonbasic P-1 substructures: Rapid structure-activity studies by solid-phase synthesis
-
Lumma Jr WC. Witherup KM, Tucker TJ, Brady SF, Sisko JT, Naylor-Olsen AM, Lewis SD, Lucas BJ, Vacca JP: Design of novel, potent, noncovalent inhibitors of thrombin with nonbasic P-1 substructures: Rapid structure-activity studies by solid-phase synthesis. J Med Chem (1998) 41:1011-1013.
-
J Med Chem (1998) 41:1011-1013.
-
-
Lumma Jr., W.C.1
-
11
-
-
0030895222
-
Design of highly potent noncovalent thrombin inhibitors that utilize a novel lipophilic binding pocket in the thrombin active site
-
Tucker TJ, Lumma WC, Mulichak AM, Chen Z, Naylor-Olsen AM, Lewis SD, Lucas R, Freidinger RM, Kuo LC. Design of highly potent noncovalent thrombin inhibitors that utilize a novel lipophilic binding pocket in the thrombin active site. J Med Chem (1997) 40:830-832.
-
J Med Chem (1997) 40:830-832.
-
-
Tucker, T.J.1
Lumma, W.C.2
Mulichak, A.M.3
Chen, Z.4
Naylor-Olsen, A.M.5
Lewis, S.D.6
Lucas, R.7
Freidinger, R.M.8
Kuo, L.C.9
-
12
-
-
0032476829
-
-
Bums CJ, Groneberg RD, Salvino JM, McGeehan G, Condon SM, Morris R, Morrissette M, Mathew R, Dambrough S, Neuenschwander K, Scotese A, Djuric SW, Ullrich J, Labaudiniere R. Nanomolar inhibitors for two distinct biological target families from a single synthetic sequence: A next step in combinatorial library design? Angew Chem Int Ed Engl (1998) 37:2848-2850.
-
Nanomolar Inhibitors for Two Distinct Biological Target Families from A Single Synthetic Sequence: A next Step in Combinatorial Library Design? Angew Chem Int Ed Engl (1998) 37:2848-2850.
-
-
Bums, C.J.1
Groneberg, R.D.2
Salvino, J.M.3
McGeehan, G.4
Condon, S.M.5
Morris, R.6
Morrissette, M.7
Mathew, R.8
Dambrough, S.9
Neuenschwander, K.10
Scotese, A.11
Djuric, S.W.12
Ullrich, J.13
Labaudiniere, R.14
-
13
-
-
0032565840
-
Solid phase synthesis of fumitremorgin, verruculogen and tryprostatin analogs based on a cyclization/cleavage strategy
-
Loevizijn A, Maarseveen JH, Stegman K, Visser GM, Koomen GJ. Solid phase synthesis of fumitremorgin, verruculogen and tryprostatin analogs based on a cyclization/cleavage strategy. Tetrahedron Lett (1998) 39:4737-4740.
-
Tetrahedron Lett (1998) 39:4737-4740.
-
-
Loevizijn, A.1
Maarseveen, J.H.2
Stegman, K.3
Visser, G.M.4
Koomen, G.J.5
-
15
-
-
0032576190
-
Solid and solution phase synthesis and biological evaluation of combinatorial sarcodictyin libraries
-
Nicolaou KG, Winssinger N, Vourtoumis D, Ohshima T, Kim S, Pfefferkorn J, Xu JY, Li T. Solid and solution phase synthesis and biological evaluation of combinatorial sarcodictyin libraries. J Am Chem Soc (1398) 120:10814-10826.
-
J Am Chem Soc (1398) 120:10814-10826.
-
-
Nicolaou, K.G.1
Winssinger, N.2
Vourtoumis, D.3
Ohshima, T.4
Kim, S.5
Pfefferkorn, J.6
Xu, J.Y.7
Li, T.8
-
17
-
-
0032497345
-
Exploring structure-activity relationships around the phosphomannose isomerase inhibitor AF-14049 via combinatorial synthesis
-
Bhandari A, Jones DG, Schullek JR, Vo K, Schunk CA, Tamanaha LL, Chen D, Yuan Z, Needels MC, Gallop MA. Exploring structure-activity relationships around the phosphomannose isomerase inhibitor AF-14049 via combinatorial synthesis. Bioorg Med Chem Lett (1998) 8:2303-2308.
-
Bioorg Med Chem Lett (1998) 8:2303-2308.
-
-
Bhandari, A.1
Jones, D.G.2
Schullek, J.R.3
Vo, K.4
Schunk, C.A.5
Tamanaha, L.L.6
Chen, D.7
Yuan, Z.8
Needels, M.C.9
Gallop, M.A.10
-
18
-
-
0031693885
-
Combinatorial synthesis and screening of a chemical library of 1,4-dihydropyridine calcium channel blockers
-
Gordeev MF, Patel DV, England BP, Jonnalagadda S, Combs JD, Gordon EM. Combinatorial synthesis and screening of a chemical library of 1,4-dihydropyridine calcium channel blockers. Bioorg Med Chem (1998) 6:883-889.
-
Bioorg Med Chem (1998) 6:883-889.
-
-
Gordeev, M.F.1
Patel, D.V.2
England, B.P.3
Jonnalagadda, S.4
Combs, J.D.5
Gordon, E.M.6
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