-
1
-
-
0031189711
-
Molecular recognition of protein-ligand complexes: Applications to drug design
-
1. Babine, R. & Bender, S. (1997) Molecular recognition of protein-ligand complexes: applications to drug design. Chem. Rev. 97, 1359-1472.
-
(1997)
Chem. Rev.
, vol.97
, pp. 1359-1472
-
-
Babine, R.1
Bender, S.2
-
2
-
-
0013662780
-
Aspartic proteinases: Structure, function, biology and biomedical implications
-
2. Takahashi, K., ed. (1994) Aspartic proteinases: structure, function, biology and biomedical implications. Adv. Exp. Med. Biol. 362.
-
(1994)
Adv. Exp. Med. Biol.
, vol.362
-
-
Takahashi, K.1
-
3
-
-
0013642459
-
Aspartic proteinases: Retroviral and cellular enzymes
-
3. James, M.N., ed. (1998) Aspartic proteinases: retroviral and cellular enzymes. Adv. Exp. Med. Biol. 436.
-
(1998)
Adv. Exp. Med. Biol.
, vol.436
-
-
James, M.N.1
-
4
-
-
0029150486
-
Discovery of inhibitors of human renin with high oral bioavailability
-
4. Hoover, D.J., Lefker, B.A., Rosati, R.L., Wester, R.T., Kleinman, E.F., Bindra, J.S., Holt, W.F., Murphy, W.R., Mangiapane, M.L., Hockel, G.M., Williams, I.H., Smith, W.H., Gumkowski, M.J., Shepard, R.M., Gardner, M.J. & Nocerini, M.R. (1995) Discovery of inhibitors of human renin with high oral bioavailability. Adv. Exp. Med. Biol. 362, 167-180.
-
(1995)
Adv. Exp. Med. Biol.
, vol.362
, pp. 167-180
-
-
Hoover, D.J.1
Lefker, B.A.2
Rosati, R.L.3
Wester, R.T.4
Kleinman, E.F.5
Bindra, J.S.6
Holt, W.F.7
Murphy, W.R.8
Mangiapane, M.L.9
Hockel, G.M.10
Williams, I.H.11
Smith, W.H.12
Gumkowski, M.J.13
Shepard, R.M.14
Gardner, M.J.15
Nocerini, M.R.16
-
5
-
-
0028986487
-
Targeting HIV-1 protease: A test of drug-design methodologies
-
5. West, M.L. & Fairlie, D.P. (1995) Targeting HIV-1 protease: a test of drug-design methodologies. Trends Pharm. Sci. 16, 67-75.
-
(1995)
Trends Pharm. Sci.
, vol.16
, pp. 67-75
-
-
West, M.L.1
Fairlie, D.P.2
-
7
-
-
0029441398
-
Inhibitors of HIV proteinase
-
7. Martin, J.A., Redshaw, S. & Thomas, G.J. (1995) Inhibitors of HIV proteinase. Prog. Med. Chem. 32, 239-287.
-
(1995)
Prog. Med. Chem.
, vol.32
, pp. 239-287
-
-
Martin, J.A.1
Redshaw, S.2
Thomas, G.J.3
-
8
-
-
0029964107
-
Current knowledge and future prospects for the use of HIV-I protease inhibitors
-
8. Moyle, G. & Gazzard, D. (1996) Current knowledge and future prospects for the use of HIV-I protease inhibitors. Drugs 51, 701-712.
-
(1996)
Drugs
, vol.51
, pp. 701-712
-
-
Moyle, G.1
Gazzard, D.2
-
9
-
-
0029564143
-
Antifungal drug targets: Candida secreted aspartyl protease and fungal wall beta-glucan synthesis
-
9. Goldman, R.C., Frost, D.J., Capobianco, J.O., Kadam, S., Rasmussen, R.R. & Abad-Zapatero, C. (1995) Antifungal drug targets: Candida secreted aspartyl protease and fungal wall beta-glucan synthesis. Infect. Agents Dis. 4, 228-247.
-
(1995)
Infect. Agents Dis.
, vol.4
, pp. 228-247
-
-
Goldman, R.C.1
Frost, D.J.2
Capobianco, J.O.3
Kadam, S.4
Rasmussen, R.R.5
Abad-Zapatero, C.6
-
10
-
-
0031852685
-
Proteases of malaria parasites: New targets for chemotherapy
-
10. Rosenthal, P.J. (1998) Proteases of malaria parasites: new targets for chemotherapy. Emerg. Infect. Dis. 4, 49-57.
-
(1998)
Emerg. Infect. Dis.
, vol.4
, pp. 49-57
-
-
Rosenthal, P.J.1
-
11
-
-
0031437464
-
Versatile and stereoselective synthesis of diamino diol dipeptide isosteres, core units of pseudopeptide HIV protease inhibitors
-
11. Benedetti, F., Miertus, S., Norbedo, S., Tossi, A. & Zlatoidsky, P. (1997) Versatile and stereoselective synthesis of diamino diol dipeptide isosteres, core units of pseudopeptide HIV protease inhibitors. J. Org. Chem. 62, 9348-9353.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 9348-9353
-
-
Benedetti, F.1
Miertus, S.2
Norbedo, S.3
Tossi, A.4
Zlatoidsky, P.5
-
12
-
-
0001117597
-
Flexible synthesis of symmetric and non-symmetric HIV-1 protease inhibitors based on all-S-diaminodiol isosteres
-
12. Tossi, A., Antcheva, N., Benedetti, F., Norbedo, S., Miertus, S. & Romeo, D. (1999) Flexible synthesis of symmetric and non-symmetric HIV-1 protease inhibitors based on all-S-diaminodiol isosteres. Peptide Protein Lett. 6, 145-148.
-
(1999)
Peptide Protein Lett.
, vol.6
, pp. 145-148
-
-
Tossi, A.1
Antcheva, N.2
Benedetti, F.3
Norbedo, S.4
Miertus, S.5
Romeo, D.6
-
13
-
-
0029411538
-
Development pseudopeptide inhibitors of HIV-1 aspartic protease: Analysis and tuning of the subsite specificity
-
13. Tossi, A., Antcheva, N., Romeo, D. & Miertus, S. (1995) Development pseudopeptide inhibitors of HIV-1 aspartic protease: analysis and tuning of the subsite specificity. Peptide Res. 8, 2-8.
-
(1995)
Peptide Res.
, vol.8
, pp. 2-8
-
-
Tossi, A.1
Antcheva, N.2
Romeo, D.3
Miertus, S.4
-
14
-
-
0030533267
-
Design of new inhibitors of HIV-1 aspartic protease
-
14. Miertus, S., Furlan, M., Tossi, A. & Romeo, D. (1996) Design of new inhibitors of HIV-1 aspartic protease. Chem. Phys. 204, 173-180.
-
(1996)
Chem. Phys.
, vol.204
, pp. 173-180
-
-
Miertus, S.1
Furlan, M.2
Tossi, A.3
Romeo, D.4
-
15
-
-
0032567678
-
A computational study of the resistance of HIV-1 aspartic protease to the inhibitors ABT-538 and VX-478 and design of new analogues
-
15. Nair, C.A., Miertus, S., Tossi, A. & Romeo, D. (1998) A computational study of the resistance of HIV-1 aspartic protease to the inhibitors ABT-538 and VX-478 and design of new analogues. Biochem. Biophys. Res. Commun. 242, 545-551.
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.242
, pp. 545-551
-
-
Nair, C.A.1
Miertus, S.2
Tossi, A.3
Romeo, D.4
-
16
-
-
0025196082
-
2 symmetric inhibitors of HIV-1 protease
-
2 symmetric inhibitors of HIV-1 protease. J. Med. Chem. 33, 2687-2689.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2687-2689
-
-
Kempf, D.J.1
Norbeck, D.W.2
Codacovi, L.3
Wang, X.C.4
Kohlbrenner, W.E.5
Wideburg, N.E.6
Paul, D.A.7
Knigge, M.F.8
Vasavanonda, S.9
Craig-Kennard, A.10
Saldivar, A.11
Rosenbrook, W.12
Clement, J.J.13
Plattner, J.J.14
Erickson, J.15
-
17
-
-
0025778148
-
Synthesis of C-2-symmetric and pseudosymmetric HIV-1 protease inhibitors from D-mannitol and D-arabitol
-
17. Chenera, B., Boehm, J.C. & Dreyer, G.B. (1991) Synthesis of C-2-symmetric and pseudosymmetric HIV-1 protease inhibitors from D-mannitol and D-arabitol. Bioorg. Med. Chem. Lett. 1, 219-222.
-
(1991)
Bioorg. Med. Chem. Lett.
, vol.1
, pp. 219-222
-
-
Chenera, B.1
Boehm, J.C.2
Dreyer, G.B.3
-
18
-
-
0026045130
-
Stereocontrolled synthesis of HIV-1 protease inhibitors with C2 axis of symmetry
-
18. Ghosh, A.K., McKee, S.P. & Thompson, W.J. (1991) Stereocontrolled synthesis of HIV-1 protease inhibitors with C2 axis of symmetry. Tetrahedron Lett. 32, 5729-5732.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 5729-5732
-
-
Ghosh, A.K.1
McKee, S.P.2
Thompson, W.J.3
-
19
-
-
0026460702
-
2-symmetric diamino alcohols and diols for use in HIV protease inhibitors
-
2-symmetric diamino alcohols and diols for use in HIV protease inhibitors. J. Org. Chem. 57, 5692-5700.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 5692-5700
-
-
Kempf, D.J.1
Sowin, T.J.2
Doherty, E.M.3
Hannick, S.M.4
Codacovi, L.5
Henry, R.F.6
Green, B.E.7
Spanton, S.G.8
Norbeck, D.W.9
-
20
-
-
0001965855
-
6]. Synthesis of C2-symmetric (1S,2R,3R,4S)-1,4-diamino-2,3-diols
-
6]. Synthesis of C2-symmetric (1S,2R,3R,4S)-1,4-diamino-2,3-diols. J. Org. Chem. 57, 28-32.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 28-32
-
-
Konradi, A.W.1
Pedersen, S.F.2
-
22
-
-
0030973649
-
2-symmetric based diols, epoxides and dideoxy derivatives of HIV protease
-
2-symmetric based diols, epoxides and dideoxy derivatives of HIV protease. Tetrahedron 53, 4769-4778.
-
(1997)
Tetrahedron
, vol.53
, pp. 4769-4778
-
-
Gurjar, M.K.1
Pal, S.2
Rao, A.V.R.3
Pariza, R.J.4
Chorgade, M.S.5
-
23
-
-
0032558614
-
Regio-and stereoselective ring opening of 2,3-epoxyalcohols with diethylaluminium azide
-
23. Benedetti, F., Berti, F. & Norbedo, S. (1998) Regio-and stereoselective ring opening of 2,3-epoxyalcohols with diethylaluminium azide. Tetrahedron Lett. 39, 7971-7974.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 7971-7974
-
-
Benedetti, F.1
Berti, F.2
Norbedo, S.3
-
24
-
-
0029757151
-
Solution NMR evidence that the HIV-1 protease catalytic aspartyl groups have different ionization states in the complex formed with the asymmetric drug KNI-272
-
24. Wang, Y.X., Freedberg, D.I., Yarnazki, T., Wingfield, P.T., Stahl, S.J., Kaufman, J.D., Kiso, Y. & Torchia, D.A. (1996) Solution NMR evidence that the HIV-1 protease catalytic aspartyl groups have different ionization states in the complex formed with the asymmetric drug KNI-272. Biochemistry 35, 9945-9950.
-
(1996)
Biochemistry
, vol.35
, pp. 9945-9950
-
-
Wang, Y.X.1
Freedberg, D.I.2
Yarnazki, T.3
Wingfield, P.T.4
Stahl, S.J.5
Kaufman, J.D.6
Kiso, Y.7
Torchia, D.A.8
-
25
-
-
0003136860
-
CADD of new pseudopeptide inhibitors of HIV-1 aspartic protease
-
Sanz, F., Giraldo J. & Manaut, F., eds. Prous Science Publishers, Barcelona, Spain
-
25. Miertus, S., Antcheva, N., Tossi, A., Bizik, F., Benedetti, F., Gennaro, R. & Romeo, D. (1995) CADD of new pseudopeptide inhibitors of HIV-1 aspartic protease. In QSAR and Molecular Modelling: Concepts, Computational Tools and Biological Applications (Sanz, F., Giraldo J. & Manaut, F., eds.), pp. 567-572. Prous Science Publishers, Barcelona, Spain.
-
(1995)
QSAR and Molecular Modelling: Concepts, Computational Tools and Biological Applications
, pp. 567-572
-
-
Miertus, S.1
Antcheva, N.2
Tossi, A.3
Bizik, F.4
Benedetti, F.5
Gennaro, R.6
Romeo, D.7
-
26
-
-
0029860834
-
An effective organic solvent system for the dissolution of amino acids
-
26. Mitin, Y. (1996) An effective organic solvent system for the dissolution of amino acids. Int. J. Peptide Protein Res. 48, 374-376.
-
(1996)
Int. J. Peptide Protein Res.
, vol.48
, pp. 374-376
-
-
Mitin, Y.1
-
27
-
-
0029087303
-
Analysis of resistance to human immunodeficiency virus type 1 protease inhibitors by using matched bacterial expression and proviral infection vectors
-
27. Maschera, B., Furfine, E. & Blair, E.D. (1995) Analysis of resistance to human immunodeficiency virus type 1 protease inhibitors by using matched bacterial expression and proviral infection vectors. J. Virol. 69,5431-5436.
-
(1995)
J. Virol.
, vol.69
, pp. 5431-5436
-
-
Maschera, B.1
Furfine, E.2
Blair, E.D.3
-
28
-
-
0029585123
-
Atom/fragment contribution method for estimating octanol/water partition coefficients
-
28. Meylan, W.H. & Howard, P.H. (1995) Atom/fragment contribution method for estimating octanol/water partition coefficients. J. Pharm. Sci. 84, 83-92.
-
(1995)
J. Pharm. Sci.
, vol.84
, pp. 83-92
-
-
Meylan, W.H.1
Howard, P.H.2
-
29
-
-
0028690038
-
Design of symmetry-based, peptidomimetic inhibitors of human immunodeficiency virus protease
-
29. Kempf, D.J. (1994) Design of symmetry-based, peptidomimetic inhibitors of human immunodeficiency virus protease. Methods Enzymol. 241, 334-354.
-
(1994)
Methods Enzymol.
, vol.241
, pp. 334-354
-
-
Kempf, D.J.1
-
30
-
-
0028328704
-
2 symmetry-based diol inhibitors of HIV-1 protease
-
2 symmetry-based diol inhibitors of HIV-1 protease. J. Am. Chem. Soc. 116, 847-855.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 847-855
-
-
Hosur, M.V.1
Bhat, T.N.2
Kempf, D.J.3
Baldwin, E.T.4
Liu, B.5
Gulnik, S.6
Wideburg, N.E.7
Norbeck, D.W.8
Appelt, K.9
Erickson, J.W.10
-
31
-
-
0029031246
-
HIV-1 protease inhibitor HOE/BAY 793, structure - Activity relationships in a series of C-2-symmetric diols
-
31. Budt, K.-H., Peyman, A., Hansen, J., Knolle, J., Meichsner, C., Paessens, A., Ruppert, D. & Stowasser, B. (1995) HIV-1 protease inhibitor HOE/BAY 793, structure - activity relationships in a series of C-2-symmetric diols. Bioorg. Med. Chem. 3, 559-571.
-
(1995)
Bioorg. Med. Chem.
, vol.3
, pp. 559-571
-
-
Budt, K.-H.1
Peyman, A.2
Hansen, J.3
Knolle, J.4
Meichsner, C.5
Paessens, A.6
Ruppert, D.7
Stowasser, B.8
-
32
-
-
0027405931
-
Symmetry-based inhibitors of HIV protease. Structure-activity studies of acylated 2,4-diamino-1,5-diphenyl-3-hydroxypentane and 2,5-diamino-1,6-diphenylhexane
-
32. Kempf, D.J., Codacovi, L., Wang, X.C., Kohlbrenner, W.E., Wideburg, N.E., Saldivar, A., Vasavanonda, S., Marsh, K.C., Bryan, P., Sham, H.L., Green, B.E., Betebenner, D.A., Erickson, J. & Norbeck, T.W. (1993) Symmetry-based inhibitors of HIV protease. Structure-activity studies of acylated 2,4-diamino-1,5-diphenyl-3-hydroxypentane and 2,5-diamino-1,6-diphenylhexane. J. Med. Chem. 36, 320-330.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 320-330
-
-
Kempf, D.J.1
Codacovi, L.2
Wang, X.C.3
Kohlbrenner, W.E.4
Wideburg, N.E.5
Saldivar, A.6
Vasavanonda, S.7
Marsh, K.C.8
Bryan, P.9
Sham, H.L.10
Green, B.E.11
Betebenner, D.A.12
Erickson, J.13
Norbeck, T.W.14
-
33
-
-
0027411473
-
A symmetric inhibitor binds HIV-1 protease asymmetrically
-
33. Dreyer, G.B., Boehm, J.C., Chenera, B., DesJarlais, R.L., Hassell, A.M., Meek, T.D. & Tomaszek, T.A. (1993) A symmetric inhibitor binds HIV-1 protease asymmetrically. Biochemistry 32, 937-947.
-
(1993)
Biochemistry
, vol.32
, pp. 937-947
-
-
Dreyer, G.B.1
Boehm, J.C.2
Chenera, B.3
DesJarlais, R.L.4
Hassell, A.M.5
Meek, T.D.6
Tomaszek, T.A.7
-
34
-
-
0029001259
-
Subsite preferences of retroviral proteinases
-
34. Dunn, B., Gustchina, A., Vlodawer, A. & Kay, J. (1994) Subsite preferences of retroviral proteinases. Methods Enzymol. 241, 254-278.
-
(1994)
Methods Enzymol.
, vol.241
, pp. 254-278
-
-
Dunn, B.1
Gustchina, A.2
Vlodawer, A.3
Kay, J.4
-
35
-
-
0030964710
-
Structure of HOE/BAY 793 complexed to human immunodeficiency virus (HIV-1) protease in two different crystal forms. Structure/function relationship and influence of crystal packing
-
35. Lange-Savage, G., Berchtold, H., Liesum, A., Budt, K.H., Peyman, A., Knolle, J., Sedlacek, J., Fabry, M. & Hilgenfeld, R. (1997) Structure of HOE/BAY 793 complexed to human immunodeficiency virus (HIV-1) protease in two different crystal forms. Structure/function relationship and influence of crystal packing. Eur. J. Biochem. 248, 313-322.
-
(1997)
Eur. J. Biochem.
, vol.248
, pp. 313-322
-
-
Lange-Savage, G.1
Berchtold, H.2
Liesum, A.3
Budt, K.H.4
Peyman, A.5
Knolle, J.6
Sedlacek, J.7
Fabry, M.8
Hilgenfeld, R.9
-
36
-
-
0028915184
-
The prediction of the lipophilicity of peptidomimetics. A comparison between experimental and theoretical lipophilicity values of renin inhibitors and their building blocks
-
36. Karajiannis, H. & van de Waterbeemd, H. (1995) The prediction of the lipophilicity of peptidomimetics. A comparison between experimental and theoretical lipophilicity values of renin inhibitors and their building blocks. Pharmaceutica Acta Helvetiae 70, 67-77.
-
(1995)
Pharmaceutica Acta Helvetiae
, vol.70
, pp. 67-77
-
-
Karajiannis, H.1
Van De Waterbeemd, H.2
|