-
1
-
-
0033964118
-
High-throughput and ultra-high-throughput screening: Solution- and cell-based approaches
-
Sundberg, S. High-throughput and ultra-high-throughput screening: solution- and cell-based approaches. Curr. Opin. Biotechnol. 11, 47-53 (2000).
-
(2000)
Curr. Opin. Biotechnol.
, vol.11
, pp. 47-53
-
-
Sundberg, S.1
-
2
-
-
0028773887
-
Structure-based drug design: Progress, results and challenges
-
Verlinde, C.L. & Hol, W.G. Structure-based drug design: progress, results and challenges. Structure 2, 577-87 (1994).
-
(1994)
Structure
, vol.2
, pp. 577-587
-
-
Verlinde, C.L.1
Hol, W.G.2
-
3
-
-
0031569368
-
Serendipity meets precision: The integration of structure-based drug design and combinatorial chemistry for efficient drug discovery
-
Salemme, F., Spurlino, J. & Bone, R. Serendipity meets precision: the integration of structure-based drug design and combinatorial chemistry for efficient drug discovery. Structure 15, 319-324 (1997).
-
(1997)
Structure
, vol.15
, pp. 319-324
-
-
Salemme, F.1
Spurlino, J.2
Bone, R.3
-
4
-
-
0026730489
-
Structure-based strategies for drug design and discovery
-
Kuntz, I. Structure-based strategies for drug design and discovery. Science 257, 1078-1082 (1992).
-
(1992)
Science
, vol.257
, pp. 1078-1082
-
-
Kuntz, I.1
-
5
-
-
0029836953
-
Discovering high affinity ligands for proteins: SAR by NMR
-
Shuker, S.B., Hajduk, P.J., Meadows, R.P. & Fesik, S.W. Discovering high affinity ligands for proteins: SAR by NMR. Science 274, 1531-1534 (1996).
-
(1996)
Science
, vol.274
, pp. 1531-1534
-
-
Shuker, S.B.1
Hajduk, P.J.2
Meadows, R.P.3
Fesik, S.W.4
-
6
-
-
0033213957
-
The SHAPES strategy: An NMR-based approach for lead generation in drug discovery
-
Fejzo, J. et al. The SHAPES strategy: an NMR-based approach for lead generation in drug discovery. Chem. Biol. 6, 755-769 (1999).
-
(1999)
Chem. Biol.
, vol.6
, pp. 755-769
-
-
Fejzo, J.1
-
7
-
-
0344558911
-
An experimental approach to mapping the binding surfaces of crystalline proteins
-
Allen, K.N. et al. An experimental approach to mapping the binding surfaces of crystalline proteins. J. Phys. Chem. 100, 2605-2611 (1996).
-
(1996)
J. Phys. Chem.
, vol.100
, pp. 2605-2611
-
-
Allen, K.N.1
-
8
-
-
0021871375
-
A computational procedure for determining energetically favorable binding sites on biologically important molecules
-
Goodford, P.J. A computational procedure for determining energetically favorable binding sites on biologically important molecules. J. Med. Chem. 28, 849-857 (1985).
-
(1985)
J. Med. Chem.
, vol.28
, pp. 849-857
-
-
Goodford, P.J.1
-
9
-
-
0027219536
-
Multiple copy simultaneous search and construction of ligands in binding sites: Application to inhibitors of HIV-1 aspartic proteinase
-
Caflish, A., Miranker, A. & Karplus, M. Multiple copy simultaneous search and construction of ligands in binding sites: application to inhibitors of HIV-1 aspartic proteinase. J. Med. Chem. 36, 2142-2167 (1993).
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2142-2167
-
-
Caflish, A.1
Miranker, A.2
Karplus, M.3
-
10
-
-
0001016942
-
Structure-based drug design
-
Kuntz, I.D., Meng, E.G. & Shoichet, B.K. Structure-based drug design. Accounts Chem. Res. 27, 117-123 (1994).
-
(1994)
Accounts Chem. Res.
, vol.27
, pp. 117-123
-
-
Kuntz, I.D.1
Meng, E.G.2
Shoichet, B.K.3
-
11
-
-
0026848170
-
In search of new lead compounds for trypanosomiasis drug desgin: A protein structure-based linked-fragment approach
-
Verlinde, C., Rudenko, G. & Hol, W. In search of new lead compounds for trypanosomiasis drug desgin: a protein structure-based linked-fragment approach. J. Comput. Aided Mol. Des. 6, 131-147 (1992).
-
(1992)
J. Comput. Aided Mol. Des.
, vol.6
, pp. 131-147
-
-
Verlinde, C.1
Rudenko, G.2
Hol, W.3
-
12
-
-
0029347588
-
Using electrospray ionization FTICR mass spectrometry to study competitive binding of inhibitors to carbonic anhydrase
-
Cheng, X. et al. Using electrospray ionization FTICR mass spectrometry to study competitive binding of inhibitors to carbonic anhydrase. J. Am. Chem. Soc. 117, 8859-8860 (1995).
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 8859-8860
-
-
Cheng, X.1
-
13
-
-
0001364796
-
Screening mixtures by affinity NMR
-
Lin, M., Shapiro, M.J. & Wareing, J.R. Screening mixtures by affinity NMR. J. Org. Chem. 62, 8930-8931 (1997).
-
(1997)
J. Org. Chem.
, vol.62
, pp. 8930-8931
-
-
Lin, M.1
Shapiro, M.J.2
Wareing, J.R.3
-
14
-
-
0034476897
-
Automated crystal mounting and data collection for protein crystallography
-
in press
-
Muchmore, S. et al. Automated crystal mounting and data collection for protein crystallography. Structure, in press.
-
Structure
-
-
Muchmore, S.1
-
15
-
-
0001928830
-
Antitrypanosomiasis drug development based on structures of glycolytic enzymes
-
ed. Veerapandian, P. Marcel Dekker, Inc, New York, NY
-
Verlinde, C., Kim, H., Berstein, B., Mande, S. & Hol, W. Antitrypanosomiasis drug development based on structures of glycolytic enzymes. In Structure-based drug design (ed. Veerapandian, P.) 365-394 (Marcel Dekker, Inc, New York, NY; 1997).
-
(1997)
Structure-based Drug Design
, pp. 365-394
-
-
Verlinde, C.1
Kim, H.2
Berstein, B.3
Mande, S.4
Hol, W.5
-
16
-
-
0031733174
-
Multifunctional potential of the plasminogen activation system in tumor invasion and metastasis
-
Reuning, U. et al. Multifunctional potential of the plasminogen activation system in tumor invasion and metastasis. Int. J. Oncol. 13, 896-906 (1998).
-
(1998)
Int. J. Oncol.
, vol.13
, pp. 896-906
-
-
Reuning, U.1
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