-
1
-
-
58149358949
-
Organic chemistry: Molecular diversity by design
-
Schreiber SL (2009) Organic chemistry: Molecular diversity by design. Nature 457:153-154.
-
(2009)
Nature
, vol.457
, pp. 153-154
-
-
Schreiber, S.L.1
-
2
-
-
33644846857
-
Small molecules: The missing link in the central dogma
-
Schreiber SL (2005) Small molecules: The missing link in the central dogma. Nat Chem Biol 1:64-66.
-
(2005)
Nat Chem Biol
, vol.1
, pp. 64-66
-
-
Schreiber, S.L.1
-
3
-
-
11144298973
-
Exploring biology with small organic molecules
-
Stockwell BR (2004) Exploring biology with small organic molecules. Nature 432:846-854.
-
(2004)
Nature
, vol.432
, pp. 846-854
-
-
Stockwell, B.R.1
-
4
-
-
33845903833
-
Drugs for bad bugs: Confronting the challenges of antibacterial discovery
-
DOI 10.1038/nrd2201, PII NRD2201
-
Payne DJ, Gwynn MN, Holmes DJ, Pompliano DL (2007) Drugs for bad bugs: Confronting the challenges of antibacterial discovery. Nat Rev Drug Discov 6:29-40. (Pubitemid 46020284)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.1
, pp. 29-40
-
-
Payne, D.J.1
Gwynn, M.N.2
Holmes, D.J.3
Pompliano, D.L.4
-
5
-
-
46849089254
-
Recent developments in fragment-based drug discovery
-
DOI 10.1021/jm8000373
-
Congreve M, Chessari G, Tisi D, Woodhead AJ (2008) Recent developments in fragment-based drug discovery. J Med Chem 51:3661-3680. (Pubitemid 351956496)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.13
, pp. 3661-3680
-
-
Congreve, M.1
Chessari, G.2
Tisi, D.3
Woodhead, A.J.4
-
6
-
-
67849113794
-
The rise of fragment-based drug discovery
-
Murray CW, Rees DC (2009) The rise of fragment-based drug discovery. Nat Chem 1:187-192.
-
(2009)
Nat Chem
, vol.1
, pp. 187-192
-
-
Murray, C.W.1
Rees, D.C.2
-
7
-
-
67649341990
-
From fragment to clinical candidate - A historical perspective
-
Chessari G, Woodhead AJ (2009) From fragment to clinical candidate-a historical perspective. Drug Discov Today 14:668-675.
-
(2009)
Drug Discov Today
, vol.14
, pp. 668-675
-
-
Chessari, G.1
Woodhead, A.J.2
-
8
-
-
34247194965
-
Virtual exploration of the chemical universe up to 11 atoms of C, N, O, F: Assembly of 26.4 million structures (110.9 million stereoisomers) and analysis for new ring systems, stereochemistry, physicochemical properties, compound classes, and drug discovery
-
DOI 10.1021/ci600423u
-
Fink T, Reymond J-L (2007) Virtual exploration of the chemical universe up to 11 atoms of C, N, O, F: Assembly of 26.4 million structures (110.9 million stereoisomers) and analysis for new ring systems, stereochemistry, physicochemical properties, compound classes, and drug discovery. J Chem Inf Model 47:342-353. (Pubitemid 46615939)
-
(2007)
Journal of Chemical Information and Modeling
, vol.47
, Issue.2
, pp. 342-353
-
-
Fink, T.1
Raymond, J.-L.2
-
9
-
-
37549048176
-
Fragment-based approaches to enzyme inhibition
-
Ciulli A, Abell C (2007) Fragment-based approaches to enzyme inhibition. Curr Opin Biotechnol 18:489-496.
-
(2007)
Curr Opin Biotechnol
, vol.18
, pp. 489-496
-
-
Ciulli, A.1
Abell, C.2
-
10
-
-
70350346470
-
Application of fragment growing and fragment linking to the discovery of inhibitors of mycobacterium tuberculosis pantothenate synthetase
-
Hung AW, et al. (2009) Application of fragment growing and fragment linking to the discovery of inhibitors of mycobacterium tuberculosis pantothenate synthetase. Angew Chem Int Ed 48:8452-8456.
-
(2009)
Angew Chem Int Ed
, vol.48
, pp. 8452-8456
-
-
Hung, A.W.1
-
11
-
-
0036051992
-
High-throughput crystallography for lead discovery in drug design
-
Blundell TL, Jhoti H, Abell C (2002) High-throughput crystallography for lead discovery in drug design. Nat Rev Drug Discov 1:45-54. (Pubitemid 37361403)
-
(2002)
Nature Reviews Drug Discovery
, vol.1
, Issue.1
, pp. 45-54
-
-
Blundell, T.L.1
Jhoti, H.2
Abell, C.3
-
12
-
-
84880296641
-
Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules
-
Galloway WRJD, Isidro-Llobet A, Spring DR (2010) Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules. Nat Commun 1:80.
-
(2010)
Nat Commun
, vol.1
, pp. 80
-
-
Wrjd, G.1
Isidro-Llobet, A.2
Spring, D.R.3
-
13
-
-
79952255911
-
Drug discovery: A question of library design
-
Hajduk PJ, Galloway WRJD, Spring DR (2011) Drug discovery: A question of library design. Nature 470:42-43.
-
(2011)
Nature
, vol.470
, pp. 42-43
-
-
Hajduk, P.J.1
Wrjd, G.2
Spring, D.R.3
-
14
-
-
33847381100
-
A decade of fragment-based drug design: Strategic advances and lessons learned
-
DOI 10.1038/nrd2220, PII NRD2220
-
Hajduk PJ, Greer J (2007) A decade of fragment-based drug design: Strategic advances and lessons learned. Nat Rev Drug Discov 6:211-219. (Pubitemid 46344625)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.3
, pp. 211-219
-
-
Hajduk, P.J.1
Greer, J.2
-
15
-
-
77952546241
-
Drugging challenging targets using fragmentbased approaches
-
Coyne AG, Scott DE, Abell C (2010) Drugging challenging targets using fragmentbased approaches. Curr Opin Chem Biol 14:299-307.
-
(2010)
Curr Opin Chem Biol
, vol.14
, pp. 299-307
-
-
Coyne, A.G.1
Scott, D.E.2
Abell, C.3
-
16
-
-
0034678033
-
Target-oriented and diversity-oriented organic synthesis in drug discovery
-
Schreiber SL (2000) Target-oriented and diversity-oriented organic synthesis in drug discovery. Science 287:1964-1969.
-
(2000)
Science
, vol.287
, pp. 1964-1969
-
-
Schreiber, S.L.1
-
18
-
-
78649527328
-
An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: Discovery of macrocyclic histone deacetylase inhibitors
-
Marcaurelle LA, et al. (2010) An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: Discovery of macrocyclic histone deacetylase inhibitors. J Am Chem Soc 132:16962-16976.
-
(2010)
J Am Chem Soc
, vol.132
, pp. 16962-16976
-
-
Marcaurelle, L.A.1
-
19
-
-
60249088794
-
A small molecule that binds hedgehog and blocks its signaling in human cells
-
Stanton BZ, et al. (2009) A small molecule that binds hedgehog and blocks its signaling in human cells. Nat Chem Biol 5:154-156.
-
(2009)
Nat Chem Biol
, vol.5
, pp. 154-156
-
-
Stanton, B.Z.1
-
20
-
-
33845208398
-
An oligomer-based approach to skeletal diversity in small-molecule synthesis
-
DOI 10.1021/ja065724a
-
Spiegel DA, Schroeder FC, Duvall JR, Schreiber SL (2006) An oligomer-based approach to skeletal diversity in small-molecule synthesis. J Am Chem Soc 128:14766-14767. (Pubitemid 44851590)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.46
, pp. 14766-14767
-
-
Spiegel, D.A.1
Schroeder, F.C.2
Duvall, J.R.3
Schreiber, S.L.4
-
21
-
-
37549020046
-
Towards the optimal screening collection: A synthesis strategy
-
Nielsen TE, Schreiber SL (2008) Towards the optimal screening collection: A synthesis strategy. Angew Chem Int Ed 47:48-56.
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 48-56
-
-
Nielsen, T.E.1
Schreiber, S.L.2
-
23
-
-
33744462355
-
Asymmetric synthesis of hydroxylated pyrrolidines, piperidines and related bioactive compounds: From N-acyliminium chemistry to N-α-carbanion chemistry
-
Huang P-Q (2006) Asymmetric synthesis of hydroxylated pyrrolidines, piperidines and related bioactive compounds: From N-acyliminium chemistry to N-α-carbanion chemistry. Synlett 8:1133-1149.
-
(2006)
Synlett
, vol.8
, pp. 1133-1149
-
-
Huang, P.-Q.1
-
24
-
-
0041350414
-
Synthesis of cyclic proline-containing peptides via ring-closing metathesis
-
DOI 10.1021/ol034370e
-
Harris PWR, Brimble MA, Gluckman PD (2003) Synthesis of cyclic proline-containing peptides via ring-closing metathesis. Org Lett 5:1847-1850. (Pubitemid 37161940)
-
(2003)
Organic Letters
, vol.5
, Issue.11
, pp. 1847-1850
-
-
Harris, P.W.R.1
Brimble, M.A.2
Gluckman, P.D.3
-
25
-
-
33845551868
-
Alkylation of amino acids without loss of the optical activity: Preparation of á-substituted proline derivatives. A case of self-reproduction of chirality
-
Seebach D, Boes M, Naef R, Schweizer WB (1983) Alkylation of amino acids without loss of the optical activity: Preparation of á-substituted proline derivatives. A case of self-reproduction of chirality. J Am Chem Soc 105:5390-5398.
-
(1983)
J Am Chem Soc
, vol.105
, pp. 5390-5398
-
-
Seebach, D.1
Boes, M.2
Naef, R.3
Schweizer, W.B.4
-
26
-
-
0032962277
-
4-Alkyl-2-trichloromethyloxazolidin-5-ones: Valuable precursors to enantiomerically pure C- and N-protected α-alkyl prolines
-
Wang H, Germanas JP (1999) 4-Alkyl-2-trichloromethyloxazolidin-5-ones: Valuable precursors to enantiomerically pure C- and N-protected α-alkyl prolines. Synlett 1999:33-36. (Pubitemid 29093052)
-
(1999)
Synlett
, Issue.1
, pp. 33-36
-
-
Wang, H.1
Germanas, J.P.2
-
27
-
-
33745806940
-
Synthesis of macrocyclic analogues of the neuroprotective agent glycyl-l-prolyl-l-glutamic acid (GPE)
-
DOI 10.1039/b605293b
-
Harris PWR, Brimble MA (2006) Synthesis of macrocyclic analogues of the neuroprotective agent glycyl-l-prolyl-l-glutamic acid (GPE). Org Biomol Chem 4:2696-2709. (Pubitemid 44034216)
-
(2006)
Organic and Biomolecular Chemistry
, vol.4
, Issue.14
, pp. 2696-2709
-
-
Harris, P.W.R.1
Brimble, M.A.2
-
28
-
-
0035903517
-
Rational molecular design and EPC synthesis of a type VI β-turn inducing peptide mimetic
-
DOI 10.1002/1521-3773(20010917)40:18<3361::AID-ANIE3361>3.0.CO;2-9
-
Hoffmann T, Lanig H, Waibel R, Gmeiner P (2001) Rational molecular design and EPC synthesis of a type VI β-turn inducing peptide mimetic. Angew Chem Int Ed 40:3361-3364. (Pubitemid 32916599)
-
(2001)
Angewandte Chemie - International Edition
, vol.40
, Issue.18
, pp. 3361-3364
-
-
Hoffmann, T.1
Lanig, H.2
Waibel, R.3
Gmeiner, P.4
-
29
-
-
70349275493
-
Oxyma: An efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion
-
Subirós-Funosas R, Prohens R, Barbas R, El-Faham A, Albericio F (2009) Oxyma: An efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion. Chem Eur J 15:9394-9403.
-
(2009)
Chem Eur J
, vol.15
, pp. 9394-9403
-
-
Subirós-Funosas, R.1
Prohens, R.2
Barbas, R.3
El-Faham, A.4
Albericio, F.5
-
30
-
-
52049093505
-
Synthesis of Sultam scaffolds via intramolecular oxa-Michael and diastereoselective Baylis-Hillman reactions
-
Zhou A, Hanson PR (2008) Synthesis of Sultam scaffolds via intramolecular oxa-Michael and diastereoselective Baylis-Hillman reactions. Org Lett 10:2951-2954.
-
(2008)
Org Lett
, vol.10
, pp. 2951-2954
-
-
Zhou, A.1
Hanson, P.R.2
-
31
-
-
2942678732
-
Decomposition of a key intermediate in ruthenium-catalyzed olefin metathesis reactions
-
DOI 10.1021/ja0488380
-
Hong SH, Day MW, Grubbs RH (2004) Decomposition of a key intermediate in ruthenium-catalyzed olefin metathesis reactions. J Am Chem Soc 126:7414-7415. (Pubitemid 38781455)
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.24
, pp. 7414-7415
-
-
Hong, S.H.1
Day, M.W.2
Grubbs, R.H.3
-
32
-
-
14844362056
-
Self-selection in olefin cross-metathesis: The effect of remote functionality
-
McNaughton BR, Bucholtz KM, Camaaño-Moure A, Miller BL (2005) Self-selection in olefin cross-metathesis: The effect of remote functionality. Org Lett 7:733-736.
-
(2005)
Org Lett
, vol.7
, pp. 733-736
-
-
McNaughton, B.R.1
Bucholtz, K.M.2
Camaaño-Moure, A.3
Miller, B.L.4
-
33
-
-
71049126548
-
Escape from flatland: Increasing saturation as an approach to improving clinical success
-
Lovering F, Bikker J, Humblet C (2009) Escape from flatland: Increasing saturation as an approach to improving clinical success. J Med Chem 52:6752-6756.
-
(2009)
J Med Chem
, vol.52
, pp. 6752-6756
-
-
Lovering, F.1
Bikker, J.2
Humblet, C.3
-
34
-
-
70350409235
-
The impact of aromatic ring count on compound developability-are too many aromatic rings a liability in drug design?
-
Ritchie TJ, Macdonald SJF (2009) The impact of aromatic ring count on compound developability-are too many aromatic rings a liability in drug design? Drug Discov Today 14:1011-1020.
-
(2009)
Drug Discov Today
, vol.14
, pp. 1011-1020
-
-
Ritchie, T.J.1
Macdonald, S.J.F.2
-
35
-
-
78650459806
-
Small molecules of different origins have distinct distributions of structural complexity that correlate with protein-binding profiles
-
Clemons PA, et al. (2010) Small molecules of different origins have distinct distributions of structural complexity that correlate with protein-binding profiles. Proc Natl Acad Sci USA 107:18787-18792.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 18787-18792
-
-
Clemons, P.A.1
-
36
-
-
13844312649
-
ZINC - A free database of commercially available compounds for virtual screening
-
Irwin JJ, Shoichet BK (2005) ZINC - A free database of commercially available compounds for virtual screening. J Chem Inf Model 45:177-182.
-
(2005)
J Chem Inf Model
, vol.45
, pp. 177-182
-
-
Irwin, J.J.1
Shoichet, B.K.2
-
37
-
-
22044441118
-
Fragment-based lead discovery: Leads by design
-
DOI 10.1016/S1359-6446(05)03511-7, PII S1359644605035117
-
Carr RAE, Congreve M, Murray CW, Rees DC (2005) Fragment-based lead discovery: Leads by design. Drug Discov Today 10:987-992. (Pubitemid 40967047)
-
(2005)
Drug Discovery Today
, vol.10
, Issue.14
, pp. 987-992
-
-
Carr, R.A.E.1
Congreve, M.2
Murray, C.W.3
Rees, D.C.4
-
38
-
-
0038512037
-
Molecular shape diversity of combinatorial libraries: A prerequisite for broad bioactivity
-
Sauer WHB, Schwarz MK (2003) Molecular shape diversity of combinatorial libraries: A prerequisite for broad bioactivity. J Chem Inf Comput Sci 43:987-1003.
-
(2003)
J Chem Inf Comput Sci
, vol.43
, pp. 987-1003
-
-
Sauer, W.H.B.1
Schwarz, M.K.2
|