-
1
-
-
3042799070
-
A planning strategy for diversity-oriented synthesis
-
DOI 10.1002/anie.200300626
-
Burke M.D.& Schreiber S. L. A planning strategy for diversity-oriented synthesis. A ngew. Chem., Int. Ed. 4 3 46 - 58 ( 2004 ). A seminal introduction to diversity-oriented synthesis (DOS) and a discussion of various planning strategies in DOS. (Pubitemid 38063470)
-
(2004)
Angewandte Chemie - International Edition
, vol.43
, Issue.1
, pp. 46-58
-
-
Burke, M.D.1
Schreiber, S.L.2
-
2
-
-
0037416141
-
The small-molecule approach to biology
-
Schreiber S.L. The small-molecule approach to biology. Chem. Eng. News. 8 1 51-61 ( 2003 ).
-
(2003)
Chem. Eng. News.
, vol.8
, Issue.1
, pp. 51-61
-
-
Schreiber, S.L.1
-
5
-
-
21144440283
-
Chemical genetics to chemical genomics: Small molecules offer big insights
-
DOI 10.1039/b312875j
-
Spring D.R. Chemical genetics to chemical genomics: Small molecules offer big insights. Chem. Soc. Rev. 34 472-482 ( 2005 ). (Pubitemid 40880427)
-
(2005)
Chemical Society Reviews
, vol.34
, Issue.6
, pp. 472-482
-
-
Spring, D.R.1
-
6
-
-
34250621337
-
Chemical genetics: Elucidating biological systems with small-molecule compounds
-
DOI 10.1038/sj.jid.5700853, PII 5700853
-
Kawasumi M.& Nghiem P. Chemical genetics: Elucidating biological systems with small-molecule compounds. J. Invest. Dermat. 127 1577-1584 ( 2007 ). (Pubitemid 46933419)
-
(2007)
Journal of Investigative Dermatology
, vol.127
, Issue.7
, pp. 1577-1584
-
-
Kawasumi, M.1
Nghiem, P.2
-
8
-
-
33745726644
-
Chemical genetics
-
Walsh D.P.& Chang Y.T. Chemical genetics. Chem. Rev. 106 2476-2530 ( 2006 ).
-
(2006)
Chem. Rev.
, vol.106
, pp. 2476-2530
-
-
Walsh, D.P.1
Chang, Y.T.2
-
10
-
-
67649103954
-
Is synthesis the main hurdle for the generation of diversity in compound libraries for screening?
-
Galloway W. R. J.D.& Spring D.R. Is synthesis the main hurdle for the generation of diversity in compound libraries for screening? Exp. Opin. Drug Discov. 4 467-472 ( 2009 ).
-
(2009)
Exp. Opin. Drug Discov.
, vol.4
, pp. 467-472
-
-
Galloway, W.R.J.D.1
Spring, D.R.2
-
11
-
-
33644839988
-
Diversity-oriented synthesis: Exploring the intersections between chemistry and biology
-
Tan D.S. Diversity-oriented synthesis: Exploring the intersections between chemistry and biology. Nat. Chem. Biol. 1 74-84 ( 2005 ).
-
(2005)
Nat. Chem. Biol.
, vol.1
, pp. 74-84
-
-
Tan, D.S.1
-
12
-
-
0344515366
-
Diversity-oriented synthesis; a challenge for synthetic chemists
-
Spring D.R. Diversity-oriented synthesis; a challenge for synthetic chemists. Org. Biomol. Chem. 1 3867-3870 ( 2003 ).
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 3867-3870
-
-
Spring, D.R.1
-
13
-
-
20444378945
-
The principle of complementarity: Chemical versus biological space
-
DOI 10.1016/j.cbpa.2005.04.006, PII S1367593105000591, Combinatorial Chemistry
-
Haggarty S.J. The principle of complementarity: Chemical versus biological space. Curr. Opin. Chem. Biol. 9 296-303 ( 2005 ). (Pubitemid 40804553)
-
(2005)
Current Opinion in Chemical Biology
, vol.9
, Issue.3
, pp. 296-303
-
-
Haggarty, S.J.1
-
14
-
-
0038512037
-
Molecular shape diversity of combinatorial libraries: A prerequisite for broad bioactivity
-
An excellent discussion of the relationship between molecular shape (scaff old) diversity and functional diversity in small molecule libraries
-
Schawrz M.K.& Sauer W.H.B. Molecular shape diversity of combinatorial libraries: Aprerequisite for broad bioactivity. J. Chem. Inf. Comput. Sci. 43 987 - 1003 ( 2003 ). An excellent discussion of the relationship between molecular shape (scaff old) diversity and functional diversity in small molecule libraries.
-
(2003)
J. Chem. Inf. Comput. Sci.
, vol.43
, pp. 987-1003
-
-
Schawrz, M.K.1
Sauer, W.H.B.2
-
15
-
-
45149106841
-
Application of combinatorial chemistry science on modern drug discovery
-
Kennedy J.P. et al. Application of combinatorial chemistry science on modern drug discovery.J. Comb. Chem. 1 0 345-354 ( 2008 ).
-
(2008)
J. Comb. Chem.
, vol.1
, Issue.0
, pp. 345-354
-
-
Kennedy, J.P.1
-
16
-
-
0043123209
-
Molecular diversity through sugar scaff olds
-
Le G.T. e t al. Molecular diversity through sugar scaff olds. Drug Discov. Today 8 701-709 ( 2003 ).
-
(2003)
Drug Discov. Today
, vol.8
, pp. 701-709
-
-
Le, G.T.1
-
18
-
-
41149097628
-
Diversity-oriented synthesis; A spectrum of approaches and results
-
DOI 10.1039/b719372f
-
Spandl R.J. Bender A.& Spring D.R. Diversity-oriented synthesis; a spectrum of approaches and results. Org. Biomol. Chem. 6 1149-1158 ( 2008 ). (Pubitemid 351432832)
-
(2008)
Organic and Biomolecular Chemistry
, vol.6
, Issue.7
, pp. 1149-1158
-
-
Spandl, R.J.1
Bender, A.2
Spring, D.R.3
-
19
-
-
0142147275
-
Generating diverse skeletons of small molecules combinatorially
-
DOI 10.1126/science.1089946
-
Burke M.D. Berger E. M.& Schreiber S. L. Generating diverse skeletons of small molecules combinatorially. Science 302 613-618 ( 2003 ). (Pubitemid 37310911)
-
(2003)
Science
, vol.302
, Issue.5645
, pp. 613-618
-
-
Burke, M.D.1
Berger, E.M.2
Schreiber, S.L.3
-
21
-
-
34447517392
-
Scaffold composition and biological relevance of screening libraries
-
DOI 10.1038/nchembio0807-442, PII NCHEMBIO0807442
-
Shelat A.A.& Guy R.K. Scaff old composition and biological relevance of screening libraries. N at. Chem. Biol. 3 442-446 ( 2007 ). (Pubitemid 47080378)
-
(2007)
Nature Chemical Biology
, vol.3
, Issue.8
, pp. 442-446
-
-
Shelat, A.A.1
Guy, R.K.2
-
22
-
-
71049126548
-
Escape from flatland: Increasing saturation as an approach to improving clinical success
-
Lovering F. Bikker J.& Humblet C. Escape from Flatland: Increasing saturation as an approach to improving clinical success.J. Med. Chem. 5 2 6752-6756 ( 2009 ).
-
(2009)
J. Med. Chem.
, vol.5
, Issue.2
, pp. 6752-6756
-
-
Lovering, F.1
Bikker, J.2
Humblet, C.3
-
23
-
-
11144320699
-
Navigating chemical space for biology and medicine
-
DOI 10.1038/nature03193
-
Lipinski C.& Hopkins A. Navigating chemical space for biology and medicine. N ature 432 855 - 861 ( 2004 ). A useful discussion of the concepts of total chemical space and biologically relevant chemical space. (Pubitemid 40037141)
-
(2004)
Nature
, vol.432
, Issue.7019
, pp. 855-861
-
-
Lipinski, C.1
Hopkins, A.2
-
26
-
-
34247109045
-
Natural products as sources of new drugs over the last 25 years
-
DOI 10.1021/np068054v
-
Newman D.J.& Cragg G. M. Natural products as sources of new drugs over the last 25 years. J Nat. Prod. 70 461-477 ( 2007 ). (Pubitemid 46595760)
-
(2007)
Journal of Natural Products
, vol.70
, Issue.3
, pp. 461-477
-
-
Newman, D.J.1
Cragg, G.M.2
-
27
-
-
33746001269
-
Antibacterial natural products in medicinal chemistry - Exodus or revival?
-
von Nussbaum F. Brands M. Hinzen B. Weigand S.& Habich D. Antibacterial natural products in medicinal chemistry - Exodus or revival? Angew. Chem., Int. Ed. 4 5 5072-5129 ( 2006 ).
-
(2006)
Angew. Chem., Int. Ed.
, vol.4
, Issue.5
, pp. 5072-5129
-
-
Von Nussbaum, F.1
Brands, M.2
Hinzen, B.3
Weigand, S.4
Habich, D.5
-
28
-
-
34547265045
-
Properties and architecture of drugs and natural products revisited
-
Schneider G.& Grabowski K. Properties and architecture of drugs and natural products revisited. Curr. Chem. Biol. 1 115-127 ( 2007 ).
-
(2007)
Curr. Chem. Biol.
, vol.1
, pp. 115-127
-
-
Schneider, G.1
Grabowski, K.2
-
29
-
-
58149358949
-
Molecular diversity by design
-
An interesting discussion of the limitations of ? traditional ? small molecule collections and how these can be addressed using diversity-driven synthetic approaches such as DOS
-
Schreiber S.L. Molecular diversity by design. Nature 4 57 153 - 154 ( 2009 ). An interesting discussion of the limitations of ? traditional ? small molecule collections and how these can be addressed using diversity-driven synthetic approaches such as DOS.
-
(2009)
Nature
, vol.457
, pp. 153-154
-
-
Schreiber, S.L.1
-
30
-
-
37549020046
-
Diversity-oriented synthesis- Towards the optimal screening collection: Asynthesis strategy
-
A useful introduction to the build-couple-pair strategy, a common strategic feature in many DOS pathways
-
Nielsen T. E.& Schreiber S. L. Diversity-oriented synthesis- Towards the optimal screening collection: Asynthesis strategy. A ngew. Chem., Int. Ed. 4 7 48 - 56 ( 2008 ). A useful introduction to the build-couple-pair strategy, a common strategic feature in many DOS pathways.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 48-56
-
-
Nielsen, T.E.1
Schreiber, S.L.2
-
31
-
-
33751544571
-
What's in a number?
-
DOI 10.1038/nrd2205, PII NRD2205
-
Drews J. What's in a number? N at. Rev. Drug Discov. 5 975 ( 2006 ). (Pubitemid 44835123)
-
(2006)
Nature Reviews Drug Discovery
, vol.5
, Issue.12
, pp. 975
-
-
Drews, J.1
-
32
-
-
33646128970
-
Breaking the spell: Drug discovery based on modulating protein-protein interactions
-
Strosberg A.D. Breaking the spell: Drug discovery based on modulating protein-protein interactions. E xpert Rev. Proteomics 1 141-143 ( 2004 ).
-
(2004)
Expert Rev. Proteomics
, vol.1
, pp. 141-143
-
-
Strosberg, A.D.1
-
33
-
-
59649093964
-
The state of the art of chemical biology
-
Schreiber S.L. The state of the art of chemical biology. Chem. Biol. Chem. 1 0 26-29 ( 2009 ).
-
(2009)
Chem. Biol. Chem.
, vol.1
, Issue.0
, pp. 26-29
-
-
Schreiber, S.L.1
-
34
-
-
77953592675
-
Stereochemical and skeletal diversity arising from amino propargylic alcohols
-
Pizzirani D. Kaya T. Clemons P. A.& Schreiber S. L. Stereochemical and skeletal diversity arising from amino propargylic alcohols. Org. Lett. 1 2 2822 - 2825 ( 2010 ).
-
(2010)
Org. Lett.
, vol.12
, pp. 2822-2825
-
-
Pizzirani, D.1
Kaya, T.2
Clemons, P.A.3
Schreiber, S.L.4
-
35
-
-
77952542911
-
Current strategies for diversity-oriented synthesis
-
Dandapani S.& Marcaurelle L.A. Current strategies for diversity-oriented synthesis. Curr. Opin. Chem. Biol. 14 362 - 370 ( 2010 ).
-
(2010)
Curr. Opin. Chem. Biol.
, vol.14
, pp. 362-370
-
-
Dandapani, S.1
Marcaurelle, L.A.2
-
36
-
-
33845903833
-
Drugs for bad bugs: Confronting the challenges of antibacterial discovery
-
DOI 10.1038/nrd2201, PII NRD2201
-
Payne D.J. Gwynn M.N. Holmes D.J.& Pompliano D.L. Drugs for bad bugs: Confronting the challenges of antibacterial discovery. Nat. Rev. Drug Discov. 6 29-40 ( 2007 ). (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
-
37
-
-
65549121692
-
Aziridines as intermediates in diversity-oriented syntheses of alkaloids
-
Taylor A.M.& Schreiber S.L. Aziridines as intermediates in diversity-oriented syntheses of alkaloids. Tet. Lett. 5 0 3230-3233 ( 2009 ).
-
(2009)
Tet. Lett.
, vol.50
, pp. 3230-3233
-
-
Taylor, A.M.1
Schreiber, S.L.2
-
38
-
-
33746047675
-
Discovery of protein phosphatase inhibitor classes by biology-oriented synthesis
-
DOI 10.1073/pnas.0601490103
-
Noren-Muller A. et al. Discovery of protein phosphatase inhibitor classes by biology-oriented synthesis. P roc. Natl Acad. Sci. USA 103 10606-10611 ( 2006 ). (Pubitemid 44078024)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.28
, pp. 10606-10611
-
-
Noren-Muller, A.1
Reis-Correa Jr., I.2
Prinz, H.3
Rosenbaum, C.4
Saxena, K.5
Schwalbe, H.J.6
Vestweber, D.7
Cagna, G.8
Schunk, S.9
Schwarz, O.10
Schiewe, H.11
Waldmann, H.12
-
40
-
-
77954772461
-
On the potential of natural products in the discovery of pharma leads: A case for reassessment
-
Danishefsky S. On the potential of natural products in the discovery of pharma leads: A case for reassessment. Nat. Prod. Rep. 27 1114-1116.
-
Nat. Prod. Rep.
, vol.27
, pp. 1114-1116
-
-
Danishefsky, S.1
-
41
-
-
28444498830
-
Charting biologically relevant chemical space: A structural classification of natural products (SCONP)
-
DOI 10.1073/pnas.0503647102
-
Koch M.A. et al. Charting biologically relevant chemical space: Astructural classifi cation of natural products (SCONP). Proc. Natl Acad. Sci. USA 1 02 17272-17277 ( 2005 ). (Pubitemid 41740856)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.48
, pp. 17272-17277
-
-
Koch, M.A.1
Schuffenhauer, A.2
Scheck, M.3
Wetzel, S.4
Casaulta, M.5
Odermatt, A.6
Ertl, P.7
Weldmann, H.8
-
42
-
-
45249123879
-
Structural diversity of organic chemistry. A scaffold analysis of the CAS Registry
-
DOI 10.1021/jo8001276
-
Lipkus A.H. e t al. Structural diversity of organic chemistry. A scaff old analysis of the CAS Registry. J. Org. Chem. 73 4443-4451 ( 2008 ). (Pubitemid 351842458)
-
(2008)
Journal of Organic Chemistry
, vol.73
, Issue.12
, pp. 4443-4451
-
-
Lipkus, A.H.1
Yuan, Q.2
Lucas, K.A.3
Funk, S.A.4
Bartelt III, W.F.5
Schenck, R.J.6
Trippe, A.J.7
-
43
-
-
77952350796
-
Multistep microwave-assisted divergent synthesis of indolo-fused pyrazino-/aiazepinoquinoxalinones on PEG support
-
Lai J. Salunke D.B.& Sun C. Multistep microwave-assisted divergent synthesis of indolo-fused pyrazino-/aiazepinoquinoxalinones on PEG support. O rg. Lett. 1 2 2174 - 2177 ( 2010 ).
-
(2010)
O rg. Lett.
, vol.12
, pp. 2174-2177
-
-
Lai, J.1
Salunke, D.B.2
Sun, C.3
-
44
-
-
0036015844
-
Teaching target-oriented and diversity-oriented organic synthesis at Harvard University
-
DOI 10.1016/S1074-5521(02)00143-6, PII S1074552102001436
-
Burke M.D.& Lalic G. Teaching target-oriented and diversity-oriented organic synthesis at Harvard University. Chem. Biol. 9 535-541 ( 2002 ). (Pubitemid 34593033)
-
(2002)
Chemistry and Biology
, vol.9
, Issue.5
, pp. 535-541
-
-
Burke, M.D.1
Lalic, G.2
-
46
-
-
34047239151
-
Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaff olds employing inter- and intramolecular mitsunobu reactions
-
Mishra J.K.& Panda G. Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaff olds employing inter- and intramolecular Mitsunobu reactions. J. Comb. Chem. 9 321-338 ( 2007 ).
-
(2007)
J. Comb. Chem.
, vol.9
, pp. 321-338
-
-
Mishra, J.K.1
Panda, G.2
-
47
-
-
4544326369
-
Synthetic strategy toward skeletal diversity via solid-supported, otherwise unstable reactive intermediates
-
DOI 10.1002/anie.200353466
-
Taylor S.J. Taylor A. M.& Schreiber S. L. Synthetic strategy toward skeletal diversity via solid-supported, Otherwise unstable reactive intermediates. Angew. Chem., Int. Ed. 4 3 1681-1685 ( 2004 ). (Pubitemid 39257862)
-
(2004)
Angewandte Chemie - International Edition
, vol.43
, Issue.13
, pp. 1681-1685
-
-
Taylor, S.J.1
Taylor, A.M.2
Schreiber, S.L.3
-
48
-
-
7444242717
-
A synthesis strategy yielding skeletally diverse small molecules combinatorially
-
DOI 10.1021/ja0457415
-
Burke M.D. Berger E. M.& Schreiber S. L. A synthesis strategy yielding skeletally diverse small molecules combinatorially. J. Am. Chem. Soc. 1 26 14095-14104 ( 2004 ). (Pubitemid 39447088)
-
(2004)
Journal of the American Chemical Society
, vol.126
, Issue.43
, pp. 14095-14104
-
-
Burke, M.D.1
Berger, E.M.2
Schreiber, S.L.3
-
49
-
-
33746720909
-
Skeletal diversity construction via a branching synthetic strategy
-
DOI 10.1039/b607710b
-
Wyatt E.E. et al. Skeletal diversity construction via a branching synthetic strategy. Chem. Commun. 3296-3298 ( 2006 ). (Pubitemid 44167928)
-
(2006)
Chemical Communications
, Issue.31
, pp. 3296-3298
-
-
Wyatt, E.E.1
Fergus, S.2
Galloway, W.R.J.D.3
Bender, A.4
Fox, D.J.5
Plowright, A.T.6
Jessiman, A.S.7
Welch, M.8
Spring, D.R.9
-
50
-
-
12344293904
-
Skeletal diversity via a folding pathway: Synthesis of indole alkaloid-like skeletons
-
DOI 10.1021/ol047945w
-
Oguri H.& Schreiber S.L. Skeletal diversity via a folding pathway: Synthesis of indole alkaloid-like skeletons. Org. Lett. 7 47-50 ( 2005 ). (Pubitemid 40138308)
-
(2005)
Organic Letters
, vol.7
, Issue.1
, pp. 47-50
-
-
Oguri, H.1
Schreiber, S.L.2
-
51
-
-
77951133670
-
Reagent based DOS: A' Click, Click, Cyclize ' strategy to probe chemical space
-
Rolfe A. Lushington G.H.& Hanson P.R. Reagent based DOS: A' Click, Click, Cyclize ' strategy to probe chemical space. Org. Biomol. Chem. 8 2198-2203.
-
Org. Biomol. Chem.
, vol.8
, pp. 2198-2203
-
-
Rolfe, A.1
Lushington, G.H.2
Hanson, P.R.3
-
52
-
-
60849102180
-
Click, click, cyclize : ADOS approach to sultams utilizing vinyl sulfonamide linchpins
-
Zhou A. Rayabarapu D.& Hanson P.R. ' Click, click, cyclize ' : ADOS approach to sultams utilizing vinyl sulfonamide linchpins. Org. Lett. 11 531-534 ( 2009 ).
-
(2009)
Org. Lett.
, vol.11
, pp. 531-534
-
-
Zhou, A.1
Rayabarapu, D.2
Hanson, P.R.3
-
53
-
-
77951837637
-
The tert-butylsulfi namide lynchpin in transition-metal-mediated multiscaff old library synthesis
-
Bauer R.A. DiBlasi C.M.& Tan D.S. The tert-butylsulfi namide lynchpin in transition-metal-mediated multiscaff old library synthesis. Org. Lett. 12 2084-2087.
-
Org. Lett.
, vol.12
, pp. 2084-2087
-
-
Bauer, R.A.1
DiBlasi, C.M.2
Tan, D.S.3
-
54
-
-
33746272686
-
Short synthesis of skeletally and stereochemically diverse small molecules by coupling petasis condensation reactions to cyclization reactions
-
DOI 10.1002/anie.200600497
-
Kumagai N. Muncipinto G.& Schreiber S. L. Short synthesis of skeletally and stereochemically diverse small molecules by coupling petasis condensation reactions to cyclization reactions. Angew. Chem., Int. Ed. 45 3635-3638 ( 2006 ). (Pubitemid 44105728)
-
(2006)
Angewandte Chemie - International Edition
, vol.45
, Issue.22
, pp. 3635-3638
-
-
Kumagai, N.1
Muncipinto, G.2
Schreiber, S.L.3
-
55
-
-
42249095476
-
Anti-MRSA agent discovery using diversity-oriented synthesis
-
Th omas G.L. e t al. Anti-MRSA agent discovery using diversity-oriented synthesis. A ngew. Chem., Int. Ed. 47 2808-2812 ( 2008 ).
-
(2008)
A ngew. Chem., Int. Ed.
, vol.47
, pp. 2808-2812
-
-
Thomas, G.L.1
-
56
-
-
3042717144
-
Complete functionalisation of small and large diameter bromopolystyrene beads; applications for solid-supported reagents, scavengers and diversity-oriented synthesis
-
Th omas G.L. Ladlow M.& Spring D.R. Complete functionalisation of small and large diameter bromopolystyrene beads; applications for solid-supported reagents, scavengers and diversity-oriented synthesis. Org. Biomol. Chem. 2 1679-1681 ( 2004 ).
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 1679-1681
-
-
Thomas, G.L.1
Ladlow, M.2
Spring, D.R.3
-
57
-
-
58149346448
-
Synthesis of natural- product-like molecules with over eighty distinct scaff olds
-
This work describes the synthesis of a library of compounds based around 84 distinct molecular scaff olds, arguably representing the current state- of-theart for scaff old diversity generated in a synthetic small molecule library
-
Morton D. Leach S. Cordier C. Warriner S.& Nelson, A. Synthesis of natural- product-like molecules with over eighty distinct scaff olds. A ngew. Chem., Int. Ed. 4 8 104 - 109 ( 2009 ). Th is work describes the synthesis of a library of compounds based around 84 distinct molecular scaff olds, arguably representing the current state- of-theart for scaff old diversity generated in a synthetic small molecule library.
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 104-109
-
-
Morton, D.1
Leach, S.2
Cordier, C.3
Warriner, S.4
Nelson, A.5
-
58
-
-
77952542304
-
Recent advances in multicomponent reactions for diversity-oriented synthesis
-
Biggs-Houck J.E. Younai A.& Shaw J.T. Recent advances in multicomponent reactions for diversity-oriented synthesis. Curr. Opin. Chem. Biol. 14 371-382.
-
Curr. Opin. Chem. Biol.
, vol.14
, pp. 371-382
-
-
Biggs-Houck, J.E.1
Younai, A.2
Shaw, J.T.3
-
59
-
-
20444383539
-
Assessment of structural diversity in combinatorial synthesis
-
DOI 10.1016/j.cbpa.2005.03.004, PII S1367593105000517, Combinatorial Chemistry
-
Fergus S. Bender A.& Spring D.R. Assessment of structural diversity in combinatorial synthesis. Curr. Opin. Chem. Biol. 9 304-309 ( 2005 ). (Pubitemid 40804554)
-
(2005)
Current Opinion in Chemical Biology
, vol.9
, Issue.3
, pp. 304-309
-
-
Fergus, S.1
Bender, A.2
Spring, D.R.3
-
60
-
-
14644431061
-
Managing molecular diversity
-
DOI 10.1039/b209064n
-
Perez J.J. Managing molecular diversity. Chem. Soc. Rev. 34 143-152 ( 2005 ). (Pubitemid 40311447)
-
(2005)
Chemical Society Reviews
, vol.34
, Issue.2
, pp. 143-152
-
-
Perez, J.J.1
-
61
-
-
10344230435
-
Molecular similarity: A key technique in molecular informatics
-
Bender A.& Glen R.C. Molecular similarity: A key technique in molecular informatics. Org. Biomol. Chem. 2 3204-3218 ( 2004 ).
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 3204-3218
-
-
Bender, A.1
Glen, R.C.2
-
62
-
-
40449141013
-
What is principal component analysis?
-
DOI 10.1038/nbt0308-303, PII NBT0308303
-
Ringner M. What is principal component analysis? N at. Biotechnol. 2 6 303-304 ( 2008 ). (Pubitemid 351355122)
-
(2008)
Nature Biotechnology
, vol.26
, Issue.3
, pp. 303-304
-
-
Ringner, M.1
-
63
-
-
68049098031
-
Interactive exploration of chemical space with scaff old hunter
-
Wetzel S. e t al. Interactive exploration of chemical space with Scaff old Hunter. Nat. Chem. Biol. 5 581-583 ( 2009 ).
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 581-583
-
-
Wetzel, S.1
-
64
-
-
68049094985
-
Bioactivity-guided mapping and navigation of chemical space
-
Renner S. et al. Bioactivity-guided mapping and navigation of chemical space. Nat. Chem. Biol. 5 585-592 ( 2009 ).
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 585-592
-
-
Renner, S.1
-
66
-
-
72249088386
-
Identification of lead compounds as antagonists of protein Bcl-x(L) with a diversity-oriented multidisciplinary approach
-
Di Micco S. e t al. Identifi cation of lead compounds as antagonists of protein Bcl-x(L) with a diversity-oriented multidisciplinary approach. J. Med. Chem. 52 7856-7867 ( 2009 ).
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7856-7867
-
-
Di Micco, S.1
-
67
-
-
0037061492
-
Dissecting glucose signalling with diversity-oriented synthesis and small-molecule microarrays
-
DOI 10.1038/416653a
-
Kuruvilla F.G. Shamji A.F. Sternson S.M. Hergenrother P.J.& Schreiber S.L. Dissecting glucose signalling with diversity-oriented synthesis and small-molecule microarrays. N ature 416 653-657 ( 2002 ). (Pubitemid 34406768)
-
(2002)
Nature
, vol.416
, Issue.6881
, pp. 653-657
-
-
Kuruvilla, F.G.1
Shamji, A.F.2
Sternson, S.M.3
Hergenrother, P.J.4
Schreiber, S.L.5
-
68
-
-
60249088794
-
A small molecule that binds Hedgehog and blocks its signaling in human cells
-
Stanton B.Z. et al. A small molecule that binds Hedgehog and blocks its signaling in human cells. Nat. Chem. Biol. 5 154-156 ( 2009 ).
-
(2009)
Nat. Chem. Biol.
, vol.5
, pp. 154-156
-
-
Stanton, B.Z.1
-
69
-
-
34447535439
-
Synthesis of diverse lactam carboxamides leading to the discovery of a new transcription-factor inhibitor
-
DOI 10.1002/anie.200700762
-
Ng P.Y. Tang Y.C. Knosp W.M. Stadler H.S.& Shaw J.T. Synthesis of diverse lactam carhoxamides leading to the discovery of a new transcriptionfactor inhibitor. Angew. Chem., Int. Ed. 4 6 5352-5355 ( 2007 ). (Pubitemid 47067632)
-
(2007)
Angewandte Chemie - International Edition
, vol.46
, Issue.28
, pp. 5352-5355
-
-
Ng, P.Y.1
Tang, Y.2
Knosp, W.M.3
Stadler, H.S.4
Shaw, J.T.5
-
70
-
-
0038713943
-
Discovery of an inhibitor of a transcription factor using small molecule microarrays and diversity-oriented synthesis
-
DOI 10.1021/ja0352698
-
Koehler A.N. Shamji A.F.& Schreiber S.L. Discovery of an inhibitor of a transcription factor using small molecule microarrays and diversity-oriented synthesis.J. Am. Chem. Soc. 125 8420-8421 ( 2003 ). (Pubitemid 36858396)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.28
, pp. 8420-8421
-
-
Koehler, A.N.1
Shamji, A.F.2
Schreiber, S.L.3
-
71
-
-
63049104834
-
Identification of an anti-MRSA dihydrofolate reductase inhibitor from a diversity-oriented synthesis
-
The authors report on the mode of action of an inhibitor of MRSA discovered from a diversity-oriented synthesis program
-
Wyatt E.E. et al. Identifi cation of an anti-MRSA dihydrofolate reductase inhibitor from a diversity-oriented synthesis. Chem. Commun. 4962 - 4964 ( 2008 ). The authors report on the mode of action of an inhibitor of MRSA discovered from a diversity-oriented synthesis program.
-
(2008)
Chem. Commun.
, pp. 4962-4964
-
-
Wyatt, E.E.1
-
72
-
-
0034678033
-
Target-oriented and diversity-oriented organic synthesis in drug discovery
-
DOI 10.1126/science.287.5460.1964
-
Schreiber S. L. Target-oriented and diversity-oriented organic synthesis in drug discovery. S cience 287 1964-1969 ( 2000 ). (Pubitemid 30158663)
-
(2000)
Science
, vol.287
, Issue.5460
, pp. 1964-1969
-
-
Schreiber, S.L.1
-
73
-
-
0034647234
-
Towards diversity-oriented, stereoselective syntheses of biaryl- or bis(aryl)metal-containing medium rings [11]
-
DOI 10.1021/ja0010507
-
Spring D.R. Krishnan S.& Schreiber S. L. Towards diversity-oriented, stereoselective syntheses of Biaryl- or Bis(aryl)metal-containing medium rings. J. Am. Chem. Soc. 1 12 5656-5657 ( 2000 ). (Pubitemid 30431093)
-
(2000)
Journal of the American Chemical Society
, vol.122
, Issue.23
, pp. 5656-5657
-
-
Spring, D.R.1
Krishnan, S.2
Schreiber, S.L.3
-
74
-
-
0037138650
-
Diversity-oriented synthesis of biaryl-containing medium rings using a one bead/one stock solution platform
-
DOI 10.1021/ja017248o
-
Spring D.R. Krishnan S. Blackwell H. E.& Schreiber S. L. Diversity oriented synthesis of biaryl-containing medium rings using a one bead/one stock solution platform. J. Am. Chem. Soc. 124 1354-1363 ( 2002 ). (Pubitemid 34169142)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.7
, pp. 1354-1363
-
-
Spring, D.R.1
Krishnan, S.2
Blackwell, H.E.3
Schreiber, S.L.4
-
75
-
-
84880301152
-
-
Broad Institute Chemical Biology Platform, Accessed 24 May 2010
-
Broad Institute Chemical Biology Platform [ http://www.broadinstitute. org/science/platforms/chemical-biology-platform/chemical-biology-platform ]. Accessed 24 May 2010.
-
-
-
-
76
-
-
84880270436
-
-
Memorial Sloan-Kettering Cancer Center,Accessed 24 May 2010
-
Memorial Sloan-Kettering Cancer Center [ http://www.mskcc.org/mskcc/ html/5804.cfm ]. Accessed 24 May 2010.
-
-
-
-
77
-
-
84880323420
-
-
The Pub Chem Project,Accessed 2 August 2010
-
The PubChem Project [ http://pubchem.ncbi.nlm.nih.gov/ ]. Accessed 2 August 2010.
-
-
-
-
78
-
-
84880262464
-
-
The NIH Common Fund Molecular Libraries and Imaging,Accessed 24 May 2010
-
The NIH Common Fund Molecular Libraries and Imaging [ http://nihroadmap. nih.gov/molecularlibraries ]. Accessed 24 May 2010.
-
-
-
-
79
-
-
84880323412
-
-
High throughput screening in academia drug discovery initiatives at the University of Kansas,Accessed 24 May 2010
-
McDonald P.R. e t al. High throughput screening in academia drug discovery initiatives at the University of kansas [ http://www.ddw-online.com/ screening/239393/high-throughput-screening-in-academia-drug-discovery- initiatives-at-the-university-of-kansas.html ] (2008). Accessed 24 May 2010.
-
-
-
McDonald, P.R.1
-
80
-
-
33847381100
-
A decade of fragment-based drug design: Strategic advances and lessons learned
-
DOI 10.1038/nrd2220, PII NRD2220
-
Hajduk P.J.& Greer J. A decade of fragment-based drug design: Strategic advances and lessons learned. Nat. Rev. Drug Discov. 6 211-219 ( 2007 ). (Pubitemid 46344625)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.3
, pp. 211-219
-
-
Hajduk, P.J.1
Greer, J.2
-
81
-
-
63749103205
-
Fragment-based ligand discovery
-
Fischer M.& Hubbard R.E. Fragment-based ligand discovery. M ol. Interv. 9 22-30 ( 2009 ).
-
(2009)
Mol. Interv.
, vol.9
, pp. 22-30
-
-
Fischer, M.1
Hubbard, R.E.2
-
82
-
-
36549033318
-
Integration of fragment screening and library design
-
DOI 10.1016/j.drudis.2007.08.005, PII S1359644607003108
-
Siegal G. Ab E.& Schultz J. Integration of fragment screening and library design. Drug Discov. Today 12 1032-1039 ( 2007 ). (Pubitemid 350180558)
-
(2007)
Drug Discovery Today
, vol.12
, Issue.23-24
, pp. 1032-1039
-
-
Siegal, G.1
Schultz, J.2
-
85
-
-
0036245954
-
Molecular characterisation of the dominant UK methicillin-resistant Staphylococcus aureus strains, EMRSA-15 and EMRSA-16
-
Moore P.C.& Lindsay J.A. Molecular characterisation of the dominant UK methicillin-resistant Staphylococcus aureus strains, EMRSA-15 and EMRSA- 16.J. Med. Microbiol. 5 1 516-521 ( 2002 ). (Pubitemid 34492981)
-
(2002)
Journal of Medical Microbiology
, vol.51
, Issue.6
, pp. 516-521
-
-
Moore, P.C.L.1
Lindsay, J.A.2
-
86
-
-
0000664092
-
Dominance of EMRSA-15 and -16
-
Johnson A.P. et al. Dominance of EMRSA-15 and -16.J. Antimicrob. Chemother. 4 8 141-156 ( 2001 ).
-
(2001)
J. Antimicrob. Chemother.
, vol.48
, pp. 141-156
-
-
Johnson, A.P.1
|