메뉴 건너뛰기




Volumn 493, Issue , 2011, Pages 509-531

Experiences in fragment-based lead discovery

Author keywords

[No Author keywords available]

Indexed keywords

HEAT SHOCK PROTEIN 70; HEAT SHOCK PROTEIN 90; LEAD; PEPTIDYLPROLYL ISOMERASE PIN1; PROTEIN KINASE; PROTEIN KINASE 1; PROTEIN KINASE 2; PROTEIN KINASE 3; RESORCINOL; UNCLASSIFIED DRUG;

EID: 79952429629     PISSN: 00766879     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-12-381274-2.00020-0     Document Type: Chapter
Times cited : (98)

References (32)
  • 6
    • 67650999672 scopus 로고    scopus 로고
    • Lessons for fragment library design: Analysis of output from multiple screening campaigns
    • I.J. Chen, and R.E. Hubbard Lessons for fragment library design: Analysis of output from multiple screening campaigns J. Comput. Aided Mol. Des 2009. 23, 603620
    • (2009) J. Comput. Aided Mol. des
    • Chen, I.J.1    Hubbard, R.E.2
  • 7
    • 67649341990 scopus 로고    scopus 로고
    • From fragment to clinical candidateA historical perspective
    • G. Chessari, and A.J. Woodhead From fragment to clinical candidateA historical perspective Drug Discov. Today 14 2009 668 675
    • (2009) Drug Discov. Today , vol.14 , pp. 668-675
    • Chessari, G.1    Woodhead, A.J.2
  • 8
    • 47749106894 scopus 로고    scopus 로고
    • Stoichiometry and physical chemistry of promiscuous aggregate-based inhibitors
    • DOI 10.1021/ja802977h
    • K.E. Coan, and B.K. Shoichet Stoichiometry and physical chemistry of promiscuous aggregate-based inhibitors J. Am. Chem. Soc. 130 2008 9606 9612 (Pubitemid 352031174)
    • (2008) Journal of the American Chemical Society , vol.130 , Issue.29 , pp. 9606-9612
    • Coan, K.E.D.1    Shoichet, B.K.2
  • 10
    • 33748325882 scopus 로고    scopus 로고
    • Drug-target residence time and its implications for lead optimization
    • DOI 10.1038/nrd2082, PII NRD2082
    • R.A. Copeland, D.L. Pompliano, and T.D. Meek Drug-target residence time and its implications for lead optimization Nat. Rev. Drug Discov. 5 2006 730 739 (Pubitemid 44323700)
    • (2006) Nature Reviews Drug Discovery , vol.5 , Issue.9 , pp. 730-739
    • Copeland, R.A.1    Pompliano, D.L.2    Meek, T.D.3
  • 12
    • 34247194965 scopus 로고    scopus 로고
    • 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
    • T. Fink, and J.L. Reymond 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 2007 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
  • 13
    • 63749103205 scopus 로고    scopus 로고
    • Fragment-based ligand discovery
    • M. Fischer, and R.E. Hubbard Fragment-based ligand discovery Mol. Interv. 9 2009 22 30
    • (2009) Mol. Interv. , vol.9 , pp. 22-30
    • Fischer, M.1    Hubbard, R.E.2
  • 15
    • 39149130730 scopus 로고    scopus 로고
    • Surface plasmon resonance based assay for the detection and characterization of promiscuous inhibitors
    • DOI 10.1021/jm700952v
    • A.M. Giannetti, B.D. Koch, and M.F. Browner Surface plasmon resonance based assay for the detection and characterization of promiscuous inhibitors J. Med. Chem. 51 2008 574 580 (Pubitemid 351252285)
    • (2008) Journal of Medicinal Chemistry , vol.51 , Issue.3 , pp. 574-580
    • Giannetti, A.M.1    Koch, B.D.2    Browner, M.F.3
  • 16
    • 33845364148 scopus 로고    scopus 로고
    • Fragment-based drug design: How big is too big?
    • DOI 10.1021/jm060511h
    • P.J. Hajduk Fragment-based drug design: How big is too big? J. Med. Chem. 49 2006 6972 6976 (Pubitemid 44885985)
    • (2006) Journal of Medicinal Chemistry , vol.49 , Issue.24 , pp. 6972-6976
    • Hajduk, P.J.1
  • 17
    • 65249117514 scopus 로고    scopus 로고
    • Identifying and characterizing binding sites and assessing druggability
    • T.A. Halgren Identifying and characterizing binding sites and assessing druggability J. Chem. Inf. Model. 49 2009 377 389
    • (2009) J. Chem. Inf. Model. , vol.49 , pp. 377-389
    • Halgren, T.A.1
  • 18
    • 1942453243 scopus 로고    scopus 로고
    • Ligand efficiency: A useful metric for lead selection
    • DOI 10.1016/S1359-6446(04)03069-7, PII S1359644604030697
    • A.L. Hopkins, C.R. Groom, and A. Alex Ligand efficiency: A useful metric for lead selection Drug Discov. Today 9 2004 430 431 (Pubitemid 38510559)
    • (2004) Drug Discovery Today , vol.9 , Issue.10 , pp. 430-431
    • Hopkins, A.L.1    Groom, C.R.2    Alex, A.3
  • 20
    • 42449142359 scopus 로고    scopus 로고
    • Fragment approaches in structure-based drug discovery
    • DOI 10.1107/S090904950705666X, PII S090904950705666X
    • R.E. Hubbard Fragment approaches in structure-based drug discovery J. Synchrotron Radiat. 15 2008 227 230 (Pubitemid 351571008)
    • (2008) Journal of Synchrotron Radiation , vol.15 , Issue.3 , pp. 227-230
    • Hubbard, R.E.1
  • 22
  • 24
    • 77955329488 scopus 로고    scopus 로고
    • Drug-target residence time: Critical information for lead optimization
    • H. Lu, and P.J. Tonge Drug-target residence time: Critical information for lead optimization Curr. Opin. Chem. Biol. 14 2010 467 474
    • (2010) Curr. Opin. Chem. Biol. , vol.14 , pp. 467-474
    • Lu, H.1    Tonge, P.J.2
  • 25
    • 33645887230 scopus 로고    scopus 로고
    • Critical review of the role of HTS in drug discovery
    • R. Macarron Critical review of the role of HTS in drug discovery Drug Discov. Today 11 2006 277 279
    • (2006) Drug Discov. Today , vol.11 , pp. 277-279
    • MacArron, R.1
  • 26
    • 77956622674 scopus 로고    scopus 로고
    • Fragment screening by surface plasmon resonance
    • I. Navratilova, and A.L. Hopkins Fragment screening by surface plasmon resonance ACS Med. Chem. Lett. 1 2010 44 48
    • (2010) ACS Med. Chem. Lett. , vol.1 , pp. 44-48
    • Navratilova, I.1    Hopkins, A.L.2
  • 29
    • 70349425790 scopus 로고    scopus 로고
    • Recent progress in fragment-based lead discovery
    • M.N. Schulz, and R.E. Hubbard Recent progress in fragment-based lead discovery Curr. Opin. Pharmacol. 9 2009 615 621
    • (2009) Curr. Opin. Pharmacol. , vol.9 , pp. 615-621
    • Schulz, M.N.1    Hubbard, R.E.2
  • 30
    • 0029836953 scopus 로고    scopus 로고
    • Discovering high-affinity ligands for proteins: SAR by NMR
    • DOI 10.1126/science.274.5292.1531
    • S.B. Shuker, P.J. Hajduk, R.P. Meadows, and S.W. Fesik Discovering high-affinity ligands for proteins: SAR by NMR Science 274 1996 1531 1534 (Pubitemid 26403929)
    • (1996) Science , vol.274 , Issue.5292 , pp. 1531-1534
    • Shuker, S.B.1    Hajduk, P.J.2    Meadows, R.P.3    Fesik, S.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.