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Volumn 14, Issue 15-16, 2009, Pages 723-725

French/European academic compound library initiative

Author keywords

[No Author keywords available]

Indexed keywords

MINOZAC; NOOTROPIC AGENT; PLANT EXTRACT; UNCLASSIFIED DRUG;

EID: 67651238448     PISSN: 13596446     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.drudis.2009.05.012     Document Type: Editorial
Times cited : (29)

References (11)
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    • 3D-QSAR and docking studies of selective GSK-3 inhibitors. Comparison with a thieno[2,3-b]pyrrolizinone derivative, a new potential lead for GSK-3 ligands
    • Lescot E., et al. 3D-QSAR and docking studies of selective GSK-3 inhibitors. Comparison with a thieno[2,3-b]pyrrolizinone derivative, a new potential lead for GSK-3 ligands. J. Chem. Inf. Model. 45 (2005) 708-715
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  • 3
    • 11144262742 scopus 로고    scopus 로고
    • New biologically active linear triterpenes from the bark of three new-caledonian Cupaniopsis species
    • Bousserouel H., et al. New biologically active linear triterpenes from the bark of three new-caledonian Cupaniopsis species. Tetrahedron 61 (2005) 845-851
    • (2005) Tetrahedron , vol.61 , pp. 845-851
    • Bousserouel, H.1
  • 4
    • 4344619713 scopus 로고    scopus 로고
    • Pharmacological inhibitors of glycogen synthase kinase 3
    • Meijer L., et al. Pharmacological inhibitors of glycogen synthase kinase 3. Trends Pharmacol. Sci. 25 (2004) 471-480
    • (2004) Trends Pharmacol. Sci. , vol.25 , pp. 471-480
    • Meijer, L.1
  • 5
    • 33646242741 scopus 로고    scopus 로고
    • Assessing the scaffold diversity of screening libraries
    • Rognan D., et al. Assessing the scaffold diversity of screening libraries. J. Chem. Inf. Model. 46 (2006) 512-524
    • (2006) J. Chem. Inf. Model. , vol.46 , pp. 512-524
    • Rognan, D.1
  • 6
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    • Managing, profiling and analyzing a library of 2.6 million compounds gathered from 32 chemical providers
    • Monge A., et al. Managing, profiling and analyzing a library of 2.6 million compounds gathered from 32 chemical providers. Mol. Divers. 10 (2006) 389-403
    • (2006) Mol. Divers. , vol.10 , pp. 389-403
    • Monge, A.1
  • 7
    • 33751286847 scopus 로고    scopus 로고
    • Use of a fluorescent polarization based high throughput assay to identify new calmodulin ligands
    • Dagher R., et al. Use of a fluorescent polarization based high throughput assay to identify new calmodulin ligands. Biochim. Biophys. Acta 1763 (2006) 1250-1255
    • (2006) Biochim. Biophys. Acta , vol.1763 , pp. 1250-1255
    • Dagher, R.1
  • 8
    • 67651239171 scopus 로고    scopus 로고
    • Hibert, M. et al. (2006) Domain therapeutics. Collections of traceable compounds and uses thereof. WO2006003329
    • Hibert, M. et al. (2006) Domain therapeutics. Collections of traceable compounds and uses thereof. WO2006003329
  • 9
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    • A novel, conformation-specific allosteric inhibitor of the tachykinin NK2 receptor (NK2R) with functionally selective properties
    • Maillet E., et al. A novel, conformation-specific allosteric inhibitor of the tachykinin NK2 receptor (NK2R) with functionally selective properties. FASEB J. 21 (2007) 2124-2134
    • (2007) FASEB J. , vol.21 , pp. 2124-2134
    • Maillet, E.1
  • 10
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    • Selective modification of alternative splicing by indole derivatives that target serine-arginine-rich protein splicing factors
    • Soret J., et al. Selective modification of alternative splicing by indole derivatives that target serine-arginine-rich protein splicing factors. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 8764-8769
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  • 11
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    • Transition therapeutics. Anti-inflammatory and protein kinase inhibitor compositions and related methods for downregulation of detrimental cellular responses and inhibition of cell death
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    • Watterson, M.D. et al. (2003) Transition therapeutics. Anti-inflammatory and protein kinase inhibitor compositions and related methods for downregulation of detrimental cellular responses and inhibition of cell death. US2003176437
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.