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Volumn 6, Issue 1, 2014, Pages

IDrug: A web-accessible and interactive drug discovery and design platform

Author keywords

3D similarity calculation; Cavity detection; Online drug design platform; Pharmacophore search; Target prediction

Indexed keywords


EID: 84902272377     PISSN: None     EISSN: 17582946     Source Type: Journal    
DOI: 10.1186/1758-2946-6-28     Document Type: Article
Times cited : (34)

References (61)
  • 1
    • 69249141491 scopus 로고    scopus 로고
    • Recent advances in computer-aided drug design
    • Recent advances in computer-aided drug design. Song CM, Lim SJ, Tong JC, Brief Bioinform 2009 10 579 591
    • (2009) Brief Bioinform , vol.10 , pp. 579-591
    • Song, C.M.1    Lim, S.J.2    Tong, J.C.3
  • 2
    • 1642357706 scopus 로고    scopus 로고
    • The many roles of computation in drug discovery
    • The many roles of computation in drug discovery. Jorgensen WL, Science 2004 303 1813 1818
    • (2004) Science , vol.303 , pp. 1813-1818
    • Jorgensen, W.L.1
  • 3
    • 45749117025 scopus 로고    scopus 로고
    • Ranking targets in structure-based virtual screening of three-dimensional protein libraries: Methods and problems
    • Ranking targets in structure-based virtual screening of three-dimensional protein libraries: methods and problems. Kellenberger E, Foata N, Rognan D, J Chem Inf Model 2008 48 1014 1025
    • (2008) J Chem Inf Model , vol.48 , pp. 1014-1025
    • Kellenberger, E.1    Foata, N.2    Rognan, D.3
  • 4
    • 80053453210 scopus 로고    scopus 로고
    • A computational approach to finding novel targets for existing drugs
    • A computational approach to finding novel targets for existing drugs. Li YY, An J, Jones SJ, PLoS Comput Biol 2011 7 1002139
    • (2011) PLoS Comput Biol , vol.7 , pp. 51002139
    • Li, Y.Y.1    An, J.2    Jones, S.J.3
  • 5
    • 33750994920 scopus 로고    scopus 로고
    • Bridging chemical and biological space: Target fishing using 2D and 3D molecular descriptors
    • Bridging chemical and biological space: "target fishing" using 2D and 3D molecular descriptors. Nettles JH, Jenkins JL, Bender A, Deng Z, Davies JW, Glick M, J Med Chem 2006 49 6802 6810
    • (2006) J Med Chem , vol.49 , pp. 6802-6810
    • Nettles, J.H.1    Jenkins, J.L.2    Bender, A.3    Deng, Z.4    Davies, J.W.5    Glick, M.6
  • 7
    • 80053324958 scopus 로고    scopus 로고
    • SHAFTS: A hybrid approach for 3D molecular similarity calculation. 1. Method and assessment of virtual screening
    • SHAFTS: a hybrid approach for 3D molecular similarity calculation. 1. Method and assessment of virtual screening. Liu X, Jiang H, Li H, J Chem Inf Model 2011 51 2372 2385
    • (2011) J Chem Inf Model , vol.51 , pp. 2372-2385
    • Liu, X.1    Jiang, H.2    Li, H.3
  • 8
    • 79960250991 scopus 로고    scopus 로고
    • LigBuilder 2: A practical de novo drug design approach
    • LigBuilder 2: a practical de novo drug design approach. Yuan Y, Pei J, Lai L, J Chem Inf Model 2011 51 1083 1091
    • (2011) J Chem Inf Model , vol.51 , pp. 1083-1091
    • Yuan, Y.1    Pei, J.2    Lai, L.3
  • 9
    • 13844320566 scopus 로고    scopus 로고
    • LigandScout: 3-D pharmacophores derived from protein-bound ligands and their use as virtual screening filters
    • LigandScout: 3-D pharmacophores derived from protein-bound ligands and their use as virtual screening filters. Wolber G, Langer T, J Chem Inf Model 2005 45 160 169
    • (2005) J Chem Inf Model , vol.45 , pp. 160-169
    • Wolber, G.1    Langer, T.2
  • 10
    • 65249167560 scopus 로고    scopus 로고
    • ShaEP: Molecular overlay based on shape and electrostatic potential
    • ShaEP: molecular overlay based on shape and electrostatic potential. Vainio MJ, Puranen JS, Johnson MS, J Chem Inf Model 2009 49 492 502
    • (2009) J Chem Inf Model , vol.49 , pp. 492-502
    • Vainio, M.J.1    Puranen, J.S.2    Johnson, M.S.3
  • 11
    • 0034934377 scopus 로고    scopus 로고
    • Pharmacophore modeling and three-dimensional database searching for drug design using catalyst
    • Pharmacophore modeling and three-dimensional database searching for drug design using catalyst. Kurogi Y, Guner OF, Curr Med Chem 2001 8 1035 1055
    • (2001) Curr Med Chem , vol.8 , pp. 1035-1055
    • Kurogi, Y.1    Guner, O.F.2
  • 12
    • 84857451391 scopus 로고    scopus 로고
    • The errors of our ways: Taking account of error in computer-aided drug design to build confidence intervals for our next 25 years
    • The errors of our ways: taking account of error in computer-aided drug design to build confidence intervals for our next 25 years. Stouch TR, J Comput Aided Mol Des 2012 26 125 134
    • (2012) J Comput Aided Mol des , vol.26 , pp. 125-134
    • Stouch, T.R.1
  • 13
    • 78651235334 scopus 로고    scopus 로고
    • Computer-aided drug design platform using PyMOL
    • Computer-aided drug design platform using PyMOL. Lill MA, Danielson ML, J Comput Aided Mol Des 2011 25 13 19
    • (2011) J Comput Aided Mol des , vol.25 , pp. 13-19
    • Lill, M.A.1    Danielson, M.L.2
  • 15
    • 84880191567 scopus 로고    scopus 로고
    • ChemMapper: A versatile web server for exploring pharmacology and chemical structure association based on molecular 3D similarity method
    • ChemMapper: a versatile web server for exploring pharmacology and chemical structure association based on molecular 3D similarity method. Gong J, Cai C, Liu X, Ku X, Jiang H, Gao D, Li H, Bioinformatics 2013 29 1827 1829
    • (2013) Bioinformatics , vol.29 , pp. 1827-1829
    • Gong, J.1    Cai, C.2    Liu, X.3    Ku, X.4    Jiang, H.5    Gao, D.6    Li, H.7
  • 16
    • 84864447594 scopus 로고    scopus 로고
    • ZINCPharmer: Pharmacophore search of the ZINC database
    • ZINCPharmer: pharmacophore search of the ZINC database. Koes DR, Camacho CJ, Nucleic Acids Res 2012 40 409 W414
    • (2012) Nucleic Acids Res , vol.40
    • Koes, D.R.1    Camacho, C.J.2
  • 18
    • 84857451273 scopus 로고    scopus 로고
    • Some thoughts on the A in computer-aided molecular design
    • Some thoughts on the "A" in computer-aided molecular design. Rarey M, J Comput Aided Mol Des 2012 26 113 114
    • (2012) J Comput Aided Mol des , vol.26 , pp. 113-114
    • Rarey, M.1
  • 19
    • 77954282775 scopus 로고    scopus 로고
    • E-LEA3D: A computational-aided drug design web server
    • e-LEA3D: a computational-aided drug design web server. Douguet D, Nucleic Acids Res 2010 38 615 W621
    • (2010) Nucleic Acids Res , vol.38
    • Douguet, D.1
  • 20
    • 84873674615 scopus 로고    scopus 로고
    • Sanjeevini: A freely accessible web-server for target directed lead molecule discovery
    • Sanjeevini: a freely accessible web-server for target directed lead molecule discovery. Jayaram B, Singh T, Mukherjee G, Mathur A, Shekhar S, Shekhar V, BMC Bioinforma 2012 13 Suppl 17 7
    • (2012) BMC Bioinforma , vol.13 , Issue.SUPPL.17 , pp. 197
    • Jayaram, B.1    Singh, T.2    Mukherjee, G.3    Mathur, A.4    Shekhar, S.5    Shekhar, V.6
  • 21
    • 33845727607 scopus 로고    scopus 로고
    • Pocket v. 2: Further developments on receptor-Based pharmacophore modeling
    • Pocket v. 2: further developments on receptor-based pharmacophore modeling. Chen J, Lai L, J Chem Inf Model 2006 46 2684 2691
    • (2006) J Chem Inf Model , vol.46 , pp. 2684-2691
    • Chen, J.1    Lai, L.2
  • 23
    • 79957771857 scopus 로고    scopus 로고
    • SHAFTS: A hybrid approach for 3D molecular similarity calculation. 2. Prospective case study in the discovery of diverse p90 ribosomal S6 protein kinase 2 inhibitors to suppress cell migration
    • SHAFTS: a hybrid approach for 3D molecular similarity calculation. 2. Prospective case study in the discovery of diverse p90 ribosomal S6 protein kinase 2 inhibitors to suppress cell migration. Lu W, Liu X, Cao X, Xue M, Liu K, Zhao Z, Shen X, Jiang H, Xu Y, Huang J, Li H, J Med Chem 2011 54 3564 3574
    • (2011) J Med Chem , vol.54 , pp. 3564-3574
    • Lu, W.1    Liu, X.2    Cao, X.3    Xue, M.4    Liu, K.5    Zhao, Z.6    Shen, X.7    Jiang, H.8    Xu, Y.9    Huang, J.10    Li, H.11
  • 25
    • 41249091782 scopus 로고    scopus 로고
    • Pybel: A Python wrapper for the OpenBabel cheminformatics toolkit
    • Pybel: a Python wrapper for the OpenBabel cheminformatics toolkit. O'Boyle NM, Morley C, Hutchison GR, Chem Cent J 2008 2 5
    • (2008) Chem Cent J , vol.2 , pp. 5
    • O'Boyle, N.M.1    Morley, C.2    Hutchison, G.R.3
  • 28
    • 13844312649 scopus 로고    scopus 로고
    • ZINC-A free database of commercially available compounds for virtual screening
    • ZINC-a free database of commercially available compounds for virtual screening. Irwin JJ, Shoichet BK, J Chem Inf Model 2005 45 177 182
    • (2005) J Chem Inf Model , vol.45 , pp. 177-182
    • Irwin, J.J.1    Shoichet, B.K.2
  • 30
    • 33846108633 scopus 로고    scopus 로고
    • BindingDB: A web-accessible database of experimentally determined protein-ligand binding affinities
    • BindingDB: a web-accessible database of experimentally determined protein-ligand binding affinities. Liu T, Lin Y, Wen X, Jorissen RN, Gilson MK, Nucleic Acids Res 2007 35 198 D201
    • (2007) Nucleic Acids Res , vol.35
    • Liu, T.1    Lin, Y.2    Wen, X.3    Jorissen, R.N.4    Gilson, M.K.5
  • 31
    • 2542530042 scopus 로고    scopus 로고
    • The PDBbind database: Collection of binding affinities for protein-ligand complexes with known three-dimensional structures
    • The PDBbind database: collection of binding affinities for protein-ligand complexes with known three-dimensional structures. Wang R, Fang X, Lu Y, Wang S, J Med Chem 2004 47 2977 2980
    • (2004) J Med Chem , vol.47 , pp. 2977-2980
    • Wang, R.1    Fang, X.2    Lu, Y.3    Wang, S.4
  • 33
    • 84877814002 scopus 로고    scopus 로고
    • Binding site detection and druggability prediction of protein targets for structure- based drug design
    • Binding site detection and druggability prediction of protein targets for structure- based drug design. Yuan Y, Pei J, Lai L, Curr Pharm Des 2013 19 2326 2333
    • (2013) Curr Pharm des , vol.19 , pp. 2326-2333
    • Yuan, Y.1    Pei, J.2    Lai, L.3
  • 34
    • 33744503192 scopus 로고    scopus 로고
    • Strategy for discovering chemical inhibitors of human cyclophilin A: Focused library design, virtual screening, chemical synthesis and bioassay
    • Strategy for discovering chemical inhibitors of human cyclophilin A: focused library design, virtual screening, chemical synthesis and bioassay. Li J, Zhang J, Chen J, Luo X, Zhu W, Shen J, Liu H, Shen X, Jiang H, J Comb Chem 2006 8 326 337
    • (2006) J Comb Chem , vol.8 , pp. 326-337
    • Li, J.1    Zhang, J.2    Chen, J.3    Luo, X.4    Zhu, W.5    Shen, J.6    Liu, H.7    Shen, X.8    Jiang, H.9
  • 35
    • 58149088865 scopus 로고    scopus 로고
    • Discovery of multitarget inhibitors by combining molecular docking with common pharmacophore matching
    • Discovery of multitarget inhibitors by combining molecular docking with common pharmacophore matching. Wei D, Jiang X, Zhou L, Chen J, Chen Z, He C, Yang K, Liu Y, Pei J, Lai L, J Med Chem 2008 51 7882 7888
    • (2008) J Med Chem , vol.51 , pp. 7882-7888
    • Wei, D.1    Jiang, X.2    Zhou, L.3    Chen, J.4    Chen, Z.5    He, C.6    Yang, K.7    Liu, Y.8    Pei, J.9    Lai, L.10
  • 36
    • 77949859256 scopus 로고    scopus 로고
    • Discovery and SAR of thiazolidine-2, 4-dione analogues as insulin-like growth factor-1 receptor (IGF-1R) inhibitors via hierarchical virtual screening
    • Discovery and SAR of thiazolidine-2, 4-dione analogues as insulin-like growth factor-1 receptor (IGF-1R) inhibitors via hierarchical virtual screening. Liu X, Xie H, Luo C, Tong L, Wang Y, Peng T, Ding J, Jiang H, Li H, J Med Chem 2010 53 2661 2665
    • (2010) J Med Chem , vol.53 , pp. 2661-2665
    • Liu, X.1    Xie, H.2    Luo, C.3    Tong, L.4    Wang, Y.5    Peng, T.6    Ding, J.7    Jiang, H.8    Li, H.9
  • 37
    • 79958173765 scopus 로고    scopus 로고
    • Acenaphtho [1, 2-b] pyrrole-Based selective fibroblast growth factor receptors 1 (FGFR1) Inhibitors: Design, synthesis, and biological activity
    • Acenaphtho [1, 2-b] pyrrole-Based selective fibroblast growth factor receptors 1 (FGFR1) Inhibitors: design, synthesis, and biological activity. Chen Z, Wang X, Zhu W, Cao X, Tong L, Li H, Xie H, Xu Y, Tan S, Kuang D, J Med Chem 2011 54 3732 3745
    • (2011) J Med Chem , vol.54 , pp. 3732-3745
    • Chen, Z.1    Wang, X.2    Zhu, W.3    Cao, X.4    Tong, L.5    Li, H.6    Xie, H.7    Xu, Y.8    Tan, S.9    Kuang, D.10
  • 38
    • 65549133951 scopus 로고    scopus 로고
    • Cyndi: A multi-objective evolution algorithm based method for bioactive molecular conformational generation
    • Cyndi: a multi-objective evolution algorithm based method for bioactive molecular conformational generation. Liu X, Bai F, Ouyang S, Wang X, Li H, Jiang H, BMC Bioinforma 2009 10 101
    • (2009) BMC Bioinforma , vol.10 , pp. 101
    • Liu, X.1    Bai, F.2    Ouyang, S.3    Wang, X.4    Li, H.5    Jiang, H.6
  • 39
    • 78049408261 scopus 로고    scopus 로고
    • Bioactive conformational generation of small molecules: A comparative analysis between force-field and multiple empirical criteria based methods
    • Bioactive conformational generation of small molecules: a comparative analysis between force-field and multiple empirical criteria based methods. Bai F, Liu X, Li J, Zhang H, Jiang H, Wang X, Li H, BMC Bioinforma 2010 11 545
    • (2010) BMC Bioinforma , vol.11 , pp. 545
    • Bai, F.1    Liu, X.2    Li, J.3    Zhang, H.4    Jiang, H.5    Wang, X.6    Li, H.7
  • 41
    • 84886494418 scopus 로고    scopus 로고
    • Discovery of Pteridin-7 (8 H)-one-based irreversible inhibitors targeting the epidermal growth factor receptor (EGFR) Kinase T790M/L858R mutant
    • Discovery of Pteridin-7 (8 H)-one-based irreversible inhibitors targeting the epidermal growth factor receptor (EGFR) Kinase T790M/L858R mutant. Zhou W, Liu X, Tu Z, Zhang L, Ku X, Bai F, Zhao Z, Xu Y, Ding K, Li H, J Med Chem 2013 56 7821 7837
    • (2013) J Med Chem , vol.56 , pp. 7821-7837
    • Zhou, W.1    Liu, X.2    Tu, Z.3    Zhang, L.4    Ku, X.5    Bai, F.6    Zhao, Z.7    Xu, Y.8    Ding, K.9    Li, H.10
  • 43
    • 84866328968 scopus 로고    scopus 로고
    • New tricks for an old natural product: Discovery of highly potent evodiamine derivatives as novel antitumor agents by systemic structure-activity relationship analysis and biological evaluations
    • New tricks for an old natural product: discovery of highly potent evodiamine derivatives as novel antitumor agents by systemic structure-activity relationship analysis and biological evaluations. Dong G, Wang S, Miao Z, Yao J, Zhang Y, Guo Z, Zhang W, Sheng C, J Med Chem 2012 55 7593 7613
    • (2012) J Med Chem , vol.55 , pp. 7593-7613
    • Dong, G.1    Wang, S.2    Miao, Z.3    Yao, J.4    Zhang, Y.5    Guo, Z.6    Zhang, W.7    Sheng, C.8
  • 44
    • 65349136650 scopus 로고    scopus 로고
    • Maximum unbiased validation (MUV) data sets for virtual screening based on PubChem bioactivity data
    • Maximum unbiased validation (MUV) data sets for virtual screening based on PubChem bioactivity data. Rohrer SG, Baumann K, J Chem Inf Model 2009 49 169 184
    • (2009) J Chem Inf Model , vol.49 , pp. 169-184
    • Rohrer, S.G.1    Baumann, K.2
  • 45
    • 84864264343 scopus 로고    scopus 로고
    • Directory of useful decoys, enhanced (DUD-E): Better ligands and decoys for better benchmarking
    • Directory of useful decoys, enhanced (DUD-E): better ligands and decoys for better benchmarking. Mysinger MM, Carchia M, Irwin JJ, Shoichet BK, J Med Chem 2012 55 6582 6594
    • (2012) J Med Chem , vol.55 , pp. 6582-6594
    • Mysinger, M.M.1    Carchia, M.2    Irwin, J.J.3    Shoichet, B.K.4
  • 46
    • 56149110450 scopus 로고    scopus 로고
    • Towards more accurate pharmacophore modeling: Multicomplex-based comprehensive pharmacophore map and most-frequent-feature pharmacophore model of CDK2
    • Towards more accurate pharmacophore modeling: multicomplex-based comprehensive pharmacophore map and most-frequent-feature pharmacophore model of CDK2. Zou J, Xie H-Z, Yang S-Y, Chen J-J, Ren J-X, Wei Y-Q, J Mol Graph Model 2008 27 430 438
    • (2008) J Mol Graph Model , vol.27 , pp. 430-438
    • Zou, J.1    Xie, H.-Z.2    Yang, S.-Y.3    Chen, J.-J.4    Ren, J.-X.5    Wei, Y.-Q.6
  • 48
    • 6444219756 scopus 로고    scopus 로고
    • Multiple targeting by the antitumor drug tamoxifen: A structure-activity study
    • Multiple targeting by the antitumor drug tamoxifen: a structure-activity study. de Medina P, Favre G, Poirot M, Curr Med Chem Anticancer Agents 2004 4 491 508
    • (2004) Curr Med Chem Anticancer Agents , vol.4 , pp. 491-508
    • De Medina, P.1    Favre, G.2    Poirot, M.3
  • 49
    • 77955799773 scopus 로고    scopus 로고
    • Identification and pharmacological characterization of cholesterol-5, 6-epoxide hydrolase as a target for tamoxifen and AEBS ligands
    • Identification and pharmacological characterization of cholesterol-5, 6-epoxide hydrolase as a target for tamoxifen and AEBS ligands. De Medina P, Paillasse MR, Segala G, Poirot M, Silvente-Poirot S, Proc Natl Acad Sci 2010 107 13520 13525
    • (2010) Proc Natl Acad Sci , vol.107 , pp. 13520-13525
    • De Medina, P.1    Paillasse, M.R.2    Segala, G.3    Poirot, M.4    Silvente-Poirot, S.5
  • 50
    • 84867116494 scopus 로고    scopus 로고
    • Hedgehog signaling is a novel therapeutic target in tamoxifen-resistant breast cancer aberrantly activated by PI3K/AKT pathway
    • Hedgehog signaling is a novel therapeutic target in tamoxifen-resistant breast cancer aberrantly activated by PI3K/AKT pathway. Ramaswamy B, Lu Y, Teng K-y, Nuovo G, Li X, Shapiro CL, Majumder S, Cancer Res 2012 72 5048 5059
    • (2012) Cancer Res , vol.72 , pp. 5048-5059
    • Ramaswamy, B.1    Lu, Y.2    Teng, K.-Y.3    Nuovo, G.4    Li, X.5    Shapiro, C.L.6    Majumder, S.7
  • 51
    • 0025838170 scopus 로고
    • The effect of toremifene therapy on serum immunoglobulin levels in breast cancer
    • The effect of toremifene therapy on serum immunoglobulin levels in breast cancer. Paavonen T, Aronen H, PyrhÖNen S, Hajba A, Andersson L, Apmis 1991 99 849 853
    • (1991) Apmis , vol.99 , pp. 849-853
    • Paavonen, T.1    Aronen, H.2    Pyrhönen, S.3    Hajba, A.4    Andersson, L.5
  • 52
    • 0032191125 scopus 로고    scopus 로고
    • Steroidal and nonsteroidal oestrogen antagonists in breast cancer: Basic and clinical appraisal
    • Steroidal and nonsteroidal oestrogen antagonists in breast cancer: basic and clinical appraisal. Favoni RE, de Cupis A, Trends Pharmacol Sci 1998 19 406 415
    • (1998) Trends Pharmacol Sci , vol.19 , pp. 406-415
    • Favoni, R.E.1    De Cupis, A.2
  • 53
    • 0027161787 scopus 로고
    • Inhibition of estrone sulfatase and 17β-hydroxysteroid dehydrogenase by antiestrogens
    • Inhibition of estrone sulfatase and 17β-hydroxysteroid dehydrogenase by antiestrogens. Santner SJ, Santen RJ, J Steroid Biochem Mol Biol 1993 45 383 390
    • (1993) J Steroid Biochem Mol Biol , vol.45 , pp. 383-390
    • Santner, S.J.1    Santen, R.J.2
  • 54
    • 0021846826 scopus 로고
    • Effects of estrogen and tamoxifen on the regulation of dihydrofolate reductase gene expression in a human breast cancer cell line
    • Effects of estrogen and tamoxifen on the regulation of dihydrofolate reductase gene expression in a human breast cancer cell line. Levine RM, Rubalcaba E, Lippman ME, Cowan KH, Cancer Res 1985 45 1644 1650
    • (1985) Cancer Res , vol.45 , pp. 1644-1650
    • Levine, R.M.1    Rubalcaba, E.2    Lippman, M.E.3    Cowan, K.H.4
  • 55
    • 0029783146 scopus 로고    scopus 로고
    • Phase II enzyme expression in rat liver in response to the antiestrogen tamoxifen
    • Phase II enzyme expression in rat liver in response to the antiestrogen tamoxifen. Nuwaysir EF, Daggett DA, Jordan VC, Pitot HC, Cancer Res 1996 56 3704 3710
    • (1996) Cancer Res , vol.56 , pp. 3704-3710
    • Nuwaysir, E.F.1    Daggett, D.A.2    Jordan, V.C.3    Pitot, H.C.4
  • 56
    • 0018848322 scopus 로고
    • The direct inhibition of prostaglandin synthetase of human breast cancer tumor tissue by tamoxifen
    • The direct inhibition of prostaglandin synthetase of human breast cancer tumor tissue by tamoxifen. Ritchie GA, Recent Results Cancer Res 1980 71 96 101
    • (1980) Recent Results Cancer Res , vol.71 , pp. 96-101
    • Ritchie, G.A.1
  • 59
    • 33947536035 scopus 로고    scopus 로고
    • MMP-2 and MMP-9 activity is regulated by estradiol and tamoxifen in cultured human breast cancer cells
    • MMP-2 and MMP-9 activity is regulated by estradiol and tamoxifen in cultured human breast cancer cells. Nilsson UW, Garvin S, Dabrosin C, Breast Cancer Res Ttreat 2007 102 253 261
    • (2007) Breast Cancer Res Ttreat , vol.102 , pp. 253-261
    • Nilsson, U.W.1    Garvin, S.2    Dabrosin, C.3
  • 60
    • 0025157132 scopus 로고
    • Leu-enkephalin, tamoxifen and ethanol interactions: Effects on motility and hepatic ethanol metabolizing enzymes
    • Leu-enkephalin, tamoxifen and ethanol interactions: effects on motility and hepatic ethanol metabolizing enzymes. Messiha FS, Gen Pharmacol 1990 21 45 48
    • (1990) Gen Pharmacol , vol.21 , pp. 45-48
    • Messiha, F.S.1
  • 61
    • 0020559112 scopus 로고
    • Antagonistic action of estrogens, flutamide, and human growth hormone on androgen-induced changes in the activities of some enzymes of hepatic steroid metabolism in the rat
    • Antagonistic action of estrogens, flutamide, and human growth hormone on androgen-induced changes in the activities of some enzymes of hepatic steroid metabolism in the rat. Lax E, Rumstadt F, Plasczyk H, Peetz A, Schriefers H, Endocrinology 1983 113 1043 1055
    • (1983) Endocrinology , vol.113 , pp. 1043-1055
    • Lax, E.1    Rumstadt, F.2    Plasczyk, H.3    Peetz, A.4    Schriefers, H.5


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