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Volumn 56, Issue 6, 2013, Pages 2581-2605

Design, synthesis, and biological evaluation of indenoisoquinoline rexinoids with chemopreventive potential

Author keywords

[No Author keywords available]

Indexed keywords

2 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)ACETIC ACID; 3 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)ACRYLIC ACID; 3 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)ACRYLONITRILE; 3 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)PROPIOLIC ACID; 3 BROMO 6 METHYL 5H INDENO[1,2 C]ISOQUINOLINE 5,11(6H)DIONE; 3 CHLORO 6 METHYL 5H INDENO[1,2 C]ISOQUINOLINE 5,11(6H)DIONE; 3 CYANO 5,11 DIHYDRO 6 METHYL 5,11 DIOXOINDENO[1,2 C]ISOQUINOLINE; 3 IODO 6 METHYL 5H INDENO[1,2 C]ISOQUINOLINE 5,11(6H) DIONE; 3,6 DIMETHYL 5H INDENO[1,2 C]ISOQUINOLINE 5,11(6H)DIONE; 5 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)BUTANOIC ACID; 5 METHYLHOMOPHTHALIC ANHYDRIDE; 6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLINE 3 CARBALDEHYDE; 6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLINE 3 CARBOXAMIDE; 6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLINE 3 CARBOXYLIC ACID; ANTINEOPLASTIC AGENT; CARBOXYL GROUP; ETHYL 1 BROMO 3 OXO 1,3 DIHYDROISOBENZOFURAN 5 CARBOXYLATE; ETHYL 1 HYDROXY 3 OXO 1,3 DIHYDROISOBENZOFURAN 5 CARBOXYLATE; ETHYL 2 CYANO 2 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)ACETATE; INDENOISOQUINOLINE REXINOID; METHYL 2 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)ACETATE; METHYL 3 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)ACRYLATE; METHYL 3 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)PROPIOLATE; METHYL 5 (6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLIN 3 YL)BUTANOATE; METHYL 5,11 DIOXO 5,11 DIHYDROINDENO[1,2 C]ISOCHROMENE 3 CARBOXYLATE; METHYL 6 [3 (1H IMIDAZOL 1 YL)PROPYL] 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLINE 3 CARBOXYLATE HYDROCHLORIDE; METHYL 6 [3 [(TERT BUTOXYCARBONYL)AMINO]PROPYL] 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLINE 3 CARBOXYLATE; METHYL 6 METHYL 5,11 DIOXO 6,11 DIHYDRO 5H INDENO[1,2 C]ISOQUINOLINE 3 CARBOXYLATE; RETINOID X RECEPTOR; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 84875712796     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm400026k     Document Type: Article
Times cited : (29)

References (75)
  • 2
    • 0023913120 scopus 로고
    • The Steroid and Thyroid Hormone Receptor Superfamily
    • Evans, R. M. The Steroid and Thyroid Hormone Receptor Superfamily Science 1988, 240, 889-895
    • (1988) Science , vol.240 , pp. 889-895
    • Evans, R.M.1
  • 6
    • 0035813186 scopus 로고    scopus 로고
    • Nuclear Receptor Minireview Series
    • Olefsky, J. M. Nuclear Receptor Minireview Series J. Biol. Chem. 2001, 276, 36863-36864
    • (2001) J. Biol. Chem. , vol.276 , pp. 36863-36864
    • Olefsky, J.M.1
  • 9
    • 1642304065 scopus 로고    scopus 로고
    • Structural Determinants of Allosteric Ligand Activation in RXR Heterodimers
    • Shulman, A. I.; Larson, C.; Mangelsdorf, D. J.; Ranganathan, R. Structural Determinants of Allosteric Ligand Activation in RXR Heterodimers Cell 2004, 116, 417-429
    • (2004) Cell , vol.116 , pp. 417-429
    • Shulman, A.I.1    Larson, C.2    Mangelsdorf, D.J.3    Ranganathan, R.4
  • 10
    • 0039937361 scopus 로고
    • H-2RIIBP, a Member of the Nuclear Hormone Receptor Superfamily that Binds to Both the Regulatory Element of Major Histocompatibility Class i Genes and the Estrogen Response Element
    • Hamada, K.; Gleason, S. L.; Levi, B. Z.; Hirschfeld, S.; Appella, E.; Ozato, K. H-2RIIBP, a Member of the Nuclear Hormone Receptor Superfamily that Binds to Both the Regulatory Element of Major Histocompatibility Class I Genes and the Estrogen Response Element Proc. Natl. Acad. Sci. U.S.A. 1989, 86, 8289-8293
    • (1989) Proc. Natl. Acad. Sci. U.S.A. , vol.86 , pp. 8289-8293
    • Hamada, K.1    Gleason, S.L.2    Levi, B.Z.3    Hirschfeld, S.4    Appella, E.5    Ozato, K.6
  • 11
    • 0028009121 scopus 로고
    • Developmental Expression of Murine Retinoid X Receptor (RXR) Genes
    • Dolle, P.; Fraulob, V.; Kastner, P.; Chambon, P. Developmental Expression of Murine Retinoid X Receptor (RXR) Genes Mech. Dev. 1994, 45, 91-104
    • (1994) Mech. Dev. , vol.45 , pp. 91-104
    • Dolle, P.1    Fraulob, V.2    Kastner, P.3    Chambon, P.4
  • 13
    • 0025270737 scopus 로고
    • Nuclear Receptor That Identifies a Novel Retinoic Acid Response Pathway
    • Mangelsdorf, D. J.; Ong, E. S.; Dyck, J. A.; Evans, R. M. Nuclear Receptor That Identifies a Novel Retinoic Acid Response Pathway Nature 1990, 345, 224-229
    • (1990) Nature , vol.345 , pp. 224-229
    • Mangelsdorf, D.J.1    Ong, E.S.2    Dyck, J.A.3    Evans, R.M.4
  • 16
    • 0029796637 scopus 로고    scopus 로고
    • Retinoids in Cancer Chemoprevention
    • Lotan, R. Retinoids in Cancer Chemoprevention FASEB J. 1996, 10, 1031-1039
    • (1996) FASEB J. , vol.10 , pp. 1031-1039
    • Lotan, R.1
  • 17
    • 0028787351 scopus 로고
    • Retinoids and Apoptosis: Implications for Cancer Chemoprevention and Therapy
    • Lotan, R. Retinoids and Apoptosis: Implications for Cancer Chemoprevention and Therapy J. Natl. Cancer Inst. 1995, 87, 1655-1657
    • (1995) J. Natl. Cancer Inst. , vol.87 , pp. 1655-1657
    • Lotan, R.1
  • 18
    • 67449132372 scopus 로고    scopus 로고
    • Therapeutic Potential of "rexinoids" in Cancer Prevention and Treatment
    • Tanaka, T.; De Luca, L. M. Therapeutic Potential of "Rexinoids" in Cancer Prevention and Treatment Cancer Res. 2009, 69, 4945-4947
    • (2009) Cancer Res. , vol.69 , pp. 4945-4947
    • Tanaka, T.1    De Luca, L.M.2
  • 19
    • 0026750804 scopus 로고
    • Retinoids in Cancer Prevention and Therapy
    • Bollag, W.; Holdener, E. E. Retinoids in Cancer Prevention and Therapy Ann. Oncol. 1992, 3, 513-526
    • (1992) Ann. Oncol. , vol.3 , pp. 513-526
    • Bollag, W.1    Holdener, E.E.2
  • 20
    • 0000417904 scopus 로고
    • Prevention and Therapy of Cancer with Retinoids in Animals and Man
    • Bollag, W.; Hartmann, H. R. Prevention and Therapy of Cancer with Retinoids in Animals and Man Cancer Surv. 1983, 2, 293-314
    • (1983) Cancer Surv. , vol.2 , pp. 293-314
    • Bollag, W.1    Hartmann, H.R.2
  • 22
    • 0036897019 scopus 로고    scopus 로고
    • Selective Retinoids and Rexinoids in Cancer Therapy and Chemoprevention
    • Zusi, F. C.; Lorenzi, M. V.; Vivat-Hannah, V. Selective Retinoids and Rexinoids in Cancer Therapy and Chemoprevention Drug Discovery Today 2002, 7, 1165-1174
    • (2002) Drug Discovery Today , vol.7 , pp. 1165-1174
    • Zusi, F.C.1    Lorenzi, M.V.2    Vivat-Hannah, V.3
  • 24
    • 0035555873 scopus 로고    scopus 로고
    • Bioavailability and Dose-Dependent Anti-Tumour Effects of 9- cis -Retinoic Acid on Human Neuroblastoma Xenografts in Rat
    • Ponthan, F.; Kogner, P.; Bjellerup, P.; Klevenvall, L.; Hassan, M. Bioavailability and Dose-Dependent Anti-Tumour Effects of 9- cis -Retinoic Acid on Human Neuroblastoma Xenografts in Rat Br. J. Cancer 2001, 85, 2004-2009
    • (2001) Br. J. Cancer , vol.85 , pp. 2004-2009
    • Ponthan, F.1    Kogner, P.2    Bjellerup, P.3    Klevenvall, L.4    Hassan, M.5
  • 26
    • 71349084776 scopus 로고    scopus 로고
    • Bexarotene: A Promising Anticancer Agent
    • Qu, L. Y.; Tang, X. W. Bexarotene: A Promising Anticancer Agent Cancer Chemother. Pharmacol. 2010, 65, 201-205
    • (2010) Cancer Chemother. Pharmacol. , vol.65 , pp. 201-205
    • Qu, L.Y.1    Tang, X.W.2
  • 31
    • 78650207455 scopus 로고    scopus 로고
    • Modification at the Lipophilic Domain of RXR Agonists Differentially Influences Activation of RXR Heterodimers
    • Ohsawa, F.; Morishita, K.; Yamada, S.; Makishima, M.; Kakuta, H. Modification at the Lipophilic Domain of RXR Agonists Differentially Influences Activation of RXR Heterodimers ACS Med. Chem. Lett. 2010, 1, 521-525
    • (2010) ACS Med. Chem. Lett. , vol.1 , pp. 521-525
    • Ohsawa, F.1    Morishita, K.2    Yamada, S.3    Makishima, M.4    Kakuta, H.5
  • 32
    • 34247526984 scopus 로고    scopus 로고
    • Triterpenoids and Rexinoids as Multifunctional Agents for the Prevention and Treatment of Cancer
    • Liby, K. T.; Yore, M. M.; Sporn, M. B. Triterpenoids and Rexinoids as Multifunctional Agents for the Prevention and Treatment of Cancer Nat. Rev. Cancer 2007, 7, 357-369
    • (2007) Nat. Rev. Cancer , vol.7 , pp. 357-369
    • Liby, K.T.1    Yore, M.M.2    Sporn, M.B.3
  • 34
    • 82355168677 scopus 로고    scopus 로고
    • Synthesis of Substituted Isoquinolines via Pd-Catalyzed Cross-Coupling Approaches
    • Todorovic, N.; Awuah, E.; Albu, S.; Ozimok, C.; Capretta, A. Synthesis of Substituted Isoquinolines via Pd-Catalyzed Cross-Coupling Approaches Org. Lett. 2011, 13, 6180-6183
    • (2011) Org. Lett. , vol.13 , pp. 6180-6183
    • Todorovic, N.1    Awuah, E.2    Albu, S.3    Ozimok, C.4    Capretta, A.5
  • 38
    • 43249094986 scopus 로고    scopus 로고
    • Enantiomerically Pure Axially Chiral Aminocarbene Complexes of Chromium
    • Meca, L.; Cisarova, I.; Drahonovsky, D.; Dvorak, D. Enantiomerically Pure Axially Chiral Aminocarbene Complexes of Chromium Organometallics 2008, 27, 1850-1858
    • (2008) Organometallics , vol.27 , pp. 1850-1858
    • Meca, L.1    Cisarova, I.2    Drahonovsky, D.3    Dvorak, D.4
  • 39
    • 0000263948 scopus 로고
    • Substituent Effects on Hydrogenation of Aromatic Rings - Hydrogenation vs Hydrogenolysis in Cyclic Analogs of Benzyl Ethers
    • Anzalone, L.; Hirsch, J. A. Substituent Effects on Hydrogenation of Aromatic Rings-Hydrogenation vs Hydrogenolysis in Cyclic Analogs of Benzyl Ethers J. Org. Chem. 1985, 50, 2128-2133
    • (1985) J. Org. Chem. , vol.50 , pp. 2128-2133
    • Anzalone, L.1    Hirsch, J.A.2
  • 40
    • 33144472888 scopus 로고    scopus 로고
    • Synthesis of Benz[ d ]indeno[1,2- b ]pyran-5,11-diones: Versatile Intermediates for the Design and Synthesis of Topoisomerase i Inhibitors
    • Morrell, A.; Antony, S.; Kohlhagen, G.; Pommier, Y.; Cushman, M. Synthesis of Benz[ d ]indeno[1,2- b ]pyran-5,11-diones: Versatile Intermediates for the Design and Synthesis of Topoisomerase I Inhibitors Bioorg. Med. Chem. Lett. 2006, 16, 1846-1849
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 1846-1849
    • Morrell, A.1    Antony, S.2    Kohlhagen, G.3    Pommier, Y.4    Cushman, M.5
  • 41
    • 36148991565 scopus 로고    scopus 로고
    • Enantioselective Synthesis of (S)-3-Carboxy-4-((carboxy)difluoromethyl) phenylalanine in Protected Form and Its Incorporation into a PTP-1B-Directed Tripeptide
    • Kang, S. U.; Yang, G.; Li, W.; Zhang, Z. Y.; Burke, T. R. Enantioselective Synthesis of (S)-3-Carboxy-4-((carboxy)difluoromethyl) phenylalanine in Protected Form and Its Incorporation Into a PTP-1B-Directed Tripeptide Chem. Biodiversity 2004, 1, 626-633
    • (2004) Chem. Biodiversity , vol.1 , pp. 626-633
    • Kang, S.U.1    Yang, G.2    Li, W.3    Zhang, Z.Y.4    Burke, T.R.5
  • 42
    • 37049059038 scopus 로고
    • Polyazanaphthalenes. IX. Synthesis of Some Folic Acid Antagonists
    • Rydon, H. N.; Undheim, K. Polyazanaphthalenes. IX. Synthesis of Some Folic Acid Antagonists J. Chem. Soc. 1962, 4689-4695
    • (1962) J. Chem. Soc. , pp. 4689-4695
    • Rydon, H.N.1    Undheim, K.2
  • 44
    • 84863113291 scopus 로고    scopus 로고
    • Identification, Synthesis, and Biological Evaluation of the Metabolites of 3-Amino-6-(3′-aminopropyl)-5 H -indeno[1,2- c ]isoquinoline-5,11-(6 H)dione (AM6-36), a Promising Rexinoid Lead Compound for the Development of Cancer Chemotherapeutic and Chemopreventive Agents
    • Chen, L.; Conda-Sheridan, M.; Reddy, P. V.; Morrell, A.; Park, E. J.; Kondratyuk, T. P.; Pezzuto, J. M.; van Breemen, R. B.; Cushman, M. Identification, Synthesis, and Biological Evaluation of the Metabolites of 3-Amino-6-(3′-aminopropyl)-5 H -indeno[1,2- c ]isoquinoline-5,11-(6 H)dione (AM6-36), a Promising Rexinoid Lead Compound for the Development of Cancer Chemotherapeutic and Chemopreventive Agents J. Med. Chem. 2012, 55, 5965-5981
    • (2012) J. Med. Chem. , vol.55 , pp. 5965-5981
    • Chen, L.1    Conda-Sheridan, M.2    Reddy, P.V.3    Morrell, A.4    Park, E.J.5    Kondratyuk, T.P.6    Pezzuto, J.M.7    Van Breemen, R.B.8    Cushman, M.9
  • 46
    • 79952006933 scopus 로고    scopus 로고
    • Structure Basis of Bigelovin as a Selective RXR Agonist with a Distinct Binding Mode
    • Zhang, H. T.; Li, L.; Chen, L. L.; Hu, L. H.; Jiang, H. L.; Shen, X. Structure Basis of Bigelovin as a Selective RXR Agonist with a Distinct Binding Mode J. Mol. Biol. 2011, 407, 13-20
    • (2011) J. Mol. Biol. , vol.407 , pp. 13-20
    • Zhang, H.T.1    Li, L.2    Chen, L.L.3    Hu, L.H.4    Jiang, H.L.5    Shen, X.6
  • 47
    • 77956220279 scopus 로고    scopus 로고
    • Identification of a Naturally Occurring Rexinoid, Honokiol, That Activates the Retinoid X Receptor
    • Kotani, H.; Tanabe, H.; Mizukami, H.; Makishima, M.; Inoue, M. Identification of a Naturally Occurring Rexinoid, Honokiol, That Activates the Retinoid X Receptor J. Nat. Prod. 2010, 73, 1332-1336
    • (2010) J. Nat. Prod. , vol.73 , pp. 1332-1336
    • Kotani, H.1    Tanabe, H.2    Mizukami, H.3    Makishima, M.4    Inoue, M.5
  • 48
    • 82255162374 scopus 로고    scopus 로고
    • Molecular Determinants of Magnolol Targeting Both RXRα and PPARγ
    • Zhang, H. T.; Xu, X.; Chen, L. L.; Chen, J.; Hu, L. H.; Jiang, H. L.; Shen, X. Molecular Determinants of Magnolol Targeting Both RXRα and PPARγ PLoS One 2011, 6, e28523
    • (2011) PLoS One , vol.6 , pp. 28523
    • Zhang, H.T.1    Xu, X.2    Chen, L.L.3    Chen, J.4    Hu, L.H.5    Jiang, H.L.6    Shen, X.7
  • 51
    • 84875716120 scopus 로고    scopus 로고
    • (accessed July 23).
    • http://www.molinspiration.com/cgi-bin/properties (accessed July 23, 2012).
    • (2012)
  • 52
    • 84875717887 scopus 로고    scopus 로고
    • (accessed July 23).
    • http://aceorganic.pearsoncmg.com/epoch-plugin/public/pKa.jsp (accessed July 23, 2012).
    • (2012)
  • 54
    • 34547661861 scopus 로고    scopus 로고
    • Comparative Performance of Several Flexible Docking Programs and Scoring Functions: Enrichment Studies for a Diverse Set of Pharmaceutically Relevant Targets
    • Zhou, Z. Y.; Felts, A. K.; Friesner, R. A.; Levy, R. M. Comparative Performance of Several Flexible Docking Programs and Scoring Functions: Enrichment Studies for a Diverse Set of Pharmaceutically Relevant Targets J. Chem. Inf. Model. 2007, 47, 1599-1608
    • (2007) J. Chem. Inf. Model. , vol.47 , pp. 1599-1608
    • Zhou, Z.Y.1    Felts, A.K.2    Friesner, R.A.3    Levy, R.M.4
  • 55
    • 67650097331 scopus 로고    scopus 로고
    • Comparison of Several Molecular Docking Programs: Pose Prediction and Virtual Screening Accuracy
    • Cross, J. B.; Thompson, D. C.; Rai, B. K.; Baber, J. C.; Fan, K. Y.; Hu, Y. B.; Humblet, C. Comparison of Several Molecular Docking Programs: Pose Prediction and Virtual Screening Accuracy J. Chem. Inf. Model. 2009, 49, 1455-1474
    • (2009) J. Chem. Inf. Model. , vol.49 , pp. 1455-1474
    • Cross, J.B.1    Thompson, D.C.2    Rai, B.K.3    Baber, J.C.4    Fan, K.Y.5    Hu, Y.B.6    Humblet, C.7
  • 57
    • 76149120388 scopus 로고    scopus 로고
    • AutoDock Vina: Improving the Speed and Accuracy of Docking with a New Scoring Function, Efficient Optimization, and Multithreading
    • Trott, O.; Olson, A. J. AutoDock Vina: Improving the Speed and Accuracy of Docking with a New Scoring Function, Efficient Optimization, and Multithreading J. Comput. Chem. 2010, 31, 455-461
    • (2010) J. Comput. Chem. , vol.31 , pp. 455-461
    • Trott, O.1    Olson, A.J.2
  • 58
    • 0037119784 scopus 로고    scopus 로고
    • Synthesis and Characterization of a New RXR Agonist Based on the 6- tert -Butyl-1,1-dimethylindanyl Structure
    • Dominguez, B.; Vega, M. J.; Sussman, F.; de Lera, A. R. Synthesis and Characterization of a New RXR Agonist Based on the 6- tert -Butyl-1,1- dimethylindanyl Structure Bioorg. Med. Chem. Lett. 2002, 12, 2607-2609
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 2607-2609
    • Dominguez, B.1    Vega, M.J.2    Sussman, F.3    De Lera, A.R.4
  • 60
    • 26444607929 scopus 로고    scopus 로고
    • Ligand Recognition by RAR and RXR Receptors: Binding and Selectivity
    • Sussman, F.; de Lera, A. R. Ligand Recognition by RAR and RXR Receptors: Binding and Selectivity J. Med. Chem. 2005, 48, 6212-6219
    • (2005) J. Med. Chem. , vol.48 , pp. 6212-6219
    • Sussman, F.1    De Lera, A.R.2
  • 61
    • 48049114021 scopus 로고    scopus 로고
    • Reduction of Lipophilicity at the Lipophilic Domain of RXR Agonists Enables Production of Subtype Preference: RXR Molecular Determinants of Magnolol Targeting Both RXRα-Preferential Agonist Possessing a Sulfonamide Moiety
    • Takamatsu, K.; Takano, A.; Yakushiji, N.; Morishita, K.; Matsuura, N.; Makishima, M.; Ali, H. I.; Akaho, E.; Tai, A.; Sasaki, K.; Kakuta, H. Reduction of Lipophilicity at the Lipophilic Domain of RXR Agonists Enables Production of Subtype Preference: RXR Molecular Determinants of Magnolol Targeting Both RXRα-Preferential Agonist Possessing a Sulfonamide Moiety ChemMedChem 2008, 3, 454-460
    • (2008) ChemMedChem , vol.3 , pp. 454-460
    • Takamatsu, K.1    Takano, A.2    Yakushiji, N.3    Morishita, K.4    Matsuura, N.5    Makishima, M.6    Ali, H.I.7    Akaho, E.8    Tai, A.9    Sasaki, K.10    Kakuta, H.11
  • 62
    • 0033855471 scopus 로고    scopus 로고
    • Structural Basis for Autorepression of Retinoid X Receptor by Tetramer Formation and the AF-2 Helix
    • Gampe, R. T.; Montana, V. G.; Lambert, M. H.; Wisely, G. B.; Milburn, M. V.; Xu, H. E. Structural Basis for Autorepression of Retinoid X Receptor by Tetramer Formation and the AF-2 Helix Genes Dev. 2000, 14, 2229-2241
    • (2000) Genes Dev. , vol.14 , pp. 2229-2241
    • Gampe, R.T.1    Montana, V.G.2    Lambert, M.H.3    Wisely, G.B.4    Milburn, M.V.5    Xu, H.E.6
  • 64
    • 12844252576 scopus 로고    scopus 로고
    • Retinoid X Receptors: X-ploring Their (Patho)Physiological Functions
    • Szanto, A.; Narkar, V.; Shen, Q.; Uray, I. P.; Davies, P. J.; Nagy, L. Retinoid X Receptors: X-ploring Their (Patho)Physiological Functions Cell Death Differ. 2004, 11 (Suppl. 2) S126-S143
    • (2004) Cell Death Differ. , vol.11 , Issue.SUPPL. 2
    • Szanto, A.1    Narkar, V.2    Shen, Q.3    Uray, I.P.4    Davies, P.J.5    Nagy, L.6
  • 65
    • 34848862778 scopus 로고    scopus 로고
    • Design of Selective Nuclear Receptor Modulators: RAR and RXR as a Case Study
    • de Lera, A. R.; Bourguet, W.; Altucci, L.; Gronemeyer, H. Design of Selective Nuclear Receptor Modulators: RAR and RXR as a Case Study Nat. Rev. Drug Discovery 2007, 6, 811-820
    • (2007) Nat. Rev. Drug Discovery , vol.6 , pp. 811-820
    • De Lera, A.R.1    Bourguet, W.2    Altucci, L.3    Gronemeyer, H.4
  • 66
    • 37249026697 scopus 로고    scopus 로고
    • Screening for Ligands of Human Retinoid X Receptor-alpha Using Ultrafiltration Mass Spectrometry
    • Liu, D.; Guo, J.; Luo, Y.; Broderick, D. J.; Schimerlik, M. I.; Pezzuto, J. M.; van Breemen, R. B. Screening for Ligands of Human Retinoid X Receptor-alpha Using Ultrafiltration Mass Spectrometry Anal. Chem. 2007, 79, 9398-9402
    • (2007) Anal. Chem. , vol.79 , pp. 9398-9402
    • Liu, D.1    Guo, J.2    Luo, Y.3    Broderick, D.J.4    Schimerlik, M.I.5    Pezzuto, J.M.6    Van Breemen, R.B.7
  • 68
    • 0032478824 scopus 로고    scopus 로고
    • Heterodimeric DNA Binding by the Vitamin D Receptor and Retinoid X Receptors Is Enhanced by 1,25-Dihydroxyvitamin D3 and Inhibited by 9- cis -Retinoic Acid. Evidence for Allosteric Receptor Interactions
    • Thompson, P. D.; Jurutka, P. W.; Haussler, C. A.; Whitfield, G. K.; Haussler, M. R. Heterodimeric DNA Binding by the Vitamin D Receptor and Retinoid X Receptors Is Enhanced by 1,25-Dihydroxyvitamin D3 and Inhibited by 9- cis -Retinoic Acid. Evidence for Allosteric Receptor Interactions J. Biol. Chem. 1998, 273, 8483-8491
    • (1998) J. Biol. Chem. , vol.273 , pp. 8483-8491
    • Thompson, P.D.1    Jurutka, P.W.2    Haussler, C.A.3    Whitfield, G.K.4    Haussler, M.R.5
  • 69
    • 0030891331 scopus 로고    scopus 로고
    • Retinoid X Receptor-Specific Ligands Synergistically Upregulate 1,25-dihydroxyvitamin D3-Dependent Transcription in Epidermal Keratinocytes in Vitro and in Vivo
    • Li, X. Y.; Xiao, J. H.; Feng, X.; Qin, L.; Voorhees, J. J. Retinoid X Receptor-Specific Ligands Synergistically Upregulate 1,25-dihydroxyvitamin D3-Dependent Transcription in Epidermal Keratinocytes in Vitro and in Vivo J. Invest. Dermatol. 1997, 108, 506-512
    • (1997) J. Invest. Dermatol. , vol.108 , pp. 506-512
    • Li, X.Y.1    Xiao, J.H.2    Feng, X.3    Qin, L.4    Voorhees, J.J.5
  • 71
    • 79955956020 scopus 로고    scopus 로고
    • Integrating Structure-Based and Ligand-Based Approaches for Computational Drug Design
    • Wilson, G. L.; Lill, M. A. Integrating Structure-Based and Ligand-Based Approaches for Computational Drug Design Future Med. Chem. 2011, 3, 735-750
    • (2011) Future Med. Chem. , vol.3 , pp. 735-750
    • Wilson, G.L.1    Lill, M.A.2
  • 73
    • 0036251738 scopus 로고    scopus 로고
    • Molecular Recognition of Agonist Ligands by RXRs
    • Egea, P. F.; Mitschler, A.; Moras, D. Molecular Recognition of Agonist Ligands by RXRs Mol. Endocrinol. 2002, 16, 987-997
    • (2002) Mol. Endocrinol. , vol.16 , pp. 987-997
    • Egea, P.F.1    Mitschler, A.2    Moras, D.3
  • 75
    • 33144480848 scopus 로고
    • Synthesis of 6-Substituted-6 H -indeno[1,2- c ]isoquinoline-5,11-diones
    • Wawzonek, S. Synthesis of 6-Substituted-6 H -indeno[1,2- c ]isoquinoline-5,11-diones Org. Prep. Proced. Int. 1982, 14, 163-168
    • (1982) Org. Prep. Proced. Int. , vol.14 , pp. 163-168
    • Wawzonek, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.