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Volumn 57, Issue 14, 2014, Pages 6259-6265

1,3,4-Oxadiazole-containing histone deacetylase inhibitors: Anticancer activities in cancer cells

Author keywords

[No Author keywords available]

Indexed keywords

1,3,4 OXADIAZOLE DERIVATIVE; ALPHA TUBULIN; ANILIDE; ANTINEOPLASTIC AGENT; DOXORUBICIN; ENTINOSTAT; HISTONE DEACETYLASE INHIBITOR; HISTONE H3; HYDROXAMIC ACID; N (2 AMINOPHENYL) 3 (4 (5 ARYL ARYLALKYL 1,3,4 OXADIAZOL 2 YL)PHENYL)ACRYLAMIDE; N (2 AMINOPHENYL) 4 ((5 (NAPHTHALEN 1 YLMETHYL) 1,3,4 OXADIAZOL 2 YL)METHYL)BENZAMIDE; N HYDROXY 3 (4 (5ARYL ARYLALKYL 1,3,4 OXADIAZOL 2 YL)PHENYL)ACRYLAMIDE; N HYDROXY 4 ((5 (NAPHTHALEN 1 YLMETHYL) 1,3,4 OXADIAZOL 2 YL)MEHTYL)BENZAMIDE; PROTEIN P21; UNCLASSIFIED DRUG; VORINOSTAT;

EID: 84904962606     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm500303u     Document Type: Article
Times cited : (125)

References (17)
  • 1
    • 33746457753 scopus 로고    scopus 로고
    • Enhanced histone acetylation and transcription: A dynamic perspective
    • Clayton, A. L.; Hazzalin, C. A.; Mahadevan, L. C. Enhanced histone acetylation and transcription: a dynamic perspective Mol. Cell 2006, 23, 289-296
    • (2006) Mol. Cell , vol.23 , pp. 289-296
    • Clayton, A.L.1    Hazzalin, C.A.2    Mahadevan, L.C.3
  • 2
    • 28044471827 scopus 로고    scopus 로고
    • Acetylation and deacetylation of non-histone proteins
    • Glozak, M. A.; Sengupta, N.; Zhang, X.; Seto, E. Acetylation and deacetylation of non-histone proteins Gene 2005, 363, 15-23
    • (2005) Gene , vol.363 , pp. 15-23
    • Glozak, M.A.1    Sengupta, N.2    Zhang, X.3    Seto, E.4
  • 3
    • 77954139965 scopus 로고    scopus 로고
    • Small-molecule chromatin-modifying agents: Therapeutic applications
    • Mai, A. Small-molecule chromatin-modifying agents: therapeutic applications Epigenomics 2010, 2, 307-324
    • (2010) Epigenomics , vol.2 , pp. 307-324
    • Mai, A.1
  • 4
    • 84935029387 scopus 로고    scopus 로고
    • Targeting HDACs in diseases: Where are we?
    • Mar 6, PMID 24382114, DOI 10.1089/ars.2013.5776.
    • Benedetti, R.; Conte, M.; Altucci, L. Targeting HDACs in diseases: where are we? Antioxid. Redox Signaling 2014, Mar 6, PMID 24382114, DOI 10.1089/ars.2013.5776.
    • (2014) Antioxid. Redox Signaling
    • Benedetti, R.1    Conte, M.2    Altucci, L.3
  • 5
    • 33846122993 scopus 로고    scopus 로고
    • Dimethyl sulfoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug
    • Marks, P. A.; Breslow, R. Dimethyl sulfoxide to vorinostat: development of this histone deacetylase inhibitor as an anticancer drug Nature Biotechnol. 2007, 25, 84-90
    • (2007) Nature Biotechnol. , vol.25 , pp. 84-90
    • Marks, P.A.1    Breslow, R.2
  • 6
    • 77749309291 scopus 로고    scopus 로고
    • Romidepsin for the treatment of cutaneous T-cell lymphoma
    • Campas-Moya, C. Romidepsin for the treatment of cutaneous T-cell lymphoma Drugs Today 2009, 45, 787-795
    • (2009) Drugs Today , vol.45 , pp. 787-795
    • Campas-Moya, C.1
  • 8
    • 84878002317 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: An attractive strategy for cancer therapy
    • Li, J.; Li, G.; Xu, W. Histone deacetylase inhibitors: an attractive strategy for cancer therapy Curr. Med. Chem. 2013, 20, 1858-1886
    • (2013) Curr. Med. Chem. , vol.20 , pp. 1858-1886
    • Li, J.1    Li, G.2    Xu, W.3
  • 9
    • 69749113873 scopus 로고    scopus 로고
    • Pyrrole-based hydroxamates and 2-aminoanilides: Histone deacetylase inhibition and cellular activities
    • references cited therein. - 1415
    • Valente, S.; Conte, M.; Tardugno, M.; Massa, S.; Nebbioso, A.; Altucci, L.; Mai, A. Pyrrole-based hydroxamates and 2-aminoanilides: histone deacetylase inhibition and cellular activities ChemMedChem 2009, 4, 1411-1415 and references cited therein.
    • (2009) ChemMedChem , vol.4 , pp. 1411
    • Valente, S.1    Conte, M.2    Tardugno, M.3    Massa, S.4    Nebbioso, A.5    Altucci, L.6    Mai, A.7
  • 11
    • 41849089386 scopus 로고    scopus 로고
    • Novel uracil-based 2-aminoanilide and 2-aminoanilide-like derivatives: Histone deacetylase inhibition and in-cell activities
    • references cited therein. - 2535
    • Mai, A.; Perrone, A.; Nebbioso, A.; Rotili, D.; Valente, S.; Tardugno, M.; Massa, S.; De Bellis, F.; Altucci, L. Novel uracil-based 2-aminoanilide and 2-aminoanilide-like derivatives: histone deacetylase inhibition and in-cell activities Bioorg. Med. Chem. Lett. 2008, 18, 2530-2535 and references cited therein.
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 2530
    • Mai, A.1    Perrone, A.2    Nebbioso, A.3    Rotili, D.4    Valente, S.5    Tardugno, M.6    Massa, S.7    De Bellis, F.8    Altucci, L.9
  • 16
    • 0034961181 scopus 로고    scopus 로고
    • Retinoic acid-induced apoptosis in leukemia cells is mediated by paracrine action of tumor-selective death ligand TRAIL
    • Altucci, L.; Rossin, A.; Raffelsberger, W.; Reitmair, A.; Chomienne, C.; Gronemeyer, H. Retinoic acid-induced apoptosis in leukemia cells is mediated by paracrine action of tumor-selective death ligand TRAIL Nature Med. 2001, 7, 680-686
    • (2001) Nature Med. , vol.7 , pp. 680-686
    • Altucci, L.1    Rossin, A.2    Raffelsberger, W.3    Reitmair, A.4    Chomienne, C.5    Gronemeyer, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.