메뉴 건너뛰기




Volumn 124, Issue 2, 2009, Pages 509-

Inhibition of HDAC6-dependent carcinogenesis: Emerging, new therapeutic options besides belinostat

(1)  Kapoor, Shailendra a  

a NONE

Author keywords

[No Author keywords available]

Indexed keywords

3 PHENYLSULFAMOYLCINNAMOHYDROXAMIC ACID; BELINOSTAT; BORTEZOMIB; CARBONIC ACID; GELDANAMYCIN; HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 6; HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID; KD 5170; PACLITAXEL; TRITHIOCARBONATE DERIVATIVE; TUBACIN; UNCLASSIFIED DRUG; VORINOSTAT; ANTINEOPLASTIC AGENT; ENZYME INHIBITOR; HISTONE DEACETYLASE;

EID: 58249094713     PISSN: 00207136     EISSN: 10970215     Source Type: Journal    
DOI: 10.1002/ijc.23975     Document Type: Letter
Times cited : (8)

References (9)
  • 1
    • 39649090731 scopus 로고    scopus 로고
    • Activity of the histone deacetylase inhibitor belinostat (PXD101) in preclinical models of prostate cancer
    • Qian X, Ara G, Mills E, LaRochelle WJ, Lichenstein HS, Jeffers M Activity of the histone deacetylase inhibitor belinostat (PXD101) in preclinical models of prostate cancer. Int J Cancer 2008;122:1400.
    • (2008) Int J Cancer , vol.122 , pp. 1400
    • Qian, X.1    Ara, G.2    Mills, E.3    LaRochelle, W.J.4    Lichenstein, H.S.5    Jeffers, M.6
  • 2
    • 0344640906 scopus 로고    scopus 로고
    • Domain-selective small-molecule inhibitor of histone deacetylase 6(HDAC 6)-mediated tubulin deacetylation
    • S J Haggarty, Domain-selective small-molecule inhibitor of histone deacetylase 6(HDAC 6)-mediated tubulin deacetylation. Proc Natl Acad Sci 2003;100:4389-94.
    • (2003) Proc Natl Acad Sci , vol.100 , pp. 4389-4394
    • Haggarty, S.J.1
  • 4
    • 35848945959 scopus 로고    scopus 로고
    • Design, synthesis, structure-selectivity relationship, and effect on human cancer cells of a novel series of histone deacetylase 6-selective inhibitors
    • Itoh Y, Suzuki T, Kouketsu A, Suzuki N, Maeda S, Yoshida M, Nakagawa H, Miyata N. Design, synthesis, structure-selectivity relationship, and effect on human cancer cells of a novel series of histone deacetylase 6-selective inhibitors. J Med Chem 2007;50:5425-38.
    • (2007) J Med Chem , vol.50 , pp. 5425-5438
    • Itoh, Y.1    Suzuki, T.2    Kouketsu, A.3    Suzuki, N.4    Maeda, S.5    Yoshida, M.6    Nakagawa, H.7    Miyata, N.8
  • 5
    • 58449105917 scopus 로고    scopus 로고
    • Hassig CA, Symons KT, Guo X, Nguyen PM, Annable T, Wash PL, Payne JE, Jenkins DA, Bonnefous C, Trotter C, Wang Y
    • Hassig CA, Symons KT, Guo X, Nguyen PM, Annable T, Wash PL, Payne JE, Jenkins DA, Bonnefous C, Trotter C, Wang Y,
  • 6
    • 49849106385 scopus 로고    scopus 로고
    • KD5170, a novel mercaptoketone-based his tone deacetylase inhibitor that exhibits broad spectrum anti tumor activity in vitro and in vivo
    • Anzola JV, et al. KD5170, a novel mercaptoketone-based his tone deacetylase inhibitor that exhibits broad spectrum anti tumor activity in vitro and in vivo. Mol Cancer Ther 2008;7:1054-65.
    • (2008) Mol Cancer Ther , vol.7 , pp. 1054-1065
    • Anzola, J.V.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.