메뉴 건너뛰기




Volumn 13, Issue 14, 2013, Pages 1999-2013

Recent progress in the development of histone deacetylase inhibitors as anti-cancer agents

Author keywords

Anticancer agent; HDAC inhibitor; Histone deacetylase (HDAC); Structure activity relationship (SAR)

Indexed keywords

2 AMINO BENZANILIDE DERIVATIVES; 2 AMINOANILIDE DERIVATIVES; ABEXINOSTAT; APICIDIN; AZUMAMIDE A; AZUMAMIDE E; BELINOSTAT; DIPHENYLMETHYLENE HYDROXAMIC ACID; ELECTROPHILIC KETONE DERIVATIVES; ENTINOSTAT; FR 235222; GIVINOSTAT; HC TOXIN; HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID DERIVATIVES; KD 5150; MACROCYCLIC DERIVATIVES; MOCETINOSTAT; PANOBINOSTAT; QUISINOSTAT; RESMINOSTAT; ROMIDEPSIN; SELENIUM DERIVATIVES; SPIRUCHOSTATIN C; SULFAMIDE DERIVATIVES; TRICHOSTATIN A; UNCLASSIFIED DRUG; VALPROIC ACID; VORINOSTAT;

EID: 84892957575     PISSN: 13895575     EISSN: 18755607     Source Type: Journal    
DOI: 10.2174/13895575113136660102     Document Type: Review
Times cited : (7)

References (108)
  • 1
    • 80053130009 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor valproic acid suppresses the growth and increases the androgen responsiveness of prostate cancer cells
    • Chou, Y. W.; Chaturvedi, N. K.; Ouyang, S.; Lin, F. F.; Kaushik, D.; Wang, J.; Kim, I.; Lin, M. F. Histone deacetylase inhibitor valproic acid suppresses the growth and increases the androgen responsiveness of prostate cancer cells. Cancer Lett., 2011, 311(2), 177-186.
    • (2011) Cancer Lett , vol.311 , Issue.2 , pp. 177-186
    • Chou, Y.W.1    Chaturvedi, N.K.2    Ouyang, S.3    Lin, F.F.4    Kaushik, D.5    Wang, J.6    Kim, I.7    Lin, M.F.8
  • 2
    • 84855432518 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors in the generation of the anti-tumour immune response
    • Leggatt, G. R.; Gabrielli, B. Histone deacetylase inhibitors in the generation of the anti-tumour immune response. Immunol Cell Biol., 2012, 90(1), 33-38.
    • (2012) Immunol Cell Biol , vol.90 , Issue.1 , pp. 33-38
    • Leggatt, G.R.1    Gabrielli, B.2
  • 3
    • 34248631385 scopus 로고    scopus 로고
    • The role of histone deacetylases (HDACs) in human cancer
    • Ropero, S.; Esteller, M. The role of histone deacetylases (HDACs) in human cancer. Mol Oncol., 2007, 1(1), 19-25.
    • (2007) Mol Oncol , vol.1 , Issue.1 , pp. 19-25
    • Ropero, S.1    Esteller, M.2
  • 4
    • 57749170458 scopus 로고    scopus 로고
    • The many roles of histone deacetylases in development and physiology: Implications for disease and therapy
    • Haberland, M.; Montgomery, R. L.; Olson, E. N. The many roles of histone deacetylases in development and physiology: implications for disease and therapy. Nat Rev Genet., 2009, 10(1), 32-42.
    • (2009) Nat Rev Genet , vol.10 , Issue.1 , pp. 32-42
    • Haberland, M.1    Montgomery, R.L.2    Olson, E.N.3
  • 5
    • 84864004364 scopus 로고    scopus 로고
    • Complex role of histone deacetylase inhibitors in the treatment of non-small-cell lung cancer
    • Neal, J. W.; Sequist, L. V. Complex role of histone deacetylase inhibitors in the treatment of non-small-cell lung cancer. J. Clin. Oncol., 2012, 30(18), 2280-2282.
    • (2012) J. Clin. Oncol , vol.30 , Issue.18 , pp. 2280-2282
    • Neal, J.W.1    Sequist, L.V.2
  • 7
    • 34547864236 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: Molecular mechanisms of action
    • Xu, W. S.; Parmigiani, R. B.; Marks, P. A. Histone deacetylase inhibitors: molecular mechanisms of action. Oncogene., 2007, 26(37), 5541-5552.
    • (2007) Oncogene , vol.26 , Issue.37 , pp. 5541-5552
    • Xu, W.S.1    Parmigiani, R.B.2    Marks, P.A.3
  • 8
    • 41149141516 scopus 로고    scopus 로고
    • Histone deacetylases: Target enzymes for cancer therapy
    • Mottet, D.; Castronovo, V. Histone deacetylases: target enzymes for cancer therapy. Clin. Exp. Metastasis., 2008, 25(2), 183-189.
    • (2008) Clin. Exp. Metastasis , vol.25 , Issue.2 , pp. 183-189
    • Mottet, D.1    Castronovo, V.2
  • 9
    • 73949121803 scopus 로고    scopus 로고
    • Inhibition of histone deacetylase activity is a novel function of the antifolate drug methotrexate
    • Yang, P. M.; Lin, J. H.; Huang, W. Y.; Lin, Y. C.; Yeh, S. H.; Chen, C. C. Inhibition of histone deacetylase activity is a novel function of the antifolate drug methotrexate. Biochem Biophys Res Commun., 2010, 391(3), 1396-1399.
    • (2010) Biochem Biophys Res Commun , vol.391 , Issue.3 , pp. 1396-1399
    • Yang, P.M.1    Lin, J.H.2    Huang, W.Y.3    Lin, Y.C.4    Yeh, S.H.5    Chen, C.C.6
  • 10
    • 78649905409 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: A chemical genetics approach to understanding cellular functions
    • Marks, P. A. Histone deacetylase inhibitors: a chemical genetics approach to understanding cellular functions. Biochim. Biophys. Acta., 2010, 1799(10-12), 717-725.
    • (2010) Biochim. Biophys. Acta , vol.1799 , Issue.10-12 , pp. 717-725
    • Marks, P.A.1
  • 11
    • 77955914870 scopus 로고    scopus 로고
    • Identification of typespecific anticancer histone deacetylase inhibitors: Road to success
    • Noureen, N.; Rashid, H.; Kalsoom, S. Identification of typespecific anticancer histone deacetylase inhibitors: road to success. Cancer Chemother. Pharmacol., 2010, 66(4), 625-633.
    • (2010) Cancer Chemother. Pharmacol , vol.66 , Issue.4 , pp. 625-633
    • Noureen, N.1    Rashid, H.2    Kalsoom, S.3
  • 12
    • 42049103914 scopus 로고    scopus 로고
    • From natural products to small molecule ketone histone deacetylase inhibitors: Development of new class specific agents
    • Jones, P.; Steinkühler, C. From natural products to small molecule ketone histone deacetylase inhibitors: development of new class specific agents. Curr. Pharm. Des., 2008, 14(6), 545-561.
    • (2008) Curr. Pharm. Des , vol.14 , Issue.6 , pp. 545-561
    • Jones, P.1    Steinkühler, C.2
  • 13
    • 77955480670 scopus 로고    scopus 로고
    • Strategies in developing promising histone deacetylase inhibitors
    • Zhang, L.; Fang, H.; Xu, W. Strategies in developing promising histone deacetylase inhibitors. Med. Res. Rev., 2010, 30(4), 585-602.
    • (2010) Med. Res. Rev , vol.30 , Issue.4 , pp. 585-602
    • Zhang, L.1    Fang, H.2    Xu, W.3
  • 14
    • 70349128205 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: Design, structureactivity relationships and therapeutic implications for cancer
    • Marson, C. M. Histone deacetylase inhibitors: design, structureactivity relationships and therapeutic implications for cancer. Anticancer Agents Med. Chem., 2009, 9(6), 661-692.
    • (2009) Anticancer Agents Med. Chem , vol.9 , Issue.6 , pp. 661-692
    • Marson, C.M.1
  • 15
    • 84055190790 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors (HDACIs). Structure--activity relationships: History and new QSAR perspectives
    • Pontiki, E.; Hadjipavlou-Litina, D. Histone deacetylase inhibitors (HDACIs). Structure--activity relationships: history and new QSAR perspectives. Med. Res. Rev., 2012, 32(1), 1-165.
    • (2012) Med. Res. Rev , vol.32 , Issue.1 , pp. 1-165
    • Pontiki, E.1    Hadjipavlou-Litina, D.2
  • 17
    • 79955678223 scopus 로고    scopus 로고
    • Developing histone deacetylase inhibitors as anti-cancer therapeutics
    • Venugopal, B.; Evans, T. R. Developing histone deacetylase inhibitors as anti-cancer therapeutics. Curr. Med, Chem., 2011, 18(11), 1658-1671.
    • (2011) Curr. Med, Chem , vol.18 , Issue.11 , pp. 1658-1671
    • Venugopal, B.1    Evans, T.R.2
  • 18
    • 84860283904 scopus 로고    scopus 로고
    • An epigenetic approach to pancreatic cancer treatment: The prospective role of histone deacetylase inhibitors
    • Tinari, N.; De Tursi, M.; Grassadonia, A.; Zilli, M.; Stuppia, L.; Iacobelli, S.; Natoli, C. An epigenetic approach to pancreatic cancer treatment: the prospective role of histone deacetylase inhibitors. Curr Cancer Drug Targets., 2012, 12(4), 439-452.
    • (2012) Curr Cancer Drug Targets , vol.12 , Issue.4 , pp. 439-452
    • Tinari, N.1    De Tursi, M.2    Grassadonia, A.3    Zilli, M.4    Stuppia, L.5    Iacobelli, S.6    Natoli, C.7
  • 19
    • 84864035147 scopus 로고    scopus 로고
    • In silico modification of suberoylanilide hydroxamic acid (SAHA) as potential inhibitor for class IIhistone deacetylase (HDAC)
    • Tambunan, U. S.; Bramantya, N.; Parikesit, A. A. In silico modification of suberoylanilide hydroxamic acid (SAHA) as potential inhibitor for class IIhistone deacetylase (HDAC). BMC Bioinformatics., 2011, 12(13), s13-S23.
    • (2011) BMC Bioinformatics , vol.12 , Issue.13
    • Tambunan, U.S.1    Bramantya, N.2    Parikesit, A.A.3
  • 20
    • 79960185557 scopus 로고    scopus 로고
    • Romidepsin (Istodax, NSC 630176, FR901228, FK228, depsipeptide): A natural product recently approved for cutaneous T-cell lymphoma
    • VanderMolen, K. M.; McCulloch, W.; Pearce, C. J.; Oberlies, N. H. Romidepsin (Istodax, NSC 630176, FR901228, FK228, depsipeptide): a natural product recently approved for cutaneous T-cell lymphoma. J Antibiot (Tokyo)., 2011, 64(8), 525-531.
    • (2011) J Antibiot (Tokyo) , vol.64 , Issue.8 , pp. 525-531
    • VanderMolen, K.M.1    McCulloch, W.2    Pearce, C.J.3    Oberlies, N.H.4
  • 21
    • 67349228774 scopus 로고    scopus 로고
    • Development of the pan-DAC inhibitor panobinostat (LBH589): Successes and challenges
    • Atadja, P. Development of the pan-DAC inhibitor panobinostat (LBH589): successes and challenges. Cancer Lett., 2009, 280(2), 233-241.
    • (2009) Cancer Lett , vol.280 , Issue.2 , pp. 233-241
    • Atadja, P.1
  • 22
    • 81555228390 scopus 로고    scopus 로고
    • Belinostat: Clinical applications in solid tumors and lymphoma
    • Molife, L. R.; de Bono, J. S. Belinostat: clinical applications in solid tumors and lymphoma. Exp. Opin. Investig. Drugs., 2011, 20(12), 1723-1732.
    • (2011) Exp. Opin. Investig. Drugs , vol.20 , Issue.12 , pp. 1723-1732
    • Molife, L.R.1    de Bono, J.S.2
  • 24
    • 79956061602 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor PCI-24781 enhances chemotherapy-induced apoptosis in multidrug-resistant sarcoma cell lines
    • Yang, C.; Choy, E.; Hornicek, F. J.; Wood, K. B.; Schwab, J. H.; Liu, X.; Mankin, H.; Duan, Z. Histone deacetylase inhibitor PCI-24781 enhances chemotherapy-induced apoptosis in multidrug-resistant sarcoma cell lines. Anticancer Res., 2011, 31(4), 1115-1123.
    • (2011) Anticancer Res , vol.31 , Issue.4 , pp. 1115-1123
    • Yang, C.1    Choy, E.2    Hornicek, F.J.3    Wood, K.B.4    Schwab, J.H.5    Liu, X.6    Mankin, H.7    Duan, Z.8
  • 25
    • 79957949655 scopus 로고    scopus 로고
    • The oral histone deacetylase inhibitor ITF2357 reduces cytokines and protects islet cells in vivo and in vitro
    • Lewis, E. C.; Blaabjerg, L.; Størling, J.; Ronn, S. G.; Mascagni, P.; Dinarello, C. A.; Mandrup-Poulsen, T. The oral histone deacetylase inhibitor ITF2357 reduces cytokines and protects islet cells in vivo and in vitro. Mol. Med., 2011, 17(5-6), 369-377.
    • (2011) Mol. Med , vol.17 , Issue.5-6 , pp. 369-377
    • Lewis, E.C.1    Blaabjerg, L.2    Størling, J.3    Ronn, S.G.4    Mascagni, P.5    Dinarello, C.A.6    Mandrup-Poulsen, T.7
  • 27
    • 77951685547 scopus 로고    scopus 로고
    • The novel inhibitor of histone deacetylase resminostat (RAS2410) inhibits proliferation and induces apoptosis in multiple myeloma (MM) cells
    • Mandl-Weber, S.; Meinel, F. G.; Jankowsky, R.; Oduncu, F.; Schmidmaier, R.; Baumann, P. The novel inhibitor of histone deacetylase resminostat (RAS2410) inhibits proliferation and induces apoptosis in multiple myeloma (MM) cells. Br. J. Haematol., 2010, 149(4), 518-528.
    • (2010) Br. J. Haematol , vol.149 , Issue.4 , pp. 518-528
    • Mandl-Weber, S.1    Meinel, F.G.2    Jankowsky, R.3    Oduncu, F.4    Schmidmaier, R.5    Baumann, P.6
  • 28
    • 45749114198 scopus 로고    scopus 로고
    • Chemistry, biology, and QSAR studies of substituted biaryl hydroxamates and mercaptoacetamides as HDAC inhibitors nanomolar potency inhibitors of pancreatic cancer cell growth
    • Kozikowski, A. P.; Chen, Y.; Gaysin, A. M.; Savoy, D. N.; Billadeau, D. D.; Kim, K. H. Chemistry, biology, and QSAR studies of substituted biaryl hydroxamates and mercaptoacetamides as HDAC inhibitors nanomolar potency inhibitors of pancreatic cancer cell growth. Chem. Med. Chem., 2008, 3(3), 487-501.
    • (2008) Chem. Med. Chem , vol.3 , Issue.3 , pp. 487-501
    • Kozikowski, A.P.1    Chen, Y.2    Gaysin, A.M.3    Savoy, D.N.4    Billadeau, D.D.5    Kim, K.H.6
  • 29
    • 49449113465 scopus 로고    scopus 로고
    • Use of the nitrile oxide cycloaddition (NOC) reaction for molecular probe generation: A new class of enzyme selective histone deacetylase inhibitors (HDACIs) showing picomolar activity at HDAC6
    • Kozikowski, A. P.; Tapadar, S.; Luchini, D. N.; Kim, K. H.; Billadeau, D. D. Use of the nitrile oxide cycloaddition (NOC) reaction for molecular probe generation: a new class of enzyme selective histone deacetylase inhibitors (HDACIs) showing picomolar activity at HDAC6. J. Med. Chem., 2008, 51(15), 4370-4373.
    • (2008) J. Med. Chem , vol.51 , Issue.15 , pp. 4370-4373
    • Kozikowski, A.P.1    Tapadar, S.2    Luchini, D.N.3    Kim, K.H.4    Billadeau, D.D.5
  • 30
    • 43049104161 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship of histone deacetylase (HDAC) inhibitors with triazole-linked cap group
    • Chen, P. C.; Patil, V.; Guerrant, W.; Green, P.; Oyelere, A. K. Synthesis and structure-activity relationship of histone deacetylase (HDAC) inhibitors with triazole-linked cap group. Bioorg. Med. Chem., 2008, 16(9), 4839-4853.
    • (2008) Bioorg. Med. Chem , vol.16 , Issue.9 , pp. 4839-4853
    • Chen, P.C.1    Patil, V.2    Guerrant, W.3    Green, P.4    Oyelere, A.K.5
  • 31
    • 70349761276 scopus 로고    scopus 로고
    • Design, synthesis and preliminary biological evaluation of N-hydroxy-4-(3-phenylpropanamido) benzamide (HPPB) derivatives as novel histone deacetylase inhibitors
    • Jiao, J.; Fang, H.; Wang, X.; Guan, P.; Yuan, Y.; Xu, W. Design, synthesis and preliminary biological evaluation of N-hydroxy-4-(3-phenylpropanamido) benzamide (HPPB) derivatives as novel histone deacetylase inhibitors. Eur. J. Med. Chem., 2009, 44(11), 4470-4476.
    • (2009) Eur. J. Med. Chem , vol.44 , Issue.11 , pp. 4470-4476
    • Jiao, J.1    Fang, H.2    Wang, X.3    Guan, P.4    Yuan, Y.5    Xu, W.6
  • 34
    • 63149180510 scopus 로고    scopus 로고
    • N-Hydroxy-(4-oxime)-cinnamide: A versatile scaffold for the synthesis of novel histone deacetylase [correction of deacetilase] (HDAC) inhibitors
    • Giannini, G.; Marzi, M.; Pezzi, R.; Brunetti, T.; Battistuzzi, G.; Marzo, M. D.; Cabri, W.; Vesci, L.; Pisano, C. N-Hydroxy-(4-oxime)-cinnamide: a versatile scaffold for the synthesis of novel histone deacetylase [correction of deacetilase] (HDAC) inhibitors. Bioorg. Med. Chem. Lett., 2009, 19(8), 2346-2349.
    • (2009) Bioorg. Med. Chem. Lett , vol.19 , Issue.8 , pp. 2346-2349
    • Giannini, G.1    Marzi, M.2    Pezzi, R.3    Brunetti, T.4    Battistuzzi, G.5    Marzo, M.D.6    Cabri, W.7    Vesci, L.8    Pisano, C.9
  • 36
  • 37
    • 65149094611 scopus 로고    scopus 로고
    • Isoxazole moiety in the linker region of HDAC inhibitors adjacent to the Zn-chelating group: Effects on HDAC biology and antiproliferative activity
    • Tapadar, S.; He, R.; Luchini, D. N.; Billadeau, D. D.; Kozikowski, AP. Isoxazole moiety in the linker region of HDAC inhibitors adjacent to the Zn-chelating group: effects on HDAC biology and antiproliferative activity. Bioorg. Med. Chem. Lett., 2009, 19(11), 3023-3026.
    • (2009) Bioorg. Med. Chem. Lett , vol.19 , Issue.11 , pp. 3023-3026
    • Tapadar, S.1    He, R.2    Luchini, D.N.3    Billadeau, D.D.4    Kozikowski, A.P.5
  • 38
    • 80052925413 scopus 로고    scopus 로고
    • The structural requirements of histone deacetylase inhibitors: Suberoylanilide hydroxamic acid analogs modified at the C3 position display isoform selectivity
    • Choi, S. E.; Weerasinghe, S. V.; Pflum, M. K. The structural requirements of histone deacetylase inhibitors: Suberoylanilide hydroxamic acid analogs modified at the C3 position display isoform selectivity. Bioorg. Med. Chem. Lett., 2011, 21(20), 6139-6142.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , Issue.20 , pp. 6139-6142
    • Choi, S.E.1    Weerasinghe, S.V.2    Pflum, M.K.3
  • 40
    • 80052555163 scopus 로고    scopus 로고
    • 2, 5-Disubstituted-1, 3, 4-oxadiazoles/thiadiazole as surface recognition moiety: Design and synthesis of novel hydroxamic acid based histone deacetylase inhibitors
    • Rajak, H.; Agarawal, A.; Parmar, P.; Thakur, B. S.; Veerasamy, R.; Sharma, P. C.; Kharya, M. D. 2, 5-Disubstituted-1, 3, 4-oxadiazoles/thiadiazole as surface recognition moiety: design and synthesis of novel hydroxamic acid based histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2011, 21(19), 5735-5738.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , Issue.19 , pp. 5735-5738
    • Rajak, H.1    Agarawal, A.2    Parmar, P.3    Thakur, B.S.4    Veerasamy, R.5    Sharma, P.C.6    Kharya, M.D.7
  • 41
    • 78650513499 scopus 로고    scopus 로고
    • Design and synthesis of aryl ether and sulfone hydroxamic acids as potent histone deacetylase (HDAC) inhibitors
    • Pabba, C.; Gregg, B. T.; Kitchen, D. B.; Chen, Z. J.; Judkins, A. Design and synthesis of aryl ether and sulfone hydroxamic acids as potent histone deacetylase (HDAC) inhibitors. Bioorg. Med. Chem. Lett., 2011, 21(1), 324-328.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , Issue.1 , pp. 324-328
    • Pabba, C.1    Gregg, B.T.2    Kitchen, D.B.3    Chen, Z.J.4    Judkins, A.5
  • 42
    • 79851512347 scopus 로고    scopus 로고
    • Structure and property based design, synthesis and biological evaluation of lactam based HDAC inhibitors
    • Choi, E.; Lee, C.; Park, J. E.; Seo, J. J.; Cho, M.; Kang, J. S.; Kim, H. M.; Park, S. K.; Lee, K.; Han, G. Structure and property based design, synthesis and biological evaluation of lactam based HDAC inhibitors. Bioorg. Med. Chem. Lett., 2011, 21(4), 1218-1221.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , Issue.4 , pp. 1218-1221
    • Choi, E.1    Lee, C.2    Park, J.E.3    Seo, J.J.4    Cho, M.5    Kang, J.S.6    Kim, H.M.7    Park, S.K.8    Lee, K.9    Han, G.10
  • 45
    • 79955455755 scopus 로고    scopus 로고
    • Development of tetrahydroisoquinoline-based hydroxamic acid derivatives: Potent histone deacetylase inhibitors with marked in vitro and in vivo antitumor activities
    • Zhang, Y.; Feng, J.; Jia, Y.; Wang, X.; Zhang, L.; Liu, C.; Fang, H.; Xu, W. Development of tetrahydroisoquinoline-based hydroxamic acid derivatives: potent histone deacetylase inhibitors with marked in vitro and in vivo antitumor activities. J. Med. Chem., 2011, 54(8), 2823-2838.
    • (2011) J. Med. Chem , vol.54 , Issue.8 , pp. 2823-2838
    • Zhang, Y.1    Feng, J.2    Jia, Y.3    Wang, X.4    Zhang, L.5    Liu, C.6    Fang, H.7    Xu, W.8
  • 48
    • 84855776224 scopus 로고    scopus 로고
    • Synthesis and biochemical analysis of 2, 2, 3, 3, 4, 4, 5, 5, 6, 6, 7, 7-dodecafluoro-N-hydroxy-octanediamides as inhibitors of human histone deacetylases
    • Henkes, L. M.; Haus, P.; Jäger, F.; Ludwig, J.; Meyer-Almes, F. J. Synthesis and biochemical analysis of 2, 2, 3, 3, 4, 4, 5, 5, 6, 6, 7, 7-dodecafluoro-N-hydroxy-octanediamides as inhibitors of human histone deacetylases. Bioorg. Med. Chem., 2012, 20(2), 985-995.
    • (2012) Bioorg. Med. Chem , vol.20 , Issue.2 , pp. 985-995
    • Henkes, L.M.1    Haus, P.2    Jäger, F.3    Ludwig, J.4    Meyer-Almes, F.J.5
  • 49
    • 84861579581 scopus 로고    scopus 로고
    • Design, synthesis and preliminary bioactivity studies of 1, 3, 4-thiadiazole hydroxamic acid derivatives as novel histone deacetylase inhibitors
    • Guan, P.; Sun, F.; Hou, X.; Wang, F.; Yi, F.; Xu, W.; Fang, H. Design, synthesis and preliminary bioactivity studies of 1, 3, 4-thiadiazole hydroxamic acid derivatives as novel histone deacetylase inhibitors. Bioorg. Med. Chem., 2012, 20(12), 3865-3872.
    • (2012) Bioorg. Med. Chem , vol.20 , Issue.12 , pp. 3865-3872
    • Guan, P.1    Sun, F.2    Hou, X.3    Wang, F.4    Yi, F.5    Xu, W.6    Fang, H.7
  • 50
    • 84861571256 scopus 로고    scopus 로고
    • Structure and property based design, synthesis and biological evaluation of lactam basedHDAC inhibitors: Part II
    • Lee, C.; Choi, E.; Cho, M.; Lee, B.; Oh, S. J.; Park, S. K.; Lee, K.; Kim, H. M.; Han, G. Structure and property based design, synthesis and biological evaluation of lactam basedHDAC inhibitors: part II. Bioorg. Med. Chem. Lett., 2012, 22(12), 4189-4192.
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , Issue.12 , pp. 4189-4192
    • Lee, C.1    Choi, E.2    Cho, M.3    Lee, B.4    Oh, S.J.5    Park, S.K.6    Lee, K.7    Kim, H.M.8    Han, G.9
  • 51
    • 84860312887 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 1-arylsulfonyl-5-(Nhydroxyacrylamide) indoles as potent histone deacetylase inhibitors with antitumor activity in vivo
    • Lai, M. J.; Huang, H. L.; Pan, S. L.; Liu, Y. M.; Peng, C. Y.; Lee, H. Y.; Yeh, T. K.; Huang, P. H.; Teng, C. M.; Chen, C. S.; Chuang, H. Y.; Liou, J. P. Synthesis and biological evaluation of 1-arylsulfonyl-5-(Nhydroxyacrylamide) indoles as potent histone deacetylase inhibitors with antitumor activity in vivo. J. Med. Chem., 2012, 55(8), 3777-3791.
    • (2012) J. Med. Chem , vol.55 , Issue.8 , pp. 3777-3791
    • Lai, M.J.1    Huang, H.L.2    Pan, S.L.3    Liu, Y.M.4    Peng, C.Y.5    Lee, H.Y.6    Yeh, T.K.7    Huang, P.H.8    Teng, C.M.9    Chen, C.S.10    Chuang, H.Y.11    Liou, J.P.12
  • 52
    • 33646548906 scopus 로고    scopus 로고
    • Rational design of non-hydroxamate histone deacetylase inhibitors
    • Suzuki, T.; Miyata, N. Rational design of non-hydroxamate histone deacetylase inhibitors. Mini. Rev. Med. Chem., 2006, 6(5), 515-526.
    • (2006) Mini. Rev. Med. Chem , vol.6 , Issue.5 , pp. 515-526
    • Suzuki, T.1    Miyata, N.2
  • 56
  • 60
    • 41849134699 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of histone deacetylase inhibitors that are based on FR235222: A cyclic tetrapeptide scaffold
    • Singh, E. K.; Ravula, S.; Pan, C. M.; Pan, P. S.; Vasko, R. C.; Lapera, S. A.; Weerasinghe, S. V.; Pflum, M. K.; McAlpine, SR. Synthesis and biological evaluation of histone deacetylase inhibitors that are based on FR235222: a cyclic tetrapeptide scaffold. Bioorg Med Chem Lett., 2008, 18(8), 2549-2554.
    • (2008) Bioorg Med Chem Lett , vol.18 , Issue.8 , pp. 2549-2554
    • Singh, E.K.1    Ravula, S.2    Pan, C.M.3    Pan, P.S.4    Vasko, R.C.5    Lapera, S.A.6    Weerasinghe, S.V.7    Pflum, M.K.8    McAlpine, S.R.9
  • 63
    • 67749142082 scopus 로고    scopus 로고
    • Design, synthesis, biological evaluation, and structural characterization of potent histone deacetylase inhibitors based on cyclic alpha/beta-tetrapeptide architectures
    • Montero, A.; Beierle, J. M.; Olsen, C. A.; Ghadiri, M. R. Design, synthesis, biological evaluation, and structural characterization of potent histone deacetylase inhibitors based on cyclic alpha/beta-tetrapeptide architectures. J. Am. Chem. Soc., 2009, 131(8), 3033-3041.
    • (2009) J. Am. Chem. Soc , vol.131 , Issue.8 , pp. 3033-3041
    • Montero, A.1    Beierle, J.M.2    Olsen, C.A.3    Ghadiri, M.R.4
  • 64
    • 72249094958 scopus 로고    scopus 로고
    • Discovery of potent and selective histone deacetylase inhibitors via focused combinatorial libraries of cyclic alpha3beta-tetrapeptides
    • Olsen, C. A.; Ghadiri, M. R. Discovery of potent and selective histone deacetylase inhibitors via focused combinatorial libraries of cyclic alpha3beta-tetrapeptides. J. Med. Chem., 2009, 52(23), 7836-7846.
    • (2009) J. Med. Chem , vol.52 , Issue.23 , pp. 7836-7846
    • Olsen, C.A.1    Ghadiri, M.R.2
  • 67
    • 77149129028 scopus 로고    scopus 로고
    • Synthesis, molecular docking and biological evaluation as HDAC nhibitors of cyclopeptide mimetics by a tandem three-component reaction and intramolecular [3+2] cycloaddition
    • Pirali, T.; Faccio, V.; Mossetti, R.; Grolla, A. A.; Di Micco, S.; Bifulco, G.; Genazzani, A. A.; Tron, G. C. Synthesis, molecular docking and biological evaluation as HDAC nhibitors of cyclopeptide mimetics by a tandem three-component reaction and intramolecular [3+2] cycloaddition. Mol. Divers., 2010, 14(1), 109-121.
    • (2010) Mol. Divers , vol.14 , Issue.1 , pp. 109-121
    • Pirali, T.1    Faccio, V.2    Mossetti, R.3    Grolla, A.A.4    Di Micco, S.5    Bifulco, G.6    Genazzani, A.A.7    Tron, G.C.8
  • 68
    • 77955430918 scopus 로고    scopus 로고
    • Histone Deacetylase Inhibitors: Synthesis of Cyclic Tetrapeptides and their Triazole Analogues
    • Singh, E. K.; Nazarova, L. A.; Lapera, S. A.; Alexander, L. D.; McAlpine, S. R. Histone Deacetylase Inhibitors: Synthesis of Cyclic Tetrapeptides and their Triazole Analogues. Tetrahedron Lett., 2010, 51(33), 4357-4360.
    • (2010) Tetrahedron Lett , vol.51 , Issue.33 , pp. 4357-4360
    • Singh, E.K.1    Nazarova, L.A.2    Lapera, S.A.3    Alexander, L.D.4    McAlpine, S.R.5
  • 69
    • 84862800182 scopus 로고    scopus 로고
    • Synthesis, evaluation and molecular modeling of cyclic tetrapeptide histone deacetylase inhibitors as anticancer agents
    • Huang, D.; Li, X.; Sun, L.; Xiu, Z.; Nishino, N. Synthesis, evaluation and molecular modeling of cyclic tetrapeptide histone deacetylase inhibitors as anticancer agents. J. Pept. Sci., 2012, 18(4), 242-251.
    • (2012) J. Pept. Sci , vol.18 , Issue.4 , pp. 242-251
    • Huang, D.1    Li, X.2    Sun, L.3    Xiu, Z.4    Nishino, N.5
  • 74
    • 65649113311 scopus 로고    scopus 로고
    • Synthesis and modeling of new benzofuranone histone deacetylase inhibitors that stimulate tumor suppressor gene expression
    • Charrier, C.; Clarhaut, J.; Gesson, J. P.; Estiu, G.; Wiest, O.; Roche, J.; Bertrand, P. Synthesis and modeling of new benzofuranone histone deacetylase inhibitors that stimulate tumor suppressor gene expression. J. Med. Chem., 2009, 52(9), 3112-3115.
    • (2009) J. Med. Chem , vol.52 , Issue.9 , pp. 3112-3115
    • Charrier, C.1    Clarhaut, J.2    Gesson, J.P.3    Estiu, G.4    Wiest, O.5    Roche, J.6    Bertrand, P.7
  • 76
    • 84857357287 scopus 로고    scopus 로고
    • Antitumor activity of new orally bioavailable 2-amino-5-(thiophen-2-yl)benzamide-series histone deacetylase inhibitors, possessing an aqueous soluble functional group as a surface recognition domain
    • Hirata, Y.; Hirata, M.; Kawaratani, Y.; Shibano, M.; Taniguchi, M.; Yasuda, M.; Ohmomo, Y.; Nagaoka, Y.; Baba, K.; Uesato, S. Antitumor activity of new orally bioavailable 2-amino-5-(thiophen-2-yl)benzamide-series histone deacetylase inhibitors, possessing an aqueous soluble functional group as a surface recognition domain. Bioorg. Med. Chem. Lett., 2012, 22(5), 1926-1930.
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , Issue.5 , pp. 1926-1930
    • Hirata, Y.1    Hirata, M.2    Kawaratani, Y.3    Shibano, M.4    Taniguchi, M.5    Yasuda, M.6    Ohmomo, Y.7    Nagaoka, Y.8    Baba, K.9    Uesato, S.10
  • 77
    • 84863983721 scopus 로고    scopus 로고
    • Design, synthesis, modeling, biological evaluation and photoaffinity labeling studies of novelseries of photoreactive benzamide probes for histone deacetylase 2
    • Vaidya, A. S.; Karumudi, B.; Mendonca, E.; Madriaga, A.; Abdelkarim, H.; van Breemen, R. B.; Petukhov, P. A. Design, synthesis, modeling, biological evaluation and photoaffinity labeling studies of novelseries of photoreactive benzamide probes for histone deacetylase 2. Bioorg. Med. Chem. Lett., 2012, 22(15), 5025-5030.
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , Issue.15 , pp. 5025-5030
    • Vaidya, A.S.1    Karumudi, B.2    Mendonca, E.3    Madriaga, A.4    Abdelkarim, H.5    van Breemen, R.B.6    Petukhov, P.A.7
  • 81
    • 84860312887 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indoles as potent histone deacetylase inhibitors with antitumor activity in vivo
    • Lai, M. J.; Huang, H. L.; Pan, S. L.; Liu, Y. M.; Peng, C. Y.; Lee, H. Y.; Yeh, T. K.; Huang, P. H.; Teng, C. M.; Chen, C. S.; Chuang, H. Y.; Liou, J. P. Synthesis and biological evaluation of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indoles as potent histone deacetylase inhibitors with antitumor activity in vivo. J. Med. Chem., 2012, 55(8), 3777-3791.
    • (2012) J. Med. Chem , vol.55 , Issue.8 , pp. 3777-3791
    • Lai, M.J.1    Huang, H.L.2    Pan, S.L.3    Liu, Y.M.4    Peng, C.Y.5    Lee, H.Y.6    Yeh, T.K.7    Huang, P.H.8    Teng, C.M.9    Chen, C.S.10    Chuang, H.Y.11    Liou, J.P.12
  • 82
    • 64049106355 scopus 로고    scopus 로고
    • Synthesis and histone deacetylase inhibitory activity of largazole analogs: Alteration of the zinc-binding domain and macrocyclic scaffold
    • Bowers, A. A.; West, N.; Newkirk, T. L.; Troutman-Youngman, A. E.; Schreiber, S. L.; Wiest, O.; Bradner, J. E.; Williams, R. M. Synthesis and histone deacetylase inhibitory activity of largazole analogs: alteration of the zinc-binding domain and macrocyclic scaffold. Org. Lett., 2009, 11(6), 1301-1304.
    • (2009) Org. Lett , vol.11 , Issue.6 , pp. 1301-1304
    • Bowers, A.A.1    West, N.2    Newkirk, T.L.3    Troutman-Youngman, A.E.4    Schreiber, S.L.5    Wiest, O.6    Bradner, J.E.7    Williams, R.M.8
  • 83
    • 80052934367 scopus 로고    scopus 로고
    • Synthesis and evaluation of aliphatic-chain hydroxamates capped with osthole derivatives as histone deacetylase inhibitors
    • Huang, W. J.; Chen, C. C.; Chao, S. W.; Yu, C. C.; Yang, C. Y.; Guh, J. H.; Lin, Y. C.; Kuo, C. I.; Yang, P.; Chang, C. I. Synthesis and evaluation of aliphatic-chain hydroxamates capped with osthole derivatives as histone deacetylase inhibitors. Eur. J. Med. Chem., 2011, 46(9), 4042-4049.
    • (2011) Eur. J. Med. Chem , vol.46 , Issue.9 , pp. 4042-4049
    • Huang, W.J.1    Chen, C.C.2    Chao, S.W.3    Yu, C.C.4    Yang, C.Y.5    Guh, J.H.6    Lin, Y.C.7    Kuo, C.I.8    Yang, P.9    Chang, C.I.10
  • 84
    • 80055086046 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors from Burkholderia thailandensis
    • Klausmeyer, P.; Shipley, S. M.; Zuck, K. M.; McCloud, T. G. Histone deacetylase inhibitors from Burkholderia thailandensis. J. Nat. Prod., 2011, 74(10), 2039-2044.
    • (2011) J. Nat. Prod , vol.74 , Issue.10 , pp. 2039-2044
    • Klausmeyer, P.1    Shipley, S.M.2    Zuck, K.M.3    McCloud, T.G.4
  • 85
    • 79960896421 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of piperamide analogues as HDAC inhibitors
    • Luo, Y.; Liu, H. M.; Su, M. B.; Sheng, L.; Zhou, Y. B.; Li, J.; Lu, W. Synthesis and biological evaluation of piperamide analogues as HDAC inhibitors. Bioorg. Med. Chem. Lett., 2011, 21(16), 4844-4846.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , Issue.16 , pp. 4844-4846
    • Luo, Y.1    Liu, H.M.2    Su, M.B.3    Sheng, L.4    Zhou, Y.B.5    Li, J.6    Lu, W.7
  • 87
    • 70349525349 scopus 로고    scopus 로고
    • Discovery, biological activity, synthesis and potential therapeutic utility of naturally occurring histone deacetylase inhibitors
    • Newkirk, T. L.; Bowers, A. A.; Williams, R. M. Discovery, biological activity, synthesis and potential therapeutic utility of naturally occurring histone deacetylase inhibitors. Nat. Prod. Rep., 2009, 26(10), 1293-1320.
    • (2009) Nat. Prod. Rep , vol.26 , Issue.10 , pp. 1293-1320
    • Newkirk, T.L.1    Bowers, A.A.2    Williams, R.M.3
  • 91
    • 65449160954 scopus 로고    scopus 로고
    • Exploring bis-(indolyl)methane moiety as an alternative and innovative CAP group in the design of histone deacetylase (HDAC) inhibitors
    • Giannini, G.; Marzi, M.; Marzo, M. D.; Battistuzzi, G.; Pezzi, R.; Brunetti, T.; Cabri, W.; Vesci, L.; Pisano, C. Exploring bis-(indolyl)methane moiety as an alternative and innovative CAP group in the design of histone deacetylase (HDAC) inhibitors. Bioorg. Med. Chem. Lett., 2009, 19(10), 2840-2843.
    • (2009) Bioorg. Med. Chem. Lett , vol.19 , Issue.10 , pp. 2840-2843
    • Giannini, G.1    Marzi, M.2    Marzo, M.D.3    Battistuzzi, G.4    Pezzi, R.5    Brunetti, T.6    Cabri, W.7    Vesci, L.8    Pisano, C.9
  • 92
  • 95
    • 77649193260 scopus 로고    scopus 로고
    • SelSA, selenium analogs of SAHA as potent histone deacetylase inhibitors
    • Desai, D.; Salli, U.; Vrana, K. E.; Amin, S. SelSA, selenium analogs of SAHA as potent histone deacetylase inhibitors. Bioorg. Med. Chem. Lett., 2010, 20(6), 2044-2047.
    • (2010) Bioorg. Med. Chem. Lett , vol.20 , Issue.6 , pp. 2044-2047
    • Desai, D.1    Salli, U.2    Vrana, K.E.3    Amin, S.4
  • 96
    • 76449103608 scopus 로고    scopus 로고
    • Fluoroalkene modification of mercaptoacetamidebased histone deacetylase inhibitors
    • Osada, S.; Sano, S.; Ueyama, M.; Chuman, Y.; Kodama, H.; Sakaguchi, K. Fluoroalkene modification of mercaptoacetamidebased histone deacetylase inhibitors. Bioorg. Med. Chem., 2010, 18(2), 605-611.
    • (2010) Bioorg. Med. Chem , vol.18 , Issue.2 , pp. 605-611
    • Osada, S.1    Sano, S.2    Ueyama, M.3    Chuman, Y.4    Kodama, H.5    Sakaguchi, K.6
  • 102
    • 84860334379 scopus 로고    scopus 로고
    • A novel series of l-2-benzyloxycarbonylamino-8-(2-pyridyl)-disulfidyloctanoic acid derivatives ashistone deacetylase inhibitors: Design, synthesis and molecular modeling study
    • Huang, D.; Li, X.; Wei, Y.; Xiu, Z. A novel series of l-2-benzyloxycarbonylamino-8-(2-pyridyl)-disulfidyloctanoic acid derivatives ashistone deacetylase inhibitors: design, synthesis and molecular modeling study. Eur. J. Med. Chem., 2012, 52, 111-122.
    • (2012) Eur. J. Med. Chem , vol.52 , pp. 111-122
    • Huang, D.1    Li, X.2    Wei, Y.3    Xiu, Z.4
  • 104
    • 84862663133 scopus 로고    scopus 로고
    • Multi-targeted hybrids based on HDAC inhibitors for anticancer drug discovery
    • Seo, S. Y. Multi-targeted hybrids based on HDAC inhibitors for anticancer drug discovery. Arch. Pharm. Res., 2012, 35(2), 197-200.
    • (2012) Arch. Pharm. Res , vol.35 , Issue.2 , pp. 197-200
    • Seo, S.Y.1
  • 105
    • 77949353758 scopus 로고    scopus 로고
    • Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer
    • Cai, X.; Zhai, H. X.; Wang, J.; Forrester, J.; Qu, H.; Yin, L.; Lai, C. J.; Bao, R.; Qian, C. Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer. J. Med. Chem., 2010, 53(5), 2000-2009.
    • (2010) J. Med. Chem , vol.53 , Issue.5 , pp. 2000-2009
    • Cai, X.1    Zhai, H.X.2    Wang, J.3    Forrester, J.4    Qu, H.5    Yin, L.6    Lai, C.J.7    Bao, R.8    Qian, C.9
  • 106
    • 45849101673 scopus 로고    scopus 로고
    • Targeting cancer and neuropathy with histone deacetylase inhibitors: Two birds with one stone?
    • Rodriguez-Menendez, V.; Tremolizzo, L.; Cavaletti, G. Targeting cancer and neuropathy with histone deacetylase inhibitors: two birds with one stone? Curr. Cancer Drug Targets, 2008, 8(4), 266-274.
    • (2008) Curr. Cancer Drug Targets , vol.8 , Issue.4 , pp. 266-274
    • Rodriguez-Menendez, V.1    Tremolizzo, L.2    Cavaletti, G.3
  • 107
    • 65449122745 scopus 로고    scopus 로고
    • Targeting histone deacetylase inhibitors for anti-malarial therapy
    • Andrews, K. T.; Tran, T. N.; Wheatley, N. C.; Fairlie, D. P. Targeting histone deacetylase inhibitors for anti-malarial therapy. Curr. Top. Med. Chem., 2009, 9(3), 292-308.
    • (2009) Curr. Top. Med. Chem , vol.9 , Issue.3 , pp. 292-308
    • Andrews, K.T.1    Tran, T.N.2    Wheatley, N.C.3    Fairlie, D.P.4
  • 108
    • 77957033927 scopus 로고    scopus 로고
    • Histone Deacetylase inhibitors: New promise in the treatment of immune and inflammatory diseases
    • Shuttleworth, S. J.; Bailey, S. G.; Townsend, P. A. Histone Deacetylase inhibitors: new promise in the treatment of immune and inflammatory diseases. Curr. Drug Targets, 2010, 11(11), 1430-1438.
    • (2010) Curr. Drug Targets , vol.11 , Issue.11 , pp. 1430-1438
    • Shuttleworth, S.J.1    Bailey, S.G.2    Townsend, P.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.