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Volumn 3, Issue 2, 2012, Pages 92-99

Hydroxamic acid - A novel molecule for anticancer therapy

Author keywords

Cancer; Histone deacetylase; Hydroxamic acid; MMP inhibitor

Indexed keywords

3 (4 AROYL 1 METHYL 1H PYRROL 2 YL) N HYDROXY 2 PROPENAMIDE; 4 (3 PYRIDYL)PHENYLHYDROXAMIC ACID; 5 PYRIDIN 2 YL THIOPHENE 2 HYDROXAMIC ACID; 7 [4 (DIMETHYLAMINO)PHENYL] N HYDROXY 4,6 DIMETHYL 7 OXOHEPTA 2,4 DIENAMIDE; AMINO SUBEROYLHYDROXAMIC ACID; ARYL ETHER HYDROXAMIC ACID; BENZOFURANONE HYDROXAMIC ACID; BIPHENYL 4 YL ACRYLOHYDROXAMIC ACID; BUTYLATED HYDROXYANISOLE; CISPLATIN; HISTONE DEACETYLASE; HISTONE DEACETYLASE INHIBITOR; HYDROXAMIC ACID; HYDROXAMIC ACID DERIVATIVE; MATRIX METALLOPROTEINASE; N (2 AMINOPHENYL) 4 [(4 PYRIDIN 3 YLPYRIMIDIN 2 YLAMINO)METHYL]BENZAMIDE; N (6 OXO 7 PHENYLHEPTYL) 2 SULFANYLETHANETHIOAMIDE; N 2 DIHYDROXYBENZAMIDE; N HYDROXY 2 [4 (NAPHTHALENE 2 YLSULFONYL)PIPERAZIN 1 YL]PYRIMIDINE 5 CARBOXAMIDE; N HYDROXY 3 PHENOXYBENZAMIDE; N HYDROXY 4 (4 PHENYLBUTYRYLAMINO)BENZAMIDE; N HYDROXY 8 OXO 9 PHENYLNONAMETHIOAMIDE; N HYDROXYBIPHENYL 3 CARBOXAMIDE; N HYDROXYHEPTAN 3 AMIDE; N HYDROXYNAPHTHALENE 1 CARBOXAMIDE; SALICYHYDROXAMIC ACID; THIAZOLE 5 HYDROXAMIC ACID; TRICHOSTATIN A; UNCLASSIFIED DRUG; UNINDEXED DRUG; VORINOSTAT;

EID: 84866433051     PISSN: 22314040     EISSN: 09762094     Source Type: Journal    
DOI: 10.4103/2231-4040.97281     Document Type: Article
Times cited : (42)

References (30)
  • 4
    • 23944487678 scopus 로고    scopus 로고
    • Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors
    • DOI 10.1021/jm0503749
    • Lu Q, Wang DS, Chen CS, Hu YD, Chen CS. Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors. J Med Chem 2005;48:5530-5 (Pubitemid 41209250)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.17 , pp. 5530-5535
    • Lu, Q.1    Wang, D.-S.2    Chen, C.-S.3    Hu, Y.-D.4    Chen, C.-S.5
  • 10
    • 62749154929 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of biphenyl-4-ylacrylohydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors
    • Dallavalle S, Cincinelli R, Nannei R, Merlini L, Morini G, Penco S, et al. Design, synthesis, and evaluation of biphenyl-4-ylacrylohydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors. Eur. J Med Chem 2009;44:1900-12
    • (2009) Eur. J Med Chem , vol.44 , pp. 1900-1912
    • Dallavalle, S.1    Cincinelli, R.2    Nannei, R.3    Merlini, L.4    Morini, G.5    Penco, S.6
  • 11
    • 65649125951 scopus 로고    scopus 로고
    • Design, synthesis, and biological activity of boronic acid-based histone deacetylase inhibitors
    • Suzuki N, Suzuki T, Ota Y, Nakano T, Kurihara M, Okuda H, et al. Design, synthesis, and biological activity of boronic acid-based histone deacetylase inhibitors. J Med Chem 2009;52:2909-22
    • (2009) J Med Chem , vol.52 , pp. 2909-2922
    • Suzuki, N.1    Suzuki, T.2    Ota, Y.3    Nakano, T.4    Kurihara, M.5    Okuda, H.6
  • 12
    • 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 JP, Estiu G, Wiest O, Roche J, et al. Synthesis and modeling of new benzofuranone histone deacetylase inhibitors that stimulate tumor suppressor gene expression. J Med Chem 2009;52:3112-5
    • (2009) J Med Chem , vol.52 , pp. 3112-3115
    • Charrier, C.1    Clarhaut, J.2    Gesson, J.P.3    Estiu, G.4    Wiest, O.5    Roche, J.6
  • 13
    • 67651155861 scopus 로고    scopus 로고
    • Antioxidant activity of NSAID hydroxamic acids
    • Koncic MZ, Rajic Z, Petric N, Zorc B. Antioxidant activity of NSAID hydroxamic acids. Acta Pharm 2000;59:235-42
    • (2000) Acta Pharm , vol.59 , pp. 235-242
    • Koncic, M.Z.1    Rajic, Z.2    Petric, N.3    Zorc, B.4
  • 14
    • 23944487678 scopus 로고    scopus 로고
    • Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors
    • DOI 10.1021/jm0503749
    • Lu Q, Wang DS, Chen CS, Hu YD, Chen CS. Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors. J Med Chem 2005;48:5530-5 (Pubitemid 41209250)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.17 , pp. 5530-5535
    • Lu, Q.1    Wang, D.-S.2    Chen, C.-S.3    Hu, Y.-D.4    Chen, C.-S.5
  • 16
    • 78650513499 scopus 로고    scopus 로고
    • Design and synthesis of aryl ether and sulfonehydroxamic acids as potent histone deacetylase (HDAC) inhibitors
    • Pabba C, Gregg BT, Kitchen DB, Chen ZJ, Judkins A. Design and synthesis of aryl ether and sulfonehydroxamic acids as potent histone deacetylase (HDAC) inhibitors. Bioorg Med Chem Lett 2011;21:324-8
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 324-328
    • Pabba, C.1    Gregg, B.T.2    Kitchen, D.B.3    Chen, Z.J.4    Judkins, A.5
  • 18
    • 59649092334 scopus 로고    scopus 로고
    • Zn(II)-dependent histone deacetylase inhibitors: Suberoylanilidehydroxamic acid and trichostatin A
    • Codd R, Braich N, Liu J, Soe CZ, Pakchung AA. Zn(II)-dependent histone deacetylase inhibitors: Suberoylanilidehydroxamic acid and trichostatin A. Int J Biochem Cell Biol 2009;41:736-9
    • (2009) Int J Biochem Cell Biol , vol.41 , pp. 736-739
    • Codd, R.1    Braich, N.2    Liu, J.3    Soe, C.Z.4    Pakchung, A.A.5
  • 19
    • 33645847864 scopus 로고    scopus 로고
    • Carbonyland sulfur-containing analogs of suberoylanilidehydroxamic acid: Potent inhibition of histone deacetylases
    • Gu W, Nusinzon I, Smith RD, Horvath CM, Silverman RB. Carbonyland sulfur-containing analogs of suberoylanilidehydroxamic acid: Potent inhibition of histone deacetylases. Bioorg Med Chem 2006;14:3320-9
    • (2006) Bioorg Med Chem , vol.14 , pp. 3320-3329
    • Gu, W.1    Nusinzon, I.2    Smith, R.D.3    Horvath, C.M.4    Silverman, R.B.5
  • 20
    • 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 BS, Veerasamy R, Sharma PC, et al. 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;21:5735-8
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 5735-5738
    • Rajak, H.1    Agarawal, A.2    Parmar, P.3    Thakur, B.S.4    Veerasamy, R.5    Sharma, P.C.6
  • 21
    • 84866406006 scopus 로고    scopus 로고
    • Design, synthesis and preliminary biological evaluation of N-hydroxy- 4-(3-phenylpropanamido)benzamide (HPPB) derivatives as novel histonedeacetylase 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 histonedeacetylase inhibitors. Eur J Med Chem 2009;30:1-7
    • (2009) Eur J Med Chem , vol.30 , pp. 1-7
    • Jiao, J.1    Fang, H.2    Wang, X.3    Guan, P.4    Yuan, Y.5    Xu, W.6
  • 22
    • 8444247447 scopus 로고    scopus 로고
    • A new route to pyrazolo[3,4-c] and [4,3-c]pyridinones via heterocyclization of vic-substituted hydroxamic acids of acetylenylpyrazoles
    • DOI 10.1016/j.tet.2004.09.104, PII S0040402004016552
    • Mshvidobadze EV, Vasilevskya SF, Elguero J. A new route to pyrazolo[3,4-c] and [4,3-c]pyridinones via heterocyclization of vicsubstituted hydroxamic acids of acetylenylpyrazoles. Tetrahedron 2004;60:11875-8 (Pubitemid 39487437)
    • (2004) Tetrahedron , vol.60 , Issue.51 , pp. 11875-11878
    • Mshvidobadze, E.V.1    Vasilevsky, S.F.2    Elguero, J.3
  • 23
    • 34247557008 scopus 로고    scopus 로고
    • Enhancement of cisplatin induced apoptosis by suberoylanilide hydroxamic acid in human oral squamous cell carcinoma cell lines
    • DOI 10.1016/j.bcp.2007.03.009, PII S0006295207001566
    • Shen J, Huang C, Jiang L, Gao F, Wang Z, Zhang Y, et al. Enhancement of cisplatin induced apoptosis by suberoylanilidehydroxamic acid in human oral squamous cell carcinoma cell lines. Bio Pharmaco 2007;73:1901-9 (Pubitemid 46677907)
    • (2007) Biochemical Pharmacology , vol.73 , Issue.12 , pp. 1901-1909
    • Shen, J.1    Huang, C.2    Jiang, L.3    Gao, F.4    Wang, Z.5    Zhang, Y.6    Bai, J.7    Zhou, H.8    Chen, Q.9
  • 25
    • 0017681527 scopus 로고
    • Mutagenicity and antibacterial activity of hydroxamic acids
    • Wang CY, Lee LH. A. Mutagenicity and antibacterial activity of hydroxamic acids. AmSocMicrobiol 1977;11:753-5 (Pubitemid 8093341)
    • (1977) Antimicrobial Agents and Chemotherapy , vol.11 , Issue.4 , pp. 753-755
    • Wang, C.Y.1    Lee, L.H.2
  • 28
    • 34248634838 scopus 로고    scopus 로고
    • Design, synthesis and utilization of a novel coupling reagent for the preparation of O-alkyl hydroxamic acids
    • DOI 10.1016/j.tetlet.2007.04.058, PII S0040403907007241
    • Kokare ND, Nagawade RR, Ranea VP, Shinde DB. Design, synthesis and utilization of a novel coupling reagent for the preparation of O-alkyl hydroxamic acids. Tetrahedron Lett 2007;48:4437-40 (Pubitemid 46776779)
    • (2007) Tetrahedron Letters , vol.48 , Issue.25 , pp. 4437-4440
    • Kokare, N.D.1    Nagawade, R.R.2    Rane, V.P.3    Shinde, D.B.4
  • 30
    • 80054793028 scopus 로고    scopus 로고
    • Potent and selective 2-naphthylsulfonamide substituted hydroxamic acid inhibitors of matrix metalloproteinase-13
    • Tommasi RA, Weiler S, McQuire LW, Rogel O, Chambers M, Clark K, et al. Potent and selective 2-naphthylsulfonamide substituted hydroxamic acid inhibitors of matrix metalloproteinase-13. Bioorg Med Chem Lett 2011;21:6440-5.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 6440-6445
    • Tommasi, R.A.1    Weiler, S.2    McQuire, L.W.3    Rogel, O.4    Chambers, M.5    Clark, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.