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Volumn 93, Issue , 2015, Pages 461-469

Synthesis and assessment of the antioxidant and antitumor properties of asymmetric curcumin analogues

Author keywords

Anti proliferate; Antioxidant; Asymmetric curcumin analogues

Indexed keywords

1 (2 HYDROXY 4 METHOXYPHENYL) 5 (3,4,5 TRIMETHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3 ETHOXY 4 HYDROXYPHENYL) 5 (4 HYDROXY 3 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3 HYDROXY 4 METHOXYPHENYL) 5 (3,4,5 TRIMETHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3 HYDROXY 4 METHOXYPHENYL) 5 (4 HYDROXY 3 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3,4 DIMETHOXYPHENYL) 5 (2 HYDROXY 4 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3,4 DIMETHOXYPHENYL) 5 (4 HYDROXY 3 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3,4 DIMETHOXYPHENYL) 5 (4 HYDROXY 3,5 DIMETHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3,4 DIMETHYLPHENYL) 5 (2 HYDROXY 4 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3,4 DIMETHYLPHENYL) 5 (4 HYDROXY 3 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3,4 DIMETHYLPHENYL) 5 (4 HYDROXY 3,5 DIMETHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (3,4,5 TRIMETHOXYPHENYL) 5 (4 HYDROXY 3,5 DIMETHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1 (4 HYDROXY 3,5 DIMETHOXYPHENYL) 5 (4 HYDROXY 3 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1,5 BIS (3 ETHOXY 4 HYDROXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1,5 BIS (3 HYDROXY 4 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1,5 BIS (3,4 DIMETHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1,5 BIS (3,4,5 TRIMETHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; 1,5 BIS (4 HYDROXY 3 METHOXYPHENYL)PENTA 1,4 DIEN 3 ONE; CARBON; CURCUMIN; FREE RADICAL; HYDROGEN; OXYGEN; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; SCAVENGER;

EID: 84923565527     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2015.02.005     Document Type: Article
Times cited : (63)

References (38)
  • 1
    • 67651028343 scopus 로고    scopus 로고
    • A simple isocratic hplc method for the simultaneous determination of curcuminoids in commercial turmeric extracts
    • W. Wichitnithad, N. Jongaroonngamsang, S. Pummuangura, P. Rojsitthisak, A simple isocratic HPLC method for the simultaneous determination of curcuminoids in commercial turmeric extracts, Phytochem. Anal. 20 (2009) 314-319.
    • (2009) Phytochem. Anal , vol.20 , pp. 314-319
    • Wichitnithad, W.1    Jongaroonngamsang, N.2    Pummuangura, S.3    Rojsitthisak, P.4
  • 2
    • 0034823149 scopus 로고    scopus 로고
    • How curcumin works preferentially with water soluble antioxidants
    • S.V. Jovanovic, S. Steenken, C.W. Boone, M.G. Simic, How curcumin works preferentially with water soluble antioxidants, J. Am. Chem. Soc. 123 (2001) 3064-3068.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 3064-3068
    • Jovanovic, S.V.1    Steenken, S.2    Boone, C.W.3    Simic, M.G.4
  • 3
    • 4143118999 scopus 로고    scopus 로고
    • Antimicrobial activity of wool fabric treated with curcumin
    • S.Y. Han, Y.Q. Yang, Antimicrobial activity of wool fabric treated with curcumin, Dyes Pigments 64 (2005) 157-161.
    • (2005) Dyes Pigments , vol.64 , pp. 157-161
    • Han, S.Y.1    Yang, Y.Q.2
  • 4
    • 0030805998 scopus 로고    scopus 로고
    • Curcumin analogs with altered potencies against hiv-1 integrase as probes for biochemical mechanisms of drug action
    • A. Mazumder, N. Neamati, S. Sunder, J. Schulz, H. Pertz, E. Eich, Y. Pommier, Curcumin analogs with altered potencies against HIV-1 integrase as probes for biochemical mechanisms of drug action, J. Med. Chem. 40 (1997) 3057-3063.
    • (1997) J. Med. Chem , vol.40 , pp. 3057-3063
    • Mazumder, A.1    Neamati, N.2    Sunder, S.3    Schulz, J.4    Pertz, H.5    Eich, E.6    Pommier, Y.7
  • 7
    • 0036837108 scopus 로고    scopus 로고
    • Gastroprotective effect of neem (azadirachta indica) bark extract: Possible involvement of h(+)-k(+)-atpase inhibition and scavenging of hydroxyl radical
    • I. Chattopadhyay, K. Biswas, U. Bandyopadhyay, R.K. Banerjee, Gastroprotective effect of Neem (Azadirachta indica) bark extract: possible involvement of H(+)-K(+)-ATPase inhibition and scavenging of hydroxyl radical, Life Sci. 71 (2002) 2845-2865.
    • (2002) Life Sci , vol.71 , pp. 2845-2865
    • Chattopadhyay, I.1    Biswas, K.2    Bandyopadhyay, U.3    Banerjee, R.K.4
  • 8
    • 64249157259 scopus 로고    scopus 로고
    • Interactions of curcumin with the pfatp6 model and the implications for its antimalarial mechanism
    • H.F. Ji, L. Shen, Interactions of curcumin with the PfATP6 model and the implications for its antimalarial mechanism, Bioorg. Med. Chem. Lett. 19 (2009) 2453-2455.
    • (2009) Bioorg. Med. Chem. Lett , vol.19 , pp. 2453-2455
    • Ji, H.F.1    Shen, L.2
  • 9
    • 79961099279 scopus 로고    scopus 로고
    • Srivastava, curcumin e the yellow magic
    • P. Archana, K.G. Ravindra, Srivastava, Curcumin e the yellow magic, Asian J. Appl. Sci. 4 (2011) 343-354.
    • (2011) Asian J. Appl. Sci , vol.4 , pp. 343-354
    • Archana, P.1    Ravindra, K.G.2
  • 11
    • 38349011007 scopus 로고    scopus 로고
    • Curcumin: Preventive and therapeutic properties in laboratory studies and clinical trials
    • A.S. Strimpakos, R.A. Sharma, Curcumin: preventive and therapeutic properties in laboratory studies and clinical trials, Antioxid. Redox Signal. 10 (2008) 511-545.
    • (2008) Antioxid. Redox Signal , vol.10 , pp. 511-545
    • Strimpakos, A.S.1    Sharma, R.A.2
  • 12
    • 33644780779 scopus 로고    scopus 로고
    • Antitumor agents 247. New 4- ethoxycarbonylethyl curcumin analogs as potential antiandrogenic agents
    • L. Lin, Q. Shi, C.Y. Su, C.C. Shih, K.H. Lee, Antitumor agents 247. New 4- ethoxycarbonylethyl curcumin analogs as potential antiandrogenic agents, Bioorg. Med. Chem. 14 (2006) 2527-2534.
    • (2006) Bioorg. Med. Chem , vol.14 , pp. 2527-2534
    • Lin, L.1    Shi, Q.2    Su, C.Y.3    Shih, C.C.4    Lee, K.H.5
  • 13
    • 84875395775 scopus 로고    scopus 로고
    • Promising curcumin-based drug design: Monocarbonyl analogues of curcumin (macs)
    • C.G. Zhao, Z.G. Liu, G. Liang, Promising curcumin-based drug design: monocarbonyl analogues of curcumin (MACs), Curr. Pharm. Des. 19 (2013) 2114-2135.
    • (2013) Curr. Pharm. des , vol.19 , pp. 2114-2135
    • Zhao, C.G.1    Liu, Z.G.2    Liang, G.3
  • 16
    • 0033862619 scopus 로고    scopus 로고
    • Cytotoxicity, antioxidant and antiinflammatory activities of curcumins ieiii from curcuma longa
    • R.S. Ramsewak, D.L. DeWitt, M.G. Nair, Cytotoxicity, antioxidant and antiinflammatory activities of curcumins IeIII from Curcuma longa, Phytomedicine 7 (2000) 303-308.
    • (2000) Phytomedicine , vol.7 , pp. 303-308
    • Ramsewak, R.S.1    Dewitt, D.L.2    Nair, M.G.3
  • 17
    • 0032479574 scopus 로고    scopus 로고
    • Inhibitory effect of curcuminoids on mcf-7 cell proliferation and structureeactivity relationships
    • A. Simon, D.P. Allais, J.L. Duroux, J.P. Basly, S. Durand-Fontanier, C. Delage, Inhibitory effect of curcuminoids on MCF-7 cell proliferation and structureeactivity relationships, Cancer Lett. 129 (1998) 111-116.
    • (1998) Cancer Lett , vol.129 , pp. 111-116
    • Simon, A.1    Allais, D.P.2    Duroux, J.L.3    Basly, J.P.4    Durand-Fontanier, S.5    Delage, C.6
  • 18
    • 84864412588 scopus 로고    scopus 로고
    • Synthesis and evaluation of antimicrobial activity of 4h-pyrimido[2,1-b]benzothiazole, pyrazole and benzylidene derivatives of cur cumin
    • P.K. Sahu, S.K. Gupta, D. Thavaselvamd, D.D. Agarwal, Synthesis and evaluation of antimicrobial activity of 4H-pyrimido[2,1-b]benzothiazole, pyrazole and benzylidene derivatives of cur cumin, Eur. J. Med. Chem. 54 (2012) 366-378.
    • (2012) Eur. J. Med. Chem , vol.54 , pp. 366-378
    • Sahu, P.K.1    Gupta, S.K.2    Thavaselvamd, D.3    Agarwal, D.D.4
  • 21
    • 84861637434 scopus 로고    scopus 로고
    • Synthesis and evaluation of curcumin-related compounds for anticancer activity
    • X.C. Wei, Synthesis and evaluation of curcumin-related compounds for anticancer activity, Eur. J. Med. Chem. 53 (2012) 235-245.
    • (2012) Eur. J. Med. Chem , vol.53 , pp. 235-245
    • Wei, X.C.1
  • 22
    • 84896523169 scopus 로고    scopus 로고
    • Synthesis of novel curcumin analogues for inhibition of 11bhydroxysteroid dehydrogenase type 1 with anti-diabetic properties
    • X.H. Yuan, Synthesis of novel curcumin analogues for inhibition of 11bhydroxysteroid dehydrogenase type 1 with anti-diabetic properties, Eur. J. Med. Chem. 77 (2014) 223-230.
    • (2014) Eur. J. Med. Chem , vol.77 , pp. 223-230
    • Yuan, X.H.1
  • 23
    • 84903958725 scopus 로고    scopus 로고
    • Curcumin-loaded guanidine functionalized pegylated i3ad mesoporous silica nanoparticles kit- 6: Practical strategy for the breast cancer therapy
    • L. Ma'mani, S. Nikzad, H. Kheiri-manjili, S. Al-Musawi, Curcumin-loaded guanidine functionalized PEGylated I3ad mesoporous silica nanoparticles KIT- 6: practical strategy for the breast cancer therapy, Eur. J. Med. Chem. 83 (2014) 646-654.
    • (2014) Eur. J. Med. Chem , vol.83 , pp. 646-654
    • Ma'Mani, L.1    Nikzad, S.2    Kheiri-Manjili, H.3    Al-Musawi, S.4
  • 25
    • 84893176418 scopus 로고    scopus 로고
    • Three-dimensional quantitative structureeactivity relationship study on antioxidant capacity of curcumin analogues
    • B.H. Chen, Z.B. Zhu, M. Chen, W.Q. Dong, Z.J. Li, Three-dimensional quantitative structureeactivity relationship study on antioxidant capacity of curcumin analogues, Mol. Struct. 1061 (2014) 134-139.
    • (2014) Mol. Struct , vol.1061 , pp. 134-139
    • Chen, B.H.1    Zhu, Z.B.2    Chen, M.3    Dong, W.Q.4    Li, Z.J.5
  • 26
    • 45849115079 scopus 로고    scopus 로고
    • Ilhami gülçin, antioxidant and radical scavenging properties of cur cumin
    • A.K. Tuba, -Ilhami Gülçin, Antioxidant and radical scavenging properties of cur cumin, Chem. Biol. Interact. 174 (2008) 27-37.
    • (2008) Chem. Biol. Interact , vol.174 , pp. 27-37
    • Tuba, A.K.1
  • 28
    • 0026592194 scopus 로고
    • Studies on curcumin and curcuminoids. XXX: Curcumin as a reducing agent and as a radical scavenger
    • H.T. Hanne, V.G. John, Studies on curcumin and curcuminoids. XXII: curcumin as a reducing agent and as a radical scavenger, Int. J. Pharm. 87 (1992) 79-87.
    • (1992) Int. J. Pharm , vol.87 , pp. 79-87
    • Hanne, H.T.1    John, V.G.2
  • 29
    • 70049118994 scopus 로고    scopus 로고
    • Ruslán álvarez-diduk, role of the reacting free radicals on the antioxidant mechanism of curcumin
    • G. Annia, Ruslán Álvarez-Diduk, Role of the reacting free radicals on the antioxidant mechanism of curcumin, Chem. Phys. 363 (2009) 13-23.
    • (2009) Chem. Phys , vol.363 , pp. 13-23
    • Annia, G.1
  • 30
    • 84862674171 scopus 로고    scopus 로고
    • The role of electron-transfer and h-atom donation on the superb antioxidant activity and free radical reaction of curcumin
    • Abolfazl Barzegar, The role of electron-transfer and H-atom donation on the superb antioxidant activity and free radical reaction of curcumin, Food Chem. 135 (2012) 1369-1376.
    • (2012) Food Chem , vol.135 , pp. 1369-1376
    • Barzegar, A.1
  • 31
    • 46049083193 scopus 로고    scopus 로고
    • Concentration dependent antioxidant/pro-oxidant activity of curcumin: Studies from aaph induced hemolysis of rbcs
    • Arnab Banerjee, Concentration dependent antioxidant/pro-oxidant activity of curcumin: studies from AAPH induced hemolysis of RBCs, Chem. Biol. Interact. 174 (2008) 134-139.
    • (2008) Chem. Biol. Interact , vol.174 , pp. 134-139
    • Banerjee, A.1
  • 32
    • 0037200362 scopus 로고    scopus 로고
    • Predicting the antioxidant activity of curcumin and curcuminoids
    • J.S. Wright, Predicting the antioxidant activity of curcumin and curcuminoids, J. Mol. Struct. 591 (2002) 207-217.
    • (2002) J. Mol. Struct , vol.591 , pp. 207-217
    • Wright, J.S.1
  • 36
    • 39149142812 scopus 로고    scopus 로고
    • Synthesis and cytotoxic activity of novel curcumin analogues
    • Q. Zhang, Y. Fu, H.W.Wang, T. Gong, Y. Qin, Synthesis and cytotoxic activity of novel curcumin analogues, Chin. Chem. Lett. 19 (2008) 281-285.
    • (2008) Chin. Chem. Lett , vol.19 , pp. 281-285
    • Zhang, Q.1    Fu, Y.2    Wang, H.W.3    Gong, T.4    Qin, Y.5
  • 37
    • 84895543431 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of allylated and prenylated mono-carbonyl analogs of curcumin as anti-inflammatory agents
    • Zhiguo Liu, Longguang Tang, Peng Zou, Yali Zhang, Zhe Wang, Qilu Fang, Lili Jiang, Gaozhi Chen, Zheng Xu, Huajie Zhang, Guang Liang, Synthesis and biological evaluation of allylated and prenylated mono-carbonyl analogs of curcumin as anti-inflammatory agents, Eur. J. Med. Chem. 74 (2014) 671-682.
    • (2014) Eur. J. Med. Chem , vol.74 , pp. 671-682
    • Liu, Z.1    Tang, L.2    Zou, P.3    Zhang, Y.4    Wang, Z.5    Fang, Q.6    Jiang, L.7    Chen, G.8    Xu, Z.9    Zhang, H.10    Liang, G.11
  • 38
    • 0030582419 scopus 로고    scopus 로고
    • Antimutagenic and anticarcinogenic activity of natural and synthetic curcuminoids
    • R.J. Anto, J. George, K.V. Dinesh Babu, K.N. Rajasekeharan, R. Kuttan, Antimutagenic and anticarcinogenic activity of natural and synthetic curcuminoids, Mutat. Res. 370 (1996) 127-131.
    • (1996) Mutat. Res , vol.370 , pp. 127-131
    • Anto, R.J.1    George, J.2    Dinesh Babu, K.V.3    Rajasekeharan, K.N.4    Kuttan, R.5


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