메뉴 건너뛰기




Volumn 87, Issue , 2014, Pages 564-577

PASS-assisted design, synthesis and antioxidant evaluation of new butylated hydroxytoluene derivatives

Author keywords

1 2 4 Triazole; 1 3 4 Thiadiazole; Butylated HydroxyToluene; Multipotent antioxidant; PASS; Thiosemicarbazide

Indexed keywords

1,1 DIPHENYL 2 PICRYLHYDRAZYL; 1,2,4 TRIAZOLE DERIVATIVE; 1,3,4 THIADIAZOLE DERIVATIVE; ANTIOXIDANT; BUTYLCRESOL; ESSENTIAL OIL; FREE RADICAL; SCAVENGER;

EID: 84949116901     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2014.10.001     Document Type: Article
Times cited : (41)

References (118)
  • 1
    • 0036086130 scopus 로고    scopus 로고
    • Free radicals in the physiological control of cell function
    • W. Droge, Free radicals in the physiological control of cell function, Physiol. Rev. 82 (2002) 47-95.
    • (2002) Physiol. Rev. , vol.82 , pp. 47-95
    • Droge, W.1
  • 2
    • 0040892873 scopus 로고    scopus 로고
    • Reactive oxygen species and biological aging: A mechanistic approach
    • C. Schoneich, Reactive oxygen species and biological aging: a mechanistic approach, Exp. Gerontol. 34 (1999) 19-34.
    • (1999) Exp. Gerontol. , vol.34 , pp. 19-34
    • Schoneich, C.1
  • 3
    • 0030174321 scopus 로고    scopus 로고
    • The role of reactive oxygen species in inflammatory disease: Evaluation of methodology
    • T. Sahinoglu, C.R. Stevens, B. Bhatt, D.R. Blake, The role of reactive oxygen species in inflammatory disease: evaluation of methodology, Methods 9 (1996) 628-634.
    • (1996) Methods , vol.9 , pp. 628-634
    • Sahinoglu, T.1    Stevens, C.R.2    Bhatt, B.3    Blake, D.R.4
  • 4
    • 12844260763 scopus 로고    scopus 로고
    • Methionine oxidation by reactive oxygen species: Reaction mechanisms and relevance to Alzheimer's disease
    • C. Schoneich, Methionine oxidation by reactive oxygen species: reaction mechanisms and relevance to Alzheimer's disease, Biochim. Biophys. Acta Proteins Proteomics 1703 (2005) 111-119.
    • (2005) Biochim. Biophys. Acta Proteins Proteomics , vol.1703 , pp. 111-119
    • Schoneich, C.1
  • 5
    • 34447547856 scopus 로고    scopus 로고
    • Relevance of anti-reactive oxygen species activity to anti-inflammatory activity of components of eviprostat a phytotherapeutic agent for benign prostatic hyperplasia
    • M. Oka, M. Tachibana, K. Noda, N. Inoue, M. Tanaka, K. Kuwabara, Relevance of anti-reactive oxygen species activity to anti-inflammatory activity of components of eviprostat, a phytotherapeutic agent for benign prostatic hyperplasia, Phytomedicine 14 (2007) 465-472.
    • (2007) Phytomedicine , vol.14 , pp. 465-472
    • Oka, M.1    Tachibana, M.2    Noda, K.3    Inoue, N.4    Tanaka, M.5    Kuwabara, K.6
  • 6
    • 0035782650 scopus 로고    scopus 로고
    • Reactive oxygen species and mitochondrial diseases
    • I.G. Kirkinezos, C.T. Moraes, Reactive oxygen species and mitochondrial diseases, Semin. Cell Dev. Biol. 12 (2001) 449-457.
    • (2001) Semin. Cell Dev. Biol. , vol.12 , pp. 449-457
    • Kirkinezos, I.G.1    Moraes, C.T.2
  • 9
    • 0030130524 scopus 로고    scopus 로고
    • Inflammation free radicals and antioxidants
    • E.M. Conner, M.B. Grisham, Inflammation, free radicals, and antioxidants, Nutrition 12 (1996) 274-277.
    • (1996) Nutrition , vol.12 , pp. 274-277
    • Conner, E.M.1    Grisham, M.B.2
  • 11
    • 79851479564 scopus 로고
    • Antioxidants: Function, types and necessity of inclusion in pet foods
    • J. Hilton, Antioxidants: function, types and necessity of inclusion in pet foods, Can. Veterinary J. 30 (1989) 682-684.
    • (1989) Can. Veterinary J. , vol.30 , pp. 682-684
    • Hilton, J.1
  • 12
    • 0039504896 scopus 로고
    • Antioxidants as food stabilizers
    • B. Stuckey, Antioxidants as Food Stabilizers, in: Handbook of Food Additives, 1972, pp. 185-221.
    • (1972) Handbook of Food Additives , pp. 185-221
    • Stuckey, B.1
  • 13
    • 0001086618 scopus 로고
    • The metabolism of 3: 5-di-tert.-butyl-4-hydroxytoluene and 3: 5-ditert.-butyl-4-hydroxybenzoic acid in the rabbit
    • J. Dacre, The metabolism of 3: 5-di-tert.-butyl-4-hydroxytoluene and 3: 5-ditert.-butyl-4-hydroxybenzoic acid in the rabbit, Biochem. J. 78 (1961) 758.
    • (1961) Biochem. J. , vol.78 , pp. 758
    • Dacre, J.1
  • 14
    • 0037871887 scopus 로고    scopus 로고
    • Antioxidant activity of obisphenols: The role of intramolecular hydrogen bonding
    • R. Amorati, M. Lucarini, V. Mugnaini, G. Pedulli, Antioxidant activity of obisphenols: the role of intramolecular hydrogen bonding, J. Org. Chem. 68 (2003) 5198-5204.
    • (2003) J. Org. Chem. , vol.68 , pp. 5198-5204
    • Amorati, R.1    Lucarini, M.2    Mugnaini, V.3    Pedulli, G.4
  • 16
    • 0020285864 scopus 로고
    • 2, 6-di-tert-butyl-4-(2-thenoyl) phenol (R-830): A novel nonsteroidal anti-inflammatory agent with antioxidant properties
    • G. Moore, K. Swingle, 2, 6-di-tert-butyl-4-(2-thenoyl) phenol (R-830): a novel nonsteroidal anti-inflammatory agent with antioxidant properties, Inflamm. Res. 12 (1982) 674-683.
    • (1982) Inflamm. Res. , vol.12 , pp. 674-683
    • Moore, G.1    Swingle, K.2
  • 17
    • 0022131227 scopus 로고
    • Functional polymers
    • P. Grosso, O. Vogl, Functional polymers, Polym. Bull. 14 (1985) 245-250.
    • (1985) Polym. Bull. , vol.14 , pp. 245-250
    • Grosso, P.1    Vogl, O.2
  • 18
    • 0033535606 scopus 로고    scopus 로고
    • Synthesis structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 2., 1, 3, 4-and 1, 2, 4-thiadiazole series 1
    • Y. Song, D. Connor, A. Sercel, R. Sorenson, R. Doubleday, P. Unangst, B. Roth, V. Beylin, R. Gilbertsen, K. Chan, Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 2. 1, 3, 4-and 1, 2, 4-thiadiazole series 1, J. Med. Chem. 42 (1999) 1161-1169.
    • (1999) J. Med. Chem. , vol.42 , pp. 1161-1169
    • Song, Y.1    Connor, D.2    Sercel, A.3    Sorenson, R.4    Doubleday, R.5    Unangst, P.6    Roth, B.7    Beylin, V.8    Gilbertsen, R.9    Chan, K.10
  • 19
    • 0032135008 scopus 로고    scopus 로고
    • Design of selective inhibitors of cyclooxygenase-2 as nonulcerogenic anti-inflammatory agents
    • L.J. Marnett, A.S. Kalgutkar, Design of selective inhibitors of cyclooxygenase-2 as nonulcerogenic anti-inflammatory agents, Curr. Opin. Chem. Biol. 2 (1998) 482-490.
    • (1998) Curr. Opin. Chem. Biol. , vol.2 , pp. 482-490
    • Marnett, L.J.1    Kalgutkar, A.S.2
  • 20
    • 0034075728 scopus 로고    scopus 로고
    • Novel antiarthritic agents with 1 2-isothiazolidine-1 1-dioxide ([gamma]-sultam) skeleton: Cytokine suppressive dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase
    • M. Inagaki, T. Tsuri, H. Jyoyama, T. Ono, K. Yamada, M. Kobayashi, Y. Hori, A. Arimura, K. Yasui, K. Ohno, Novel antiarthritic agents with 1, 2-isothiazolidine-1, 1-dioxide ([gamma]-sultam) skeleton: cytokine suppressive dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase, J. Med. Chem. 43 (2000) 2040-2048.
    • (2000) J. Med. Chem. , vol.43 , pp. 2040-2048
    • Inagaki, M.1    Tsuri, T.2    Jyoyama, H.3    Ono, T.4    Yamada, K.5    Kobayashi, M.6    Hori, Y.7    Arimura, A.8    Yasui, K.9    Ohno, K.10
  • 21
    • 84891550643 scopus 로고    scopus 로고
    • Discovery of potential anti-infectives against Staphylococcus aureus using a caenorhabditis elegans infection model
    • C. Kong, W.A. Yehye, N.A. Rahman, M.-W. Tan, S. Nathan, Discovery of potential anti-infectives against Staphylococcus aureus using a caenorhabditis elegans infection model, BMC Complem. Altern. Med. 14 (2014) 4.
    • (2014) BMC Complem. Altern. Med. , vol.14 , pp. 4
    • Kong, C.1    Yehye, W.A.2    Rahman, N.A.3    Tan, M.-W.4    Nathan, S.5
  • 22
    • 0020082284 scopus 로고
    • Effect of anti-inflammatory thiosemicarbazone indoles on hyaluronidase acid phosphatase and trypsin
    • S. Kaur, B. Ali, Effect of anti-inflammatory thiosemicarbazone indoles on hyaluronidase, acid phosphatase and trypsin, Pharmacology 24 (1982) 162-168.
    • (1982) Pharmacology , vol.24 , pp. 162-168
    • Kaur, S.1    Ali, B.2
  • 23
    • 0021061361 scopus 로고
    • Thiosemicarbazones of 2-acetylpyridine, 2-acetylquinoline, 1-and 3-acetylisoquinoline and related compounds as inhibitors of clinically significant bacteria in vitro
    • A. Dobek, D. Klayman, E. Dickson Jr., J. Scovill, C. Oster, Thiosemicarbazones of 2-acetylpyridine, 2-acetylquinoline, 1-and 3-acetylisoquinoline and related compounds as inhibitors of clinically significant bacteria in vitro, Arzneim. 33 (1983) 1583-1591.
    • (1983) Arzneim. , vol.33 , pp. 1583-1591
    • Dobek, A.1    Klayman, D.2    Dickson, Jr.E.3    Scovill, J.4    Oster, C.5
  • 24
    • 0028206669 scopus 로고
    • Synthesis of new 7-substituted 4-methylcoumarin derivatives of antimicrobial activity
    • A.I. Eid, F.A. Ragab, S.L. El-Ansary, S.M. El-Gazayerly, F.E. Mourad, Synthesis of new 7-substituted 4-methylcoumarin derivatives of antimicrobial activity, Arch. Pharm. 327 (1994) 211-213.
    • (1994) Arch. Pharm. , vol.327 , pp. 211-213
    • Eid, A.I.1    Ragab, F.A.2    El-Ansary, S.L.3    El-Gazayerly, S.M.4    Mourad, F.E.5
  • 26
    • 0036176817 scopus 로고    scopus 로고
    • Synthesis and antiinflammatory activity of 1-acylthiosemicarbazides 1, 3, 4-oxadiazoles, 1, 3, 4-thiadiazoles and 1, 2, 4-triazole-3-thiones
    • E. Palaska, G. Sahin, P. Kelicen, N.T. Durlu, G. Altinok, Synthesis and antiinflammatory activity of 1-acylthiosemicarbazides, 1, 3, 4-oxadiazoles, 1, 3, 4-thiadiazoles and 1, 2, 4-triazole-3-thiones, Il Farm. 57 (2002) 101-107.
    • (2002) Il Farm. , vol.57 , pp. 101-107
    • Palaska, E.1    Sahin, G.2    Kelicen, P.3    Durlu, N.T.4    Altinok, G.5
  • 27
    • 57349151615 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activities of 124-triazole and 1, 3,4-thiadiazole derivatives of 5-amino-2-hydroxybenzoic acid
    • S. Hussain, J. Sharma, M. Amir, Synthesis and antimicrobial activities of 1,2,4-triazole and 1,3,4-thiadiazole derivatives of 5-amino-2-hydroxybenzoic acid, E. J. Chem. 5 (2008) 963-968.
    • (2008) E. J. Chem. , vol.5 , pp. 963-968
    • Hussain, S.1    Sharma, J.2    Amir, M.3
  • 28
    • 70549092095 scopus 로고    scopus 로고
    • Synthesis of some new thiosemicarbazide and 1, 3,4-thiadiazole heterocycles bearing benzo[b] Thiophene nucleus as a potent antitubercular and antimicrobial agents
    • S.L. Vasoya, D.J. Paghdar, P.T. Chovatia, H.S. Joshi, Synthesis of some new thiosemicarbazide and 1,3,4-thiadiazole heterocycles bearing benzo[b] Thiophene nucleus as a potent antitubercular and antimicrobial agents, J. Sci. Islam.Repub. Iran 16 (2005) 33-36.
    • (2005) J. Sci. Islam.Repub. Iran , vol.16 , pp. 33-36
    • Vasoya, S.L.1    Paghdar, D.J.2    Chovatia, P.T.3    Joshi, H.S.4
  • 29
    • 33947589666 scopus 로고    scopus 로고
    • Anticancer neuroprotective activities and computational studies of 2-amino-1 3,4-thiadiazole based compound
    • W. Rzeski, J. Matysiak, M. Kandefer-Szerszen, Anticancer, neuroprotective activities and computational studies of 2-amino-1,3,4-thiadiazole based compound, Bioorg. Med. Chem. 15 (2007) 3201-3207.
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 3201-3207
    • Rzeski, W.1    Matysiak, J.2    Kandefer-Szerszen, M.3
  • 30
    • 33745177793 scopus 로고    scopus 로고
    • Synthesis, Reactions, and Anticancer Activity of Some 1, 3,4-thiadiazole/thiadiazine Derivatives of Carbazole
    • T.M. Abdel-Rahman, Synthesis, reactions, and anticancer activity of some 1,3,4-thiadiazole/thiadiazine derivatives of carbazole, Phosphorus Sulfur Silicon Relat. Elem. 181 (2006) 1737-1754.
    • (2006) Phosphorus Sulfur Silicon Relat. Elem. , vol.181 , pp. 1737-1754
    • Abdel-Rahman, T.M.1
  • 31
    • 77957856848 scopus 로고    scopus 로고
    • Syn thesis, antioxidant activities and urease inhibition of some new 1, 2, 4-triazole and 1, 3, 4-thiadiazole derivatives
    • I. Khan, S. Ali, S. Hameed, N. Rama, M. Hussain, A. Wadood, R. Uddin, Z. Ul-Haq, A. Khan, Synthesis, antioxidant activities and urease inhibition of some new 1, 2, 4-triazole and 1, 3, 4-thiadiazole derivatives, Eur. J. Med. Chem. 45 (2010) 5200-5207.
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 5200-5207
    • Khan, I.1    Ali, S.2    Hameed, S.3    Rama, N.4    Hussain, M.5    Wadood, A.6    Uddin, R.7    Ul-Haq, Z.8    Khan, A.9
  • 32
    • 33644749178 scopus 로고    scopus 로고
    • Design, syn thesis, and biological evaluation of substituted 3-alkylthio-4,5-diaryl-4H-1 2,4-triazoles as selective COX-2 inhibitors
    • L. Navidpour, H. Shafaroodi, K. Abdi, M. Amini, M.H. Ghahremani, A.R. Dehpour, A. Shafiee, Design, synthesis, and biological evaluation of substituted 3-alkylthio-4,5-diaryl-4H-1,2,4-triazoles as selective COX-2 inhibitors, Bioorg. Med. Chem. 14 (2006) 2507-2517.
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 2507-2517
    • Navidpour, L.1    Shafaroodi, H.2    Abdi, K.3    Amini, M.4    Ghahremani, M.H.5    Dehpour, A.R.6    Shafiee, A.7
  • 33
    • 6344291043 scopus 로고    scopus 로고
    • Synthesis and potential antimycotic activity of 4-substituted-3-(thiophene-2-yl-methyl)-delta2-1 2,4-triazoline-5-thiones
    • M. Wujec, M. Pitucha, M. Dobosz, U. Kosikowska, A. Malm, Synthesis and potential antimycotic activity of 4-substituted-3-(thiophene-2-yl-methyl)-delta2-1,2,4-triazoline-5-thiones, Acta Pharm. Short. Commun. 54 (2004) 251-260.
    • (2004) Acta Pharm. Short. Commun. , vol.54 , pp. 251-260
    • Wujec, M.1    Pitucha, M.2    Dobosz, M.3    Kosikowska, U.4    Malm, A.5
  • 34
    • 0035857407 scopus 로고    scopus 로고
    • Predicting the activity of phenolic antioxidants: Theoretical method, analysis of substituent effects, and application to major families of antioxidants
    • J. Wright, E. Johnson, G. DiLabio, Predicting the activity of phenolic antioxidants: theoretical method, analysis of substituent effects, and application to major families of antioxidants, J. Am. Chem. Soc. 123 (2001) 1173-1183.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 1173-1183
    • Wright, J.1    Johnson, E.2    Dilabio, G.3
  • 35
    • 23744500296 scopus 로고    scopus 로고
    • Structure-activity relationships and rational design strategies for radical-scavenging antioxidants
    • H. Zhang, Structure-activity relationships and rational design strategies for radical-scavenging antioxidants, Curr. Comp. Aided Drug Des. 1 (2005) 257-273.
    • (2005) Curr. Comp. Aided Drug Des. , vol.1 , pp. 257-273
    • Zhang, H.1
  • 36
    • 33745815173 scopus 로고    scopus 로고
    • Multipotent antioxidants: From screening to design
    • H.-Y. Zhang, D.-P. Yang, G.-Y. Tang, Multipotent antioxidants: from screening to design, Drug Discov. Today 11 (2006) 749-754.
    • (2006) Drug Discov. Today , vol.11 , pp. 749-754
    • Zhang, H.-Y.1    Yang, D.-P.2    Tang, G.-Y.3
  • 37
    • 0035091785 scopus 로고    scopus 로고
    • Effect of para-substituents of phenolic antioxidants
    • T. Kajiyama, Y. Ohkatsu, Effect of para-substituents of phenolic antioxidants, Polym. Degrad. Stab. 71 (2001) 445-452.
    • (2001) Polym. Degrad. Stab. , vol.71 , pp. 445-452
    • Kajiyama, T.1    Ohkatsu, Y.2
  • 38
    • 0028120449 scopus 로고
    • Bond dissociation enthalpy of.alpha.-tocopherol and other phenolic antioxidants
    • M. Lucarini, G.F. Pedulli, M. Cipollone, Bond dissociation enthalpy of.alpha.-tocopherol and other phenolic antioxidants, J. Org. Chem. 59 (1994) 5063-5070.
    • (1994) J. Org. Chem. , vol.59 , pp. 5063-5070
    • Lucarini, M.1    Pedulli, G.F.2    Cipollone, M.3
  • 40
    • 61849161313 scopus 로고    scopus 로고
    • On the energetics of phenol antioxidants activity
    • E. Klein, V. Luke-s, Z. Cibulkov-a, On the energetics of phenol antioxidants activity, Pet. Coal 47 (2005).
    • (2005) Pet. Coal , pp. 47
    • Klein, E.1    Lukes, V.2    Cibulkova, Z.3
  • 41
    • 0033852366 scopus 로고    scopus 로고
    • Assessing antioxidant and prooxidant activities of phenolic compounds
    • L.R. Fukumoto, G. Mazza, Assessing antioxidant and prooxidant activities of phenolic compounds, J. Agric. food Chem. 48 (2000) 3597-3604.
    • (2000) J. Agric. Food Chem. , vol.48 , pp. 3597-3604
    • Fukumoto, L.R.1    Mazza, G.2
  • 42
    • 0031232088 scopus 로고    scopus 로고
    • Kinetics and mechanisms of antioxidant activity using the DPPH. Free radical method Lebensm. und
    • V. Bondet, W. Brand-Williams, C. Berset, Kinetics and mechanisms of antioxidant activity using the DPPH. Free radical method, Lebensm. und Technologie 30 (1997) 609-615.
    • (1997) Technologie , vol.30 , pp. 609-615
    • Bondet, V.1    Brand-Williams, W.2    Berset, C.3
  • 45
    • 0029203718 scopus 로고
    • Chain-breaking stabilizers in polymers: The current status
    • J. Pospísil, S. Nespurek, Chain-breaking stabilizers in polymers: the current status, Polym. Degrad. Stab. 49 (1995) 99-110.
    • (1995) Polym. Degrad. Stab. , vol.49 , pp. 99-110
    • Pospísil, J.1    Nespurek, S.2
  • 46
    • 34748883874 scopus 로고    scopus 로고
    • Radical scavenging activity prediction of o-coumaric acid thioamide
    • Z. Velkov, E. Balabanova, A. Tadjer, Radical scavenging activity prediction of o-coumaric acid thioamide, J. Mol. Struct. Theochem 821 (2007) 133-138.
    • (2007) J. Mol. Struct. Theochem , vol.821 , pp. 133-138
    • Velkov, Z.1    Balabanova, E.2    Tadjer, A.3
  • 47
    • 79955428884 scopus 로고    scopus 로고
    • A comparison of some properties of C14;O and C14;S bonds
    • K.B. Wiberg, Y. Wang, A comparison of some properties of C14;O and C14;S bonds, Arkivoc 5 (2011) 45-56.
    • (2011) Arkivoc , vol.5 , pp. 45-56
    • Wiberg, K.B.1    Wang, Y.2
  • 48
    • 34248225425 scopus 로고    scopus 로고
    • First principle study of the structure of conjugated amides and thioamides
    • Z. Velkov, Y. Velkov, E. Balabanova, A. Tadjer, First principle study of the structure of conjugated amides and thioamides, Int. J. Quantum Chem. 107 (2007) 1765-1771.
    • (2007) Int. J. Quantum Chem. , vol.107 , pp. 1765-1771
    • Velkov, Z.1    Velkov, Y.2    Balabanova, E.3    Tadjer, A.4
  • 49
    • 0033572950 scopus 로고    scopus 로고
    • Bond dissociation energies of the NeH bond and rate constants for the reaction with alkyl, alkoxyl, and peroxyl radicals of phenothiazines and related compounds
    • M. Lucarini, P. Pedrielli, G.F. Pedulli, L. Valgimigli, D. Gigmes, P. Tordo, Bond dissociation energies of the NeH bond and rate constants for the reaction with alkyl, alkoxyl, and peroxyl radicals of phenothiazines and related compounds, J. Am. Chem. Soc. 121 (1999) 11546-11553.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 11546-11553
    • Lucarini, M.1    Pedrielli, P.2    Pedulli, G.F.3    Valgimigli, L.4    Gigmes, D.5    Tordo, P.6
  • 51
    • 0345529031 scopus 로고    scopus 로고
    • Modeling the co-antioxidant behavior of monofunctional phenols. Applications to some relevant compounds
    • R. Amorati, F. Ferroni, G.F. Pedulli, L. Valgimigli, Modeling the co-antioxidant behavior of monofunctional phenols. Applications to some relevant compounds, J. Org. Chem. 68 (2003) 9654-9658.
    • (2003) J. Org. Chem. , vol.68 , pp. 9654-9658
    • Amorati, R.1    Ferroni, F.2    Pedulli, G.F.3    Valgimigli, L.4
  • 52
    • 0033578691 scopus 로고    scopus 로고
    • Poly methoxy phenols in solution: OeH bond dissociation enthalpies, structures, and hydrogen bonding
    • M.I. de Heer, H.G. Korth, P. Mulder, Poly methoxy phenols in solution: OeH bond dissociation enthalpies, structures, and hydrogen bonding, J. Org. Chem. 64 (1999) 6969-6975.
    • (1999) J. Org. Chem. , vol.64 , pp. 6969-6975
    • De Heer, M.I.1    Korth, H.G.2    Mulder, P.3
  • 53
    • 33745672314 scopus 로고    scopus 로고
    • Sources of natural phenolic antioxidants
    • B. Dimitrios, Sources of natural phenolic antioxidants, Trends Food Sci. Technol. 17 (2006) 505-512.
    • (2006) Trends Food Sci. Technol. , vol.17 , pp. 505-512
    • Dimitrios, B.1
  • 54
    • 0034654215 scopus 로고    scopus 로고
    • Hydrogen atom abstraction kinetics from intramolecularly hydrogen bonded ubiquinol-0 and other (poly)methoxy phenols
    • M.I. de Heer, P. Mulder, H.-G. Korth, K.U. Ingold, J. Lusztyk, Hydrogen atom abstraction kinetics from intramolecularly hydrogen bonded ubiquinol-0 and other (poly)methoxy phenols, J. Am. Chem. Soc. 122 (2000) 2355-2360.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 2355-2360
    • De Heer, M.I.1    Mulder, P.2    Korth, H.-G.3    Ingold, K.U.4    Lusztyk, J.5
  • 55
    • 0035404019 scopus 로고    scopus 로고
    • Biological activities of curcuma longa L Mem-orias do
    • C. Araujo, L. Leon, Biological activities of curcuma longa L, Mem-orias do Inst. Oswaldo Cruz 96 (2001) 723-728.
    • (2001) Inst. Oswaldo Cruz , vol.96 , pp. 723-728
    • Araujo, C.1    Leon, L.2
  • 57
    • 0036154958 scopus 로고    scopus 로고
    • Effect of meta-substituents of phenolic antioxidantseproposal of secondary substituent effect
    • T. Kajiyama, Y. Ohkatsu, Effect of meta-substituents of phenolic antioxidantseproposal of secondary substituent effect, Polym. Degrad. Stab. 75 (2002) 535-542.
    • (2002) Polym. Degrad. Stab. , vol.75 , pp. 535-542
    • Kajiyama, T.1    Ohkatsu, Y.2
  • 58
    • 21844439716 scopus 로고    scopus 로고
    • Free radical scavenging alleviates the biomechanical impairment of gamma radiation sterilized bone tissue
    • O. Akkus, R.M. Belaney, P. Das, Free radical scavenging alleviates the biomechanical impairment of gamma radiation sterilized bone tissue, J. Orthop. Res. 23 (2005) 838-845.
    • (2005) J. Orthop. Res. , vol.23 , pp. 838-845
    • Akkus, O.1    Belaney, R.M.2    Das, P.3
  • 61
    • 84888798824 scopus 로고    scopus 로고
    • PASS-predicted vitex negundo activity: Antioxidant and antiproliferative properties on human hepatoma cells-an in vitro study
    • F.A. Kadir, N.M. Kassim, M.A. Abdulla, W.A. Yehye, PASS-predicted vitex negundo activity: antioxidant and antiproliferative properties on human hepatoma cells-an in vitro study, BMC Complem. Altern. Med. 13 (2013) 343.
    • (2013) BMC Complem. Altern. Med. , vol.13 , pp. 343
    • Kadir, F.A.1    Kassim, N.M.2    Abdulla, M.A.3    Yehye, W.A.4
  • 62
    • 0037241423 scopus 로고    scopus 로고
    • Prediction of biological activity spectra for substances: Evaluation on the diverse sets of drug-like structures
    • A.V. Stepanchikova, A.A. Lagunin, D.A. Filimonov, V.V. Poroikov, Prediction of biological activity spectra for substances: evaluation on the diverse sets of drug-like structures, Curr. Med. Chem. 10 (2003) 225-233.
    • (2003) Curr. Med. Chem. , vol.10 , pp. 225-233
    • Stepanchikova, A.V.1    Lagunin, A.A.2    Filimonov, D.A.3    Poroikov, V.V.4
  • 63
    • 0035913046 scopus 로고    scopus 로고
    • Discriminating between drugs and nondrugs by prediction of activity spectra for substances (PASS)
    • S. Anzali, G. Barnickel, B. Cezanne, M. Krug, D. Filimonov, V. Poroikov, Discriminating between drugs and nondrugs by prediction of activity spectra for substances (PASS), J. Med. Chem. 44 (2001) 2432-2437.
    • (2001) J. Med. Chem. , vol.44 , pp. 2432-2437
    • Anzali, S.1    Barnickel, G.2    Cezanne, B.3    Krug, M.4    Filimonov, D.5    Poroikov, V.6
  • 64
    • 84907934923 scopus 로고    scopus 로고
    • PASS-predicted hepatoprotective activity of Caesalpinia sappan in thioacetamide-induced liver fibrosis in rats
    • F. Kadir, N.B.M. Kassim, M.A. Abdulla, B. Kamalidehghan, F. Ahmadipour, W. Yehye, PASS-predicted hepatoprotective activity of Caesalpinia sappan in thioacetamide-induced liver fibrosis in rats, Sci. World J. (2014) 1-12.
    • (2014) Sci. World J. , pp. 1-12
    • Kadir, F.1    Kassim, N.B.M.2    Abdulla, M.A.3    Kamalidehghan, B.4    Ahmadipour, F.5    Yehye, W.6
  • 65
    • 0035991962 scopus 로고    scopus 로고
    • In vitro activities of position 2 substitutionbearing 6-nitro-and 6-amino-benzothiazoles and their corresponding anthranilic acid derivatives against leishmania infantum and trichomonas vaginalis
    • F. Delmas, C. Di Giorgio, M. Robin, N. Azas, M. Gasquet, C. Detang, M. Costa, P. Timon-David, J.-P. Galy, In vitro activities of position 2 substitutionbearing 6-nitro-and 6-amino-benzothiazoles and their corresponding anthranilic acid derivatives against leishmania infantum and trichomonas vaginalis, Antimicrob. Agents Chemother. 46 (2002) 2588-2594.
    • (2002) Antimicrob. Agents Chemother. , vol.46 , pp. 2588-2594
    • Delmas, F.1    Di Giorgio, C.2    Robin, M.3    Azas, N.4    Gasquet, M.5    Detang, C.6    Costa, M.7    Timon-David, P.8    Galy, J.-P.9
  • 67
    • 2542434992 scopus 로고    scopus 로고
    • In vitro activity of the b-carboline alkaloids harmane, harmine, and harmaline toward parasites of the species leishmania infantum
    • C. Di Giorgio, F. Delmas, E. Ollivier, R. Elias, G. Balansard, P. Timon-David, In vitro activity of the b-carboline alkaloids harmane, harmine, and harmaline toward parasites of the species leishmania infantum, Exp. Parasitol. 106 (2004) 67-74.
    • (2004) Exp. Parasitol. , vol.106 , pp. 67-74
    • Di Giorgio, C.1    Delmas, F.2    Ollivier, E.3    Elias, R.4    Balansard, G.5    Timon-David, P.6
  • 68
    • 84949127760 scopus 로고    scopus 로고
    • Synthesis characterization and activity prediction of some new class of hydroxytriazenes
    • P.K. Baroliya, P. Joshi, R. Chauhan, A. Goswami, Synthesis, characterization and activity prediction of some new class of hydroxytriazenes, Int. J. Chem. Sci. Technol. 1 (2011) 1-4.
    • (2011) Int. J. Chem. Sci. Technol. , vol.1 , pp. 1-4
    • Baroliya, P.K.1    Joshi, P.2    Chauhan, R.3    Goswami, A.4
  • 70
    • 0005158420 scopus 로고
    • Magnetic and spectroscopic properties of copper(II) complexes with 1-salicoyl-4-phenylthiosemicarbazide
    • N.T. Akinchan, D.X. West, Y. Yang, M.M. Salberg, T.L. Klein, Magnetic and spectroscopic properties of copper(II) complexes with 1-salicoyl-4-phenylthiosemicarbazide, Transit. Metal. Chem. 20 (1995) 481-484.
    • (1995) Transit. Metal. Chem. , vol.20 , pp. 481-484
    • Akinchan, N.T.1    West, D.X.2    Yang, Y.3    Salberg, M.M.4    Klein, T.L.5
  • 71
    • 67349276592 scopus 로고    scopus 로고
    • Copper(II) and uranyl(II) complexes with acylthiosemicarbazide: Syn thesis, characterization, antibacterial activity and effects on the growth of promyelocytic leukemia cells HL-60
    • M.V. Angelusiu, G.L. Almajan, T. Rosu, M. Negoiu, E.-R. Almajan, J. Roy, Copper(II) and uranyl(II) complexes with acylthiosemicarbazide: synthesis, characterization, antibacterial activity and effects on the growth of promyelocytic leukemia cells HL-60, Eur. J. Med. Chem. 44 (2009) 3323-3329.
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 3323-3329
    • Angelusiu, M.V.1    Almajan, G.L.2    Rosu, T.3    Negoiu, M.4    Almajan, E.-R.5    Roy, J.6
  • 73
    • 23644451984 scopus 로고    scopus 로고
    • 4-Substituted aryl bromides coupling with 4-methoxybenzene-1-thiol by means of copper catalysts
    • J. Jampílek, M. Dolezal, J. Kunes, I. Raich, F. Li-ska, 4-Substituted aryl bromides coupling with 4-methoxybenzene-1-thiol by means of copper catalysts, Chem. Pap. 59 (2005) 178-181.
    • (2005) Chem. Pap. , vol.59 , pp. 178-181
    • Jampílek, J.1    Dolezal, M.2    Kunes, J.3    Raich, I.4    Liska, F.5
  • 74
    • 27144537231 scopus 로고    scopus 로고
    • Prooxidant and antioxidant activity of vitamin e analogues and troglitazone
    • S. Tafazoli, J.S. Wright, P.J. O'Brien, Prooxidant and antioxidant activity of vitamin e analogues and troglitazone, Chem. Res. Toxicol. 18 (2005) 1567-1574.
    • (2005) Chem. Res. Toxicol. , vol.18 , pp. 1567-1574
    • Tafazoli, S.1    Wright, J.S.2    O'Brien, P.J.3
  • 75
    • 0032968521 scopus 로고    scopus 로고
    • The importance of lipid solubility in antioxidants and free radical generating systems for determining lipoprotein peroxidation
    • H. Massaeli, S. Sobrattee, G.N. Pierce, The importance of lipid solubility in antioxidants and free radical generating systems for determining lipoprotein peroxidation, Free Radic. Biol. Med. 26 (1999) 1524-1530.
    • (1999) Free Radic. Biol. Med. , vol.26 , pp. 1524-1530
    • Massaeli, H.1    Sobrattee, S.2    Pierce, G.N.3
  • 76
    • 78649316934 scopus 로고    scopus 로고
    • Molecular properties prediction, synthesis and antimicrobial activity of some newer oxadiazole derivatives
    • M.A. Bakht, M.S. Yar, S.G. Abdel-Hamid, S.I. Al Qasoumi, A. Samad, Molecular properties prediction, synthesis and antimicrobial activity of some newer oxadiazole derivatives, Eur. J. Med. Chem. 45 (2010) 5862-5869.
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 5862-5869
    • Bakht, M.A.1    Yar, M.S.2    Abdel-Hamid, S.G.3    Al Qasoumi, S.I.4    Samad, A.5
  • 77
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • C.A. Lipinski, F. Lombardo, B.W. Dominy, P.J. Feeney, Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings, Adv. Drug Deliv. Rev. 23 (1997) 3-25.
    • (1997) Adv. Drug Deliv. Rev. , vol.23 , pp. 3-25
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 78
    • 78651080738 scopus 로고    scopus 로고
    • A comparative study on the molecular descriptors for predicting drug-likeness of small molecules
    • H. Mishra, N. Singh, T. Lahiri, K. Misra, A comparative study on the molecular descriptors for predicting drug-likeness of small molecules, Bioinformation 3 (2009) 384-388.
    • (2009) Bioinformation , vol.3 , pp. 384-388
    • Mishra, H.1    Singh, N.2    Lahiri, T.3    Misra, K.4
  • 80
    • 0000262640 scopus 로고    scopus 로고
    • A new atom-additive method for calculating partition coefficients
    • R. Wang, Y. Fu, L. Lai, A new atom-additive method for calculating partition coefficients, J. Chem. Inf. Comput. Sci. 37 (1997) 615-621.
    • (1997) J. Chem. Inf. Comput. Sci. , vol.37 , pp. 615-621
    • Wang, R.1    Fu, Y.2    Lai, L.3
  • 81
    • 0032811868 scopus 로고    scopus 로고
    • Rapid calculation of polar molecular surface area and its application to the prediction of transport phenomena. 2. Prediction of blood-brain barrier penetration
    • D.E. Clark, Rapid calculation of polar molecular surface area and its application to the prediction of transport phenomena. 2. Prediction of blood-brain barrier penetration, J. Pharm. Sci. 88 (1999) 815-821.
    • (1999) J. Pharm. Sci. , vol.88 , pp. 815-821
    • Clark, D.E.1
  • 83
    • 55949129945 scopus 로고    scopus 로고
    • DPPH antioxidant assay revisited
    • O.P. Sharma, T.K. Bhat, DPPH antioxidant assay revisited, Food Chem. 113 (2009) 1202-1205.
    • (2009) Food Chem. , vol.113 , pp. 1202-1205
    • Sharma, O.P.1    Bhat, T.K.2
  • 84
    • 79952538928 scopus 로고    scopus 로고
    • Oily Press Lipid Library Bridgewater, England
    • E. Frankel, Lipid oxidation, Oily Press Lipid Library Bridgewater, England, 2005, pp. 1-470.
    • (2005) Lipid Oxidation , pp. 1-470
    • Frankel, E.1
  • 86
    • 3843083954 scopus 로고    scopus 로고
    • Syntheses and evaluation of antioxidant activity of sydnonyl substituted thiazolidinone and thiazoline derivatives
    • M.H. Shih, F.Y. Ke, Syntheses and evaluation of antioxidant activity of sydnonyl substituted thiazolidinone and thiazoline derivatives, Bioorg. Med. Chem. 12 (2004) 4633-4643.
    • (2004) Bioorg. Med. Chem. , vol.12 , pp. 4633-4643
    • Shih, M.H.1    Ke, F.Y.2
  • 87
    • 33646814916 scopus 로고    scopus 로고
    • Synthesis and oxidant properties of novel (5-bromobenzofuran-2-yl)(3-methyl-3-mesitylcyclobutyl)ketonethiosemicarbazone
    • F. Karatas, M. Koca, H. Kara, S. Servi, Synthesis and oxidant properties of novel (5-bromobenzofuran-2-yl)(3-methyl-3-mesitylcyclobutyl)ketonethiosemicarbazone, Eur. J. Med. Chem. 41 (2006) 664-669.
    • (2006) Eur. J. Med. Chem. , vol.41 , pp. 664-669
    • Karatas, F.1    Koca, M.2    Kara, H.3    Servi, S.4
  • 88
    • 57849088639 scopus 로고    scopus 로고
    • Syntheses and evaluation of glucosyl aryl thiosemicarbazide and glucosyl thiosemicarbazone derivatives as antioxidant and anti-dyslipidemic agents
    • S. Ghosh, A.K. Misra, G. Bhatia, M.M. Khan, A.K. Khanna, Syntheses and evaluation of glucosyl aryl thiosemicarbazide and glucosyl thiosemicarbazone derivatives as antioxidant and anti-dyslipidemic agents, Bioorg. Med. Chem. Lett. 19 (2009) 386-389.
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 386-389
    • Ghosh, S.1    Misra, A.K.2    Bhatia, G.3    Khan, M.M.4    Khanna, A.K.5
  • 89
    • 44649140390 scopus 로고    scopus 로고
    • Synthesis, crystal structure and biological activity of 1-(1H-benzoimidazol-2-yl)-ethanone thiosemicarbazone and its cobalt complex
    • M. Poyraz, M. Sari, F. Demirci, M. Kosar, S. Demirayak, O. Buyükgüngor, Synthesis, crystal structure and biological activity of 1-(1H-benzoimidazol-2-yl)-ethanone thiosemicarbazone and its cobalt complex, Polyhedron 27 (2008) 2091-2096.
    • (2008) Polyhedron , vol.27 , pp. 2091-2096
    • Poyraz, M.1    Sari, M.2    Demirci, F.3    Kosar, M.4    Demirayak, S.5    Buyükgüngor, O.6
  • 90
    • 42149101677 scopus 로고    scopus 로고
    • Synthesis and antioxidant properties of novel N-methyl-1, 3, 4-thiadiazol-2-amine and 4-methyl-2H-1, 2, 4-triazole-3 (4H)-thione derivatives of benzimidazole class
    • C. Kus, G. Ayhan-KIlcIgil, S. Ozbey, F. Kaynak, M. Kaya, T. Çoban, B. Can-Eke, Synthesis and antioxidant properties of novel N-methyl-1, 3, 4-thiadiazol-2-amine and 4-methyl-2H-1, 2, 4-triazole-3 (4H)-thione derivatives of benzimidazole class, Bioorg. Med. Chem. 16 (2008) 4294-4303.
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 4294-4303
    • Kus, C.1    Ayhan-Kilcigil S Ozbey F Kaynak, G.2    Kaya, M.3    Çoban, T.4    Can-Eke, B.5
  • 91
    • 34250229804 scopus 로고
    • Radical arylation of thiosemicarbazide and acetone thiosemicarbazone by aryldiazonium borofluorides
    • B.V. Kopylova, R.G. Gasanov, R.K. Freidlina, Radical arylation of thiosemicarbazide and acetone thiosemicarbazone by aryldiazonium borofluorides, Russ. Chem. Bull. 30 (1981) 1059-1062.
    • (1981) Russ. Chem. Bull. , vol.30 , pp. 1059-1062
    • Kopylova, B.V.1    Gasanov, R.G.2    Freidlina, R.K.3
  • 93
    • 84902665620 scopus 로고    scopus 로고
    • Synthesis and antioxidant activity evaluation of new compounds from hydrazinecarbothioamide and 1, 2,4-triazole class containing diarylsulfone and 2,4-difluorophenyl moieties
    • S.F. Barbuceanu, D.C. Ilies, G. Saramet, V. Uivarosi, C. Draghici, V. Radulescu, Synthesis and antioxidant activity evaluation of new compounds from hydrazinecarbothioamide and 1,2,4-triazole class containing diarylsulfone and 2,4-difluorophenyl moieties, Int. J. Mol. Sci. 15 (2014) 10908-10925.
    • (2014) Int. J. Mol. Sci. , vol.15 , pp. 10908-10925
    • Barbuceanu, S.F.1    Ilies, D.C.2    Saramet, G.3    Uivarosi, V.4    Draghici, C.5    Radulescu, V.6
  • 94
    • 0033116118 scopus 로고    scopus 로고
    • Chain-breaking fused heterocyclic antioxidants: Antioxidant activities of phenothiazines compared to related compounds
    • T. Nishiyama, T. Yamaguchi, T. Fukui, K. Tomii, Chain-breaking fused heterocyclic antioxidants: antioxidant activities of phenothiazines compared to related compounds, Polym. Degrad. Stab. 64 (1999) 33-38.
    • (1999) Polym. Degrad. Stab. , vol.64 , pp. 33-38
    • Nishiyama, T.1    Yamaguchi, T.2    Fukui, T.3    Tomii, K.4
  • 95
    • 0000775778 scopus 로고    scopus 로고
    • Bond dissociation energies of O-H bonds in substituted phenols from equilibration studies
    • M. Lucarini, P. Pedrielli, G. Pedulli, S. Cabiddu, C. Fattuoni, Bond dissociation energies of O-H bonds in substituted phenols from equilibration studies, J. Org. Chem. 61 (1996) 9259-9263.
    • (1996) J. Org. Chem. , vol.61 , pp. 9259-9263
    • Lucarini, M.1    Pedrielli, P.2    Pedulli, G.3    Cabiddu, S.4    Fattuoni, C.5
  • 96
    • 0034598350 scopus 로고    scopus 로고
    • Antioxidant function of phenethyl-5-bromo-pyridyl thiourea compounds with potent anti-HIV activity
    • Y. Dong, T. Venkatachalam, R. Narla, V. Trieu, E. Sudbeck, F. Uckun, Antioxidant function of phenethyl-5-bromo-pyridyl thiourea compounds with potent anti-HIV activity, Bioorg. Med. Chem. Lett. 10 (2000) 87-90.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 87-90
    • Dong, Y.1    Venkatachalam, T.2    Narla, R.3    Trieu, V.4    Sudbeck, E.5    Uckun, F.6
  • 97
    • 0008129222 scopus 로고    scopus 로고
    • Acrylamides as phenolic antioxidants for acrylqnitrile-butadiene rubber compounds
    • S.N. Lawandy, A.B. Shehata, A.F. Younan, Acrylamides as phenolic antioxidants for acrylqnitrile-butadiene rubber compounds, Polym. Plast. Technol. Eng. 35 (1996) 813-825.
    • (1996) Polym. Plast. Technol. Eng. , vol.35 , pp. 813-825
    • Lawandy, S.N.1    Shehata, A.B.2    Younan, A.F.3
  • 98
    • 0037290312 scopus 로고    scopus 로고
    • Differences in the antioxidant activity of plant and mammalian lignans
    • H.B. Niemeyer, M. Metzler, Differences in the antioxidant activity of plant and mammalian lignans, J. Food Eng. 56 (2003) 255-256.
    • (2003) J. Food Eng. , vol.56 , pp. 255-256
    • Niemeyer, H.B.1    Metzler, M.2
  • 99
    • 57449110347 scopus 로고    scopus 로고
    • Reaction of phenols with the 2,2-diphenyl-1-picrylhydrazyl radical. Kinetics and DFT calculations applied to determine ArO-h bond dissociation enthalpies and reaction mechanism
    • C.F. Mario, D. Carmelo, D.M. Iain, A.D. Gino, K.U. Ingold, Reaction of phenols with the 2,2-diphenyl-1-picrylhydrazyl radical. Kinetics and DFT calculations applied to determine ArO-h bond dissociation enthalpies and reaction mechanism, J. Org. Chem. 73 (2008) 9270-9282.
    • (2008) J. Org. Chem. , vol.73 , pp. 9270-9282
    • Mario, C.F.1    Carmelo, D.2    Iain, D.M.3    Gino, A.D.4    Ingold, K.U.5
  • 100
    • 33845377128 scopus 로고
    • Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenols
    • G. Burton, T. Doba, E. Gabe, L. Hughes, F. Lee, L. Prasad, K. Ingold, Autoxidation of biological molecules. 4. Maximizing the antioxidant activity of phenols, J. Am. Chem. Soc. 107 (1985) 7053-7065.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 7053-7065
    • Burton, G.1    Doba, T.2    Gabe, E.3    Hughes, L.4    Lee, F.5    Prasad, L.6    Ingold, K.7
  • 101
    • 0020074850 scopus 로고
    • Autoxidation of biological molecules. 1. Antioxidant activity of vitamin e and related chain-breaking phenolic antioxidants in vitro
    • G. Burton, K. Ingold, Autoxidation of biological molecules. 1. Antioxidant activity of vitamin E and related chain-breaking phenolic antioxidants in vitro, J. Am. Chem. Soc. 103 (1981) 6472-6477.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 6472-6477
    • Burton, G.1    Ingold, K.2
  • 102
    • 0036019820 scopus 로고    scopus 로고
    • The second stable conformation of the methoxy groups of o-dimethoxybenzene: Stabilization of perpendicular conformation by CH-O interaction
    • S. Tsuzuki, H. Houjou, Y. Nagawa, K. Hiratani, The second stable conformation of the methoxy groups of o-dimethoxybenzene: stabilization of perpendicular conformation by CH-O interaction, J. Chem. Soc. Perkin Trans. 2 (2002) 1271-1273.
    • (2002) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 1271-1273
    • Tsuzuki, S.1    Houjou, H.2    Nagawa, Y.3    Hiratani, K.4
  • 103
    • 0035857407 scopus 로고    scopus 로고
    • Predicting the activity of phenolic antioxidants: Theoretical method, analysis of substituent effects, and application to major families of antioxidants
    • J.S. Wright, E.R. Johnson, G.A. DiLabio, Predicting the activity of phenolic antioxidants: theoretical method, analysis of substituent effects, and application to major families of antioxidants, J. Am. Chem. Soc. 123 (2001) 1173-1183.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 1173-1183
    • Wright, J.S.1    Johnson, E.R.2    Dilabio, G.A.3
  • 104
    • 84986452937 scopus 로고
    • Vitamin E: Or why we don't go rancid1
    • K. Ingold, G. Burton, Vitamin E: or why we don't go rancid1, J. Chin. Chem. Soc. 39 (1992) 199-204.
    • (1992) J. Chin. Chem. Soc. , vol.39 , pp. 199-204
    • Ingold, K.1    Burton, G.2
  • 105
    • 31344432053 scopus 로고    scopus 로고
    • Phospholipase A2 reactive oxygen species, and lipid peroxidation in cerebral ischemia
    • R. Muralikrishna Adibhatla, J. Hatcher, Phospholipase A2, reactive oxygen species, and lipid peroxidation in cerebral ischemia, Free Radic. Biol. Med. 40 (2006) 376-387.
    • (2006) Free Radic. Biol. Med. , vol.40 , pp. 376-387
    • Muralikrishna Adibhatla, R.1    Hatcher, J.2
  • 107
    • 0031853711 scopus 로고    scopus 로고
    • Effects of vitamin e and/or C on reactive oxygen species-related lead toxicity in the rat sperm
    • P.-C. Hsu, M.-Y. Liu, C.-C. Hsu, L.-Y. Chen, Y. Leon Guo, Effects of vitamin E and/or C on reactive oxygen species-related lead toxicity in the rat sperm, Toxicology 128 (1998) 169-179.
    • (1998) Toxicology , vol.128 , pp. 169-179
    • Hsu, P.-C.1    Liu, M.-Y.2    Hsu, C.-C.3    Chen, L.-Y.4    Leon Guo, Y.5
  • 108
    • 34547633812 scopus 로고    scopus 로고
    • Comparative evaluation of various total antioxidant capacity assays applied to phenolic compounds with the CUPRAC assay
    • R. Apak, K. Guclu, B. Demirata, M. Ozyurek, S. Çelik, B. Bektasoglu, K. Berker, D. Ozyurt, Comparative evaluation of various total antioxidant capacity assays applied to phenolic compounds with the CUPRAC assay, Molecules 12 (2007) 1496-1547.
    • (2007) Molecules , vol.12 , pp. 1496-1547
    • Apak, R.1    Guclu, K.2    Demirata, B.3    Ozyurek, M.4    Çelik, S.5    Bektasoglu, B.6    Berker, K.7    Ozyurt, D.8
  • 109
    • 20844445334 scopus 로고    scopus 로고
    • Standardized methods for the determination of antioxidant capacity and phenolics in foods and dietary supplements
    • R.L. Prior, X. Wu, K. Schaich, Standardized methods for the determination of antioxidant capacity and phenolics in foods and dietary supplements, J. Agric. Food Chem. 53 (2005) 4290-4302.
    • (2005) J. Agric. Food Chem. , vol.53 , pp. 4290-4302
    • Prior, R.L.1    Wu, X.2    Schaich, K.3
  • 110
    • 77954106917 scopus 로고    scopus 로고
    • Influence of "remote" intramolecular hydrogen bonds on the stabilities of phenoxyl radicals and benzyl cations
    • M.C. Foti, R. Amorati, G.F. Pedulli, C. Daquino, D.A. Pratt, K.U. Ingold, Influence of "remote" intramolecular hydrogen bonds on the stabilities of phenoxyl radicals and benzyl cations, J. Org. Chem. 75 (2010) 4434-4440.
    • (2010) J. Org. Chem. , vol.75 , pp. 4434-4440
    • Foti, M.C.1    Amorati, R.2    Pedulli, G.F.3    Daquino, C.4    Pratt, D.A.5    Ingold, K.U.6
  • 111
    • 0037181273 scopus 로고    scopus 로고
    • Development and validation of oxygen radical absorbance capacity assay for lipophilic antioxidants using randomly methylated-cyclodextrin as the solubility enhancer
    • D. Huang, B. Ou, M. Hampsch-Woodill, J. Flanagan, E. Deemer, Development and validation of oxygen radical absorbance capacity assay for lipophilic antioxidants using randomly methylated-cyclodextrin as the solubility enhancer, J. Agric. Food Chem. 50 (2002) 1815-1821.
    • (2002) J. Agric. Food Chem. , vol.50 , pp. 1815-1821
    • Huang, D.1    Ou, B.2    Hampsch-Woodill, M.3    Flanagan, J.4    Deemer, E.5
  • 112
    • 0034492226 scopus 로고    scopus 로고
    • Lipid oxidation in oil in water emulsions: Impact of molecular environment on chemical reactions in heterogeneous food systems
    • D. McClements, E. Decker, Lipid oxidation in oil in water emulsions: impact of molecular environment on chemical reactions in heterogeneous food systems, J. Food Sci. 65 (2000) 1270-1282.
    • (2000) J. Food Sci. , vol.65 , pp. 1270-1282
    • McClements, D.1    Decker, E.2
  • 114
    • 18444376420 scopus 로고    scopus 로고
    • Bruker AXS Inc Wisconsin USA
    • M. Bruker, APEX2 and SAINT, Bruker AXS Inc, Wisconsin, USA, 2007.
    • (2007) APEX2 and SAINT
    • Bruker, M.1
  • 116
    • 0036664108 scopus 로고    scopus 로고
    • X-Seedda software tool for supramolecular crystallography
    • L.J. Barbour, X-Seedda software tool for supramolecular crystallography, J. Supramol. Chem. 1 (2001) 189-191.
    • (2001) J. Supramol. Chem. , vol.1 , pp. 189-191
    • Barbour, L.J.1
  • 117
    • 36949063535 scopus 로고
    • Antioxidant determination by the use of a stable free radical
    • M.S. Blois, Antioxidant determination by the use of a stable free radical, Nature 181 (1958) 1199-1200.
    • (1958) Nature , vol.181 , pp. 1199-1200
    • Blois, M.S.1
  • 118
    • 36349025741 scopus 로고    scopus 로고
    • Antioxidant from maize and maize fermented by marasmiellus sp. As stabiliser of lipid-rich foods
    • M. Daker, N. Abdullah, S. Vikineswary, P.C. Goh, U.R. Kuppusamy, Antioxidant from maize and maize fermented by marasmiellus sp. as stabiliser of lipid-rich foods, Food Chem. 107 (2008) 1092-1098.
    • (2008) Food Chem. , vol.107 , pp. 1092-1098
    • Daker, M.1    Abdullah, N.2    Vikineswary, S.3    Goh, P.C.4    Kuppusamy, U.R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.