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Volumn 8, Issue 5, 2012, Pages 942-946

Antioxidant activity of new benzo[de]quinolines and lactams: 2DQuantitative structure-activity relationships

Author keywords

2D QSAR; Antioxidant agent; Benzo de quinoline; Hydroxyketolactam; Lactam

Indexed keywords

8,9 DIHYDRO 7H BENZO[DE]PYRROLO[1,2 A]QUINOLINE 7,10(7AH) DIONE; ANTIOXIDANT; DISSOLVED OXYGEN; KETONE DERIVATIVE; LACTAM DERIVATIVE; METHANOL; MOLECULAR SCAFFOLD; PYROGALLOL; QUINOLINE DERIVATIVE; RADICAL; SUPEROXIDE; UNCLASSIFIED DRUG;

EID: 84865758394     PISSN: 15734064     EISSN: 18756638     Source Type: Journal    
DOI: 10.2174/157340612802084216     Document Type: Article
Times cited : (6)

References (24)
  • 1
    • 0027201993 scopus 로고
    • The pineal hormone melatonin inhibits DNA-adduct formation induced by the chemical carcinogen safrole in vivo
    • Tan, D.X.; Pöeggeler, B.; Reiter, R.J.; Chen, L.D.; Chen, S.; Lucien, M.L.; Barlow-Walden, L.R. The pineal hormone melatonin inhibits DNA-adduct formation induced by the chemical carcinogen safrole in vivo. Cancer Lett., 1993, 70, 65-71. (Pubitemid 23219861)
    • (1993) Cancer Letters , vol.70 , Issue.1-2 , pp. 65-71
    • Tan, D.-X.1    Poeggeler, B.2    Reiter, R.J.3    Chen, L.-D.4    Chen, S.5    Manchester, L.C.6    Barlow-Walden, L.R.7
  • 2
    • 0028178826 scopus 로고
    • Both physiological and pharmacological levels of melatonin reduce DNA adduct formation induced by the carcinogen safrole
    • Tan, D.X.; Reiter, R.J.; Chen, L.D.; Pöeggeler, B.; Lucien, M.L.; Barlow-Walden, L.R. Both physiological and pharmacological levels of melatonin reduce DNA adduct formation induced by the carcinogen safrole. Carcinogenesis, 1994, 15, 215-218. (Pubitemid 24121651)
    • (1994) Carcinogenesis , vol.15 , Issue.2 , pp. 215-218
    • Tan, D.-X.1    Reiter, R.J.2    Chen, L.-D.3    Poeggeler, B.4    Manchester, L.C.5    Barlow-Walden, L.R.6
  • 3
    • 0028924029 scopus 로고
    • Potent protective effect of melatonin on in vivo paraquat-induced oxidative damage in rats
    • DOI 10.1016/0024-3205(94)00417-Q
    • Melchiorri, D.; Reiter, R.J.; Attia, A.M.; Hara, M.; Burgos, A.; Nistico, G. Potent protective effect of melatonin on in vivo paraquat-induced oxidative damage in rats. Life Sci., 1995, 56, 83-89. (Pubitemid 24380187)
    • (1995) Life Sciences , vol.56 , Issue.2 , pp. 83-89
    • Melchiorri, D.1    Reiter, R.J.2    Attia, A.M.3    Hara, M.4    Burgos, A.5    Nistico, G.6
  • 4
    • 0029082155 scopus 로고
    • Melatonin reduces kainate-induced lipid peroxidation in homogenates of different brain regions
    • Melchiorri, D.; Reiter, R.J.; Sewerynek, E.; Chen, L.D.; Nistico, G. Melatonin reduces kainate-induced lipid peroxidation in homogenates of different brain regions. FASEB J., 1995, 9, 1205-1210.
    • (1995) FASEB J. , vol.9 , pp. 1205-1210
    • Melchiorri, D.1    Reiter, R.J.2    Sewerynek, E.3    Chen, L.D.4    Nistico, G.5
  • 5
    • 0034469566 scopus 로고    scopus 로고
    • Melatonin and tryptophan derivatives as free radical scavengers and antioxidants
    • Reiter, R.J.; Tan, D.X.; Cabrera, J.; D'Arpa, D. Melatonin and tryptophan derivatives as free radical scavengers and antioxidants. Adv. Exp. Med. Biol., 1999, 467, 379-387.
    • (1999) Adv. Exp. Med. Biol. , vol.467 , pp. 379-387
    • Reiter, R.J.1    Tan, D.X.2    Cabrera, J.3    D'Arpa, D.4
  • 6
    • 0033027481 scopus 로고    scopus 로고
    • Structure-activity relationships in a series of melatonin analogues with the low-density lipoprotein oxidation model
    • DOI 10.1016/S0891-5849(99)00020-9, PII S0891594999000209
    • Gozzo, A.; Lesieur, D.; Duriez, P.; Fruchart, J.C.; Teissier, E. Structure-activity relationships in a series of melatonin analogues with the low-density lipoprotein oxidation model. Free Radical Bio. Med., 1999, 26, 1538-1543. (Pubitemid 29308023)
    • (1999) Free Radical Biology and Medicine , vol.26 , Issue.11-12 , pp. 1538-1543
    • Gozzo, A.1    Lesieur, D.2    Duriez, P.3    Fruchart, J.-C.4    Teissier, E.5
  • 12
    • 84986487093 scopus 로고
    • Studies on pyrrolidinones Derivatives of 1, 2, 351010a-Hexahydrobenz [f]indolizine-310-dione
    • Rigo, B.; Kolocouris, N. Studies on pyrrolidinones. Derivatives of 1,2,3,5,10,10a-Hexahydrobenz [f]indolizine-3,10-dione. J. Het. Chem., 1983, 20, 893-898.
    • (1983) J Het Chem , vol.20 , pp. 893-898
    • Rigo, B.1    Kolocouris, N.2
  • 13
    • 33646101043 scopus 로고    scopus 로고
    • Studies on pyrrolidinones. Oxidations and rearrangements in the hexahydrobenz [f]indolizine-3, 10-dione series
    • Bourry, A.; Couturier, D.; Sanz, G.; Van Hijfte, L.; Hénichart, J.P.; Rigo, B. Studies on pyrrolidinones. Oxidations and rearrangements in the hexahydrobenz [f]indolizine-3,10-dione series. Tetrahedron, 2006, 62, 4400-4407.
    • (2006) Tetrahedron , vol.62 , pp. 4400-4407
    • Bourry, A.1    Couturier, D.2    Sanz, G.3    Van Hijfte, L.4    Hénichart, J.P.5    Rigo, B.6
  • 14
    • 84963950818 scopus 로고    scopus 로고
    • Study of the by-products of benzo [f]indolizines syntheses: A quest towards structural diversity
    • Rigo, B.; Akué-Gédu, R. Study of the by-products of benzo [f]indolizines syntheses: a quest towards structural diversity. Targets Het. Syst., 2006, 10, 232-265.
    • (2006) Targets Het. Syst. , vol.10 , pp. 232-265
    • Rigo, B.1    Akué-Gédu, R.2
  • 15
    • 27544497542 scopus 로고    scopus 로고
    • Oxidation of liposomal membrane suppressed by flavonoids: Quantitative structure-activity relationship
    • DOI 10.1016/j.bmc.2005.07.047, PII S096808960500619X
    • Rackova, L.; Firakova, S.; Kostalova, D.; Stefek, M.; Sturdik, E.; Majekova, M. Oxidation of liposomal membrane suppressed by flavonoids: Quantitative structure-activity relationships. Bioorg. Med. Chem., 2005, 13, 6477-6484. (Pubitemid 41539311)
    • (2005) Bioorganic and Medicinal Chemistry , vol.13 , Issue.23 , pp. 6477-6484
    • Rackova, L.1    Firakova, S.2    Kostalova, D.3    Stefek, M.4    Sturdik, E.5    Majekova, M.6
  • 16
    • 33646095778 scopus 로고    scopus 로고
    • Free radicals scavenging and antioxidant activities of substituted hexahydropyridoindoles. Quantitative structure-activity relationships
    • Rackova, L.; Snirc, V.; Majekova, M.; Majek, P.; Stefek, M. Free radicals scavenging and antioxidant activities of substituted hexahydropyridoindoles. Quantitative structure-activity relationships. J. Med. Chem., 2006, 49, 2543-2548.
    • (2006) J. Med. Chem. , vol.49 , pp. 2543-2548
    • Rackova, L.1    Snirc, V.2    Majekova, M.3    Majek, P.4    Stefek, M.5
  • 17
    • 19544372282 scopus 로고    scopus 로고
    • Antioxidant and antiproliferative activity of curcumin semicarbazone
    • DOI 10.1016/j.bmcl.2005.04.001, PII S0960894X05004439
    • Dutta, S.; Padhye, S.; Priyadarsini, K.I.; Newton, C. Antioxidant and antiproliferative activity of curcumin semicarbazone. Bioorg. Med. Chem. Lett., 2005, 15, 2738-2744. (Pubitemid 40732210)
    • (2005) Bioorganic and Medicinal Chemistry Letters , vol.15 , Issue.11 , pp. 2738-2744
    • Dutta, S.1    Padhye, S.2    Priyadarsini, K.I.3    Newton, C.4
  • 18
    • 70749090893 scopus 로고    scopus 로고
    • Studies on pyrrolidinones. on the application of coppercatalyzed arylation of methyl pyroglutamate to obtain a new benzo [de]quinoline scaffold
    • Ghinet, A.; Oudir, S.; Hénichart, J.P.; Rigo, B.; Pommery, N.; Gautret, P. Studies on pyrrolidinones. On the application of coppercatalyzed arylation of methyl pyroglutamate to obtain a new benzo [de]quinoline scaffold. Tetrahedron, 2010, 66, 215-221.
    • (2010) Tetrahedron , vol.66 , pp. 215-221
    • Ghinet, A.1    Oudir, S.2    Hénichart, J.P.3    Rigo, B.4    Pommery, N.5    Gautret, P.6
  • 19
    • 84986524579 scopus 로고
    • New dehydration in the pyrrolo [1,2-b]isoquinoline series. Preparation and structural identification of 3,5- dihydrobenz [f]indolizin-3-one
    • Rigo, B.; Tulier, E.; Barbry, D.; Couturier, D.; Warin, V.; Lamiot, J.; Baert, F. New dehydration in the pyrrolo [1,2-b]isoquinoline series. Preparation and structural identification of 3,5- dihydrobenz [f]indolizin-3-one. J. Het. Chem., 1990, 27, 1383-1386.
    • (1990) J. Het. Chem. , vol.27 , pp. 1383-1386
    • Rigo, B.1    Tulier, E.2    Barbry, D.3    Couturier, D.4    Warin, V.5    Lamiot, J.6    Baert, F.7
  • 21
    • 76749085210 scopus 로고    scopus 로고
    • Studies on the Lossen-type rearrangement of N-(3-phenylpropionyloxy) phtalimide and N-tosyloxy derivatives with several nucleophiles
    • Chanmiya Sheikh, M.; Takagi, S.; Ogasawara, A.; Ohira, M.; Miyatake, R.; Abe, H.; Yoshimura, T.; Morita, H. Studies on the Lossen-type rearrangement of N-(3-phenylpropionyloxy)phtalimide and N-tosyloxy derivatives with several nucleophiles. Tetrahedron, 2010, 66, 2132-2140.
    • (2010) Tetrahedron , vol.66 , pp. 2132-2140
    • Chanmiya Sheikh, M.1    Takagi, S.2    Ogasawara, A.3    Ohira, M.4    Miyatake, R.5    Abe, H.6    Yoshimura, T.7    Morita, H.8
  • 23
    • 0141502213 scopus 로고    scopus 로고
    • Potent mammalian cerebroprotection and neuronal cell death inhibition are afforded by a synthetic antioxidant analogue of marine invertebrate cell protectant ovothiols
    • DOI 10.1046/j.1460-9568.2003.02846.x
    • Vamecq, J.; Maurois, P.; Bac, P.; Bailly, F.; Bernier, J.L.; Stables, J.P.; Husson, I.; Gressens, P. Potent mammalian cerebroprotection and neuronal cell death inhibition are afforded by a synthetic antioxidant analogue of marine invertebrate cell protectant ovothiols. Eur. J. Neurosci., 2003, 18, 1110-1120. (Pubitemid 37115033)
    • (2003) European Journal of Neuroscience , vol.18 , Issue.5 , pp. 1110-1120
    • Vamecq, J.1    Maurois, P.2    Bac, P.3    Bailly, F.4    Bernier, J.-L.5    Stables, J.P.6    Husson, I.7    Gressens, P.8
  • 24
    • 0016272750 scopus 로고
    • Involvement of superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase
    • Marklund, S.; Marklund, G. Involvement of superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur. J. Biochem., 1974, 47, 469-474.
    • (1974) Eur. J. Biochem. , vol.47 , pp. 469-474
    • Marklund, S.1    Marklund, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.