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Volumn 33, Issue , 2016, Pages 35-44

Pro-apoptotic effect of new quinolone 7- ethyl 9-ethyl-6-oxo-6,9-dihydro[1,2,5]selenadiazolo [3,4-h]quinoline-7-carboxylate on cervical cancer cell line HeLa alone/with UVA irradiation

Author keywords

Apoptosis; Cell cycle arrest; HeLa cells; Quinolone derivative; UVA irradiation

Indexed keywords

7 ETHYL 9 ETHYL 6 OXO 6,9 DIHYDRO[1,2,5]SELENADIAZOLO[3,4 H]QUINOLINE 7 CARBOXYLATE; CASPASE 3; QUINOLONE DERIVATIVE; REACTIVE OXYGEN METABOLITE; UNCLASSIFIED DRUG; 7-ETHYL 9-ETHYL-6-OXO-6,9-DIHYDRO(1,2,5)SELENADIAZOLO(3,4-H)QUINOLINE-7-CARBOXYLATE; ANTINEOPLASTIC AGENT; ORGANOSELENIUM DERIVATIVE;

EID: 84959500097     PISSN: 08872333     EISSN: 18793177     Source Type: Journal    
DOI: 10.1016/j.tiv.2016.02.012     Document Type: Article
Times cited : (6)

References (66)
  • 1
    • 34548761462 scopus 로고    scopus 로고
    • Photosensitizing potential of ciprofloxacin at ambient level of UV radiation
    • Agrawal N.R., Ray M., Farooq A.P., Hans R. Photosensitizing potential of ciprofloxacin at ambient level of UV radiation. Photochem. Photobiol. 2007, 83:1226-1236.
    • (2007) Photochem. Photobiol. , vol.83 , pp. 1226-1236
    • Agrawal, N.R.1    Ray, M.2    Farooq, A.P.3    Hans, R.4
  • 2
    • 84898948830 scopus 로고    scopus 로고
    • Mechanism of quinolone action and resistance
    • Aldred K.J., Kerns R.J., Osheroff N. Mechanism of quinolone action and resistance. Biochemistry 2014, 53:1565-1574.
    • (2014) Biochemistry , vol.53 , pp. 1565-1574
    • Aldred, K.J.1    Kerns, R.J.2    Osheroff, N.3
  • 8
    • 77956614176 scopus 로고    scopus 로고
    • Application of the Gould-Jacobs reaction to 4-amino-2,1,3- benzoselenadiazole
    • Bella M., Schultz M., Milata V., Koňariková K., Breza M. Application of the Gould-Jacobs reaction to 4-amino-2,1,3- benzoselenadiazole. Tetrahedron 2010, 66:8169-8174.
    • (2010) Tetrahedron , vol.66 , pp. 8169-8174
    • Bella, M.1    Schultz, M.2    Milata, V.3    Koňariková, K.4    Breza, M.5
  • 10
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 1976, 72:248-254.
    • (1976) Anal. Biochem. , vol.72 , pp. 248-254
    • Bradford, M.M.1
  • 11
    • 0033134745 scopus 로고    scopus 로고
    • In vitro photogenotoxic activity of clinafloxacin: a paradigm predicting photocarcinogenicity
    • Bulera S., Theiss J., Festerling T., de la Iglesia F. In vitro photogenotoxic activity of clinafloxacin: a paradigm predicting photocarcinogenicity. Toxicol. Appl. Pharmacol. 1999, 156:222-230.
    • (1999) Toxicol. Appl. Pharmacol. , vol.156 , pp. 222-230
    • Bulera, S.1    Theiss, J.2    Festerling, T.3    de la Iglesia, F.4
  • 13
    • 68549097938 scopus 로고    scopus 로고
    • Induction of mitotic arrest and apoptosis by a novel synthetic quinolone analogue, CWC-8, via intrinsic and extrinsic apoptotic pathways in human osteogenic sarcoma U-2 OS cells
    • Chang Y.H., Yang J.S., Kuo S.C., Chung J.G. Induction of mitotic arrest and apoptosis by a novel synthetic quinolone analogue, CWC-8, via intrinsic and extrinsic apoptotic pathways in human osteogenic sarcoma U-2 OS cells. Anticancer Res. 2009, 29:3139-3148.
    • (2009) Anticancer Res. , vol.29 , pp. 3139-3148
    • Chang, Y.H.1    Yang, J.S.2    Kuo, S.C.3    Chung, J.G.4
  • 14
    • 84866462308 scopus 로고    scopus 로고
    • The newly synthesized 2-(3-hydroxy-5-methoxyphenyl)-6,7-methylenedioxyquinolin-4-one triggers cell apoptosis through induction of oxidative stress and upregulation of the p38 MAPK signaling pathway in HL-60 human leukemia cells
    • Cheng Y.Y., Yang J.S., Tsai S.C., Liaw C.C., Chung J.G., Huang L.J., Lee K.H., Lu C.C., Chien H.C., Tsuzuki M., Kuo S.C. The newly synthesized 2-(3-hydroxy-5-methoxyphenyl)-6,7-methylenedioxyquinolin-4-one triggers cell apoptosis through induction of oxidative stress and upregulation of the p38 MAPK signaling pathway in HL-60 human leukemia cells. Oncol. Rep. 2012, 28:1482-1490.
    • (2012) Oncol. Rep. , vol.28 , pp. 1482-1490
    • Cheng, Y.Y.1    Yang, J.S.2    Tsai, S.C.3    Liaw, C.C.4    Chung, J.G.5    Huang, L.J.6    Lee, K.H.7    Lu, C.C.8    Chien, H.C.9    Tsuzuki, M.10    Kuo, S.C.11
  • 15
  • 16
    • 0037375444 scopus 로고    scopus 로고
    • 4-Hydroxymethyl- and 4-methoxymethylfuro[2,3-h]quinolin-2(1H)-ones: synthesis and biological properties
    • Chilin A., Marzano F., Baccichetti M., Simonato A., Guiotto A. 4-Hydroxymethyl- and 4-methoxymethylfuro[2,3-h]quinolin-2(1H)-ones: synthesis and biological properties. Bioorg. Med. Chem. 2003, 11:1311-1318.
    • (2003) Bioorg. Med. Chem. , vol.11 , pp. 1311-1318
    • Chilin, A.1    Marzano, F.2    Baccichetti, M.3    Simonato, A.4    Guiotto, A.5
  • 17
    • 70350026142 scopus 로고    scopus 로고
    • The synthesized 2-(2-fluorophenyl)-6,7-methylenedioxyquinolin-4-one (CHM-1) promoted G2/M arrest through inhibition of CDK1 and induced apoptosis through the mitochondrial dependent pathway in CT-26 murine colorectal adenocarcinoma cells
    • Chou L., Yang J., Huang L., Wu H., Lu C., Chiang J., Chen K., Kuo S., Chung J. The synthesized 2-(2-fluorophenyl)-6,7-methylenedioxyquinolin-4-one (CHM-1) promoted G2/M arrest through inhibition of CDK1 and induced apoptosis through the mitochondrial dependent pathway in CT-26 murine colorectal adenocarcinoma cells. J. Gastroenterol. 2009, 44:1055-1063.
    • (2009) J. Gastroenterol. , vol.44 , pp. 1055-1063
    • Chou, L.1    Yang, J.2    Huang, L.3    Wu, H.4    Lu, C.5    Chiang, J.6    Chen, K.7    Kuo, S.8    Chung, J.9
  • 19
    • 33747089883 scopus 로고    scopus 로고
    • Biological evaluation of newly synthesized quinoline-5,8-quinones as Cdc25B inhibitors
    • Cossy J., Belotti D., Brisson M., Skoko J.J., Wipf P., Lazo J.S. Biological evaluation of newly synthesized quinoline-5,8-quinones as Cdc25B inhibitors. Bioorg. Med. Chem. 2006, 14:6283-6287.
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 6283-6287
    • Cossy, J.1    Belotti, D.2    Brisson, M.3    Skoko, J.J.4    Wipf, P.5    Lazo, J.S.6
  • 20
    • 70349256451 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new heterocyclic quinolinones as anti-parasite and anti-HIV drug candidates
    • Darque A., Dumetre A., Hutter S., Casano G., Robin M., Pannecouque C., Azas N. Synthesis and biological evaluation of new heterocyclic quinolinones as anti-parasite and anti-HIV drug candidates. Bioorg. Med. Chem. Lett. 2009, 19:5962-5964.
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 5962-5964
    • Darque, A.1    Dumetre, A.2    Hutter, S.3    Casano, G.4    Robin, M.5    Pannecouque, C.6    Azas, N.7
  • 21
    • 0036581843 scopus 로고    scopus 로고
    • Synthesis, photochemical synthesis and antitumor evaluation of novel derivatives of thieno[3',2':4,5]thieno[2,3-c]quinolones
    • Dogan J.K., Slade N., Zamola B., Pavelič K., Karminski-Zamola G. Synthesis, photochemical synthesis and antitumor evaluation of novel derivatives of thieno[3',2':4,5]thieno[2,3-c]quinolones. Chem. Pharm. Bull.(Tokyo) 2002, 50:656-660.
    • (2002) Chem. Pharm. Bull.(Tokyo) , vol.50 , pp. 656-660
    • Dogan, J.K.1    Slade, N.2    Zamola, B.3    Pavelič, K.4    Karminski-Zamola, G.5
  • 24
  • 27
    • 33750456981 scopus 로고    scopus 로고
    • Evaluation of 3-carboxy-4(1H)-quinolones as inhibitors of human protein kinase CK2
    • Golub A., Yakovenko O., Bdzhola V., Sapelkin V., Zien P., Yarmoluk S. Evaluation of 3-carboxy-4(1H)-quinolones as inhibitors of human protein kinase CK2. J. Med. Chem. 2006, 49:6443-6450.
    • (2006) J. Med. Chem. , vol.49 , pp. 6443-6450
    • Golub, A.1    Yakovenko, O.2    Bdzhola, V.3    Sapelkin, V.4    Zien, P.5    Yarmoluk, S.6
  • 28
    • 27244455909 scopus 로고    scopus 로고
    • Ciprofloxacin-induced cytotoxicity and apoptosis in HeLa cells
    • Gürbay A., Osman M., Favier A., Hincal F. Ciprofloxacin-induced cytotoxicity and apoptosis in HeLa cells. Toxicol. Mech. Methods 2005, 15:339-342.
    • (2005) Toxicol. Mech. Methods , vol.15 , pp. 339-342
    • Gürbay, A.1    Osman, M.2    Favier, A.3    Hincal, F.4
  • 30
    • 84863169837 scopus 로고    scopus 로고
    • A novel synthetic 2-(3-methoxyphenyl)-6,7-methylenedioxoquinolin-4-one arrests the G2/M phase arrest via Cdc25c and induces apoptosis through caspase- and mitochondria-dependent pathways in TSGH8301 human bladder cancer cells
    • Hsu S.C., Yu C.C., Yang J.S., Lai K.C., Wu S.H., Lin J.J., Kuo J.H., Yang S.T., Huang C.C., Kuo S.C., Chung J.G. A novel synthetic 2-(3-methoxyphenyl)-6,7-methylenedioxoquinolin-4-one arrests the G2/M phase arrest via Cdc25c and induces apoptosis through caspase- and mitochondria-dependent pathways in TSGH8301 human bladder cancer cells. Int. J. Oncol. 2012, 40:731-738.
    • (2012) Int. J. Oncol. , vol.40 , pp. 731-738
    • Hsu, S.C.1    Yu, C.C.2    Yang, J.S.3    Lai, K.C.4    Wu, S.H.5    Lin, J.J.6    Kuo, J.H.7    Yang, S.T.8    Huang, C.C.9    Kuo, S.C.10    Chung, J.G.11
  • 31
    • 0031726906 scopus 로고    scopus 로고
    • Synthesis and antiplatelet activity of phenyl quinolones
    • Huang L., Hsieh M., Teng C., Lee K., Kuo S. Synthesis and antiplatelet activity of phenyl quinolones. Bioorg. Med. Chem. 1998, 6:1657-1662.
    • (1998) Bioorg. Med. Chem. , vol.6 , pp. 1657-1662
    • Huang, L.1    Hsieh, M.2    Teng, C.3    Lee, K.4    Kuo, S.5
  • 33
    • 78650643607 scopus 로고    scopus 로고
    • Effect of new synthetically prepared quinolone ethyl-1,4-dihydro-8-nitro-4-oxoquinoline-3- carboxylate on human leukemia cell line HL-60 without/with presence of UVA irradiation
    • Jantová S., Letašiová S., Koňariková K., Milata V., Brezová V. Effect of new synthetically prepared quinolone ethyl-1,4-dihydro-8-nitro-4-oxoquinoline-3- carboxylate on human leukemia cell line HL-60 without/with presence of UVA irradiation. Acta Chim. Slov. 2010, 3:51-72.
    • (2010) Acta Chim. Slov. , vol.3 , pp. 51-72
    • Jantová, S.1    Letašiová, S.2    Koňariková, K.3    Milata, V.4    Brezová, V.5
  • 35
    • 84881186678 scopus 로고    scopus 로고
    • New uses for old drugs: attempts to convert quinolone antibacterials into potential anticancer agents containing ruthenium
    • Kljun J., Bratsos I., Alessio E., Psomas G., Repnik U., Butinar M., Turk B., Turel I. New uses for old drugs: attempts to convert quinolone antibacterials into potential anticancer agents containing ruthenium. Inorg. Chem. 2013, 52:9039-9052.
    • (2013) Inorg. Chem. , vol.52 , pp. 9039-9052
    • Kljun, J.1    Bratsos, I.2    Alessio, E.3    Psomas, G.4    Repnik, U.5    Butinar, M.6    Turk, B.7    Turel, I.8
  • 36
    • 33745526474 scopus 로고    scopus 로고
    • Berberine-antiproliferative activity in vitro and induction of apoptosis/necrosis of the U937 and B16 cells
    • Letašiová S., Jantová S., Čipák L., Múčková M. Berberine-antiproliferative activity in vitro and induction of apoptosis/necrosis of the U937 and B16 cells. Cancer Lett. 2006, 239:254-262.
    • (2006) Cancer Lett. , vol.239 , pp. 254-262
    • Letašiová, S.1    Jantová, S.2    Čipák, L.3    Múčková, M.4
  • 37
    • 0032524848 scopus 로고    scopus 로고
    • Cyclic AMP and cyclic GMP phosphodiesterase inhibition by an antiplatelet agent, 6-[(3-methylene-2-oxo-5-phenyl-5-tetrahydrofuranyl)methoxy]quinolinone (CCT-62)
    • Liao C., Tzeng C., Teng C. Cyclic AMP and cyclic GMP phosphodiesterase inhibition by an antiplatelet agent, 6-[(3-methylene-2-oxo-5-phenyl-5-tetrahydrofuranyl)methoxy]quinolinone (CCT-62). Eur. J. Pharmacol. 1998, 349:107-114.
    • (1998) Eur. J. Pharmacol. , vol.349 , pp. 107-114
    • Liao, C.1    Tzeng, C.2    Teng, C.3
  • 38
    • 84891372288 scopus 로고    scopus 로고
    • Dovitinib induces mitotic defects and activates the G2 DNA damage checkpoint
    • Man W.Y., Mak J.P., Poon R.Y. Dovitinib induces mitotic defects and activates the G2 DNA damage checkpoint. J. Cell. Mol. Med. 2014, 18:143-155.
    • (2014) J. Cell. Mol. Med. , vol.18 , pp. 143-155
    • Man, W.Y.1    Mak, J.P.2    Poon, R.Y.3
  • 39
    • 0030908382 scopus 로고    scopus 로고
    • DNA damage and cytotoxicity induced in mammalian cells by a tetramethylfuroquinolinone derivative
    • Marzano C., Severin E., Pani B., Guiotto A., Bordin F. DNA damage and cytotoxicity induced in mammalian cells by a tetramethylfuroquinolinone derivative. Environ. Mol. Mutagen. 1997, 29:256-264.
    • (1997) Environ. Mol. Mutagen. , vol.29 , pp. 256-264
    • Marzano, C.1    Severin, E.2    Pani, B.3    Guiotto, A.4    Bordin, F.5
  • 40
    • 33947361191 scopus 로고    scopus 로고
    • The farnesyl transferase inhibitor, tipifarnib, is a potent inhibitor of the MDR1 gene product, P-glycoprotein, and demonstrates significant cytotoxic synergism against human leukemia cell lines
    • Medeiros B., Landau H., Morrow M., Lockerbie R., Pitts T., Eckhardt S. The farnesyl transferase inhibitor, tipifarnib, is a potent inhibitor of the MDR1 gene product, P-glycoprotein, and demonstrates significant cytotoxic synergism against human leukemia cell lines. Leukemia 2007, 21:739-746.
    • (2007) Leukemia , vol.21 , pp. 739-746
    • Medeiros, B.1    Landau, H.2    Morrow, M.3    Lockerbie, R.4    Pitts, T.5    Eckhardt, S.6
  • 44
    • 67651180850 scopus 로고    scopus 로고
    • Synthesis and in vitro anti-lung cancer activity of novel 1,3,4,8-tetrahydropyrrolo [4, 3, 2-de]quinolin-8(1H)-one alkaloid analogs
    • Nadkarni D., Wang F., Wang W., Rayburn E., Ezell S., Murugesan S., Velu S., Zhang R. Synthesis and in vitro anti-lung cancer activity of novel 1,3,4,8-tetrahydropyrrolo [4, 3, 2-de]quinolin-8(1H)-one alkaloid analogs. Med. Chem. 2009, 227-236.
    • (2009) Med. Chem. , pp. 227-236
    • Nadkarni, D.1    Wang, F.2    Wang, W.3    Rayburn, E.4    Ezell, S.5    Murugesan, S.6    Velu, S.7    Zhang, R.8
  • 45
    • 0024697032 scopus 로고
    • Use of quinolones in chlamydial infection
    • Oriel J. Use of quinolones in chlamydial infection. Rev. Infect. Dis. 1989, 11(Suppl. 5):S1273-S1276.
    • (1989) Rev. Infect. Dis. , vol.11 , pp. S1273-S1276
    • Oriel, J.1
  • 47
    • 79955751294 scopus 로고    scopus 로고
    • A phase II study of gefitinib and irradiation in children with newly diagnosed brainstem gliomas: a report from the pediatric brain tumor consortium
    • Pollack I.F., Stewart C.F., Kocak M., Poussaint T.Y., Broniscer A., Douglas J.G., Kun L.E., Boyett J.M., Geyer J.R. A phase II study of gefitinib and irradiation in children with newly diagnosed brainstem gliomas: a report from the pediatric brain tumor consortium. Neuro-Oncology 2011, 13:290-297.
    • (2011) Neuro-Oncology , vol.13 , pp. 290-297
    • Pollack, I.F.1    Stewart, C.F.2    Kocak, M.3    Poussaint, T.Y.4    Broniscer, A.5    Douglas, J.G.6    Kun, L.E.7    Boyett, J.M.8    Geyer, J.R.9
  • 48
    • 0035902990 scopus 로고    scopus 로고
    • Quinolones and their N-oxides as inhibitors of photosystem II and the cytochrome b(6)/f-complex
    • Reil E., Hofle G., Draber W., Oettmeier W. Quinolones and their N-oxides as inhibitors of photosystem II and the cytochrome b(6)/f-complex. Biochim. Biophys. Acta, Bioenerg. 2001, 1506:127-132.
    • (2001) Biochim. Biophys. Acta, Bioenerg. , vol.1506 , pp. 127-132
    • Reil, E.1    Hofle, G.2    Draber, W.3    Oettmeier, W.4
  • 49
    • 61849154200 scopus 로고    scopus 로고
    • Apoptosis induced by 2-acetyl-3-(6methoxybenzo-thiazo)-2-yl-aminoacrylonitrile in human leukemia cells involves ROS mitochondrial mediated death signaling and activation of p38 MAPK
    • Repický A., Jantová S., Čipák L. Apoptosis induced by 2-acetyl-3-(6methoxybenzo-thiazo)-2-yl-aminoacrylonitrile in human leukemia cells involves ROS mitochondrial mediated death signaling and activation of p38 MAPK. Cancer Lett. 2009, 277:55-63.
    • (2009) Cancer Lett. , vol.277 , pp. 55-63
    • Repický, A.1    Jantová, S.2    Čipák, L.3
  • 50
    • 0036952539 scopus 로고    scopus 로고
    • Screening for ocular phototoxicity
    • Roberts J.E. Screening for ocular phototoxicity. Int. J. Toxicol. 2002, 21:491-500.
    • (2002) Int. J. Toxicol. , vol.21 , pp. 491-500
    • Roberts, J.E.1
  • 54
    • 74949119366 scopus 로고    scopus 로고
    • Fluoroquinolone antibacterials: a review on chemistry, microbiology and therapeutic prospects
    • Sharma P.C., Jain A., Jain S. Fluoroquinolone antibacterials: a review on chemistry, microbiology and therapeutic prospects. Acta Pol. Pharm. 2009, 66:587-604.
    • (2009) Acta Pol. Pharm. , vol.66 , pp. 587-604
    • Sharma, P.C.1    Jain, A.2    Jain, S.3
  • 55
    • 84878802813 scopus 로고    scopus 로고
    • Design, synthesis, biological evaluation, and molecular docking studies of quinolone derivatives as potential antitumor topoisomerase I inhibitors
    • Shou K.J., Li J., Jin Y., Lv Y.W. Design, synthesis, biological evaluation, and molecular docking studies of quinolone derivatives as potential antitumor topoisomerase I inhibitors. Chem. Pharm. Bull.(Tokyo) 2013, 61:631-636.
    • (2013) Chem. Pharm. Bull.(Tokyo) , vol.61 , pp. 631-636
    • Shou, K.J.1    Li, J.2    Jin, Y.3    Lv, Y.W.4
  • 58
    • 84868119898 scopus 로고    scopus 로고
    • Stable radical trianions from reversibly formed sigma-dimers of selenadiazoloquinolones studied by in situ EPR/UV-vis spectroelectrochemistry and quantum chemical calculations
    • Staško A., Lušpai K., Barbieriková Z., Rimarčík J., Vagánek A., Lukeš V., Bella M., Milata V., Zalibera M., Rapta P., Brezová V. Stable radical trianions from reversibly formed sigma-dimers of selenadiazoloquinolones studied by in situ EPR/UV-vis spectroelectrochemistry and quantum chemical calculations. J. Phys. Chem. A 2012, 116:9919-9927.
    • (2012) J. Phys. Chem. A , vol.116 , pp. 9919-9927
    • Staško, A.1    Lušpai, K.2    Barbieriková, Z.3    Rimarčík, J.4    Vagánek, A.5    Lukeš, V.6    Bella, M.7    Milata, V.8    Zalibera, M.9    Rapta, P.10    Brezová, V.11
  • 59
    • 84875384373 scopus 로고    scopus 로고
    • Novel quinolone substituted thiazolidin-4-ones as anti-inflammatory, anticancer agents: design, synthesis and biological screening
    • Suthar S.K., Jaiswal V., Lohan S., Bansal S., Chaudhary A., Tiwari A., Alex A.T., Joeph A. Novel quinolone substituted thiazolidin-4-ones as anti-inflammatory, anticancer agents: design, synthesis and biological screening. Eur. J. Med. Chem. 2013, 63:589-602.
    • (2013) Eur. J. Med. Chem. , vol.63 , pp. 589-602
    • Suthar, S.K.1    Jaiswal, V.2    Lohan, S.3    Bansal, S.4    Chaudhary, A.5    Tiwari, A.6    Alex, A.T.7    Joeph, A.8
  • 61
    • 81855194397 scopus 로고    scopus 로고
    • MG-2477, a new tubulin inhibitor, induces autophagy through inhibition of the Akt/mTOR pathaway and delayed apoptosis in A549 cells
    • Viola G., Bortolozzi R., Hamel E., Moro S., Brun P., Castagliuolo I., Ferlin M.G., Basso G. MG-2477, a new tubulin inhibitor, induces autophagy through inhibition of the Akt/mTOR pathaway and delayed apoptosis in A549 cells. Biochem. Pharmacol. 2012, 83:16-26.
    • (2012) Biochem. Pharmacol. , vol.83 , pp. 16-26
    • Viola, G.1    Bortolozzi, R.2    Hamel, E.3    Moro, S.4    Brun, P.5    Castagliuolo, I.6    Ferlin, M.G.7    Basso, G.8
  • 62
    • 0025773284 scopus 로고
    • Important role of oxygen metabolites in quinolone antibacterial agent-induced cutaneous phototoxicity in mice
    • Wagai N., Tawara K. Important role of oxygen metabolites in quinolone antibacterial agent-induced cutaneous phototoxicity in mice. Arch. Toxicol. 1991, 65:495-499.
    • (1991) Arch. Toxicol. , vol.65 , pp. 495-499
    • Wagai, N.1    Tawara, K.2
  • 63
    • 0035829462 scopus 로고    scopus 로고
    • Antitumor agents. 211. Fluorinated 2-phenyl-4-quinolone derivatives as antimitotic antitumor agents
    • Xia Y., Yang Z., Xia P., Hackl T., Hamel E., Mauger A., Wu J., Lee K. Antitumor agents. 211. Fluorinated 2-phenyl-4-quinolone derivatives as antimitotic antitumor agents. J. Med. Chem. 2001, 44:3932-3936.
    • (2001) J. Med. Chem. , vol.44 , pp. 3932-3936
    • Xia, Y.1    Yang, Z.2    Xia, P.3    Hackl, T.4    Hamel, E.5    Mauger, A.6    Wu, J.7    Lee, K.8
  • 64
    • 0034762479 scopus 로고    scopus 로고
    • In vitro method for prediction of the phototoxic potentials of fluoroquinolones
    • Yamamoto T., Tsurumaki Y., Takei M., Hosaka M., Oomori Y. In vitro method for prediction of the phototoxic potentials of fluoroquinolones. Toxicol. in Vitro 2001, 15:721-727.
    • (2001) Toxicol. in Vitro , vol.15 , pp. 721-727
    • Yamamoto, T.1    Tsurumaki, Y.2    Takei, M.3    Hosaka, M.4    Oomori, Y.5
  • 65
    • 70349410539 scopus 로고    scopus 로고
    • Discovery of a novel series of quinolone and naphthyridine derivatives as potential topoisomerase I inhibitors by scaffold modification
    • You Q., Li, Huang C., Yang Q., Wang X., Guo Q., Chen X., He X., Li T., Chern J. Discovery of a novel series of quinolone and naphthyridine derivatives as potential topoisomerase I inhibitors by scaffold modification. J. Med. Chem. 2009, 52:5649-5661.
    • (2009) J. Med. Chem. , vol.52 , pp. 5649-5661
    • You, Q.1    Li2    Huang, C.3    Yang, Q.4    Wang, X.5    Guo, Q.6    Chen, X.7    He, X.8    Li, T.9    Chern, J.10
  • 66
    • 84873750558 scopus 로고    scopus 로고
    • Pharmacophore-based drug design and biological evaluation of novel ABCB1 inhibitors
    • Zhang S.L., Wei Y.X., Li Q., Sun H.P., Peng H., You Q.D. Pharmacophore-based drug design and biological evaluation of novel ABCB1 inhibitors. Chem. Biol. Drug Des. 2013, 81:349-358.
    • (2013) Chem. Biol. Drug Des. , vol.81 , pp. 349-358
    • Zhang, S.L.1    Wei, Y.X.2    Li, Q.3    Sun, H.P.4    Peng, H.5    You, Q.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.