메뉴 건너뛰기




Volumn 170, Issue 2-3, 2009, Pages 1173-1178

Assessment of cytotoxic and cytogenetic effects of a 1,2,5-thiadiazole derivative on CHO-K1 cells. Its application as corrosion inhibitor

Author keywords

CHO K1 cells; Corrosion inhibitor; Cytotoxicity; Genotoxicity; Phenanthro 9,10 c 1,2,5 thiadiazole 1,1 dioxide

Indexed keywords

ADVERSE EFFECT; CHO-K1 CELLS; CHROMOSOMAL ABERRATION; COLONY FORMATION; CONCENTRATION OF; CONCENTRATION RANGES; CYTOGENETIC EFFECTS; CYTOTOXIC; DOSE-DEPENDENT; EXPOSURE TESTS; GENOTOXIC; GENOTOXICITIES; GENOTOXICITY; HUMAN HEALTH; INHIBITION EFFECT; MITOTIC INDEX; NEUTRAL RED; PHENANTHRO[9,10-C]-1,2,5-THIADIAZOLE 1,1-DIOXIDE; THIADIAZOLES; THRESHOLD LEVELS; WORK FOCUS;

EID: 69049084452     PISSN: 03043894     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2009.05.107     Document Type: Article
Times cited : (23)

References (35)
  • 1
    • 38549121376 scopus 로고    scopus 로고
    • Inactivation of human neutrophil elastase by 1,2,5-thiadiazolidin-3-one 1,1 dioxide-based sulfonamides
    • Li Y., Yang Q., Dou D., Alliston K.R., and Groutas W.C. Inactivation of human neutrophil elastase by 1,2,5-thiadiazolidin-3-one 1,1 dioxide-based sulfonamides. Bioorg. Med. Chem. 16 (2008) 692-698
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 692-698
    • Li, Y.1    Yang, Q.2    Dou, D.3    Alliston, K.R.4    Groutas, W.C.5
  • 3
    • 33845499876 scopus 로고    scopus 로고
    • Design and synthesis of novel derivatives of the muscarinic agonist tetra(ethylene glycol)(3-methoxy-1,2,5-thiadiazol-4-yl) [3-(1-methyl-1,2,5,6-tetrahydropyrid-3-yl)-1,2,5-thiadiazol-4-yl] ether (CDD-0304): effects of structural modifications on the binding and activity at muscarinic receptor subtypes and chimeras
    • Frederick R., Tejada P.I.N., Xu M., Wu C., Katz T., Dorsey J., Rieman M., Lawlor E., Warrier M., and Messer W.S. Design and synthesis of novel derivatives of the muscarinic agonist tetra(ethylene glycol)(3-methoxy-1,2,5-thiadiazol-4-yl) [3-(1-methyl-1,2,5,6-tetrahydropyrid-3-yl)-1,2,5-thiadiazol-4-yl] ether (CDD-0304): effects of structural modifications on the binding and activity at muscarinic receptor subtypes and chimeras. J. Med. Chem. 49 (2006) 7518-7531
    • (2006) J. Med. Chem. , vol.49 , pp. 7518-7531
    • Frederick, R.1    Tejada, P.I.N.2    Xu, M.3    Wu, C.4    Katz, T.5    Dorsey, J.6    Rieman, M.7    Lawlor, E.8    Warrier, M.9    Messer, W.S.10
  • 4
    • 62549153106 scopus 로고    scopus 로고
    • Synthesis, antimicrobial and cytotoxic activities of 1,3,4-oxidiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles
    • Padmavathi V., Sudhakar G., Reddy A., Padmaja P., and Kondaiah A.S. Synthesis, antimicrobial and cytotoxic activities of 1,3,4-oxidiazoles, 1,3,4-thiadiazoles and 1,2,4-triazoles. Eur. J. Med. Chem. 44 (2008) 2106-2112
    • (2008) Eur. J. Med. Chem. , vol.44 , pp. 2106-2112
    • Padmavathi, V.1    Sudhakar, G.2    Reddy, A.3    Padmaja, P.4    Kondaiah, A.S.5
  • 6
    • 0038644076 scopus 로고    scopus 로고
    • Palladium-catalyzed cross-coupling reaction of resin-bound chlorotriazines
    • Bork J.T., Lee J.W., and Chang Y.T. Palladium-catalyzed cross-coupling reaction of resin-bound chlorotriazines. Tetrahedron Lett. 44 (2003) 6141-6144
    • (2003) Tetrahedron Lett. , vol.44 , pp. 6141-6144
    • Bork, J.T.1    Lee, J.W.2    Chang, Y.T.3
  • 7
    • 43849090987 scopus 로고    scopus 로고
    • The electronic states of 1,2,5-thiadiazole studied by VUV absorption spectroscopy and ab initio configuration interaction methods
    • Palmer M.H. The electronic states of 1,2,5-thiadiazole studied by VUV absorption spectroscopy and ab initio configuration interaction methods. J. Chem. Phys. 348 (2008) 130-142
    • (2008) J. Chem. Phys. , vol.348 , pp. 130-142
    • Palmer, M.H.1
  • 8
    • 38849159097 scopus 로고    scopus 로고
    • A new type of light-emitting naphtho[2,3-c][1,2,5] thiadiazole derivatives: synthesis, photophysical characterization and transporting properties
    • Peng W., Duan L., Zhang D., Qiao J., Wang L., Wang R., Dong G., and Qiu Y. A new type of light-emitting naphtho[2,3-c][1,2,5] thiadiazole derivatives: synthesis, photophysical characterization and transporting properties. J. Mater. Chem. 18 (2008) 806-818
    • (2008) J. Mater. Chem. , vol.18 , pp. 806-818
    • Peng, W.1    Duan, L.2    Zhang, D.3    Qiao, J.4    Wang, L.5    Wang, R.6    Dong, G.7    Qiu, Y.8
  • 9
    • 0036589259 scopus 로고    scopus 로고
    • Aril-aril bond formation one century after the discovery of the Ullmann reaction
    • Hassan J., Sévignon M., Gozzi C., Schulz E., and Lemaire M. Aril-aril bond formation one century after the discovery of the Ullmann reaction. Chem. Rev. 102 (2002) 1359-1470
    • (2002) Chem. Rev. , vol.102 , pp. 1359-1470
    • Hassan, J.1    Sévignon, M.2    Gozzi, C.3    Schulz, E.4    Lemaire, M.5
  • 10
    • 51549104040 scopus 로고    scopus 로고
    • Evaluation of some non-toxic thiadiazole derivatives as bronze corrosion inhibitors in aqueous solution
    • Varvara S., Muresan L.M., Rahmouni K., and Takenouti H. Evaluation of some non-toxic thiadiazole derivatives as bronze corrosion inhibitors in aqueous solution. Corros. Sci. 50 (2008) 2596-2604
    • (2008) Corros. Sci. , vol.50 , pp. 2596-2604
    • Varvara, S.1    Muresan, L.M.2    Rahmouni, K.3    Takenouti, H.4
  • 11
    • 34547896257 scopus 로고    scopus 로고
    • The inhibiting effect of 3-methyl 1,2,4-triazole 5-thione on corrosion of copper in 3% NaCl in presence of sulphide
    • Rahmouni K., Hajjaji H., Keddam M., Srhiri A., and Takenouti H. The inhibiting effect of 3-methyl 1,2,4-triazole 5-thione on corrosion of copper in 3% NaCl in presence of sulphide. Electrochim. Acta 52 (2007) 7519-7528
    • (2007) Electrochim. Acta , vol.52 , pp. 7519-7528
    • Rahmouni, K.1    Hajjaji, H.2    Keddam, M.3    Srhiri, A.4    Takenouti, H.5
  • 12
    • 33947189997 scopus 로고    scopus 로고
    • Electrochemical and spectroscopic evidences of corrosion inhibition of bronze by a triazole derivative
    • Dermaj A., Hajjaji N., Joiret S., Rahmouni K., Srhiri A., Takenouti A., and Vivier A. Electrochemical and spectroscopic evidences of corrosion inhibition of bronze by a triazole derivative. Electrochim. Acta 52 (2007) 4654-4662
    • (2007) Electrochim. Acta , vol.52 , pp. 4654-4662
    • Dermaj, A.1    Hajjaji, N.2    Joiret, S.3    Rahmouni, K.4    Srhiri, A.5    Takenouti, A.6    Vivier, A.7
  • 13
    • 2442569657 scopus 로고    scopus 로고
    • Aminotriazole as corrosion inhibitor of Cu-30Ni alloy in 3% NaCl in presence of ammoniac
    • Es-Salah K., Keddam M., Rahmouni K., Srhiri A., and Takenouti H. Aminotriazole as corrosion inhibitor of Cu-30Ni alloy in 3% NaCl in presence of ammoniac. Electrochim. Acta 49 (2004) 2771-2778
    • (2004) Electrochim. Acta , vol.49 , pp. 2771-2778
    • Es-Salah, K.1    Keddam, M.2    Rahmouni, K.3    Srhiri, A.4    Takenouti, H.5
  • 14
    • 0033633878 scopus 로고    scopus 로고
    • Some results of a research in the problem. Inhibitors of metal corrosion. Toxicology and industrial hygiene
    • Paustovskaya V.V. Some results of a research in the problem. Inhibitors of metal corrosion. Toxicology and industrial hygiene. Prot. Met. 1 (2000) 89-93
    • (2000) Prot. Met. , vol.1 , pp. 89-93
    • Paustovskaya, V.V.1
  • 15
    • 0034144649 scopus 로고    scopus 로고
    • Inhibitive action of the octyl esters of 4- and 5-carboxybenzotriazole for copper corrosion in sulphate solutions
    • Huynh N., Bottle S.E., Notova T., and Schweinsberg D.P. Inhibitive action of the octyl esters of 4- and 5-carboxybenzotriazole for copper corrosion in sulphate solutions. Corros. Sci. 42 (2000) 259-274
    • (2000) Corros. Sci. , vol.42 , pp. 259-274
    • Huynh, N.1    Bottle, S.E.2    Notova, T.3    Schweinsberg, D.P.4
  • 16
    • 0037048813 scopus 로고    scopus 로고
    • Evaluation of non-toxic corrosion inhibitors for copper in sulphuric acid
    • Stupnisek-Lisac E., Gazivoda A., and Madzarac M. Evaluation of non-toxic corrosion inhibitors for copper in sulphuric acid. Electrochim. Acta 47 (2002) 4189-4194
    • (2002) Electrochim. Acta , vol.47 , pp. 4189-4194
    • Stupnisek-Lisac, E.1    Gazivoda, A.2    Madzarac, M.3
  • 17
    • 33746610203 scopus 로고    scopus 로고
    • Efficient formation of polycyclic aromatic systems fused to a thiadiazole ring using strong Lewis or Bronsted acids
    • Svartman E.L., Rozas M.F., Piro O.E., Castellano E., and Mirífico M.V. Efficient formation of polycyclic aromatic systems fused to a thiadiazole ring using strong Lewis or Bronsted acids. Synthesis 14 (2006) 2313-2318
    • (2006) Synthesis , vol.14 , pp. 2313-2318
    • Svartman, E.L.1    Rozas, M.F.2    Piro, O.E.3    Castellano, E.4    Mirífico, M.V.5
  • 18
    • 0001502264 scopus 로고
    • Synthesen von Heterocyclen, 64. Mitt. : Über Reaktionen mit Schwefelsäurediamid
    • Vorriether H.K., and Ziegler E. Synthesen von Heterocyclen, 64. Mitt. : Über Reaktionen mit Schwefelsäurediamid. Monatsh. Chem. 96 (1965) 216-219
    • (1965) Monatsh. Chem. , vol.96 , pp. 216-219
    • Vorriether, H.K.1    Ziegler, E.2
  • 19
    • 17044395830 scopus 로고    scopus 로고
    • Cadmium chloride-induced DNA and lysosomal damage in a hepatoma cell line
    • Fotakis G., Cemeli E., Anderson D., and Timbrell J.A. Cadmium chloride-induced DNA and lysosomal damage in a hepatoma cell line. Toxicol. In Vitro 19 (2005) 481-489
    • (2005) Toxicol. In Vitro , vol.19 , pp. 481-489
    • Fotakis, G.1    Cemeli, E.2    Anderson, D.3    Timbrell, J.A.4
  • 21
    • 33846222118 scopus 로고    scopus 로고
    • International Workshop on the Standardisation of Genotoxicity Test Procedures
    • Kirkland D.J., Galloway S.M., and Sofuni T. International Workshop on the Standardisation of Genotoxicity Test Procedures. Mutat. Res. 312 (2004) 205-209
    • (2004) Mutat. Res. , vol.312 , pp. 205-209
    • Kirkland, D.J.1    Galloway, S.M.2    Sofuni, T.3
  • 22
    • 0025973329 scopus 로고
    • In vitro sensitivity assays in cancer: a review, analysis, and prognosis
    • Hoffman R.M. In vitro sensitivity assays in cancer: a review, analysis, and prognosis. J. Clin. Lab. Anal. 5 (1991) 133-143
    • (1991) J. Clin. Lab. Anal. , vol.5 , pp. 133-143
    • Hoffman, R.M.1
  • 23
    • 0022391554 scopus 로고
    • A simple quantitative procedure using monolayer culture for toxicity assays
    • Borenfreud E., and Puerner J.A. A simple quantitative procedure using monolayer culture for toxicity assays. J. Tissue Cult. Methods 9 (1984) 7-9
    • (1984) J. Tissue Cult. Methods , vol.9 , pp. 7-9
    • Borenfreud, E.1    Puerner, J.A.2
  • 24
    • 84981834288 scopus 로고
    • The chromosome number of man
    • Tjio J., and Levan A. The chromosome number of man. Hereditas 42 (1956) 1-6
    • (1956) Hereditas , vol.42 , pp. 1-6
    • Tjio, J.1    Levan, A.2
  • 25
    • 0024509914 scopus 로고
    • Suspect spindle poisons: analysis of c-mitotic effects in mouse bone
    • Miller B.M., and Adler I.D. Suspect spindle poisons: analysis of c-mitotic effects in mouse bone. Mutagenesis 4 (1989) 208-221
    • (1989) Mutagenesis , vol.4 , pp. 208-221
    • Miller, B.M.1    Adler, I.D.2
  • 27
    • 0035937242 scopus 로고    scopus 로고
    • The behaviour of copper anodes in aqueous thiourea-containing sulphuric acid solutions. Open circuit potentials and electrochemical kinetics
    • Bolzán A.E., Wakenge I.B., Piatti R.C.V., Salvarezza R.C., and Arvía A.J. The behaviour of copper anodes in aqueous thiourea-containing sulphuric acid solutions. Open circuit potentials and electrochemical kinetics. J. Electroanal. Chem. 501 (2001) 241-252
    • (2001) J. Electroanal. Chem. , vol.501 , pp. 241-252
    • Bolzán, A.E.1    Wakenge, I.B.2    Piatti, R.C.V.3    Salvarezza, R.C.4    Arvía, A.J.5
  • 29
    • 69049086957 scopus 로고    scopus 로고
    • J.B. Wright, U.S. Patent 3,115,496 (December 24, 1963) [CA 60, 5512c (1964)].
    • J.B. Wright, U.S. Patent 3,115,496 (December 24, 1963) [CA 60, 5512c (1964)].
  • 32
    • 0039178097 scopus 로고    scopus 로고
    • Sulfamides in the synthesis of heterocyclic compounds
    • Gazieva G.A., Kravchenko A.N., and Lebedev O.V. Sulfamides in the synthesis of heterocyclic compounds. Russ. Chem. Rev. 69 (2000) 221-230
    • (2000) Russ. Chem. Rev. , vol.69 , pp. 221-230
    • Gazieva, G.A.1    Kravchenko, A.N.2    Lebedev, O.V.3
  • 35
    • 0032465960 scopus 로고    scopus 로고
    • Identification of rodent carcinogens and non-carcinogens using genetic toxicity test: premises, promises and performance, regulatory
    • Zieger E. Identification of rodent carcinogens and non-carcinogens using genetic toxicity test: premises, promises and performance, regulatory. Toxicol. Pharmacol. 28 (1998) 85-95
    • (1998) Toxicol. Pharmacol. , vol.28 , pp. 85-95
    • Zieger, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.