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Volumn 56, Issue 3, 2006, Pages 239-248

Synthesis and evaluation of antimicrobial and anticonvulsant activities of some new 3-[2-(5-aryl-1,3,4-oxadiazol-2-yl/4-carbethoxymethylthiazol-2-yl)imino- 4-thiazolidinon-5-ylidene]-5-substituted/nonsubstituted 1H-indole-2-ones and investigation of their structure-activity relationships

Author keywords

1H Indole 2 one 3 ylidene derivatives, antimicrobial and anticonvulsant activities, 5 substituted nonsubstituted, synthesis; Anticonvulsants; Antimicrobials

Indexed keywords

1H INDOLE 2 ONE DERIVATIVE; 2 [(1,3,4 OXADIAZOL 2 YL)IMINO] 4 THIAZOLIDINONE (DI,II) DERIVATIVE; 2 [(4 CARBETHOXYMETHYL THIAZOL YLIMINO] 4 THIAZOLIDINONE DERIVATIVE; 2 [(CHLOROACETYL)AMINO] 1,3,4 OXADIAZOLE (CI,II) DERIVATIVE; 4 CARBETHOXYMETHYL 2 [(CHLOROACETYL)AMINO]THIAZOLE DERIVATIVE; CEFUROXIME; INDOLE DERIVATIVE; PENTETRAZOLE; UNCLASSIFIED DRUG;

EID: 33645470717     PISSN: 00044172     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0031-1296716     Document Type: Article
Times cited : (11)

References (33)
  • 1
    • 0030774342 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of 5-aryl-2-[(α-chloro- α-phenylacetyl/α-bromopropionyl)amino]-1,3,4-oxadiazoles and 2-[(5-aryl-1,3,4-oxadiazol-2-yl)imino]-5-phenyl/methyl-4-thiazolidinones
    • Ates, Ö., Kocabalkanli, A., Ötük, G. et al., Synthesis and antibacterial activity of 5-aryl-2-[(α-chloro-α-phenylacetyl/ α-bromopropionyl)amino]-1,3,4-oxadiazoles and 2-[(5-aryl-1,3,4-oxadiazol- 2-yl)imino]-5-phenyl/methyl-4-thiazolidinones. Arzneim.-Forsch./Drug Res. 47, 1134 (1997)
    • (1997) Arzneim.-Forsch./Drug Res. , vol.47 , pp. 1134
    • Ates, Ö.1    Kocabalkanli, A.2    Ötük, G.3
  • 2
    • 0031416408 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of novel imidazo[2,1-b]thiazolyl acetylaminohydrazono 4-thiazolidinones
    • Ulusoy, N., Çapan, G., Ergenç, N. et al., Synthesis and antimicrobial activity of novel imidazo[2,1-b]thiazolyl acetylamino]hydrazono 4-thiazolidinones. Acta Pharm.Sci. XXXIX, 181 (1997)
    • (1997) Acta Pharm. Sci. , vol.39 , pp. 181
    • Ulusoy, N.1    Çapan, G.2    Ergenç, N.3
  • 3
    • 0042143804 scopus 로고    scopus 로고
    • Mannich reaction products of 5-arylidene-2-phenylimino-4-thiazolidinones as anticonvulsants
    • Gahane, D. R., Khapekar, K. D., Sharma, V. C. et al., Mannich reaction products of 5-arylidene-2-phenylimino-4-thiazolidinones as anticonvulsants. Indian J. Pharm. Sci. 60, 275 (1998)
    • (1998) Indian J. Pharm. Sci. , vol.60 , pp. 275
    • Gahane, D.R.1    Khapekar, K.D.2    Sharma, V.C.3
  • 4
    • 0033945344 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of 4-carbethoxymethyl-2-[(α- haloacyl)amino]thiazoles and 5-nonsubstituted/substituted 2-[(4- carbethoxymethylthiazol-2-yl)imino]-4-thiazolidinones
    • Ateş, Ö., Altintaş, H., Ötük, G., Synthesis and antimicrobial activity of 4-carbethoxymethyl-2-[(α-haloacyl)amino] thiazoles and 5-nonsubstituted/substituted 2-[(4-carbethoxymethylthiazol-2-yl) imino]-4-thiazolidinones. Arzneim.-Forsch./Drug Res. 50, 569 (2000)
    • (2000) Arzneim.-Forsch./Drug Res. , vol.50 , pp. 569
    • Ateş, Ö.1    Altintaş, H.2    Ötük, G.3
  • 5
    • 0008609437 scopus 로고
    • 7-Aminothiazolylacetamidocephalosporanic acid derivatives
    • Ref. C.A. 87, 152245t (1977)
    • Heymes, R., 7-Aminothiazolylacetamidocephalosporanic acid derivatives. Ger. Offen. 2,700,552 (1977); Ref. C.A. 87, 152245t (1977)
    • (1977) Ger. Offen. , vol.2 , Issue.700 , pp. 552
    • Heymes, R.1
  • 6
    • 33645469004 scopus 로고    scopus 로고
    • Preparation of antibacterial ammonia cephalosporins. Jpn. Kokai Tokkyo Koho JP 08, 283, 274 (1995); Ref. C.A. 126, 74673p (1997)
    • Korea, S., Preparation of antibacterial ammonia cephalosporins. Jpn. Kokai Tokkyo Koho JP 08,283,274 (1995); Ref. C.A. 126, 74673p (1997)
    • Korea, S.1
  • 7
    • 33645462709 scopus 로고    scopus 로고
    • Synthesis of 2-arylimino-5-[5′-amino-1′-(4″- chlorophenyl)-1′,2′,3′-triazol-4′-yl]-1,3,4-oxadiazoles
    • Ref. C.A. 129, 67738 (1998)
    • Dong, H. S., Zhang, Z. Y., Hui, X. P. et al., Synthesis of 2-arylimino-5-[5′-amino-1′-(4″-chlorophenyl)-1′, 2′,3′-triazol-4′-yl]-1,3,4-oxadiazoles. Youji Huaxue 18, 253 (1998); Ref. C.A. 129, 67738 (1998)
    • (1998) Youji Huaxue , vol.18 , pp. 253
    • Dong, H.S.1    Zhang, Z.Y.2    Hui, X.P.3
  • 8
    • 0344232163 scopus 로고
    • Synthesis of some substituted 1,3,4-oxadiazoles, their antibacterial and antiamebic activity
    • Ref. C.A. 115, 49539g (1991)
    • Kachroo, P. L., Gupta, R., Gupta, S. C. et al., Synthesis of some substituted 1,3,4-oxadiazoles, their antibacterial and antiamebic activity. Natl. Acad. Sci. Lett. (India) 13, 125 (1991); Ref. C.A. 115, 49539g (1991)
    • (1991) Natl. Acad. Sci. Lett. (India) , vol.13 , pp. 125
    • Kachroo, P.L.1    Gupta, R.2    Gupta, S.C.3
  • 9
    • 0032999494 scopus 로고    scopus 로고
    • Synthesis and antiinflammatory activity of some new 6-methoxy-α- methyl-2-naphthaleneacetic acid derivatives
    • Ref. C.A. 131, 5225 (1999)
    • Amir, M., Oberoi, A., Alam, S., Synthesis and antiinflammatory activity of some new 6-methoxy-α-methyl-2-naphthaleneacetic acid derivatives. Indian J. Chem. Sect. B: Org. Chem. Incl. Med. Chem. 38, 237 (1999); Ref. C.A. 131, 5225 (1999)
    • (1999) Indian J. Chem. Sect. B: Org. Chem. Incl. Med. Chem. , vol.38 , pp. 237
    • Amir, M.1    Oberoi, A.2    Alam, S.3
  • 10
    • 0016230908 scopus 로고
    • Synthesis and structure-activity relationships of a series of antibacterially active 5-(5-nitro-2-furfurylidene) thiazolones, 5-(5-nitro-2-furylpropenylidene)thiazolones and 6-(5-nitro-2-furyl)-4H-1,3- thiazinones
    • Akerblom, E. B., Synthesis and structure-activity relationships of a series of antibacterially active 5-(5-nitro-2-furfurylidene) thiazolones, 5-(5-nitro-2-furylpropenylidene)thiazolones and 6-(5-nitro-2-furyl)-4H-1,3- thiazinones. J. Med. Chem. 17, 609 (1974)
    • (1974) J. Med. Chem. , vol.17 , pp. 609
    • Akerblom, E.B.1
  • 11
    • 0018726862 scopus 로고
    • Synthesis and properties of 3-(2′-carbomethoxyfuryl-5′-yl) methyl-2,4-dioxothiazolidine and their derivatives
    • Ref. C.A. 92, 146660m (1980)
    • Kirichenko, B. M., Steblyuk, P. M., Vladzimirskaya, E. V. et al., Synthesis and properties of 3-(2′-carbomethoxyfuryl-5′-yl)methyl-2, 4-dioxothiazolidine and their derivatives. Farm.Zh. (Kiev) 5, 39 (1979); Ref. C.A. 92, 146660m (1980)
    • (1979) Farm.Zh. (Kiev) , vol.5 , pp. 39
    • Kirichenko, B.M.1    Steblyuk, P.M.2    Vladzimirskaya, E.V.3
  • 12
    • 0022411217 scopus 로고
    • Synthesis of some 3-(benzimidazol-2-ylmethyl)thiazolidinone derivatives as potential antimicrobial agents
    • Rida, S. M., Salama, H. M., Labouta, I. M. et al., Synthesis of some 3-(benzimidazol-2-ylmethyl)thiazolidinone derivatives as potential antimicrobial agents. Pharmazie 40, 727 (1985)
    • (1985) Pharmazie , vol.40 , pp. 727
    • Rida, S.M.1    Salama, H.M.2    Labouta, I.M.3
  • 13
    • 0018694512 scopus 로고
    • Some transformations of the antimicrobial drug ciminal
    • Ref. C.A. 92, 128788 (1980)
    • Tkachuk, B. V., Some transformations of the antimicrobial drug ciminal. Farm. Zh. (Kiev) 5, 46 (1979); Ref. C.A. 92, 128788 (1980)
    • (1979) Farm. Zh. (Kiev) , vol.5 , pp. 46
    • Tkachuk, B.V.1
  • 14
    • 0018391491 scopus 로고
    • Synthesis of 3-hydroxy-3-phenacyloxindole analogs
    • Popp, F. D., Donigan, B. E., Synthesis of 3-hydroxy-3-phenacyloxindole analogs. J. Pharm. Sci. 68, 519 (1979)
    • (1979) J. Pharm. Sci. , vol.68 , pp. 519
    • Popp, F.D.1    Donigan, B.E.2
  • 15
    • 0001473151 scopus 로고
    • Potential anticonvulsants. III. The condensation of isatin with cyclic ketones
    • Popp, F. D., Parson, R., Donigan, B. E., Potential anticonvulsants. III. The condensation of isatin with cyclic ketones. J. Heterocycl. Chem. 17, 1329 (1980)
    • (1980) J. Heterocycl. Chem. , vol.17 , pp. 1329
    • Popp, F.D.1    Parson, R.2    Donigan, B.E.3
  • 16
    • 0031876447 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of 3-hydrazono-1H-2- indolinones with antituberculosis activity
    • Karali, N., Terzioglu, N., Gürsoy, A., Synthesis and structure-activity relationships of 3-hydrazono-1H-2-indolinones with antituberculosis activity. Arzneim.-Forsch./Drug Res. 48, 758 (1998)
    • (1998) Arzneim.-Forsch./Drug Res. , vol.48 , pp. 758
    • Karali, N.1    Terzioglu, N.2    Gürsoy, A.3
  • 22
    • 0036841462 scopus 로고    scopus 로고
    • Collaborative evaluation of optimal antifungal susceptibility testing conditions for dermatophytes
    • Fernandez, T. B., Cabanes, F. J., Carillo-Munoz A. et al., Collaborative evaluation of optimal antifungal susceptibility testing conditions for dermatophytes. J. Clin. Microbiol. 40, 3999 (2002)
    • (2002) J. Clin. Microbiol. , vol.40 , pp. 3999
    • Fernandez, T.B.1    Cabanes, F.J.2    Carillo-Munoz, A.3
  • 23
    • 0034863428 scopus 로고    scopus 로고
    • In vitro activities of 10 antifungal drugs against 508 dermatophyte strains
    • Fernandez, T. B., Carillo A. J., Martin, E. et al., In vitro activities of 10 antifungal drugs against 508 dermatophyte strains. Antimicrob. Agents Chemother. 45, 2524 (2001)
    • (2001) Antimicrob. Agents Chemother. , vol.45 , pp. 2524
    • Fernandez, T.B.1    Carillo, A.J.2    Martin, E.3
  • 24
    • 0042413558 scopus 로고    scopus 로고
    • Clinical and laboratory investigations in vitro susceptibility testing of ciclopirox, terbinafine, ketoconazole and itraconazole against dermatophytes and nondermatophytes and in vitro evaluation of combination antifungal activity
    • Gupta, A. K., Kohli, Y., Clinical and laboratory investigations in vitro susceptibility testing of ciclopirox, terbinafine, ketoconazole and itraconazole against dermatophytes and nondermatophytes and in vitro evaluation of combination antifungal activity. Br. J. Dermatol. 149, 296 (2003)
    • (2003) Br. J. Dermatol. , vol.149 , pp. 296
    • Gupta, A.K.1    Kohli, Y.2
  • 25
    • 0026464766 scopus 로고
    • Collaborative comparision of broth macrodilution and microdilution antifungal susceptibility tests
    • Espinel-Ingroff, A., Kigh, C. W., Kerkering, T. M. et al., Collaborative comparision of broth macrodilution and microdilution antifungal susceptibility tests. J. Clin. Microbiol., 30, 3138 (1992)
    • (1992) J. Clin. Microbiol. , vol.30 , pp. 3138
    • Espinel-Ingroff, A.1    Kigh, C.W.2    Kerkering, T.M.3
  • 26
    • 0029795520 scopus 로고    scopus 로고
    • Comparision of a spectrophotometric microdilution method with RPMI-2% glucose with the national commitee for clinical laboratory standard reference macrodilution method M 27-P for in vitro susceptibility testing of amphotreicin B, Flucytosine and fluconazole against Candida albicans
    • Rodriguez-Tudela, J. L., Berenguer, J., Martinez-Suare J. V. et al., Comparision of a spectrophotometric microdilution method with RPMI-2% glucose with the national commitee for clinical laboratory standard reference macrodilution method M 27-P for in vitro susceptibility testing of amphotreicin B, Flucytosine and fluconazole against Candida albicans. Antimicrob. Agents Chemother. 40, 1998 (1996)
    • (1996) Antimicrob. Agents Chemother. , vol.40 , pp. 1998
    • Rodriguez-Tudela, J.L.1    Berenguer, J.2    Martinez-Suare, J.V.3
  • 27
    • 0027988607 scopus 로고
    • Antiepileptic effects of inhibitors of nitric oxide synthase examined in pentylenetetrazol-induced seizures in rats
    • Osonoe, K., Mori, N., Suzuki, K. et al., Antiepileptic effects of inhibitors of nitric oxide synthase examined in pentylenetetrazol-induced seizures in rats. Brain Res. 663, 338 (1994)
    • (1994) Brain Res. , vol.663 , pp. 338
    • Osonoe, K.1    Mori, N.2    Suzuki, K.3
  • 28
    • 0036318617 scopus 로고    scopus 로고
    • Sythesis of new 2,5-Disubstituted-1,3,4-thiadiazoles and preliminary evalulation of anticonvulsant and antimicrobial activities
    • Dogan, H. N., Duran, A., Rollas, S. et al., Sythesis of new 2,5-Disubstituted-1,3,4-thiadiazoles and preliminary evalulation of anticonvulsant and antimicrobial activities. Bioorg. Med. Chem. 10, 2893 (2002)
    • (2002) Bioorg. Med. Chem. , vol.10 , pp. 2893
    • Dogan, H.N.1    Duran, A.2    Rollas, S.3
  • 30
    • 0030774342 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of 5-aryl-2-[α-chloro-(- phenylacetyl/α-bromopropionyl)amino]-1,3,4-oxadiazoles and 2-[(5-aryl-1,3,4-oxadiazol-2-yl)imino]-5-phenyl/methyl-4-thiazolidinones
    • Ateş, Ö., Kocabalkanli, A., Saniş, G. Ö. et al., Synthesis and antibacterial activity of 5-aryl-2-[(α-chloro-(- phenylacetyl/α-bromopropionyl)amino]-1,3,4-oxadiazoles and 2-[(5-aryl-1,3,4-oxadiazol-2-yl)imino]-5-phenyl/methyl-4-thiazolidinones. Arzneim.-Forsch./Drug Res. 47, 1134 (1997)
    • (1997) Arzneim.-Forsch./Drug Res. , vol.47 , pp. 1134
    • Ateş, Ö.1    Kocabalkanli, A.2    Saniş, G.Ö.3
  • 31
    • 85023380111 scopus 로고
    • Preparation of some 3-(2-arylimino-4-oxo-5-thiazolidinylidene)oxindoles
    • Ref. C.A. 54, 17376d (1960)
    • Rao, R. P., Preparation of some 3-(2-arylimino-4-oxo-5- thiazolidinylidene)oxindoles. J. Sci. Ind. Res. 19B, 29 (1960); Ref. C.A. 54, 17376d (1960)
    • (1960) J. Sci. Ind. Res. , vol.19 B , pp. 29
    • Rao, R.P.1
  • 32
    • 0021931687 scopus 로고
    • Chinazolinone. 4. Mitteilung: Synthese von derivaten des 2-Methyl-3-(4-oxothiazolidin-2-ylidenamino)-4(3H)-chinazolinons
    • Büyüktimkin, S., Chinazolinone. 4. Mitteilung: Synthese von Derivaten des 2-Methyl-3-(4-oxothiazolidin-2-ylidenamino)-4(3H)-chinazolinons. Pharmazie 40, 393 (1985)
    • (1985) Pharmazie , vol.40 , pp. 393
    • Büyüktimkin, S.1
  • 33
    • 0037210321 scopus 로고    scopus 로고
    • Synthesis and primary cytotoxicity evaluation of new 5-nitroindole-2,3- dione derivatives
    • Karali, N., Synthesis and primary cytotoxicity evaluation of new 5-nitroindole-2,3-dione derivatives. Eur. J. Med. Chem. 37, 909 (2002)
    • (2002) Eur. J. Med. Chem. , vol.37 , pp. 909
    • Karali, N.1


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