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      KCI등재 SCIE SCOPUS

      Antibacterial, Antifungal and Anticonvulsant Evaluation of Novel Newly Synthesized 1-[2-(1H-Tetrazol-5-yl)ethyl]-1H-benzo[d][1, 2,3]triazoles

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      https://www.riss.kr/link?id=A104665900

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      다국어 초록 (Multilingual Abstract)

      Several novel 1-[2-(1H-tetrazol-5-yl) ethyl]-1H-benzo[d][1,2,3]triazoles (3a-h) have been synthesized
      by the condensation of 1-[2-(1H-tetrazol-5-yl)-ethyl]-1H-benzotriazole (2) and appropriate
      acid chlorides. 1-[2-(1H-tetrazol-5-yl)-ethyl]-1H-benzotriazole (2) was synthesized by
      reacting 3-(1H-benzo[d][1,2,3]triazol-1-yl)propanenitrile with sodium azide and ammonium
      chloride in the presence of dimethylformamide. The synthesized compounds were characterized
      by IR and PMR analysis. The titled compounds were evaluated for their in vitro antibacterial
      and antifungal activity by the cup plate method and anticonvulsant activity evaluated by the
      maximal electroshock induced convulsion method in mice. All synthesized compounds exhibited
      moderate antibacterial activity against Bacillus subtilis and moderate antifungal activity
      against Candida albicans. Compounds 5-(2-(1 H-benzo[d][1,2,3]triazo-1-yl)ethyl)-1H-tetrazol-
      1-yl)(4-aminophenyl)methanone 3d and 5-(2-(1 H-benzo[d][1,2,3]triazo-1-yl)ethyl)-1H-tetrazol-
      1-yl)(2-aminophenyl)methanone 3e elicited excellent anticonvulsant activity.
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      Several novel 1-[2-(1H-tetrazol-5-yl) ethyl]-1H-benzo[d][1,2,3]triazoles (3a-h) have been synthesized by the condensation of 1-[2-(1H-tetrazol-5-yl)-ethyl]-1H-benzotriazole (2) and appropriate acid chlorides. 1-[2-(1H-tetrazol-5-yl)-ethyl]-1H-benzotri...

      Several novel 1-[2-(1H-tetrazol-5-yl) ethyl]-1H-benzo[d][1,2,3]triazoles (3a-h) have been synthesized
      by the condensation of 1-[2-(1H-tetrazol-5-yl)-ethyl]-1H-benzotriazole (2) and appropriate
      acid chlorides. 1-[2-(1H-tetrazol-5-yl)-ethyl]-1H-benzotriazole (2) was synthesized by
      reacting 3-(1H-benzo[d][1,2,3]triazol-1-yl)propanenitrile with sodium azide and ammonium
      chloride in the presence of dimethylformamide. The synthesized compounds were characterized
      by IR and PMR analysis. The titled compounds were evaluated for their in vitro antibacterial
      and antifungal activity by the cup plate method and anticonvulsant activity evaluated by the
      maximal electroshock induced convulsion method in mice. All synthesized compounds exhibited
      moderate antibacterial activity against Bacillus subtilis and moderate antifungal activity
      against Candida albicans. Compounds 5-(2-(1 H-benzo[d][1,2,3]triazo-1-yl)ethyl)-1H-tetrazol-
      1-yl)(4-aminophenyl)methanone 3d and 5-(2-(1 H-benzo[d][1,2,3]triazo-1-yl)ethyl)-1H-tetrazol-
      1-yl)(2-aminophenyl)methanone 3e elicited excellent anticonvulsant activity.

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      참고문헌 (Reference)

      1 "Tetrazole analogues of cyclolinopeptide A synthesis conformation and biology" 63 : 343-357, 2002

      2 "Synthesis of novel substituted tetrazoles"

      3 "Synthesis and antinociceptive activity of some substituted 5,2,1,2,3,4 tetrahydrocarbazol9 yl ethyl tetrazol1 yl alkanones" 40 : 1359-1364, 2005

      4 "Synthesis and analgesic evaluation of some 5beta 10phenothiazinyl ethyl 1acyl 1,2,3,4 tetrazoles" 39 : 273-279, 2004

      5 "Synthesis and Anti Inflam matory activity of some 10,1Acyl 1h Tetrazol 5 yl Ethyl 10h Phenothiazines" 45 : 235-240, 2003

      6 "Study of somederivatives of the benzotriazole nucleus" 240-247, 1980

      7 "Reactive oxygen scavenger efect of pyrimidines benzotri azoles and related compounds" 22 : 937-942, 2002

      8 "Novel thiazolinyl thiazolidinonyl thiadiazolyl and oxadiazolyl benzotriazole derivatives with potential antiinflammatory activity and minimum ulcerogenic effect" 55 : 900-906, 2000

      9 "Medical Laboratory Technology" Mcraw Hill 2 : 674-675, 1996

      10 "Handbook of Experimental Pharmacology" 125-127, 2004

      1 "Tetrazole analogues of cyclolinopeptide A synthesis conformation and biology" 63 : 343-357, 2002

      2 "Synthesis of novel substituted tetrazoles"

      3 "Synthesis and antinociceptive activity of some substituted 5,2,1,2,3,4 tetrahydrocarbazol9 yl ethyl tetrazol1 yl alkanones" 40 : 1359-1364, 2005

      4 "Synthesis and analgesic evaluation of some 5beta 10phenothiazinyl ethyl 1acyl 1,2,3,4 tetrazoles" 39 : 273-279, 2004

      5 "Synthesis and Anti Inflam matory activity of some 10,1Acyl 1h Tetrazol 5 yl Ethyl 10h Phenothiazines" 45 : 235-240, 2003

      6 "Study of somederivatives of the benzotriazole nucleus" 240-247, 1980

      7 "Reactive oxygen scavenger efect of pyrimidines benzotri azoles and related compounds" 22 : 937-942, 2002

      8 "Novel thiazolinyl thiazolidinonyl thiadiazolyl and oxadiazolyl benzotriazole derivatives with potential antiinflammatory activity and minimum ulcerogenic effect" 55 : 900-906, 2000

      9 "Medical Laboratory Technology" Mcraw Hill 2 : 674-675, 1996

      10 "Handbook of Experimental Pharmacology" 125-127, 2004

      11 "Halogenated benzimidazolesand benzotriazoles as inhibitors of the NTPase helicaseactivities of hepatitis C and related viruses" 270 : 1645-1653, 2003

      12 "Cytotoxicity anti tumoral and antimycobacterial activity of tetrazole and oxadiazole derivatives" 60 : 396-397, 2005

      13 "Anticonvulsantactivity of some trimethoxy-benzylidene-2-Thiohydantionderivatives" 449-450, 1973

      14 "Analgesic and Anti Antimicrobial and Anticonvulsant Activities of 1,21H Tetrazol5 yl ethyl 1H benzo d 1,2,3 triazoles 540 Epileptic activity of N Mannich bases of Some Substituted Benztriazoles" 2 : 445-449, 2004

      15 "A note on the antitubercular activities of 1 aryl 5benzylsulfanyltetrazoles" 338 : 385-389, 2005

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2001-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1998-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.96 0.2 1.44
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.07 0.87 0.439 0.05
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