메뉴 건너뛰기




Volumn 50, Issue 1, 2000, Pages 48-54

Synthesis and biological evaluation of indole containing derivatives of thiosemicarbazide and their cyclic 1,2,4-triazole and 1,3,4-thiadiazole analogs

Author keywords

1,2,4 Triazoles, analogs, synthesis; 1,3,4 Thiadiazoles, analogs, synthesis; Indole containing thiosemicarbazides, antifungal activity, antimicrobial activity, antiphage activity

Indexed keywords

1,3,4 THIADIAZOLE DERIVATIVE; THIOSEMICARBAZIDE; TRIAZOLE DERIVATIVE;

EID: 0033968284     PISSN: 00044172     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0031-1300163     Document Type: Article
Times cited : (79)

References (27)
  • 1
    • 0026730087 scopus 로고
    • Novel 1,2,4-oxadiazoles and 1,2,4-thiadiazoles as dual 5-lipoxygenase and cycloxygenase inhibitors
    • [1] Unangst, P. C, Shrum, G. P., Connor, D.T. et al., Novel 1,2,4-oxadiazoles and 1,2,4-thiadiazoles as Dual 5-Lipoxygenase and cycloxygenase Inhibitors. Med. Chem. 35, 3691 (1992)
    • (1992) Med. Chem. , vol.35 , pp. 3691
    • Unangst, P.C.1    Shrum, G.P.2    Connor, D.T.3
  • 2
    • 0027221539 scopus 로고
    • Design of 5-(3,5-Di-tert-butyI-4-hydroxyphenylj-1,3,4-thiadiazoles, 1,3,4-oxadiazoles and 1,2,4-triazoles as orally-active nonulcerogenic antinflammatory agents
    • [2] Mullican, M. D., Wilson, M. W., Connor, D. T. et al., Design of 5-(3,5-Di-tert-butyI-4-hydroxyphenylj-1,3,4-thiadiazoles, 1,3,4-oxadiazoles and 1,2,4-triazoles as orally-active nonulcerogenic antinflammatory agents. J. Med. Chem. 36, 1090 (1993)
    • (1993) J. Med. Chem. , vol.36 , pp. 1090
    • Mullican, M.D.1    Wilson, M.W.2    Connor, D.T.3
  • 3
    • 0027301137 scopus 로고
    • 1,3,4-Oxadiazole, 1,3,4-thiadiazole and 1,2,4-triazole analogs of the Fenamates: In vitro inhibition of cycloxygenase and 5-lipoxygenase activities
    • [3] Boschelli, D. H., Connor, D. T., Bornemeier, D. A. et al., 1,3,4-oxadiazole, 1,3,4-thiadiazole and 1,2,4-triazole analogs of the Fenamates: In vitro inhibition of cycloxygenase and 5-lipoxygenase activities. J. Med. Chem. 36, 1802 (1993)
    • (1993) J. Med. Chem. , vol.36 , pp. 1802
    • Boschelli, D.H.1    Connor, D.T.2    Bornemeier, D.A.3
  • 4
    • 33947481778 scopus 로고
    • Antiviral Chemotherapy. I. The activity of pyridine and quinoline derivatives against Neurovaccinia in mice
    • [4] Jones, D. H., Slack, R., Squires, S. et al., Antiviral Chemotherapy. I. The activity of pyridine and quinoline derivatives against Neurovaccinia in mice. J. Med. Chem. 8, 676 (1965)
    • (1965) J. Med. Chem. , vol.8 , pp. 676
    • Jones, D.H.1    Slack, R.2    Squires, S.3
  • 5
    • 0015790823 scopus 로고
    • Synthesis and Antiviral activity of 1,2,4-triazole-3-thiocarboxamide and 1,2,4-triazole-3-carboxamidine ribonucleosides
    • [5] Witkowski, J. T., Robins, R. K., Khare, G. P. et al., Synthesis and Antiviral activity of 1,2,4-triazole-3-thiocarboxamide and 1,2,4-triazole-3-carboxamidine ribonucleosides. J. Med. Chem. 16, 935 (1973)
    • (1973) J. Med. Chem. , vol.16 , pp. 935
    • Witkowski, J.T.1    Robins, R.K.2    Khare, G.P.3
  • 6
    • 0016294444 scopus 로고
    • Synthesis of compounds with potential fungicidal activity
    • [6] Shams El-Dine, S. A., Hazzaa, A. A. B., Synthesis of compounds with potential fungicidal activity. Pharmazie 29, 761 (1974)
    • (1974) Pharmazie , vol.29 , pp. 761
    • Shams El-Dine, S.A.1    Hazzaa, A.A.B.2
  • 7
    • 0008886753 scopus 로고    scopus 로고
    • Japan. Kokai 77 25,028, 24 Feb 1977
    • [7] Misato, T., Ko, K., Honma, Y. et al., Japan. Kokai 77 25,028, 24 Feb 1977
    • Misato, T.1    Ko, K.2    Honma, Y.3
  • 9
    • 0008887117 scopus 로고    scopus 로고
    • U.S. patent 4,160,838, 10 July 1979
    • [9 ] Van Reet, G., Heeres, I, Wals, L.,U.S. patent 4,160,838, 10 July 1979
    • Van Reet, G.1    Heeres, I.2    Wals, L.3
  • 10
    • 0024893414 scopus 로고
    • Synthesis of Benzimidazole derivatives as potential antimicrobial agents
    • [10] Habib, N. S., Abdel-Hamid, S., El-Hawash, M., Synthesis of Benzimidazole derivatives as potential antimicrobial agents. II Farmaco 44, 1225 (1989)
    • (1989) II Farmaco , vol.44 , pp. 1225
    • Habib, N.S.1    Abdel-Hamid, S.2    El-Hawash, M.3
  • 11
    • 0028791168 scopus 로고
    • Antifungal agents. 9. 3-Aryl-4-[α-(1H-imidazol-1-y1)arylmethyl]pyr-roles: A new Class of Potent Anti-Candida Agents
    • [11] Liu, M-C., Lin, T-S., Penketh, P. et al., Antifungal agents. 9. 3-Aryl-4-[α-(1H-imidazol-1-y1)arylmethyl]pyr-roles: A new Class of Potent Anti-Candida Agents. J. Med. Chem. 38, 4232 (1995)
    • (1995) J. Med. Chem. , vol.38 , pp. 4232
    • Liu, M.-C.1    Lin, T.-S.2    Penketh, P.3
  • 12
    • 0028966766 scopus 로고
    • Synthesis of new alkylaminoalkyl thiosemicarbazones of 3-acetylindole and their effect on DNA synthesis and cell proliferation
    • [12] Siatra-Papastaikoudi, T., Tsotinis, A., Raptopoulou, C. P. et al., Synthesis of new alkylaminoalkyl thiosemicarbazones of 3-acetylindole and their effect on DNA synthesis and cell proliferation. Eur. J. Med. Chem. 30, 107 (1995)
    • (1995) Eur. J. Med. Chem. , vol.30 , pp. 107
    • Siatra-Papastaikoudi, T.1    Tsotinis, A.2    Raptopoulou, C.P.3
  • 14
    • 0022521637 scopus 로고
    • Syntheses and in vitro antimicrobial evaluation of some benzimidazol-2-ylmethylthioureas, benzimidozol-2-ylacetylthioscmicarbazides and products of their condensation with monochloroacetic acid
    • [14] Rida, A. M., Labouta, I. M., Salama, H. M. et al., Syntheses and In vitro Antimicrobial Evaluation of some Benzimidazol-2-ylmethylthioureas, Benzimidozol-2-ylacetylthioscmicarbazides and Products of their Condensation with Monochloroacetic acid. Pharmazie 41, 475 (1986)
    • (1986) Pharmazie , vol.41 , pp. 475
    • Rida, A.M.1    Labouta, I.M.2    Salama, H.M.3
  • 15
    • 0025322672 scopus 로고
    • Synthesis of some new hydrazides, hydrazones, thiosemicarbazides, thiadiazoles, triazoles and their derivatives as possible antimicrobial
    • [15] Gürsoy, A., Demirayak, S., Cesur, Z. et al., Synthesis of some new hydrazides, hydrazones, thiosemicarbazides, thiadiazoles, triazoles and their derivatives as possible antimicrobial. Pharmazie 45, 246 (1990)
    • (1990) Pharmazie , vol.45 , pp. 246
    • Gürsoy, A.1    Demirayak, S.2    Cesur, Z.3
  • 16
    • 0020066039 scopus 로고
    • Biologically active indole derivatives
    • [16] Krishna, C., Joshi, K.C., Chand, P., Biologically active indole derivatives. Pharmazie 37, 1 (1982)
    • (1982) Pharmazie , vol.37 , pp. 1
    • Krishna, C.1    Joshi, K.C.2    Chand, P.3
  • 17
    • 0024337836 scopus 로고
    • Novel indolecarboxamidotetrazoles as potential antiallergy agents
    • [17] Unangst, P. C., Connor, D. T., Stabler, S.R. et al., Novel indolecarboxamidotetrazoles as potential antiallergy agents. J. Med. Chem. 32, 1360 (1989)
    • (1989) J. Med. Chem. , vol.32 , pp. 1360
    • Unangst, P.C.1    Connor, D.T.2    Stabler, S.R.3
  • 18
    • 0024571761 scopus 로고
    • Synthesis, structure and antifungal activity of 3-(2'-nitrovinyl) indoles
    • [18] Canoira, L., Gonzalo Rodriguez, J., Subirats, J. B. et al., Synthesis, Structure and antifungal activity of 3-(2'-nitrovinyl) indoles. Eur. J. Med. Chem. 24, 39 (1989)
    • (1989) Eur. J. Med. Chem. , vol.24 , pp. 39
    • Canoira, L.1    Gonzalo Rodriguez, J.2    Subirats, J.B.3
  • 19
    • 0008946721 scopus 로고    scopus 로고
    • Jpn. Kokai Tokkyo Koho JP 01 31,762 [89 31,762], 2 Feb 1989
    • [19] Masanori, S., Toshiharu, O., Hiroko, T. et al., Jpn. Kokai Tokkyo Koho JP 01 31,762 [89 31,762], 2 Feb 1989
    • Masanori, S.1    Toshiharu, O.2    Hiroko, T.3
  • 20
    • 0030904909 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of indole containing derivatives of 1,3,4-thiadiazole, 1,2,4-triazole and their open-chain counterparts
    • [20] Tsotinis, A., Varvaresou, A., Calogeropoulou, T. el al., Synthesis and antimicrobial evaluation of indole containing derivatives of 1,3,4-thiadiazole, 1,2,4-triazole and their open-chain counterparts. Arzneim. Forsch./ Drug Res. 47 (1), 307 (1997)
    • (1997) Arzneim. Forsch./ Drug Res. , vol.47 , Issue.1 , pp. 307
    • Tsotinis, A.1    Varvaresou, A.2    Calogeropoulou, T.3
  • 21
    • 0032580690 scopus 로고    scopus 로고
    • Synthesis, lipophilicity and biological evaluation of Indole containing derivatives of 1,3,4-Thiadiazole and 1,2,4-Triazole
    • [2l] Varvaresou, A., Siatra-Papastaikoudi, T., Tsotinis A. et al., Synthesis, Lipophilicity and Biological Evaluation of Indole containing Derivatives of 1,3,4-Thiadiazole and 1,2,4-Triazole. II Farmaco 53, 320 (1998 )
    • (1998) II Farmaco , vol.53 , pp. 320
    • Varvaresou, A.1    Siatra-Papastaikoudi, T.2    Tsotinis, A.3
  • 22
    • 0008896072 scopus 로고    scopus 로고
    • Pallas 2.0, PrologP 5.1, CompuDrug Chemistry Ltd., Budapest, Hungary
    • [22] Pallas 2.0, PrologP 5.1, CompuDrug Chemistry Ltd., Budapest, Hungary
  • 24
    • 0008896638 scopus 로고    scopus 로고
    • Antiphage activity in extracts of plants growing in Greece
    • [24] Delitheos, A., Tiligada, E., Yiannitsaros, A. et al., Antiphage Activity in extracts of plants growing in Greece. Phytomedicine 4, 115 (1997)
    • (1997) Phytomedicine , vol.4 , pp. 115
    • Delitheos, A.1    Tiligada, E.2    Yiannitsaros, A.3
  • 25
    • 37049122667 scopus 로고
    • N-Alkylation of Indole and Pyrroles in Dimethyl Sulfoxide
    • [25] Heaney, H., Ley, S.V., N-Alkylation of Indole and Pyrroles in Dimethyl Sulfoxide. J. C. S. Perkin 1, 499 (1973)
    • (1973) J. C. S. Perkin , vol.1 , pp. 499
    • Heaney, H.1    Ley, S.V.2
  • 26
    • 21344477359 scopus 로고
    • Synthesis of derivatives of 1,3,4 oxa(thia)diazole and 1,2,4-triazole containing 3-indolylmethyl radicals
    • [26] Kelarev, V. L, Karakhanov, R. A., Gasanov, S. S. et al., Synthesis of derivatives of 1,3,4 oxa(thia)diazole and 1,2,4-triazole containing 3-indolylmethyl radicals. J. Org. Chem. USSR 29, 323 (1993)
    • (1993) J. Org. Chem. USSR , vol.29 , pp. 323
    • Kelarev, V.L.1    Karakhanov, R.A.2    Gasanov, S.S.3
  • 27
    • 0023546523 scopus 로고
    • Hydrophobicity and central nervous system agents: On the principle of minimum hydrophobicity in drug design
    • [27] Mansch, C., Bjorkroth, J.P., Leo, A., Hydrophobicity and Central Nervous System Agents: On the Principle of Minimum Hydrophobicity in Drug Design. J. Pharm. Sci. 76, 663 (1993)
    • (1993) J. Pharm. Sci. , vol.76 , pp. 663
    • Mansch, C.1    Bjorkroth, J.P.2    Leo, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.