메뉴 건너뛰기




Volumn 29, Issue 6, 2010, Pages 265-274

Synthesis and antitubercular evaluation of new bis-1,2,3-triazoles derived from D-mannitol

Author keywords

1,2,3 Triazole; Antitubercular activity; D mannitol; Drugs

Indexed keywords

MYCOBACTERIUM TUBERCULOSIS; TETRA;

EID: 77957847018     PISSN: 07328303     EISSN: 15322327     Source Type: Journal    
DOI: 10.1080/07328303.2010.511749     Document Type: Article
Times cited : (17)

References (18)
  • 1
    • 77957854892 scopus 로고    scopus 로고
    • http://www.who.int/tb/en/.
  • 6
    • 0028783851 scopus 로고
    • 1-(Fluorobenzyl)-4-amino-1H-1, 2, 3-triazolo[4, 5-c]pyridines: Synthesis and anticonvulsant activity
    • Kelley, J. L.; Koble, C. S.; Davis, R. G.; McLean, E. W.; Soroko, F. E.; Cooper, B. R. 1-(Fluorobenzyl)-4-amino-1H-1, 2, 3-triazolo[4, 5-c]pyridines: synthesis and anticonvulsant activity. J. Med. Chem. 1995, 38, 4131-4134.
    • (1995) J. Med. Chem. , vol.38 , pp. 4131-4134
    • Kelley, J.L.1    Koble, C.S.2    Davis, R.G.3    McLean, E.W.4    Soroko, F.E.5    Cooper, B.R.6
  • 8
    • 0037294865 scopus 로고    scopus 로고
    • Synthesis and investigation of tuberculosis inhibition activities of some 1,2,3-triazole derivatives
    • DOI 10.1016/S0223-5234(02)01445-9
    • Dabak, K.; Sezer, O.; Akar, A.; Anac, O. Synthesis and investigation of tuberculosis inhibition activities of some 1, 2, 3-triazole derivatives. Eur. J. Med. Chem. 2003, 38, 215-218. (Pubitemid 36288475)
    • (2003) European Journal of Medicinal Chemistry , vol.38 , Issue.2 , pp. 215-218
    • Dabak, K.1    Sezer, O.2    Akar, A.3    Anac, O.4
  • 11
    • 36148997680 scopus 로고    scopus 로고
    • Synthesis and evaluation of 1-Alkyl-4-phenyl-[1, 2, 3]-triazole derivatives as antimycobacterial agent
    • Gallardo, H.; Conte, G.; Bryk, F.; Lourenço, M. C. S.; Costa, M. S.; Ferreira, V. F. J. Synthesis and evaluation of 1-Alkyl-4-phenyl-[1, 2, 3]-triazole derivatives as antimycobacterial agent. Braz. Chem. Soc. 2007, 18, 1285-1291.
    • (2007) Braz. Chem. Soc. , vol.18 , pp. 1285-1291
    • Gallardo, H.1    Conte, G.2    Bryk, F.3    Lourenço, M.C.S.4    Costa, M.S.5    Ferreira, V.F.J.6
  • 13
    • 33746674339 scopus 로고    scopus 로고
    • Synthesis of α,ω-diazidoalditol derivatives via both bis- or tris-cyclic sulfites and peracetylated α,ω-dibromoalditols as bielectrophilic intermediates
    • DOI 10.1081/CAR-120030470, PII NTABVBDLM8PRUHAA
    • Glacon, V.; Benazza, M.; El Anzi, A.; Beaupere, D.; Demailly, G. J. ω-Diazidoalditol Derivitives via Both bis- or tris-cyclic sulfites and Peracetylated, ω-Dibromoalditols as Bielectrophilic Intermediates. Carbohydr. Chem. 2004, 23, 95-110. (Pubitemid 44161418)
    • (2004) Journal of Carbohydrate Chemistry , vol.23 , Issue.2-3 , pp. 95-110
    • Glacon, V.1    Benazza, M.2    Anzi, A.3    Beaupere, D.4    Demailly, G.5
  • 14
    • 0348109450 scopus 로고    scopus 로고
    • The growing impact of click chemistry on drug discovery
    • DOI 10.1016/S1359-6446(03)02933-7, PII S1359644603029337
    • Kolb, H. C.; Sharpless, K. B. The growing impact of click chemistry on drug discovery. Drug Discov Today. 2003, 8, 1128-1137. (Pubitemid 37547919)
    • (2003) Drug Discovery Today , vol.8 , Issue.24 , pp. 1128-1137
    • Kolb, H.C.1    Sharpless, K.B.2
  • 15
    • 17644414186 scopus 로고    scopus 로고
    • I-catalyzed azide-alkyne cycloaddition reaction
    • DOI 10.1002/anie.200461496
    • Rodionov, V. O.; Fokin, V. V.; Finn, M. G. Mechanism of the ligand-free CuI-catalyzed azide-alkyne cycloaddition reaction. Angew. Chem. Int. Ed. 2005, 44, 2210-2215. (Pubitemid 40560884)
    • (2005) Angewandte Chemie - International Edition , vol.44 , Issue.15 , pp. 2210-2215
    • Rodionov, V.O.1    Fokin, V.V.2    Finn, M.G.3
  • 16
    • 60049087880 scopus 로고
    • Measurement of sensitivity of the tuberculous bacillus to antibacillary drugs by the method of proportions. Methodology, resistance criteria, results and interpretation
    • Canetti, G., Rist, N.; Grosset, J. Measurement of sensitivity of the tuberculous bacillus to antibacillary drugs by the method of proportions. Methodology, resistance criteria, results and interpretation. Rev. Tuberculosis Pneumol. 1963, 27, 217-272.
    • (1963) Rev. Tuberculosis Pneumol , vol.27 , pp. 217-272
    • Canetti, G.R.N.1    Grosset, J.2
  • 18
    • 2442551918 scopus 로고    scopus 로고
    • Comparison of flow cytometric and Alamar Blue tests with the proportional method for testing susceptibility of Mycobacterium tuberculosis to rifampin and isoniazid
    • Reis, R. S.; Neves, I. Jr; Lourenço, S. L. S.; Fonseca, L. S.; Lourenço, M. C. S. Comparison of flow cytometric and Alamar Blue tests with the proportional method for testing susceptibility of Mycobacterium tuberculosis to rifampin and isoniazid. J. Clin. Microbiol. 2004, 42, 2247-2248.
    • (2004) J. Clin. Microbiol. , vol.42 , pp. 2247-2248
    • Reis, R.S.1    Neves Jr., I.2    Lourenço, S.L.S.3    Fonseca, L.S.4    Lourenço, M.C.S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.