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Volumn 15, Issue 4, 2011, Pages 1017-1024

Targeting tuberculosis through a small focused library of 1, 2, 3-triazoles

Author keywords

Click chemistry; Triazoles; Tuberculosis

Indexed keywords

(1 BENZYL 1H 1,2,3 TRIAZOL 4 YL)METHANOL; 1 (2 ETHOXY 2 OXOETHYL) 1H 1,2,3 TRIAZOLE 4 CARBOXYLIC ACID; 1 BENZYL 1H 1,2,3 TRIAZOLE 4 CARBOXYLIC ACID; 1 BENZYL 4 PHENYL 1H 1,2,3 TRIAZOLE; 1,2,3 TRIAZOLE; 4 PHENYL 1 (3 PHENYLPROPYL) 1H 1,2,3 TRIAZOLE; [1 (3 PHENYLPROPYL) 1H 1,2,3 TRIAZOL 4 YL]METHANOL; BENZYL 4 OCTYL 1H 1,2,3 TRIAZOLE; BENZYL 4 PENTYL 1H 1,2,3 TRIAZOLE; BENZYL 4 PROYL 1H 1,2,3 TRIAZOLE; ECONAZOLE; ETHYL 2 (4 OCTYL 1H 1,2,3 TRIAZOL 1 YL)ACETATE; ETHYL 2 (4 PENTYL 1H 1,2,3 TRIAZOL 1 YL)ACETATE; ETHYL 2 (4 PHENYL 1H 1,2,3 TRIAZOL 1 YL)ACETATE; ETHYL 2 (4 PROPYL 1H 1,2,3 TRIAZOL 1 YL)ACETATE; ETHYL 2 [4 (HYDROXYMETHYL) 1H 1,2,3 TRIAZOL 1 YL]ACETATE; FLUCONAZOLE; METHYL 1 (3 PHENYLPROPYL) 1H 1,2,3 TRIAZOLE 4 CARBOXYLATE; METHYL 1 BENZYL 1H 1,2,3 TRIAZOLE 4 CARBOXYLATE; RIFAMPICIN; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG;

EID: 84855219978     PISSN: 13811991     EISSN: 1573501X     Source Type: Journal    
DOI: 10.1007/s11030-011-9319-0     Document Type: Article
Times cited : (47)

References (44)
  • 1
    • 0141853344 scopus 로고    scopus 로고
    • Tuberculosis
    • DOI 10.1016/S0140-6736(03)14333-4
    • Frieden TR, Sterling TR, Munsiff SS, Watt CJ, Dye C (2003) Tuberculosis. Lancet 362:887-899. doi:10.1016/S0140-6736(03)14333-4 (Pubitemid 37130100)
    • (2003) Lancet , vol.362 , Issue.9387 , pp. 887-899
    • Frieden, T.R.1    Sterling, T.R.2    Munsiff, S.S.3    Watt, C.J.4    Dye, C.5
  • 2
    • 32444444955 scopus 로고
    • Tuberculosis on the increase
    • WHO
    • WHO (1993) Tuberculosis on the increase. World Health Forum 14:1-94
    • (1993) World Health Forum , vol.14 , pp. 1-94
  • 3
    • 0037841362 scopus 로고    scopus 로고
    • The global situation of MDR-TB
    • DOI 10.1016/S1472-9792(02)00058-6
    • Espinal MA (2003) The global situation of MDR-TB. Tuberculosis 83:44-51. doi:10.1016/S1472-9792(02)00058-6 (Pubitemid 36686747)
    • (2003) Tuberculosis , vol.83 , Issue.1-3 , pp. 44-51
    • Espinal, M.A.1
  • 5
    • 0035806725 scopus 로고    scopus 로고
    • Detention and mandatory treatment for tuberculosis patients in Russia
    • DOI 10.1016/S0140-6736(01)05587-8
    • Coker R (2001) Detention and mandatory treatment for tuberculosis patients in Russia. Lancet 358:349-350. doi:10.1016/S0140-6736(01)05587-8 (Pubitemid 32739092)
    • (2001) Lancet , vol.358 , Issue.9279 , pp. 349-350
    • Coker, R.1
  • 6
    • 0011523808 scopus 로고    scopus 로고
    • World Health Organization, WHO/CDS/TB/2002.295.World Health Organization, Geneva, Switzerland
    • World Health Organization (2002) Global tuberculosis control: surveillance, planning, financing. WHO/CDS/TB/2002.295.World Health Organization, Geneva, Switzerland
    • (2002) Global Tuberculosis Control: Surveillance, Planning, Financing
  • 8
    • 33847681052 scopus 로고    scopus 로고
    • Antituberculosis drugs: Ten years of research
    • DOI 10.1016/j.bmc.2007.01.030, PII S0968089607000442
    • JaninYL (2007) Antituberculosis drugs: ten years of research.Bioorg Med Chem 15:2479-2513. doi:10.1016/j.bmc.2007.01.030 (Pubitemid 46367698)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.7 , pp. 2479-2513
    • Janin, Y.L.1
  • 9
    • 77952915341 scopus 로고    scopus 로고
    • Lipoic acid metabolism in microbial pathogens
    • doi:10.1128/MMBR.00008-10
    • Spalding MD, Prigge ST (2010) Lipoic acid metabolism in microbial pathogens.Microbiol Mol Biol Rev 74:200-228. doi:10.1128/MMBR.00008-10
    • (2010) Microbiol Mol Biol Rev , vol.74 , pp. 200-228
    • Spalding, M.D.1    Prigge, S.T.2
  • 10
    • 0345701347 scopus 로고    scopus 로고
    • Genes required for mycobacterial growth defined by high density mutagenesis
    • DOI 10.1046/j.1365-2958.2003.03425.x
    • Sassetti CM, Boyd DH, Rubin EJ (2003) Genes required for mycobacterial growth defined by high density mutagenesis. Mol Microbiol 48:77-84. doi:10.1046/j.1365-2958.2003.03425.x (Pubitemid 36411469)
    • (2003) Molecular Microbiology , vol.48 , Issue.1 , pp. 77-84
    • Sassetti, C.M.1    Boyd, D.H.2    Rubin, E.J.3
  • 12
    • 33646093721 scopus 로고    scopus 로고
    • Dual inhibition of mycobacterial fatty acid biosynthesis and degradation by 2-alkynoic acids
    • doi:10.1016/j.chembiol.2006.01.005
    • Morbidoni HR, Vilcheze C, Kremer L, Bittman R, Sacchettini JC, Jacobs WR Jr (2006) Dual inhibition of mycobacterial fatty acid biosynthesis and degradation by 2-alkynoic acids. Chem Biol 13:297-307. doi:10.1016/j.chembiol. 2006.01.005
    • (2006) Chem Biol , vol.13 , pp. 297-307
    • Morbidoni, H.R.1    Vilcheze, C.2    Kremer, L.3    Bittman, R.4    Sacchettini, J.C.5    Jacobs Jr., W.R.6
  • 13
    • 0038410325 scopus 로고    scopus 로고
    • Inactivation of the inhA-encoded fatty acid synthase II (FASII) enoyl- acyl carrier protein reductase induces accumulation of the FASI end products and cell lysis of Mycobacterium smegmatis
    • DOI 10.1128/JB.182.14.4059-4067.2000
    • Vilcheze C, Morbidoni HR, WeisbrodTR, IwamotoH, Kuo M, Sacchettini JC, JacobsWR Jr (2000) Inactivation of the inhA-encoded fatty acid synthase II (FASII) enoyl-acyl carrier protein reductase induces accumulation of the FASI end products and cell lysis of Mycobacterium smegmatis. J Bacteriol 182:4059-4067. doi:10. 1128/JB.186.13.4051-4055.2004 (Pubitemid 30436569)
    • (2000) Journal of Bacteriology , vol.182 , Issue.14 , pp. 4059-4067
    • Vilcheze, C.1    Morbidoni, H.R.2    Weisbrod, T.R.3    Iwamoto, H.4    Kuo, M.5    Sacchettini, J.C.6    Jacobs Jr., W.R.7
  • 14
    • 38949097460 scopus 로고    scopus 로고
    • Inhibitors of FabI, an enzyme drug target in the bacterial fatty acid biosynthesis pathway
    • doi:10.1021/ar700156e
    • Lu H, Tonge PJ (2008) Inhibitors of FabI, an enzyme drug target in the bacterial fatty acid biosynthesis pathway. Acc Chem Res 41:11-20. doi:10.1021/ar700156e
    • (2008) Acc Chem Res , vol.41 , pp. 11-20
    • Lu, H.1    Tonge, P.J.2
  • 16
    • 53249084552 scopus 로고    scopus 로고
    • New anti-tuberculosis drugs with novel mechanisms of action
    • doi:10.2174/092986708785132906
    • Rivers EC, Mancera RL (2008) New anti-tuberculosis drugs with novel mechanisms of action. Curr Med Chem 15:1956-1967. doi:10.2174/092986708785132906
    • (2008) Curr Med Chem , vol.15 , pp. 1956-1967
    • Rivers, E.C.1    Mancera, R.L.2
  • 17
    • 0036775336 scopus 로고    scopus 로고
    • Azole antifungals are potent inhibitors of cytochrome P450 mono-oxygenases and bacterial growth in mycobacteria and streptomycetes
    • McLean KJ, MarshallKR, Richmond A, Hunter IS, FowlerK, Kieser T, Gurcha SS, Besra GS, Munro AW (2002) Azole antifungals are potent inhibitors of cytochrome P450 mono-oxygenases and bacterial growth in mycobacteria and streptomycetes. Microbiology 148:2937-2949 (Pubitemid 35243693)
    • (2002) Microbiology , vol.148 , Issue.10 , pp. 2937-2949
    • McLean, K.J.1    Marshall, K.R.2    Richmond, A.3    Hunter, I.S.4    Fowler, K.5    Kieser, T.6    Gurcha, S.S.7    Besra, G.S.8    Munro, A.W.9
  • 18
    • 24944503971 scopus 로고    scopus 로고
    • 37Rv
    • DOI 10.1016/j.femsle.2005.07.022, PII S0378109705004830
    • Ahmad Z, Sharma S, Khuller GK (2005) In vitro and ex vivo antimycobacterial potential of azole drugs against Mycobacterium tuberculosis H37Rv. FEMS Microbiol Lett 251:19-22. doi:10.1016/j.femsle.2005.07.022 (Pubitemid 41306223)
    • (2005) FEMS Microbiology Letters , vol.251 , Issue.1 , pp. 19-22
    • Ahmad, Z.1    Sharma, S.2    Khuller, G.K.3
  • 19
    • 33646227650 scopus 로고    scopus 로고
    • The potential of azole antifungals against latent/persistent tuberculosis
    • doi:10.1111/j.1574-6968.2006.00224.x
    • Ahmad Z, Sharma S, Khuller GK (2006) The potential of azole antifungals against latent/persistent tuberculosis. FEMSMicrobiol Lett 258:200-203. doi:10.1111/j.1574-6968.2006.00224.x
    • (2006) FEMSMicrobiol Lett , vol.258 , pp. 200-203
    • Ahmad, Z.1    Sharma, S.2    Khuller, G.K.3
  • 20
    • 33746489403 scopus 로고    scopus 로고
    • Azole antifungals as novel chemotherapeutic agents against murine tuberculosis
    • DOI 10.1111/j.1574-6968.2006.00350.x
    • Ahmad Z, Sharma S, Khuller GK (2006) Azole antifungals as novel chemotherapeutic agents against murine tuberculosis. FEMS Microbiol Lett 261:181-186. doi:10.1111/j.1574-6968.2006.00350.x (Pubitemid 44134150)
    • (2006) FEMS Microbiology Letters , vol.261 , Issue.2 , pp. 181-186
    • Ahmad, Z.1    Sharma, S.2    Khuller, G.K.3
  • 21
    • 67349280375 scopus 로고    scopus 로고
    • SARstudy of clubbed [1, 2, 4]-triazolylwith fluorobenzimidazoles as antimicrobial and antituberculosis agents
    • doi:10.1016/j.ejmech.2008.12.001
    • Jadhav GR, Shaikh MU, Kale RP, Shiradkar MR, Gill CH (2009) SARstudy of clubbed [1, 2, 4]-triazolylwith fluorobenzimidazoles as antimicrobial and antituberculosis agents. Eur JMed Chem 44:2930-2935. doi:10.1016/j.ejmech.2008. 12.001
    • (2009) Eur JMed Chem , vol.44 , pp. 2930-2935
    • Jadhav, G.R.1    Shaikh, M.U.2    Kale, R.P.3    Shiradkar, M.R.4    Gill, C.H.5
  • 22
    • 34547761440 scopus 로고    scopus 로고
    • Synthesis of some 4-arylidenamino-4H-1,2,4-triazole-3-thiols and their antituberculosis activity
    • DOI 10.1080/14756360601178424, PII 779968382
    • Ozdemir A, Turan-Zitouni G, Kaplancikli ZA, Chevallet P (2007) Synthesis of some 4-arylidenamino-4H-1, 2, 4-triazole-3- thiols and their antituberculosis activity. JEnzyme InhibMedChem 22:511-516. doi:10.1080/14756360601178424 (Pubitemid 47225716)
    • (2007) Journal of Enzyme Inhibition and Medicinal Chemistry , vol.22 , Issue.4 , pp. 511-516
    • Ozdemir, A.1    Turan-Zitouni, G.2    Kaplancikli, Z.A.3    Chevallet, P.4
  • 23
    • 18444394637 scopus 로고    scopus 로고
    • Synthesis and antituberculosis activity of new 3-alkylsulfanyl-1,2,4- triazole derivatives
    • DOI 10.1080/14756360500043471
    • Kaplancikli ZA, Turan-Zitouni G, Chevallet P (2005) Synthesis and antituberculosis activity of new 3-alkylsulfanyl-1, 2, 4-triazole derivatives. J Enzyme Inhib Med Chem 20:179-182. doi:10.1080/14756360500043471 (Pubitemid 40645507)
    • (2005) Journal of Enzyme Inhibition and Medicinal Chemistry , vol.20 , Issue.2 , pp. 179-182
    • Kaplancikli, Z.A.1    Turan-Zitouni, G.2    Chevallet, P.3
  • 25
    • 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 (2003) Synthesis and investigation of tuberculosis inhibition activities of some 1, 2, 3-triazole derivatives. Eur J Med Chem 38:215-218. doi:10.1016/S0223-5234(02)01445-9 (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
  • 27
    • 55749092597 scopus 로고    scopus 로고
    • Clubbed [1, 2, 3] triazoles by fluorine benzimidazole: A novel approach to H37Rv inhibitors as a potential treatment for tuberculosis
    • doi:10.1016/j.bmcl.2008.09.096
    • Gill C, Jadhav G, Shaikh M, Kale R, Ghawalkar A, Nagargoje D, Shiradkar M (2008) Clubbed [1, 2, 3] triazoles by fluorine benzimidazole: a novel approach to H37Rv inhibitors as a potential treatment for tuberculosis. Bioorg Med Chem Lett 18:6244-6247. doi:10.1016/j.bmcl.2008.09.096
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 6244-6247
    • Gill, C.1    Jadhav, G.2    Shaikh, M.3    Kale, R.4    Ghawalkar, A.5    Nagargoje, D.6    Shiradkar, M.7
  • 28
    • 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 HC, Sharpless KB (2003) The growing impact of click chemistry on drug discovery. Drug Discov Today 8:1128-1137. doi:10.1016/S1359-6446(03)02933-7 (Pubitemid 37547919)
    • (2003) Drug Discovery Today , vol.8 , Issue.24 , pp. 1128-1137
    • Kolb, H.C.1    Sharpless, K.B.2
  • 29
    • 39549111477 scopus 로고    scopus 로고
    • Click chemistry reactions in medicinal chemistry: Applications of the 1,3-dipolar cycloaddition between azides and alkynes
    • DOI 10.1002/med.20107
    • Tron GC, Pirali T, Billington RA, Canonico PL, Sorba G, Genazzani AA (2008) Click chemistry reactions in medicinal chemistry: applications of the 1, 3-dipolar cycloaddition between azides and alkynes. Med Res Rev 28:278-308. doi:10.1002/med.20107 (Pubitemid 351281190)
    • (2008) Medicinal Research Reviews , vol.28 , Issue.2 , pp. 278-308
    • Tron, G.C.1    Pirali, T.2    Billington, R.A.3    Canonico, P.L.4    Sorba, G.5    Genazzani, A.A.6
  • 30
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • DOI 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
    • Rostovtsev VV, Green LG, Fokin VV, Sharpless KB (2002) A stepwise Hüisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew Chem Int Ed Engl 41:2596-2599. doi:10.1002/1521-3773(20020715)41:14 (Pubitemid 34803480)
    • (2002) Angewandte Chemie - International Edition , vol.41 , Issue.14 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 31
    • 33744966628 scopus 로고    scopus 로고
    • A new solvent system for efficient synthesis of 1,2,3-triazoles
    • DOI 10.1016/j.tetlet.2006.05.079, PII S0040403906010045
    • Lee B-Y, Park SR, JeonHB, KimKS (2006) Anewsolvent system for efficient synthesis of 1, 2, 3-triazoles. Tetrahedron Lett 47:5105-5109. doi:10.1016/j.tetlet.2006.05.079 (Pubitemid 43867620)
    • (2006) Tetrahedron Letters , vol.47 , Issue.29 , pp. 5105-5109
    • Lee, B.-Y.1    Park, S.R.2    Jeon, H.B.3    Kim, K.S.4
  • 32
    • 35348874803 scopus 로고    scopus 로고
    • Solution- and solid-phase synthesis of triazole oligomers that display protein-like functionality
    • DOI 10.1021/jo701292h
    • Angelo NG, Arora PS (2007) Solution- and solid-phase synthesis of triazole oligomers that display protein-like functionality. J Org Chem 72:7963-7967. doi:10.1021/jo701292h (Pubitemid 47582582)
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.21 , pp. 7963-7967
    • Angelo, N.G.1    Arora, P.S.2
  • 33
    • 77953869940 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of glycal-derived novel tetrahydrofuran 1, 2, 3-triazoles by 'click' chemistry
    • doi:10.1016/j.carres.2010.03.031
    • VijayaRaghava Reddy L, Venkat Reddy P, Mishra NN, Shukla PK, Yadav G, Srivastava R, Shaw AK (2010) Synthesis and biological evaluation of glycal-derived novel tetrahydrofuran 1, 2, 3-triazoles by 'click' chemistry. Carbohydr Res 345:1515-1521. doi:10.1016/j.carres.2010.03.031
    • (2010) Carbohydr Res , vol.345 , pp. 1515-1521
    • Vijayaraghava Reddy, L.1    Venkat Reddy, P.2    Mishra, N.N.3    Shukla, P.K.4    Yadav, G.5    Srivastava, R.6    Shaw, A.K.7
  • 34
    • 77952855073 scopus 로고    scopus 로고
    • Automated synthesis of a 96 product-sized library of triazole derivatives using a solid phase supported copper catalyst
    • doi:10.3390/molecules15053087
    • Jlalia I, Beauvineau C, Beauvière S, ÖnenE, AufortM, Beauvineau A, KhabaE, Herscovici J, Meganem F, GirardC (2010) Automated synthesis of a 96 product-sized library of triazole derivatives using a solid phase supported copper catalyst. Molecules 15:3087-3120. doi:10.3390/ molecules15053087
    • (2010) Molecules , vol.15 , pp. 3087-3120
    • Jlalia, I.1    Beauvineau, C.2    Beauvière, S.3    Önen, E.4    Aufort, M.5    Beauvineau, A.6    Khaba, E.7    Herscovici, J.8    Meganem, F.9    Girard, C.10
  • 35
    • 36849088097 scopus 로고    scopus 로고
    • Click chemistry as amacrocyclization tool in the solid-phase synthesis of small cyclic peptides
    • doi:10.1021/ol702228u
    • Turner RA, OliverAG, Lokey RS (2007) Click chemistry as amacrocyclization tool in the solid-phase synthesis of small cyclic peptides. Org Lett 9:5011-5014. doi:10.1021/ol702228u
    • (2007) Org Lett , vol.9 , pp. 5011-5014
    • Turner, R.A.1    Oliver, A.G.2    Lokey, R.S.3
  • 37
    • 77957888281 scopus 로고    scopus 로고
    • 'Click' assembly of selective inhibitors for MAO-A
    • doi:10.1016/j.bmcl.2010.08.104
    • Jia Z, Zhu Q (2010) 'Click' assembly of selective inhibitors for MAO-A. Bioorg Med Chem Lett 20:6222-6225. doi:10.1016/j.bmcl.2010.08.104
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 6222-6225
    • Jia, Z.1    Zhu, Q.2
  • 38
    • 52149091210 scopus 로고    scopus 로고
    • Synthesis of spiroacetal-triazoles as privileged natural product-like scaffolds using "click chemistry"
    • doi:10.1039/b808454h
    • Choi KW, Brimble MA (2008) Synthesis of spiroacetal-triazoles as privileged natural product-like scaffolds using "click chemistry". Org Biomol Chem 6:3518-3526. doi:10.1039/b808454h
    • (2008) Org Biomol Chem , vol.6 , pp. 3518-3526
    • Choi, K.W.1    Brimble, M.A.2
  • 39
    • 77949485158 scopus 로고    scopus 로고
    • Oxazolomycins: Natural product lead structures for novel antibacterials by click fragment conjugation
    • doi:10. 1016/j.bmcl.2010.02.066
    • Bagwell CL, Moloney MG, Yaqoob M (2010) Oxazolomycins: natural product lead structures for novel antibacterials by click fragment conjugation. Bioorg Med Chem Lett 20:2090-2094. doi:10. 1016/j.bmcl.2010.02.066
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 2090-2094
    • Bagwell, C.L.1    Moloney, M.G.2    Yaqoob, M.3
  • 41
    • 0033986977 scopus 로고    scopus 로고
    • Use of genomics and combinatorial chemistry in the development of new antimycobacterial drugs
    • DOI 10.1016/S0006-2952(99)00253-1, PII S0006295299002531
    • Barry CEIII, Slayden RA, Sampson AE, Lee RE (2000) Use of genomics and combinatorial chemistry in the development of new antimycobacterial drugs. Biochem Pharmacol 59:221-231. doi:10. 1016/S0006-2952(99)00253-1 (Pubitemid 30001748)
    • (2000) Biochemical Pharmacology , vol.59 , Issue.3 , pp. 221-231
    • Barry III, C.E.1    Slayden, R.A.2    Sampson, A.E.3    Lee, R.E.4
  • 43
    • 9444260351 scopus 로고    scopus 로고
    • A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction
    • Appukkuttan P, Dehaen W, Fokin VV, Van der Eycken E (2004) A microwave-assisted click chemistry synthesis of 1, 4-disubstituted 1, 2, 3-triazoles via a copper(I)-catalyzed three-component reaction. Org Lett 6:4223-4225. doi:10.1021/ol048341v (Pubitemid 39563449)
    • (2004) Organic Letters , vol.6 , Issue.23 , pp. 4223-4225
    • Appukkuttan, P.1    Dehaen, W.2    Fokin, V.V.3    Van Der Eycken, E.4
  • 44
    • 0025784808 scopus 로고
    • Cytotoxicity of T-2 toxin and its metabolites determined with the neutral red cell viability assay
    • Babich H, Borenfreund E (1991) Cytotoxicity of T-2 toxin and its metabolites determined with the neutral red cell viability assay. Appl Environ Microbiol 57:2101-2103
    • (1991) Appl Environ Microbiol , vol.57 , pp. 2101-2103
    • Babich, H.1    Borenfreund, E.2


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