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Volumn 22, Issue 10, 2013, Pages 4700-4707

New carbodithioate derivatives: Synthesis, characterization, and in vitro antibacterial, antifungal, antitubercular, and antimalarial activity

Author keywords

2,3 Dioxoindoline; Antimalarial activities; Antitubercular; Carbodithioate; Isatin; Ultrasound

Indexed keywords

2 (2,3 DIOXOINDOLIN 1 YL)ETHYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 2 (5 BROMO 2,3 DIOXOINDOLIN 1 YL)ETHYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 2 (5 BROMO 2,3 DIOXOINDOLIN 1 YL)PROPYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 2 (5 CHLORO 2,3 DIOXOINDOLIN 1 YL)ETHYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 2 (5 CHLORO 2,3 DIOXOINDOLIN 1 YL)PROPYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 2 (5 FLUORO 2,3 DIOXOINDOLIN 1 YL)ETHYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 2 (5 FLUORO 2,3 DIOXOINDOLIN 1 YL)PROPYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 2 (5 N NITRO 2,3 DIOXOINDOLIN 1 YL)ETHYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 2 (5 NITRO 2,3 DIOXOINDOLIN 1 YL)PROPYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 3 (2,3 DIOXOINDOLIN 1 YL)PROPYL 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBODITHIOATE; 4 (3,4 DICHLOROPHENYL)PIPERAZINE 1 CARBOTHIOIC DITHIOPEROXYANHYDRIDE; AMPICILLIN; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; CARBODITHIOATE DERIVATIVE; CIPROFLOXACIN; ETHAMBUTOL; ISONIAZID; NORFLOXACIN; NYSTATIN; PYRAZINAMIDE; RIFAMPICIN; THIOCARBAMIC ACID DERIVATIVE; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG;

EID: 84883448376     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-013-0472-0     Document Type: Article
Times cited : (13)

References (60)
  • 1
    • 80054909846 scopus 로고    scopus 로고
    • 1, 3-dihydro-2H-indol-2-ones derivatives: Design, synthesis, in vitro antibacterial, antifungal and antitubercular study
    • 21981980 10.1016/j.ejmech.2011.09.023 1:CAS:528:DC%2BC3MXhtlKkurzI
    • Akhaja TN, Raval JP (2011) 1, 3-dihydro-2H-indol-2-ones derivatives: design, synthesis, in vitro antibacterial, antifungal and antitubercular study. Eur J Med Chem 46:5573-5579
    • (2011) Eur J Med Chem , vol.46 , pp. 5573-5579
    • Akhaja, T.N.1    Raval, J.P.2
  • 2
    • 84863099283 scopus 로고    scopus 로고
    • Design, synthesis and in vitro evaluation of tetrahydropyrimidine-isatin hybrids as potential antitubercular and antimalarial agents
    • 10.1016/j.cclet.2012.05.004 1:CAS:528:DC%2BC38XptFCmtro%3D
    • Akhaja TN, Raval JP (2012a) Design, synthesis and in vitro evaluation of tetrahydropyrimidine-isatin hybrids as potential antitubercular and antimalarial agents. Chin Chem Lett 23:785-788
    • (2012) Chin Chem Lett , vol.23 , pp. 785-788
    • Akhaja, T.N.1    Raval, J.P.2
  • 3
    • 84859005110 scopus 로고    scopus 로고
    • Design, synthesis, in vitro evaluation of tetrahydropyrimidine-isatin hybrids as potential antibacterial, antifungal and anti-tubercular agents
    • 10.1016/j.cclet.2012.01.040 1:CAS:528:DC%2BC38XksVyqt70%3D
    • Akhaja TN, Raval JP (2012b) Design, synthesis, in vitro evaluation of tetrahydropyrimidine-isatin hybrids as potential antibacterial, antifungal and anti-tubercular agents. Chin Chem Lett 23:446-449
    • (2012) Chin Chem Lett , vol.23 , pp. 446-449
    • Akhaja, T.N.1    Raval, J.P.2
  • 4
    • 0025366722 scopus 로고
    • Comparison of improved BACTEC and Lowenstein-Jensen media for culture of mycobacteria from clinical specimens
    • 2116446 1:STN:280:DyaK3czjvVektw%3D%3D
    • Anargyros P, Astill DS, Lim IS (1990) Comparison of improved BACTEC and Lowenstein-Jensen media for culture of mycobacteria from clinical specimens. J Clin Microbiol 28:1288-1291
    • (1990) J Clin Microbiol , vol.28 , pp. 1288-1291
    • Anargyros, P.1    Astill, D.S.2    Lim, I.S.3
  • 5
    • 84883466206 scopus 로고
    • Synthesis of Some N,NDisubstituted Carbamodithioic Acid Esters Tested for Antifungal Activity
    • Ates, Cesur N, Guener H, Uzun M, Kiraz M, Kaya D (1995) Synthesis of Some N,NDisubstituted Carbamodithioic Acid Esters Tested for Antifungal Activity. ChemInform, 26
    • (1995) ChemInform , pp. 26
    • Ates1    Cesur, N.2    Guener, H.3    Uzun, M.4    Kiraz, M.5    Kaya, D.6
  • 6
    • 0026607504 scopus 로고
    • The Invention of Chemical Reactions: The Last Five Years
    • 10.1016/S0040-4020(01)88519-7 1:CAS:528:DyaK38XitlCksLs%3D
    • Barton DHR (1992) The Invention of Chemical Reactions: the Last Five Years. Tetrahedron 48:2529-2544
    • (1992) Tetrahedron , vol.48 , pp. 2529-2544
    • Barton, D.H.R.1
  • 7
    • 58049189252 scopus 로고    scopus 로고
    • Ultrasound assisted reactions of steroid analogous of anticipated biological activities
    • 19081283 10.1016/j.ultsonch.2008.10.012 1:CAS:528:DC%2BD1MXjvFaqtw%3D%3D
    • Bejan V, Moldoveanu C, Mangalagiu II (2009) Ultrasound assisted reactions of steroid analogous of anticipated biological activities. Ultrason Sonochem 16:312-315
    • (2009) Ultrason Sonochem , vol.16 , pp. 312-315
    • Bejan, V.1    Moldoveanu, C.2    Mangalagiu, I.I.3
  • 8
    • 0002865018 scopus 로고    scopus 로고
    • Synthesis of F-alkyl N-sulfonyl carbamates and thiocarbamates
    • 10.1016/S0022-1139(99)00096-2 1:CAS:528:DyaK1MXlvVCmsro%3D
    • Beji M, Sbihi H, Baklouti A, Cambon A (1999) Synthesis of F-alkyl N-sulfonyl carbamates and thiocarbamates. J Fluorine Chem 99:17-24
    • (1999) J Fluorine Chem , vol.99 , pp. 17-24
    • Beji, M.1    Sbihi, H.2    Baklouti, A.3    Cambon, A.4
  • 9
    • 0037180972 scopus 로고    scopus 로고
    • Spontaneous formation of thiuram disulfides in solutions of iron(III) dithiocarbamates
    • 11853487 10.1021/jf011143n 1:CAS:528:DC%2BD38XnvVGktg%3D%3D
    • Bergendorff O, Hansson C (2002) Spontaneous formation of thiuram disulfides in solutions of iron(III) dithiocarbamates. J Agric Food Chem 50:1092-1096
    • (2002) J Agric Food Chem , vol.50 , pp. 1092-1096
    • Bergendorff, O.1    Hansson, C.2
  • 10
    • 37049085421 scopus 로고
    • Structure-activity relations. Part 6. The alkaline hydrolysis of 3-methyl-5-methylidene- and 3,5-dimethylthiazolidine-2,4-diones. The addition of thiols to 3-methyl-5-methylidenethiazolidine-2,4-dione
    • Bowden K, Chana RS (1990) Structure-activity relations. Part 6. The alkaline hydrolysis of 3-methyl-5-methylidene- and 3,5-dimethylthiazolidine-2,4- diones. The addition of thiols to 3-methyl-5-methylidenethiazolidine-2,4-dione. J Chem Soc Perk T 2, 2163-2166
    • (1990) J Chem Soc Perk T , vol.2 , pp. 2163-2166
    • Bowden, K.1    Chana, R.S.2
  • 11
    • 15044361072 scopus 로고    scopus 로고
    • Synthesis and in vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains
    • 15780632 10.1016/j.bmcl.2005.01.083 1:CAS:528:DC%2BD2MXisVCnur4%3D
    • Cao SL, Feng YP, Jiang YY, Liu SY, Ding GY, Li RT (2005) Synthesis and in vitro antitumor activity of 4(3H)-quinazolinone derivatives with dithiocarbamate side chains. Bioorg Med Chem Lett 15:1915-1917
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 1915-1917
    • Cao, S.L.1    Feng, Y.P.2    Jiang, Y.Y.3    Liu, S.Y.4    Ding, G.Y.5    Li, R.T.6
  • 12
    • 0027715676 scopus 로고
    • Synthesis, characterization and biological evaluation of 2-methyl-3-(N- substituted thiocarbamoylthio)acetamido-4(3H)-quinazolinones
    • 1:CAS:528:DyaK2cXntVSrtr4%3D
    • Capan G, Ergenc N, Buyuktimkin S, Yulug N (1993) SSynthesis, characterization and biological evaluation of 2-methyl-3-(N- substituted thiocarbamoylthio)acetamido-4(3H)-quinazolinones. Sci Pharm 61:243-250
    • (1993) Sci Pharm , vol.61 , pp. 243-250
    • Capan, G.1    Ergenc, N.2    Buyuktimkin, S.3    Yulug, N.4
  • 13
    • 45849148082 scopus 로고    scopus 로고
    • New uses for old copper-binding drugs: Converting the pro-angiogenic copper to a specific cancer cell death inducer
    • 18479220 10.1517/14728222.12.6.739 1:CAS:528:DC%2BD1cXlvFSjsrk%3D
    • Chen D, Dou QP (2008) New uses for old copper-binding drugs: converting the pro-angiogenic copper to a specific cancer cell death inducer. Expert Opin Ther Targets 12:739-748
    • (2008) Expert Opin Ther Targets , vol.12 , pp. 739-748
    • Chen, D.1    Dou, Q.P.2
  • 14
    • 28844475908 scopus 로고    scopus 로고
    • Synthesis of some new substituted triazolyl dithiocarbanilates and their pharmaceutical use
    • 1:CAS:528:DC%2BD3MXhs1Sms7g%3D
    • Chourasia MRT, Devendra (1999) Synthesis of some new substituted triazolyl dithiocarbanilates and their pharmaceutical use. Indian J Phys Nat Sci 15:15-21
    • (1999) Indian J Phys Nat Sci , vol.15 , pp. 15-21
    • Chourasia, M.R.T.1    Devendra2
  • 15
    • 33645222276 scopus 로고    scopus 로고
    • Power ultrasound in organic synthesis: Moving cavitational chemistry from academia to innovative and large-scale applications
    • 16444299 10.1039/b503848k 1:CAS:528:DC%2BD28Xot1ajsQ%3D%3D
    • Cravotto G, Cintas P (2006) Power ultrasound in organic synthesis: moving cavitational chemistry from academia to innovative and large-scale applications. Chem Soc Rev 35:180-196
    • (2006) Chem Soc Rev , vol.35 , pp. 180-196
    • Cravotto, G.1    Cintas, P.2
  • 16
    • 4243854308 scopus 로고
    • Radical chemistry associated with the thiocarbonyl group
    • 10.1021/cr00097a001 1:CAS:528:DyaL1MXmtFeqsbg%3D
    • Crich D, Quintero L (1989) Radical chemistry associated with the thiocarbonyl group. Chem Rev 89:1413-1432
    • (1989) Chem Rev , vol.89 , pp. 1413-1432
    • Crich, D.1    Quintero, L.2
  • 17
    • 36349012493 scopus 로고    scopus 로고
    • Targeting of nuclear factor-B and proteasome by dithiocarbamate complexes with metals
    • 10.2174/138161207782110390 1:CAS:528:DC%2BD2sXhtlarurnF
    • Cvek B, Dvorak Z (2007) Targeting of nuclear factor-B and proteasome by dithiocarbamate complexes with metals. Curr Pharm Design 13:3155-3167
    • (2007) Curr Pharm Design , vol.13 , pp. 3155-3167
    • Cvek, B.1    Dvorak, Z.2
  • 18
    • 4243621386 scopus 로고
    • In vitro techniques for antimalarial development and evaluation
    • W. Peters W.H.G. Richards (eds) Springer Berlin
    • Desjardins RE (1984) In vitro techniques for antimalarial development and evaluation. In: Peters W, Richards WHG (eds) Handbook of experimental pharmacology. Springer, Berlin, pp 179-200
    • (1984) Handbook of Experimental Pharmacology , pp. 179-200
    • Desjardins, R.E.1
  • 19
    • 0006017177 scopus 로고
    • Dunn Ad RW-D Ellis Horwood, Chichester, UK
    • Dunn Ad RW-D (1989) Carbon disulphide in organic chemistry. Ellis Horwood, Chichester, UK, pp 226-367
    • (1989) Carbon Disulphide in Organic Chemistry , pp. 226-367
  • 20
    • 0033603405 scopus 로고    scopus 로고
    • The chemistry of thiocyanic esters
    • 10.1016/S0040-4020(99)00386-5 1:CAS:528:DyaK1MXktVegurs%3D
    • Erian AW, Sherif SM (1999) The chemistry of thiocyanic esters. Tetrahedron 55:7957-8024
    • (1999) Tetrahedron , vol.55 , pp. 7957-8024
    • Erian, A.W.1    Sherif, S.M.2
  • 21
    • 0032804784 scopus 로고    scopus 로고
    • Synthesis and in vitro antifungal activity of some N,N-disubstituted dithiocarbamic acid esters derived from 2-methylquinazolinones
    • 10464978 1:CAS:528:DyaK1MXmsVGls7o%3D
    • Farghaly AO, Moharram AM (1999) Synthesis and in vitro antifungal activity of some N,N-disubstituted dithiocarbamic acid esters derived from 2-methylquinazolinones. Boll Chim Farm 138:280-289
    • (1999) Boll Chim Farm , vol.138 , pp. 280-289
    • Farghaly, A.O.1    Moharram, A.M.2
  • 22
    • 77954314740 scopus 로고    scopus 로고
    • Synthesis and in vitro antimycobacterial activity of balofloxacin ethylene isatin derivatives
    • 20493593 10.1016/j.ejmech.2010.04.027 1:CAS:528:DC%2BC3cXnsVWjsr4%3D
    • Feng LS, Liu ML, Wang B, Chai Y, Hao XQ, Meng S, Guo HY (2010) Synthesis and in vitro antimycobacterial activity of balofloxacin ethylene isatin derivatives. Eur J Med Chem 45:3407-3412
    • (2010) Eur J Med Chem , vol.45 , pp. 3407-3412
    • Feng, L.S.1    Liu, M.L.2    Wang, B.3    Chai, Y.4    Hao, X.Q.5    Meng, S.6    Guo, H.Y.7
  • 23
    • 0033233191 scopus 로고    scopus 로고
    • The inhibition of NF-kappaB activation pathways and the induction of apoptosis by dithiocarbamates in T cells are blocked by the glutathione precursor N-acetyl-L-cysteine
    • 1:CAS:528:DC%2BD3cXhtF2lsLw%3D
    • Fernandez PC, Machado J Jr, Heussler VT, Botteron C, Palmer GH, Dobbelaere DA. (1999) The inhibition of NF-kappaB activation pathways and the induction of apoptosis by dithiocarbamates in T cells are blocked by the glutathione precursor N-acetyl-L-cysteine. Biol Chem 380:1383-1394
    • (1999) Eur J Med Chem , vol.380 , pp. 1383-1394
    • Fernandez, P.C.1    Machado, Jr.J.2    Heussler, V.T.3    Botteron, C.4    Palmer, G.H.5    Dobbelaere, D.A.6
  • 24
    • 78149412000 scopus 로고    scopus 로고
    • An efficient synthesis of 3-substituted indole derivates under ultrasound irradiation
    • 21044854 10.1016/j.ultsonch.2010.09.007 1:CAS:528:DC%2BC3cXhtl2gtbfM
    • Fu Z, Shao H (2011) An efficient synthesis of 3-substituted indole derivates under ultrasound irradiation. Ultrason Sonochem 18:520-526
    • (2011) Ultrason Sonochem , vol.18 , pp. 520-526
    • Fu, Z.1    Shao, H.2
  • 26
    • 0342980850 scopus 로고    scopus 로고
    • 5-Nitroimidazole derivatives as possible antibacterial and antifungal agents
    • 10668184 10.1016/S0014-827X(99)00109-3
    • Günay NS, Çapan G, Ulusoy N, Ergenç N, Ötük G, Kaya D (1999) 5-Nitroimidazole derivatives as possible antibacterial and antifungal agents. Il Farmaco 54:826-831
    • (1999) Il Farmaco , vol.54 , pp. 826-831
    • Günay, N.S.1    Çapan, G.2    Ulusoy, N.3    Ergenç, N.4    Ötük, G.5    Kaya, D.6
  • 27
    • 0037075792 scopus 로고    scopus 로고
    • Synthesis and antimycobacterial activity of 6-arylpurines: The requirements for the N-9 substituent in active antimycobacterial purines
    • 11882008 10.1021/jm0110284 1:CAS:528:DC%2BD38XhtVWksr4%3D
    • Gundersen LL, Nissen-Meyer J, Spilsberg B (2002) Synthesis and antimycobacterial activity of 6-arylpurines: the requirements for the N-9 substituent in active antimycobacterial purines. J Med Chem 45:1383-1386
    • (2002) J Med Chem , vol.45 , pp. 1383-1386
    • Gundersen, L.L.1    Nissen-Meyer, J.2    Spilsberg, B.3
  • 28
    • 0029837235 scopus 로고    scopus 로고
    • Synthesis and antifungal activity of new carbamodithioic acid esters derived from 3-acetylcoumarin
    • 10.1016/0223-5234(96)89561-4
    • Gürsoy A, Ateş Ö, Karali N, Cesur N, Kiraz M (1996) Synthesis and antifungal activity of new carbamodithioic acid esters derived from 3-acetylcoumarin. Eur J Med Chem 31:643-646
    • (1996) Eur J Med Chem , vol.31 , pp. 643-646
    • Gürsoy, A.1    Ateş, Ö.2    Karali, N.3    Cesur, N.4    Kiraz, M.5
  • 29
    • 33750090398 scopus 로고    scopus 로고
    • Synthesis, antimycobacterial and antitumor activities of new (1, 1-dioxido-3-oxo-1, 2-benzisothiazol-2(3H)-yl)methyl N, N-disubstituted dithiocarbamate/O-alkyldithiocarbonate derivatives
    • 16931027 10.1016/j.bmc.2006.07.065
    • Güzel Ö, Salman A (2006) Synthesis, antimycobacterial and antitumor activities of new (1, 1-dioxido-3-oxo-1, 2-benzisothiazol-2(3H)-yl) methyl N, N-disubstituted dithiocarbamate/O-alkyldithiocarbonate derivatives. Bioorg Med Chem 14:7804-7815
    • (2006) Bioorg Med Chem , vol.14 , pp. 7804-7815
    • Güzel, Ö.1    Salman, A.2
  • 30
    • 49449097238 scopus 로고    scopus 로고
    • The many roles for fluorine in medicinal chemistry
    • 18570365 10.1021/jm800219f 1:CAS:528:DC%2BD1cXns1WjtLo%3D
    • Hagmann WK (2008) The many roles for fluorine in medicinal chemistry. J Med Chem 51:4359-4369
    • (2008) J Med Chem , vol.51 , pp. 4359-4369
    • Hagmann, W.K.1
  • 31
    • 77954608527 scopus 로고    scopus 로고
    • Synthesis of dithiocarbamate by Markovnikov addition reaction in aqueous medium
    • 10.1039/c004711b 1:CAS:528:DC%2BC3cXotlyru7w%3D
    • Halimehjani AZ, Marjani K, Ashouri A (2010) Synthesis of dithiocarbamate by Markovnikov addition reaction in aqueous medium. Green Chem 12:1306-1310
    • (2010) Green Chem , vol.12 , pp. 1306-1310
    • Halimehjani, A.Z.1    Marjani, K.2    Ashouri, A.3
  • 33
    • 67650427150 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of novel dithiocarbamate substituted chromones
    • 19410339 10.1016/j.ejmech.2009.04.004 1:CAS:528:DC%2BD1MXoslGhs7o%3D
    • Huang W, Ding Y, Miao Y, Liu MZ, Li Y, Yang GF (2009) Synthesis and antitumor activity of novel dithiocarbamate substituted chromones. Eur J Med Chem 44:3687-3696
    • (2009) Eur J Med Chem , vol.44 , pp. 3687-3696
    • Huang, W.1    Ding, Y.2    Miao, Y.3    Liu, M.Z.4    Li, Y.5    Yang, G.F.6
  • 36
    • 0018704491 scopus 로고
    • Synchronization of plasmodium falciparum erythrocytic stages in culture
    • 383936 10.2307/3280287 1:STN:280:DyaL3c%2FgvVGmtg%3D%3D
    • Lambros C, Vanderberg JP (1979) Synchronization of plasmodium falciparum erythrocytic stages in culture. J Parasitol 65:418-420
    • (1979) J Parasitol , vol.65 , pp. 418-420
    • Lambros, C.1    Vanderberg, J.P.2
  • 38
    • 78149409104 scopus 로고    scopus 로고
    • Potassium sorbate as an efficient and green catalyst for Knoevenagel condensation
    • 20932793 10.1016/j.ultsonch.2010.09.003 1:CAS:528:DC%2BC3cXhtl2gtbbO
    • Liu Q, Ai H, Li Z (2011) Potassium sorbate as an efficient and green catalyst for Knoevenagel condensation. Ultrason Sonochem 18:477-479
    • (2011) Ultrason Sonochem , vol.18 , pp. 477-479
    • Liu, Q.1    Ai, H.2    Li, Z.3
  • 39
    • 8444223066 scopus 로고    scopus 로고
    • Drug permeation in biomembranes: In vitro and in silico prediction and influence of physicochemical properties
    • 15324921 10.1016/j.ejps.2004.05.009
    • Mälkiä A, Murtomäki L, Urtti A, Kontturi K (2004) Drug permeation in biomembranes: in vitro and in silico prediction and influence of physicochemical properties. Eur J Pharm Sci 23:13-47
    • (2004) Eur J Pharm Sci , vol.23 , pp. 13-47
    • Mälkiä, A.1    Murtomäki, L.2    Urtti, A.3    Kontturi, K.4
  • 42
    • 1542787706 scopus 로고    scopus 로고
    • Synthesis of polystyrene-supported dithiocarbamates and their complexation with metal ions
    • 10.1002/app.13623 1:CAS:528:DC%2BD2cXhslOlsbo%3D
    • Mcclain A, Hsieh YL (2004) Synthesis of polystyrene-supported dithiocarbamates and their complexation with metal ions. J Appl Polym Sci 92:218-225
    • (2004) J Appl Polym Sci , vol.92 , pp. 218-225
    • McClain, A.1    Hsieh, Y.L.2
  • 44
    • 31544461215 scopus 로고    scopus 로고
    • Dithiocarbamates: Functional and versatile linkers for the formation of self-assembled monolayers
    • 16401114 10.1021/la052952u 1:CAS:528:DC%2BD2MXht1yiur%2FI
    • Morf P, Raimondi F, Nothofer HG, Schnyder B, Yasuda A, Wessels JM, Jung TA (2006) Dithiocarbamates: functional and versatile linkers for the formation of self-assembled monolayers. Langmuir 22:658-663
    • (2006) Langmuir , vol.22 , pp. 658-663
    • Morf, P.1    Raimondi, F.2    Nothofer, H.G.3    Schnyder, B.4    Yasuda, A.5    Wessels, J.M.6    Jung, T.A.7
  • 45
    • 70350052996 scopus 로고    scopus 로고
    • A one-pot preparation of cyanamide from dithiocarbamate using molecular iodine
    • 10.1039/b914283p 1:CAS:528:DC%2BD1MXht1ags7%2FI
    • Nath J, Patel BK, Jamir L, Sinha UB, Satyanarayana KVVV (2009) A one-pot preparation of cyanamide from dithiocarbamate using molecular iodine. Green Chem 11:1503-1506
    • (2009) Green Chem , vol.11 , pp. 1503-1506
    • Nath, J.1    Patel, B.K.2    Jamir, L.3    Sinha, U.B.4    Satyanarayana, K.5
  • 46
    • 28844498721 scopus 로고    scopus 로고
    • Synthesis of new triazolyl-N,N-dialkyldithiocarbamates as antifungal agents
    • 16350843 10.1007/BF02978200 1:CAS:528:DC%2BD2MXhtlGmsrjM
    • Ozkirimli S, Apak T, Kiraz M, Yegenoglu Y (2005) Synthesis of new triazolyl-N,N-dialkyldithiocarbamates as antifungal agents. Arch Pharm Res 28:1213-1218
    • (2005) Arch Pharm Res , vol.28 , pp. 1213-1218
    • Ozkirimli, S.1    Apak, T.2    Kiraz, M.3    Yegenoglu, Y.4
  • 49
    • 0018262277 scopus 로고
    • Drug sensitivity of Plasmodium falciparum. An in vitro microtechnique
    • 74500 10.1016/S0140-6736(78)90365-3 1:STN:280:DyaE1c%2FptV2lsA%3D%3D
    • Rieckmann KH, Campbell GH, Campbell GH, Sax LJ, LJ Sax, Mrema JE, Je M (1978) Drug sensitivity of Plasmodium falciparum. An in vitro microtechnique. Lancet 1:22-23
    • (1978) Lancet , vol.1 , pp. 22-23
    • Rieckmann, K.H.1    Campbell, G.H.2    Campbell, G.H.3    Sax, L.J.4    Lj, S.5    Mrema, J.E.6    Je, M.7
  • 50
    • 33644843388 scopus 로고    scopus 로고
    • Disulfiram, an old drug with new potential therapeutic uses for human cancers and fungal infections
    • 10.1039/b504392a 1:CAS:528:DC%2BD2MXntlCmsbk%3D
    • Sauna ZE, Shukla S, Ambudkar SV (2005) Disulfiram, an old drug with new potential therapeutic uses for human cancers and fungal infections. Mol BioSys 1:127-134
    • (2005) Mol BioSys , vol.1 , pp. 127-134
    • Sauna, Z.E.1    Shukla, S.2    Ambudkar, S.V.3
  • 51
    • 0015359007 scopus 로고
    • Carcinostatic and antimicrobial activity of acylated N-hemiacetals, aminals and aminomethyl esters of dithiocarbamic acid. 18. Cytostatics
    • 10.1002/ardp.19723050606 1:STN:280:DyaE383lt1WgsQ%3D%3D
    • Schonenberger H, Lippert P (1972) Carcinostatic and antimicrobial activity of acylated N-hemiacetals, aminals and aminomethyl esters of dithiocarbamic acid. 18. Cytostatics. Arch Pharm 305:427-441
    • (1972) Arch Pharm , vol.305 , pp. 427-441
    • Schonenberger, H.1    Lippert, P.2
  • 53
    • 0017311840 scopus 로고
    • Human malaria parasites in continuous culture
    • 781840 10.1126/science.781840 1:STN:280:DyaE283ks1Wqug%3D%3D
    • Trager W, Jensen J (1976) Human malaria parasites in continuous culture. Science 193:673-675
    • (1976) Science , vol.193 , pp. 673-675
    • Trager, W.1    Jensen, J.2
  • 54
    • 46449136571 scopus 로고    scopus 로고
    • A simple biphasic route to water soluble dithiocarbamate functionalized quantum dots
    • 10.1039/b803618g 1:CAS:528:DC%2BD1cXnvFygsL0%3D
    • Wang J, Xu J, Goodman MD, Chen Y, Cai M, Shinar J, Lin Z (2008) A simple biphasic route to water soluble dithiocarbamate functionalized quantum dots. J Mater Chem 18:3270-3274
    • (2008) J Mater Chem , vol.18 , pp. 3270-3274
    • Wang, J.1    Xu, J.2    Goodman, M.D.3    Chen, Y.4    Cai, M.5    Shinar, J.6    Lin, Z.7
  • 55
    • 0032533882 scopus 로고    scopus 로고
    • Analysis of the Dithiocarbamate Fungicides Ziram, Maneb, and Zineb and the Flotation Agent Ethylxanthogenate by Ion-Pair Reversed-Phase HPLC
    • 10.1021/ac980626w 1:CAS:528:DyaK1cXmsVKqtL8%3D
    • Weissmahr KW, Houghton CL, Sedlak DL (1998) Analysis of the Dithiocarbamate Fungicides Ziram, Maneb, and Zineb and the Flotation Agent Ethylxanthogenate by Ion-Pair Reversed-Phase HPLC. Anal Chem 70:4800-4804
    • (1998) Anal Chem , vol.70 , pp. 4800-4804
    • Weissmahr, K.W.1    Houghton, C.L.2    Sedlak, D.L.3
  • 57
    • 0242484473 scopus 로고
    • The synthesis of some dialkylaminoalkyl arylthiourethans and thioureas1
    • 10.1021/ja01855a068 1:CAS:528:DyaH38XislWm
    • Wood TF, Gardner JH (1941) The synthesis of some dialkylaminoalkyl arylthiourethans and thioureas1. J Am Chem Soc 63:2741-2742
    • (1941) J Am Chem Soc , vol.63 , pp. 2741-2742
    • Wood, T.F.1    Gardner, J.H.2
  • 58
    • 0037147596 scopus 로고    scopus 로고
    • Studies on synthesis and biological activities of novel triazole compounds containing N, N-dialkyldithiocarbamate
    • 10.5012/bkcs.2002.23.12.1699 1:CAS:528:DC%2BD3sXis1OhsQ%3D%3D
    • Xu LZ, Jiao K, Zhang SS, Kuang SP (2002) Studies on synthesis and biological activities of novel triazole compounds containing N, N-dialkyldithiocarbamate. Bull Korean Chem Soc 23:1699
    • (2002) Bull Korean Chem Soc , vol.23 , pp. 1699
    • Xu, L.Z.1    Jiao, K.2    Zhang, S.S.3    Kuang, S.P.4
  • 59
    • 0030802574 scopus 로고    scopus 로고
    • On the trail of xanthates: Some new chemistry from an old functional group
    • 10.1002/anie.199706721
    • Zard SZ (1997) On the trail of xanthates: some new chemistry from an old functional group. Angew Chem Int Ed Engl 36:672-685
    • (1997) Angew Chem Int Ed Engl , vol.36 , pp. 672-685
    • Zard, S.Z.1
  • 60
    • 14944342626 scopus 로고    scopus 로고
    • Facile synthesis of novel ionic liquids containing dithiocarbamate
    • 10.1081/SCC-200049773 1:CAS:528:DC%2BD2MXis1yltL8%3D
    • Zhang D, Chen J, Liang Y, Zhou H (2005) Facile synthesis of novel ionic liquids containing dithiocarbamate. Synth Commun 35:521-526
    • (2005) Synth Commun , vol.35 , pp. 521-526
    • Zhang, D.1    Chen, J.2    Liang, Y.3    Zhou, H.4


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