메뉴 건너뛰기




Volumn 80, Issue 4, 2012, Pages 789-823

Biological activities of 2-mercaptobenzothiazole derivatives: A review

Author keywords

2 mercaptobenzothiazoles (mbt); 2 sulfanyl 1; 3 benzothiazoles; Anti inflammatory activity; Antimicrobial activity; Heat shock protein 90; Monoamine oxidase

Indexed keywords

2 MERCAPTOBENZOTHIAZOLE; 2 MERCAPTOBENZOTHIAZOLE DERIVATIVE; AMINE OXIDASE (FLAVIN CONTAINING); ARACHIDONATE 5 LIPOXYGENASE; CARBONATE DEHYDRATASE; CATHEPSIN D; CHEMOKINE RECEPTOR CCR3; CHOLESTEROL ACYLTRANSFERASE; CYCLOOXYGENASE 2; ERGOSTEROL; HEAT SHOCK PROTEIN 90; LEUKOTRIENE; OMEPRAZOLE; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR; SEROTONIN 1A RECEPTOR; STRESS ACTIVATED PROTEIN KINASE; UNCLASSIFIED DRUG;

EID: 84870901194     PISSN: 00368709     EISSN: 22180532     Source Type: Journal    
DOI: 10.3797/scipharm.1204-27     Document Type: Review
Times cited : (103)

References (127)
  • 2
    • 34548448749 scopus 로고
    • 3-(2-Alkylthio-6-benzothiazolylamino-methyl)-6-bromo-2-benzothiazohnones and their antimicrobial activity
    • http://dx.doi.org/10.1002/chin.199119162
    • Holbova E, Sidoova E, Zemanova M, Drobnicova I. 3-(2-Alkylthio-6-benzothiazolylamino-methyl)-6-bromo-2-benzothiazohnones and their antimicrobial activity. Chem Papers. 1990; 44: 363-368. http://dx.doi.org/10.1002/chin.199119162
    • (1990) Chem Papers , vol.44 , pp. 363-368
    • Holbova, E.1    Sidoova, E.2    Zemanova, M.3    Drobnicova, I.4
  • 3
    • 0010188964 scopus 로고    scopus 로고
    • S-Acyl derivatives of benzothiazole-2-thiol: A convenient method for the synthesis of amides and carbamates
    • http://dx.doi.org/10.1002/chin.199742171
    • Lee JH, Kim JD. S-Acyl derivatives of benzothiazole-2-thiol: A convenient method for the synthesis of amides and carbamates. Bull Korean Chem Soc. 1997; 18: 442-443. http://dx.doi.org/10.1002/chin.199742171
    • (1997) Bull Korean Chem Soc , vol.18 , pp. 442-443
    • Lee, J.H.1    Kim, J.D.2
  • 4
    • 0035200947 scopus 로고    scopus 로고
    • Efficient synthesis of 2-(thiocyanomethylthio) benzothiazole
    • http://dx.doi.org/10.1002/chin.199713098
    • Muthusubramanian L, Rao VS, Mitra RB. Efficient synthesis of 2-(thiocyanomethylthio) benzothiazole. J Cleaner Prod. 2001; 9: 65-67. http://dx.doi.org/10.1002/chin.199713098
    • (2001) J Cleaner Prod , vol.9 , pp. 65-67
    • Muthusubramanian, L.1    Rao, V.S.2    Mitra, R.B.3
  • 5
    • 0033020475 scopus 로고    scopus 로고
    • Convenient synthesis of chloromethyl thioaromatics
    • http://dx.doi.org/10.1080/00397919908086063
    • Ramadas K, Janarthanan N. Convenient synthesis of chloromethyl thioaromatics. Synth Commun. 1999; 29: 1003-1007. http://dx.doi.org/10.1080/00397919908086063
    • (1999) Synth Commun , vol.29 , pp. 1003-1007
    • Ramadas, K.1    Janarthanan, N.2
  • 6
    • 0344504628 scopus 로고
    • The preparation and properties of mercaptobenzothiazole, its homologs and derivatives
    • http://dx.doi.org/10.1021/ja01663a023
    • Sebrell LB, Boord CE. The preparation and properties of mercaptobenzothiazole, its homologs and derivatives. J Am Chem Soc. 1923; 45: 2390-2399. http://dx.doi.org/10.1021/ja01663a023
    • (1923) J Am Chem Soc , vol.45 , pp. 2390-2399
    • Sebrell, L.B.1    Boord, C.E.2
  • 7
    • 0346790175 scopus 로고
    • Researches on mercaptobenzothiazoles
    • http://dx.doi.org/10.1021/ja01406a015
    • Teppema J, Sebrell LB. Researches on mercaptobenzothiazoles. J Am Chem Soc. 1927; 49: 1748-1758. http://dx.doi.org/10.1021/ja01406a015
    • (1927) J Am Chem Soc , vol.49 , pp. 1748-1758
    • Teppema, J.1    Sebrell, L.B.2
  • 8
    • 1842397427 scopus 로고
    • A method for the preparation of 2-mercaptobenzothiazole
    • http://dx.doi.org/10.1021/ja01327a065
    • Dunbrook RF, Zimmermann MH. A method for the preparation of 2-mercaptobenzothiazole. J Am Chem Soc. 1934; 56: 2734-2736. http://dx.doi.org/10.1021/ja01327a065
    • (1934) J Am Chem Soc , vol.56 , pp. 2734-2736
    • Dunbrook, R.F.1    Zimmermann, M.H.2
  • 9
    • 84917773693 scopus 로고
    • http://dx.doi.org/10.1021/ie50294a006
    • Magill PL. Formamide. Ind Eng Chem. 1934; 26: 611-614. http://dx.doi.org/10.1021/ie50294a006
    • (1934) Formamide. Ind Eng Chem , vol.26 , pp. 611-614
    • Magill, P.L.1
  • 13
    • 77954557873 scopus 로고    scopus 로고
    • Dynamic covalent chemistry of disulfides offers a highly efficient synthesis of diverse benzofused nitrogen-sulfur heterocycles in one pot
    • http://dx.doi.org/10.1021/cc100042v
    • Zhu N, Zhang F, Liu G. Dynamic covalent chemistry of disulfides offers a highly efficient synthesis of diverse benzofused nitrogen-sulfur heterocycles in one pot. J Comb Chem. 2010; 12: 531-540. http://dx.doi.org/10.1021/cc100042v
    • (2010) J Comb Chem , vol.12 , pp. 531-540
    • Zhu, N.1    Zhang, F.2    Liu, G.3
  • 14
    • 5444239745 scopus 로고    scopus 로고
    • Ortho-selective nucleophilic aromatic substitution reactions of polyhaloanilines with potassium/sodium O-ethyl xanthate: A convenient access to halogenated 2(3H)-benzothiazolethiones
    • http://dx.doi.org/10.1021/jo049056s
    • Zhu L, Zhang M. Ortho-selective nucleophilic aromatic substitution reactions of polyhaloanilines with potassium/sodium O-ethyl xanthate: A convenient access to halogenated 2(3H)-benzothiazolethiones. J Org Chem. 2004; 69: 7371-7374. http://dx.doi.org/10.1021/jo049056s
    • (2004) J Org Chem , vol.69 , pp. 7371-7374
    • Zhu, L.1    Zhang, M.2
  • 15
    • 19644388300 scopus 로고    scopus 로고
    • A convenient synthesis of 2-mercapto and 2-chlorobenzothiazoles
    • http://dx.doi.org/10.1002/jhet.5570420440
    • Zhu L, Zhang M, Dai M. A convenient synthesis of 2-mercapto and 2-chlorobenzothiazoles. J Heterocycl Chem. 2005; 42: 727-730. http://dx.doi.org/10.1002/jhet.5570420440
    • (2005) J Heterocycl Chem , vol.42 , pp. 727-730
    • Zhu, L.1    Zhang, M.2    Dai, M.3
  • 16
    • 33846971212 scopus 로고    scopus 로고
    • Improved synthesis of 2-(3H) benzothiazolethiones under microwave irradiation
    • http://dx.doi.org/10.1080/00397910601038665
    • Hung W, Tan Y, Ding MW, Yang GF. Improved synthesis of 2-(3H) benzothiazolethiones under microwave irradiation. Synth Commun. 2007; 37: 369-376. http://dx.doi.org/10.1080/00397910601038665
    • (2007) Synth Commun , vol.37 , pp. 369-376
    • Hung, W.1    Tan, Y.2    Ding, M.W.3    Yang, G.F.4
  • 17
    • 33846970855 scopus 로고    scopus 로고
    • Fly-ash-supported synthesis of 2-mercaptobenzothiazole derivatives under microwave irradiation
    • http://dx.doi.org/10.1080/00397910601055073
    • Narkhede HP, More UB, Dalal DS, Pawar NS, Moore DH, Mahulika PP. Fly-ash-supported synthesis of 2-mercaptobenzothiazole derivatives under microwave irradiation. Synth Commun. 2007; 37: 573-577. http://dx.doi.org/10.1080/00397910601055073
    • (2007) Synth Commun , vol.37 , pp. 573-577
    • Narkhede, H.P.1    More, U.B.2    Dalal, D.S.3    Pawar, N.S.4    Moore, D.H.5    Mahulika, P.P.6
  • 18
    • 0029764388 scopus 로고    scopus 로고
    • Convenient strategies for the preparation of modified 2(3H)-benzothiazolethiones
    • http://dx.doi.org/10.1002/chin.199703174
    • Chaudhuri NC. Convenient strategies for the preparation of modified 2(3H)-benzothiazolethiones. Synth Commun. 1996; 26: 3783-3790. http://dx.doi.org/10.1002/chin.199703174
    • (1996) Synth Commun , vol.26 , pp. 3783-3790
    • Chaudhuri, N.C.1
  • 19
    • 0034729932 scopus 로고    scopus 로고
    • Synthesis and reactivity of benzoxa(thia)zol-2-thiones: New route to 2-alkylthiobenzoxa (thia)zoles
    • http://dx.doi.org/10.1002/chin.200042111
    • Harizi A, Romdhane A, Mighri Z. Synthesis and reactivity of benzoxa(thia)zol-2-thiones: new route to 2-alkylthiobenzoxa (thia)zoles. Tetrahedron Lett. 2000; 41: 5833-5835. http://dx.doi.org/10.1002/chin.200042111
    • (2000) Tetrahedron Lett , vol.41 , pp. 5833-5835
    • Harizi, A.1    Romdhane, A.2    Mighri, Z.3
  • 20
    • 79956128921 scopus 로고    scopus 로고
    • Synthesis of 2-thio-substituted benzothiazoles via a domino condensation/S-arylation/ heterocyclization process
    • http://dx.doi.org/dx.doi.org/10.1021/jo200535e
    • Shi L, Liu X, Zhang H, Jiang Y, Ma D. Synthesis of 2-thio-substituted benzothiazoles via a domino condensation/S-arylation/ heterocyclization process. J Org Chem. 2011; 76: 4200-4204. http://dx.doi.org/dx.doi.org/10.1021/jo200535e
    • (2011) J Org Chem , vol.76 , pp. 4200-4204
    • Shi, L.1    Liu, X.2    Zhang, H.3    Jiang, Y.4    Ma, D.5
  • 21
    • 79958858521 scopus 로고    scopus 로고
    • Synthesis of 2-mercaptobenzothiazoles via DBU-promoted tandem reaction of o-haloanilines and carbon disulfide
    • http://dx.doi.org/10.1021/ol2011105
    • Wang F, Cai S, Wang Z, Xi C. Synthesis of 2-mercaptobenzothiazoles via DBU-promoted tandem reaction of o-haloanilines and carbon disulfide. Org Lett. 2011; 13: 3202-3205. http://dx.doi.org/10.1021/ol2011105
    • (2011) Org Lett , vol.13 , pp. 3202-3205
    • Wang, F.1    Cai, S.2    Wang, Z.3    Xi, C.4
  • 22
    • 0031282209 scopus 로고    scopus 로고
    • Biodegradation and toxicity of benzothiazole
    • http://dx.doi.org/10.1016/S0043-1354(97)00138-3
    • Wever HD and Veractert H. Biodegradation and toxicity of benzothiazole. Wat Res. 1997; 31: 2673-2684. http://dx.doi.org/10.1016/S0043-1354(97)00138-3
    • (1997) Wat Res , vol.31 , pp. 2673-2684
    • Wever, H.D.1    Veractert, H.2
  • 23
    • 18744396703 scopus 로고    scopus 로고
    • Human health risk assessment of 2-mercaptobenzothiazole in drinking water
    • Whittaker MH, Gebhart AM, Miller TC, Hammer F. Human health risk assessment of 2-mercaptobenzothiazole in drinking water. Toxicol Ind Health. 2004; 20: 149-163. http://www.ncbi.nlm.nih.gov/pubmed/15941012
    • (2004) Toxicol Ind Health , vol.20 , pp. 149-163
    • Whittaker, M.H.1    Gebhart, A.M.2    Miller, T.C.3    Hammer, F.4
  • 24
    • 66149101235 scopus 로고    scopus 로고
    • Cancer risks in chemical production workers exposed to 2-mercaptobenzothiazole
    • http://dx.doi.org/10.1136/oem.2008.041400
    • Sorahan T. Cancer risks in chemical production workers exposed to 2-mercaptobenzothiazole. Occup Environ Med. 2009; 66: 269-273. http://dx.doi.org/10.1136/oem.2008.041400
    • (2009) Occup Environ Med , vol.66 , pp. 269-273
    • Sorahan, T.1
  • 25
    • 33947341255 scopus 로고
    • Researches on thiazoles. II. The nitration and reduction of 2-mercaptobenzothiazole and its substituted derivatives
    • http://dx.doi.org/10.1021/ja01406a018
    • Teppema J, Sebrell LB. Researches on thiazoles. II. The nitration and reduction of 2-mercaptobenzothiazole and its substituted derivatives. J Am Chem Soc. 1927; 9: 1779-1785. http://dx.doi.org/10.1021/ja01406a018
    • (1927) J Am Chem Soc , vol.9 , pp. 1779-1785
    • Teppema, J.1    Sebrell, L.B.2
  • 26
    • 0006746797 scopus 로고
    • The action of chlorine on 2-mercaptobenzothiazole in aqueous acetic acid
    • http://dx.doi.org/10.1021/ja01212a509
    • Findlay SP, Dougherty G. The action of chlorine on 2-mercaptobenzothiazole in aqueous acetic acid. J Am Chem Soc. 1946; 68: 1666-1666. http://dx.doi.org/10.1021/ja01212a509
    • (1946) J Am Chem Soc , vol.68 , pp. 1666
    • Findlay, S.P.1    Dougherty, G.2
  • 27
    • 4243593008 scopus 로고
    • 2-Mercaptobenzothiazole derivatives. Part I. The reaction of di(benzothiazol-2-yl) disulphide with olefins
    • http://dx.doi.org/10.1039/JR9520004232
    • Moore CG. 2-Mercaptobenzothiazole derivatives. Part I. The reaction of di(benzothiazol-2-yl) disulphide with olefins. J Chem Soc. 1952; 4232-4237. http://dx.doi.org/10.1039/JR9520004232
    • (1952) J Chem Soc , pp. 4232-4237
    • Moore, C.G.1
  • 28
    • 0001783277 scopus 로고
    • 2-Mercaptobenzothiazole derivatives. Part II. The thermal decomposition and isomerisation of 2-alkyl- and 2-alkenyl-thiobenzothiazoles and 3-alkyl- and 3-alkenyl-2-thiobenzothiazolines
    • http://dx.doi.org/10.1039/JR9520004237
    • Moore CG, Waight ES. 2-Mercaptobenzothiazole derivatives. Part II. The thermal decomposition and isomerisation of 2-alkyl- and 2-alkenyl-thiobenzothiazoles and 3-alkyl- and 3-alkenyl-2-thiobenzothiazolines. J Chem Soc. 1952; 4237-4251. http://dx.doi.org/10.1039/JR9520004237
    • (1952) J Chem Soc , pp. 4237-4251
    • Moore, C.G.1    Waight, E.S.2
  • 29
    • 33947448061 scopus 로고
    • Chloro-substituted unsaturated alkylmercapto thiazoles
    • http://dx.doi.org/10.1021/ja01099a050
    • D'Amico JJ. Chloro-substituted unsaturated alkylmercapto thiazoles. J Am Chem Soc. 1953; 75: 681-682. http://dx.doi.org/10.1021/ja01099a050
    • (1953) J Am Chem Soc , vol.75 , pp. 681-682
    • D'Amico, J.J.1
  • 30
    • 0343204283 scopus 로고
    • Derivatives of thiazolethiols
    • http://dx.doi.org/10.1021/ja01576a054
    • D'Amico JJ, Harman MW, Cooper RH. Derivatives of thiazolethiols. J Am Chem Soc. 1957; 79: 5270-5276. http://dx.doi.org/10.1021/ja01576a054
    • (1957) J Am Chem Soc , vol.79 , pp. 5270-5276
    • D'Amico, J.J.1    Harman, M.W.2    Cooper, R.H.3
  • 31
    • 37049065553 scopus 로고
    • The alkylation of mercaptobenzothiazoles
    • http://dx.doi.org/10.1039/JR9580000854
    • Morgan KJ. The alkylation of mercaptobenzothiazoles. J Chem Soc. 1958; 166: 854-858. http://dx.doi.org/10.1039/JR9580000854
    • (1958) J Chem Soc , vol.166 , pp. 854-858
    • Morgan, K.J.1
  • 32
    • 0001678050 scopus 로고
    • Study of the Michael and Mannich reactions with benzothiazole-2-thiol
    • http://dx.doi.org/10.1021/jo00804a006
    • Halasa AF, Smith GEP. Study of the Michael and Mannich reactions with benzothiazole-2-thiol. J Org Chem. 1971; 36: 636-641. http://dx.doi.org/10.1021/jo00804a006
    • (1971) J Org Chem , vol.36 , pp. 636-641
    • Halasa, A.F.1    Smith, G.E.P.2
  • 33
    • 84858188072 scopus 로고    scopus 로고
    • S-Acyl and N-acyl derivatives of benzothiazole-2-thiol: An example of acyl group rearrangement
    • http://dx.doi.org/10.1002/chin.200749151
    • Lee JH, Park SH, Lee H. S-Acyl and N-acyl derivatives of benzothiazole-2-thiol: An example of acyl group rearrangement. Bull Korean Chem Soc. 2007; 28: 1211-1214. http://dx.doi.org/10.1002/chin.200749151
    • (2007) Bull Korean Chem Soc , vol.28 , pp. 1211-1214
    • Lee, J.H.1    Park, S.H.2    Lee, H.3
  • 34
    • 0028107908 scopus 로고
    • A novel approach to cephalosporins from allenylazetidinones: A new cyclization strategy via tandem cuprate addition-sulfenylation
    • http://dx.doi.org/10.1021/jo00096a045
    • Kant J, Roth JA, Fuller CA, Walker DG, Benigni DA, Farina V. A novel approach to cephalosporins from allenylazetidinones: A new cyclization strategy via tandem cuprate addition-sulfenylation. J Org Chem. 1994; 59: 4956-4966. http://dx.doi.org/10.1021/jo00096a045
    • (1994) J Org Chem , vol.59 , pp. 4956-4966
    • Kant, J.1    Roth, J.A.2    Fuller, C.A.3    Walker, D.G.4    Benigni, D.A.5    Farina, V.6
  • 35
    • 70350165284 scopus 로고    scopus 로고
    • Intra- and intermolecular C-S bond formation using a single catalytic system: First direct access to arylthiobenzothiazoles
    • http://dx.doi.org/10.1021/ol9017535
    • Murru S, Ghosh H, Sahoo SK, Patel BK. Intra- and intermolecular C-S bond formation using a single catalytic system: First direct access to arylthiobenzothiazoles. Org Lett. 2009; 2: 4254-4257. http://dx.doi.org/10.1021/ol9017535
    • (2009) Org Lett , vol.2 , pp. 4254-4257
    • Murru, S.1    Ghosh, H.2    Sahoo, S.K.3    Patel, B.K.4
  • 36
    • 65249094847 scopus 로고    scopus 로고
    • Three-component synthesis of 2-aryl-4-arylthio-tetrahydro-2H-pyrans via the Prins cyclization
    • http://dx.doi.org/10.1016/j.tetlet.2009.03.176
    • Yadav JS, Reddy BVS, Reddy YJ, Reddy NS. Three-component synthesis of 2-aryl-4-arylthio-tetrahydro-2H-pyrans via the Prins cyclization. Tetrahedron Lett. 2009; 50: 2877-2880. http://dx.doi.org/10.1016/j.tetlet.2009.03.176
    • (2009) Tetrahedron Lett , vol.50 , pp. 2877-2880
    • Yadav, J.S.1    Reddy, B.V.S.2    Reddy, Y.J.3    Reddy, N.S.4
  • 37
    • 84961980729 scopus 로고    scopus 로고
    • Copper-mediated C-H activation/C-S cross-coupling of heterocycles with thiols
    • http://dx.doi.org/10.1021/jo2017444
    • Ranjit S, Lee R, Heryadi D, Shen C, Wu J, Zhang P, Huang KW, Liu X. Copper-mediated C-H activation/C-S cross-coupling of heterocycles with thiols. J Org Chem. 2011; 76: 8999-9007. http://dx.doi.org/10.1021/jo2017444
    • (2011) J Org Chem , vol.76 , pp. 8999-9007
    • Ranjit, S.1    Lee, R.2    Heryadi, D.3    Shen, C.4    Wu, J.5    Zhang, P.6    Huang, K.W.7    Liu, X.8
  • 38
    • 79956128921 scopus 로고    scopus 로고
    • Synthesis of 2-thio-substituted benzothiazoles via a domino condensation/S-arylation/heterocyclization process
    • http://dx.doi.org/10.1021/jo200535e
    • Shi L, Liu X, Zhang H, Jiang Y, Ma D. Synthesis of 2-thio-substituted benzothiazoles via a domino condensation/S-arylation/heterocyclization process. J Org Chem. 2011; 76: 4200-4204. http://dx.doi.org/10.1021/jo200535e
    • (2011) J Org Chem , vol.76 , pp. 4200-4204
    • Shi, L.1    Liu, X.2    Zhang, H.3    Jiang, Y.4    Ma, D.5
  • 39
    • 79957688474 scopus 로고    scopus 로고
    • S-arylation of mercaptobenzimidazoles using Cu(I) catalysts-experimental and theoretical observations
    • http://dx.doi.org/10.1002/chin.201142121
    • Sekar R, Srinivasan M, Marcelis ATM, Sambandam A. S-arylation of mercaptobenzimidazoles using Cu(I) catalysts-experimental and theoretical observations. Tetrahedron Lett. 2011; 52: 3347-3352. http://dx.doi.org/10.1002/chin.201142121
    • (2011) Tetrahedron Lett , vol.52 , pp. 3347-3352
    • Sekar, R.1    Srinivasan, M.2    Marcelis, A.T.M.3    Sambandam, A.4
  • 40
    • 84870915397 scopus 로고
    • US Patent 2,343,538, Mar. 7, 1944, Application No.: 366,885, Nov. 23
    • Ebelke WH. Thiazyl sulfamine derivatives. US Patent 2,343,538, Mar. 7, 1944, Application No.: 366,885, Nov. 23, 1940.
    • (1940) Thiazyl Sulfamine Derivatives
    • Ebelke, W.H.1
  • 41
    • 84870884848 scopus 로고
    • US Patent 2,304,568, Dec. 8, 1942, Application No.: 334,178, May 9
    • Hanalick RS. Vulcanization accelerator. US Patent 2,304,568, Dec. 8, 1942, Application No.: 334,178, May 9 1940.
    • (1940) Vulcanization Accelerator
    • Hanalick, R.S.1
  • 43
    • 84870887618 scopus 로고
    • US Patent 2,560,021, Jul. 10, 1951, Application No.: 100,594, June 21
    • Smith GEP. N-Isobutenyl-2-benzothiazole sulfenamide. US Patent 2,560,021, Jul. 10, 1951, Application No.: 100,594, June 21, 1949.
    • (1949) N-Isobutenyl-2-benzothiazole Sulfenamide
    • Smith, G.E.P.1
  • 44
    • 33947490158 scopus 로고
    • Derivatives of 1,1-dimethyl-3-oxobutylthiocyanate. I. 1,4-Dihydro-1-(2-mercaptobenzothiazol-6-yl)-2-thioxo-4,4,6-trimethylpyrimidine
    • http://dx.doi.org/10.1021/je60018a053
    • D'Amico JJ, Tung CC, Campbell RH, Mullins DD. Derivatives of 1,1-dimethyl-3-oxobutylthiocyanate. I. 1,4-Dihydro-1-(2-mercaptobenzothiazol-6-yl)-2-thioxo-4,4,6-trimethylpyrimidine. J Chem Eng Data. 1963; 8: 446-450. http://dx.doi.org/10.1021/je60018a053
    • (1963) J Chem Eng Data , vol.8 , pp. 446-450
    • D'Amico, J.J.1    Tung, C.C.2    Campbell, R.H.3    Mullins, D.D.4
  • 45
    • 0001309678 scopus 로고
    • 2-Substituted thiobenzothiazole and related compounds. I. Novel methods for the preparation of 2,2'-thiobis(benzothiazoles), 2-(N,N-disubstitued amino)benzothiazoles, and related compounds
    • http://dx.doi.org/10.1021/jo01022a010
    • D'Amico JJ, Webster ST, Campbell RH, Twine CE. 2-Substituted thiobenzothiazole and related compounds. I. Novel methods for the preparation of 2,2'-thiobis(benzothiazoles), 2-(N,N-disubstitued amino)benzothiazoles, and related compounds. J Org Chem. 1965; 30: 3625-3527. http://dx.doi.org/10.1021/jo01022a010
    • (1965) J Org Chem , vol.30 , pp. 3527-3625
    • D'Amico, J.J.1    Webster, S.T.2    Campbell, R.H.3    Twine, C.E.4
  • 48
    • 0018747812 scopus 로고
    • Antiviral activity of benzothiazole and benzothiazolinethione derivatives in cell cultures
    • Rada B, Holbova E, Mikulasek S, Sidoova E, Gvozdjakova A. Antiviral activity of benzothiazole and benzothiazolinethione derivatives in cell cultures. Acta Virol. 1979; 23: 203-209. http://www.ncbi.nlm.nih.gov/pubmed/41432
    • (1979) Acta Virol , vol.23 , pp. 203-209
    • Rada, B.1    Holbova, E.2    Mikulasek, S.3    Sidoova, E.4    Gvozdjakova, A.5
  • 49
    • 0024892287 scopus 로고
    • Inhibition of yeast-mycelium transformation by 2-alkylthio-6-amino- and 2-alkylthio-6-formamidobenzothiazoles and their in vitro antifungal activity
    • http://dx.doi.org/10.1007/BF02814461
    • Kuchta T, Bujdakova H, Sidoova E. Inhibition of yeast-mycelium transformation by 2-alkylthio-6-amino- and 2-alkylthio-6-formamidobenzothiazoles and their in vitro antifungal activity. Folia Microbiol. 1989; 34: 504-510. http://dx.doi.org/10.1007/BF02814461
    • (1989) Folia Microbiol , vol.34 , pp. 504-510
    • Kuchta, T.1    Bujdakova, H.2    Sidoova, E.3
  • 50
    • 0017888504 scopus 로고
    • Antimicrobial effects of some benzothiazole derivatives
    • Foltinova P, Sutoris V, Blockinger G, Ebringer L. Antimicrobial effects of some benzothiazole derivatives. Folia Microbiol. 1978; 23: 225-228. http://www.ncbi.nlm.nih.gov/pubmed/669490
    • (1978) Folia Microbiol , vol.23 , pp. 225-228
    • Foltinova, P.1    Sutoris, V.2    Blockinger, G.3    Ebringer, L.4
  • 51
    • 0040621083 scopus 로고
    • Organic sulfur compounds
    • New York: Academic Press
    • Owens RG. Organic sulfur compounds. In: Fungicides, an advanced treatise. Volume II. New York: Academic Press, 1969: 161-165.
    • (1969) Fungicides, An Advanced Treatise , vol.2 , pp. 161-165
    • Owens, R.G.1
  • 52
    • 0343875958 scopus 로고
    • Prevention of the bacterial oxidation of rubber
    • http://dx.doi.org/10.1126/science.97.2510.144
    • Dimond AE, Horsfall JG. Prevention of the bacterial oxidation of rubber. Science. 1963; 97: 144-145. http://dx.doi.org/10.1126/science.97.2510.144
    • (1963) Science , vol.97 , pp. 144-145
    • Dimond, A.E.1    Horsfall, J.G.2
  • 54
    • 0027103741 scopus 로고
    • Ergosterol depletion and 4-methyl sterols accumulation in the yeast Saccharomyces cerevisiae treated with an antigungal, 6-amino-2-n-pentylthiobenzothiazole
    • Kutcha T, Bartkova K, Kubinec R. Ergosterol depletion and 4-methyl sterols accumulation in the yeast Saccharomyces cerevisiae treated with an antigungal, 6-amino-2-n-pentylthiobenzothiazole. Biochem Biophys Res Comm. 1992; 189: 85-91. http://www.ncbi.nlm.nih.gov/pubmed/1449509
    • (1992) Biochem Biophys Res Comm , vol.189 , pp. 85-91
    • Kutcha, T.1    Bartkova, K.2    Kubinec, R.3
  • 55
    • 0027971961 scopus 로고
    • Antifungal activity of a new benzothiazole derivative against Candida in vitro and in vivo
    • http://dx.doi.org/10.1016/0924-8579(94)90030-2
    • Bujdakova H, Muckova M. Antifungal activity of a new benzothiazole derivative against Candida in vitro and in vivo. Antimicrob Agents 1994; 4: 303-308. http://dx.doi.org/10.1016/0924-8579(94)90030-2
    • (1994) Antimicrob Agents , vol.4 , pp. 303-308
    • Bujdakova, H.1    Muckova, M.2
  • 56
    • 0029072581 scopus 로고
    • Inhibition of sterol 4-demethylation in Candida albicans by 6-amino-2-n-pentylthiobenzo- thiazole, a novel mechanism of action for an antifungal agent
    • http://dx.doi.org/10.1128/AAC.39.7.1538
    • Kuchta T, Leka C, Farkas P, Bujdakova H, Belajova E, Russel NJ. Inhibition of sterol 4-demethylation in Candida albicans by 6-amino-2-n-pentylthiobenzo- thiazole, a novel mechanism of action for an antifungal agent. Antimicrob Agents Chemother. 1995; 39: 1538-1541. http://dx.doi.org/10.1128/AAC.39.7.1538
    • (1995) Antimicrob Agents Chemother , vol.39 , pp. 1538-1541
    • Kuchta, T.1    Leka, C.2    Farkas, P.3    Bujdakova, H.4    Belajova, E.5    Russel, N.J.6
  • 57
    • 0027327305 scopus 로고
    • Anti-Candida activity of four antifungal benzothiazoles
    • http://dx.doi.org/10.1111/j.1574-6968.1993.tb06471.x
    • Budjakova H, Kuchta T, Sidoova E, Gvozdjakova A. Anti-Candida activity of four antifungal benzothiazoles. FEMS Microbiol Lett. 1993; 112: 329-334. http://dx.doi.org/10.1111/j.1574-6968.1993.tb06471.x
    • (1993) FEMS Microbiol Lett , vol.112 , pp. 329-334
    • Budjakova, H.1    Kuchta, T.2    Sidoova, E.3    Gvozdjakova, A.4
  • 58
    • 0029320521 scopus 로고
    • Efficacy of 6-amino-2-n-pentylthiobenzothiazole on Trichophyton in vitro and in vivo
    • Bujdakova H, Mackova M, Klobusicky M, Sidoova E. Efficacy of 6-amino-2-n-pentylthiobenzothiazole on Trichophyton in vitro and in vivo. Mycopathologia. 1995; 130: 141-145. http://www.ncbi.nlm.nih.gov/pubmed/7566067
    • (1995) Mycopathologia , vol.130 , pp. 141-145
    • Bujdakova, H.1    Mackova, M.2    Klobusicky, M.3    Sidoova, E.4
  • 59
    • 4344610021 scopus 로고    scopus 로고
    • New anti-Candidous 2-alkylthio-6-aminobenzothiazoles
    • http://dx.doi.org/10.3390/feb97p2
    • Sidoova E, Loos D, Budjakova H, Kallova J. New anti-Candidous 2-alkylthio-6-aminobenzothiazoles. Molecules. 1997; 2: 36-42. http://dx.doi.org/10.3390/feb97p2
    • (1997) Molecules , vol.2 , pp. 36-42
    • Sidoova, E.1    Loos, D.2    Budjakova, H.3    Kallova, J.4
  • 60
    • 0024617608 scopus 로고
    • Relation between the chemical structure of substances and their antimicrobial action against atypical strains. II. 6-acycloamido-2-alkylthiobenzothiazoles, quantitative relation to their effectiveness spectrum
    • Machacek M, Kunes J, Sidoova E, Odlerova Z, Waisser K. Relation between the chemical structure of substances and their antimicrobial action against atypical strains. II. 6-acycloamido-2-alkylthiobenzothiazoles, quantitative relation to their effectiveness spectrum. Cesk Farm. 1989; 38: 9-15. http://www.ncbi.nlm.nih.gov/pubmed/2743430
    • (1989) Cesk Farm , vol.38 , pp. 9-15
    • Machacek, M.1    Kunes, J.2    Sidoova, E.3    Odlerova, Z.4    Waisser, K.5
  • 61
    • 0028199903 scopus 로고
    • Correlation between biological activity and the structure of 6-amino-2-R-thiobenzothiazoles. Anti-yeast activity and inhibition of photochemical activity of chloroplasts
    • Kralova K, Bujdakova H, Kuchta T, Loos D. Correlation between biological activity and the structure of 6-amino-2-R-thiobenzothiazoles. Anti-yeast activity and inhibition of photochemical activity of chloroplasts. Pharmazie. 1994; 49: 460-461. http://www.ncbi.nlm.nih.gov/pubmed/8047551
    • (1994) Pharmazie , vol.49 , pp. 460-461
    • Kralova, K.1    Bujdakova, H.2    Kuchta, T.3    Loos, D.4
  • 62
    • 0024643447 scopus 로고
    • Inhibition of Candida albicans transformation from the yeast form to the mycelial form by 2-alkylthio-6-amino- and 2-alkylthio-6-formamido-benzothiazoles
    • Kuchta T, Strakova H, Sidoova E. [Inhibition of Candida albicans transformation from the yeast form to the mycelial form by 2-alkylthio-6-amino- and 2-alkylthio-6-formamido-benzothiazoles]. Cesk Farm. 1989; 38: 139-140. http://www.ncbi.nlm.nih.gov/pubmed/2673553
    • (1989) Cesk Farm , vol.38 , pp. 139-140
    • Kuchta, T.1    Strakova, H.2    Sidoova, E.3
  • 63
    • 4243510084 scopus 로고
    • Antimycobacterially active 2-alkylthio-6-formamidobenzothiazoles and 6-formamido-2-benzothiazolmethione
    • http://dx.doi.org/10.1002/chin.199119163
    • Sidoova E, Odlerova Z. Antimycobacterially active 2-alkylthio-6-formamidobenzothiazoles and 6-formamido-2-benzothiazolmethione. Chem Papers. 1990; 44: 375-380. http://dx.doi.org/10.1002/chin.199119163
    • (1990) Chem Papers , vol.44 , pp. 375-380
    • Sidoova, E.1    Odlerova, Z.2
  • 64
    • 0024214154 scopus 로고
    • Biological side-effects of potential anti-tubercular agents. XIV. Relation between the chemical structure, antitubercular activity and hepatotoxicity of 2-alkylthio-6-(2-chlorobenzamido) benzothiazoles
    • Waisser K, Dolezal M, Sidoova E, Odlerova Z, Drsata J. [Biological side-effects of potential anti-tubercular agents. XIV. Relation between the chemical structure, antitubercular activity and hepatotoxicity of 2-alkylthio-6-(2-chlorobenzamido) benzothiazoles]. Cesk Farm. 1988; 37: 437-439. http://www.ncbi.nlm.nih.gov/pubmed/3149912
    • (1988) Cesk Farm , vol.37 , pp. 437-439
    • Waisser, K.1    Dolezal, M.2    Sidoova, E.3    Odlerova, Z.4    Drsata, J.5
  • 65
    • 0024472011 scopus 로고
    • Antifungal activity of 6-acetamido-2-alkylthiobenzothiasoles in vitro
    • Kuchta T, Sidoova E. [Antifungal activity of 6-acetamido-2-alkylthiobenzothiasoles in vitro]. Cesk Farm. 1989; 38: 310-311. http://www.ncbi.nlm.nih.gov/pubmed/2611910
    • (1989) Cesk Farm , vol.38 , pp. 310-311
    • Kuchta, T.1    Sidoova, E.2
  • 66
    • 78651405064 scopus 로고
    • 3-Substituted 6-bromo-2-benzothiazolinones and their antialgal and plant growth regulating activity
    • http://dx.doi.org/10.1002/chin.199304170
    • Sidoova E, Gvozdjakova A, Kralova K, Mitterhauszerova L. 3-Substituted 6-bromo-2-benzothiazolinones and their antialgal and plant growth regulating activity. Chem Papers. 1992; 46: 112-115. http://dx.doi.org/10.1002/chin.199304170
    • (1992) Chem Papers , vol.46 , pp. 112-115
    • Sidoova, E.1    Gvozdjakova, A.2    Kralova, K.3    Mitterhauszerova, L.4
  • 67
    • 33750496902 scopus 로고    scopus 로고
    • Microwave-assisted, one pot synthesis and fungicidal activity of polyfluorinated 2-benzylthiobenzothiazoles
    • http://dx.doi.org/10.1016/j.bmc.2006.09.016
    • Huang W, Yang GF. Microwave-assisted, one pot synthesis and fungicidal activity of polyfluorinated 2-benzylthiobenzothiazoles. Bioorg Med Chem. 2006; 14: 8280-8285. http://dx.doi.org/10.1016/j.bmc.2006.09.016
    • (2006) Bioorg Med Chem , vol.14 , pp. 8280-8285
    • Huang, W.1    Yang, G.F.2
  • 68
    • 0028225665 scopus 로고
    • Antifungal activity of 3(2-alkylthio-6-benzothiazolylaminomethyl)-2-benzothiazolines in vitro
    • Bujdakova H, Kralova K, Sidoova E. Antifungal activity of 3(2-alkylthio-6-benzothiazolylaminomethyl)-2-benzothiazolines in vitro. Pharmzie. 1994; 49: 375-376. http://www.ncbi.nlm.nih.gov/pubmed/8016186
    • (1994) Pharmzie , vol.49 , pp. 375-376
    • Bujdakova, H.1    Kralova, K.2    Sidoova, E.3
  • 69
    • 0028872143 scopus 로고
    • Antifungal and antialgal activity of 3-(2-alkylthio-6-benzothiazolylaminomethyl)-2-benzoxazolinethiones
    • Bujdakova H, Kralova K, Sidoova E. Antifungal and antialgal activity of 3-(2-alkylthio-6-benzothiazolylaminomethyl)-2-benzoxazolinethiones. Pharmzie. 1995; 50: 156-158. http://www.ncbi.nlm.nih.gov/pubmed/7700973
    • (1995) Pharmzie , vol.50 , pp. 156-158
    • Bujdakova, H.1    Kralova, K.2    Sidoova, E.3
  • 70
    • 4344646711 scopus 로고    scopus 로고
    • 3-(2-Alkylsulfanyl-6-benzothiazolylaminomethyl)-2-benzoxazolethiones-synthesis and photosynthesis-inhibiting activity in spinach chloroplasts
    • http://dx.doi.org/10.3390/40300073
    • Sidoova E, Kralova K, Loos D. 3-(2-Alkylsulfanyl-6-benzothiazolylaminomethyl)-2-benzoxazolethiones-synthesis and photosynthesis-inhibiting activity in spinach chloroplasts. Molecules. 1999; 4: 73-80. http://dx.doi.org/10.3390/40300073
    • (1999) Molecules , vol.4 , pp. 73-80
    • Sidoova, E.1    Kralova, K.2    Loos, D.3
  • 71
    • 4344575702 scopus 로고    scopus 로고
    • Synthesis of 2-(6-acetamidobenzothiazolethio)acetic acid esters as photosynthesis inhibitors
    • http://dx.doi.org/10.3390/30400135
    • Sidoova E, Kralova K, Loos D. Synthesis of 2-(6-acetamidobenzothiazolethio)acetic acid esters as photosynthesis inhibitors. Molecules. 1998; 3: 135-140. http://dx.doi.org/10.3390/30400135
    • (1998) Molecules , vol.3 , pp. 135-140
    • Sidoova, E.1    Kralova, K.2    Loos, D.3
  • 72
    • 0024897404 scopus 로고
    • Effects of nitrification inhibitors on germination of various seeds in soil
    • http://dx.doi.org/10.1007/BF00263170
    • Bremner JM, Krogmeier MJ. Effects of nitrification inhibitors on germination of various seeds in soil. Biol Fertil Soils. 1989; 8: 369-372. http://dx.doi.org/10.1007/BF00263170
    • (1989) Biol Fertil Soils , vol.8 , pp. 369-372
    • Bremner, J.M.1    Krogmeier, M.J.2
  • 73
    • 0023228430 scopus 로고
    • Relation between chemical structure, antitubercular activity and hepatotoxicity of 2-alkylthio-6-benzamidobenzothiazoles
    • Waisser K, Sidoova E, Odlerova Z, Gockeritz W, Drsata J. [Relation between chemical structure, antitubercular activity and hepatotoxicity of 2-alkylthio-6-benzamidobenzothiazoles]. Pharmazie. 1987; 42: 536-537. http://www.ncbi.nlm.nih.gov/pubmed/3124140
    • (1987) Pharmazie , vol.42 , pp. 536-537
    • Waisser, K.1    Sidoova, E.2    Odlerova, Z.3    Gockeritz, W.4    Drsata, J.5
  • 74
    • 0022003897 scopus 로고
    • Relation between the chemical structure of substances and their antimycobacterial activity against atypical strains. I. 2-Aklylthio-6-aminobenzothiazol
    • Sidoova E, Odlerova Z, Waisser K. [Relation between the chemical structure of substances and their antimycobacterial activity against atypical strains. I. 2-Aklylthio-6-aminobenzothiazol]. Cesk Farm. 1985; 34: 7-9. http://www.ncbi.nlm.nih.gov/pubmed/3986934
    • (1985) Cesk Farm , vol.34 , pp. 7-9
    • Sidoova, E.1    Odlerova, Z.2    Waisser, K.3
  • 75
    • 0009976079 scopus 로고
    • Correlation of structural parameters with antituberculotic activity in a group of 2-benzamidobenzothiazoles
    • http://dx.doi.org/10.1135/cccc19912978
    • Waisser K, Kunes J, Odlerova Z. Correlation of structural parameters with antituberculotic activity in a group of 2-benzamidobenzothiazoles. Collect Czech Chem Commun. 1991; 56: 2978-2985. http://dx.doi.org/10.1135/cccc19912978
    • (1991) Collect Czech Chem Commun , vol.56 , pp. 2978-2985
    • Waisser, K.1    Kunes, J.2    Odlerova, Z.3
  • 76
    • 0028000150 scopus 로고
    • Toxicity of 2-mercaptobenzothiazole towards bacterial growth and respiration
    • De Wever H, De Moor K, Verachtert H. Toxicity of 2-mercaptobenzothiazole towards bacterial growth and respiration. Appl Microbiol Biotechnol. 1994; 42: 631-635. http://www.ncbi.nlm.nih.gov/pubmed/7765737
    • (1994) Appl Microbiol Biotechnol , vol.42 , pp. 631-635
    • de Wever, H.1    de Moor, K.2    Verachtert, H.3
  • 77
    • 0014841196 scopus 로고
    • 2-Mercaptobenzothiazole, an inhibitor of dopamine fl-hydroxylase
    • Johnson GA, Boukma SJ, Platz PA. 2-Mercaptobenzothiazole, an inhibitor of dopamine fl-hydroxylase. J Pharm Pharmacol. 1970; 22: 710-712. http://www.ncbi.nlm.nih.gov/pubmed/4394766
    • (1970) J Pharm Pharmacol , vol.22 , pp. 710-712
    • Johnson, G.A.1    Boukma, S.J.2    Platz, P.A.3
  • 78
    • 0009632629 scopus 로고
    • Screening of tryptophan synthase inhibitors as leads of herbicide candidates
    • Shuto A, Ohgai M, Eto M. Screening of tryptophan synthase inhibitors as leads of herbicide candidates. J Pestic Sci. 1989; 14: 69-74.
    • (1989) J Pestic Sci , vol.14 , pp. 69-74
    • Shuto, A.1    Ohgai, M.2    Eto, M.3
  • 79
    • 0343120517 scopus 로고
    • The effect of selected industrial biocides on lactate metabolism in Desulfovibrio desulfuricans
    • Czechhowski M, Rossmoore HW. The effect of selected industrial biocides on lactate metabolism in Desulfovibrio desulfuricans. Dev Ind Microbiol. 1981; 22: 797-804.
    • (1981) Dev Ind Microbiol , vol.22 , pp. 797-804
    • Czechhowski, M.1    Rossmoore, H.W.2
  • 81
    • 0032029505 scopus 로고    scopus 로고
    • Synthesis, antimicrobial activity and bleaching effect of some reaction products of 4-oxa-4H-benzopyran-3-carboxaldehydes with aminobenzothiazoles and hydrazides
    • http://dx.doi.org/10.1002/chin.199836178
    • El-Shaaer HM, Foltinova P, Lacova M, Chovancova J, Stankovicova H. Synthesis, antimicrobial activity and bleaching effect of some reaction products of 4-oxa-4H-benzopyran-3-carboxaldehydes with aminobenzothiazoles and hydrazides. Farmaco. 1998; 53: 224-232. http://dx.doi.org/10.1002/chin.199836178
    • (1998) Farmaco , vol.53 , pp. 224-232
    • El-Shaaer, H.M.1    Foltinova, P.2    Lacova, M.3    Chovancova, J.4    Stankovicova, H.5
  • 82
    • 0345981079 scopus 로고    scopus 로고
    • Synthesis of some new 1-[5′-{(2-benzothiazolylthio) methyl}-1′,3′,4′-thiadiazol-2′-yl]-4-substituted-3-chloro-2-azetidinones: Antimicrobal agents
    • Guru N, Srivastava SD. Synthesis of some new 1-[5′-{(2-benzothiazolylthio) methyl}-1′,3′,4′-thiadiazol-2′-yl]-4-substituted-3-chloro-2-azetidinones: Antimicrobal agents. J Sci Ind Res. 2001; 60: 601-605.
    • (2001) J Sci Ind Res , vol.60 , pp. 601-605
    • Guru, N.1    Srivastava, S.D.2
  • 83
    • 2342640065 scopus 로고    scopus 로고
    • Synthesis of some new 2-mercaptobenzothiazolyl-2-oxoazetidines as antimicrobial and anthelmintic agents
    • http://dx.doi.org/10.1002/chin.200508138
    • Srivastava SK, Yadav R, Srivastava SD. Synthesis of some new 2-mercaptobenzothiazolyl-2-oxoazetidines as antimicrobial and anthelmintic agents. J Indian Chem Soc. 2004; 81: 342-343. http://dx.doi.org/10.1002/chin.200508138
    • (2004) J Indian Chem Soc , vol.81 , pp. 342-343
    • Srivastava, S.K.1    Yadav, R.2    Srivastava, S.D.3
  • 84
    • 28244482586 scopus 로고    scopus 로고
    • Rapid and efficient synthesis of some biological active 2-azetidinones under microwave irradiation
    • http://dx.doi.org/10.1002/chin.200605088
    • Desai KG, Desai KR. Rapid and efficient synthesis of some biological active 2-azetidinones under microwave irradiation. Indian J Chem. 2005; 44B: 2093-2096. http://dx.doi.org/10.1002/chin.200605088
    • (2005) Indian J Chem , vol.44 B , pp. 2093-2096
    • Desai, K.G.1    Desai, K.R.2
  • 85
    • 0037131751 scopus 로고    scopus 로고
    • Heterocyclic benzazole derivatives with antimycobacterial in vitro activity
    • http://dx.doi.org/10.1016/S0960-894X(02)00697-2
    • Koci J, Klimesova V, Waisser K, Kaustova J, Dahse HM, Mollmann U. Heterocyclic benzazole derivatives with antimycobacterial in vitro activity. Bioorg Med Chem Lett. 2002; 12: 3275-3278. http://dx.doi.org/10.1016/S0960-894X(02)00697-2
    • (2002) Bioorg Med Chem Lett , vol.12 , pp. 3275-3278
    • Koci, J.1    Klimesova, V.2    Waisser, K.3    Kaustova, J.4    Dahse, H.M.5    Mollmann, U.6
  • 86
    • 17844410934 scopus 로고    scopus 로고
    • Facile synthesis of 2-(substitutedbenzylsulfanyl)-benzothiazoles and their antimicrobial activity screening
    • http://dx.doi.org/10.1002/jhet.5570420124
    • Ramnathan VK, Kotha VSRSK, Kotarkonda RG. Facile synthesis of 2-(substitutedbenzylsulfanyl)-benzothiazoles and their antimicrobial activity screening. J Heterocycl Chem. 2005; 42: 153-156. http://dx.doi.org/10.1002/jhet.5570420124
    • (2005) J Heterocycl Chem , vol.42 , pp. 153-156
    • Ramnathan, V.K.1    Kotha, V.S.R.S.K.2    Kotarkonda, R.G.3
  • 87
    • 3142554176 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of some benzazole derivatives
    • http://dx.doi.org/10.1002/chin.200418107
    • Karali N, Cesur N, Gursoy A, Ates O, Ozden S, Otuk G, Birteksoz S. Synthesis and antimicrobial activity of some benzazole derivatives. Indian J Chem. 2004; 43B: 212-216. http://dx.doi.org/10.1002/chin.200418107
    • (2004) Indian J Chem , vol.43 B , pp. 212-216
    • Karali, N.1    Cesur, N.2    Gursoy, A.3    Ates, O.4    Ozden, S.5    Otuk, G.6    Birteksoz, S.7
  • 88
    • 33750496835 scopus 로고    scopus 로고
    • Neat reaction technology for the synthesis of 4-oxo-thiazolidines derived from 2-SH-benzothiazole and antimicrobial screening of some synthesized 4-thiazolidinones
    • Desai KG, Raval JP, Desai KR. Neat reaction technology for the synthesis of 4-oxo-thiazolidines derived from 2-SH-benzothiazole and antimicrobial screening of some synthesized 4-thiazolidinones. J Iranian Chem Soc. 2006; 3: 233-241.
    • (2006) J Iranian Chem Soc , vol.3 , pp. 233-241
    • Desai, K.G.1    Raval, J.P.2    Desai, K.R.3
  • 89
    • 1842710920 scopus 로고    scopus 로고
    • Synthesis and biological activity of 4-oxothiazolidines and their 5-arylidenes
    • http://dx.doi.org/10.1002/chin.200422150
    • Srivastava SK, Yadav R, Srivastava SD. Synthesis and biological activity of 4-oxothiazolidines and their 5-arylidenes. Indian J Chem. 2004; 43B: 399-405. http://dx.doi.org/10.1002/chin.200422150
    • (2004) Indian J Chem , vol.43 B , pp. 399-405
    • Srivastava, S.K.1    Yadav, R.2    Srivastava, S.D.3
  • 90
    • 23844499699 scopus 로고    scopus 로고
    • Synthesis, antimicrobial and anti-inflammatory activities of 4-oxothiazolidines and their 5-arylidenes
    • http://dx.doi.org/10.1002/chin.200544145
    • Yadav R, Srivastava SD, Srivastava SK. Synthesis, antimicrobial and anti-inflammatory activities of 4-oxothiazolidines and their 5-arylidenes. Indian J Chem. 2005; 44B: 1262-1266. http://dx.doi.org/10.1002/chin.200544145
    • (2005) Indian J Chem , vol.44 B , pp. 1262-1266
    • Yadav, R.1    Srivastava, S.D.2    Srivastava, S.K.3
  • 91
    • 0037294820 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of benzimidazole/benzothiazole and benzoxazole derivatives as cyclooxygenase inhibitors
    • http://dx.doi.org/10.1016/S0960-894X(02)01006-5
    • Paramshivappa R, Kumar PP, Rao PVS, Rao AS. Design, synthesis and biological evaluation of benzimidazole/benzothiazole and benzoxazole derivatives as cyclooxygenase inhibitors. Bioorg Med Chem Lett. 2003; 13: 657-660. http://dx.doi.org/10.1016/S0960-894X(02)01006-5
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 657-660
    • Paramshivappa, R.1    Kumar, P.P.2    Rao, P.V.S.3    Rao, A.S.4
  • 92
    • 84857234671 scopus 로고    scopus 로고
    • Alam MS. Synthesis of novel 2-mercaptobenzothiazole and 1,2,3-triazole based bis-heterocycles: Their anti-inflammatory and anti-nociceptive activities
    • http://dx.doi.org/10.1016/j.ejmech.2012.01.032
    • Shafi S, Alam MM, Mulakayala N, Mulakayala C, Vanaja G, Kalle AM, Pallu R, Alam MS. Synthesis of novel 2-mercaptobenzothiazole and 1,2,3-triazole based bis-heterocycles: Their anti-inflammatory and anti-nociceptive activities. Eur J Med Chem. 2012; 49: 324-333. http://dx.doi.org/10.1016/j.ejmech.2012.01.032
    • (2012) Eur J Med Chem , vol.49 , pp. 324-333
    • Shafi, S.1    Alam, M.M.2    Mulakayala, N.3    Mulakayala, C.4    Vanaja, G.5    Kalle, A.M.6    Pallu, R.7
  • 94
    • 0026775999 scopus 로고
    • Benzothiazole hydroxy ureas as inhibitors of 5-lipoxygenase: Use of the hydroxyurea moiety as a replacement for hydroxamic acid
    • http://dx.doi.org/10.1021/jm00095a012
    • Greco MN, Hageman WE, Powell ET, Tighe JJ, Persicot FJ. Benzothiazole hydroxy ureas as inhibitors of 5-lipoxygenase: Use of the hydroxyurea moiety as a replacement for hydroxamic acid. J Med Chem. 1992; 35: 3180-3183. http://dx.doi.org/10.1021/jm00095a012
    • (1992) J Med Chem , vol.35 , pp. 3180-3183
    • Greco, M.N.1    Hageman, W.E.2    Powell, E.T.3    Tighe, J.J.4    Persicot, F.J.5
  • 95
    • 30144433528 scopus 로고    scopus 로고
    • Chemical inhibitors of TNF signal transduction in human neutrophils point to distinct steps in cell activation
    • Han H, Roberts J, Lou O, Muller WA, Nathan N, Nathan C. Chemical inhibitors of TNF signal transduction in human neutrophils point to distinct steps in cell activation. J Leukoc Biol. 2006; 79: 147-154. http://www.ncbi.nlm.nih.gov/pubmed/16275893
    • (2006) J Leukoc Biol , vol.79 , pp. 147-154
    • Han, H.1    Roberts, J.2    Lou, O.3    Muller, W.A.4    Nathan, N.5    Nathan, C.6
  • 96
    • 77956921560 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of some novel 2-mercaptobenzothiazoles carrying 1,3,4-oxadiazole, 1,3,4-thiadiazole and 1,2,4-triazole moieties
    • Azam MA, Suresh B, Kalsi SS, Antony AS. Synthesis and biological evaluation of some novel 2-mercaptobenzothiazoles carrying 1,3,4-oxadiazole, 1,3,4-thiadiazole and 1,2,4-triazole moieties. S Afr J Chem. 2010; 63: 114-122.
    • (2010) S Afr J Chem , vol.63 , pp. 114-122
    • Azam, M.A.1    Suresh, B.2    Kalsi, S.S.3    Antony, A.S.4
  • 97
    • 79959431717 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of some 1,3,4-oxadiazole incorporated 2-mercaptobenzothiazoles
    • Azam MA, Suresh B, Thomas A. Synthesis and biological evaluation of some 1,3,4-oxadiazole incorporated 2-mercaptobenzothiazoles. Indian J Heterocycl Chem. 2010; 20: 77-80.
    • (2010) Indian J Heterocycl Chem , vol.20 , pp. 77-80
    • Azam, M.A.1    Suresh, B.2    Thomas, A.3
  • 98
    • 84856752951 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of some novel 2-mercaptobenzothiazoles carrying 2-pyrazoline
    • Azam MA, Suresh B. Synthesis and biological evaluation of some novel 2-mercaptobenzothiazoles carrying 2-pyrazoline. J Sci Ind Res. 2012: 71: 113-119.
    • (2012) J Sci Ind Res , vol.71 , pp. 113-119
    • Azam, M.A.1    Suresh, B.2
  • 101
    • 2742600319 scopus 로고    scopus 로고
    • Biological evaluation of some new nitrophenoxy/halophenoxyacetyl/propionyl-2-mercaptobenzothiazoles
    • http://dx.doi.org/10.1002/chin.199740156
    • Khare PK, Srivastava SD, Mukaraya DK. Biological evaluation of some new nitrophenoxy/halophenoxyacetyl/propionyl-2-mercaptobenzothiazoles. J Indian Chem Soc. 1996; 73: 627-628. http://dx.doi.org/10.1002/chin.199740156
    • (1996) J Indian Chem Soc , vol.73 , pp. 627-628
    • Khare, P.K.1    Srivastava, S.D.2    Mukaraya, D.K.3
  • 102
    • 0000293559 scopus 로고
    • Synthesis and studies of 3-[2-benzothiazolyl/benzoimidazolyl/benzoxazolylthio)methyl]-1,2,4-triazolo[3,4b][1,3,4]thiadiazole-6-yl substitutedphenyl as possible anthelmintics
    • http://dx.doi.org/10.1002/chin.199228162
    • Hussain MI, Kumar V. Synthesis and studies of 3-[2-benzothiazolyl/benzoimidazolyl/benzoxazolylthio)methyl]-1,2,4-triazolo[3,4b][1,3,4]thiadiazole-6-yl substitutedphenyl as possible anthelmintics. Indian J Chem. 1992; 31B: 673-676. http://dx.doi.org/10.1002/chin.199228162
    • (1992) Indian J Chem , vol.31 B , pp. 673-676
    • Hussain, M.I.1    Kumar, V.2
  • 103
    • 77956910903 scopus 로고
    • Synthesis and studies of (2-benzothiazolyl/benzimidazolyl/benzoxazolylthio)-acetic acid[(3-pyridyl)[substitutedphenyl)azo]methylenehydrazides as possible anthelmintics
    • http://dx.doi.org/10.1002/chin.199347198
    • Hussain MI, Kumar V. Synthesis and studies of (2-benzothiazolyl/benzimidazolyl/benzoxazolylthio)-acetic acid[(3-pyridyl)[substitutedphenyl)azo]methylenehydrazides as possible anthelmintics. Indian J Chem. 1993; 32B: 905-907. http://dx.doi.org/10.1002/chin.199347198
    • (1993) Indian J Chem , vol.32 B , pp. 905-907
    • Hussain, M.I.1    Kumar, V.2
  • 105
    • 0342707138 scopus 로고
    • Carbonic anhydrase inhibitors. I. Benzothiazole derivatives
    • http://dx.doi.org/10.1021/jo01105a053
    • Korman J. Carbonic anhydrase inhibitors. I. Benzothiazole derivatives. J Org Chem. 1958; 23: 1768-1771. http://dx.doi.org/10.1021/jo01105a053
    • (1958) J Org Chem , vol.23 , pp. 1768-1771
    • Korman, J.1
  • 111
    • 0348017505 scopus 로고    scopus 로고
    • Structure-activity relationships of 2-(benzothiazolylthio)acetamide class of CCR3 selective antagonist
    • http://dx.doi.org/10.1002/chin.200345213
    • Naya A, Kobayashi K, Ishikawa M, Ohwaki K, Saeki T, Noguchi K, Ohtake N. Structure-activity relationships of 2-(benzothiazolylthio)acetamide class of CCR3 selective antagonist. Chem Pharm Bull. 2003; 51: 697-701. http://dx.doi.org/10.1002/chin.200345213
    • (2003) Chem Pharm Bull , vol.51 , pp. 697-701
    • Naya, A.1    Kobayashi, K.2    Ishikawa, M.3    Ohwaki, K.4    Saeki, T.5    Noguchi, K.6    Ohtake, N.7
  • 112
    • 49449095466 scopus 로고    scopus 로고
    • Synthesis of new arylpiperazinylalkylthio-benzimidazole, benzothiazole or benzoxazole derivatives as potent and selective 5-HT1A serotonin receptor ligands
    • http://dx.doi.org/10.1021/jm800176x
    • Siracusa MA, Salerno L, Modica MN, Pittala V, Romeo G, Amato ME Nowak M, Bojarski AJ, Mereghetti I, Cagnotto A, Mennini T. Synthesis of new arylpiperazinylalkylthio-benzimidazole, benzothiazole or benzoxazole derivatives as potent and selective 5-HT1A serotonin receptor ligands. J Med Chem. 2008; 51: 4529-4538. http://dx.doi.org/10.1021/jm800176x
    • (2008) J Med Chem , vol.51 , pp. 4529-4538
    • Siracusa, M.A.1    Salerno, L.2    Modica, M.N.3    Pittala, V.4    Romeo, G.5    Amato, M.E.6    Nowak, M.7    Bojarski, A.J.8    Mereghetti, I.9    Cagnotto, A.10    Mennini, T.11
  • 113
    • 77949486625 scopus 로고    scopus 로고
    • A rationale for the activity profile of arylpiperazinylthioalkyls as 5-HT1A-serotonin and α1-adrenergic receptor ligands
    • http://dx.doi.org/10.1016/j.ejmech.2010.01.034
    • Sharma BK, Sarbhai K, Singh P. A rationale for the activity profile of arylpiperazinylthioalkyls as 5-HT1A-serotonin and α1-adrenergic receptor ligands. Eur J Med Chem. 2010; 45: 1927-1934. http://dx.doi.org/10.1016/j.ejmech.2010.01.034
    • (2010) Eur J Med Chem , vol.45 , pp. 1927-1934
    • Sharma, B.K.1    Sarbhai, K.2    Singh, P.3
  • 119
    • 70349638300 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2-mercapto-1,3-benzothiazole derivatives with potential antimicrobial activity
    • http://dx.doi.org/10.1002/ardp.200900092
    • Franchini C, Muraglia M, Corbo F, Florio MA, Mola AD, Rosato A, Matucci R, Nesi M, van Bambeke F, Vitali C. Synthesis and biological evaluation of 2-mercapto-1,3-benzothiazole derivatives with potential antimicrobial activity. Arch Pharm. 2009; 342: 605-613. http://dx.doi.org/10.1002/ardp.200900092
    • (2009) Arch Pharm , vol.342 , pp. 605-613
    • Franchini, C.1    Muraglia, M.2    Corbo, F.3    Florio, M.A.4    Mola, A.D.5    Rosato, A.6    Matucci, R.7    Nesi, M.8    van Bambeke, F.9    Vitali, C.10
  • 120
    • 79851516168 scopus 로고    scopus 로고
    • Synthesis, structure-activity relationships and preliminary antitumor evaluation of benzothiazole-2-thiol derivatives as novel apoptosis inducers
    • http://dx.doi.org/10.1016/j.bmcl.2010.12.124
    • Wang Z, Shi XH, Wangb J, Zhou T, Xu YZ, Huang TT, Li YF, Zhao YL, Yang L, Yang SY, Yu LT, Wei YQ. Synthesis, structure-activity relationships and preliminary antitumor evaluation of benzothiazole-2-thiol derivatives as novel apoptosis inducers. Bioorg Med Chem Lett. 2011; 21: 1097-1101. http://dx.doi.org/10.1016/j.bmcl.2010.12.124
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 1097-1101
    • Wang, Z.1    Shi, X.H.2    Wangb, J.3    Zhou, T.4    Xu, Y.Z.5    Huang, T.T.6    Li, Y.F.7    Zhao, Y.L.8    Yang, L.9    Yang, S.Y.10    Yu, L.T.11    Wei, Y.Q.12
  • 121
    • 26444495595 scopus 로고    scopus 로고
    • Inhibitors of apoptosis in lymphocytes: Synthesis and biological evaluation of compounds related to Pifithrin-α
    • http://dx.doi.org/10.1021/jm0502034
    • Barchechath SD, Tawatao RI, Corr M, Carson DA, Cottam HB. Inhibitors of apoptosis in lymphocytes: Synthesis and biological evaluation of compounds related to Pifithrin-α. J Med Chem. 2005; 48: 6409-6422. http://dx.doi.org/10.1021/jm0502034
    • (2005) J Med Chem , vol.48 , pp. 6409-6422
    • Barchechath, S.D.1    Tawatao, R.I.2    Corr, M.3    Carson, D.A.4    Cottam, H.B.5
  • 123
    • 0033530132 scopus 로고    scopus 로고
    • Synthesis and structure, activity relationships of novel small molecule cathepsin D inhibitors
    • http://dx.doi.org/10.1016/S0960-894X(99)00433-3
    • Dumas J, Brittelli D, Chen J, Dixon B, Hatoum-Mokdad H. Synthesis and structure, activity relationships of novel small molecule cathepsin D inhibitors. Bioorg Med Chem Lett. 1999; 9: 2531-2536. http://dx.doi.org/10.1016/S0960-894X(99)00433-3
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 2531-2536
    • Dumas, J.1    Brittelli, D.2    Chen, J.3    Dixon, B.4    Hatoum-Mokdad, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.