메뉴 건너뛰기




Volumn , Issue , 2013, Pages

Biological aspects of emerging benzothiazoles: A short review

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84885596231     PISSN: 20909063     EISSN: 20909071     Source Type: Journal    
DOI: 10.1155/2013/345198     Document Type: Review
Times cited : (74)

References (50)
  • 1
    • 79851516168 scopus 로고    scopus 로고
    • Synthesis, structure-activity relationships and preliminary antitumor evaluation of benzothiazole-2-thiol derivatives as novel apoptosis inducers
    • 2-s2.0-79851516168 10.1016/j.bmcl.2010.12.124
    • Wang Z., Shi X., Wang J., Zhou T., Xu Y.-Z., Huang T.-T., Li Y.-F., Zhao Y.-L., Yang L., Yang S.-Y., Yu L.-T., Wei Y.-Q., Synthesis, structure-activity relationships and preliminary antitumor evaluation of benzothiazole-2-thiol derivatives as novel apoptosis inducers. Bioorganic and Medicinal Chemistry Letters 2011 21 4 1097 1101 2-s2.0-79851516168 10.1016/j.bmcl.2010.12.124
    • (2011) Bioorganic and Medicinal Chemistry Letters , vol.21 , Issue.4 , pp. 1097-1101
    • Wang, Z.1    Shi, X.2    Wang, 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
  • 2
    • 84655163397 scopus 로고    scopus 로고
    • Synthesis and cytotoxic evaluation of thiourea and N -bis-benzothiazole derivatives: A novel class of cytotoxic agents
    • 2-s2.0-84655163397 10.1016/j.bmcl.2011.10.106
    • Kumbhare R. M., Dadmal T., Kosurkar U., Sridhar V., Rao J. V., Synthesis and cytotoxic evaluation of thiourea and N -bis-benzothiazole derivatives: a novel class of cytotoxic agents. Bioorganic and Medicinal Chemistry Letters 2012 22 1 453 455 2-s2.0-84655163397 10.1016/j.bmcl.2011.10.106
    • (2012) Bioorganic and Medicinal Chemistry Letters , vol.22 , Issue.1 , pp. 453-455
    • Kumbhare, R.M.1    Dadmal, T.2    Kosurkar, U.3    Sridhar, V.4    Rao, J.V.5
  • 3
    • 32144455908 scopus 로고    scopus 로고
    • Synthesis, X-ray crystallographic analysis, and antitumor activity of N-(benzothiazole-2-yl)-1-(fluorophenyl)-O,O-dialkyl-α-aminophosphonates
    • DOI 10.1016/j.bmcl.2005.12.041, PII S0960894X05015829
    • Jin L., Song B., Zhang G., Xu R., Zhang S., Gao X., Hu D., Yang S., Synthesis, X-ray crystallographic analysis, and antitumor activity of N -(benzothiazole-2-yl)-1-(fluorophenyl)- O, O -dialkyl- α -aminophosphonates. Bioorganic and Medicinal Chemistry Letters 2006 16 6 1537 1543 2-s2.0-32144455908 10.1016/j.bmcl.2005.12.041 (Pubitemid 43204236)
    • (2006) Bioorganic and Medicinal Chemistry Letters , vol.16 , Issue.6 , pp. 1537-1543
    • Jin, L.1    Song, B.2    Zhang, G.3    Xu, R.4    Zhang, S.5    Gao, X.6    Hu, D.7    Yang, S.8
  • 4
    • 77349118931 scopus 로고    scopus 로고
    • Synthesis, characterization and biological evaluation of some thiourea derivatives bearing benzothiazole moiety as potential antimicrobial and anticancer agents
    • 2-s2.0-77349118931 10.1016/j.ejmech.2009.12.016
    • Saeed S., Rashid N., Jones P. G., Ali M., Hussain R., Synthesis, characterization and biological evaluation of some thiourea derivatives bearing benzothiazole moiety as potential antimicrobial and anticancer agents. European Journal of Medicinal Chemistry 2010 45 4 1323 1331 2-s2.0-77349118931 10.1016/j.ejmech.2009.12.016
    • (2010) European Journal of Medicinal Chemistry , vol.45 , Issue.4 , pp. 1323-1331
    • Saeed, S.1    Rashid, N.2    Jones, P.G.3    Ali, M.4    Hussain, R.5
  • 5
    • 77957844111 scopus 로고    scopus 로고
    • Synthesis and anticancer activity evaluation of 4-thiazolidinones containing benzothiazole moiety
    • 2-s2.0-77957844111 10.1016/j.ejmech.2010.08.008
    • Havrylyuk D., Mosula L., Zimenkovsky B., Vasylenko O., Gzella A., Lesyk R., Synthesis and anticancer activity evaluation of 4-thiazolidinones containing benzothiazole moiety. European Journal of Medicinal Chemistry 2010 45 11 5012 5021 2-s2.0-77957844111 10.1016/j.ejmech.2010.08.008
    • (2010) European Journal of Medicinal Chemistry , vol.45 , Issue.11 , pp. 5012-5021
    • Havrylyuk, D.1    Mosula, L.2    Zimenkovsky, B.3    Vasylenko, O.4    Gzella, A.5    Lesyk, R.6
  • 6
    • 73949084441 scopus 로고    scopus 로고
    • Hybrid pharmacophore design and synthesis of isatin-benzothiazole analogs for their anti-breast cancer activity
    • 2-s2.0-73949084441 10.1016/j.bmc.2009.08.068
    • Solomon V. R., Hu C., Lee H., Hybrid pharmacophore design and synthesis of isatin-benzothiazole analogs for their anti-breast cancer activity. Bioorganic and Medicinal Chemistry Letters 2009 17 21 7585 7592 2-s2.0-73949084441 10.1016/j.bmc.2009.08.068
    • (2009) Bioorganic and Medicinal Chemistry Letters , vol.17 , Issue.21 , pp. 7585-7592
    • Solomon, V.R.1    Hu, C.2    Lee, H.3
  • 8
    • 84857519061 scopus 로고    scopus 로고
    • Synthesis and anticancer evaluation of 2-phenyl thiaolidinone substituted 2-phenyl benzothiazole-6-carboxylic acid derivatives
    • 2-s2.0-84857519061 10.1016/j.jscs.2012.02.001
    • Prabhu P., Panneerselvam T., Shastry C. S., Sivakumar A., Pande S., Synthesis and anticancer evaluation of 2-phenyl thiaolidinone substituted 2-phenyl benzothiazole-6-carboxylic acid derivatives. Journal of Saudi Chemical Society 2012 2-s2.0-84857519061 10.1016/j.jscs.2012.02.001
    • (2012) Journal of Saudi Chemical Society
    • Prabhu, P.1    Panneerselvam, T.2    Shastry, C.S.3    Sivakumar, A.4    Pande, S.5
  • 10
    • 38349165553 scopus 로고    scopus 로고
    • A QSAR study and molecular design of benzothiazole derivatives as potent anticancer agents
    • 2-s2.0-38349165553 10.1007/s11426-007-0107-8
    • Chen J., Qian L., Shen Y., Chen L., Zheng K., A QSAR study and molecular design of benzothiazole derivatives as potent anticancer agents. Science in China B 2008 51 2 111 119 2-s2.0-38349165553 10.1007/s11426-007-0107-8
    • (2008) Science in China B , vol.51 , Issue.2 , pp. 111-119
    • Chen, J.1    Qian, L.2    Shen, Y.3    Chen, L.4    Zheng, K.5
  • 11
    • 30444437324 scopus 로고    scopus 로고
    • 1 2-(3,4-dimethoxyphenyl)-5- fluorobenzothiazole (GW 610, NSC 721648), a simple fluorinated 2-arylbenzothiazole, shows potent and selective inhibitory activity against lung, colon, and breast cancer cell lines
    • DOI 10.1021/jm050942k
    • Mortimer C. G., Wells G., Crochard J., Stone E. L., Bradshaw T. D., Stevens M. F. G., Westwell A. D., Antitumor benzothiazoles. 26.1 2-(3,4-dimethoxyphenyl)-5- fluorobenzothiazole (GW 610, NSC 721648), a simple fluorinated 2-arylbenzothiazole, shows potent and selective inhibitory activity against lung, colon, and breast cancer cell lines. Journal of Medicinal Chemistry 2006 49 1 179 185 2-s2.0-30444437324 10.1021/jm050942k (Pubitemid 43077331)
    • (2006) Journal of Medicinal Chemistry , vol.49 , Issue.1 , pp. 179-185
    • Mortimer, C.G.1    Wells, G.2    Crochard, J.-P.3    Stone, E.L.4    Bradshaw, T.D.5    Stevens, M.F.G.6    Westwell, A.D.7
  • 14
    • 84871443319 scopus 로고    scopus 로고
    • A facile green synthesis and in vitro antimicrobial activity 4H-pyrimido[2,1-b][1,3]benzothiazole derivatives using aluminum trichloride under solvent free conditions
    • 2-s2.0-82755167926 10.1007/s00044-011-9908-6
    • Sahu P. K., Sahu P. K., Lal J., Thavaselvam D., Agarwal D., A facile green synthesis and in vitro antimicrobial activity 4H-pyrimido[2,1-b][1,3] benzothiazole derivatives using aluminum trichloride under solvent free conditions. Medicinal Chemistry Research 2012 21 11 3826 3834 2-s2.0-82755167926 10.1007/s00044-011-9908-6
    • (2012) Medicinal Chemistry Research , vol.21 , Issue.11 , pp. 3826-3834
    • Sahu, P.K.1    Sahu, P.K.2    Lal, J.3    Thavaselvam, D.4    Agarwal, D.5
  • 15
    • 84861918298 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of pyrazolinones and pyrazoles having benzothiazole moiety
    • 2-s2.0-79953701971 10.1007/s00044-011-9642-0
    • Amir M., Javed S. A., Zaheen Hassan M., Synthesis and antimicrobial activity of pyrazolinones and pyrazoles having benzothiazole moiety. Medicinal Chemistry Research 2012 21 7 1261 1270 2-s2.0-79953701971 10.1007/s00044-011- 9642-0
    • (2012) Medicinal Chemistry Research , vol.21 , Issue.7 , pp. 1261-1270
    • Amir, M.1    Javed, S.A.2    Zaheen Hassan, M.3
  • 16
    • 85027927846 scopus 로고    scopus 로고
    • Synthesis, characterization and antimicrobial activity of thiazole, benzothiazole and pyrimidine derivatives bearing sydnone moieties
    • 2-s2.0-84859507703 10.1007/s11094-012-0712-5
    • Asundaria S. T., Patel K. C., Synthesis, characterization and antimicrobial activity of thiazole, benzothiazole and pyrimidine derivatives bearing sydnone moieties. Pharmaceutical Chemistry Journal 2012 45 12 725 731 2-s2.0-84859507703 10.1007/s11094-012-0712-5
    • (2012) Pharmaceutical Chemistry Journal , vol.45 , Issue.12 , pp. 725-731
    • Asundaria, S.T.1    Patel, K.C.2
  • 17
    • 84871431899 scopus 로고    scopus 로고
    • Synthesis of novel 2-[4-(4-substitutedbenzamido/phenylacetamido)phenyl] benzothiazoles as antimicrobial agents
    • 2-s2.0-82655178442 10.1007/s00044-011-9918-4
    • Bolelli K., Yalcin I., Ertan-Bolelli T., Özgen S., Kaynak-Onurdag F., Yildiz I., Aki E., Synthesis of novel 2-[4-(4-substitutedbenzamido/ phenylacetamido)phenyl]benzothiazoles as antimicrobial agents. Medicinal Chemistry Research 2012 21 11 3818 3825 2-s2.0-82655178442 10.1007/s00044-011- 9918-4
    • (2012) Medicinal Chemistry Research , vol.21 , Issue.11 , pp. 3818-3825
    • Bolelli, K.1    Yalcin, I.2    Ertan-Bolelli, T.3    Özgen, S.4    Kaynak-Onurdag, F.5    Yildiz, I.6    Aki, E.7
  • 18
    • 79952039611 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of 2H-pyrimido[2,1-b]benzothiazol-2- ones
    • 2-s2.0-79952039611 10.1007/s11164-010-0211-9
    • Sharma P. K., Kumar M., Mohan V., Synthesis and antimicrobial activity of 2H-pyrimido[2,1-b]benzothiazol-2- ones. Research on Chemical Intermediates 2010 36 8 985 993 2-s2.0-79952039611 10.1007/s11164-010-0211-9
    • (2010) Research on Chemical Intermediates , vol.36 , Issue.8 , pp. 985-993
    • Sharma, P.K.1    Kumar, M.2    Mohan, V.3
  • 19
    • 34047153255 scopus 로고    scopus 로고
    • 3D-QSAR and molecular docking studies on benzothiazole derivatives as Candida albicans N-myristoyltransferase inhibitors
    • DOI 10.1016/j.ejmech.2006.11.001, PII S0223523406003928
    • Sheng C., Zhu J., Zhang W., Zhang M., Ji H., Song Y., Xu H., Yao J., Miao Z., Zhou Y., Zhu J., Lü J., 3D-QSAR and molecular docking studies on benzothiazole derivatives as Candida albicans N -myristoyltransferase inhibitors. European Journal of Medicinal Chemistry 2007 42 4 477 486 2-s2.0-34047153255 10.1016/j.ejmech.2006.11.001 (Pubitemid 46517787)
    • (2007) European Journal of Medicinal Chemistry , vol.42 , Issue.4 , pp. 477-486
    • Sheng, C.1    Zhu, J.2    Zhang, W.3    Zhang, M.4    Ji, H.5    Song, Y.6    Xu, H.7    Yao, J.8    Miao, Z.9    Zhou, Y.10    Zhu, J.11    Lu, J.12
  • 20
    • 77954349191 scopus 로고    scopus 로고
    • Synthesis and evaluation of some new benzothiazole derivatives as potential antimicrobial agents
    • 2-s2.0-77954349191 10.1016/j.ejmech.2010.03.019
    • Soni B. S., Ranawat M., Sharma R., Bhandari A., Sharma S., Synthesis and evaluation of some new benzothiazole derivatives as potential antimicrobial agents. European Journal of Medicinal Chemistry 2010 45 7 2938 2942 2-s2.0-77954349191 10.1016/j.ejmech.2010.03.019
    • (2010) European Journal of Medicinal Chemistry , vol.45 , Issue.7 , pp. 2938-2942
    • Soni, B.S.1    Ranawat, M.2    Sharma, R.3    Bhandari, A.4    Sharma, S.5
  • 21
    • 84864412588 scopus 로고    scopus 로고
    • Synthesis and evaluation of antimicrobial activity of 4H-pyrimido[2,1-b] benzothiazole, pyrazole and benzylidene derivatives of curcumin
    • Sahu P. K., Sahu P. K., Gupta S. K., Thavaselvam D., Agarwal D. D., Synthesis and evaluation of antimicrobial activity of 4H-pyrimido[2,1-b] benzothiazole, pyrazole and benzylidene derivatives of curcumin. European Journal of Medicinal Chemistry 2012 54 366 378
    • (2012) European Journal of Medicinal Chemistry , vol.54 , pp. 366-378
    • Sahu, P.K.1    Sahu, P.K.2    Gupta, S.K.3    Thavaselvam, D.4    Agarwal, D.D.5
  • 22
    • 84946496007 scopus 로고    scopus 로고
    • Synthesis, characterization and comparative study the microbial activity of some heterocyclic compounds containing oxazole and benzothiazole moieties
    • 10.1016/j.jscs.2012.04.010
    • Tomi I. H. R., Tomma J. H., Daraji A., Al-Dujaili A., Synthesis, characterization and comparative study the microbial activity of some heterocyclic compounds containing oxazole and benzothiazole moieties. Journal of Saudi Chemical Society 2012 10.1016/j.jscs.2012.04.010
    • (2012) Journal of Saudi Chemical Society
    • Tomi, I.H.R.1    Tomma, J.H.2    Daraji, A.3    Al-Dujaili, A.4
  • 23
    • 84855579910 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of novel 2-substituted benzimidazole, benzoxazole and benzothiazole derivatives
    • 2-s2.0-84855579910 10.1016/j.arabjc.2011.12.006
    • Padalkar V. S., Borse B. N., Gupta V. D., Phatangare K. R., Patil V. S., Umape P. G., Sekar N., Synthesis and antimicrobial activity of novel 2-substituted benzimidazole, benzoxazole and benzothiazole derivatives. Arabian Journal of Chemistry 2012 2-s2.0-84855579910 10.1016/j.arabjc.2011.12.006
    • (2012) Arabian Journal of Chemistry
    • Padalkar, V.S.1    Borse, B.N.2    Gupta, V.D.3    Phatangare, K.R.4    Patil, V.S.5    Umape, P.G.6    Sekar, N.7
  • 24
    • 84861564569 scopus 로고    scopus 로고
    • Benzothiazole incorporated thiazolidin-4-ones and azetidin-2-ones derivatives: Synthesis and in vitro antimicrobial evaluation
    • 10.1016/j.arabjc.2012.04.004
    • Gilani S., Nagarajan K., Dixit S. P., Taleuzzaman M., Khan S. A., Benzothiazole incorporated thiazolidin-4-ones and azetidin-2-ones derivatives: synthesis and in vitro antimicrobial evaluation. Arabian Journal of Medicinal Chemistry 2012 10.1016/j.arabjc.2012.04.004
    • (2012) Arabian Journal of Medicinal Chemistry
    • Gilani, S.1    Nagarajan, K.2    Dixit, S.P.3    Taleuzzaman, M.4    Khan, S.A.5
  • 25
    • 84866352524 scopus 로고    scopus 로고
    • Synthesis of benzothiazole derivatives having acetamido and carbothioamido pharmacophore as anticonvulsant agents
    • 2-s2.0-80052770018 10.1007/s00044-011-9791-1
    • Amir M., Asif S., Ali I., Hassan M. Z., Synthesis of benzothiazole derivatives having acetamido and carbothioamido pharmacophore as anticonvulsant agents. Medicinal Chemistry Research 2012 21 9 2661 2670 2-s2.0-80052770018 10.1007/s00044-011-9791-1
    • (2012) Medicinal Chemistry Research , vol.21 , Issue.9 , pp. 2661-2670
    • Amir, M.1    Asif, S.2    Ali, I.3    Hassan, M.Z.4
  • 26
    • 84866392970 scopus 로고    scopus 로고
    • Design, synthesis, and anticonvulsant evaluation of some novel 1, 3 benzothiazol-2-yl hydrazones/acetohydrazones
    • 2-s2.0-79961107382 10.1007/s00044-011-9768-0
    • Kumar P., Shrivastava B., Pandeya S. N., Tripathi L., Stables J. P., Design, synthesis, and anticonvulsant evaluation of some novel 1, 3 benzothiazol-2-yl hydrazones/acetohydrazones. Medicinal Chemistry Research 2012 21 9 2428 2442 2-s2.0-79961107382 10.1007/s00044-011-9768-0
    • (2012) Medicinal Chemistry Research , vol.21 , Issue.9 , pp. 2428-2442
    • Kumar, P.1    Shrivastava, B.2    Pandeya, S.N.3    Tripathi, L.4    Stables, J.P.5
  • 27
    • 84881125748 scopus 로고    scopus 로고
    • Synthesis of substituted benzo[ d ]thiazol-2-ylcarbamates as potential anticonvulsants
    • 10.1007/s00044-012-0434-y
    • Navale A., Pawar S., Deodhar M., Kale A., Synthesis of substituted benzo[ d ]thiazol-2-ylcarbamates as potential anticonvulsants. Medicinal Chemistry Research 2013 22 9 4316 4321 10.1007/s00044-012-0434-y
    • (2013) Medicinal Chemistry Research , vol.22 , Issue.9 , pp. 4316-4321
    • Navale, A.1    Pawar, S.2    Deodhar, M.3    Kale, A.4
  • 29
    • 42949094253 scopus 로고    scopus 로고
    • N-{[(6-Substituted-1,3-benzothiazole-2-yl)amino]carbonothioyl}-2/ 4-substituted benzamides: Synthesis and pharmacological evaluation
    • DOI 10.1016/j.ejmech.2007.07.008, PII S022352340700298X
    • Rana A., Siddiqui N., Khan S. A., Haque S. E., Bhat M. A., N -{[(6-Substituted-1,3-benzothiazole-2-yl)amino]carbonothioyl}-2/4-substituted benzamides: synthesis and pharmacological evaluation. European Journal of Medicinal Chemistry 2008 43 5 1114 1122 2-s2.0-42949094253 10.1016/j.ejmech. 2007.07.008 (Pubitemid 351615243)
    • (2008) European Journal of Medicinal Chemistry , vol.43 , Issue.5 , pp. 1114-1122
    • Rana, A.1    Siddiqui, N.2    Khan, S.A.3    Ehtaishamul Haque, S.4    Bhat, M.A.5
  • 30
    • 34347369280 scopus 로고    scopus 로고
    • Synthesis of benzothiazole semicarbazones as novel anticonvulsants-The role of hydrophobic domain
    • DOI 10.1016/j.bmcl.2007.05.048, PII S0960894X0700618X
    • Siddiqui N., Rana A., Khan S. A., Haque S. E., Bhat M. A., Synthesis of benzothiazole semicarbazones as novel anticonvulsants-the role of hydrophobic domain. Bioorganic and Medicinal Chemistry Letters 2007 17 15 4178 4182 2-s2.0-34347369280 10.1016/j.bmcl.2007.05.048 (Pubitemid 47021404)
    • (2007) Bioorganic and Medicinal Chemistry Letters , vol.17 , Issue.15 , pp. 4178-4182
    • Siddiqui, N.1    Rana, A.2    Khan, S.A.3    Bhat, M.A.4    Haque, S.E.5
  • 31
    • 72149100457 scopus 로고    scopus 로고
    • Synthesis, anticonvulsant activity and 3D-QSAR study of some prop-2-eneamido and 1-acetyl-pyrazolin derivatives of aminobenzothiazole
    • 2-s2.0-72149100457 10.1016/j.ejmech.2009.09.037
    • Amnerkar N. D., Bhusari K. P., Synthesis, anticonvulsant activity and 3D-QSAR study of some prop-2-eneamido and 1-acetyl-pyrazolin derivatives of aminobenzothiazole. European Journal of Medicinal Chemistry 2010 45 1 149 159 2-s2.0-72149100457 10.1016/j.ejmech.2009.09.037
    • (2010) European Journal of Medicinal Chemistry , vol.45 , Issue.1 , pp. 149-159
    • Amnerkar, N.D.1    Bhusari, K.P.2
  • 32
    • 84868239948 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of N -(substituted benzothiazol-2-yl) amides as anticonvulsant and neuroprotective
    • 10.1016/j.ejmech.2012.10.002
    • Hassan M. Z., Khan S. A., Amir M., Design, synthesis and evaluation of N -(substituted benzothiazol-2-yl)amides as anticonvulsant and neuroprotective. European Journal of Medicinal Chemistry 2012 58 206 213 10.1016/j.ejmech.2012. 10.002
    • (2012) European Journal of Medicinal Chemistry , vol.58 , pp. 206-213
    • Hassan, M.Z.1    Khan, S.A.2    Amir, M.3
  • 34
    • 33845603888 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant activity of sulfonamide derivatives- hydrophobic domain
    • DOI 10.1016/j.bmcl.2006.09.053, PII S0960894X06011103
    • Siddiqui N., Pandeya S. N., Khan S. A., Stables J., Rana A., Alam M., Arshad M. F., Bhat M. A., Synthesis and anticonvulsant activity of sulfonamide derivatives-hydrophobic domain. Bioorganic and Medicinal Chemistry Letters 2007 17 1 255 259 2-s2.0-33845603888 10.1016/j.bmcl.2006.09.053 (Pubitemid 44959955)
    • (2007) Bioorganic and Medicinal Chemistry Letters , vol.17 , Issue.1 , pp. 255-259
    • Siddiqui, N.1    Pandeya, S.N.2    Khan, S.A.3    Stables, J.4    Rana, A.5    Alam, M.6    Arshad, Md.F.7    Bhat, M.A.8
  • 36
    • 84871150692 scopus 로고    scopus 로고
    • Synthesis, crystal structure and antidiabetic activity of substituted (E)-3-(Benzo [ d ]thiazol-2-ylamino) phenylprop-2-en-1-one
    • 10.1016/j.ejmech.2012.11.020
    • Patil V. S., Nandre K. P., Ghosh S., Rao V. J., Chopade B. A., BSridharf B., Bhosale S. V., Synthesis, crystal structure and antidiabetic activity of substituted (E)-3-(Benzo [ d ]thiazol-2-ylamino) phenylprop-2-en-1-one. European Journal of Medicinal Chemistry 2013 59 304 309 10.1016/j.ejmech.2012.11.020
    • (2013) European Journal of Medicinal Chemistry , vol.59 , pp. 304-309
    • Patil, V.S.1    Nandre, K.P.2    Ghosh, S.3    Rao, V.J.4    Chopade, B.A.5    Bsridharf, B.6    Bhosale, S.V.7
  • 37
    • 33644916083 scopus 로고    scopus 로고
    • Benzothiazole derivatives as novel inhibitors of human 11 β - hydroxysteroid dehydrogenase type 1
    • 2-s2.0-33644916083 10.1016/j.mce.2005.10.022
    • Su X., Vicker N., Ganeshapillai D., Smith A., Purohit A., Reed M. J., Potter B. V. L., Benzothiazole derivatives as novel inhibitors of human 11 β-hydroxysteroid dehydrogenase type 1. Molecular and Cellular Endocrinology 2006 248 1-2 214 217 2-s2.0-33644916083 10.1016/j.mce.2005.10.022
    • (2006) Molecular and Cellular Endocrinology , vol.248 , Issue.1-2 , pp. 214-217
    • Su, X.1    Vicker, N.2    Ganeshapillai, D.3    Smith, A.4    Purohit, A.5    Reed, M.J.6    Potter, B.V.L.7
  • 38
    • 33744937911 scopus 로고    scopus 로고
    • Synthesis and biological activity of [[(heterocycloamino)alkoxy]benzyl]- 2, 4-thiazolidinediones as PPARγ agonists
    • DOI 10.1007/BF02968589
    • Jeon R., Kim Y., Cheon Y., Ryu J., Synthesis and biological activity of [[(heterocycloamino)alkoxy]benzyl]-2, 4-thiazolidinediones as PPAR γ agonists. Archives of Pharmacal Research 2006 29 5 394 399 2-s2.0-33744937911 10.1007/BF02968589 (Pubitemid 43846209)
    • (2006) Archives of Pharmacal Research , vol.29 , Issue.5 , pp. 394-399
    • Jeon, R.1    Kim, Y.-J.2    Cheon, Y.3    Ryu, J.-H.4
  • 41
    • 84860143979 scopus 로고    scopus 로고
    • A broad study of two new promising antimycobacterial drugs: Ag(I) and Au(I) complexes with 2-(2-thienyl)benzothiazole
    • 2-s2.0-84860143979 10.1016/j.poly.2012.03.016
    • Pereira G. A., Massabni A. C., Castellano E. E., Costa L. A. S., Leite C. Q. F., Pavan F. R., Cuin A., A broad study of two new promising antimycobacterial drugs: Ag(I) and Au(I) complexes with 2-(2-thienyl) benzothiazole. Polyhedron 2012 38 1 291 296 2-s2.0-84860143979 10.1016/j.poly.2012.03.016
    • (2012) Polyhedron , vol.38 , Issue.1 , pp. 291-296
    • Pereira, G.A.1    Massabni, A.C.2    Castellano, E.E.3    Costa, L.A.S.4    Leite, C.Q.F.5    Pavan, F.R.6    Cuin, A.7
  • 42
    • 84655162157 scopus 로고    scopus 로고
    • Novel 2-(2-(4-aryloxybenzylidene) hydrazinyl)benzothiazole derivatives as anti-tubercular agents
    • 2-s2.0-84655162157 10.1016/j.bmcl.2011.10.064
    • Telvekar V. N., Bairwa V. K., Satardekar K., Bellubi A., Novel 2-(2-(4-aryloxybenzylidene) hydrazinyl)benzothiazole derivatives as anti-tubercular agents. Bioorganic and Medicinal Chemistry Letters 2012 22 1 649 652 2-s2.0-84655162157 10.1016/j.bmcl.2011.10.064
    • (2012) Bioorganic and Medicinal Chemistry Letters , vol.22 , Issue.1 , pp. 649-652
    • Telvekar, V.N.1    Bairwa, V.K.2    Satardekar, K.3    Bellubi, A.4
  • 43
    • 0000831203 scopus 로고
    • Antituberculous compounds. III. Benzothiazole and benzoxazole derivatives
    • 2-s2.0-0000831203
    • Katz L., Antituberculous compounds. III. Benzothiazole and benzoxazole derivatives. Journal of the American Chemical Society 1953 75 3 712 714 2-s2.0-0000831203
    • (1953) Journal of the American Chemical Society , vol.75 , Issue.3 , pp. 712-714
    • Katz, L.1
  • 44
    • 53549091061 scopus 로고    scopus 로고
    • Discovery of novel nitrobenzothiazole inhibitors for Mycobacterium tuberculosis ATP phosphoribosyl transferase (HisG) through virtual screening
    • 2-s2.0-53549091061 10.1021/jm800328v
    • Cho Y., Ioerger T. R., Sacchettini J. C., Discovery of novel nitrobenzothiazole inhibitors for Mycobacterium tuberculosis ATP phosphoribosyl transferase (HisG) through virtual screening. Journal of Medicinal Chemistry 2008 51 19 5984 5992 2-s2.0-53549091061 10.1021/jm800328v
    • (2008) Journal of Medicinal Chemistry , vol.51 , Issue.19 , pp. 5984-5992
    • Cho, Y.1    Ioerger, T.R.2    Sacchettini, J.C.3
  • 46
    • 84857234671 scopus 로고    scopus 로고
    • Synthesis of novel 2-mercapto benzothiazole and 1,2,3-triazole based bis-heterocycles: Their anti-inflammatory and anti-nociceptive activities
    • 2-s2.0-84857234671 10.1016/j.ejmech.2012.01.032
    • Shafi S., Alam M. M., Mulakayala N., Mulakayala C., Vanaja G., Kalle A. M., Pallu R., Alam M. S., Synthesis of novel 2-mercapto benzothiazole and 1,2,3-triazole based bis-heterocycles: their anti-inflammatory and anti-nociceptive activities. European Journal of Medicinal Chemistry 2012 49 324 333 2-s2.0-84857234671 10.1016/j.ejmech.2012.01.032
    • (2012) European Journal of Medicinal Chemistry , 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    Alam, M.S.8
  • 47
    • 0037784006 scopus 로고    scopus 로고
    • Novel thiazolyl, thiazolinyl and benzothiazolyl Schiff bases as possible lipoxygenase's inhibitors and anti-inflammatory agents
    • DOI 10.1016/S0014-827X(03)00065-X
    • Geronikaki A., Hadjipavlou-Litina D., Amourgianou M., Novel thiazolyl, thiazolinyl and benzothiazolyl Schiff bases as possible lipoxygenase's inhibitors and anti-inflammatory agents. Farmaco 2003 58 7 489 495 2-s2.0-0037784006 10.1016/S0014-827X(03)00065-X (Pubitemid 36765349)
    • (2003) Farmaco , vol.58 , Issue.7 , pp. 489-495
    • Geronikaki, A.1    Hadjipavlou-Litina, D.2    Amourgianou, M.3
  • 48
    • 3242778619 scopus 로고    scopus 로고
    • Synthesis and antileishmanial activity of (1,3-benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives
    • DOI 10.1016/j.ejmech.2004.04.006, PII S022352340400100X
    • Delmas F., Avellaneda A., Giorgio C. D., Robin M., De Clercq E., Timon-David P., Galy J.-P., Synthesis and antileishmanial activity of (1,3-benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives. European Journal of Medicinal Chemistry 2004 39 8 685 690 2-s2.0-3242778619 10.1016/j.ejmech. 2004.04.006 (Pubitemid 38970082)
    • (2004) European Journal of Medicinal Chemistry , vol.39 , Issue.8 , pp. 685-690
    • Delmas, F.1    Avellaneda, A.2    Di Giorgio, C.3    Robin, M.4    De Clercq, E.5    Timon-David, P.6    Galy, J.-P.7
  • 49
    • 64249140117 scopus 로고    scopus 로고
    • Synthesis and antioxidant potential of novel synthetic benzophenone analogues
    • 2-s2.0-64249140117 10.1016/j.ejmech.2008.09.010
    • Tzanova T., Gerova M., Petrov O., Karaivanova M., Bagrel D., Synthesis and antioxidant potential of novel synthetic benzophenone analogues. European Journal of Medicinal Chemistry 2009 44 6 2724 2730 2-s2.0-64249140117 10.1016/j.ejmech.2008.09.010
    • (2009) European Journal of Medicinal Chemistry , vol.44 , Issue.6 , pp. 2724-2730
    • Tzanova, T.1    Gerova, M.2    Petrov, O.3    Karaivanova, M.4    Bagrel, D.5
  • 50
    • 67650069151 scopus 로고    scopus 로고
    • Synthesis, antioxidant properties and radioprotective effects of new benzothiazoles and thiadiazoles
    • 2-s2.0-67650069151 10.1016/j.bmc.2009.05.039
    • Cressier D., Prouillac C., Hernandez P., Amourette C., Diserbo M., Lion C., Rima G., Synthesis, antioxidant properties and radioprotective effects of new benzothiazoles and thiadiazoles. Bioorganic and Medicinal Chemistry 2009 17 14 5275 5284 2-s2.0-67650069151 10.1016/j.bmc.2009.05.039
    • (2009) Bioorganic and Medicinal Chemistry , vol.17 , Issue.14 , pp. 5275-5284
    • Cressier, D.1    Prouillac, C.2    Hernandez, P.3    Amourette, C.4    Diserbo, M.5    Lion, C.6    Rima, G.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.