메뉴 건너뛰기




Volumn 124, Issue , 2016, Pages 1093-1104

Synthesis and evaluation of novel hybrids β-carboline-4-thiazolidinones as potential antitumor and antiviral agents

Author keywords

4 Thiazolidinone; Antitumor; Antiviral; Carboline

Indexed keywords

1 (2 CHLOROPHENYL) N' (4 OXOTHIAZOLIDIN 2 YLIDENE) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; 1 (2 FLUOROPHENYL) N' (4 OXO 3 PHENYLTHIAZOLIDIN 2 YLIDENE) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; 1 (2 FLUOROPHENYL) N' (4 OXOTHIAZOLIDIN 2 YLIDENE) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; 1 (3 NITROPHENYL) N' (4 OXO 3 PHENYLTHIAZOLIDIN 2 YLIDENE) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; 1 (3 NITROPHENYL) N' (4 OXOTHIAZOLIDIN 2 YLIDENE) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; 1 (4 DIMETHYLAMINOPHENYL) N' (4 OXO 3 PHENYLTHIAZOLIDIN 2 YLIDENE) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; 1 (4 METHOXYPHENYL) N' (4 OXOTHIAZOLIDIN 2 YLIDENE) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; 1 [4 (DIMETHYLAMINO)PHENYL] N' (4 OXOTHIAZOLIDIN 2 YLIDENE) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; 4 THIAZOLIDINONE DERIVATIVE; ACICLOVIR; ANTIVIRUS AGENT; BETA CARBOLINE DERIVATIVE; COLCHICINE; CYTOTOXIC AGENT; DOXORUBICIN; N (4 OXO 2 PHENYLTHIAZOLIDIN 3 YL) 1 (2 FLUOROPHENYL) 9H PYRIDO[3,4 B]INDOLE 3 CARBOXAMIDE; N (4 OXO 2 PHENYLTHIAZOLIDIN 3 YL) 1 (3 NITROPHENYL) 9H PYRIDO[3,4 B]INDOLE 3 CARBOXAMIDE; N (4 OXO 2 PHENYLTHIAZOLIDIN 3 YL) 1 (4 DIMETHYLAMINOPHENYL) 9H PYRIDO[3,4 B]INDOLE 3 CARBOXAMIDE; N (4 OXO 2 PHENYLTHIAZOLIDIN 3 YL) 1 PHENYL 9H PYRIDO[3,4 B]INDOLE 3 CARBOXAMIDE; N (4 OXO 2 THIENYLTHIAZOLIDIN 3 YL) 1 PHENYL 9H PYRIDO[3,4 B]INDOLE 3 CARBOXAMIDE; N [4 OXO 2 (2 CHLOROPHENYL)THIAZOLIDIN 3 YL] 1 PHENYL 9H PYRIDO[3,4 B]INDOLE 3 CARBOXAMIDE; N' (3 ETHYL 4 OXOTHIAZOLIDIN 2 YLIDENE) 1 (2 CHLOROPHENYL) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; N' (3 ETHYL 4 OXOTHIAZOLIDIN 2 YLIDENE) 1 (2 FLUOROPHENYL) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; N' (3 ETHYL 4 OXOTHIAZOLIDIN 2 YLIDENE) 1 (3 NITROPHENYL) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; N' (3 ETHYL 4 OXOTHIAZOLIDIN 2 YLIDENE) 1 (4 DIMETHYLAMINOPHENYL) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; N' (3 ETHYL 4 OXOTHIAZOLIDIN 2 YLIDENE) 1 (4 METHOXYPHENYL) 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; N' (3 ETHYL 4 OXOTHIAZOLIDIN 2 YLIDENE) 1 PHENYL 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; N' (4 OXO 3 PHENYLTHIAZOLIDIN 2 YLIDENE) 1 PHENYL 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; N' [4 OXOTHIAZOLIDIN 2 YLIDENE] 1 PHENYL 9H PYRIDO[3,4 B]INDOLE 3 CARBOHYDRAZIDE; PHOSPHATIDYLSERINE; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; CARBOLINE DERIVATIVE;

EID: 84993965476     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2016.10.018     Document Type: Article
Times cited : (45)

References (48)
  • 3
    • 84861578387 scopus 로고    scopus 로고
    • Synthesis and anti-leishmanial activity of 1-aryl-β-carboline derivatives against Leishmania donovani
    • [3] Gohil, V.M., Brahmbhatt, K.G., Loiseau, P.M., Bhutani, K.K., Synthesis and anti-leishmanial activity of 1-aryl-β-carboline derivatives against Leishmania donovani. Bioorg. Med. Chem. Lett. 22 (2012), 3905–3907.
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 3905-3907
    • Gohil, V.M.1    Brahmbhatt, K.G.2    Loiseau, P.M.3    Bhutani, K.K.4
  • 6
    • 84908407171 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of novel tacrine-(β-carboline) hybrids as multifunctional agents for the treatment of Alzheimer's disease
    • [6] Jin-Shuai, L., Sai-Sai, X., Su-Yi, L., Long-Fei, P., Xiao-Bing, W., Ling-Yi, K., Design, synthesis and evaluation of novel tacrine-(β-carboline) hybrids as multifunctional agents for the treatment of Alzheimer's disease. Bioorg. Med. Chem. 22 (2014), 6089–6104.
    • (2014) Bioorg. Med. Chem. , vol.22 , pp. 6089-6104
    • Jin-Shuai, L.1    Sai-Sai, X.2    Su-Yi, L.3    Long-Fei, P.4    Xiao-Bing, W.5    Ling-Yi, K.6
  • 7
    • 77951143986 scopus 로고    scopus 로고
    • A class of 3S-2-aminoacyltetrahydro-β-carboline-3-carboxylic acids: their facile synthesis, inhibition for platelet activation, and high in vivo anti-thrombotic potency
    • [7] Liu, J., Jiang, X., Zhao, M., Zhang, X., Zheng, M., Peng, L., Peng, S., A class of 3S-2-aminoacyltetrahydro-β-carboline-3-carboxylic acids: their facile synthesis, inhibition for platelet activation, and high in vivo anti-thrombotic potency. J. Med. Chem. 53 (2010), 3106–3116.
    • (2010) J. Med. Chem. , vol.53 , pp. 3106-3116
    • Liu, J.1    Jiang, X.2    Zhao, M.3    Zhang, X.4    Zheng, M.5    Peng, L.6    Peng, S.7
  • 8
    • 79958263530 scopus 로고    scopus 로고
    • A class of oral N-[(1S,3S)-1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carbonyl]-N-(amino-acid-acyl) hydrazine: discovery, synthesis, in vitro anti-platelet aggregation/in vivo anti-thrombotic evaluation and 3D QSAR analysis
    • [8] Yao, K., Zhao, M., Zhang, X., Wang, Y., Li, L., Zheng, M., Peng, S., A class of oral N-[(1S,3S)-1-methyl-1,2,3,4-tetrahydro-β-carboline-3-carbonyl]-N-(amino-acid-acyl) hydrazine: discovery, synthesis, in vitro anti-platelet aggregation/in vivo anti-thrombotic evaluation and 3D QSAR analysis. Eur. J. Med. Chem. 46 (2011), 3237–3249.
    • (2011) Eur. J. Med. Chem. , vol.46 , pp. 3237-3249
    • Yao, K.1    Zhao, M.2    Zhang, X.3    Wang, Y.4    Li, L.5    Zheng, M.6    Peng, S.7
  • 9
    • 79958281343 scopus 로고    scopus 로고
    • Stimulation, protection and regeneration of dopaminergic neurons by 9-methyl-β-carboline: a new anti-Parkinson drug?
    • [9] Polanski, W., Reichmann, H., Gille, G., Stimulation, protection and regeneration of dopaminergic neurons by 9-methyl-β-carboline: a new anti-Parkinson drug?. Expert Rev. Neurother. 11 (2011), 845–860.
    • (2011) Expert Rev. Neurother. , vol.11 , pp. 845-860
    • Polanski, W.1    Reichmann, H.2    Gille, G.3
  • 10
    • 84908699102 scopus 로고    scopus 로고
    • Computational & experimental evaluation of the structure/activity relationship of β-carbolines as DYRK1A inhibitors
    • [10] Drung, B., Scholz, C., Barbosa, V.A., Nazari, A., Sarragiotto, M.H., Schmidt, B., Computational & experimental evaluation of the structure/activity relationship of β-carbolines as DYRK1A inhibitors. Bioorg. Med. Chem. Lett. 24 (2014), 4854–4860.
    • (2014) Bioorg. Med. Chem. Lett. , vol.24 , pp. 4854-4860
    • Drung, B.1    Scholz, C.2    Barbosa, V.A.3    Nazari, A.4    Sarragiotto, M.H.5    Schmidt, B.6
  • 11
    • 84941242782 scopus 로고    scopus 로고
    • Selectivity profiling and biological activity of novel β-carbolines as potent and selective DYRK1 Kinase inhibitors
    • [11] Rüben, K., Wurzlbauer, A., Walte, A., Sippl, W., Bracher, F., Becker, W., Selectivity profiling and biological activity of novel β-carbolines as potent and selective DYRK1 Kinase inhibitors. PLoS One 10:7 (2015), 1–18.
    • (2015) PLoS One , vol.10 , Issue.7 , pp. 1-18
    • Rüben, K.1    Wurzlbauer, A.2    Walte, A.3    Sippl, W.4    Bracher, F.5    Becker, W.6
  • 12
    • 77955983637 scopus 로고    scopus 로고
    • A class of novel carboline intercalators: their synthesis, in vitro anti-proliferation, in vivo anti-tumor action, and 3D QSAR analysis
    • [12] Wu, J., Li, C., Zhao, M., Wang, W., Wang, Y., Peng, S., A class of novel carboline intercalators: their synthesis, in vitro anti-proliferation, in vivo anti-tumor action, and 3D QSAR analysis. Bioorg. Med. Chem. 18 (2010), 6220–6229.
    • (2010) Bioorg. Med. Chem. , vol.18 , pp. 6220-6229
    • Wu, J.1    Li, C.2    Zhao, M.3    Wang, W.4    Wang, Y.5    Peng, S.6
  • 13
    • 77954298116 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of novel β-carbolines as potent cytotoxic and DNA intercalating agents
    • [13] Chen, Z., Cao, R., Shi, B., Yi, W., Yu, L., Song, H., Ren, Z., Synthesis and biological evaluation of novel β-carbolines as potent cytotoxic and DNA intercalating agents. Chem. Pharm. Bull. 58 (2010), 901–907.
    • (2010) Chem. Pharm. Bull. , vol.58 , pp. 901-907
    • Chen, Z.1    Cao, R.2    Shi, B.3    Yi, W.4    Yu, L.5    Song, H.6    Ren, Z.7
  • 14
    • 84871544584 scopus 로고    scopus 로고
    • Design, synthesis and in vitro and in vivo antitumor activities of novel bivalent β-carbolines
    • [14] Shi, B., Cao, R., Fan, W., Guo, L., Ma, Q., Chen, X., Zhang, G., Qiu, L., Song, H., Design, synthesis and in vitro and in vivo antitumor activities of novel bivalent β-carbolines. Eur. J. Med. Chem. 60 (2013), 10–22.
    • (2013) Eur. J. Med. Chem. , vol.60 , pp. 10-22
    • Shi, B.1    Cao, R.2    Fan, W.3    Guo, L.4    Ma, Q.5    Chen, X.6    Zhang, G.7    Qiu, L.8    Song, H.9
  • 15
    • 84880314440 scopus 로고    scopus 로고
    • Pharmacophore modeling and QSAR analysis of novel β-carboline derivatives as antitumor agents
    • [15] Chourasiya, R.K., Rao, A.R., Agrawal, R.K., Pharmacophore modeling and QSAR analysis of novel β-carboline derivatives as antitumor agents. Lett. Drug Des. Discov. 10 (2013), 572–584.
    • (2013) Lett. Drug Des. Discov. , vol.10 , pp. 572-584
    • Chourasiya, R.K.1    Rao, A.R.2    Agrawal, R.K.3
  • 16
    • 84884271207 scopus 로고    scopus 로고
    • 2-alkylated quaternary β-carbolines as novel antitumor agents
    • [16] Zhang, G., Cao, R., Guo, L., Ma, Q., Fan, W., Chen, X., Li, J., Shao, G., Qiu, L., Ren, Z., Synthesis and structure-activity relationships of N2-alkylated quaternary β-carbolines as novel antitumor agents. Eur. J. Med. Chem. 65 (2013), 21–31.
    • (2013) Eur. J. Med. Chem. , vol.65 , pp. 21-31
    • Zhang, G.1    Cao, R.2    Guo, L.3    Ma, Q.4    Fan, W.5    Chen, X.6    Li, J.7    Shao, G.8    Qiu, L.9    Ren, Z.10
  • 17
    • 84896475860 scopus 로고    scopus 로고
    • Synthesis of β-carboline–benzimidazole conjugates using lanthanum nitrate as a catalyst and their biological evaluation
    • [17] Kovvuri, J., Reddy, V.S., Vidyasagarb, K., Nagesh, N., Synthesis of β-carboline–benzimidazole conjugates using lanthanum nitrate as a catalyst and their biological evaluation. Org. Biomol. Chem. 12 (2014), 2370–2387.
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 2370-2387
    • Kovvuri, J.1    Reddy, V.S.2    Vidyasagarb, K.3    Nagesh, N.4
  • 18
    • 84946490196 scopus 로고    scopus 로고
    • Design and synthesis of dithiocarbamate linked β-carboline derivatives: DNA topoisomerase II inhibition with DNA binding and apoptosis inducing ability
    • [18] Kamal, A., Sathish, M., Nayak, V.L., Srinivasulu, V., Kavitha, B., Tangella, Y., Thummuri, D., Bagul, C., Shankaraiah, N., Nagesh, N., Design and synthesis of dithiocarbamate linked β-carboline derivatives: DNA topoisomerase II inhibition with DNA binding and apoptosis inducing ability. Bioorg. Med. Chem. 23 (2015), 5511–5526.
    • (2015) Bioorg. Med. Chem. , vol.23 , pp. 5511-5526
    • Kamal, A.1    Sathish, M.2    Nayak, V.L.3    Srinivasulu, V.4    Kavitha, B.5    Tangella, Y.6    Thummuri, D.7    Bagul, C.8    Shankaraiah, N.9    Nagesh, N.10
  • 20
    • 84948467383 scopus 로고    scopus 로고
    • Design and synthesis of C3-tethered 1,2,3-triazolo-β-carboline derivatives: anticancer activity, DNA-binding ability, viscosity and molecular modeling studies
    • [20] Shankaraiah, N., Jadala, C., Nekkanti, S., Senwar, K.R., Nagesh, N., Shrivastava, S., Naidu, V., Sathish, M., Kamal, A., Design and synthesis of C3-tethered 1,2,3-triazolo-β-carboline derivatives: anticancer activity, DNA-binding ability, viscosity and molecular modeling studies. Bioorg. Chem. 64 (2016), 42–50.
    • (2016) Bioorg. Chem. , vol.64 , pp. 42-50
    • Shankaraiah, N.1    Jadala, C.2    Nekkanti, S.3    Senwar, K.R.4    Nagesh, N.5    Shrivastava, S.6    Naidu, V.7    Sathish, M.8    Kamal, A.9
  • 21
    • 77955427418 scopus 로고    scopus 로고
    • Synthesis and evaluation of β-carboline derivatives as inhibitors of human immunodeficiency virus
    • [21] Brahmbhatt, K.G., Ahmed, N., Sabde, S., Mitra, D., Singh, I.P., Bhutani, K.K., Synthesis and evaluation of β-carboline derivatives as inhibitors of human immunodeficiency virus. Bioorg. Med. Chem. Lett. 20 (2010), 4416–4419.
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 4416-4419
    • Brahmbhatt, K.G.1    Ahmed, N.2    Sabde, S.3    Mitra, D.4    Singh, I.P.5    Bhutani, K.K.6
  • 22
    • 84939885330 scopus 로고    scopus 로고
    • In-silico design and study of novel piperazinyl β-carbolines as inhibitor of HIV-1 reverse transcriptase
    • [22] Ashok, P., Sharma, H., Lathiya, H., Chander, S., Murugesan, S., In-silico design and study of novel piperazinyl β-carbolines as inhibitor of HIV-1 reverse transcriptase. Med. Chem. Res. 24 (2014), 513–522.
    • (2014) Med. Chem. Res. , vol.24 , pp. 513-522
    • Ashok, P.1    Sharma, H.2    Lathiya, H.3    Chander, S.4    Murugesan, S.5
  • 23
    • 84923914777 scopus 로고    scopus 로고
    • Design, synthesis of new β-carboline derivatives and their selective anti-HIV-2 activity
    • [23] Ashok, P., Chander, S., Balzarini, J., Pannecouque, C., Design, synthesis of new β-carboline derivatives and their selective anti-HIV-2 activity. Bioorg. Med. Chem. Lett. 25 (2015), 1232–1235.
    • (2015) Bioorg. Med. Chem. Lett. , vol.25 , pp. 1232-1235
    • Ashok, P.1    Chander, S.2    Balzarini, J.3    Pannecouque, C.4
  • 24
    • 84954378688 scopus 로고    scopus 로고
    • C ring may be dispensable for β-carboline: design, synthesis, and bioactivities evaluation of tryptophan analog derivatives based on the biosynthesis of β-carboline alkaloids
    • [24] Huang, Y., Liu, Y., Liu, Y., Song, H., Wang, Q., C ring may be dispensable for β-carboline: design, synthesis, and bioactivities evaluation of tryptophan analog derivatives based on the biosynthesis of β-carboline alkaloids. Bioorg. Med. Chem. 24 (2016), 462–473.
    • (2016) Bioorg. Med. Chem. , vol.24 , pp. 462-473
    • Huang, Y.1    Liu, Y.2    Liu, Y.3    Song, H.4    Wang, Q.5
  • 25
    • 84908364564 scopus 로고    scopus 로고
    • A review on recent developments of indole-containing antiviral agents Review Article
    • [25] Zhang, M.Z., Chen, Q., Yang, G.F., A review on recent developments of indole-containing antiviral agents Review Article. Eur. J. Med. Chem. 89 (2015), 421–441.
    • (2015) Eur. J. Med. Chem. , vol.89 , pp. 421-441
    • Zhang, M.Z.1    Chen, Q.2    Yang, G.F.3
  • 26
    • 84939489234 scopus 로고    scopus 로고
    • Novel halogenated 3-deazapurine, 7-deazapurine and alkylated 9-deazapurine derivatives of l-ascorbic or imino-l-ascorbic acid: synthesis, antitumour and antiviral activity evaluations
    • [26] Babić, M.S., Makuc, D., Plavec, J., Martinović, T., Pavelić, S.K., Pavelić, K., Snoeck, R., Andrei, G., Schols, D., Wittine, K., Mintas, M., Novel halogenated 3-deazapurine, 7-deazapurine and alkylated 9-deazapurine derivatives of l-ascorbic or imino-l-ascorbic acid: synthesis, antitumour and antiviral activity evaluations. Eur. J. Med. Chem. 102 (2015), 288–302.
    • (2015) Eur. J. Med. Chem. , vol.102 , pp. 288-302
    • Babić, M.S.1    Makuc, D.2    Plavec, J.3    Martinović, T.4    Pavelić, S.K.5    Pavelić, K.6    Snoeck, R.7    Andrei, G.8    Schols, D.9    Wittine, K.10    Mintas, M.11
  • 28
    • 85057444720 scopus 로고    scopus 로고
    • Bioactive nucleoside analogues possessing selected five-membered azaheterocyclic bases
    • [28] Zeidler, J., Baraniak, D., Ostrowski, T., Bioactive nucleoside analogues possessing selected five-membered azaheterocyclic bases. Eur. J. Med. Chem. 97 (2015), 409–418.
    • (2015) Eur. J. Med. Chem. , vol.97 , pp. 409-418
    • Zeidler, J.1    Baraniak, D.2    Ostrowski, T.3
  • 32
    • 84903372416 scopus 로고    scopus 로고
    • Synthesis and antitumoral activity of novel 3-(2-substituted-1,3,4-oxadiazol-5-yl) and 3-(5-substituted-1,2,4-triazol-3-yl) β-carboline derivatives
    • [32] Formagio, A.S.N., Tonin, L.T.D., Foglio, M.A., Madjarof, C., De Carvalho, J.E., Da Costa, W.F., Cardoso, F.P., Sarragiotto, M.H., Synthesis and antitumoral activity of novel 3-(2-substituted-1,3,4-oxadiazol-5-yl) and 3-(5-substituted-1,2,4-triazol-3-yl) β-carboline derivatives. Bioorg.Med. Chem. 16 (2008), 9660–9667.
    • (2008) Bioorg.Med. Chem. , vol.16 , pp. 9660-9667
    • Formagio, A.S.N.1    Tonin, L.T.D.2    Foglio, M.A.3    Madjarof, C.4    De Carvalho, J.E.5    Da Costa, W.F.6    Cardoso, F.P.7    Sarragiotto, M.H.8
  • 34
    • 70349774236 scopus 로고    scopus 로고
    • Synthesis and antiviral activity of β-carboline derivatives bearing a substituted carbohydrazide at C-3 against poliovirus and herpes simplex virus (HSV-1)
    • [34] Formagio, A.S.N., Santos, P.R., Zanoli, K., Ueda-Nakamura, T., Tonin, L.T.D., Nakamura, C.V., Sarragiotto, M.H., Synthesis and antiviral activity of β-carboline derivatives bearing a substituted carbohydrazide at C-3 against poliovirus and herpes simplex virus (HSV-1). Eur. J. Med. Chem. 44 (2009), 4695–4701.
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 4695-4701
    • Formagio, A.S.N.1    Santos, P.R.2    Zanoli, K.3    Ueda-Nakamura, T.4    Tonin, L.T.D.5    Nakamura, C.V.6    Sarragiotto, M.H.7
  • 35
    • 84924871525 scopus 로고    scopus 로고
    • Effect of 1-(phenyl)-N-(4-methoxybenzylidene)-9H-pyrido[3,4-b] indole-3-carbohydrazide on in vitro poliovirus replication
    • [35] Santos, P.R., Formagio, A.S.N., Dias Filho, B.P., Sarragiotto, M.H., Nakamura, C.V., Nakamura, T.U., Effect of 1-(phenyl)-N-(4-methoxybenzylidene)-9H-pyrido[3,4-b] indole-3-carbohydrazide on in vitro poliovirus replication. Acta Pharm. 65 (2015), 75–81.
    • (2015) Acta Pharm. , vol.65 , pp. 75-81
    • Santos, P.R.1    Formagio, A.S.N.2    Dias Filho, B.P.3    Sarragiotto, M.H.4    Nakamura, C.V.5    Nakamura, T.U.6
  • 36
    • 43049161063 scopus 로고    scopus 로고
    • 4-Thiazolidinone – a biologically active scaffold
    • [36] Verma, A., Saraf, S.K., 4-Thiazolidinone – a biologically active scaffold. Eur. J. Med. Chem. 43 (2008), 897–905.
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 897-905
    • Verma, A.1    Saraf, S.K.2
  • 37
    • 84861188772 scopus 로고    scopus 로고
    • Recent developments and biological activities of thiazolidinone derivatives: a review
    • [37] Jain, A.K., Vaidya, A., Ravichandran, V., Kashaw, S.K., Agrawal, R.K., Recent developments and biological activities of thiazolidinone derivatives: a review. Bioorg. Med. Chem. 20 (2012), 3378–3395.
    • (2012) Bioorg. Med. Chem. , vol.20 , pp. 3378-3395
    • Jain, A.K.1    Vaidya, A.2    Ravichandran, V.3    Kashaw, S.K.4    Agrawal, R.K.5
  • 39
    • 84899889800 scopus 로고    scopus 로고
    • Optimization of 2-(3-(arylalkyl amino carbonyl) phenyl)-3-(2- methoxyphenyl)-4-thiazolidinone derivatives as potent antitumor growth and metastasis agents
    • [39] Wu, J., Yu, L., Yang, F., Li, J., Wang, P., Zhou, W., Qin, L., Li, Y., Luo, J., Yi, Z., Liu, M., Chen, Y., Optimization of 2-(3-(arylalkyl amino carbonyl) phenyl)-3-(2- methoxyphenyl)-4-thiazolidinone derivatives as potent antitumor growth and metastasis agents. Eur. J. Med. Chem. 80 (2014), 340–351.
    • (2014) Eur. J. Med. Chem. , vol.80 , pp. 340-351
    • Wu, J.1    Yu, L.2    Yang, F.3    Li, J.4    Wang, P.5    Zhou, W.6    Qin, L.7    Li, Y.8    Luo, J.9    Yi, Z.10    Liu, M.11    Chen, Y.12
  • 42
    • 84897463577 scopus 로고    scopus 로고
    • Synergistic action by multi-targeting compounds produces a potent compound combination for human NSCLC both in vitro and in vivo
    • [42] Zhang, C., Zhai, S., Li, X., Zhang, Q., Wu, L., Liu, Y., Jiang, C., Zhou, H., Li, F., Zhang, S., Su, G., Zhang, B., Yan, B., Synergistic action by multi-targeting compounds produces a potent compound combination for human NSCLC both in vitro and in vivo. Cell Death Dis., 5, 2014, 1138.
    • (2014) Cell Death Dis. , vol.5 , pp. 1138
    • Zhang, C.1    Zhai, S.2    Li, X.3    Zhang, Q.4    Wu, L.5    Liu, Y.6    Jiang, C.7    Zhou, H.8    Li, F.9    Zhang, S.10    Su, G.11    Zhang, B.12    Yan, B.13
  • 43
    • 84897386255 scopus 로고    scopus 로고
    • Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids
    • [43] Nepali, K., Sharma, S., Sharma, M., Bedi, P.M.S., Dhar, K.L., Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids. Eur. J. Med. Chem. 77 (2014), 422–487.
    • (2014) Eur. J. Med. Chem. , vol.77 , pp. 422-487
    • Nepali, K.1    Sharma, S.2    Sharma, M.3    Bedi, P.M.S.4    Dhar, K.L.5
  • 45
    • 84873204498 scopus 로고    scopus 로고
    • Gene expression profiling from a prostate cancer PC-3 cell line treated with salinomycin predicts cell cycle arrest and endoplasmic reticulum stress
    • [45] Kim, K.Y., Seo, Y.K., Yu, S.N., Kim, S.H., Suh, P.G., Ji, J.H., Park, Y.M., Ahn, S.C., Gene expression profiling from a prostate cancer PC-3 cell line treated with salinomycin predicts cell cycle arrest and endoplasmic reticulum stress. J. Canc. Sci. Ther. 5 (2013), 23–30.
    • (2013) J. Canc. Sci. Ther. , vol.5 , pp. 23-30
    • Kim, K.Y.1    Seo, Y.K.2    Yu, S.N.3    Kim, S.H.4    Suh, P.G.5    Ji, J.H.6    Park, Y.M.7    Ahn, S.C.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.