메뉴 건너뛰기




Volumn 124, Issue , 2016, Pages 608-621

Synthesis and biological evaluation of new benzimidazole-thiazolidinedione hybrids as potential cytotoxic and apoptosis inducing agents

Author keywords

Annexin; Apoptosis; Benzimidazole; Cell migration; MitoSOX; Thiazolidinedione

Indexed keywords

2 (5 ((1 METHYL 1H BENZO[D]IMIDAZOL 2 YL)METHYLENE) 2,4 DIOXOTHIAZOLIDIN 3 YL) N (4 PHENYLTHIAZOL 2 YL)ACETAMIDE; 2,4 THIAZOLIDINEDIONE DERIVATIVE; 4',6 DIAMIDINO 2 PHENYLINDOLE; ACRIDINE ORANGE; BENZIMIDAZOLE DERIVATIVE; CYTOTOXIC AGENT; ETHIDIUM BROMIDE; F ACTIN; FLUORESCEIN ISOTHIOCYANATE; FLUOROURACIL; LIPOCORTIN 5; PROPIDIUM IODIDE; RHODAMINE 123; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT;

EID: 84986317261     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2016.08.029     Document Type: Article
Times cited : (84)

References (50)
  • 1
    • 0036911505 scopus 로고    scopus 로고
    • New chemotherapeutic agents: update of major chemoradiation trials in solid tumors
    • [1] Curran, W.J., New chemotherapeutic agents: update of major chemoradiation trials in solid tumors. Oncology 63 (2002), 29–38.
    • (2002) Oncology , vol.63 , pp. 29-38
    • Curran, W.J.1
  • 2
    • 34250308322 scopus 로고    scopus 로고
    • Apoptosis: a review of programmed cell death
    • [2] Elmore, S., Apoptosis: a review of programmed cell death. Toxicol. Pathol. 35 (2007), 495–516.
    • (2007) Toxicol. Pathol. , vol.35 , pp. 495-516
    • Elmore, S.1
  • 3
    • 58149296552 scopus 로고    scopus 로고
    • Tumor resistance to apoptosis
    • [3](a) Fulda, S., Tumor resistance to apoptosis. Int. J. Cancer 124 (2009), 511–515.
    • (2009) Int. J. Cancer , vol.124 , pp. 511-515
    • Fulda, S.1
  • 4
    • 33746886979 scopus 로고    scopus 로고
    • Extrinsic versus intrinsic apoptosis pathways in anticancer chemotherapy
    • [3](b) Fulda, S., Debatin, K.-M., Extrinsic versus intrinsic apoptosis pathways in anticancer chemotherapy. Oncogene 25 (2006), 4798–4811.
    • (2006) Oncogene , vol.25 , pp. 4798-4811
    • Fulda, S.1    Debatin, K.-M.2
  • 5
    • 28544443984 scopus 로고    scopus 로고
    • Promoting apoptosis as a strategy for cancer drug discovery
    • [4](a) Fesik, S.W., Promoting apoptosis as a strategy for cancer drug discovery. Nat. Rev. Cancer 5 (2005), 876–885.
    • (2005) Nat. Rev. Cancer , vol.5 , pp. 876-885
    • Fesik, S.W.1
  • 6
    • 20344385260 scopus 로고    scopus 로고
    • Targeting apoptosis pathways in cancer therapy
    • [4](b) Ghobrial, I.M., Witzig, T.E., Adjei, A.A., Targeting apoptosis pathways in cancer therapy. CA Cancer J. Clin. 55 (2005), 178–194.
    • (2005) CA Cancer J. Clin. , vol.55 , pp. 178-194
    • Ghobrial, I.M.1    Witzig, T.E.2    Adjei, A.A.3
  • 7
    • 84965034325 scopus 로고    scopus 로고
    • Targeting cell death signalling in cancer: minimising ‘Collateral damage’
    • [4](c) Fox, J.L., MacFarlane, M., Targeting cell death signalling in cancer: minimising ‘Collateral damage’. Br. J. Cancer 115 (2016), 5–11.
    • (2016) Br. J. Cancer , vol.115 , pp. 5-11
    • Fox, J.L.1    MacFarlane, M.2
  • 8
    • 84964461716 scopus 로고    scopus 로고
    • Design, synthesis and apoptosis inducing effect of novel (Z)-3-(3′-methoxy-4′-(2-amino-2-oxoethoxy)-benzylidene)indolin-2-ones as potential antitumour agents
    • [4](d) Senwar, K.R., Reddy, T.S., Thummuri, D., Sharma, P., Naidu, V.G.M., Srinivasulu, G., Shankaraiah, N., Design, synthesis and apoptosis inducing effect of novel (Z)-3-(3′-methoxy-4′-(2-amino-2-oxoethoxy)-benzylidene)indolin-2-ones as potential antitumour agents. Eur. J. Med. Chem. 118 (2016), 34–46.
    • (2016) Eur. J. Med. Chem. , vol.118 , pp. 34-46
    • Senwar, K.R.1    Reddy, T.S.2    Thummuri, D.3    Sharma, P.4    Naidu, V.G.M.5    Srinivasulu, G.6    Shankaraiah, N.7
  • 9
    • 84939785456 scopus 로고    scopus 로고
    • Spirooxindole-derived morpholine-fused-1,2,3-triazoles: design, synthesis, cytotoxicity and apoptosis inducing studies
    • [4](e) Senwar, K.R., Sharma, P., Reddy, T.S., Jeengar, M.K., Nayak, V.L., Naidu, V.G.M., Kamal, A., Shankaraiah, N., Spirooxindole-derived morpholine-fused-1,2,3-triazoles: design, synthesis, cytotoxicity and apoptosis inducing studies. Eur. J. Med. Chem. 102 (2015), 413–424.
    • (2015) Eur. J. Med. Chem. , vol.102 , pp. 413-424
    • Senwar, K.R.1    Sharma, P.2    Reddy, T.S.3    Jeengar, M.K.4    Nayak, V.L.5    Naidu, V.G.M.6    Kamal, A.7    Shankaraiah, N.8
  • 11
    • 84875232365 scopus 로고    scopus 로고
    • Thiazolidine-2,4-diones: progress towards multifarious applications
    • [5](a) Jain, V.S., Vora, D.K., Ramaa, C.S., Thiazolidine-2,4-diones: progress towards multifarious applications. Bioorg. Med. Chem. 21 (2013), 1599–1620.
    • (2013) Bioorg. Med. Chem. , vol.21 , pp. 1599-1620
    • Jain, V.S.1    Vora, D.K.2    Ramaa, C.S.3
  • 13
    • 84861611610 scopus 로고    scopus 로고
    • Synthesis, hypoglycemic and hypolipidemic activities of novel thiazolidinedione derivatives containing thiazole/triazole/oxadiazole ring
    • [6](a) Iqbal, A.K.M., Khan, A.Y., Kalashetti, M.B., Belavagi, N.S., Gong, Y.-D., Khazi, I.A.M., Synthesis, hypoglycemic and hypolipidemic activities of novel thiazolidinedione derivatives containing thiazole/triazole/oxadiazole ring. Eur. J. Med. Chem. 53 (2012), 308–315.
    • (2012) Eur. J. Med. Chem. , vol.53 , pp. 308-315
    • Iqbal, A.K.M.1    Khan, A.Y.2    Kalashetti, M.B.3    Belavagi, N.S.4    Gong, Y.-D.5    Khazi, I.A.M.6
  • 14
    • 84964490230 scopus 로고    scopus 로고
    • Molecular docking assisted 3D-QSAR study of benzylidene-2,4-thiazolidinedione derivatives as PTP-1B inhibitors for the management of type-2 diabetes mellitus
    • [6](b) Verma, S.K., Thareja, S., Molecular docking assisted 3D-QSAR study of benzylidene-2,4-thiazolidinedione derivatives as PTP-1B inhibitors for the management of type-2 diabetes mellitus. RSC Adv. 6 (2016), 33857–33867.
    • (2016) RSC Adv. , vol.6 , pp. 33857-33867
    • Verma, S.K.1    Thareja, S.2
  • 15
    • 80053250964 scopus 로고    scopus 로고
    • Synthesis, characterization and antimicrobial activity evaluation of new 2,4-thiazolidinediones bearing imidazo[2,1-b][1,3,4]thiadiazole moiety
    • [7](a) Alagawadi, K.R., Alegaon, S.G., Synthesis, characterization and antimicrobial activity evaluation of new 2,4-thiazolidinediones bearing imidazo[2,1-b][1,3,4]thiadiazole moiety. Arab. J. Chem. 4 (2011), 465–472.
    • (2011) Arab. J. Chem. , vol.4 , pp. 465-472
    • Alagawadi, K.R.1    Alegaon, S.G.2
  • 16
    • 79958256411 scopus 로고    scopus 로고
    • Synthesis of new chalcone derivatives bearing 2,4-thiazolidinedione and benzoic acid moieties as potential anti-bacterial agents
    • [7](b) Liu, X.-F., Zheng, C.-J., Sun, L.-P., Liu, X.-K., Piao, H.-R., Synthesis of new chalcone derivatives bearing 2,4-thiazolidinedione and benzoic acid moieties as potential anti-bacterial agents. Eur. J. Med. Chem. 46 (2011), 3469–3473.
    • (2011) Eur. J. Med. Chem. , vol.46 , pp. 3469-3473
    • Liu, X.-F.1    Zheng, C.-J.2    Sun, L.-P.3    Liu, X.-K.4    Piao, H.-R.5
  • 20
    • 84888139352 scopus 로고    scopus 로고
    • Studies on the synthetic and structural aspects of benzosuberones bearing 2,4-thiazolidenone moiety as potential anti-cancer agents
    • [9](b) Nagarapu, L., Yadagiri, B., Bantu, R., Kumar, C.G., Pombala, S., Nanubolu, J., Studies on the synthetic and structural aspects of benzosuberones bearing 2,4-thiazolidenone moiety as potential anti-cancer agents. Eur. J. Med. Chem. 71 (2014), 91–97.
    • (2014) Eur. J. Med. Chem. , vol.71 , pp. 91-97
    • Nagarapu, L.1    Yadagiri, B.2    Bantu, R.3    Kumar, C.G.4    Pombala, S.5    Nanubolu, J.6
  • 21
    • 84870155584 scopus 로고    scopus 로고
    • 2H-chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents
    • [9](c) Azizmohammadi, M., Khoobi, M., Ramazani, A., Emami, S., Zarrin, A., Firuzi, O., Miri, R., Shafiee, A., 2H-chromene derivatives bearing thiazolidine-2,4-dione, rhodanine or hydantoin moieties as potential anticancer agents. Eur. J. Med. Chem. 59 (2013), 15–22.
    • (2013) Eur. J. Med. Chem. , vol.59 , pp. 15-22
    • Azizmohammadi, M.1    Khoobi, M.2    Ramazani, A.3    Emami, S.4    Zarrin, A.5    Firuzi, O.6    Miri, R.7    Shafiee, A.8
  • 22
    • 84903786971 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new rhodanine analogues bearing 2-chloroquinoline and benzo[h]quinoline scaffolds as anticancer agents
    • [9](d) Ramesh, V., Rao, B.A., Sharma, P., Swarna, B., Thummuri, D., Srinivas, K., Naidu, V.G.M., Rao, V.J., Synthesis and biological evaluation of new rhodanine analogues bearing 2-chloroquinoline and benzo[h]quinoline scaffolds as anticancer agents. Eur. J. Med. Chem. 83 (2014), 569–580.
    • (2014) Eur. J. Med. Chem. , vol.83 , pp. 569-580
    • Ramesh, V.1    Rao, B.A.2    Sharma, P.3    Swarna, B.4    Thummuri, D.5    Srinivas, K.6    Naidu, V.G.M.7    Rao, V.J.8
  • 23
    • 66149157824 scopus 로고    scopus 로고
    • Peroxisome proliferator-activated receptor gamma in bladder cancer: a promising therapeutic target
    • [10] Mansure, J.J., Nassim, R., Kassouf, W., Peroxisome proliferator-activated receptor gamma in bladder cancer: a promising therapeutic target. Cancer Biol. Ther. 8 (2009), 6–15.
    • (2009) Cancer Biol. Ther. , vol.8 , pp. 6-15
    • Mansure, J.J.1    Nassim, R.2    Kassouf, W.3
  • 25
    • 84855758265 scopus 로고    scopus 로고
    • 3,5-disubstituted-thiazolidine-2,4-dione analogs as anticancer agents: design, synthesis and biological characterization
    • [12] Liu, K., Rao, W., Parikh, H., Li, Q., Guo, T.L., Grant, S., Kellogg, G.E., Zhang, S., 3,5-disubstituted-thiazolidine-2,4-dione analogs as anticancer agents: design, synthesis and biological characterization. Eur. J. Med. Chem. 47 (2012), 125–136.
    • (2012) Eur. J. Med. Chem. , vol.47 , pp. 125-136
    • Liu, K.1    Rao, W.2    Parikh, H.3    Li, Q.4    Guo, T.L.5    Grant, S.6    Kellogg, G.E.7    Zhang, S.8
  • 28
    • 84937431709 scopus 로고    scopus 로고
    • Structure activity relationship (SAR) study of benzimidazole scaffold for different biological activities: a mini-review
    • [15] Yadav, G., Ganguly, S., Structure activity relationship (SAR) study of benzimidazole scaffold for different biological activities: a mini-review. Eur. J. Med. Chem. 97 (2015), 419–443.
    • (2015) Eur. J. Med. Chem. , vol.97 , pp. 419-443
    • Yadav, G.1    Ganguly, S.2
  • 30
    • 84978529182 scopus 로고    scopus 로고
    • New (E)-1-alkyl-1H-benzo[d]imidazol-2-yl)methylene)indolin-2-ones: synthesis, in vitro cytotoxicity evaluation and apoptosis inducing studies
    • [16](b) Sharma, P., Thummuri, D., Reddy, T.S., Senwar, K.R., Naidu, V.G.M., Srinivasulu, G., Bharghava, S.K., Shankaraiah, N., New (E)-1-alkyl-1H-benzo[d]imidazol-2-yl)methylene)indolin-2-ones: synthesis, in vitro cytotoxicity evaluation and apoptosis inducing studies. Eur. J. Med. Chem. 122 (2016), 584–600.
    • (2016) Eur. J. Med. Chem. , vol.122 , pp. 584-600
    • Sharma, P.1    Thummuri, D.2    Reddy, T.S.3    Senwar, K.R.4    Naidu, V.G.M.5    Srinivasulu, G.6    Bharghava, S.K.7    Shankaraiah, N.8
  • 31
    • 84898400145 scopus 로고    scopus 로고
    • Pd-catalyzed aryl C–H activation and tandem ortho-hydroxylation/alkoxylation of 2-aryl benzimidazoles: cytotoxicity and DNA-binding studies
    • [16](c) Kamal, A., Srinivasulu, V., Sathish, M., Tangella, Y., Nayak, V.L., Rao, M.P.N., Shankaraiah, N., Nagesh, N., Pd-catalyzed aryl C–H activation and tandem ortho-hydroxylation/alkoxylation of 2-aryl benzimidazoles: cytotoxicity and DNA-binding studies. Asian J. Org. Chem. 3 (2014), 68–76.
    • (2014) Asian J. Org. Chem. , vol.3 , pp. 68-76
    • Kamal, A.1    Srinivasulu, V.2    Sathish, M.3    Tangella, Y.4    Nayak, V.L.5    Rao, M.P.N.6    Shankaraiah, N.7    Nagesh, N.8
  • 34
    • 38949125112 scopus 로고    scopus 로고
    • Hybrid molecules with a dual mode of action: dream or reality?
    • [18] Meunier, B., Hybrid molecules with a dual mode of action: dream or reality?. Acc. Chem. Res. 41 (2008), 69–77.
    • (2008) Acc. Chem. Res. , vol.41 , pp. 69-77
    • Meunier, B.1
  • 35
    • 84928974863 scopus 로고    scopus 로고
    • A one-pot ‘click’ reaction from spiro-epoxides catalyzed by Cu(I)-pyrrolidinyl-oxazole-carboxamide
    • [19](a) Senwar, K.R., Sharma, P., Nekkanti, S., Sathish, M., Kamal, A., Sridhar, B., Shankaraiah, N., A one-pot ‘click’ reaction from spiro-epoxides catalyzed by Cu(I)-pyrrolidinyl-oxazole-carboxamide. New. J. Chem. 39 (2015), 3973–3981.
    • (2015) New. J. Chem. , vol.39 , pp. 3973-3981
    • Senwar, K.R.1    Sharma, P.2    Nekkanti, S.3    Sathish, M.4    Kamal, A.5    Sridhar, B.6    Shankaraiah, N.7
  • 36
    • 85027942620 scopus 로고    scopus 로고
    • Design and synthesis of C3-pyrazole/chalcone linked β-carboline hybrids: antitopoisomerase I, DNA interactive and apoptosis inducing anticancer agents
    • [19](b) Kamal, A., Srinivasulu, V., Nayak, V.L., Sathish, M., Shankaraiah, N., Bagul, C., Reddy, N.V.S., Rangaraj, N., Nagesh, N., Design and synthesis of C3-pyrazole/chalcone linked β-carboline hybrids: antitopoisomerase I, DNA interactive and apoptosis inducing anticancer agents. ChemMedChem 9 (2014), 2084–2098.
    • (2014) ChemMedChem , vol.9 , pp. 2084-2098
    • Kamal, A.1    Srinivasulu, V.2    Nayak, V.L.3    Sathish, M.4    Shankaraiah, N.5    Bagul, C.6    Reddy, N.V.S.7    Rangaraj, N.8    Nagesh, N.9
  • 37
    • 33846641698 scopus 로고    scopus 로고
    • Solid-phase synthesis of a library of pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones with potential antitubercular activity
    • [19](c) A. Kamal, K. L. Reddy, V. Devaiah, N. Shankaraiah, G. S. K. Reddy, S. Raghavan, Solid-phase synthesis of a library of pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones with potential antitubercular activity J. Comb. Chem. 9(2007) 29–42.
    • (2007) J. Comb. Chem. , vol.9 , pp. 29-42
    • Kamal, A.1    Reddy, K.L.2    Devaiah, V.3    Shankaraiah, N.4    Reddy, G.S.K.5    Raghavan, S.6
  • 39
    • 84935883110 scopus 로고    scopus 로고
    • Structure–activity relationship and pharmacokinetic studies of 1,5-diheteroarylpenta-1,4-dien-3-ones: a class of promising curcumin-based anticancer agents
    • [21] Wang, R., Chen, C., Zhang, X., Zhang, C., Zhong, Q., Chen, G., Zhang, Q., Zheng, S., Wang, G., Chen, Q.-H., Structure–activity relationship and pharmacokinetic studies of 1,5-diheteroarylpenta-1,4-dien-3-ones: a class of promising curcumin-based anticancer agents. J. Med. Chem. 58 (2015), 4713–4726.
    • (2015) J. Med. Chem. , vol.58 , pp. 4713-4726
    • Wang, R.1    Chen, C.2    Zhang, X.3    Zhang, C.4    Zhong, Q.5    Chen, G.6    Zhang, Q.7    Zheng, S.8    Wang, G.9    Chen, Q.-H.10
  • 40
    • 84942590646 scopus 로고    scopus 로고
    • 2O-mediated isatin spiro-epoxide ring opening with NaCN: synthesis of novel 3-tetrazolylmethyl-3-hydroxy-oxindole hybrids and their anticancer evaluation
    • [22] Sharma, P., Senwar, K.R., Jeengar, M.K., Reddy, T.S., Naidu, V.G.M., Kamal, A., Shankaraiah, N., H2O-mediated isatin spiro-epoxide ring opening with NaCN: synthesis of novel 3-tetrazolylmethyl-3-hydroxy-oxindole hybrids and their anticancer evaluation. Eur. J. Med. Chem. 104 (2015), 11–24.
    • (2015) Eur. J. Med. Chem. , vol.104 , pp. 11-24
    • Sharma, P.1    Senwar, K.R.2    Jeengar, M.K.3    Reddy, T.S.4    Naidu, V.G.M.5    Kamal, A.6    Shankaraiah, N.7
  • 41
    • 34347218991 scopus 로고    scopus 로고
    • In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro
    • [23](a) Liang, C.-C., Park, A.Y., Guan, J.-L., In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro. Nat. Protoc. 2 (2007), 329–333.
    • (2007) Nat. Protoc. , vol.2 , pp. 329-333
    • Liang, C.-C.1    Park, A.Y.2    Guan, J.-L.3
  • 42
    • 84938371554 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of 1,3-diphenyl-1H-pyrazole derivatives containing benzimidazole skeleton as potential anticancer and apoptosis inducing agents
    • [23](b) Reddy, T.S., Kulhari, H., Reddy, V.G., Bansal, V., Kamal, A., Shukla, R., Design, synthesis and biological evaluation of 1,3-diphenyl-1H-pyrazole derivatives containing benzimidazole skeleton as potential anticancer and apoptosis inducing agents. Eur. J. Med. Chem. 101 (2015), 790–805.
    • (2015) Eur. J. Med. Chem. , vol.101 , pp. 790-805
    • Reddy, T.S.1    Kulhari, H.2    Reddy, V.G.3    Bansal, V.4    Kamal, A.5    Shukla, R.6
  • 43
    • 42049092972 scopus 로고    scopus 로고
    • Regulation of actin assembly associated with protrusion and adhesion in cell migration
    • [24](a) Clainche, C.L., Carlier, M.F., Regulation of actin assembly associated with protrusion and adhesion in cell migration. Physiol. Rev. 88 (2008), 489–513.
    • (2008) Physiol. Rev. , vol.88 , pp. 489-513
    • Clainche, C.L.1    Carlier, M.F.2
  • 44
    • 84963804488 scopus 로고    scopus 로고
    • Synthesis of (Z)-1-(1,3-diphenyl-1H-pyrazol-4-yl)-3-(phenylamino)prop-2-en-1-one derivatives as potential anticancer and apoptosis inducing agents
    • [24](b) Reddy, T.S., Reddy, V.G., Kulhari, H., Shukla, R., Kamal, A., Bansal, V., Synthesis of (Z)-1-(1,3-diphenyl-1H-pyrazol-4-yl)-3-(phenylamino)prop-2-en-1-one derivatives as potential anticancer and apoptosis inducing agents. Eur. J. Med. Chem. 117 (2016), 157–166.
    • (2016) Eur. J. Med. Chem. , vol.117 , pp. 157-166
    • Reddy, T.S.1    Reddy, V.G.2    Kulhari, H.3    Shukla, R.4    Kamal, A.5    Bansal, V.6
  • 45
    • 77953021503 scopus 로고    scopus 로고
    • Cucurbitacin B induces apoptosis and S phase cell cycle arrest in BEL-7402 human hepatocellular carcinoma cells and is effective via oral administration
    • [25] Chan, K.T., Meng, F.Y., Li, Q., Ho, C.Y., Lam, T.S., To, Y., Lee, W.H., Li, M., Chu, K.H., Toh, M., Cucurbitacin B induces apoptosis and S phase cell cycle arrest in BEL-7402 human hepatocellular carcinoma cells and is effective via oral administration. Cancer Lett. 294 (2010), 118–124.
    • (2010) Cancer Lett. , vol.294 , pp. 118-124
    • Chan, K.T.1    Meng, F.Y.2    Li, Q.3    Ho, C.Y.4    Lam, T.S.5    To, Y.6    Lee, W.H.7    Li, M.8    Chu, K.H.9    Toh, M.10
  • 46
    • 84893283159 scopus 로고    scopus 로고
    • Synthesis of novel ring-A fused hybrids of oleanolic acid with capabilities to arrest cell cycle and induce apoptosis in breast cancer cells
    • [26] Mallavadhani, U.V., Vanga, N.R., Jeengar, M.K., Naidu, V.G.M., Synthesis of novel ring-A fused hybrids of oleanolic acid with capabilities to arrest cell cycle and induce apoptosis in breast cancer cells. Eur. J. Med. Chem. 74 (2014), 398–404.
    • (2014) Eur. J. Med. Chem. , vol.74 , pp. 398-404
    • Mallavadhani, U.V.1    Vanga, N.R.2    Jeengar, M.K.3    Naidu, V.G.M.4
  • 47
    • 0025046988 scopus 로고
    • Time-resolved fluorescence of DAPI in solution and bound to polydeoxynucleotides
    • [27] Barcellona, M.L., Cardiel, G., Gratton, E., Time-resolved fluorescence of DAPI in solution and bound to polydeoxynucleotides. Biochem. Biophys. Res. Commun. 170 (1990), 270–280.
    • (1990) Biochem. Biophys. Res. Commun. , vol.170 , pp. 270-280
    • Barcellona, M.L.1    Cardiel, G.2    Gratton, E.3
  • 48
    • 84983197442 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of pyrazolo–triazole hybrids as cytotoxic and apoptosis inducing agents
    • [28] Reddy, T.S., Kulhari, H., Reddy, V.G., Rao, A.V.S., Bansal, V., Kamal, A., Shukla, R., Synthesis and biological evaluation of pyrazolo–triazole hybrids as cytotoxic and apoptosis inducing agents. Org. Biomol. Chem. 13 (2015), 10136–10149.
    • (2015) Org. Biomol. Chem. , vol.13 , pp. 10136-10149
    • Reddy, T.S.1    Kulhari, H.2    Reddy, V.G.3    Rao, A.V.S.4    Bansal, V.5    Kamal, A.6    Shukla, R.7
  • 49
    • 80051512168 scopus 로고    scopus 로고
    • Withaferin A-induced apoptosis in human breast cancer cells is mediated by reactive oxygen species
    • [29](a) Hahm, E.-R., Moura, M.B., Kelley, E.E., Houten, B.V., Shiva, S., Singh, S.V., Withaferin A-induced apoptosis in human breast cancer cells is mediated by reactive oxygen species. PLoS One, 6, 2011, e23354.
    • (2011) PLoS One , vol.6 , pp. e23354
    • Hahm, E.-R.1    Moura, M.B.2    Kelley, E.E.3    Houten, B.V.4    Shiva, S.5    Singh, S.V.6
  • 50
    • 84896874935 scopus 로고    scopus 로고
    • Polyphenol-rich apple (Malus domestica L.) peel extract attenuates arsenic trioxide induced cardiotoxicity in H9c2 cells via its antioxidant activity
    • [29](b) Vineetha, V.P., Girija, S., Soumya, R.S., Raghu, K.G., Polyphenol-rich apple (Malus domestica L.) peel extract attenuates arsenic trioxide induced cardiotoxicity in H9c2 cells via its antioxidant activity. Food Funct. 5 (2014), 502–511.
    • (2014) Food Funct. , vol.5 , pp. 502-511
    • Vineetha, V.P.1    Girija, S.2    Soumya, R.S.3    Raghu, K.G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.