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Volumn 64, Issue , 2013, Pages 285-291

Synthesis and in vitro anticancer studies of novel C-2 arylidene congeners of lantadenes

Author keywords

COMPARE analysis; Cytotoxicity; Lantadenes; NCI

Indexed keywords

2 (3 NITROBENZYLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 (3 PHENYLPROP 2 EN 1 YLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 (4 CHLOROBENZYLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 (4 DIMETHYLAMINOBENZYLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 (4 FLUOROBENZYLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 (4 HYDROXY 3 METHOXYBENZYLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 (4 METHOXYBENZYLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 (4 METHYLBENZYLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 (PYRIDINE 4 YLMETHYLIDENE) 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 2 BENZYLIDENE 22 BETA HYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; 22BETA [(2 METHYL 1 OXO 2 BUTENYL)OXY] 3BETA HYDROXYOLEAN 12 EN 28 OIC ACID; 22BETA [(3 METHYL 1 OXO 2 BUTENYL)OXY] 3BETA HYDROXYOLEAN 12 EN 28 OIC ACID; 22BETA HYDROXYOLEAN 12 EN 28 OIC ACID; 3BETA,22BETA DIHYDROXY 3 OXOOLEAN 12 EN 28 OIC ACID; ANTINEOPLASTIC AGENT; CISPLATIN; LANTADENE A; LANTADENE B; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84877078781     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2013.04.009     Document Type: Article
Times cited : (19)

References (19)
  • 1
    • 35148836262 scopus 로고    scopus 로고
    • Natural triterpenoids from Cecropia lyratiloba are cytotoxic to both sensitive and multidrug resistant leukemia cell lines
    • G.G. Rocha, M. Simões, K.A. Lúcio, R.R. Oliveira, M.A.C. Kaplan, and C.R. Gattass Natural triterpenoids from Cecropia lyratiloba are cytotoxic to both sensitive and multidrug resistant leukemia cell lines Bioorg. Med. Chem. 15 2007 7355 7360
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 7355-7360
    • Rocha, G.G.1    Simões, M.2    Lúcio, K.A.3    Oliveira, R.R.4    Kaplan, M.A.C.5    Gattass, C.R.6
  • 2
    • 0028895005 scopus 로고
    • Inhibitory effects of Lantadenes and related triterpinoids on Epstein-Barr virus activation
    • A. Inada, T. Nakanishi, H. Tokuda, H. Nishino, A. Iwashina, and O.P. Sharma Inhibitory effects of Lantadenes and related triterpinoids on Epstein-Barr virus activation Planta Med. 61 1995 558 559
    • (1995) Planta Med. , vol.61 , pp. 558-559
    • Inada, A.1    Nakanishi, T.2    Tokuda, H.3    Nishino, H.4    Iwashina, A.5    Sharma, O.P.6
  • 3
    • 0030751659 scopus 로고    scopus 로고
    • Anti-tumor promoting activities of lantadenes on mouse skin tumors and mouse hepatic tumors
    • A. Inada, T. Nakanishi, H. Tokuda, H. Nishino, A. Iwashina, and O.P. Sharma Anti-tumor promoting activities of lantadenes on mouse skin tumors and mouse hepatic tumors Planta Med. 63 1997 272 274
    • (1997) Planta Med. , vol.63 , pp. 272-274
    • Inada, A.1    Nakanishi, T.2    Tokuda, H.3    Nishino, H.4    Iwashina, A.5    Sharma, O.P.6
  • 4
    • 42049086093 scopus 로고    scopus 로고
    • Chemopreventive activity of lantadenes on two-stage carcinogenesis model in Swiss albino mice: AP-1 (c-jun), NF kB (p65) and p55 expression by ELISA and immunohistochemical localization
    • J. Kaur, M. Sharma, P.D. Sharma, and M.P. Bansal Chemopreventive activity of lantadenes on two-stage carcinogenesis model in Swiss albino mice: AP-1 (c-jun), NF kB (p65) and p55 expression by ELISA and immunohistochemical localization Mol. Cell. Biochem. 314 2008 1 8
    • (2008) Mol. Cell. Biochem. , vol.314 , pp. 1-8
    • Kaur, J.1    Sharma, M.2    Sharma, P.D.3    Bansal, M.P.4
  • 5
    • 81755184640 scopus 로고    scopus 로고
    • Antitumor activity of Lantadenes in DMBA/TPA induced skin tumors in mice: Expression of transcription factors
    • J. Kaur, M. Sharma, P.D. Sharma, and M.P. Bansal Antitumor activity of Lantadenes in DMBA/TPA induced skin tumors in mice: expression of transcription factors Am. J. Biomed. Sci. 2 2010 79 90
    • (2010) Am. J. Biomed. Sci. , vol.2 , pp. 79-90
    • Kaur, J.1    Sharma, M.2    Sharma, P.D.3    Bansal, M.P.4
  • 6
    • 84879024885 scopus 로고    scopus 로고
    • Synthesis, selective cancer cytotoxicity and mechanistic studies of novel analogs of lantadenes
    • (Epub ahead of print)
    • N.K. Tailor, V. Jaiswal, S.S. Lan, H.B. Lee, and M. Sharma Synthesis, selective cancer cytotoxicity and mechanistic studies of novel analogs of lantadenes Anticancer Agents Med. Chem. 2012 Dec 24 (Epub ahead of print)
    • (2012) Anticancer Agents Med. Chem.
    • Tailor, N.K.1    Jaiswal, V.2    Lan, S.S.3    Lee, H.B.4    Sharma, M.5
  • 7
    • 34447637984 scopus 로고    scopus 로고
    • Lantadene A-induced apoptosis in human leukemia HL-60 cells
    • M. Sharma, P.D. Sharma, M.P. Bansal, and J. Singh Lantadene A-induced apoptosis in human leukemia HL-60 cells Ind. J. Pharmacol. 39 2007 140 144
    • (2007) Ind. J. Pharmacol. , vol.39 , pp. 140-144
    • Sharma, M.1    Sharma, P.D.2    Bansal, M.P.3    Singh, J.4
  • 8
    • 49049120810 scopus 로고    scopus 로고
    • Lantadenes and their esters as potential antitumor agents
    • M. Sharma, P.D. Sharma, and M.P. Bansal Lantadenes and their esters as potential antitumor agents J. Nat. Prod. 71 2008 1222 1227
    • (2008) J. Nat. Prod. , vol.71 , pp. 1222-1227
    • Sharma, M.1    Sharma, P.D.2    Bansal, M.P.3
  • 9
    • 34250689896 scopus 로고    scopus 로고
    • Synthesis, cytotoxicity and antitumor activity of Lantadene A congeners
    • M. Sharma, P.D. Sharma, M.P. Bansal, and J. Singh Synthesis, cytotoxicity and antitumor activity of Lantadene A congeners Chem. Biodiver. 4 2007 932 939
    • (2007) Chem. Biodiver. , vol.4 , pp. 932-939
    • Sharma, M.1    Sharma, P.D.2    Bansal, M.P.3    Singh, J.4
  • 10
    • 33947537738 scopus 로고    scopus 로고
    • Synthesis and antitumor activity of novel pentacyclic triterpenoid Lantadene D
    • M. Sharma, P.D. Sharma, and M.P. Bansal Synthesis and antitumor activity of novel pentacyclic triterpenoid Lantadene D Lett. Drug Des. Discov. 4 2007 201 206
    • (2007) Lett. Drug Des. Discov. , vol.4 , pp. 201-206
    • Sharma, M.1    Sharma, P.D.2    Bansal, M.P.3
  • 11
    • 79951743402 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of Lantadene A congener with hydroxyl functionality in ring A as an antitumour agent
    • M. Sharma, A. Rakhi, N. Dalal, and N. Sharma Design, synthesis and evaluation of Lantadene A congener with hydroxyl functionality in ring A as an antitumour agent Nat. Prod. Res. 25 2011 387 396
    • (2011) Nat. Prod. Res. , vol.25 , pp. 387-396
    • Sharma, M.1    Rakhi, A.2    Dalal, N.3    Sharma, N.4
  • 13
    • 0028906786 scopus 로고
    • Some practical considerations and applications of the national cancer institute in vitro anticancer drug discovery screen
    • M.R. Boyd, and K.D. Paull Some practical considerations and applications of the national cancer institute in vitro anticancer drug discovery screen Drug Develop. Res. 34 1995 91 104
    • (1995) Drug Develop. Res. , vol.34 , pp. 91-104
    • Boyd, M.R.1    Paull, K.D.2
  • 14
    • 77952117909 scopus 로고    scopus 로고
    • Analysis of FDA-approved anti-cancer agents in the NCI 60 panel of human Tumor cell lines
    • S.L. Holbeck, J.M. Collins, and J.H. Doroshow Analysis of FDA-approved anti-cancer agents in the NCI 60 panel of human Tumor cell lines Mol. Cancer Ther. 9 2010 1451 1460
    • (2010) Mol. Cancer Ther. , vol.9 , pp. 1451-1460
    • Holbeck, S.L.1    Collins, J.M.2    Doroshow, J.H.3
  • 17
    • 33749028694 scopus 로고    scopus 로고
    • Optimization of lantadene isolation and preparation of 22β-hydroxy oleanonic acid
    • M. Sharma, and P.D. Sharma Optimization of lantadene isolation and preparation of 22β-hydroxy oleanonic acid Chem. Nat. Comp. 42 2006 442 444
    • (2006) Chem. Nat. Comp. , vol.42 , pp. 442-444
    • Sharma, M.1    Sharma, P.D.2
  • 19
    • 33749011163 scopus 로고    scopus 로고
    • The NCI60 human tumour cell line anticancer drug screen
    • R.H. Shoemaker The NCI60 human tumour cell line anticancer drug screen Nat. Rev. Cancer 6 2006 813 823
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 813-823
    • Shoemaker, R.H.1


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