메뉴 건너뛰기




Volumn 77, Issue , 2014, Pages 258-268

Development of bivalent oleanane-type triterpenes as potent HCV entry inhibitors

Author keywords

Dimer; Echinocystic acid; HCV entry inhibitor; Triterpene

Indexed keywords

1,2,3 TRI [[N (3BETA,16ALPHA DIHYDROXYL OLEAN 12 EN 28 OYL)AMINO]METHYL (1H 1,2,3 TRIAZOL 4 YL)]PROPANE; 2,2,2 TRI [[N (3BETA,16ALPHA DIHYDROXYL OLEAN 12 EN 28 OYL)AMINO]METHYL (1H 1,2,3 TRIAZOL 4 YL)METHYL]ETHANOL; ANTIVIRUS AGENT; ECHINOCYSTIC ACID; N (3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) (1 BENZYL 1H 1,2,3 TRIAZOL 4 YL)METHYLAMINE; N (3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) (1 ETHYL 1H 1,2,3 TRIAZOL 4-YL)METHYLAMINE; N (3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) (1 PROPYL 1H 1,2,3 TRIAZOL 4 YL)METHYLAMIN; N (3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1 (3 HYDROXYPROPYL) 1H 1,2,3 TRIAZOL 4 YL]METHYLAMINE; N (3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28- YL) [1 (2 HYDROXYETHYL) 1H 1,2,3 TRIAZOL 4 YL]METHYLAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) 1,12 DIAMINODODECANE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) 1,3 DIAMINOPROPANE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) 1,4 DIAMINOBUTANE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) 1,5 DIAMINE 3 OXAPENTANE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) 1,6 DIAMINOHEXANE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' (ETHANE 1,2 DIYL)BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' (HEXANE 1,6 DIYL)BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' (PENTANE 1,5 DIYL)BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' (PROPANE 1,4 DIYL)BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' [(2,5 DIMETHOXY 1,4 PHENYLENE)BIS(METHYLENE)]BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' [(2,5 DIMETHYL 1,4 PHENYLENE)BIS(METHYLENE)]BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' [1,2 PHENYLENEBIS(METHYLENE)]BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' [1,3 PHENYLENEBIS(METHYLENE)]BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' [1,4 PHENYLENEBIS(ETHANE 2,1 DIYL)]BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' [1,4 PHENYLENEBIS(METHYLENE)]BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' [OXYBIS(ETHANE 2,1DIYL)](1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL) [1,1' [[[OXYBIS(ETHANE 2,1DIYL)]BIS(OXY)]BIS(ETHANE 2,1 DIYL)]BIS(1H 1,2,3 TRIAZOLE 4,1 DIYL)]DIMETHANAMINE; N,N' BIS(3BETA,16ALPHA DIHYDROXY OLEAN 12 EN 28 OYL)TETRAETHYLENE GLYCOL BISAMINE; TETRA [[N (3BETA,16ALPHA DIHYDROXYL OLEAN 12 EN 28 OYL)AMINO]METHYL (1H 1,2,3 TRIAZOL 4 YL)METHYL]METHANE; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; OLEANANE; OLEANOLIC ACID; TRITERPENE;

EID: 84896536482     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2014.03.017     Document Type: Article
Times cited : (32)

References (18)
  • 1
    • 0033839753 scopus 로고    scopus 로고
    • Assessment of long-term outcomes of community-acquired hepatitis C infection in a cohort with sera stored from 1971 to 1975
    • A.J. Rodger, S. Roberts, A. Lanigan, S. Bowden, T. Brown, N. Crofts, Assessment of long-term outcomes of community-acquired hepatitis C infection in a cohort with sera stored from 1971 to 1975, Hepatology 32 (2000) 582-587.
    • (2000) Hepatology , vol.32 , pp. 582-587
    • Rodger, A.J.1    Roberts, S.2    Lanigan, A.3    Bowden, S.4    Brown, T.5    Crofts, N.6
  • 3
    • 84856371566 scopus 로고    scopus 로고
    • New Merck and Vertex drugs raise standard of care in hepatitis C
    • C. Sheridan, New Merck and Vertex drugs raise standard of care in hepatitis C, Nature Biotechnology 29 (2011) 553-554.
    • (2011) Nature Biotechnology , vol.29 , pp. 553-554
    • Sheridan, C.1
  • 5
    • 0036139972 scopus 로고    scopus 로고
    • New therapeutic strategies for hepatitis C
    • DOI 10.1053/jhep.2002.30531
    • A.M. Di Bisceglie, J. McHutchison, C.M. Rice, New therapeutic strategies for hepatitis C, Hepatology 35 (2002) 224-231. (Pubitemid 34032564)
    • (2002) Hepatology , vol.35 , Issue.1 , pp. 224-231
    • Di, B.A.M.1    McHutchison, J.2    Rice, C.M.3
  • 6
    • 79958830099 scopus 로고    scopus 로고
    • Hepatitis C virus resistance to protease inhibitors
    • P. Halfon, S. Locarnini, Hepatitis C virus resistance to protease inhibitors, Journal of Hepatology 55 (2011) 192-206.
    • (2011) Journal of Hepatology , vol.55 , pp. 192-206
    • Halfon, P.1    Locarnini, S.2
  • 7
    • 84855246805 scopus 로고    scopus 로고
    • Future treatment of chronic hepatitis C with direct acting antivirals: Is resistance important?
    • P. Halfon, C. Sarrazin, Future treatment of chronic hepatitis C with direct acting antivirals: is resistance important? Liver International 32 (2012) 79-87.
    • (2012) Liver International , vol.32 , pp. 79-87
    • Halfon, P.1    Sarrazin, C.2
  • 8
    • 61549095016 scopus 로고    scopus 로고
    • Screening of small-molecule compounds as inhibitors of HCV entry
    • J. Yang, D. Zhou, F. Wong-Staal, Screening of small-molecule compounds as inhibitors of HCV entry, Methods in Molecular Biology 510 (2009) 295-304.
    • (2009) Methods in Molecular Biology , vol.510 , pp. 295-304
    • Yang, J.1    Zhou, D.2    Wong-Staal, F.3
  • 16
    • 78650917501 scopus 로고    scopus 로고
    • Measuring antiviral activity of benzimidazole molecules that alter IRES RNA structure with an infectious hepatitis C virus chimera expressing Renilla luciferase
    • S. Liu, C.A. Nelson, L. Xiao, L. Lu, P.P. Seth, D.R. Davis, C.H. Hagedorn, Measuring antiviral activity of benzimidazole molecules that alter IRES RNA structure with an infectious hepatitis C virus chimera expressing Renilla luciferase, Antiviral Research 89 (2011) 54-63.
    • (2011) Antiviral Research , vol.89 , pp. 54-63
    • Liu, S.1    Nelson, C.A.2    Xiao, L.3    Lu, L.4    Seth, P.P.5    Davis, D.R.6    Hagedorn, C.H.7
  • 17
    • 0036956250 scopus 로고    scopus 로고
    • The biological action of saponins in animal systems: A review
    • DOI 10.1079/BJN2002725
    • G. Francis, Z. Kerem, H.P.S. Makkar, K. Becker, The biological action of saponins in animal systems: a review, British Journal of Nutrition 88 (2002) 587-605. (Pubitemid 36082888)
    • (2002) British Journal of Nutrition , vol.88 , Issue.6 , pp. 587-605
    • Francis, G.1    Kerem, Z.2    Makkar, H.P.S.3    Becker, K.4
  • 18
    • 0030560967 scopus 로고    scopus 로고
    • Characterization of a hemagglutinin-specific inhibitor of influenza A virus
    • DOI 10.1006/viro.1996.0628
    • G. Luo, R. Colonno, M. Krystal, Characterization of a hemagglutinin-specific inhibitor of influenza A virus, Virology 226 (1996) 66-76. (Pubitemid 26414395)
    • (1996) Virology , vol.226 , Issue.1 , pp. 66-76
    • Luo, G.1    Colonno, R.2    Krystal, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.