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Volumn 38, Issue 3, 2010, Pages 701-709

Pseudo-peptides derived from isomannide: Inhibitors of serine proteases

Author keywords

Dengue; Hepatitis C; Isomannide; Oxazolones; Serine protease

Indexed keywords

1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 2 NAPHTHYLACRYLAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 2 THIOPHENYLACRYLAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 3,4 DIMETHOXYCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 3,4 METHYLENEDIOXYCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 4 BROMOCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 4 CHLOROCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 4 FLUOROCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 4 METHYLCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO 4 TRIFLUOROMETHYLCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 ACETAMIDO CINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 2 THIOPHENYLACRYLAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 3 PYRIDYLACRYLAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 3,4 DIMETHOXYCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 3,4 METHYLENEDIOXYCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 4 BROMOCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 4 CHLOROCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 4 FLUOROCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 4 METHOXYCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO 4 TRIFLUOROMETHYLCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS [2 BENZAMIDO CINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; 1,4:3,6 DIANHYDRO 2,5 BIS N [2 ACETAMIDO 4 CYANOCINNAMAMIDO] 2,5 DIDEOXY LEVO IDITIOL; ALPHA INTERFERON; ANTIVIRUS AGENT; PSEUDOPEPTIDE; THIOPHENE; UNCLASSIFIED DRUG;

EID: 77951667433     PISSN: 09394451     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00726-009-0273-4     Document Type: Article
Times cited : (20)

References (43)
  • 1
    • 3142641019 scopus 로고
    • Synthesis of polynitro-2, 6-dioxabicyclo[3.3.0]octanes
    • 10.1080/00397918908051042 10.1080/00397918908051042 1:CAS:528: DyaK3cXpvFSmsw%3D%3D
    • TG Archibald K Baum 1989 Synthesis of polynitro-2, 6-dioxabicyclo[3.3.0] octanes Synth Commun 19 1493 1498 10.1080/00397918908051042 10.1080/ 00397918908051042 1:CAS:528:DyaK3cXpvFSmsw%3D%3D
    • (1989) Synth Commun , vol.19 , pp. 1493-1498
    • Archibald, T.G.1    Baum, K.2
  • 2
    • 47049112231 scopus 로고    scopus 로고
    • Combinations of 2'-C-methylcytidine analogues with interferon-α 2b and triple combination with ribavirin in the hepatitis C virus replicon system
    • 1:CAS:528:DC%2BD1cXnvFCltbk%3D 18610555
    • L Bassit J Grier M Bennett RF Schinazi 2008 Combinations of 2'-C-methylcytidine analogues with interferon-α 2b and triple combination with ribavirin in the hepatitis C virus replicon system Antivir Chem Chemother 19 25 31 1:CAS:528:DC%2BD1cXnvFCltbk%3D 18610555
    • (2008) Antivir Chem Chemother , vol.19 , pp. 25-31
    • Bassit, L.1    Grier, J.2    Bennett, M.3    Schinazi, R.F.4
  • 3
    • 0036007677 scopus 로고    scopus 로고
    • Study on dry-media microwave azalactone synthesis on different supported KF catalysts: Influence of textural and acid-base properties of supports
    • FM Bautista JM Campelo A Garcia D Luna JM Marinas AA Romero 2002 Study on dry-media microwave azalactone synthesis on different supported KF catalysts: influence of textural and acid-base properties of supports J Chem Soc Perkin Trans 2 227 234
    • (2002) J Chem Soc Perkin Trans , vol.2 , pp. 227-234
    • Bautista, F.M.1    Campelo, J.M.2    Garcia, A.3    Luna, D.4    Marinas, J.M.5    Romero, A.A.6
  • 4
    • 0024372153 scopus 로고
    • Detection of a trypsin-like serine protease domain in flaviviruses and pestiviruses
    • DOI 10.1016/0042-6822(89)90639-9
    • JF Bazan RJ Fletterick 1989 Detection of a trypsin-like serine protease domain in flaviviruses and pestiviruses Virology 171 637 639 10.1016/0042-6822(89)90639-9 10.1016/0042-6822(89)90639-9 1:CAS:528: DyaL1MXlt12ms7w%3D 2548336 (Pubitemid 19210412)
    • (1989) Virology , vol.171 , Issue.2 , pp. 637-639
    • Bazan, J.F.1    Fletterick, R.J.2
  • 5
    • 0000651334 scopus 로고
    • Structural and catalytic models of trypsin-like viral proteases
    • 1:CAS:528:DyaK3MXks1Oisb8%3D
    • JF Bazan RJ Fletterick 1990 Structural and catalytic models of trypsin-like viral proteases Semin Virol 1 311 322 1:CAS:528:DyaK3MXks1Oisb8%3D
    • (1990) Semin Virol , vol.1 , pp. 311-322
    • Bazan, J.F.1    Fletterick, R.J.2
  • 6
    • 0141520355 scopus 로고    scopus 로고
    • Efficient, stereoselective synthesis of oxazolo[3,2-a]pyrazin-5-ones: Novel bicyclic lactam scaffolds from the bicyclocondensation of 3-aza-1,5-ketoacids and amino alcohols
    • DOI 10.1021/ol030065h
    • JR Bencsik T Kercher M O'Sullivan JA Josey 2003 Efficient, stereoselective synthesis of oxazolo[3, 2-a]pyrazin-5-ones: novel bicyclic lactam scaffolds from the bicyclocondensation of 3-aza-1, 5-keto acids and amino alcohols Org Lett 54 2727 2730 10.1021/ol030065h 10.1021/ol030065h (Pubitemid 37140851)
    • (2003) Organic Letters , vol.5 , Issue.15 , pp. 2727-2730
    • Bencsik, J.R.1    Kercher, T.2    O'Sullivan, M.3    Josey, J.A.4
  • 8
    • 0024421391 scopus 로고
    • Prevalence of antibodies to hepatitis C virus in Spanish patients with hepatocellular carcinoma and hepatic cirrhosis
    • J Bruix X Cavalet J Costa M Ventura M Bruguera R Castillo JM Barrera G Ercilla JM Sanchez-Tapias M Vall C Bru J Rodes 1989 Prevalence of antibodies to hepatitis C virus in Spanish patients with hepatocellular carcinoma and hepatic cirrhosis Lancet 2 1004 1006 10.1016/S0140-6736(89)91015-5 10.1016/S0140- 6736(89)91015-5 1:STN:280:DyaK3c%2Fkt1Ojsw%3D%3D 2572739 (Pubitemid 19257915)
    • (1989) Lancet , vol.2 , Issue.8670 , pp. 1004-1006
    • Bruix, J.1    Calvet, X.2    Costa, J.3    Ventura, M.4    Bruguera, M.5    Castillo, R.6    Barrera, J.M.7    Ercilla, G.8    Sanchez-Tapias, J.M.9    Vall, M.10    Bru, C.11    Rodes, J.12
  • 9
    • 0043011003 scopus 로고    scopus 로고
    • 3 and KCN with alkyl halides and tosylates
    • DOI 10.1021/jo026838h
    • 3 and KCN with alkyl halides and tosylates J Org Chem 68 6710 6715 10.1021/jo026838h 10.1021/jo026838h 1:CAS:528:DC%2BD3sXlslKnt7Y%3D 12919037 (Pubitemid 37010979)
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.17 , pp. 6710-6715
    • Chiappe, C.1    Pieraccini, D.2    Saullo, P.3
  • 10
    • 0042338525 scopus 로고    scopus 로고
    • Efficient synthesis of enantiopure pyrrolizidinone amino acid
    • DOI 10.1021/jo034739d
    • E Dietrich WD Lubell 2003 Efficient synthesis of enantiopure pyrrolizidinone amino acid J Org Chem 68 6988 6996 10.1021/jo034739d 10.1021/jo034739d 1:CAS:528:DC%2BD3sXmsVehu7Y%3D 12946139 (Pubitemid 37071778)
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.18 , pp. 6988-6996
    • Dietrich, E.1    Lubell, W.D.2
  • 11
    • 0034583251 scopus 로고    scopus 로고
    • Ionic liquids: Green solvents for the future
    • 10.1351/pac200072071391 10.1351/pac200072071391 1:CAS:528: DC%2BD3cXotFKqsLs%3D
    • MJ Earle KR Seddon 2000 Ionic liquids: green solvents for the future Pure Appl Chem 72 1391 1398 10.1351/pac200072071391 10.1351/pac200072071391 1:CAS:528:DC%2BD3cXotFKqsLs%3D
    • (2000) Pure Appl Chem , vol.72 , pp. 1391-1398
    • Earle, M.J.1    Seddon, K.R.2
  • 13
    • 35348829315 scopus 로고    scopus 로고
    • Darunavir, a conceptually new HIV-1 protease inhibitor for the treatment of drug-resistant HIV
    • DOI 10.1016/j.bmc.2007.09.010, PII S0968089607007833
    • AK Ghosh ZL Dawson H Mitsuya 2007 Darunavir, a conceptually new HIV-1 protease inhibitor for the treatment of drug-resistant HIV Bioorg Med Chem 15 7576 7580 10.1016/j.bmc.2007.09.010 10.1016/j.bmc.2007.09.010 1:CAS:528:DC%2BD2sXhtF2msL%2FJ 17900913 (Pubitemid 47575929)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.24 , pp. 7576-7580
    • Ghosh, A.K.1    Dawson, Z.L.2    Mitsuya, H.3
  • 14
    • 30744464347 scopus 로고    scopus 로고
    • Enantioselective heterogeneous catalytic production of alpha-amino acids
    • 10.1007/s11144-006-0004-8 10.1007/s11144-006-0004-8 1:CAS:528: DC%2BD28XksFKmug%3D%3D
    • M Gomes Jr R Hernandez-Valdes CESJ Marques ML Bastos DAG Aranda OAC Antunes 2006 Enantioselective heterogeneous catalytic production of alpha-amino acids React Kinet Catal Lett 87 19 24 10.1007/s11144-006-0004-8 10.1007/s11144-006-0004-8 1:CAS:528:DC%2BD28XksFKmug%3D%3D
    • (2006) React Kinet Catal Lett , vol.87 , pp. 19-24
    • Gomes Jr., M.1    Hernandez-Valdes, R.2    Cesj, M.3    Bastos, M.L.4    Aranda, D.A.G.5    Antunes, O.A.C.6
  • 15
    • 0024341494 scopus 로고
    • N-terminal domains of putative helicases of flavi- and pestiviruses may be serine proteases
    • 10.1093/nar/17.10.3889 10.1093/nar/17.10.3889 1:CAS:528: DyaL1MXktlGksbs%3D 2543956
    • AE Gorbalenya AP Donchenko EV Kunin VM Blinov 1989 N-terminal domains of putative helicases of flavi- and pestiviruses may be serine proteases Nucleic Acids Res 17 3889 3897 10.1093/nar/17.10.3889 10.1093/nar/17.10.3889 1:CAS:528:DyaL1MXktlGksbs%3D 2543956
    • (1989) Nucleic Acids Res , vol.17 , pp. 3889-3897
    • Gorbalenya, A.E.1    Donchenko, A.P.2    Kunin, E.V.3    Blinov, V.M.4
  • 16
    • 40549101840 scopus 로고    scopus 로고
    • Relative replication capacity and selective advantage profiles of protease inhibitor-resistant hepatitis C virus (HCV) NS3 protease mutants in the HCV genotype 1b replicon system
    • DOI 10.1128/AAC.01149-07
    • Y He MS King DJ Kempf L Lu HB Lim P Krishnan W Kati T Middleton A Molla 2008 Relative replication capacity and selective advantage profiles of protease inhibitor-resistant hepatitis C virus (HCV) NS3 protease mutants in the HCV genotype 1b replicon system Antimicrob Agents Chemother 52 1101 1110 10.1128/AAC.01149-07 10.1128/AAC.01149-07 1:CAS:528:DC%2BD1cXivFalt70%3D 18086851 (Pubitemid 351358394)
    • (2008) Antimicrobial Agents and Chemotherapy , vol.52 , Issue.3 , pp. 1101-1110
    • He, Y.1    King, M.S.2    Kempf, D.J.3    Lu, L.4    Lim, H.B.5    Krishnan, P.6    Kati, W.7    Middleton, T.8    Molla, A.9
  • 17
    • 4544298375 scopus 로고    scopus 로고
    • Production of L-DOPA under heterogeneous asymmetric catalysis
    • 10.1016/j.catcom.2004.07.018 10.1016/j.catcom.2004.07.018 1:CAS:528:DC%2BD2cXns1yqtbw%3D
    • R Hernandez Valdes L Puzer M Gomes CESJ Marques DAG Aranda ML Bastos AL Gemal OAC Antunes 2004 Production of L-DOPA under heterogeneous asymmetric catalysis Catal Commun 5 631 634 10.1016/j.catcom.2004.07.018 10.1016/j.catcom.2004.07.018 1:CAS:528:DC%2BD2cXns1yqtbw%3D
    • (2004) Catal Commun , vol.5 , pp. 631-634
    • Hernandez Valdes, R.1    Puzer, L.2    Gomes, M.3    Cesj, M.4    Aranda, D.A.G.5    Bastos, M.L.6    Gemal, A.L.7    Antunes, O.A.C.8
  • 18
    • 33947444931 scopus 로고
    • The structures of the anhydromannitols of Brigl and Gr.ovrddot.uner
    • 10.1021/ja01210a004 10.1021/ja01210a004 1:CAS:528:DyaH28Xitl2jsg%3D%3D
    • RC Hockett HG Fletcher Jr EL Sheffield RM Goepp Jr S Soltzberg 1946 The structures of the anhydromannitols of Brigl and Gr.ovrddot.uner J Am Chem Soc 68 930 935 10.1021/ja01210a004 10.1021/ja01210a004 1:CAS:528:DyaH28Xitl2jsg%3D%3D
    • (1946) J Am Chem Soc , vol.68 , pp. 930-935
    • Hockett, R.C.1    Fletcher Jr, H.G.2    Sheffield, E.L.3    Goepp, Jr.R.M.4    Soltzberg, S.5
  • 19
    • 0034607838 scopus 로고    scopus 로고
    • Formation of isoquinoline and 1-azetine derivatives via novel photocyclization of substituted α-dehydrophenylalanines
    • DOI 10.1016/S0040-4020(00)00188-5, PII S0040402000001885
    • H Hoshina K Kubo A Morita T Sakurai 2000 Formation of isoquinoline and 1-azetine derivatives via novel photocyclization of substituted α-dehydrophenylalanines Tetrahedron 56 2941 2951 10.1016/S0040-4020(00) 00188-5 10.1016/S0040-4020(00)00188-5 1:CAS:528:DC%2BD3cXjt1CisLc%3D (Pubitemid 30253992)
    • (2000) Tetrahedron , vol.56 , Issue.19 , pp. 2941-2951
    • Hoshina, H.1    Kubo, K.2    Morita, A.3    Sakurai, T.4
  • 20
    • 0028822273 scopus 로고
    • Efficient kg-scale synthesis of thrombin inhibitor CRC 220
    • 10.1016/0040-4020(95)00765-Z 10.1016/0040-4020(95)00765-Z 1:CAS:528:DyaK2MXptVyqtLk%3D
    • H Jendralla B Seuring J Herchen B Kulitzscher J Wunner W Stueber R Koschinsky 1995 Efficient kg-scale synthesis of thrombin inhibitor CRC 220 Tetrahedron 51 12047 12068 10.1016/0040-4020(95)00765-Z 10.1016/0040-4020(95) 00765-Z 1:CAS:528:DyaK2MXptVyqtLk%3D
    • (1995) Tetrahedron , vol.51 , pp. 12047-12068
    • Jendralla, H.1    Seuring, B.2    Herchen, J.3    Kulitzscher, B.4    Wunner, J.5    Stueber, W.6    Koschinsky, R.7
  • 21
    • 8444233615 scopus 로고    scopus 로고
    • Inhibition of subgenomic hepatitis C virus RNA in Huh-7 cells: Ribavirin induces mutagenesis in HCV RNA
    • DOI 10.1111/j.1365-2893.2004.00531.x
    • T Kanda O Yokosuka F Imazeki M Tanaka Y Shino H Shimada T Tomonaga F Nomura K Nagao T Ochiai H Saisho 2004 Inhibition of subgenomic hepatitis C virus RNA in Huh-7 cells: ribavirin induces mutagenesis in HCV RNA J Viral Hepat 11 479 487 10.1111/j.1365-2893.2004.00531.x 10.1111/j.1365-2893.2004.00531.x 1:STN:280:DC%2BD2crnsFSnsw%3D%3D 15500548 (Pubitemid 39486611)
    • (2004) Journal of Viral Hepatitis , vol.11 , Issue.6 , pp. 479-487
    • Kanda, T.1    Yokosuka, O.2    Imazeki, F.3    Tanaka, M.4    Shino, Y.5    Shimada, H.6    Tomonaga, T.7    Nomura, F.8    Nagao, K.9    Ochiai, T.10    Saisho, H.11
  • 22
    • 0001026099 scopus 로고
    • Novel molecular design for second-harmonic generation: Azlactone derivatives
    • 10.1021/j100040a031 10.1021/j100040a031 1:CAS:528:DyaK2MXnvFOlt7g%3D
    • M Kitazawa R Higuchi M Takahashi T Wada H Sasabe 1995 Novel molecular design for second-harmonic generation: azlactone derivatives J Phys Chem 99 14784 14792 10.1021/j100040a031 10.1021/j100040a031 1:CAS:528:DyaK2MXnvFOlt7g%3D
    • (1995) J Phys Chem , vol.99 , pp. 14784-14792
    • Kitazawa, M.1    Higuchi, R.2    Takahashi, M.3    Wada, T.4    Sasabe, H.5
  • 23
    • 77951665390 scopus 로고
    • US Patent 4 659 857
    • Kuhn DG (1987) US Patent 4 659 857
    • (1987)
    • Kuhn, D.G.1
  • 24
    • 0037073935 scopus 로고    scopus 로고
    • 1 Cation effects on halide nucleophilicity in a series of bis(trifluoromethylsulfonyl)imide ionic liquids
    • DOI 10.1021/jo026113d
    • NL Lancaster PA Salter T Welton GB Young 2002 Nucleophilicity in ionic liquids. 2. Cation effects on halide nucleophilicity in a series of bis(trifluoromethylsulfonyl)imide ionic liquids J Org Chem 67 8855 8861 10.1021/jo026113d 10.1021/jo026113d 1:CAS:528:DC%2BD38XosFCqtbw%3D 12467399 (Pubitemid 35471106)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.25 , pp. 8855-8861
    • Lancaster, N.L.1    Salter, P.A.2    Welton, T.3    Young, G.B.4
  • 25
    • 0035824539 scopus 로고    scopus 로고
    • Activity of Recombinant Dengue 2 Virus NS3 Protease in the Presence of a Truncated NS2B Co-factor, Small Peptide Substrates, and Inhibitors
    • DOI 10.1074/jbc.M107360200
    • D Leung K Schroder H White N-X Fang MJ Stoermer G Abbenante JL Martin PR Young DP Fairlie 2001 Activity of recombinant dengue 2 virus NS3 protease in the presence of a truncated NS2B co-factor, small peptide substrates, and inhibitors J Biol Chem 276 45762 45771 10.1074/jbc.M107360200 10.1074/jbc.M107360200 1:CAS:528:DC%2BD3MXptVynu7s%3D 11581268 (Pubitemid 37370814)
    • (2001) Journal of Biological Chemistry , vol.276 , Issue.49 , pp. 45762-45771
    • Leung, D.1    Schroder, K.2    White, H.3    Fang, N.-X.4    Stoermer, M.J.5    Abbenante, G.6    Martin, J.L.7    Young, P.R.8    Fairlie, D.P.9
  • 27
    • 0033236368 scopus 로고    scopus 로고
    • The effect of anions in the coordination sphere of Mg complexes of N-acetyldehydrophenylalanyl-(S)-valine on the diastereoselectivity of hydrogenation
    • 10.1007/BF02494812 10.1007/BF02494812 1:CAS:528:DyaK1MXotVGmu7w%3D
    • IN Lisichkina OM Ushakova MO Alekseeva AS Peregudov VM Belikov 1999 The effect of anions in the coordination sphere of Mg complexes of N-acetyldehydrophenylalanyl-(S)-valine on the diastereoselectivity of hydrogenation Russ Chem Bull 48 1682 1684 10.1007/BF02494812 10.1007/BF02494812 1:CAS:528:DyaK1MXotVGmu7w%3D
    • (1999) Russ Chem Bull , vol.48 , pp. 1682-1684
    • Lisichkina, I.N.1    Ushakova, O.M.2    Alekseeva, M.O.3    Peregudov, A.S.4    Belikov, V.M.5
  • 28
    • 0345188811 scopus 로고    scopus 로고
    • Replication of subgenomic hepatitis C virus RNAs in a hepatoma cell line
    • DOI 10.1126/science.285.5424.110
    • V Lohmann F Korner J-O Koch U Herian L Theilmann R Bartenschlager 1999 Replication of subgenomic hepatitis C virus RNAs in a hepatoma cell line Science 285 110 113 10.1126/science.285.5424.110 10.1126/science.285.5424.110 1:CAS:528:DyaK1MXksVCqurk%3D 10390360 (Pubitemid 29307577)
    • (1999) Science , vol.285 , Issue.5424 , pp. 110-113
    • Lohmann, V.1    Korner, F.2    Koch, J.-O.3    Herian, U.4    Theilmann, L.5    Bartenschlager, R.6
  • 29
    • 0037369066 scopus 로고    scopus 로고
    • Viral and cellular determinants of hepatitis C virus RNA replication in cell culture
    • DOI 10.1128/JVI.77.5.3007-3019.2003
    • V Lohmann S Hoffmann U Herian F Penin R Bartenschlager 2003 Viral and cellular determinants of hepatitis C virus RNA replication in cell culture J Virol 77 3007 3019 10.1128/JVI.77.5.3007-3019.2003 10.1128/JVI.77.5.3007-3019. 2003 1:CAS:528:DC%2BD3sXhsVOhtbs%3D 12584326 (Pubitemid 36228086)
    • (2003) Journal of Virology , vol.77 , Issue.5 , pp. 3007-3019
    • Lohmann, V.1    Hoffmann, S.2    Herian, U.3    Penin, F.4    Bartenschlager, R.5
  • 30
    • 0031579460 scopus 로고    scopus 로고
    • Asymmetric synthesis of L-thienylalanines
    • DOI 10.1016/S0957-4166(97)00016-5, PII S0957416697000165
    • J Meiwes M Schudok G Kretzschmar 1997 Asymmetric synthesis of l-thienylalanines Tetrahedron Asymmetry 8 527 536 10.1016/S0957-4166(97)00016-5 10.1016/S0957-4166(97)00016-5 1:CAS:528:DyaK2sXhvVartrk%3D (Pubitemid 27085441)
    • (1997) Tetrahedron Asymmetry , vol.8 , Issue.4 , pp. 527-536
    • Meiwes, J.1    Schudok, M.2    Kretzschmar, G.3
  • 33
    • 21244494905 scopus 로고    scopus 로고
    • Pseudo-peptides derived from isomannide as potential inhibitors of serine proteases
    • DOI 10.1007/s00726-004-0146-9
    • EMF Muri M Gomes Jr MG Albuquerque EFF Cunha RB Alencastro JS Williamson OAC Antunes 2005 Pseudo-peptides derived from isomannide as potential inhibitors of serine proteases Amino Acids 28 413 419 10.1007/s00726-004-0146-9 10.1007/s00726-004-0146-9 1:CAS:528:DC%2BD2MXlt1Kmtb0%3D 15662562 (Pubitemid 40884733)
    • (2005) Amino Acids , vol.28 , Issue.4 , pp. 413-419
    • Muri, E.M.F.1    Gomes Jr., M.2    Albuquerque, M.G.3    Da Cunha, E.F.F.4    De Alencastro, R.B.5    Williamson, J.S.6    Antunes, O.A.C.7
  • 35
    • 0347627365 scopus 로고    scopus 로고
    • Calcium acetate catalyzed synthesis of 4-arylidene-2-phenyl-5(4H)- oxazolones under solvent-free conditions
    • DOI 10.1016/j.tetlet.2003.10.125
    • S Paul P Nanda R Gupta A Loupy 2004 Calcium acetate-catalyzed synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones under solvent-free conditions Tetrahedron Lett 45 425 427 10.1016/j.tetlet.2003.10.125 10.1016/j.tetlet.2003. 10.125 1:CAS:528:DC%2BD3sXpslOjtrY%3D (Pubitemid 37542291)
    • (2004) Tetrahedron Letters , vol.45 , Issue.2 , pp. 425-427
    • Paul, S.1    Nanda, P.2    Gupta, R.3    Loupy, A.4
  • 36
    • 0000785501 scopus 로고
    • Reactions in polyphosphoric acid. I. New stereospecific synthesis of the E isomers of 2-phenyl-4-arylmethylene-2-oxazolin-5-ones
    • 10.1021/jo00866a037 10.1021/jo00866a037 1:CAS:528:DyaE28XptVSntQ%3D%3D
    • YS Rao 1976 Reactions in polyphosphoric acid. I. New stereospecific synthesis of the E isomers of 2-phenyl-4-arylmethylene-2-oxazolin-5-ones J Org Chem 41 722 725 10.1021/jo00866a037 10.1021/jo00866a037 1:CAS:528: DyaE28XptVSntQ%3D%3D
    • (1976) J Org Chem , vol.41 , pp. 722-725
    • Rao, Y.S.1
  • 37
    • 0030463241 scopus 로고    scopus 로고
    • Synthesis of some new 2-methyl-4-(substituted benzylidene)1-phenyl-1,2,4 triazolo [3,4-b] 1,3,4 thiadiazole as potential AChE inhibitory agents
    • S Sen K Shanker 1996 Synthesis of some new 2-methyl-4-(substituted benzylidene) 1-phenyl-1, 2, 4 triazolo[3, 4,-b]1, 3, 4-thiadiazole as potential AChE inhibitory agents Boll Chim Farm 135 465 467 1:CAS:528:DyaK2sXhtVWqtLo%3D 9081295 (Pubitemid 27055389)
    • (1996) Bollettino Chimico Farmaceutico , vol.135 , Issue.8 , pp. 465-467
    • Sen, S.1    Shanker, K.2
  • 38
    • 1842725794 scopus 로고
    • Syntheses from pyridinecarboxaldehydes. I. 6H- and 7H-pyridines
    • 10.1016/0040-4020(66)80098-4 10.1016/0040-4020(66)80098-4 1:CAS:528:DyaF28XktlKrtg%3D%3D
    • G Slater AW Somerville 1966 Syntheses from pyridinecarboxaldehydes. I. 6H- and 7H-pyridines Tetrahedron 22 35 42 10.1016/0040-4020(66)80098-4 10.1016/0040-4020(66)80098-4 1:CAS:528:DyaF28XktlKrtg%3D%3D
    • (1966) Tetrahedron , vol.22 , pp. 35-42
    • Slater, G.1    Somerville, A.W.2
  • 39
    • 0010244354 scopus 로고    scopus 로고
    • The use of new ionic liquids in two-phase catalytic hydrogenation reaction by rhodium complexes
    • DOI 10.1016/0277-5387(95)00365-7
    • PAZ Suarez JEL Dullius S Einloft RF De Souza J Dupont 1996 The use of new ionic liquids in two-phase catalytic hydrogenation reaction by rhodium complexes Polyhedron 15 1217 1219 10.1016/0277-5387(95)00365-7 10.1016/0277-5387(95)00365-7 1:CAS:528:DyaK28XotVykug%3D%3D (Pubitemid 126331166)
    • (1996) Polyhedron , vol.15 , Issue.7 , pp. 1217-1219
    • Suarez, P.A.Z.1    Dullius, J.E.L.2    Einloft, S.3    De Souza, R.F.4    Dupont, J.5
  • 40
    • 33947143397 scopus 로고    scopus 로고
    • Microwave-promoted ring opening reaction of azlactones
    • 10.2174/157017807780037360 10.2174/157017807780037360 1:CAS:528:DC%2BD2sXjtlCjsr0%3D
    • RH Valdes DAG Aranda HM Alvarez OAC Antunes 2007 Microwave-promoted ring opening reaction of azlactones Lett Org Chem 4 35 38 10.2174/157017807780037360 10.2174/157017807780037360 1:CAS:528:DC%2BD2sXjtlCjsr0%3D
    • (2007) Lett Org Chem , vol.4 , pp. 35-38
    • Valdes, R.H.1    Aranda, D.A.G.2    Alvarez, H.M.3    Antunes, O.A.C.4
  • 41
    • 0026649670 scopus 로고
    • Compounds from Danshen. 6. A modified synthesis of (±)- β-aryllactic acid
    • 10.1055/s-1992-26228
    • Wong HNC, Xu ZL, Chang HM, Lee CM (1992) Compounds from Danshen. 6. A modified synthesis of (±)- β-aryllactic acid. Synthesis (8):793-797. doi: 10.1055/s-1992-26228
    • (1992) Synthesis , Issue.8 , pp. 793-797
    • Wong, H.N.C.1    Xu, Z.L.2    Chang, H.M.3    Lee, C.M.4
  • 43
    • 0034616194 scopus 로고    scopus 로고
    • Purified NS2B/NS3 serine protease of dengue virus type 2 exhibits cofactor NS2B dependence for cleavage of substrates with dibasic amino acids in vitro
    • DOI 10.1074/jbc.275.14.9963
    • R Yusof S Clum M Wetzel HM Murthy R Padmanabhan 2000 Purified NS2B/NS3 serine protease of dengue virus type 2 exhibits cofactor NS2B dependence for cleavage of substrates with dibasic amino acids in vitro J Biol Chem 275 9963 9969 10.1074/jbc.275.14.9963 10.1074/jbc.275.14.9963 1:CAS:528: DC%2BD3cXisFSqu7s%3D 10744671 (Pubitemid 30202042)
    • (2000) Journal of Biological Chemistry , vol.275 , Issue.14 , pp. 9963-9969
    • Yusof, R.1    Clum, S.2    Wetzel, M.3    Murthy, H.M.K.4    Padmanabhan, R.5


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