-
1
-
-
39849110713
-
Hepatitis C Virus (HCV) Infection: A Systemic Disease
-
For a recent review, see the following
-
For a recent review, see the following: Craxe, A.; Laffi, G.; Zignego, A. L. Hepatitis C Virus (HCV) Infection: A Systemic Disease Mol. Aspects Med. 2008, 29, 85-95
-
(2008)
Mol. Aspects Med.
, vol.29
, pp. 85-95
-
-
Crax, A.1
Laffi, G.2
Zignego, A.L.3
-
2
-
-
0024509701
-
Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome
-
Choo, Q.-L.; Kuo, G.; Weiner, A. J.; Overby, L. R.; Bradley, D. W.; Houghton, M. Isolation of a cDNA Clone Derived from a Blood-Borne Non-A, Non-B Viral Hepatitis Genome Science 1989, 244, 359-362 (Pubitemid 19117877)
-
(1989)
Science
, vol.244
, Issue.4902
, pp. 359-362
-
-
Choo, Q.-L.1
Kuo, G.2
Weiner, A.J.3
Overby, L.R.4
Bradley, D.W.5
Houghton, M.6
-
3
-
-
33644547392
-
Antiviral therapy for chronic hepatitis C: Past, present, and future
-
For a review, see the following
-
For a review, see the following: Hayashi, N.; Takehara, T. Antiviral Therapy for Chronic Hepatitis C: Past, Present, and Future J. Gastroenterol. 2006, 41, 17-27
-
(2006)
J. Gastroenterol.
, vol.41
, pp. 17-27
-
-
Hayashi, N.1
Takehara, T.2
-
4
-
-
36749001029
-
The way forward in HCV treatment - Finding the right path
-
DOI 10.1038/nrd2411, PII NRD2411
-
For recent reviews, see the following: Manns, M. P.; Foster, G. R.; Rockstroh, J. K.; Zeuzem, S.; Zoulim, F.; Houghton, M. The Way Forward in HCV Treatment: Finding the Right Path Nat. Rev. Drug Discovery 2007, 6, 991-1000 (Pubitemid 350201789)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.12
, pp. 991-1000
-
-
Manns, M.P.1
Foster, G.R.2
Rockstroh, J.K.3
Zeuzem, S.4
Zoulim, F.5
Houghton, M.6
-
5
-
-
36749073433
-
The design of drugs for HIV and HCV
-
DOI 10.1038/nrd2424, PII NRD2424
-
De Clercq, E. The Design of Drugs for HIV and HCV Nat. Rev. Drug Discovery 2007, 6, 1001-1018 (Pubitemid 350213865)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.12
, pp. 1001-1018
-
-
De Clercq, E.1
-
6
-
-
70350102158
-
Helicase inhibitors as specifically targeted antiviral therapy for hepatitis C
-
Belon, C. A.; Frick, D. N. Helicase Inhibitors as Specifically Targeted Antiviral Therapy for Hepatitis C Future Virol. 2009, 4, 277-293
-
(2009)
Future Virol.
, vol.4
, pp. 277-293
-
-
Belon, C.A.1
Frick, D.N.2
-
7
-
-
84984532074
-
Structure-Based Discovery of Triphenylmethane Derivatives as Inhibitors of Hepatitis C Virus Helicase
-
For recent representative work, see the following
-
For recent representative work, see the following: Chen, C.-S.; Chiou, C.-T.; Chen, G. S.; Chen, S.-C.; Hu, C.-Y.; Chi, W.-K.; Chu, Y.-D.; Hwang, L.-H.; Chen, P.-J.; Chen, D.-S.; Liaw, S.-H.; Chern, J.-W. Structure-Based Discovery of Triphenylmethane Derivatives as Inhibitors of Hepatitis C Virus Helicase J. Med. Chem. 2009, 52, 2716-2723
-
(2009)
J. Med. Chem.
, vol.52
, pp. 2716-2723
-
-
Chen, C.-S.1
Chiou, C.-T.2
Chen, G.S.3
Chen, S.-C.4
Hu, C.-Y.5
Chi, W.-K.6
Chu, Y.-D.7
Hwang, L.-H.8
Chen, P.-J.9
Chen, D.-S.10
Liaw, S.-H.11
Chern, J.-W.12
-
8
-
-
66249127534
-
Inhibition of subgenomic hepatitis C virus RNA replication by acridone derivatives: Identification of an NS3 helicase inhibitor
-
Manfroni, G.; Paeshuyse, J.; Massari, S.; Zanoli, S.; Gatto, B.; Maga, G.; Tabarrini, O.; Cecchetti, V.; Fravolini, A.; Neyts, J. Inhibition of Subgenomic Hepatitis C Virus RNA Replication by Acridone Derivatives: Identification of an NS3 Helicase Inhibitor J. Med. Chem. 2009, 52, 3354-3365
-
(2009)
J. Med. Chem.
, vol.52
, pp. 3354-3365
-
-
Manfroni, G.1
Paeshuyse, J.2
Massari, S.3
Zanoli, S.4
Gatto, B.5
Maga, G.6
Tabarrini, O.7
Cecchetti, V.8
Fravolini, A.9
Neyts, J.10
-
9
-
-
71049182299
-
Novel Macrocyclic Inhibitors of Hepatitis C NS3/4A Protease Featuring a 2-Amino-1,3-thiazole as a P4 Carbamate Replacement
-
Di Francesco, M. E.; Dessole, G.; Nizi, E.; Pace, P.; Koch, U.; Fiore, F.; Pesci, S.; Di Muzio, J.; Monteagudo, E.; Rowley, M.; Summa, V. Novel Macrocyclic Inhibitors of Hepatitis C NS3/4A Protease Featuring a 2-Amino-1,3-thiazole as a P4 Carbamate Replacement J. Med. Chem. 2009, 52, 7014-7028
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7014-7028
-
-
Di Francesco, M.E.1
Dessole, G.2
Nizi, E.3
Pace, P.4
Koch, U.5
Fiore, F.6
Pesci, S.7
Di Muzio, J.8
Monteagudo, E.9
Rowley, M.10
Summa, V.11
-
10
-
-
71049150926
-
Pyrazolo[1,5- a ]pyrimidine-Based Inhibitors of HCV Polymerase
-
Popovici-Muller, J.; Shipps, G. W., Jr.; Rosner, K. E.; Deng, Y.; Wang, T.; Curran, P. J.; Brown, M. A.; Siddiqui, M. A.; Cooper, A. B.; Duca, J.; Cable, M.; Girijavallabhan, V. Pyrazolo[1,5- a ]pyrimidine-Based Inhibitors of HCV Polymerase Bioorg. Med. Chem. Lett. 2009, 19, 6331-6336
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6331-6336
-
-
Popovici-Muller, J.1
Shipps Jr., G.W.2
Rosner, K.E.3
Deng, Y.4
Wang, T.5
Curran, P.J.6
Brown, M.A.7
Siddiqui, M.A.8
Cooper, A.B.9
Duca, J.10
Cable, M.11
Girijavallabhan, V.12
-
11
-
-
72049106897
-
Discovery of Benzimidazole-diamide Finger Loop (Thumb Pocket I) Allosteric Inhibitors of HCV NS5B Polymerase: Implementing parallel synthesis for rapid linker optimization
-
Goulet, S.; Poupart, M.-A.; Gillard, J.; Poirier, M.; Kukolj, G.; Beaulieu, P. L. Discovery of Benzimidazole-diamide Finger Loop (Thumb Pocket I) Allosteric Inhibitors of HCV NS5B Polymerase: Implementing Parallel Synthesis for Rapid Linker Optimization Bioorg. Med. Chem. Lett. 2010, 20, 196-200
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 196-200
-
-
Goulet, S.1
Poupart, M.-A.2
Gillard, J.3
Poirier, M.4
Kukolj, G.5
Beaulieu, P.L.6
-
12
-
-
73549084951
-
Synthesis, anti-hcv, antioxidant, and peroxynitrite inhibitory activity of fused benzosuberone derivatives
-
Farghaly, T. A.; Hafez, N. A. A.; Ragab, E. A.; Awad, H. M.; Abdalla, M. M. Synthesis, Anti-HCV, Antioxidant, and Peroxynitrite Inhibitory Activity of Fused Benzosuberone Derivatives Eur. J. Med. Chem. 2010, 45, 492-500
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 492-500
-
-
Farghaly, T.A.1
Hafez, N.A.A.2
Ragab, E.A.3
Awad, H.M.4
Abdalla, M.M.5
-
13
-
-
17444388557
-
Design, synthesis, and antiviral activity of adenosine 5′-phosphonate analogues as chain terminators against hepatitis C virus
-
DOI 10.1021/jm049029u
-
Koh, Y.-h.; Shim, J. H.; Wu, J. Z.; Zhong, W.; Hong, Z.; Girardet, J.-L. Design, Synthesis, and Antiviral Activity of Adenosine 5′-Phosphonate Analogues as Chain Terminators against Hepatitis C Virus J. Med. Chem. 2005, 48, 2867-2875 (Pubitemid 40548101)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.8
, pp. 2867-2875
-
-
Koh, Y.-H.1
Shim, J.H.2
Wu, J.Z.3
Zhong, W.4
Hong, Z.5
Girardet, J.-L.6
-
14
-
-
35848930168
-
First example of phosphoramidate approach applied to a 4′-substituted purine nucleoside (4′-Azidoadenosine): Conversion of an inactive nucleoside to a submicromolar compound versus hepatitis C virus
-
DOI 10.1021/jm070362i
-
Perrone, P.; Daverio, F.; Valente, R.; Rajyaguru, S.; Martin, J. A.; Lévsque, V.; Le Pogam, S.; Najera, I.; Klumpp, K.; Smith, D. B.; McGuigan, C. First Example of Phosphoramidate Approach Applied to a 4′-Substituted Purine Nucleoside (4′-Azidoadenosine): Conversion of an Inactive Nucleoside to a Submicromolar Compound versus Hepatitis C Virus J. Med. Chem. 2007, 50, 5463-5470 (Pubitemid 350057856)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.22
, pp. 5463-5470
-
-
Perrone, P.1
Daverio, F.2
Valente, R.3
Rajyaguru, S.4
Martin, J.A.5
Leveque, V.6
Le Pogam, S.7
Najera, I.8
Klumpp, K.9
Smith, D.B.10
McGuigan, C.11
-
15
-
-
12444326148
-
Synthesis of 9-(2-β-C-methyl-β-d-ribofuranosyl)-6-substituted purine derivatives as inhibitors of HCV RNA replication
-
DOI 10.1016/j.bmcl.2004.11.020, PII S0960894X04013691
-
Ding, Y.; Girardet, J.-L.; Hong, Z.; Lai, V. C. H.; An, H.; Koh, Y.-h.; Shaw, S. Z.; Zhong, W. Synthesis of 9-(2-β- C -Methyl-β- d -ribofuranosyl)-6-substituted Purine Derivatives as Inhibitors of HCV RNA Replication Bioorg. Med. Chem. Lett. 2005, 15, 709-713 (Pubitemid 40143152)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.3
, pp. 709-713
-
-
Ding, Y.1
Girardet, J.-L.2
Hong, Z.3
Lai, V.C.H.4
An, H.5
Koh, Y.-H.6
Shaw, S.Z.7
Zhong, W.8
-
16
-
-
34748890056
-
5′-O-Masked 2′-deoxyadenosine analogues as lead compounds for hepatitis C virus (HCV) therapeutic agents
-
DOI 10.1016/j.bmc.2007.08.025, PII S0968089607007195
-
Ikejiri, M.; Ohshima, T.; Kato, K.; Toyama, M.; Murata, T.; Shimotohno, K.; Maruyama, T. 5′- O -Masked 2′-Deoxyadenosine Analogues as Lead Compounds for Hepatitis C Virus (HCV) Therapeutic Agents Bioorg. Med. Chem. 2007, 15, 6882-6892 (Pubitemid 47470047)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.22
, pp. 6882-6892
-
-
Ikejiri, M.1
Ohshima, T.2
Kato, K.3
Toyama, M.4
Murata, T.5
Shimotohno, K.6
Maruyama, T.7
-
17
-
-
24744436849
-
Cytostatic 6-arylpurine nucleosides. 6. SAR in anti-HCV and cytostatic activity of extended series of 6-hetarylpurine ribonucleosides
-
DOI 10.1021/jm050335x
-
Hocek, M.; Nau , P.; Pohl, R.; Votruba, I.; Furman, P. A.; Tharnish, P. M.; Otto, M. J. Cytostatic 6-Arylpurine Nucleosides. 6. SAR in Anti-HCV and Cytostatic Activity of Extended Series of 6-Hetarylpurine Ribonucleosides J. Med. Chem. 2005, 48, 5869-5873 (Pubitemid 41298356)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.18
, pp. 5869-5873
-
-
Hocek, M.1
Naus, P.2
Pohl, R.3
Votruba, I.4
Furman, P.A.5
Tharnish, P.M.6
Otto, M.J.7
-
18
-
-
64349110092
-
Discovery of Novel Arylethynyltriazole Ribonucleosides with Selective and Effective Antiviral and Antiproliferative Activity
-
Wan, J.; Xia, Y.; Liu, Y.; Wang, M.; Rocchi, P.; Yao, J.; Qu, F.; Neyts, J.; Iovanna, J. L.; Peng, L. Discovery of Novel Arylethynyltriazole Ribonucleosides with Selective and Effective Antiviral and Antiproliferative Activity J. Med. Chem. 2009, 52, 1144-1155
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1144-1155
-
-
Wan, J.1
Xia, Y.2
Liu, Y.3
Wang, M.4
Rocchi, P.5
Yao, J.6
Qu, F.7
Neyts, J.8
Iovanna, J.L.9
Peng, L.10
-
19
-
-
59449099742
-
Synthesis and Anti-Hepatitis B Virus and Anti-Hepatitis C Virus Activities of 7-Deazaneplanocin A Analogues in Vitro
-
Kim, H.-J.; Sharon, A.; Bal, C.; Wang, J.; Allu, M.; Huang, Z.; Murray, M. G.; Bassit, L.; Schinazi, R. F.; Korba, B.; Chu, C. K. Synthesis and Anti-Hepatitis B Virus and Anti-Hepatitis C Virus Activities of 7-Deazaneplanocin A Analogues in Vitro J. Med. Chem. 2009, 52, 206-213
-
(2009)
J. Med. Chem.
, vol.52
, pp. 206-213
-
-
Kim, H.-J.1
Sharon, A.2
Bal, C.3
Wang, J.4
Allu, M.5
Huang, Z.6
Murray, M.G.7
Bassit, L.8
Schinazi, R.F.9
Korba, B.10
Chu, C.K.11
-
20
-
-
0015523596
-
Broad-Spectrum Antiviral Activity of Virazole: 1-β- d -Ribofuranosyl-1,2,4-triazole-3-carboxamide
-
Sidewell, R. W.; Huffman, J. H.; Khare, G. P.; Allen, L. B.; Witkowski, J. T.; Robins, R. K. Broad-Spectrum Antiviral Activity of Virazole: 1-β- d -Ribofuranosyl-1,2,4-triazole-3-carboxamide Science 1972, 177, 705-706
-
(1972)
Science
, vol.177
, pp. 705-706
-
-
Sidewell, R.W.1
Huffman, J.H.2
Khare, G.P.3
Allen, L.B.4
Witkowski, J.T.5
Robins, R.K.6
-
21
-
-
0034532953
-
The broad-spectrum antiviral ribonucleoside ribavirin is an RNA virus mutagen
-
DOI 10.1038/82191
-
Crotty, S.; Maag, D.; Arnold, J. J; Zhong, W.; Lau, J. Y. N.; Hong, Z.; Andino, R.; Cameron, C. E. The Broad-Spectrum Antiviral Ribonucleoside Ribavirin Is an RNA Virus Mutagen Nat. Med. 2000, 6, 1375-1379 (Pubitemid 32001022)
-
(2000)
Nature Medicine
, vol.6
, Issue.12
, pp. 1375-1379
-
-
Crotty, S.1
Maag, D.2
Arnold, J.J.3
Zhong, W.4
Lau, J.Y.N.5
Hong, Z.6
Andino, R.7
Cameron, C.E.8
-
22
-
-
34848908030
-
Ribavirin: Analytical determinations since the origin until today
-
DOI 10.1016/j.jpba.2007.06.004, PII S0731708507003238
-
Bosch, M. E.; Sánchez, A. J. R.; Rojas, F. S.; Ojeda, C. B. Ribavirin: Analytical Determinations Since the Origin until Today J. Pharm. Biomed. Anal. 2007, 45, 185-193 (Pubitemid 47513418)
-
(2007)
Journal of Pharmaceutical and Biomedical Analysis
, vol.45
, Issue.2
, pp. 185-193
-
-
Bosch, M.E.1
Sanchez, A.J.R.2
Rojas, F.S.3
Ojeda, C.B.4
-
23
-
-
79953788767
-
-
U.S. Patent 0,223,783 A1.
-
Xu, B.; Zhu, Q.; Cho, H.-J.; Fathi, R.; Yang, Z.; Sandrasagra, A.; Liu, Y. 3,4-Disubstituted Coumarin and Quinolone Compounds. U.S. Patent 0,223,783 A1, 2006.
-
(2006)
3,4-Disubstituted Coumarin and Quinolone Compounds
-
-
Xu, B.1
Zhu, Q.2
Cho, H.-J.3
Fathi, R.4
Yang, Z.5
Sandrasagra, A.6
Liu, Y.7
-
24
-
-
79953791324
-
-
U.S. Patent 0,180,950 A1.
-
Wu, J.; Yang, Z.; Fathi, R.; Zhu, Q. 4-Thio Coumarins. U.S. Patent 0,180,950 A1, 2004.
-
(2004)
4-Thio Coumarins
-
-
Wu, J.1
Yang, Z.2
Fathi, R.3
Zhu, Q.4
-
25
-
-
79953783039
-
-
U.S. Patent 0,312,406 A1.
-
Hsieh, H.-P.; Hsu, T.-A.; Yeh, J.-Y.; Horng, J.-T.; Shih, S.-R.; Chang, S.-Y.; Chao, Y.-S. Coumarin Compounds and Their Use for Treating Viral Infection. U.S. Patent 0,312,406 A1, 2009.
-
(2009)
Coumarin Compounds and Their Use for Treating Viral Infection
-
-
Hsieh, H.-P.1
Hsu, T.-A.2
Yeh, J.-Y.3
Horng, J.-T.4
Shih, S.-R.5
Chang, S.-Y.6
Chao, Y.-S.7
-
26
-
-
41149136756
-
Identification and characterization of coumestans as novel HCV NS5B polymerase inhibitors
-
DOI 10.1093/nar/gkm1178
-
Kaushik-Basu, N.; Bopda-Waffo, A.; Talele, T. T.; Basu, A.; Costa, P. R. R.; da Silva, A. J. M.; Sarafianos, S. G.; No l, F. Identification and Characterization of Coumestans as Novel HCV NS5B Polymerase Inhibitors Nucleic Acids Res. 2008, 36, 1482-1496 (Pubitemid 351426102)
-
(2008)
Nucleic Acids Research
, vol.36
, Issue.5
, pp. 1482-1496
-
-
Kaushik-Basu, N.1
Bopda-Waffo, A.2
Talele, T.T.3
Basu, A.4
Costa, P.R.R.5
Da Silva, A.J.M.6
Sarafianos, S.G.7
Noel, F.8
-
27
-
-
38149026447
-
Synthesis of New Benzimidazole-Coumarin Conjugates as Anti-Hepatitis C Virus Agents
-
Hwu, J. R.; Singha, R.; Hong, S. C.; Chang, Y. H.; Das, A. R.; Vliegen, I.; De Clercq, E.; Neyts, J. Synthesis of New Benzimidazole-Coumarin Conjugates as Anti-Hepatitis C Virus Agents Antiviral Res. 2008, 77, 157-162
-
(2008)
Antiviral Res.
, vol.77
, pp. 157-162
-
-
Hwu, J.R.1
Singha, R.2
Hong, S.C.3
Chang, Y.H.4
Das, A.R.5
Vliegen, I.6
De Clercq, E.7
Neyts, J.8
-
28
-
-
64349103355
-
Structure-activity relationship of new anti-hepatitis C virus agents: Heterobicycle coumarin conjugates
-
Neyts, J.; De Clercq, E.; Singha, R.; Chang, Y. H.; Das, A. R.; Chakraborty, S. K.; Hong, S. C.; Tsay, S.-C.; Hsu, M.-H.; Hwu, J. R. Structure-activity Relationship of New Anti-Hepatitis C Virus Agents: Heterobicycle Coumarin Conjugates J. Med. Chem. 2009, 52, 1486-1490
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1486-1490
-
-
Neyts, J.1
De Clercq, E.2
Singha, R.3
Chang, Y.H.4
Das, A.R.5
Chakraborty, S.K.6
Hong, S.C.7
Tsay, S.-C.8
Hsu, M.-H.9
Hwu, J.R.10
-
29
-
-
34547484265
-
Molecular hybridization: A useful tool in the design of new drug prototypes
-
DOI 10.2174/092986707781058805
-
For a review, see the following: Viegas-Junior, C.; Danuello, A.; Bolzani, V. D. S.; Barreiro, E. J.; Fraga, C. A. M. Molecular Hybridization: A Useful Tool in the Design of New Drug Prototypes Curr. Med. Chem. 2007, 14, 1829-1852 (Pubitemid 47163402)
-
(2007)
Current Medicinal Chemistry
, vol.14
, Issue.17
, pp. 1829-1852
-
-
Viegas-Junior, C.1
Danuello, A.2
Da Silva Bolzani, V.3
Barreiro, E.J.4
Fraga, C.A.M.5
-
30
-
-
0003448576
-
-
In, 3 rd ed.; The Royal Society of Chemistry: Cambridge, U.K.,; Chapter 3.
-
Blackburn, G. M.; Gait, M. J.; Loakes, D.; Williams, D. M. In Nucleic Acids in Chemistry and Biology, 3 rd ed.; The Royal Society of Chemistry: Cambridge, U.K., 2006; Chapter 3.
-
(2006)
Nucleic Acids in Chemistry and Biology
-
-
Blackburn, G.M.1
Gait, M.J.2
Loakes, D.3
Williams, D.M.4
-
31
-
-
84982068675
-
Nucleoside Syntheses, XXII Nucleoside Synthesis with Trimethylsilyl Triflate and Perchlorate as Catalysts
-
Vorbr ggen, H.; Krolikiewicz, K.; Bennua, B. Nucleoside Syntheses, XXII Nucleoside Synthesis with Trimethylsilyl Triflate and Perchlorate as Catalysts Chem. Ber. 1981, 114, 1234-1255
-
(1981)
Chem. Ber.
, vol.114
, pp. 1234-1255
-
-
Vorbrggen, H.1
Krolikiewicz, K.2
Bennua, B.3
-
32
-
-
0003520774
-
-
7 th ed.; John Wiley & Sons: New York,; p.
-
Silverstein, R. M.; Webster, F. X.; Kiemle, D. J. Spectrometric Identification of Organic Compounds, 7 th ed.; John Wiley & Sons: New York, 2005; p 98.
-
(2005)
Spectrometric Identification of Organic Compounds
, pp. 98
-
-
Silverstein, R.M.1
Webster, F.X.2
Kiemle, D.J.3
-
33
-
-
0028332138
-
Synthesis and biologic evaluation of 8-substituted derivatives of nebularine (9-β-D-ribofuranosylpurine)
-
Secrist, J. A., III; Shortnacy-Fowler, A.; Bennett, L. L., Jr.; Montgomery, J. A. Synthesis and Biologic Evaluation of 8-Substituted Derivatives of Nebularine (9-β- d -Ribofuranosylpurine) Nucleosides Nucleotides 1994, 13, 1017-1029 (Pubitemid 24160981)
-
(1994)
Nucleosides and Nucleotides
, vol.13
, Issue.5
, pp. 1017-1029
-
-
Secrist III, J.A.1
Shortnacy-Fowler, A.2
Bennett Jr., L.L.3
Montgomery, J.A.4
-
34
-
-
0015528142
-
Studies on the Conformation of Purine Nucleosides and Their 5′-Phosphates
-
Ikehara, M.; Uesugi, S.; Yoshida, K. Studies on the Conformation of Purine Nucleosides and Their 5′-Phosphates Biochemistry 1972, 11, 830-836
-
(1972)
Biochemistry
, vol.11
, pp. 830-836
-
-
Ikehara, M.1
Uesugi, S.2
Yoshida, K.3
-
36
-
-
0000978075
-
Purine Nucleosides. VII. Direct Bromination of Adenosine, Deoxyadenosine, Guanosine, and Related Purine Nucleosides
-
Holmes, R. E.; Robins, R. K. Purine Nucleosides. VII. Direct Bromination of Adenosine, Deoxyadenosine, Guanosine, and Related Purine Nucleosides J. Am. Chem. Soc. 1964, 86, 1242-1245
-
(1964)
J. Am. Chem. Soc.
, vol.86
, pp. 1242-1245
-
-
Holmes, R.E.1
Robins, R.K.2
-
37
-
-
0014851361
-
Studies of Nucleosides and Nucleotides - XLI: Purine Cyclonucleosides - 8 Selective Sulfonylation of 8-Bromoadenosine Derivatives and an Alternate Synthesis of 8,2′-And 8,3′- S -Cyclonucleosides
-
Ikehara, M.; Kaneko, M. Studies of Nucleosides and Nucleotides - XLI: Purine Cyclonucleosides - 8 Selective Sulfonylation of 8-Bromoadenosine Derivatives and an Alternate Synthesis of 8,2′-And 8,3′- S -Cyclonucleosides Tetrahedron 1970, 26, 4251-4259
-
(1970)
Tetrahedron
, vol.26
, pp. 4251-4259
-
-
Ikehara, M.1
Kaneko, M.2
-
38
-
-
0003909885
-
-
In, 2 nd ed.; John Wiley & Sons: West Sussex, England,; Chapter 2.
-
Thomas, G. In Medicinal Chemistry. An Introduction, 2 nd ed.; John Wiley & Sons: West Sussex, England, 2007; Chapter 2.
-
(2007)
Medicinal Chemistry. An Introduction
-
-
Thomas, G.1
-
39
-
-
28144445057
-
Adenosine kinase inhibitors. 6. Synthesis, water solubility, and antinociceptive activity of 5-phenyl-7-(5-deoxy-β-d-ribofuranosyl) pyrrolo[2,3-d]pyrimidines substituted at C4 with glycinamides and related compounds
-
DOI 10.1021/jm050394a
-
Bookser, B. C.; Ugarkar, B. G.; Matelich, M. C.; Lemus, R. H.; Allan, M; Tsuchiya, M.; Nakane, M.; Nagahisa, A.; Wiesner, J. B.; Erion, M. D. Adenosine Kinase Inhibitors. 6. Synthesis, Water Solubility, and Antinociceptive Activity of 5-Phenyl-7-(5-deoxy-β- d -ribofuranosyl)pyrrolo[2,3- d ]pyrimidines Substituted at C4 with Glycinamides and Related Compounds J. Med. Chem. 2005, 48, 7808-7820 (Pubitemid 41698820)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.24
, pp. 7808-7820
-
-
Bookser, B.C.1
Ugarkar, B.G.2
Matelich, M.C.3
Lemus, R.H.4
Allan, M.5
Tsuchiya, M.6
Nakane, M.7
Nagahisa, A.8
Wiesner, J.B.9
Erion, M.D.10
-
40
-
-
0345188811
-
Replication of subgenomic hepatitis C virus RNAs in a hepatoma cell line
-
DOI 10.1126/science.285.5424.110
-
Lohmann, V.; Körner, F.; Koch, J.-O.; Herian, U.; Theilmann, L.; Bartenschlager, R. Replication of Subgenomic Hepatitis C Virus RNAs in a Hepatoma Cell Line Science 1999, 285, 110-113 (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
-
41
-
-
33646015668
-
The Non-Immunosuppressive Cyclosporin DEBIO-025 Is a Potent Inhibitor of Hepatitis C Virus Replication in Vitro
-
Paeshuyse, J.; Kaul, A.; De Clercq, E.; Rosenwirth, B.; Dumont, J.-M.; Scalfaro, P.; Bartenschlager, R.; Neyts, J. The Non-Immunosuppressive Cyclosporin DEBIO-025 Is a Potent Inhibitor of Hepatitis C Virus Replication in Vitro Hepatology 2006, 43, 761-770
-
(2006)
Hepatology
, vol.43
, pp. 761-770
-
-
Paeshuyse, J.1
Kaul, A.2
De Clercq, E.3
Rosenwirth, B.4
Dumont, J.-M.5
Scalfaro, P.6
Bartenschlager, R.7
Neyts, J.8
-
42
-
-
0028817654
-
Acyl CoA: Cholesterol Acyltransferase (ACAT) Inhibitors: Ureas Bearing Heterocyclic Groups Bioisosteric for an Imidazole
-
Wilde, R. G.; Billheimer, J. T.; Germain, S. J.; Gillies, P. J.; Higley, C. A.; Kezar, H. S., III; Maduskuie, T. P.; Shimshick, E. S.; Wexler, R. R. Acyl CoA: Cholesterol Acyltransferase (ACAT) Inhibitors: Ureas Bearing Heterocyclic Groups Bioisosteric for an Imidazole Bioorg. Med. Chem. Lett. 1995, 5, 167-172
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 167-172
-
-
Wilde, R.G.1
Billheimer, J.T.2
Germain, S.J.3
Gillies, P.J.4
Higley, C.A.5
Iii, S.K.H.6
Maduskuie, T.P.7
Shimshick, E.S.8
Wexler, R.R.9
-
43
-
-
0036928061
-
A convenient and improved Baylis-Hillman synthesis of 3-substututed 2H-1-benzopyran-2-ones
-
Kaye, P. T.; Musa, M. A. A Convenient and Improved Baylis-Hillman Synthesis of 3-Substututed 2 H -1-Benzopyran-2-ones Synthesis 2002, 2701-2706 (Pubitemid 36034429)
-
(2002)
Synthesis
, Issue.18
, pp. 2701-2706
-
-
Kaye, P.T.1
Musa, M.A.2
|