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Houghton, M.6
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0037064091
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(b) For recent disclosures of other non-nucleoside HCV NS5B polymerase inhibitors, see: Dhanak D., Duffy K.J., Johnston V.K., Lin-Goerke J., Darcy M., Shaw A.N., Gu B., Silverman C., Gates A.T., Nonnemacher M.R., Earnshaw D.L., Casper D.J., Kaura A., Baker A., Greenwood C., Gutshall L.L., Maley D., DelVecchio A., Macarron R., Hofmann G.A., Alnoah Z., Cheng H.-Y., Chan G., Khandekar S., Keenan R.M., Sarisky R.T. J. Biol. Chem. 277:2002;38322 (c) Chan L., Reddy T.J., Proulx M., Das S.K., Pereira O., Wang W., Siddiqui A., Yannopoulos C.G., Poisson C., Turcotte N., Drouin A., Alaoui-Ismaili M.H., Bethell R., Hamel M., L'Heureux L., Bilimoria D., Nguyen-Ba N. J. Med. Chem. 46:2003;1283.
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Dhanak, D.1
Duffy, K.J.2
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Lin-Goerke, J.4
Darcy, M.5
Shaw, A.N.6
Gu, B.7
Silverman, C.8
Gates, A.T.9
Nonnemacher, M.R.10
Earnshaw, D.L.11
Casper, D.J.12
Kaura, A.13
Baker, A.14
Greenwood, C.15
Gutshall, L.L.16
Maley, D.17
Delvecchio, A.18
MacArron, R.19
Hofmann, G.A.20
Alnoah, Z.21
Cheng, H.-Y.22
more..
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0037431376
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(b) For recent disclosures of other non-nucleoside HCV NS5B polymerase inhibitors, see: Dhanak D., Duffy K.J., Johnston V.K., Lin-Goerke J., Darcy M., Shaw A.N., Gu B., Silverman C., Gates A.T., Nonnemacher M.R., Earnshaw D.L., Casper D.J., Kaura A., Baker A., Greenwood C., Gutshall L.L., Maley D., DelVecchio A., Macarron R., Hofmann G.A., Alnoah Z., Cheng H.-Y., Chan G., Khandekar S., Keenan R.M., Sarisky R.T. J. Biol. Chem. 277:2002;38322 (c) Chan L., Reddy T.J., Proulx M., Das S.K., Pereira O., Wang W., Siddiqui A., Yannopoulos C.G., Poisson C., Turcotte N., Drouin A., Alaoui-Ismaili M.H., Bethell R., Hamel M., L'Heureux L., Bilimoria D., Nguyen-Ba N. J. Med. Chem. 46:2003;1283.
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Sarisky, R.T.4
Chan, L.5
Reddy, T.J.6
Proulx, M.7
Das, S.K.8
Pereira, O.9
Wang, W.10
Siddiqui, A.11
Yannopoulos, C.G.12
Poisson, C.13
Turcotte, N.14
Drouin, A.15
Alaoui-Ismaili, M.H.16
Bethell, R.17
Hamel, M.18
L'Heureux, L.19
Bilimoria, D.20
Nguyen-Ba, N.21
more..
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12
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85030917437
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note
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11a A more detailed description of this assay will be published else where (McKercher, G. et al.).
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13
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85030932916
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note
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9,11a.
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14
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85030917827
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US patents 6,448,281 B1 and 6,479,508 B1, 2002, to Boehringer Ingelheim (Canada) Ltd.
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(a) Austel, V., Beaulieu, P. L., Fazal, G., Gillard, J., Kukolj, G. US patents 6,448,281 B1 and 6,479,508 B1, 2002, to Boehringer Ingelheim (Canada) Ltd.
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Austel, V.1
Beaulieu, P.L.2
Fazal, G.3
Gillard, J.4
Kukolj, G.5
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15
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85030921770
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EP 1 162 196 A1, 2001
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(b) A recent patent application from Japan Tobacco Inc. also discloses derivatives of benzimidazole 5-carboxylic acids as HCV polymerase inhibitors: Hashimoto, H., Mizutani, K., Yishida, A. EP 1 162 196 A1, 2001.
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Hashimoto, H.1
Mizutani, K.2
Yishida, A.3
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16
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85030930314
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note
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2O (v/v). Data acquisition was performed at 600 MHz and 300 K using methods similar to those reported previously: LaPlante, S. R.; Cameron, D. R.; Aubry, N.; LeFebvre, S.; Kukolj, G.; Maurice, R.; Thibeault, D.; Lamarre, D.; Llinas-Brunet, M. J. Biol. Chem. 1999, 274, 18618. A soluble form of the polymerase, NS5BΔ21, lacking C-terminal 21 amino acids was used: Ferrari, E.; Wright-Minogue, J.; Fang, J. W. S.; Baroudy, B. M.; Lau, J. Y. N.; Hong, Z. J. Virol. 1999, 73, 1649.
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0345188811
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Körner, F.2
Koch, J.O.3
Herian, U.4
Theilmann, L.5
Bartenschlager, R.6
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18
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84943408843
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(a) Grimmet, M. R.; In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon: Oxford, 1984; Vol. 5, p 457.
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Grimmet, R.M.1
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0043240483
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(c) For the use of oxone® in the synthesis of benzimidazoles from aldehydes and 1,2-phenylenediamines see: Beaulieu P.L., Haché B., von Moos E. Synthesis. 2003;1683.
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Synthesis
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Beaulieu, P.L.1
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