公开(公告)号：WO2008011337A1

公开(公告)日：2008-01-24

申请号：PCT/US2007/073422

申请日：2007-07-13

Applicant: ABBOTT LABORATORIES ,  WAGNER, Rolf ,  DONNER, Pamela L. ,  KEMPF, Dale J. ,  MARING, Clarence J. ,  STOLL, Vincent S. ,  KU, Yi-yin ,  PU, Yu-ming

Inventor： WAGNER, Rolf ,  DONNER, Pamela L. ,  KEMPF, Dale J. ,  MARING, Clarence J. ,  STOLL, Vincent S. ,  KU, Yi-yin ,  PU, Yu-ming

IPC: C07D495/04 ,  A61K31/505 ,  A61P31/12

CPC classification number: C07D495/04

Abstract: The present invention provides HCV polymerase inhibiting compounds having the formula (I) where R 1 is cyclobutyl-N(R a )-, n is 1, 2, 3 or 4, and at least one R 5 is R a SO 2 N(R j )alkyl-. In a non-limiting example, a compound of the present invention is N-[(3-{1-[(cyclobutyl)amino]-4-hydroxy-2-oxo-1,2-dihydro-quinolin-3-yl}-1,1-dioxo-1,4-dihydro-1?λ 6 -thieno[2,3-e][1,2,4]thiadiazin-7-yl)meth yl]methane-sulfonamide. The present invention also features compositions comprising the compounds of the present invention or pharmaceutically acceptable salts, stereoisomers or tautomers thereof, and methods of using the same to treat or prevent HCV infection.

Abstract translation: 本发明提供具有式（I）的HCV聚合酶抑制化合物，其中R 1是

公开(公告)号：WO2005019191A2

公开(公告)日：2005-03-03

申请号：PCT/US2004/027000

申请日：2004-08-19

Applicant: ABBOTT LABORATORIES ,  HUTCHINSON, Douglas, K. ,  BELLETTINI, John, R. ,  BETEBENNER, David, A. ,  BISHOP, Richard, D. ,  BORCHARDT, Thomas, B. ,  BOSSE, Todd, D. ,  CINK, Russell, D. ,  FLENTGE, Charles, A. ,  GATES, Bradley, D. ,  GREEN, Brian, E. ,  HINMAN, Mira, M. ,  HUANG, Peggy, P. ,  KLEIN, Larry, L. ,  KRUEGER, Allan, C. ,  LARSON, Daniel, P. ,  LEANNA, M., Robert ,  LIU, Dachun ,  MADIGAN, Darold, L. ,  MCDANIEL, Keith, F. ,  RANDOLPH, John, T. ,  ROCKWAY, Todd, W. ,  ROSENBERG, Teresa, A. ,  STEWART, Kent, D. ,  STOLL, Vincent, S. ,  WAGNER, Rolf ,  YEUNG, Ming, C.

Inventor： HUTCHINSON, Douglas, K. ,  BELLETTINI, John, R. ,  BETEBENNER, David, A. ,  BISHOP, Richard, D. ,  BORCHARDT, Thomas, B. ,  BOSSE, Todd, D. ,  CINK, Russell, D. ,  FLENTGE, Charles, A. ,  GATES, Bradley, D. ,  GREEN, Brian, E. ,  HINMAN, Mira, M. ,  HUANG, Peggy, P. ,  KLEIN, Larry, L. ,  KRUEGER, Allan, C. ,  LARSON, Daniel, P. ,  LEANNA, M., Robert ,  LIU, Dachun ,  MADIGAN, Darold, L. ,  MCDANIEL, Keith, F. ,  RANDOLPH, John, T. ,  ROCKWAY, Todd, W. ,  ROSENBERG, Teresa, A. ,  STEWART, Kent, D. ,  STOLL, Vincent, S. ,  WAGNER, Rolf ,  YEUNG, Ming, C.

IPC: C07D285/00

CPC classification number: C07D417/12 ,  C07D285/24 ,  C07D285/30 ,  C07D513/04

Abstract: Compounds having the formula (I) are hepatitis C (HCV) polymerase inhibitors. Also disclosed are a composition and method for inhibiting hepatitis C (HCV) polymerase, processes for making the compounds, and synthetic intermediates employed in the processes.

Abstract translation: 具有式（I）的化合物是丙型肝炎（HCV）聚合酶抑制剂。 还公开了用于抑制丙型肝炎（HCV）聚合酶的组合物和方法，用于制备化合物的方法和在该方法中使用的合成中间体。

公开(公告)号：WO2009029123A1

公开(公告)日：2009-03-05

申请号：PCT/US2007/087514

申请日：2007-12-14

Applicant: ABBOTT LABORATORIES ,  REILLY, Edward, B. ,  LACY, Susan, E. ,  FUNG, Emma ,  BELK, Jonathan, P. ,  ROGUSKA, Michael ,  STOLL, Vincent, S. ,  JAKOB, Clarissa

Inventor： REILLY, Edward, B. ,  LACY, Susan, E. ,  FUNG, Emma ,  BELK, Jonathan, P. ,  ROGUSKA, Michael ,  STOLL, Vincent, S. ,  JAKOB, Clarissa

IPC: C07K16/28

CPC classification number: C07K16/2863 ,  C07K2317/21 ,  C07K2317/34 ,  C07K2317/565 ,  C07K2317/622 ,  C07K2317/74 ,  C07K2317/92

Abstract: The present invention relates to antibodies and antigen-binding portions thereof that bind to and activate an erythropoietin receptor. The invention also relates to nucleic acid sequences encoding such antibodies and antigen-binding portions. The present invention further relates to methods of activating the endogenous activity of an erythropoietin receptor in a mammal using said antibodies and antigen-binding portions, methods of treatment, as well as pharmaceutical compositions comprising said antibodies and antigen-binding portions. The invention further provides compositions and crystals of an erythropoietin receptor in complex with an anti-erythropoietin receptor antibody. Specifically, the high-resolution structure provides binding sites defined by the structure coordinated determined herein.

Abstract translation: 本发明涉及结合并激活促红细胞生成素受体的抗体及其抗原结合部分。 本发明还涉及编码这种抗体和抗原结合部分的核酸序列。 本发明还涉及使用所述抗体和抗原结合部分，治疗方法以及包含所述抗体和抗原结合部分的药物组合物来激活哺乳动物中促红细胞生成素受体的内源性活性的方法。 本发明还提供与抗促红细胞生成素受体抗体复合的促红细胞生成素受体的组合物和晶体。 具体地，高分辨率结构提供由本文确定的结构所定义的结合位点。

公开(公告)号：WO0128996A3

公开(公告)日：2001-11-29

申请号：PCT/US0027910

申请日：2000-10-10

Applicant: ABBOTT LAB ,  MARING CLARENCE J ,  GIRANDA VINCENT L ,  KEMPF DALE J ,  STOLL VINCENT S ,  SUN MINGHUA ,  ZHAO CHEN ,  GU YU GUI ,  HANESSIAN STEPHEN ,  WANG GARY T ,  KRUEGER ALLAN C ,  CHEN HUI-JU ,  CHEN YUANWEI ,  DEGOEY DAVID A ,  FLOSI WILLIAM J ,  GRAMPOVNIK DAVID J ,  KATI WARREN M ,  KENNEDY APRIL L ,  KLEIN LARRY L ,  LIN ZHEN ,  MADIGAN DAROLD L

Inventor： MARING CLARENCE J ,  GIRANDA VINCENT L ,  KEMPF DALE J ,  STOLL VINCENT S ,  SUN MINGHUA ,  ZHAO CHEN ,  GU YU GUI ,  HANESSIAN STEPHEN ,  WANG GARY T ,  KRUEGER ALLAN C ,  CHEN HUI-JU ,  CHEN YUANWEI ,  DEGOEY DAVID A ,  FLOSI WILLIAM J ,  GRAMPOVNIK DAVID J ,  KATI WARREN M ,  KENNEDY APRIL L ,  KLEIN LARRY L ,  LIN ZHEN ,  MADIGAN DAROLD L

IPC: C07D401/12 ,  A61K31/357 ,  A61K31/40 ,  A61K31/401 ,  A61K31/4025 ,  A61K31/405 ,  A61K31/415 ,  A61K31/4155 ,  A61K31/4178 ,  A61K31/42 ,  A61K31/422 ,  A61K31/425 ,  A61K31/427 ,  A61K31/4439 ,  A61K31/5377 ,  A61K31/66 ,  A61K31/662 ,  A61P31/00 ,  A61P31/12 ,  A61P31/16 ,  A61P43/00 ,  C07D20060101 ,  C07D207/00 ,  C07D207/12 ,  C07D207/16 ,  C07D207/26 ,  C07D207/32 ,  C07D207/327 ,  C07D207/38 ,  C07D207/46 ,  C07D303/16 ,  C07D403/04 ,  C07D403/06 ,  C07D405/04 ,  C07D405/06 ,  C07D407/06 ,  C07D407/12 ,  C07D409/06 ,  C07D413/04 ,  C07D413/06 ,  C07D417/04 ,  C07D417/06 ,  C07D521/00 ,  C07F9/40 ,  C07F9/572

CPC classification number: C07D207/16 ,  C07D207/26 ,  C07D207/327 ,  C07D207/38 ,  C07D207/46 ,  C07D231/12 ,  C07D233/56 ,  C07D249/08 ,  C07D303/16 ,  C07D403/04 ,  C07D405/04 ,  C07D405/06 ,  C07D409/06 ,  C07D413/04 ,  C07D417/04 ,  C07D417/06

Abstract: Enantiomerically enriched compounds having the absolute stereochemistry of the formula (I) or a pharmaceutically acceptable salt, ester or prodrug thereof, which are useful for inhibiting neuraminidases from disease-causing microorganisms, especially, influenza neuraminidase. Also disclosed are compositions and methods for preventing and treating diseases caused by microorganisms having a neuraminidase, processes for preparing the compounds and synthetic intermediates used in these processes.