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Extract from the Register of European Patents

EP About this file: EP1465862

EP1465862 - CYCLOALKYL KETOAMIDES DERIVATIVES USEFUL AS CATHEPSIN K INHIBITORS [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  22.12.2006
Database last updated on 15.06.2024
Most recent event   Tooltip22.12.2006Application deemed to be withdrawnpublished on 24.01.2007  [2007/04]
Applicant(s)For all designated states
SMITHKLINE BEECHAM CORPORATION
One Franklin Plaza
Philadelphia, PA 19101 / US
[N/P]
Former [2004/42]For all designated states
SmithKline Beecham Corporation
One Franklin Plaza
Philadelphia, PA 19101 / US
Inventor(s)01 / CATALANO, John, George, GlaxoSmithKline
Five Moore Drive, P.O. Box 13398
Research Triangle Park, NC 27709 / US
02 / DEATON, David, Norman, GlaxoSmithKline
Five Moore Drive, P.O. Box 13398
Research Triangle Park, NC 27709 / US
03 / MILLER, Aaron, Bayne, GlaxoSmithKline
Five Moore Drive, P.O. Box 13398
Research Triangle Park, NC 27709 / US
04 / TAVARES, Francis, Xavier, GlaxoSmithKline
Five Moore Drive, P.O. Box 13398
Research Triangle Park, NC 27709 / US
 [2004/42]
Representative(s)Cooke, Tracey
GlaxoSmithKline
Global Patents (CN925.1)
980 Great West Road
Brentford, Middlesex TW8 9GS / GB
[N/P]
Former [2004/42]Cooke, Tracey (GB)
GlaxoSmithKline Corporate Intellectual Property (CN9.25.1) 980 Great West Road
GB-Brentford, Middlesex TW8 9GS / GB
Application number, filing date03703836.115.01.2003
[2004/42]
WO2003US01271
Priority number, dateUS20020349812P17.01.2002         Original published format: US 349812 P
[2004/42]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO03062192
Date:31.07.2003
Language:EN
[2003/31]
Type: A1 Application with search report 
No.:EP1465862
Date:13.10.2004
Language:EN
The application published by WIPO in one of the EPO official languages on 31.07.2003 takes the place of the publication of the European patent application.
[2004/42]
Search report(s)International search report - published on:EP31.07.2003
ClassificationIPC:C07C271/34, C07C271/22, C07D295/20, C07D213/30, C07C275/14, C07D231/38, C07D231/56, C07D213/40, C07D277/66, C07D277/22, C07D263/58, C07D285/08, C07D239/46, C07D495/04, C07D239/34
[2004/42]
CPC:
C07D213/30 (EP,US); A61P19/00 (EP); A61P19/08 (EP);
A61P19/10 (EP); A61P43/00 (EP); C07C271/22 (EP,US);
C07C271/34 (EP,US); C07C275/16 (EP,US); C07D213/40 (EP,US);
C07D231/40 (EP,US); C07D233/84 (EP,US); C07D237/14 (EP,US);
C07D239/34 (EP,US); C07D239/38 (EP,US); C07D239/42 (EP,US);
C07D263/58 (EP,US); C07D277/24 (EP,US); C07D277/34 (EP,US);
C07D285/08 (EP,US); C07D295/215 (EP,US); C07D417/12 (EP,US);
C07D495/04 (EP,US); C07C2601/04 (EP,US); C07C2601/08 (EP,US);
C07C2601/14 (EP,US) (-)
Designated contracting statesAT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HU,   IE,   IT,   LI,   LU,   MC,   NL,   PT,   SE,   SI,   SK,   TR [2004/42]
Extension statesALNot yet paid
LT09.07.2004
LV09.07.2004
MKNot yet paid
RO09.07.2004
TitleGerman:CYCLOALKYL-KETOAMIDEN DERIVATE UND IHRE VERWENDUNG ALS CATHEPSIN-K-INHIBITOREN[2004/42]
English:CYCLOALKYL KETOAMIDES DERIVATIVES USEFUL AS CATHEPSIN K INHIBITORS[2004/42]
French:DERIVES DE CETOAMIDES A SUBSTITUTION CYCLOALKYLE, UTILES COMME INHIBITEURS DE CATHEPSINE K[2004/42]
Entry into regional phase09.07.2004National basic fee paid 
09.07.2004Designation fee(s) paid 
09.07.2004Examination fee paid 
Examination procedure21.07.2003Request for preliminary examination filed
International Preliminary Examining Authority: EP
09.07.2004Amendment by applicant (claims and/or description)
09.07.2004Examination requested  [2004/42]
01.08.2006Application deemed to be withdrawn, date of legal effect  [2007/04]
06.09.2006Despatch of communication that the application is deemed to be withdrawn, reason: renewal fee not paid in time  [2007/04]
Fees paidRenewal fee
07.01.2005Renewal fee patent year 03
Penalty fee
Additional fee for renewal fee
31.01.200604   M06   Not yet paid
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Cited inInternational search[A]WO9616079  (TAKEDA CHEMICAL INDUSTRIES LTD [JP], et al) [A] 1-52 * page 58 - page 62; claim 1 *;
 [A]WO9212140  (GEORGIA TECH RES INST [US]) [A] 1 * claim 1 *;
 [A]  - LALONDE J M ET AL, "USE A PAPAIN AS A MODEL FOR THE STRUCTURE-BASED DESIGN OF CATHEPSIN K INHIBITORS: CRYSTAL STRUCTURES OF TWO PAPAIN-INHIBITOR COMPLEXES DEMONSTRATE BINDING TO S-SUBSITES", JOURNAL OF MEDICINAL CHEMISTRY, AMERICAN CHEMICAL SOCIETY. WASHINGTON, US, (1998), vol. 41, ISSN 0022-2623, pages 4567 - 4576, XP001041629 [A] 1 * the whole document *

DOI:   http://dx.doi.org/10.1021/jm980249f
The EPO accepts no responsibility for the accuracy of data originating from other authorities; in particular, it does not guarantee that it is complete, up to date or fit for specific purposes.