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Extract from the Register of European Patents

EP About this file: EP1797084

EP1797084 - NOVEL HETEROCYCLIC NF-kB INHIBITORS [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  16.08.2013
Database last updated on 14.09.2024
Most recent event   Tooltip16.08.2013Application deemed to be withdrawnpublished on 18.09.2013  [2013/38]
Applicant(s)For all designated states
4SC Discovery GmbH
Am Klopferspitz 19a
82152 Planegg-Martinsried / DE
[2012/14]
Former [2007/25]For all designated states
4SC AG
Am Klopferspitz 19a
82152 Martinsried / DE
Inventor(s)01 / LEBAN, Johann
Kopernikusweg 5
82152 Planegg / DE
02 / SCHMITT, Harald
Fuststr. 8
55116 Mainz / DE
03 / WOLF, Kristina
Johannishöhe 60
82288 Kottgeisering / DE
04 / PEGORARO, Stefano
Röntgenstr. 35
82125 Planegg / DE
05 / WUZIK, Andreas
Schlehenweg 9
86836 Untermeitingen / DE
 [2007/33]
Former [2007/25]01 / LEBAN, Johann
Kirchenstr. 25
82110 Germering / DE
02 / SCHMITT, Harald
Fuststr. 8
55116 Mainz / DE
03 / WOLF, Kristina
Margaretenplatz 4
81373 München / DE
04 / PEGORARO, Stefano
Röntgenstr. 35
82125 Planegg / DE
05 / WUZIK, Andreas
Hoher Ifen-Weg 7
86836 Untermeitingen / DE
Representative(s)Kilger, Ute, et al
Boehmert & Boehmert
Anwaltspartnerschaft mbB
Pettenkoferstrasse 22
80336 München / DE
[N/P]
Former [2009/45]Kilger, Ute, et al
Forrester & Boehmert Pettenkoferstrasse 20-22
80336 München / DE
Former [2009/42]Kilger, Ute, et al
Boehmert & Boehmert Helene-Lange-Strasse 3
14469 Potsdam / DE
Former [2008/35]Vossius & Partner
Siebertstrasse 3
81675 München / DE
Former [2007/25]Vossius & Partner
Siebertstrasse 4
81675 München / DE
Application number, filing date05769860.729.07.2005
[2007/25]
WO2005EP08261
Priority number, dateEP2004002236320.09.2004         Original published format: EP 04022363
US20040612794P27.09.2004         Original published format: US 612794 P
[2007/25]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report
No.:WO2006032322
Date:30.03.2006
Language:EN
[2006/13]
Type: A1 Application with search report 
No.:EP1797084
Date:20.06.2007
Language:EN
The application published by WIPO in one of the EPO official languages on 30.03.2006 takes the place of the publication of the European patent application.
[2007/25]
Search report(s)International search report - published on:EP30.03.2006
ClassificationIPC:C07D417/14, C07D417/12, A61K31/4535, C07D495/04, C07D487/04, A61P25/28, A61P35/00, C07D277/56, C07D413/12, C07D417/04, C07D263/48, C07D211/62, C07D473/34, C07D513/04, A61K31/454
[2007/25]
CPC:
C07D263/48 (EP,US); A61P1/00 (EP); A61P1/16 (EP);
A61P11/00 (EP); A61P13/12 (EP); A61P17/00 (EP);
A61P17/06 (EP); A61P17/10 (EP); A61P17/14 (EP);
A61P19/00 (EP); A61P21/04 (EP); A61P25/00 (EP);
A61P25/08 (EP); A61P25/12 (EP); A61P25/16 (EP);
A61P25/28 (EP); A61P27/16 (EP); A61P31/00 (EP);
A61P31/04 (EP); A61P31/12 (EP); A61P35/00 (EP);
A61P37/08 (EP); A61P9/00 (EP); A61P9/10 (EP);
C07D277/56 (EP,US); C07D401/14 (EP,US); C07D413/06 (EP,US);
C07D413/12 (EP,US); C07D413/14 (EP,US); C07D417/04 (EP,US);
C07D417/06 (EP,US); C07D417/12 (EP,US); C07D417/14 (EP,US);
C07D487/04 (EP,US); C07D491/04 (EP,US); C07D495/04 (EP,US) (-)
Designated contracting statesAT,   BE,   BG,   CH,   CY,   CZ,   DE,   DK,   EE,   ES,   FI,   FR,   GB,   GR,   HU,   IE,   IS,   IT,   LI,   LT,   LU,   LV,   MC,   NL,   PL,   PT,   RO,   SE,   SI,   SK,   TR [2007/25]
Extension statesALNot yet paid
BANot yet paid
HRNot yet paid
MKNot yet paid
YUNot yet paid
TitleGerman:NEUE HETEROCYCLISCHE NF-KB-INHIBITOREN[2007/25]
English:NOVEL HETEROCYCLIC NF-kB INHIBITORS[2007/25]
French:NOUVEAUX INHIBITEURS HÉTÉROCYCLIQUES DU NF-kB[2007/25]
Entry into regional phase19.04.2007National basic fee paid 
19.04.2007Designation fee(s) paid 
19.04.2007Examination fee paid 
Examination procedure06.03.2006Request for preliminary examination filed
International Preliminary Examining Authority: EP
19.04.2007Examination requested  [2007/25]
04.12.2008Despatch of a communication from the examining division (Time limit: M06)
12.06.2009Reply to a communication from the examining division
15.03.2011Despatch of a communication from the examining division (Time limit: M06)
26.09.2011Reply to a communication from the examining division
14.11.2012Despatch of a communication from the examining division (Time limit: M04)
26.03.2013Application deemed to be withdrawn, date of legal effect  [2013/38]
02.05.2013Despatch of communication that the application is deemed to be withdrawn, reason: reply to the communication from the examining division not received in time  [2013/38]
Divisional application(s)EP10193705.0  / EP2343293
The date of the Examining Division's first communication in respect of the earliest application for which a communication has been issued is  04.12.2008
Fees paidRenewal fee
31.07.2007Renewal fee patent year 03
31.07.2008Renewal fee patent year 04
27.07.2009Renewal fee patent year 05
14.07.2010Renewal fee patent year 06
12.07.2011Renewal fee patent year 07
26.07.2012Renewal fee patent year 08
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Cited inInternational search[PX]WO2005003128  (MERCK PATENT GMBH [DE], et al) [PX] 1-16 * Claims 1-15, 17; Formulae (I), (V2), (VI); examples; Table 1 *;
 [X]EP1352650  (INST MED MOLECULAR DESIGN INC [JP]) [X] 1-22 * Claims 1-18; Compounds 180-223 *;
 [A]WO2004014882  (AXYS PHARMACEUTICALS [US], et al) [A] 1-22 * the whole document *;
 [X]WO9715567  (THOMAE GMBH DR K [DE]) [X] 1-16 * Claims 1-9; Formula (I); examples 1(4), 1(5), 2(1), 2(2), 4(4), 6 *;
 [X]WO2004058750  (METRIS THERAPEUTICS LTD [GB], et al) [X] 1-6,8-12,15-17,22 * Claims 1-38; Formulae (II), (III); compounds 8a-f; Table 5 *;
 [X]WO2004058751  (METRIS THERAPEUTICS LTD [GB], et al) [X] 1-12,15,16 * Claims 1-33, 38-42; Formulae (II), (III); compounds 8a-e *;
 [X]WO2004041815  (MERCK PATENT GMBH [DE], et al) [X] 1-6,8-12,15,16,19 * Claims 1-8, 11-13, 18-19; Formula (I); example 7 *;
 [X]FR2270848  (CLIN MIDY [FR]) [X] 6,8,15,16,20 * Claims 1-13; Formulae (I) and (II); examples 13-44 *;
 [X]FR1516777  (INNOTHERA LAB SA) [X] 6,8 * Claim 1; Formulae (I) and (V); examples 37-38 *;
 [X]WO2004018453  (DAINIPPON PHARMACEUTICAL CO [JP], et al) [X] 6,7,9,12 * Formula (2); Preparations A-23, A-58, A-67, A-68, B-77, B-78 *;
 [X]DE10208256  (BAYER AG [DE]) [X] 6-8,12,15,16,20 * Claims 1-13; Formula (I); Compound 5 *;
 [PX]WO2005058887  (HOFFMANN LA ROCHE [CH], et al) [PX] 6,7,15,16 * Claims 1-21; formula (I); examples *
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DOI:   http://dx.doi.org/10.1016/S0960-894X(00)00152-9
 [X]  - LANGE U E W ET AL, "Synthesis of Highly potent and Selective Hetaryl Ureas as Integrin avb3-Receptor Antagonists", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, OXFORD, GB, (2002), vol. 12, ISSN 0960-894X, pages 1379 - 1382, XP002289253 [X] 6,8,15,16,20 * Compounds 23a and 25a *

DOI:   http://dx.doi.org/10.1016/S0960-894X(02)00161-0
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DOI:   http://dx.doi.org/10.1016/S0223-5234(97)86181-8
 [X]  - EKAMBARESWARA RAO K ET AL, "Synthesis of Novel Thiazole-Containing DNA Minor Groove Binding Oligopeptides Related to the Antibiotic Distamycin", JOURNAL OF ORGANIC CHEMISTRY, AMERICAN CHEMICAL SOCIETY. EASTON, US, (1990), vol. 55, no. 2, ISSN 0022-3263, pages 728 - 737, XP002255609 [X] 6,8 * Compound 30 *

DOI:   http://dx.doi.org/10.1021/jo00289a057
 [X]  - R. KUMAR, J. WILLIAM LOWN, "Synthesis and Antitumot Cytotoxicity Evalutation of Novel Thiazole-Containing Glycosylated Polyamides", EUR. J. ORG. CHEM., (2003), vol. 24, pages 4842 - 4851, XP002346491 [X] 6,8,15,16,20 * Compounds 26-27 *

DOI:   http://dx.doi.org/10.1002/ejoc.200300532
 [X]  - AI. KHALAF ET AL., "Distamycin Analogues with Enhanced Lipophilicity : Synthesis and Antimicrobial Activity", J. MED. CHEM., (20040305), vol. 47, no. 8, pages 2133 - 2156, XP002346492 [X] 6,8 * Compounds 28-29 *

DOI:   http://dx.doi.org/10.1021/jm031089x
 [X]  - WIPF P ET AL, "Total Synthesis of (-)-Muscoride A", JOURNAL OF ORGANIC CHEMISTRY, AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, US, (1996), vol. 61, ISSN 0022-3263, pages 6517 - 6522, XP002199739 [X] 6 * Compound 9 *

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DOI:   http://dx.doi.org/10.1016/S0960-894X(00)00594-1
 [X]  - R.J. BOYCE, G. PATTENDEN, "Naturally Occuring 4-Methylthiazolines. A total Synthesis of (-)-[4R,4S']-Didehyrdomirabazole A", TETRAHEDRON, (1995), vol. 51, no. 26, pages 7313 - 7320, XP002346493 [X] 6 * Compounds 3, 9 and 13 *

DOI:   http://dx.doi.org/10.1016/0040-4020(95)00355-C
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DOI:   http://dx.doi.org/10.1021/jo00096a012
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DOI:   http://dx.doi.org/10.1021/jo00127a030
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DOI:   http://dx.doi.org/10.1002/hlca.200390154
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DOI:   http://dx.doi.org/10.1016/S0960-894X(00)80330-3
ExaminationWO2005118579
 WO2004067521
 WO03004020
 WO0220010
 EP0870765
 EP0934938
 US2002010316
 EP0994108
 WO0024724
 US5510478
 US4731446
 WO03099316
    - OGISHIMA M ET AL, "Z-338 facilitates acetylcholine release from enteric neurons due to blockade of muscarinic autoreceptors in guinea pig stomach", JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, AMERICAN SOCIETY FOR PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, US, (20000101), vol. 294, no. 1, ISSN 0022-3565, pages 33 - 37, XP002962156
    - CRANK,G. AND FOULIS,M.J., "Derivatives of 2-Aminooxazoles Showing Antiinflammatory Activity", J. MED. CHEM., (1971), vol. 14, no. 11, pages 1075 - 1077
    - L. FELIU ET AL., "Synthesis of Methyl 2-Acetylamino-5-(1,3-dithian-2-yl)thiazole-4- carboxylate", HETEROCYCLES, (1997), vol. 45, no. 7, pages 1299 - 1308, XP001525809

DOI:   http://dx.doi.org/10.3987/COM-97-7805
    - ROHTASH KUMAR ET AL, "Synthesis of Novel Thiazole-Containing BIS-1-Chloromethyl-5-Hydroxy-1,2-Dihydro-3H-Benz(e)Indole(seco-CBI)-Polyamide Conjugates as Anticancer Agents", HETEROCYCLIC COMMUNICATIONS, FREUND PUBLISHING HOUSE, TEL AVIV, (20020101), ISSN 0793-0283, pages 521 - 530, XP009145534
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.