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Extract from the Register of European Patents

EP About this file: EP2147912

EP2147912 - Styrylquinolines, their process of preparation and their therapeutic uses [Right-click to bookmark this link]
StatusThe application is deemed to be withdrawn
Status updated on  11.03.2011
Database last updated on 25.09.2024
Most recent event   Tooltip11.03.2011Application deemed to be withdrawnpublished on 13.04.2011  [2011/15]
Applicant(s)For all designated states
BioAlliance Pharma
49, boulevard du Général Martial Valin
75015 Paris / FR
[2010/04]
Inventor(s)01 / Soma, Emilienne
3, rue Fagon, Appartement 44
75013 Paris / FR
02 / Thibault, Laurent
37, allée des Chevreuils
91330 Yerres / FR
03 / Michaut, Mathieu
109, route Burkel
67400 Illkirch / FR
04 / Wermuth, Camille, Georges
3, rue de la Côté d'Azur
67100 Strasbourg / FR
05 / Giethlen, Bruno
12, route des Romains
67120 Altorf / FR
 [2010/04]
Representative(s)Domenego, Bertrand
Cabinet Lavoix
2, Place d'Estienne d'Orves
75441 Paris Cedex 09 / FR
[N/P]
Former [2010/04]Domenego, Bertrand
Cabinet Lavoix 2, place d'Estienne d'Orves
75441 Paris Cedex 09 / FR
Application number, filing date08161000.823.07.2008
[2010/04]
Filing languageEN
Procedural languageEN
PublicationType: A1 Application with search report 
No.:EP2147912
Date:27.01.2010
Language:EN
[2010/04]
Search report(s)(Supplementary) European search report - dispatched on:EP29.12.2008
ClassificationIPC:C07D215/14, A61K31/47, A61P31/18
[2010/04]
CPC:
C07D215/14 (EP); A61P31/18 (EP)
Designated contracting states[2010/39]
Former [2010/04]AT,  BE,  BG,  CH,  CY,  CZ,  DE,  DK,  EE,  ES,  FI,  FR,  GB,  GR,  HR,  HU,  IE,  IS,  IT,  LI,  LT,  LU,  LV,  MC,  MT,  NL,  NO,  PL,  PT,  RO,  SE,  SI,  SK,  TR 
TitleGerman:Styrylchinoline, Herstellungsverfahren dafür und therapeutische Anwendungen[2010/04]
English:Styrylquinolines, their process of preparation and their therapeutic uses[2010/04]
French:Styrylquinolines, leur procédé de préparation et leurs utilisations thérapeutiques[2010/04]
Examination procedure28.07.2010Application deemed to be withdrawn, date of legal effect  [2011/15]
22.09.2010Despatch of communication that the application is deemed to be withdrawn, reason: examination fee not paid in time  [2011/15]
Fees paidPenalty fee
Additional fee for renewal fee
31.07.201003   M06   Not yet paid
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Responsibility for the accuracy, completeness or quality of the data displayed under the link provided lies entirely with the Unified Patent Court.
Documents cited:Search[X]WO2006129134  (BIOALLIANCE PHARMA [FR], et al) [X] 1-15 * page 10, lines 24, 27;; page 2, line 27 - page 3, line 13; claims 3,4 *;
 [X]DE1902595  (SOC D ETUDES PROD CHIMIQUE) [X] 1-7 * page 2, 1st paragraph; page 4, lines 3,4 and initial product of example 2 *;
 [X]  - LEONARD ET AL, "Exploring molecular shape analysis of styrylquinoline derivatives as HIV-1 integrase inhibitors", EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, EDITIONS SCIENTIFIQUE ELSEVIER, PARIS, FR, (20080101), vol. 43, no. 1, ISSN 0223-5234, pages 81 - 92, XP022423016 [X] 1-15 * page 82, paragraph before "2. Materials and methods"; compounds 2-23,35,36, especially compound 21 *

DOI:   http://dx.doi.org/10.1016/j.ejmech.2007.02.021
 [X]  - XIAO-HUI MA ET AL, "Exploring binding mode for styrylquinoline HIV-1 integrase inhibitors using comparative molecular field analysis and docking studies", ACTA PHARMACOLOGICA SINICA, (2004), vol. 25, no. 7, pages 950 - 958, XP009109792 [X] 1-15 * page 951, 1st full paragraph; table 2, compound SQ21 *
 [X]  - PODESZWA ET AL, "Investigating the antiproliferative activity of quinoline-5,8-diones and styrylquinolinecarboxylic acids on tumor cell lines", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, PERGAMON, ELSEVIER SCIENCE, GB, (20071012), vol. 17, no. 22, ISSN 0960-894X, pages 6138 - 6141, XP022297113 [X] 1-15 * page 6141, 2nd paragraph;;; examples 16,28,30,31 *

DOI:   http://dx.doi.org/10.1016/j.bmcl.2007.09.040
 [X]  - ZOUHIRI F ET AL, "HIV-1 replication inhibitors of the styrylquinoline class: introduction of an additional carboxyl group at the C-5 position of the quinoline", TETRAHEDRON LETTERS, ELSEVIER, AMSTERDAM, (20050328), vol. 46, no. 13, ISSN 0040-4039, pages 2201 - 2205, XP004846709 [X] 1-15 * page 2201, right column, 1st complete paragraph; table 1 (p. 2203), compound 3b *

DOI:   http://dx.doi.org/10.1016/j.tetlet.2005.02.033
 [X]  - ZOUHIRI F ET AL, "STRUCTURE-ACTIVITY RELATIONSHIPS AND BINDING MODE OF STYRYLQUINOLINES AS POTENT INHIBITORS OF HIV-1 INTEGRASE AND REPLICATION OF HIV-1 IN CELL CULTURE", JOURNAL OF MEDICINAL CHEMISTRY, US AMERICAN CHEMICAL SOCIETY. WASHINGTON, (20000101), vol. 43, ISSN 0022-2623, pages 1533 - 1540, XP000926747 [X] 1-15 * page 1533, right column, end of paragraph; table 1, compound 29 *

DOI:   http://dx.doi.org/10.1021/jm990467o
 [X]  - J. POLANSKI ET AL, "fragment based approach for the investigation of HIV-1 integrase inhibition", LETTERS IN DRUG DESIGN & DISCOVERY, (2007), vol. 4, pages 99 - 105, XP009109802 [X] 1-15 * table 1, compounds 15, 16a, 16b *

DOI:   http://dx.doi.org/10.2174/157018007779422532
by applicantWO9845269
    - POMMIER Y, NAT REV DRUG DISCOV, (2005), vol. 4, pages 236 - 248
    - JOHNSON AA ET AL., MOL PHARMACOL., (2007), vol. 71, no. 3, pages 893 - 901
    - Handbook of Chemistry and Physics, CRC PRESS, INC., (1995), vol. 1996, pages 2 - 25
    - Remington's Pharmaceutical Sciences, MACK PUBLISHING COMPANY, (1985), page 1418
    - MEEK ET AL., CHEM. ENGINEERING, (1969), vol. 14, pages 388 - 391
    - PRZYSTAL ET AL., J.HETEROCYD. CHEM, (1967), vol. 4, pages 131 - 2
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.