FR2835186B1 - Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases - Google Patents

Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases

Info

Publication number
FR2835186B1
FR2835186B1 FR0200951A FR0200951A FR2835186B1 FR 2835186 B1 FR2835186 B1 FR 2835186B1 FR 0200951 A FR0200951 A FR 0200951A FR 0200951 A FR0200951 A FR 0200951A FR 2835186 B1 FR2835186 B1 FR 2835186B1
Authority
FR
France
Prior art keywords
beta
heterocyclic compounds
novel heterocyclic
compounds active
lactamases inhibitors
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
FR0200951A
Other languages
English (en)
French (fr)
Other versions
FR2835186A1 (fr
Inventor
Jozsef Aszodi
Maxime Lampilas
Claude Fromentin
David Alan Rowlands
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Ireland Pharmaceuticals
Original Assignee
Aventis Pharma SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27619669&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=FR2835186(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Aventis Pharma SA filed Critical Aventis Pharma SA
Priority to FR0200951A priority Critical patent/FR2835186B1/fr
Priority to JO2002138A priority patent/JO2646B1/en
Priority to TW092101133A priority patent/TWI293071B/zh
Priority to ES03709903T priority patent/ES2356813T3/es
Priority to YU65804A priority patent/RS52137B/sr
Priority to PT03709903T priority patent/PT1480644E/pt
Priority to SI200332240T priority patent/SI2279737T1/sl
Priority to CNB2007100015952A priority patent/CN100563653C/zh
Priority to EP10177533A priority patent/EP2279737B1/fr
Priority to PCT/FR2003/000243 priority patent/WO2003063864A2/fr
Priority to BR122015020406A priority patent/BR122015020406B8/pt
Priority to PT101775336T priority patent/PT2279737E/pt
Priority to JP2003563554A priority patent/JP4472346B2/ja
Priority to EP03709903A priority patent/EP1480644B1/fr
Priority to UY27626A priority patent/UY27626A1/es
Priority to UA20040807144A priority patent/UA80271C2/uk
Priority to CNB038028786A priority patent/CN100482225C/zh
Priority to AT03709903T priority patent/ATE484281T1/de
Priority to DE60334527T priority patent/DE60334527D1/de
Priority to NZ533936A priority patent/NZ533936A/en
Priority to MYPI20030260A priority patent/MY140638A/en
Priority to DK03709903.3T priority patent/DK1480644T3/da
Priority to PL371601A priority patent/PL220725B1/pl
Priority to HRP20040686AA priority patent/HRP20040686B1/hr
Priority to EA200400981A priority patent/EA007220B1/ru
Priority to CA2474043A priority patent/CA2474043C/fr
Priority to ARP030100226A priority patent/AR038234A1/es
Priority to AU2003214335A priority patent/AU2003214335B2/en
Priority to CNA2008101667591A priority patent/CN101406471A/zh
Priority to KR1020047011594A priority patent/KR100979079B1/ko
Priority to BRPI0307267A priority patent/BRPI0307267B8/pt
Priority to DK10177533.6T priority patent/DK2279737T3/da
Priority to MXPA04006621A priority patent/MXPA04006621A/es
Priority to SI200331935T priority patent/SI1480644T1/sl
Priority to HK05109272.5A priority patent/HK1077205B/xx
Priority to ES10177533T priority patent/ES2401855T3/es
Priority to PE2003000080A priority patent/PE20030969A1/es
Priority to OA1200400200A priority patent/OA12761A/fr
Publication of FR2835186A1 publication Critical patent/FR2835186A1/fr
Priority to MA27777A priority patent/MA26351A1/fr
Priority to CR7387A priority patent/CR7387A/es
Priority to ZA2004/05607A priority patent/ZA200405607B/en
Priority to EC2004005193A priority patent/ECSP045193A/es
Priority to IL163167A priority patent/IL163167A/en
Priority to TNP2004000137A priority patent/TNSN04137A1/fr
Priority to US10/898,754 priority patent/US7612087B2/en
Priority to CO04071440A priority patent/CO5601014A2/es
Priority to NO20043587A priority patent/NO335195B1/no
Application granted granted Critical
Publication of FR2835186B1 publication Critical patent/FR2835186B1/fr
Priority to HK07111190.8A priority patent/HK1105864B/xx
Priority to US12/434,270 priority patent/US20090215747A1/en
Priority to US12/610,562 priority patent/US20100048528A1/en
Priority to CY20101101192T priority patent/CY1111061T1/el
Priority to CL2011000009A priority patent/CL2011000009A1/es
Priority to US13/161,783 priority patent/US20110245254A1/en
Priority to CR20120356A priority patent/CR20120356A/es
Priority to CY20131100090T priority patent/CY1114417T1/el
Priority to ARP150101838A priority patent/AR100790A2/es
Priority to CY2016042C priority patent/CY2016042I2/el
Priority to NL300847C priority patent/NL300847I2/nl
Priority to BE2016C069C priority patent/BE2016C069I2/fr
Priority to FR16C1019C priority patent/FR16C1019I2/fr
Priority to LTPA2016037C priority patent/LTC1480644I2/lt
Priority to HUS1600055C priority patent/HUS1600055I1/hu
Priority to NO2016024C priority patent/NO2016024I1/no
Anticipated expiration legal-status Critical
Priority to NO2025027C priority patent/NO2025027I1/no
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/439Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4995Pyrazines or piperazines forming part of bridged ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
FR0200951A 2002-01-28 2002-01-28 Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases Expired - Lifetime FR2835186B1 (fr)

Priority Applications (64)

Application Number Priority Date Filing Date Title
FR0200951A FR2835186B1 (fr) 2002-01-28 2002-01-28 Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
JO2002138A JO2646B1 (en) 2002-01-28 2002-12-29 New differentiated cyclic compounds as beta - lactam inhibitors
TW092101133A TWI293071B (en) 2002-01-28 2003-01-20 New heterocyclic compounds, which are active as inhibitors of beta-lactamases
ES03709903T ES2356813T3 (es) 2002-01-28 2003-01-27 Nuevos compuestos heterocíclicos, activos como inhibidores de beta-lactamasas.
YU65804A RS52137B (sr) 2002-01-28 2003-01-27 Nova heterociklična jedinjenja aktivna kao inhibitori beta-laktamaze
PT03709903T PT1480644E (pt) 2002-01-28 2003-01-27 Compostos heterociclícos, activos como inibidores de beta-lactamases
SI200332240T SI2279737T1 (sl) 2002-01-28 2003-01-27 Heterociklične spojine, učinkovite kot inhibitorji beta-laktamaz
CNB2007100015952A CN100563653C (zh) 2002-01-28 2003-01-27 具有β-内酰胺酶抑制剂活性的杂环化合物
EP10177533A EP2279737B1 (fr) 2002-01-28 2003-01-27 Composés hétérocycliques, actifs comme inhibiteurs de béta-lactamases
PCT/FR2003/000243 WO2003063864A2 (fr) 2002-01-28 2003-01-27 Composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
BR122015020406A BR122015020406B8 (pt) 2002-01-28 2003-01-27 uso de compostos de formula i como inibidores de beta-lactamases e composições farmaceuticas
PT101775336T PT2279737E (pt) 2002-01-28 2003-01-27 Compostos heterocíclicos, activos como inibidores de beta-lactamases
JP2003563554A JP4472346B2 (ja) 2002-01-28 2003-01-27 ベータ−ラクタマーゼの阻害剤として活性である新規な複素環化合物
EP03709903A EP1480644B1 (fr) 2002-01-28 2003-01-27 Composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
UY27626A UY27626A1 (es) 2002-01-28 2003-01-27 Nuevos compuestos heterocíclos, activos como inhibidores de beta-lactamasas
UA20040807144A UA80271C2 (uk) 2002-01-28 2003-01-27 Застосування гетероциклічних сполук як інгібіторів бета-лактамази
CNB038028786A CN100482225C (zh) 2002-01-28 2003-01-27 具有β-内酰胺酶抑制剂活性的新的杂环化合物
AT03709903T ATE484281T1 (de) 2002-01-28 2003-01-27 Heterocyclische verbindungen die als beta- lactamasehemmer aktiv sind
DE60334527T DE60334527D1 (de) 2002-01-28 2003-01-27 Heterocyclische verbindungen die als beta-lactamasehemmer aktiv sind
NZ533936A NZ533936A (en) 2002-01-28 2003-01-27 Novel heterocyclic compounds, which are active as inhibitors of beta-lactamases
MYPI20030260A MY140638A (en) 2002-01-28 2003-01-27 New heterocyclic compounds, which are active as inhibitors of beta-lactamases
DK03709903.3T DK1480644T3 (da) 2002-01-28 2003-01-27 Heterocykliske forbindelser, der er aktive som inhibitorer af beta-lactamaser
PL371601A PL220725B1 (pl) 2002-01-28 2003-01-27 Zastosowanie związków heterocyklicznych aktywnych jako inhibitor β-laktamazy do wytwarzania leku do leczenia infekcji bakteryjnych u człowieka lub zwierząt, oraz zawierająca je kompozycja farmaceutyczna
HRP20040686AA HRP20040686B1 (hr) 2002-01-28 2003-01-27 Novi heterocikliäśki spojevi koji djeluju kao inhibitori beta-laktamaza
EA200400981A EA007220B1 (ru) 2002-01-28 2003-01-27 Новое применение гетероциклических соединений, активных в качестве ингибиторов бета-лактамаз, и содержащие их фармацевтические композиции
CA2474043A CA2474043C (fr) 2002-01-28 2003-01-27 Composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
ARP030100226A AR038234A1 (es) 2002-01-28 2003-01-27 Compuestos heterociclicos, activos como inhibidores de beta-lactamasas
AU2003214335A AU2003214335B2 (en) 2002-01-28 2003-01-27 Heterocyclic compounds which are active as inhibitors of beta lactamases
CNA2008101667591A CN101406471A (zh) 2002-01-28 2003-01-27 具有β-内酰胺酶抑制剂活性的新的杂环化合物
KR1020047011594A KR100979079B1 (ko) 2002-01-28 2003-01-27 베타 락타마제의 억제제로서 활성인 헤테로사이클릭 화합물을 함유하는 약제학적 조성물
BRPI0307267A BRPI0307267B8 (pt) 2002-01-28 2003-01-27 uso de compostos inibidores de beta-lactamases e composições farmacêuticas para terapia antibacteriana
DK10177533.6T DK2279737T3 (da) 2002-01-28 2003-01-27 Heterocycliske forbindelser, der er aktive som beta-lactamaseinhibitorer
MXPA04006621A MXPA04006621A (es) 2002-01-28 2003-01-27 Nuevos compuestos heterociclicos, activos como inhibidores de beta-lactamasas.
SI200331935T SI1480644T1 (sl) 2002-01-28 2003-01-27 Heterociklične spojine, učinkovite kot inhibitorji beta-laktamaz
HK05109272.5A HK1077205B (en) 2002-01-28 2003-01-27 Novel heterocyclic compounds which are active as inhibitors of beta+lactamases
ES10177533T ES2401855T3 (es) 2002-01-28 2003-01-27 Compuestos heterocíclicos, activos como inhibidores de beta-lactamasas
PE2003000080A PE20030969A1 (es) 2002-01-28 2003-01-27 Compuestos heterociclicos, activos inhibidores de beta-lactamasas
OA1200400200A OA12761A (fr) 2002-01-28 2003-01-27 Nouveaux composés héterocycliques, actifs comme inhibiteurs de béta-lactamases.
MA27777A MA26351A1 (fr) 2002-01-28 2004-07-12 Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta+lactamases
CR7387A CR7387A (es) 2002-01-28 2004-07-13 Nuevos compuestos heterociclicos activos como inhibidores de las beta- lactamasas
ZA2004/05607A ZA200405607B (en) 2002-01-28 2004-07-14 Heterocyclic compounds which are active as inhibitors of beta-lactamases
EC2004005193A ECSP045193A (es) 2002-01-28 2004-07-15 "nuevos compuestos heterociclicos, activos como inhibidores de beta-lactamasas"
IL163167A IL163167A (en) 2002-01-28 2004-07-22 Heterocyclic compounds which are active as inhibitors of beta lactamases
TNP2004000137A TNSN04137A1 (fr) 2002-01-28 2004-07-23 Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
US10/898,754 US7612087B2 (en) 2002-01-28 2004-07-26 Heterocyclic compounds as inhibitors of beta-lactamases
CO04071440A CO5601014A2 (es) 2002-01-28 2004-07-26 Nuevos compuestos heterociclicos, activos como inhibidores de beta-lactamasas
NO20043587A NO335195B1 (no) 2002-01-28 2004-08-27 Anvendelse av heterocykliske forbindelser som er aktive som inhibitorer av betalaktamaser samt farmasøytisk blanding derav.
HK07111190.8A HK1105864B (en) 2002-01-28 2007-10-17 Heterocyclic compounds which are active as inhibitors of beta-lactamases
US12/434,270 US20090215747A1 (en) 2002-01-28 2009-05-01 Heterocyclic compounds as inhibitors of beta-lactamases
US12/610,562 US20100048528A1 (en) 2002-01-28 2009-11-02 Heterocyclic compounds as inhibitors of beta-lactamases
CY20101101192T CY1111061T1 (el) 2002-01-28 2010-12-23 Νεες ετεροκυκλικες ενωσεις δραστικες ως αναστολεις των βητα-λακταμασων
CL2011000009A CL2011000009A1 (es) 2002-01-28 2011-01-05 Composicion farmaceutica que comprende un compuesto derivado de (diaza)- u (oxa-aza)-biciclo-octano en combinacion con un antibiotico de beta-lactamina; y el uso de la composicion para inhibir la produccion de beta-lactamasa en una terapia antibacteriana. (divisional de la solicitud 134-2003)
US13/161,783 US20110245254A1 (en) 2002-01-28 2011-06-16 Heterocyclic compounds as inhibitors of beta-lactamases
CR20120356A CR20120356A (es) 2002-01-28 2012-06-28 Nuevos compuestos heterocíclicos activos como inhibidores de beta-lactamasas
CY20131100090T CY1114417T1 (el) 2002-01-28 2013-01-31 Ετεροκυκλικες ενωσεις, δραστικες ως αναστολεις των βητα-λακταμασων
ARP150101838A AR100790A2 (es) 2002-01-28 2015-06-10 COMPUESTOS HETEROCÍCLICOS, ACTIVOS COMO INHIBIDORES DE b-LACTAMAS
CY2016042C CY2016042I2 (el) 2002-01-28 2016-12-06 Νεες ετεροκυκλικες ενωσεις δραστικες ως αναστολεις των βητα-λακταμασων
NL300847C NL300847I2 (enExample) 2002-01-28 2016-12-08
BE2016C069C BE2016C069I2 (enExample) 2002-01-28 2016-12-12
FR16C1019C FR16C1019I2 (fr) 2002-01-28 2016-12-13 Composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
LTPA2016037C LTC1480644I2 (lt) 2002-01-28 2016-12-13 Nauji heterocikliniai junginiai, veiksmingi kaip beta-laktamazės slopikliai
HUS1600055C HUS1600055I1 (hu) 2002-01-28 2016-12-13 Béta-laktamáz-inhibitor aktivitással rendelkezõ új heterociklusos vegyületek
NO2016024C NO2016024I1 (no) 2002-01-28 2016-12-15 Farmasøytisk blanding eller assosisjon som inneholder som aktive ingredienser: (1) ceftazidim eller et salt derav, og (2) avibaktam eller et farmasøytisk akseptabelt salt derav
NO2025027C NO2025027I1 (no) 2002-01-28 2025-06-13 Pharmaceutical mixture or association that includes as active ingredients: (1) ceftazidime or a salt thereof, and (2) avibactam or a pharmaceutically acceptable salt thereof - forlenget.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0200951A FR2835186B1 (fr) 2002-01-28 2002-01-28 Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases

Publications (2)

Publication Number Publication Date
FR2835186A1 FR2835186A1 (fr) 2003-08-01
FR2835186B1 true FR2835186B1 (fr) 2006-10-20

Family

ID=27619669

Family Applications (2)

Application Number Title Priority Date Filing Date
FR0200951A Expired - Lifetime FR2835186B1 (fr) 2002-01-28 2002-01-28 Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
FR16C1019C Active FR16C1019I2 (fr) 2002-01-28 2016-12-13 Composes heterocycliques, actifs comme inhibiteurs de beta-lactamases

Family Applications After (1)

Application Number Title Priority Date Filing Date
FR16C1019C Active FR16C1019I2 (fr) 2002-01-28 2016-12-13 Composes heterocycliques, actifs comme inhibiteurs de beta-lactamases

Country Status (44)

Country Link
US (4) US7612087B2 (enExample)
EP (2) EP1480644B1 (enExample)
JP (1) JP4472346B2 (enExample)
KR (1) KR100979079B1 (enExample)
CN (3) CN100563653C (enExample)
AR (2) AR038234A1 (enExample)
AT (1) ATE484281T1 (enExample)
AU (1) AU2003214335B2 (enExample)
BE (1) BE2016C069I2 (enExample)
BR (1) BRPI0307267B8 (enExample)
CA (1) CA2474043C (enExample)
CL (1) CL2011000009A1 (enExample)
CO (1) CO5601014A2 (enExample)
CR (2) CR7387A (enExample)
CY (3) CY1111061T1 (enExample)
DE (1) DE60334527D1 (enExample)
DK (2) DK2279737T3 (enExample)
EA (1) EA007220B1 (enExample)
EC (1) ECSP045193A (enExample)
ES (2) ES2401855T3 (enExample)
FR (2) FR2835186B1 (enExample)
HR (1) HRP20040686B1 (enExample)
HU (1) HUS1600055I1 (enExample)
IL (1) IL163167A (enExample)
JO (1) JO2646B1 (enExample)
LT (1) LTC1480644I2 (enExample)
MA (1) MA26351A1 (enExample)
MX (1) MXPA04006621A (enExample)
MY (1) MY140638A (enExample)
NL (1) NL300847I2 (enExample)
NO (3) NO335195B1 (enExample)
NZ (1) NZ533936A (enExample)
OA (1) OA12761A (enExample)
PE (1) PE20030969A1 (enExample)
PL (1) PL220725B1 (enExample)
PT (2) PT1480644E (enExample)
RS (1) RS52137B (enExample)
SI (2) SI2279737T1 (enExample)
TN (1) TNSN04137A1 (enExample)
TW (1) TWI293071B (enExample)
UA (1) UA80271C2 (enExample)
UY (1) UY27626A1 (enExample)
WO (1) WO2003063864A2 (enExample)
ZA (1) ZA200405607B (enExample)

Families Citing this family (88)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2812635B1 (fr) * 2000-08-01 2002-10-11 Aventis Pharma Sa Nouveaux composes heterocycliques, preparation et utilisation comme medicaments notamment comme anti- bacteriens
FR2835186B1 (fr) * 2002-01-28 2006-10-20 Aventis Pharma Sa Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
FR2844273B1 (fr) 2002-09-05 2008-04-04 Aventis Pharma Sa Nouveaux composes heterocycliques, procede et intermediaires de preparation et utilisation comme medicament, notamment comme inhibiteurs de beta-lactamases et anti-bacteriens.
FR2848210B1 (fr) * 2002-12-06 2007-10-19 Aventis Pharma Sa Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments, notamment comme anti-bacteriens et inhibiteurs de beta-lactamases
US7439253B2 (en) 2002-12-06 2008-10-21 Novexel Heterocyclic compounds, their preparation and their use as medicaments, in particular as antibacterials and beta-lactamase inhibitors
US8900637B2 (en) * 2005-12-02 2014-12-02 Lupin Limited Stable taste masked formulations of cephalosporins
EP2484680B1 (en) * 2005-12-07 2013-06-26 Basilea Pharmaceutica AG Useful Combinations of Monobactam Antibiotics with beta-Lac-tamase Inhibitors
JP5539717B2 (ja) * 2006-07-14 2014-07-02 塩野義製薬株式会社 オキシム化合物およびその使用
BRPI0717348A2 (pt) * 2006-10-23 2013-10-15 Irm Llc Composições e processos para inibir captecina proteases
JP5323063B2 (ja) * 2007-05-31 2013-10-23 塩野義製薬株式会社 オキシイミノ化合物およびその使用
FR2921060B1 (fr) * 2007-09-14 2012-06-15 Novexel Nouveau procede de preparation d'une piperidine disubsituee et nouveaux intermediaires
JP5038509B2 (ja) 2008-01-18 2012-10-03 メルク・シャープ・エンド・ドーム・コーポレイション β−ラクタマーゼ阻害剤
WO2009114921A1 (en) * 2008-03-17 2009-09-24 Dmitrienko Gary I INHIBITORS OF CLASS B AND CLASS D β-LACTAMASES
FR2930553B1 (fr) * 2008-04-29 2010-05-21 Novexel Composes azabicycliques, leur preparation et leur utilisation comme medicaments, notamment inhibiteurs de beta-lactamases
WO2009151152A1 (en) * 2008-06-11 2009-12-17 Shionogi & Co., Ltd. Oxycarbamoyl compounds and the use thereof
FR2936798B1 (fr) * 2008-10-03 2012-09-28 Novexel Nouveaux composes heterocycliques azotes, leur preparation et leur utilisation comme medicaments antibacteriens.
FR2937034B1 (fr) * 2008-10-10 2012-11-23 Novexel Nouveaux composes heterocycliques azotes, leur preparation et leur utilisation comme medicaments antibacteriens
FR2936951B1 (fr) * 2008-10-10 2010-12-03 Novexel Nouvelles combinaisons de composes heterocycliques azotes antibacteriens avec d'autres composes antibacteriens et leur utilisation comme medicaments
FR2951171A1 (fr) 2009-10-09 2011-04-15 Novexel Nouveau sel de sodium d'un compose azabicyclique sous forme enantiomere cristallisee et nouvelles formes polymorphes et pseudopolymorphes ainsi que leur preparation
AU2014244235B2 (en) * 2009-10-09 2016-04-21 Pfizer Ireland Pharmaceuticals Polymorphic and pseudopolymorphic forms of a pharmaceutical compound
RU2599791C2 (ru) 2010-08-10 2016-10-20 Ремпекс Фармасьютикэлз, Инч. Циклические бороновые кислотно-эфирные производные и их использование в терапии
US8772490B2 (en) 2010-12-22 2014-07-08 Meiji Seika Pharma Co., Ltd. Optically active diazabicyclooctane derivatives and process for preparing the same
SI2657234T1 (sl) * 2010-12-22 2017-06-30 Meiji Seika Pharma Co., Ltd. Derivat optično-aktivnega diazabiciklooktana in metoda za njegovo izdelavo
CA2780403C (en) * 2011-06-17 2020-04-21 Forest Laboratories Holdings Ltd. Processes for preparing heterocyclic compounds including trans-7-oxo-6-(sulphooxy)-1,6-diazabicyclo[3,2,1]octane-2-carboxamide and salts thereof
RU2636147C1 (ru) * 2011-08-27 2017-11-21 Вокхардт Лимитед Производные 1,6-диазабицикло[3,2,1]октан-7-она и их применение при лечении бактериальных инфекционных болезней
US20130053565A1 (en) * 2011-08-29 2013-02-28 University Of Utah Research Foundation Substituted 3-piperidone compounds
US9102683B2 (en) 2011-08-29 2015-08-11 University Of Utah Research Foundation Heterocyclic compounds
WO2013033461A1 (en) 2011-08-31 2013-03-07 Rempex Pharmaceuticals, Inc. Heterocyclic boronic acid ester derivatives and therapeutic uses thereof
US8969567B2 (en) * 2011-09-13 2015-03-03 Wockhardt Ltd. Nitrogen containing compounds and their use
US8754102B2 (en) * 2011-09-13 2014-06-17 Wockhardt Ltd. Nitrogen containing compounds and their use
US8796257B2 (en) 2011-12-02 2014-08-05 Naeja Pharmaceutical Inc. Bicyclic compounds and their use as antibacterial agents and β-lactamase inhibitors
US9505761B2 (en) 2011-12-02 2016-11-29 Fedora Pharmaceuticals Inc. Bicyclic compounds and their use as antibacterial agents and beta-lactamase inhibitors
WO2013149121A1 (en) 2012-03-30 2013-10-03 Cubist Pharmaceuticals, Inc. 1,3,4-oxadiazole and 1,3,4-thiadiazole beta-lactamase inhibitors
AU2013237869A1 (en) 2012-03-30 2014-10-23 Cubist Pharmaceuticals, Inc. Isoxazole beta-lactamase inhibitors
US8916709B2 (en) 2012-03-30 2014-12-23 Cubist Pharmaceuticals, Inc. 1,2,4-oxadiazole and 1,2,4-thiadiazole β-lactamase inhibitors
US8969570B2 (en) 2012-03-30 2015-03-03 Cubist Pharmaceuticals, Inc. Beta-lactamase inhibitors
AR090539A1 (es) * 2012-04-02 2014-11-19 Astrazeneca Ab COMPUESTOS INHIBIDORES DE b LACTAMASA
US9156858B2 (en) 2012-05-23 2015-10-13 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
TWI565707B (zh) 2012-05-30 2017-01-11 明治製菓藥業股份有限公司 新穎β-內醯胺酶抑制劑及其製造方法
US10561675B2 (en) 2012-06-06 2020-02-18 Rempex Pharmaceuticals, Inc. Cyclic boronic acid ester derivatives and therapeutic uses thereof
EP2961751B1 (en) * 2012-08-25 2018-03-21 Wockhardt Limited 1,6- diazabicyclo [3,2,1]octan- 7- one derivatives and their use in the treatment of bacterial infections
UA111925C2 (uk) * 2012-12-11 2016-06-24 Федора Фармасьютікалз Інк. БІЦИКЛІЧНІ СПОЛУКИ ТА ЇХ ВИКОРИСТАННЯ ЯК АНТИБАКТЕРІАЛЬНИХ АГЕНТІВ ТА ІНГІБІТОРІВ β-ЛАКТАМАЗИ
JP6324409B2 (ja) 2013-01-04 2018-05-16 レンペックス・ファーマシューティカルズ・インコーポレイテッド ボロン酸誘導体及びその治療的使用
AU2014204045B2 (en) 2013-01-04 2018-10-18 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
US9241947B2 (en) 2013-01-04 2016-01-26 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
US9101638B2 (en) 2013-01-04 2015-08-11 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
EP2970338A1 (en) 2013-03-14 2016-01-20 Merck Sharp & Dohme Corp. Crystalline form of a beta-lactamase inhibitor
TWI644908B (zh) 2013-09-24 2018-12-21 明治製菓藥業股份有限公司 二氮雜二環辛烷衍生物之製法及其中間體
WO2015051101A1 (en) 2013-10-02 2015-04-09 Cubist Pharmaceuticals, Inc. B-lactamase inhibitor picoline salt
KR102388529B1 (ko) 2013-10-08 2022-04-20 메이지 세이카 파루마 가부시키가이샤 디아자비시클로옥탄 유도체의 결정과 그의 제조법
KR20160115941A (ko) * 2014-02-20 2016-10-06 욱크하르트 리미티드 항세균제를 포함하는 제약학적 조합
CN103896936A (zh) * 2014-03-20 2014-07-02 西安交通大学 (5s,6r)氯唑西林青霉噻唑酸盐及其制备方法和应用
WO2015171398A1 (en) 2014-05-05 2015-11-12 Rempex Pharmaceuticals, Inc. Salts and polymorphs of cyclic boronic acid ester derivatives and therapeutic uses thereof
RS59488B1 (sr) 2014-05-05 2019-12-31 Rempex Pharmaceuticals Inc Sinteza boronatnih soli i njihove upotrebe
JP6672176B2 (ja) 2014-05-19 2020-03-25 レンペックス・ファーマシューティカルズ・インコーポレイテッド ボロン酸誘導体およびその治療的使用
CN104059083B (zh) * 2014-05-27 2017-01-04 浙江工业大学 一种手性二环己内酰胺类化合物的不对称合成方法
AU2015284307A1 (en) 2014-07-01 2017-02-02 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
US9968593B2 (en) 2014-11-17 2018-05-15 Entasis Therapeutics Limited Combination therapy for treatment of resistant bacterial infections
US10662205B2 (en) 2014-11-18 2020-05-26 Qpex Biopharma, Inc. Cyclic boronic acid ester derivatives and therapeutic uses thereof
RU2732129C2 (ru) 2014-12-05 2020-09-11 Мейдзи Сейка Фарма Ко., Лтд. Способ производства кристаллов производного диазабициклооктана и стабильного лиофилизированного препарата
US20180051041A1 (en) 2015-03-17 2018-02-22 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
JP6767392B2 (ja) * 2015-05-07 2020-10-14 ミュタビリスMutabilis 複素環式化合物及び細菌感染の治療又は予防におけるその使用
CN107531709B (zh) * 2015-09-16 2020-10-23 吉林四环制药有限公司 β-内酰胺酶抑制剂及其用途
EA201890847A1 (ru) 2015-10-02 2018-08-31 Легокем Байосайенсез, Инк. Композиции и способы ингибирования бета-лактамазы
WO2017156458A1 (en) 2016-03-11 2017-09-14 University Of South Florida Beta-lactamase inhibitors, formulations, and uses thereof
EP3156400B1 (en) 2016-05-27 2019-05-15 Valoralia I Más D, SL Dihydrooxadiazine compounds for treating infections and cancer
JP7060245B2 (ja) 2016-06-30 2022-04-26 キューペックス バイオファーマ, インコーポレイテッド ボロン酸誘導体およびその治療的使用
CN106279163A (zh) * 2016-08-12 2017-01-04 上海龙翔生物医药开发有限公司 一种合成阿维巴坦及其中间体光学异构体的方法
CN107789355B (zh) * 2016-09-07 2022-04-12 湘北威尔曼制药股份有限公司 含有哌拉西林的复方药物组合物及其应用
SMT202200397T1 (it) 2016-09-16 2022-11-18 Entasis Therapeutics Ltd Composti inibitori di beta-lattamasi
JOP20190061A1 (ar) * 2016-09-28 2019-03-26 Novartis Ag مثبطات بيتا-لاكتاماز
CN106699756B (zh) * 2016-12-30 2019-10-29 淄博鑫泉医药技术服务有限公司 β内酰胺酶抑制剂阿维巴坦的合成方法
MX2019009362A (es) 2017-02-06 2019-10-22 Mutabilis Compuestos heterociclicos novedosos y sus usos en la prevencion o el tratamiento de infecciones bacterianas.
PT3630111T (pt) 2017-05-08 2022-03-01 Entasis Therapeutics Inc Compostos e métodos de tratamento de infeções bacterianas
WO2018234962A1 (en) 2017-06-20 2018-12-27 Wockhardt Limited Process for o-sulfonation of 1,6-diazabicyclo[3.2.1]octane compounds
CA3078627A1 (en) 2017-10-11 2019-04-18 Qpex Biopharma, Inc. Boronic acid derivatives and synthesis thereof
CN109678856B (zh) * 2017-10-18 2020-09-25 新发药业有限公司 一种阿维巴坦中间体的制备方法
TW201925201A (zh) * 2017-11-10 2019-07-01 日商鹽野義製藥股份有限公司 二氮雜二環辛烷衍生物
EP3781576B1 (en) 2018-04-20 2024-06-12 Qpex Biopharma, Inc. Boronic acid derivatives and therapeutic uses thereof
DK3833665T3 (da) 2018-08-09 2023-10-09 Antabio Sas Diazabicyclooctanoner som hæmmere af serin-beta-lactamaser
US11905286B2 (en) 2018-08-09 2024-02-20 Antabio Sas Diazabicyclooctanones as inhibitors of serine beta-lactamases
CN109942579B (zh) * 2019-04-18 2021-06-22 成都千禧莱医药科技有限公司 β-内酰胺酶抑制剂含脲双环化合物及其制备方法和应用
WO2022047603A1 (en) 2020-09-01 2022-03-10 Ningxia Academy Of Agriculture And Forestry Sciences Beta-lactamase inhibitors and their preparation
WO2022047790A1 (en) * 2020-09-07 2022-03-10 Ningxia Academy Of Agriculture And Forestry Sciences Amidine substituted bicyclic compounds, their preparation, their use as antibacterial agents and beta-lactamase inhibitors
EP4146651A4 (en) 2021-05-07 2024-06-05 Ningxia Academy of Agriculture and Forestry Sciences SULFONYLAMIDINE SUBSTITUTED COMPOUNDS AND THEIR USE AS BETA-LACTAMASE INHIBITORS
WO2023060369A1 (en) * 2021-10-11 2023-04-20 Ningxia Academy Of Agriculture And Forestry Sciences Novel carbimidate substituted bicyclic compounds and their use as beta-lactamase inhibitors
KR20240041506A (ko) 2022-09-23 2024-04-01 주식회사 경보제약 아비박탐 나트륨 염의 안정한 일수화물 형태 및 그의 제조 방법
CN116375706B (zh) * 2023-02-22 2025-02-14 时森海(杭州)医药科技有限公司 阿维巴坦钠关键中间体及其制备方法

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0260057A3 (en) 1986-09-02 1989-02-01 The University Of Melbourne 2-oxo-4-carboxy-pyrimidines
JP2955358B2 (ja) 1989-06-09 1999-10-04 ファルマシア・アンド・アップジョン・カンパニー 中枢神経系活性を有する複素環系アミン
FR2676230B1 (fr) 1991-05-07 1993-08-27 Centre Nat Rech Scient Nouveaux derives de pyrrolo [1,4]-benzodiazepines, leur procede de preparation et medicaments les contenant.
JPH05339263A (ja) 1992-06-08 1993-12-21 Wakunaga Pharmaceut Co Ltd ジヒドロピリジン誘導体
DK1227103T3 (da) 1993-09-29 2006-11-27 Univ Maryland Nukleosider og nukleotider med forstörrede ringe
WO1995018129A1 (en) * 1993-12-29 1995-07-06 Pfizer Inc. Diazabicyclic neurokinin antagonists
EP0702004A2 (de) 1994-09-15 1996-03-20 Ciba-Geigy Ag 2,9-Diamino- und 2-amino-8-carbamoyl-4-hydroxy-alkansäureamid-derivative
GB9505538D0 (en) 1995-03-18 1995-05-03 Ciba Geigy Ag New compounds
SE9504618D0 (sv) 1995-12-22 1995-12-22 Astra Ab New Compounds
HUP9900973A3 (en) * 1996-01-03 2000-04-28 Smithkline Beecham Plc Carbamoyloxy derivatives of mutiline with antibacterial activity, pharmaceutical compns. contg. them and process for preparing the said compds.
UA51716C2 (uk) 1996-07-08 2002-12-16 Авентіс Фармасьютікалз Продактс Інк. Сполуки, що мають гіпотензивну, кардіопротекторну, анти-ішемічну та антиліполітичну властивості, фармацевтична композиція та способи лікування
DE19627431A1 (de) * 1996-07-08 1998-01-15 Bayer Ag Heterocyclisch kondensierte Pyridine
HUP0001741A3 (en) * 1996-08-02 2000-11-28 Smithkline Beecham Plc Azabicyclic carbamoyloxy mutilin derivatives for antibacterial use, process for preparing them, pharmaceuticals contg. them and their use
TW527355B (en) 1997-07-02 2003-04-11 Bristol Myers Squibb Co Inhibitors of farnesyl protein transferase
US5994340A (en) * 1997-08-29 1999-11-30 Synphar Laboratories, Inc. Azetidinone derivatives as β-lactamase inhibitors
US6197339B1 (en) 1997-09-30 2001-03-06 Pharmacia & Upjohn Company Sustained release tablet formulation to treat Parkinson's disease
UY25225A1 (es) * 1997-10-29 2000-12-29 Smithkline Beecham Plc Derivados de pleuromutilina utiles como agentes antimicrobianos
US6329389B1 (en) 1998-04-08 2001-12-11 Takeda Chemical Industries, Ltd. Amine compounds, their production and use
WO2000000479A1 (en) 1998-06-30 2000-01-06 Du Pont Pharmaceuticals Company 1,3-benzodiazepin-2-ones and 1,3-benzoxazepin-2-ones useful as hiv reverse transcriptase inhibitors
GB9818731D0 (en) 1998-08-27 1998-10-21 Univ Portsmouth Compounds
CA2354774C (en) 1998-12-18 2009-05-26 Schering Corporation Farnesyl protein transferase inhibitors
CO5180550A1 (es) 1999-04-19 2002-07-30 Smithkline Beecham Corp Inhibidores de fab i
EP1227090A4 (en) 1999-10-07 2002-11-20 Tadeka Chemical Ind Ltd AMINE DERIVATIVES
US20030105118A1 (en) 2000-04-18 2003-06-05 Shuji Masumoto Tricyclic quinazolinediones
FR2812635B1 (fr) * 2000-08-01 2002-10-11 Aventis Pharma Sa Nouveaux composes heterocycliques, preparation et utilisation comme medicaments notamment comme anti- bacteriens
WO2002067937A1 (en) 2001-02-22 2002-09-06 School Of Pharmacy, University Of London Indoline and tetrahydro-quinolines as prodrugs for tumour treatment
FR2825705B1 (fr) * 2001-06-08 2005-05-20 Aventis Pharma Sa Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments, notamment comme anti-bacteriens
FR2835186B1 (fr) 2002-01-28 2006-10-20 Aventis Pharma Sa Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
US7439253B2 (en) * 2002-12-06 2008-10-21 Novexel Heterocyclic compounds, their preparation and their use as medicaments, in particular as antibacterials and beta-lactamase inhibitors

Also Published As

Publication number Publication date
WO2003063864A3 (fr) 2004-03-11
CR7387A (es) 2010-10-25
TNSN04137A1 (fr) 2007-03-12
NO20043587L (no) 2004-08-27
CY2016042I1 (el) 2017-03-15
CR20120356A (es) 2012-10-05
HK1077205A1 (zh) 2006-02-10
KR20040081473A (ko) 2004-09-21
CA2474043A1 (fr) 2003-08-07
JO2646B1 (en) 2012-06-17
EA007220B1 (ru) 2006-08-25
US20090215747A1 (en) 2009-08-27
ATE484281T1 (de) 2010-10-15
LTPA2016037I1 (lt) 2017-01-10
CA2474043C (fr) 2011-08-02
DE60334527D1 (de) 2010-11-25
BRPI0307267B1 (pt) 2016-02-10
AR100790A2 (es) 2016-11-02
NL300847I2 (enExample) 2017-01-03
US20100048528A1 (en) 2010-02-25
OA12761A (fr) 2006-07-04
PL220725B1 (pl) 2015-12-31
EA200400981A1 (ru) 2005-02-24
DK2279737T3 (da) 2013-02-11
EP1480644B1 (fr) 2010-10-13
HRP20040686A2 (en) 2004-12-31
NO2016024I2 (no) 2016-12-15
ES2356813T3 (es) 2011-04-13
UY27626A1 (es) 2003-08-29
CL2011000009A1 (es) 2011-03-25
KR100979079B1 (ko) 2010-08-31
UA80271C2 (uk) 2007-09-10
PT1480644E (pt) 2011-01-17
CN100482225C (zh) 2009-04-29
CN100563653C (zh) 2009-12-02
YU65804A (sh) 2006-08-17
NO335195B1 (no) 2014-10-20
LTC1480644I2 (lt) 2018-09-10
BRPI0307267B8 (pt) 2021-05-25
AR038234A1 (es) 2005-01-05
MA26351A1 (fr) 2004-10-01
MXPA04006621A (es) 2004-10-04
US20050020572A1 (en) 2005-01-27
ECSP045193A (es) 2004-08-27
JP4472346B2 (ja) 2010-06-02
NO2025027I1 (no) 2025-06-13
NZ533936A (en) 2007-05-31
NO2016024I1 (no) 2016-12-15
RS52137B (sr) 2012-08-31
CN1994301A (zh) 2007-07-11
MY140638A (en) 2010-01-15
CN101406471A (zh) 2009-04-15
IL163167A (en) 2010-04-15
PT2279737E (pt) 2013-02-01
BR0307267A (pt) 2004-12-07
BE2016C069I2 (enExample) 2022-05-17
FR16C1019I1 (fr) 2017-02-03
PL371601A1 (pl) 2005-06-27
CO5601014A2 (es) 2006-01-31
HRP20040686B1 (hr) 2013-02-28
AU2003214335B2 (en) 2007-04-05
HK1105864A1 (zh) 2008-02-29
FR2835186A1 (fr) 2003-08-01
HUS1600055I1 (hu) 2017-01-30
CY2016042I2 (el) 2017-03-15
US20110245254A1 (en) 2011-10-06
SI1480644T1 (sl) 2011-03-31
FR16C1019I2 (fr) 2017-12-29
EP2279737A1 (fr) 2011-02-02
SI2279737T1 (sl) 2013-07-31
EP1480644A2 (fr) 2004-12-01
PE20030969A1 (es) 2003-12-12
TW200303305A (en) 2003-09-01
JP2005523897A (ja) 2005-08-11
US7612087B2 (en) 2009-11-03
ES2401855T3 (es) 2013-04-25
EP2279737B1 (fr) 2012-10-31
CY1114417T1 (el) 2016-08-31
ZA200405607B (en) 2005-09-28
CN1655781A (zh) 2005-08-17
WO2003063864A2 (fr) 2003-08-07
TWI293071B (en) 2008-02-01
CY1111061T1 (el) 2015-06-11
DK1480644T3 (da) 2011-01-24

Similar Documents

Publication Publication Date Title
FR2835186B1 (fr) Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases
ATE328036T1 (de) Polyolefinzusammensetzung mit hoher zähigkeit
AU2003258045A1 (en) Novel gamma-lactams as beta-secretase inhibitors
AUPS019702A0 (en) Condensed heterocyclic compounds
DE60313872D1 (de) Pyrazoloä1,5-aüpyrimidine als hemmstoffe cyclin-abhängiger kinasen
ITBO20030081A1 (it) Pacchetto di sigarette.
NO20022649D0 (no) Heterocykliske dihydropyrimidiner som kaliumkanal inhibitorer
IL174375A0 (en) Novel heterocyclic compounds as hsp90-inhibitors
DE60315862D1 (de) Dihydropyridinonderivate als hne-inhibitoren
IS7509A (is) Þíoxantínafleiður sem mergperoxídasatálmar
IL183599A0 (en) Novel hydantoin derivatives as metalloproteinase inhibitors
IL183667A0 (en) Novel hydantoin derivatives as metalloproteinase inhibitors
ZA200705068B (en) Hydantoin derivatives useful as metalloproteinase inhibitors
AU2003212310A1 (en) (4,2-disubstituted-thiazol-5-yl)amine compounds as pde7 inhibitors
DK1492934T3 (da) Dørenhed
NO20054854D0 (no) Femrings heterocykliske derivater
IS7795A (is) Pyrrólafleiður sem efnasambönd gegn sveppagerlum
FR2844273B1 (fr) Nouveaux composes heterocycliques, procede et intermediaires de preparation et utilisation comme medicament, notamment comme inhibiteurs de beta-lactamases et anti-bacteriens.
DE60324703D1 (de) Barbitursäure derivaten.
ATE427945T1 (de) Imidazolderivate
IS8042A (is) Benz[1,2,5]thíadíazól efnasambönd
AU2003280578A1 (en) Heterocyclic compounds
HK1089770A (en) Novel heterocyclic compounds as hsp90-inhibitors
SE0201185D0 (sv) Heterocyclic compounds
SE0203606D0 (sv) Heterocyclic compounds

Legal Events

Date Code Title Description
CA Change of address
TP Transmission of property
TP Transmission of property

Owner name: ASTRA ZENECA HOLDING FRANCE, FR

Effective date: 20140610

PLFP Fee payment

Year of fee payment: 15

PLFP Fee payment

Year of fee payment: 16

TP Transmission of property

Owner name: PFIZER IRELAND PHARMACEUTICALS, IE

Effective date: 20170830

PLFP Fee payment

Year of fee payment: 17

PLFP Fee payment

Year of fee payment: 19

PLFP Fee payment

Year of fee payment: 20