AR054467A1 - Metodo para inhibir las enzimas beta-lactamasas de clase d en el tratamiento de infeccion bacteriana en un paciente - Google Patents

Metodo para inhibir las enzimas beta-lactamasas de clase d en el tratamiento de infeccion bacteriana en un paciente

Info

Publication number
AR054467A1
AR054467A1 ARP060102292A ARP060102292A AR054467A1 AR 054467 A1 AR054467 A1 AR 054467A1 AR P060102292 A ARP060102292 A AR P060102292A AR P060102292 A ARP060102292 A AR P060102292A AR 054467 A1 AR054467 A1 AR 054467A1
Authority
AR
Argentina
Prior art keywords
treatment
beta
class
enzymes
optionally substituted
Prior art date
Application number
ARP060102292A
Other languages
English (en)
Inventor
Aranapakam Mudumbai Venkatesan
Tarek Suhayi Mansour
Original Assignee
Wyeth Corp
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
Application filed by Wyeth Corp filed Critical Wyeth Corp
Publication of AR054467A1 publication Critical patent/AR054467A1/es

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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/424Oxazoles condensed with heterocyclic ring systems, e.g. clavulanic acid
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/429Thiazoles condensed with heterocyclic ring systems
    • A61K31/43Compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula, e.g. penicillins, penems
    • 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)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (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)
  • Engineering & Computer Science (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Penemes tricíclicos de 6-alquilideno con actividad como inhibidores de enzimas clases D. Las beta-lactamasas hidrolizan los antibioticos beta-lactámicos, y como tales sirven como la causa primaria de resistencia bacteriana cuando se combinan con los antibioticos beta-lactama, los compuestos de la presente suministran un tratamiento efectivo contra las infecciones bacteriales que amenazan la vida. Estos compuestos suministrados son de formula (1), son utiles para el tratamiento de infecciones bacterianas que tienen asociada junto con esta la enzima Clase D, en donde: uno de A y B denota hidrogeno y el otro grupo heteroarilo tricíclicos fusionado opcionalmente sustituido; y X es S u O. Reivindicacion 1: Un método para inhibir las enzimas de Clase D en el tratamiento de para inhibir las enzimas de Clase D en el tratamiento de infeccion bacterial en un paciente en necesidad de éste, caracterizado por comprender suministrar una cantidad efectiva de un compuesto de formula (1), en donde: uno de A y B denotan hidrogeno y el otro un grupo heteroarilo tricíclico fusionado opcionalmente sustituido; X es S u O; R5 es H, alquilo C1-6, cicloalquilo C5-6, alquiloC1-6CHR30CO; y R3 es hidrogeno, alquilo C1-6, cicloalquilo C5-6, arilo opcionalmente sustituido o heteroarilo opcionalmente sustituido; o una sal farmacéuticamente aceptable o éster hidrolizable in vivo de esta.
ARP060102292A 2005-06-01 2006-06-01 Metodo para inhibir las enzimas beta-lactamasas de clase d en el tratamiento de infeccion bacteriana en un paciente AR054467A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US68622105P 2005-06-01 2005-06-01

Publications (1)

Publication Number Publication Date
AR054467A1 true AR054467A1 (es) 2007-06-27

Family

ID=37836305

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP060102292A AR054467A1 (es) 2005-06-01 2006-06-01 Metodo para inhibir las enzimas beta-lactamasas de clase d en el tratamiento de infeccion bacteriana en un paciente

Country Status (14)

Country Link
US (1) US20060276446A1 (es)
EP (1) EP1885358A2 (es)
JP (1) JP2008542376A (es)
CN (1) CN101189010A (es)
AR (1) AR054467A1 (es)
AU (1) AU2006287938A1 (es)
BR (1) BRPI0611491A2 (es)
CA (1) CA2610478A1 (es)
GT (1) GT200600235A (es)
MX (1) MX2007015173A (es)
PE (1) PE20070010A1 (es)
SV (1) SV2007002555A (es)
TW (1) TW200716104A (es)
WO (1) WO2007030166A2 (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR039774A1 (es) * 2002-05-01 2005-03-02 Wyeth Corp 6-alquiliden-penems biciclicos como inhibidores de beta-lactamasas
AR039475A1 (es) * 2002-05-01 2005-02-23 Wyeth Corp 6-alquiliden-penems triciclicos como inhibidores de beta-lactamasa
TW200716102A (en) * 2005-06-01 2007-05-01 Wyeth Corp Bicyclic 6-alkylidene-penems as class-D β -lactamases inhibitors
US8524304B2 (en) 2005-11-23 2013-09-03 The Coca-Cola Company High-potency sweetener composition with probiotics/prebiotics and compositions sweetened therewith
US8512789B2 (en) 2005-11-23 2013-08-20 The Coca-Cola Company High-potency sweetener composition with dietary fiber and compositions sweetened therewith
US8945652B2 (en) 2005-11-23 2015-02-03 The Coca-Cola Company High-potency sweetener for weight management and compositions sweetened therewith
JP2012121809A (ja) * 2009-02-26 2012-06-28 Eisai R & D Management Co Ltd 多環式化合物の製造法およびその中間体
US20110288063A1 (en) * 2010-05-19 2011-11-24 Naeja Pharmaceutical Inc. Novel fused bridged bicyclic heteroaryl substituted 6-alkylidene penems as potent beta-lactamase inhibitors
CN104341345B (zh) * 2014-10-24 2016-03-23 海门海康生物医药科技有限公司 一种2-甲氧基-6-酮-5,6,7,8-四氢喹啉的合成方法
JP7413346B2 (ja) 2019-03-06 2024-01-15 第一三共株式会社 ピロロピラゾール誘導体

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995028935A1 (en) * 1994-04-25 1995-11-02 Smithkline Beecham Plc Pharmaceutical formulations containing a beta-lactamase inhibiting penem in combination with a beta-lactam antibiotic and their use in the treatment of bacterial infections
US20040132706A1 (en) * 2001-10-05 2004-07-08 Daniela Salvemini Composition comprising a catalyst for the dismutation of superoxide and use of the composition for preventing and treating hypotension
AR039774A1 (es) * 2002-05-01 2005-03-02 Wyeth Corp 6-alquiliden-penems biciclicos como inhibidores de beta-lactamasas
US20040132708A1 (en) * 2002-05-01 2004-07-08 Wyeth Process for preparing 6-alkylidene penem derivatives
AR039475A1 (es) * 2002-05-01 2005-02-23 Wyeth Corp 6-alquiliden-penems triciclicos como inhibidores de beta-lactamasa
AR039476A1 (es) * 2002-05-01 2005-02-23 Wyeth Corp Proceso para preparar derivados de 6-alquiliden penem
TW200716102A (en) * 2005-06-01 2007-05-01 Wyeth Corp Bicyclic 6-alkylidene-penems as class-D β -lactamases inhibitors

Also Published As

Publication number Publication date
WO2007030166A2 (en) 2007-03-15
CN101189010A (zh) 2008-05-28
AU2006287938A1 (en) 2007-03-15
GT200600235A (es) 2007-03-29
EP1885358A2 (en) 2008-02-13
BRPI0611491A2 (pt) 2010-12-21
US20060276446A1 (en) 2006-12-07
CA2610478A1 (en) 2007-03-15
SV2007002555A (es) 2007-02-02
WO2007030166A3 (en) 2007-05-24
MX2007015173A (es) 2008-02-15
JP2008542376A (ja) 2008-11-27
PE20070010A1 (es) 2007-01-12
TW200716104A (en) 2007-05-01

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