MA32025B1 - Inhibiteurs des beta-lactamases - Google Patents

Inhibiteurs des beta-lactamases

Info

Publication number
MA32025B1
MA32025B1 MA33026A MA33026A MA32025B1 MA 32025 B1 MA32025 B1 MA 32025B1 MA 33026 A MA33026 A MA 33026A MA 33026 A MA33026 A MA 33026A MA 32025 B1 MA32025 B1 MA 32025B1
Authority
MA
Morocco
Prior art keywords
beta
lactamase inhibitors
compounds
lactam antibiotics
lactam
Prior art date
Application number
MA33026A
Other languages
Arabic (ar)
English (en)
Inventor
Timothy A Blizzard
Helen Chen
Candido Gude
Jeffrey D Hermes
Jason E Imbriglio
Seongkon Kim
Jane Y Wu
Sookhee Ha
Christopher J Mortko
Ian Mangion
Nelo Rivera
Rebecca T Ruck
Michael Shevlin
Original Assignee
Merck Sharp & Dohme
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 Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of MA32025B1 publication Critical patent/MA32025B1/fr

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
    • A61K31/468-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D211/78Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Emergency Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pyrrole Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Immobilizing And Processing Of Enzymes And Microorganisms (AREA)

Abstract

L'invention concerne des bêta-lactames bicycliques substitués de la formule i : (i), sont des inhibiteurs de b-lactamase, a, x, r1 et r2 étant décrits par les présentes. Les composés et les sels de qualité pharmaceutique de ceux-ci s'utilisent dans le traitement d'infections bactériennes en combinaison avec des antibiotiques de b-lactame. En particulier, les composés peuvent être utilisés avec des antibiotiques de b-lactame (par exemple l'imipenème, la pipéracilline ou la ceftazidime) contre des micro-organismes résistants aux antibiotiques de b-lactame dus à la présence des b-lactamases.
MA33026A 2008-01-18 2010-07-16 Inhibiteurs des beta-lactamases MA32025B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1153308P 2008-01-18 2008-01-18
PCT/US2009/031047 WO2009091856A2 (fr) 2008-01-18 2009-01-15 Inhibiteurs de bêta-lactamase

Publications (1)

Publication Number Publication Date
MA32025B1 true MA32025B1 (fr) 2011-01-03

Family

ID=40642204

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33026A MA32025B1 (fr) 2008-01-18 2010-07-16 Inhibiteurs des beta-lactamases

Country Status (38)

Country Link
US (2) US8487093B2 (fr)
EP (2) EP2231667B1 (fr)
JP (3) JP5038509B2 (fr)
KR (2) KR101648728B1 (fr)
CN (2) CN101918407B (fr)
AU (1) AU2009206119C1 (fr)
BR (1) BRPI0906871B1 (fr)
CA (1) CA2712783C (fr)
CO (1) CO6331438A2 (fr)
CR (1) CR11626A (fr)
CY (5) CY1114900T1 (fr)
DK (2) DK2231667T3 (fr)
DO (1) DOP2010000218A (fr)
EC (2) ECSP10010345A (fr)
ES (2) ES2433744T3 (fr)
FR (3) FR20C1031I2 (fr)
HN (1) HN2010001395A (fr)
HR (2) HRP20131123T1 (fr)
HU (2) HUS000513I2 (fr)
IL (1) IL206395A (fr)
LT (3) LTC2231667I2 (fr)
LU (1) LUC00165I2 (fr)
MA (1) MA32025B1 (fr)
ME (1) ME02089B (fr)
MX (1) MX2010007823A (fr)
MY (1) MY162532A (fr)
NI (1) NI201000115A (fr)
NL (3) NL301051I2 (fr)
NO (3) NO2020024I1 (fr)
NZ (1) NZ586861A (fr)
PL (2) PL2666774T3 (fr)
PT (2) PT2231667E (fr)
RS (2) RS53862B1 (fr)
RU (1) RU2445314C9 (fr)
SI (2) SI2231667T1 (fr)
UA (1) UA101966C2 (fr)
WO (1) WO2009091856A2 (fr)
ZA (1) ZA201005333B (fr)

Families Citing this family (107)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101918407B (zh) * 2008-01-18 2014-02-26 默沙东公司 β-内酰胺酶抑制剂
KR102205755B1 (ko) 2010-08-10 2021-01-22 렘펙스 파머수티클스 인코퍼레이티드 고리형 보론산 에스터 유도체의 결정 형태
US8772490B2 (en) * 2010-12-22 2014-07-08 Meiji Seika Pharma Co., Ltd. Optically active diazabicyclooctane derivatives and process for preparing the same
SG191320A1 (en) 2010-12-22 2013-07-31 Meiji Seika Pharma Co Ltd Optically-active diazabicyclooctane derivative and method for manufacturing same
TWI565706B (zh) * 2011-06-17 2017-01-11 阿斯特捷利康公司 用於製備包括反-7-酮基-6-(磺酸氧基)-1,6-二氮雜雙環[3,2,1]辛烷-2-甲醯胺之雜環化合物及其鹽類之方法
JP5666743B2 (ja) * 2011-08-27 2015-02-12 ウォックハート リミテッド 1,6−ジアザビシクロ[3,2,1]オクタン−7−オン誘導体および細菌感染の処置におけるそれらの使用
RU2570423C2 (ru) * 2011-08-30 2015-12-10 Вокхардт Лимитед Производные 1,6-диазабицикло[3.2.1]октан-7-она и их применение при лечении бактериальных инфекций
WO2013033461A1 (fr) 2011-08-31 2013-03-07 Rempex Pharmaceuticals, Inc. Dérivés d'ester d'acide boronique hétérocyclique et leurs utilisations thérapeutiques
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
EP2800568A4 (fr) 2012-01-06 2015-06-10 Univ South Florida Compositions, procédés d'utilisation et procédés de traitement
TW201343646A (zh) 2012-03-30 2013-11-01 Cubist Pharm Inc 異□唑β-內醯胺酶抑制劑
US8969570B2 (en) * 2012-03-30 2015-03-03 Cubist Pharmaceuticals, Inc. Beta-lactamase inhibitors
SG11201406123TA (en) 2012-03-30 2014-10-30 Cubist Pharm Inc 1,3,4-OXADIAZOLE AND 1,3,4-THIADIAZOLE β-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
AR090539A1 (es) * 2012-04-02 2014-11-19 Astrazeneca Ab COMPUESTOS INHIBIDORES DE b LACTAMASA
US9790527B2 (en) 2012-05-08 2017-10-17 Codexis, Inc. Engineered proline hydroxylase polypeptides
US9156858B2 (en) 2012-05-23 2015-10-13 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
WO2013180197A1 (fr) 2012-05-30 2013-12-05 Meiji Seikaファルマ株式会社 NOUVEL INHIBITEUR DE β-LACTAMASE ET PROCÉDÉ DE PRODUCTION DE CELUI-CI
US10561675B2 (en) 2012-06-06 2020-02-18 Rempex Pharmaceuticals, Inc. Cyclic boronic acid ester derivatives and therapeutic uses thereof
WO2014033560A1 (fr) * 2012-08-25 2014-03-06 Wockhardt Limited Dérivés de 1,6-diazabicyclo[3,2,1]octan-7-one et leur utilisation dans le traitement d'infections bactériennes
JPWO2014069351A1 (ja) * 2012-11-01 2016-09-08 株式会社カネカ 光学活性二環式ウレア化合物の製造方法
PT2928898T (pt) 2012-12-07 2021-07-05 Venatorx Pharmaceuticals Inc Inibidores de beta-lactamase
UA111925C2 (uk) * 2012-12-11 2016-06-24 Федора Фармасьютікалз Інк. БІЦИКЛІЧНІ СПОЛУКИ ТА ЇХ ВИКОРИСТАННЯ ЯК АНТИБАКТЕРІАЛЬНИХ АГЕНТІВ ТА ІНГІБІТОРІВ β-ЛАКТАМАЗИ
US9101638B2 (en) 2013-01-04 2015-08-11 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
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
JP2016509594A (ja) 2013-01-04 2016-03-31 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
JP6346904B2 (ja) 2013-01-10 2018-06-20 ベナトルクス ファーマシューティカルズ,インク. ベータ−ラクタマーゼ阻害剤
CA2904082C (fr) * 2013-03-08 2017-10-03 Wockhardt Limited Procede de preparation de (2s, 5r)-7-oxo-6-sulfoxy-2-[((3r)- pyrrolidine- 3-carbonyl)-hydrazinocarbonyl]-1,6-diaza-bicyclo[3.2.1]octane
NZ711329A (en) * 2013-03-08 2016-06-24 Wockhardt Ltd A process for preparation of (2s, 5r)- sulfuric acid mono-{ [(4-aminopiperidin-4-yl) carbonyl]-7-oxo-1,6-diaza-bicyclo[3.2.1]-oct-6-yl} ester
KR101774132B1 (ko) 2013-03-08 2017-09-01 욱크하르트 리미티드 (2s, 5r)-7-옥소-6-술포옥시-2-[((3r)-피페리딘-3-카보닐)-히드라지노 카보닐]-1,6-디아자-비사이클로[3.2.1]-옥탄의 제조 방법
US9567335B2 (en) * 2013-03-08 2017-02-14 Wockhardt Limited Process for sodium salt of (2S, 5R)-2-carboxamido-7-oxo-6-sulfooxy -1,6-diaza-bicyclo[3.2.1]octane
US9657021B2 (en) * 2013-03-08 2017-05-23 Wockhardt Limited Process for preparation of (2S, 5R)-7-oxo-6-sulphooxy-2[((3R)-piperidine-3-carbonyl)-hydrazino carbonyl]-1,6-diaza-bicyclo [3.2.1]-octane
WO2014135931A1 (fr) * 2013-03-08 2014-09-12 Wockhardt Limited Procédé pour la préparation du (2s, 5r)-7-oxo-6-sulfo-oxy-2-[((3r)-pipéridine-3-carbonyl)-hydrazino carbonyl]-1,6-diaza-bicyclo[3.2.1]octane
US9120795B2 (en) 2013-03-14 2015-09-01 Cubist Pharmaceuticals, Inc. Crystalline form of a β-lactamase inhibitor
WO2014151958A1 (fr) 2013-03-14 2014-09-25 VenatoRx Pharmaceuticals, Inc. Inhibiteurs de bêta-lactamase
MX362348B (es) 2013-06-10 2019-01-11 Merck Sharp & Dohme Preparacion de 4-((1r,2s,5r)-6-(benciloxi)-7-oxo-1,6-diazabiciclo[ 3.2.1]octano-2-carboxamido)piperidin-1-carboxilato de ter-butilo.
NZ718009A (en) 2013-09-24 2018-03-23 Meiji Seika Pharma Co Ltd Process for producing diazabicyclooctane derivative and intermediate thereof
US9120796B2 (en) 2013-10-02 2015-09-01 Cubist Pharmaceuticals, Inc. B-lactamase inhibitor picoline salt
CN105612159A (zh) * 2013-10-08 2016-05-25 明治制果药业株式会社 二氮杂二环辛烷衍生物的结晶及其制备方法
US9604986B2 (en) 2013-11-26 2017-03-28 Wockhardt Limited Polymorphs and process for preparation of (2S, 5R)-7-oxo-N-[(2S)-pyrrolidin-2-yl-methyloxy]-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide
WO2015148379A1 (fr) 2014-03-24 2015-10-01 Novartis Ag Composés organiques monobactam pour le traitement d'infections bactériennes
WO2015150891A1 (fr) * 2014-03-29 2015-10-08 Wockhardt Limited Procédé de préparation de mono-[2-(5-azétidin-3-ylméthyl-[1,3,4]oxadiazol-2-yl)-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester d'acide sulfurique trans
IN2014MU01196A (fr) * 2014-03-29 2015-10-02 Wockhardt Ltd
US9687497B1 (en) 2014-05-05 2017-06-27 Rempex Pharmaceuticals, Inc. Salts and polymorphs of cyclic boronic acid ester derivatives and therapeutic uses thereof
FI3604316T3 (fi) 2014-05-05 2024-02-29 Melinta Therapeutics Inc Boronaattisuolojen synteesi
AU2015264418A1 (en) 2014-05-19 2016-11-10 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
RU2686740C2 (ru) 2014-06-11 2019-04-30 Венаторкс Фармасьютикалс, Инк. Ингибиторы бета-лактамазы
US9511142B2 (en) 2014-06-11 2016-12-06 VenatoRx Pharmaceuticals, Inc. Beta-lactamase inhibitors
EA201692301A1 (ru) 2014-07-01 2017-06-30 Ремпекс Фармасьютикалз, Инк. Производные бороновой кислоты и их терапевтическое применение
DK3221313T3 (en) * 2014-11-17 2019-04-08 Entasis Therapeutics Ltd COMBINATION THERAPY FOR TREATING INFECTIONS WITH RESISTANT BACTERIA
WO2016081297A1 (fr) 2014-11-18 2016-05-26 Rempex Pharmaceuticals, Inc. Dérivés d'esters d'acide boronique cycliques et leurs utilisations thérapeutiques
WO2016089718A1 (fr) 2014-12-02 2016-06-09 Merck Sharp & Dohme Corp. Procédé pour la préparation de 4-((2s,5r)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamido)-pipéridine-1-carboxylate de tert-butyle et ses analogues
TWI691499B (zh) 2014-12-05 2020-04-21 日商明治製菓藥業股份有限公司 二氮雜雙環辛烷衍生物之結晶及安定的凍結乾燥製劑的製造法
US20180051041A1 (en) 2015-03-17 2018-02-22 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
CA2980109A1 (fr) 2015-03-31 2016-10-06 Mutabilis Composes heterocycliques et leur utilisation dans la prevention ou le traitement d'infections bacteriennes
CA2983674A1 (fr) * 2015-05-07 2016-11-10 Mutabilis Composes heterocycliques et leur utilisation dans la prevention ou le traitement d'infections bacteriennes
CN108472284A (zh) 2015-09-11 2018-08-31 维纳拓尔斯制药公司 β-内酰胺酶抑制剂
EP3281942A4 (fr) * 2015-09-16 2018-08-15 Xuanzhu Pharma Co., Ltd. Inhibiteur de ss-lactamase et son application
CA3000087A1 (fr) 2015-10-02 2017-04-06 Legochem Biosciences, Inc. Compositions et methodes pour inhiber la beta-lactamase
WO2017100537A1 (fr) 2015-12-10 2017-06-15 VenatoRx Pharmaceuticals, Inc. Inhibiteurs de bêta-lactamases
WO2017098425A1 (fr) * 2015-12-11 2017-06-15 Wockhardt Limited Composés contenant du 7-oxo-6-(sulfo-oxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide et leur utilisation dans le traitement d'infections bactériennes
EP3411359B1 (fr) 2016-02-04 2021-10-13 Merck Sharp & Dohme Corp. Procédés de préparation de dérivés d'hydroxylamine utiles dans la préparation d'agents anti-infectieux
CN108778270B (zh) * 2016-03-31 2021-07-30 吉林四环制药有限公司 一种抗菌组合物及其用途
SG11201809575TA (en) 2016-06-09 2018-11-29 Codexis Inc Biocatalysts and methods for hydroxylation of chemical compounds
UA124464C2 (uk) 2016-06-30 2021-09-22 Кьюпекс Біофарма, Інк. Похідні боронової кислоти та їх терапевтичні застосування
WO2018027062A1 (fr) 2016-08-04 2018-02-08 VenatoRx Pharmaceuticals, Inc. Composés contenant du bore
KR102537340B1 (ko) * 2016-09-16 2023-05-26 엔타시스 테라퓨틱스 리미티드 베타-락타마제 억제제 화합물
EP3515915B1 (fr) * 2016-09-19 2021-08-04 Merck Sharp & Dohme Corp. Procédé de préparation d'intermédiaires d'hydroxyurée inhibiteurs des bêta-lactamases
JOP20190061A1 (ar) * 2016-09-28 2019-03-26 Novartis Ag مثبطات بيتا-لاكتاماز
CN108078982B (zh) * 2016-11-21 2020-02-07 天津大学 脯氨酸衍生物在制备β-内酰胺酶抑制剂中的用途
ES3015371T3 (en) 2017-03-06 2025-05-05 Venatorx Pharmaceuticals Inc Solid forms and combination compositions comprising a beta-lactamase inhibitor and uses thereof
CN108619141B (zh) * 2017-03-16 2021-09-10 山东轩竹医药科技有限公司 一种抗菌组合物及其用途
MA48743A (fr) 2017-05-08 2020-04-08 Entasis Therapeutics Inc Composés et méthodes de traitement d'infections bactériennes
US10085999B1 (en) * 2017-05-10 2018-10-02 Arixa Pharmaceuticals, Inc. Beta-lactamase inhibitors and uses thereof
WO2018218190A1 (fr) 2017-05-26 2018-11-29 VenatoRx Pharmaceuticals, Inc. Inhibiteurs de protéines de liaison à la pénicilline
EP3630783A4 (fr) 2017-05-26 2021-03-03 Venatorx Pharmaceuticals, Inc. Inhibiteurs protéiques de liaison à la pénicilline
KR20200030584A (ko) 2017-07-21 2020-03-20 앤타바이오 에스에이에스 화합물
CN109568323B (zh) * 2017-09-29 2022-09-30 吉林四环制药有限公司 抗菌组合物及其用途
EP3694864B1 (fr) 2017-10-11 2025-03-05 Qpex Biopharma, Inc. Dérivés d'acide boronique et synthèse de ces derniers
ES2928152T3 (es) 2017-12-01 2022-11-15 Qilu Pharmaceutical Co Ltd Forma cristalina de un inhibidor de beta-lactamasa y método de preparación de la misma
CN109956941B (zh) * 2017-12-25 2020-08-04 新发药业有限公司 一种阿维巴坦的简便制备方法
EP3744722A4 (fr) 2018-01-25 2021-11-03 Suzhou Sinovent Pharmaceuticals Co., Ltd. INHIBITEUR DE ß-LACTAMASE ET SON UTILISATION
WO2019204419A1 (fr) 2018-04-20 2019-10-24 The Medicines Company (San Diego), Llc Dérivés d'acide boronique et leurs utilisations thérapeutiques
EP3572411A1 (fr) 2018-05-21 2019-11-27 Antabio SAS Dérivés de thiazole comme inhibiteurs de métallo-bêta-lactamases
WO2019226931A1 (fr) 2018-05-25 2019-11-28 VenatoRx Pharmaceuticals, Inc. Inhibiteurs de protéine de liaison à la pénicilline
EP3670512A1 (fr) * 2018-12-18 2020-06-24 Antabio SAS Diazabicyclooctanones comme inhibiteurs de sérine beta-lactamases
CA3110111A1 (fr) * 2018-08-09 2020-02-13 Antabio Sas Diazabicyclooctanones en tant qu'inhibiteurs de beta-lactamases a serine
US11905286B2 (en) 2018-08-09 2024-02-20 Antabio Sas Diazabicyclooctanones as inhibitors of serine beta-lactamases
EP3854786B1 (fr) 2018-09-21 2026-02-18 UBE Corporation Procédé de production de dérivés d'acide aminé
WO2020072442A1 (fr) * 2018-10-01 2020-04-09 Arixa Pharmaceuticals, Inc. Dérivés de relebactam et utilisations associées
CN111072660B (zh) * 2018-10-22 2021-05-18 新发药业有限公司 一种瑞来巴坦的简便制备方法
WO2020112542A1 (fr) 2018-11-29 2020-06-04 VenatoRx Pharmaceuticals, Inc. Compositions mixtes comprenant un inhibiteur de bêta-lactamase et leurs utilisations
CN113614084A (zh) 2019-03-12 2021-11-05 阿里萨制药公司 阿维巴坦衍生物的晶型
WO2020219405A1 (fr) * 2019-04-26 2020-10-29 Merck Sharp & Dohme Corp. Procédé de préparation d'intermédiaires utiles pour la fabrication de (2s,5r)-7-oxo-n-pipéridin-4-yl-6-(sulfoxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide
JP7647110B2 (ja) * 2020-01-22 2025-03-18 日油株式会社 ポリエーテルエステル化合物
AU2021266715A1 (en) 2020-05-05 2022-11-17 Qpex Biopharma, Inc. Boronic acid derivatives and synthesis, polymorphic forms, and therapeutic uses thereof
EP4146650B1 (fr) 2020-09-01 2026-01-21 Ningxia Academy of Agriculture and Forestry Sciences Inhibiteurs de bêta-lactamase et leur préparation
WO2022047790A1 (fr) * 2020-09-07 2022-03-10 Ningxia Academy Of Agriculture And Forestry Sciences Composés bicycliques substitués par amidine, leur préparation, leur utilisation comme agents antibactériens et inhibiteurs de bêta-lactamase
CN111943950B (zh) * 2020-09-10 2022-03-29 山东安信制药有限公司 一种瑞来巴坦的制备方法
EP4146651B1 (fr) 2021-05-07 2026-03-04 Ningxia Academy of Agriculture and Forestry Sciences Composés substitués de sulfonylamidine et leur utilisation en tant qu'inhibiteurs de bêta-lactamase
US11814385B2 (en) * 2021-06-25 2023-11-14 University Of South Florida Small molecule inhibitors targeting Clostridioides difficile sporulation
WO2023220324A1 (fr) * 2022-05-11 2023-11-16 The Regents Of The University Of Colorado A Body Corporate Composition antibiotique et ses procédés d'utilisation
CN117384169B (zh) * 2022-07-05 2025-10-17 福安药业集团重庆三禾兴医药科技有限公司 一类噻唑胺-二氮杂双环辛酮缀合衍生物及其用途
GB202306833D0 (en) 2023-05-09 2023-06-21 Adjutec Pharma As Therapy
GB202306826D0 (en) 2023-05-09 2023-06-21 Adjutec Pharma As Therapy

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4880793A (en) 1978-07-24 1989-11-14 Merck & Co., Inc. Combination of thienamycin-type antibiotics with dipeptidase inhibitors
US5071843A (en) 1978-07-24 1991-12-10 Merck & Co., Inc. Combination of 2-substituted carbapenems with dipeptidase inhibitors
US4616038A (en) 1978-07-24 1986-10-07 Merck & Co., Inc. Combination of thienamycin-type antibiotics with dipeptidase inhibitors
US4539208A (en) 1980-09-17 1985-09-03 Merck & Co., Inc. Combination of thienamycin-type antibiotics with dipeptidase inhibitors
DE59206796D1 (de) 1991-04-11 1996-08-29 Hoffmann La Roche Beta-Lactame
ATE177099T1 (de) 1993-12-29 1999-03-15 Pfizer Diazabicyclische neurokinin antagonisten
JP3199300B2 (ja) 1994-05-09 2001-08-13 三共株式会社 1−メチルカルバペネム誘導体
KR100386993B1 (ko) 1995-12-21 2003-12-18 상꾜 가부시키가이샤 1-메틸카르바페넴유도체
JP2965922B2 (ja) * 1995-12-21 1999-10-18 三共株式会社 1−メチルカルバペネム誘導体
JP2955276B2 (ja) 1997-06-19 1999-10-04 三共株式会社 1−メチルカルバペネム誘導体を含有する抗菌剤
JP4490517B2 (ja) 1998-03-19 2010-06-30 富山化学工業株式会社 5−デオキシ−5−アルカノイルアミノ−β−D−アロフラノシルウロン酸誘導体またはその塩、それらを含有する抗真菌剤及びキチン合成酵素阻害剤
MXPA02000246A (es) 1999-07-06 2003-08-20 Methylgene Inc Inhibidores de °-lactamasa de sulfonamidometil fosfonato.
CN1217932C (zh) * 1999-08-10 2005-09-07 英国生物技术药物有限公司 抗菌剂
FR2812635B1 (fr) 2000-08-01 2002-10-11 Aventis Pharma Sa Nouveaux composes heterocycliques, preparation et utilisation comme medicaments notamment comme anti- bacteriens
IL155931A0 (en) 2000-11-16 2003-12-23 Sankyo Co 1-methylcarbapenem derivatives and pharmaceutical compositions containing the same
JP2002212182A (ja) * 2000-11-16 2002-07-31 Sankyo Co Ltd 1−メチルカルバペネム誘導体
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
JP2004043438A (ja) 2002-05-15 2004-02-12 Sankyo Co Ltd 1−メチルカルバペネム誘導体を含有する医薬
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
WO2005009943A2 (fr) * 2003-07-09 2005-02-03 Paratek Pharmaceuticals, Inc. Composes de tetracycline substitues
US6984652B2 (en) * 2003-09-05 2006-01-10 Warner-Lambert Company Llc Gyrase inhibitors
WO2005033129A1 (fr) 2003-10-01 2005-04-14 Bayer Healthcare Ag Macrocycles d'amide antibacteriens
EP1751527A2 (fr) 2004-02-24 2007-02-14 SSCI, Inc. Analyse et criblage de formes solides au moyen de la fonction de distribution de paires atomiques
HRP20110841T1 (hr) * 2005-12-07 2012-01-31 Basilea Pharmaceutica Ag Korisni monobaktamski antibiotici
CA2664296A1 (fr) 2006-09-27 2008-04-03 Merck & Co., Inc. Nouveaux inhibiteurs de beta-lactamase
CN101918407B (zh) * 2008-01-18 2014-02-26 默沙东公司 β-内酰胺酶抑制剂

Also Published As

Publication number Publication date
FR20C1030I1 (fr) 2020-02-10
AU2009206119A1 (en) 2009-07-23
SI2231667T1 (sl) 2013-12-31
LTC2666774I2 (lt) 2022-01-25
HRP20131123T1 (hr) 2013-12-20
IL206395A0 (en) 2010-12-30
DK2231667T3 (da) 2013-12-16
LTC2231667I2 (lt) 2021-07-26
ES2433744T3 (es) 2013-12-12
PL2231667T3 (pl) 2014-01-31
LTPA2020517I1 (lt) 2020-07-27
HUS2000023I1 (hu) 2021-03-29
JP2011207900A (ja) 2011-10-20
LTPA2020518I1 (lt) 2020-07-27
KR101648728B1 (ko) 2016-08-17
EP2666774B1 (fr) 2015-01-07
RS53862B1 (sr) 2015-08-31
PT2666774E (pt) 2015-04-13
KR20100130176A (ko) 2010-12-10
US8487093B2 (en) 2013-07-16
JP5038509B2 (ja) 2012-10-03
US20110294777A1 (en) 2011-12-01
ZA201005333B (en) 2011-04-28
RU2445314C9 (ru) 2013-04-10
CR11626A (es) 2010-09-13
WO2009091856A2 (fr) 2009-07-23
CY1116243T1 (el) 2017-03-15
ME02089B (fr) 2014-04-30
HRP20150269T1 (hr) 2015-04-24
HN2010001395A (es) 2012-11-12
BRPI0906871B1 (pt) 2021-09-28
RS53052B (sr) 2014-04-30
FR20C1031I2 (fr) 2022-07-29
CN102827067B (zh) 2015-09-23
CN101918407B (zh) 2014-02-26
SI2666774T1 (sl) 2015-04-30
ECSP10010568A (es) 2010-11-30
JP5597164B2 (ja) 2014-10-01
NO2020022I1 (no) 2020-08-10
LTPA2020516I1 (lt) 2020-07-27
DOP2010000218A (es) 2010-08-31
HUS000504I2 (hu) 2021-03-29
NO2020023I1 (no) 2020-08-10
CN102827067A (zh) 2012-12-19
NL301051I2 (nl) 2020-09-03
NL301052I2 (nl) 2026-02-03
IL206395A (en) 2015-04-30
MX2010007823A (es) 2010-08-10
NL301050I2 (nl) 2020-09-03
JP5422020B2 (ja) 2014-02-19
KR101800610B1 (ko) 2017-11-23
HK1186180A1 (en) 2014-03-07
UA101966C2 (xx) 2013-05-27
BRPI0906871A2 (pt) 2020-07-28
JP2012214475A (ja) 2012-11-08
DK2666774T3 (en) 2015-03-23
EP2231667A2 (fr) 2010-09-29
AU2009206119C1 (en) 2016-05-26
CA2712783C (fr) 2013-03-19
EP2666774A1 (fr) 2013-11-27
FR20C1030I2 (fr) 2021-08-27
AU2009206119B2 (en) 2012-06-07
FR20C1032I1 (fr) 2020-02-10
HUS000513I2 (hu) 2021-03-29
CO6331438A2 (es) 2011-10-20
CY2020025I1 (el) 2020-11-25
ES2533826T3 (es) 2015-04-15
NI201000115A (es) 2011-07-08
KR20160099117A (ko) 2016-08-19
CY1114900T1 (el) 2016-12-14
HUS2000024I1 (hu) 2021-03-29
NZ586861A (en) 2011-12-22
US20130274475A1 (en) 2013-10-17
CA2712783A1 (fr) 2009-07-23
CY2020023I1 (el) 2020-11-25
ECSP10010345A (es) 2010-08-31
CY2020024I2 (el) 2020-11-25
FR20C1031I1 (fr) 2020-02-10
HK1143809A1 (en) 2011-01-14
JP2011510012A (ja) 2011-03-31
PL2666774T3 (pl) 2015-06-30
NO2020024I1 (no) 2020-08-10
MY162532A (en) 2017-06-15
LUC00165I2 (fr) 2021-08-16
CY2020023I2 (el) 2020-11-25
CY2020025I2 (el) 2020-11-25
WO2009091856A3 (fr) 2009-12-03
CN101918407A (zh) 2010-12-15
CY2020024I1 (el) 2020-11-25
RU2445314C1 (ru) 2012-03-20
EP2231667B1 (fr) 2013-09-04
FR20C1032I2 (fr) 2022-07-29
PT2231667E (pt) 2013-12-13

Similar Documents

Publication Publication Date Title
MA32025B1 (fr) Inhibiteurs des beta-lactamases
WO2008039420A3 (fr) Nouveaux inhibiteurs de bêta-lactamase
MA37383A1 (fr) Compose heterobicycliques comme inhibiteurs de la beta lactamase
Aswapokee et al. A sulfone β-lactam compound which acts as a β-lactamase inhibitor
MA32727B1 (fr) Pyrazolylaminopyridines au titre d'inhibiteurs de fak
JO2646B1 (en) New differentiated cyclic compounds as beta - lactam inhibitors
NZ600134A (en) Methylsulfonylmethane (msm) for treatment of drug resistant microorganisms
WO2005004799A3 (fr) Inhibiteurs de $g(b)-lactamases et methodes d'utilisation de ces inhibiteurs
JO3588B1 (ar) مشتقات 3-تترازوليل -بنزين- 1، 2-ثنائي سلفوناميد كمثبطات ميتالو -بيتا- لاكتاماز
CN103648496A (zh) 包含β-内酰胺抗生素、舒巴坦和β-内酰胺酶抑制剂的药物组合物
NO20076076L (no) Bicykliske 6-alkyliden-penems som klasse-D beta-laktamase inhibitorer
Majewski et al. Syntheses and biological evaluations of highly functionalized hydroxamate containing and N-methylthio monobactams as anti-tuberculosis and β-lactamase inhibitory agents
WO2007004028A3 (fr) Procedes de preparation de penemes et de leurs intermediaires
WO2003020732A3 (fr) 7-alkylidene-3-substitues-3-cephem-4-carboxylates utilises en tant qu'inhibiteurs de $g(b)-lactamase
WO2007030166A3 (fr) 6-ALKYLIDENE-PENEMS TRICYCLIQUES, INHIBITEURS DES ß-LACTAMASES DE CLASSE D
WO2008073142A3 (fr) Nouveaux inhibiteurs de la beta-lactamase
Thirunavukkarasu et al. Clinical evaluation of ceftriaxone and tazobactam in canine urinary tract infection
TW200727897A (en) Bicyclic 6-alkylidene-penem β-lactamase inhibitors and β-lactam antibiotic combination: a broad spectrum antibiotic
EP2124935A2 (fr) Combinaison antibactérienne et son utilisation
WO2007139729A8 (fr) Nouveaux inhibiteurs de bêta-lactamases de type sulfonamidométhylphosphonate
EA202191461A1 (ru) Комбинированные композиции, содержащие ингибитор -лактамазы, и пути их применения
Sobia et al. Class B-Type Beta-Lactamases: Treatment Strategies
MA53270B1 (fr) Diazabicyclooctanones comme inhibiteurs de sérine beta-lactamases
TW200738235A (en) Tricyclic 6-alkylidene-penem β-lactamase inhibitors and β-lactam antibiotic combination: a broad spectrum antibiotic
MA39085B1 (fr) Combinaison de cineol et d'amoxicilline pour une utilisation dans le traitement d'une infection bacterienne