[go: up one dir, main page]

FR20C1030I2 - Inhibiteurs de beta-lactamase - Google Patents

Inhibiteurs de beta-lactamase

Info

Publication number
FR20C1030I2
FR20C1030I2 FR20C1030C FR20C1030C FR20C1030I2 FR 20C1030 I2 FR20C1030 I2 FR 20C1030I2 FR 20C1030 C FR20C1030 C FR 20C1030C FR 20C1030 C FR20C1030 C FR 20C1030C FR 20C1030 I2 FR20C1030 I2 FR 20C1030I2
Authority
FR
France
Prior art keywords
beta
lactamase inhibitors
lactamase
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.)
Active
Application number
FR20C1030C
Other languages
English (en)
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.)
Organon Pharma UK Ltd
Merck Sharp and Dohme LLC
Original Assignee
Merck Sharp and Dohme Ltd
Merck Sharp and Dohme LLC
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
Publication of FR20C1030I1 publication Critical patent/FR20C1030I1/fr
Application filed by Merck Sharp and Dohme Ltd, Merck Sharp and Dohme LLC filed Critical Merck Sharp and Dohme Ltd
Application granted granted Critical
Publication of FR20C1030I2 publication Critical patent/FR20C1030I2/fr
Active 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
    • A61K31/468-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)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Emergency Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (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)
FR20C1030C 2008-01-18 2020-07-10 Inhibiteurs de beta-lactamase Active FR20C1030I2 (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 (2)

Publication Number Publication Date
FR20C1030I1 FR20C1030I1 (fr) 2020-02-10
FR20C1030I2 true FR20C1030I2 (fr) 2021-08-27

Family

ID=40642204

Family Applications (3)

Application Number Title Priority Date Filing Date
FR20C1030C Active FR20C1030I2 (fr) 2008-01-18 2020-07-10 Inhibiteurs de beta-lactamase
FR20C1031C Active FR20C1031I2 (fr) 2008-01-18 2020-07-10 Inhibiteurs de beta-lactamase
FR20C1032C Active FR20C1032I2 (fr) 2008-01-18 2020-07-10 Inhibiteurs de beta-lactamase

Family Applications After (2)

Application Number Title Priority Date Filing Date
FR20C1031C Active FR20C1031I2 (fr) 2008-01-18 2020-07-10 Inhibiteurs de beta-lactamase
FR20C1032C Active FR20C1032I2 (fr) 2008-01-18 2020-07-10 Inhibiteurs de beta-lactamase

Country Status (38)

Country Link
US (2) US8487093B2 (fr)
EP (2) EP2666774B1 (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) FR20C1030I2 (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 (2) NL301051I2 (fr)
NO (3) NO2020022I1 (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 (105)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI2231667T1 (sl) * 2008-01-18 2013-12-31 Merck Sharp & Dohme Corp. Beta laktamazni inhibitorji
BR112013003045B1 (pt) 2010-08-10 2021-08-31 Rempex Pharmaceuticals, Inc. Composto e respectivo uso, composição farmacêutica, recipiente estéril e método para preparar composição farmacêutica para administração
US8772490B2 (en) * 2010-12-22 2014-07-08 Meiji Seika Pharma Co., Ltd. Optically active diazabicyclooctane derivatives and process for preparing the same
CN104892490B (zh) * 2010-12-22 2017-07-21 明治制果药业株式会社 用于制备光学活性二氮杂环辛烷衍生物的中间体化合物的化合物
WO2012172368A1 (fr) * 2011-06-17 2012-12-20 Astrazeneca Ab Procédé de préparation de composés hétérocycliques, notamment le trans-7-oxo-6-(sulphooxy)-1,6-diazabicyclo[3,2,1]octane-2-carboxamide et ses sels
KR101512738B1 (ko) * 2011-08-27 2015-04-17 욱크하르트 리미티드 1,6-디아자-비시클로[3,2,1]옥탄-7-온 유도체 및 세균 감염 치료에서의 그 유도체의 용도
JP5677634B2 (ja) 2011-08-30 2015-02-25 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
US9012491B2 (en) 2011-08-31 2015-04-21 Rempex Pharmaceuticals, Inc. Heterocyclic boronic acid ester derivatives and therapeutic uses thereof
US9505761B2 (en) 2011-12-02 2016-11-29 Fedora Pharmaceuticals Inc. Bicyclic compounds and their use as antibacterial agents and beta-lactamase inhibitors
US8796257B2 (en) 2011-12-02 2014-08-05 Naeja Pharmaceutical Inc. Bicyclic compounds and their use as antibacterial agents and β-lactamase inhibitors
AU2013207510A1 (en) 2012-01-06 2014-07-31 The Regents Of The University Of California Compositions, methods of use, and methods of treatment
US8969570B2 (en) * 2012-03-30 2015-03-03 Cubist Pharmaceuticals, Inc. 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
SG11201406120SA (en) * 2012-03-30 2014-10-30 Cubist Pharm Inc ISOXAZOLE β-LACTAMASE INHIBITORS
MX2014011827A (es) * 2012-03-30 2015-02-20 Cubist Pharm Inc Inhibidores de 1,3,4 - oxadiazol y 1,3,4 - tiadiazol b-lactamasa.
AR090539A1 (es) 2012-04-02 2014-11-19 Astrazeneca Ab COMPUESTOS INHIBIDORES DE b LACTAMASA
WO2013169725A2 (fr) 2012-05-08 2013-11-14 Codexis, Inc. Biocatalyseurs et procédés pour l'hydroxylation de composés chimiques
US9156858B2 (en) 2012-05-23 2015-10-13 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
UA117734C2 (uk) 2012-05-30 2018-09-25 Мейдзі Сейка Фарма Ко., Лтд. НОВИЙ ІНГІБІТОР β-ЛАКТАМАЗИ І СПОСІБ ЙОГО ОДЕРЖАННЯ
US10561675B2 (en) 2012-06-06 2020-02-18 Rempex Pharmaceuticals, Inc. Cyclic boronic acid ester derivatives and therapeutic uses thereof
BR112015003592B1 (pt) * 2012-08-25 2020-04-14 Wockhardt Ltd derivados de 1,6-diazabiciclo[3,2,1]octan-7-ona e seu uso no tratamento de infecções bacterianas
US20150315145A1 (en) * 2012-11-01 2015-11-05 Kaneka Corporation Process for producing optically active bicyclic urea compound
KR102147420B1 (ko) * 2012-12-07 2020-08-25 베나토알엑스 파마슈티컬스, 인크. 베타-락타마제 억제제
UA111925C2 (uk) * 2012-12-11 2016-06-24 Федора Фармасьютікалз Інк. БІЦИКЛІЧНІ СПОЛУКИ ТА ЇХ ВИКОРИСТАННЯ ЯК АНТИБАКТЕРІАЛЬНИХ АГЕНТІВ ТА ІНГІБІТОРІВ β-ЛАКТАМАЗИ
MX2015008627A (es) 2013-01-04 2015-09-23 Rempex Pharmaceuticals Inc Derivados de acido boronico y usos terapeuticos de los mismos.
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
CA2894891A1 (fr) 2013-01-04 2014-07-10 Rempex Pharmaceuticals, Inc. Derives d'acide boronique et leurs utilisations therapeutiques
WO2014110442A1 (fr) 2013-01-10 2014-07-17 VenatoRx Pharmaceuticals, Inc. Inhibiteurs de bêta-lactamase
CN105143224A (zh) * 2013-03-08 2015-12-09 沃克哈特有限公司 一种制备(2s,5r)-硫酸单-{[(4-氨基哌啶-4-基)羰基]-7-氧代-1,6-二氮杂-双环[3.2.1]-辛-6-基}酯的方法
AU2013380573B2 (en) * 2013-03-08 2016-07-07 Wockhardt Limited A process for sodium salt of (2S, 5R)-2-carboxamido-7-oxo-6-sulfooxy -1,6-diaza-bicyclo[3.2.1]octane
CN105143225A (zh) 2013-03-08 2015-12-09 沃克哈特有限公司 一种制备(2s,5r)-7-氧代-6-磺酰氧基-2-[((3r)-哌啶-3-羰基)-肼基羰基]-1,6-二氮杂-双环[3.2.1]辛烷的方法
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
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
US9624222B2 (en) * 2013-03-08 2017-04-18 Wockhardt Limited Process for preparation of (2S, 5R)-7-oxo-6-sulphooxy-2-[((3R)-pyrrolidine-3-carbonyl)-hydrazino carbonyl]-1,6-diaza-bicyclo[3.2.1]octance
US9120795B2 (en) 2013-03-14 2015-09-01 Cubist Pharmaceuticals, Inc. Crystalline form of a β-lactamase inhibitor
EP2970340B1 (fr) 2013-03-14 2020-02-12 Venatorx Pharmaceuticals, Inc. Inhibiteurs de bêta-lactamase
AU2014278556B2 (en) * 2013-06-10 2018-07-19 Merck Sharp & Dohme Llc Preparation of tert-butyl 4-((1R,2S,5R)-6- (benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2- carboxamido)piperidine-1-carboxylate
MY176278A (en) 2013-09-24 2020-07-27 Meiji Seika Pharma Co Ltd Process for producing diazabicyclooctane derivative and intermediate thereof
WO2015051101A1 (fr) * 2013-10-02 2015-04-09 Cubist Pharmaceuticals, Inc. Sel picoline inhibiteur de b-lactamase
NZ757221A (en) 2013-10-08 2021-12-24 Meiji Seika Pharma Co Ltd Crystalline forms of diazabicyclooctane derivative and production process thereof
WO2015079329A2 (fr) * 2013-11-26 2015-06-04 Wockhardt Limited Procédé de préparation de (2s, 5r)-7-oxo-n-[(2s)-pyrrolidin-2-yl-méthyloxy]-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide
ES2719136T3 (es) 2014-03-24 2019-07-08 Novartis Ag Compuestos orgánicos de monobactam para el tratamiento de infecciones bacterianas
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
WO2015150890A1 (fr) * 2014-03-29 2015-10-08 Wockhardt Limited Procédé de préparation de mono-{2-(5-(3-amino-propyl)-[1,3,4]oxadiazol-2-yl]-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl}ester d'acide sulfurique trans
US9687497B1 (en) 2014-05-05 2017-06-27 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
KR20170007448A (ko) 2014-05-19 2017-01-18 렘펙스 파머수티클스 인코퍼레이티드 보론산 유도체 및 그의 치료적 용도
KR102396753B1 (ko) 2014-06-11 2022-05-12 베나토알엑스 파마슈티컬스, 인크. 베타-락타마제 억제제
US9511142B2 (en) 2014-06-11 2016-12-06 VenatoRx Pharmaceuticals, Inc. Beta-lactamase inhibitors
EP3164406B1 (fr) 2014-07-01 2024-12-25 Qpex Biopharma, Inc. Dérivés d'acide boronique et leurs utilisations thérapeutiques
SI3221313T1 (sl) 2014-11-17 2019-04-30 Entasis Therapeutics Limited Kombinacijska terapija za zdravljenje okužb z rezistentnimi bakterijami
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
BR112017010445B8 (pt) 2014-12-05 2024-02-27 Meiji Seika Pharma Co Ltd Processo de produção de cristais de derivado de diazabiciclo-octano e preparação liofilizada estável
US20180051041A1 (en) 2015-03-17 2018-02-22 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
US10570131B2 (en) 2015-03-31 2020-02-25 Mutabilis Heterocyclic compounds and their use in preventing or treating bacterial infections
MX2017014080A (es) * 2015-05-07 2018-07-06 Mutabilis Compuestos heterociclicos y su uso en la prevencion o tratamiento de las infecciones bacterianas.
EP3347008B1 (fr) 2015-09-11 2022-03-09 Venatorx Pharmaceuticals, Inc. Inhibiteurs de bêta-lactamases
EP3281942A4 (fr) * 2015-09-16 2018-08-15 Xuanzhu Pharma Co., Ltd. Inhibiteur de ss-lactamase et son application
CN108137567A (zh) 2015-10-02 2018-06-08 乐高化学生物科学股份有限公司 用于抑制β-内酰胺酶的组合物和方法
WO2017100537A1 (fr) 2015-12-10 2017-06-15 VenatoRx Pharmaceuticals, Inc. Inhibiteurs de bêta-lactamases
EP3386982A1 (fr) * 2015-12-11 2018-10-17 The 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
US10472345B2 (en) 2016-02-04 2019-11-12 Merck Sharp & Dohme Corp. Methods of preparing hydroxylamine derivatives useful in the preparation of anti-infective agents
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
WO2017213758A1 (fr) 2016-06-09 2017-12-14 Codexis, Inc. Biocatalyseurs et procédés d'hydroxylation de composés chimiques
US10294249B2 (en) 2016-06-30 2019-05-21 Qpex Biopharma, Inc. Boronic acid derivatives and therapeutic uses thereof
WO2018027062A1 (fr) 2016-08-04 2018-02-08 VenatoRx Pharmaceuticals, Inc. Composés contenant du bore
SMT202200397T1 (it) * 2016-09-16 2022-11-18 Entasis Therapeutics Ltd Composti inibitori di beta-lattamasi
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
PL3592362T3 (pl) 2017-03-06 2025-06-23 VenatoRx Pharmaceuticals, Inc. Postacie stałe i kompozycje skojarzone zawierające inhibitor beta-laktamaz i ich zastosowania
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
CN110709081B (zh) 2017-05-08 2023-09-22 恩塔西斯治疗公司 用于治疗细菌感染的化合物及方法
US10085999B1 (en) 2017-05-10 2018-10-02 Arixa Pharmaceuticals, Inc. Beta-lactamase inhibitors and uses thereof
US11267826B2 (en) 2017-05-26 2022-03-08 VenatoRx Pharmaceuticals, Inc. Penicillin-binding protein inhibitors
US11332485B2 (en) 2017-05-26 2022-05-17 VenatoRx Pharmaceuticals, Inc. Penicillin-binding protein inhibitors
SG11202000217QA (en) 2017-07-21 2020-02-27 Antabio Sas Chemical compounds
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
US11286270B2 (en) 2017-10-11 2022-03-29 Qpex Biopharma, Inc. Boronic acid derivatives and synthesis thereof
EP3719020B1 (fr) 2017-12-01 2022-09-21 Qilu Pharmaceutical Co., Ltd. Forme cristalline d'un inhibiteur de beta-lactamase et son procédé de préparation
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
EP3781576B1 (fr) 2018-04-20 2024-06-12 Qpex Biopharma, Inc. 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
US11905286B2 (en) 2018-08-09 2024-02-20 Antabio Sas Diazabicyclooctanones as inhibitors of serine beta-lactamases
EP3670512A1 (fr) * 2018-12-18 2020-06-24 Antabio SAS Diazabicyclooctanones comme inhibiteurs de sérine beta-lactamases
EP3833665B1 (fr) * 2018-08-09 2023-07-19 Antabio SAS Diazabicyclooctanones comme inhibiteurs de sérine beta-lactamases
US11897844B2 (en) * 2018-09-21 2024-02-13 Api Corporation Method for producing amino acid derivatives
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
SG11202108905UA (en) 2019-03-12 2021-09-29 Arixa Pharmaceuticals Inc Crystalline form of an avibactam derivative
CN114206851B (zh) 2019-04-26 2025-02-11 默沙东有限责任公司 可用于制备(2s,5r)-7-氧代-n-哌啶-4-基-6-(硫酸基)-1,6-二氮杂双环[3.2.1]辛烷-2-甲酰胺的中间体的制备方法
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
EP4146650A4 (fr) 2020-09-01 2024-01-17 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
EP4146651A4 (fr) 2021-05-07 2024-06-05 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
US20250302846A1 (en) * 2022-05-11 2025-10-02 The Regents Of The University Of Colorado A Body Corporate Antibiotic composition and methods of use thereof
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
US4616038A (en) 1978-07-24 1986-10-07 Merck & Co., Inc. Combination of thienamycin-type antibiotics with dipeptidase inhibitors
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
US4539208A (en) 1980-09-17 1985-09-03 Merck & Co., Inc. Combination of thienamycin-type antibiotics with dipeptidase inhibitors
ES2090393T3 (es) 1991-04-11 1996-10-16 Hoffmann La Roche Beta-lactamas.
CZ282567B6 (cs) 1993-12-29 1997-08-13 Pfizer Inc. Diazabicyklické sloučeniny a farmaceutické prostředky na jejich bázi
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
DE69623497T2 (de) 1995-12-21 2003-05-28 Sankyo Co., Ltd. 1-methylcarbapenem-derivate
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
JP4226818B2 (ja) 1999-07-06 2009-02-18 メチルジーン・インコーポレーテッド ベータ−ラクタマーゼのスルフォンアミドメチルホスホン酸阻害剤
WO2001010834A2 (fr) 1999-08-10 2001-02-15 British Biotech Pharmaceuticals Limited Agents antibacteriens
FR2812635B1 (fr) * 2000-08-01 2002-10-11 Aventis Pharma Sa Nouveaux composes heterocycliques, preparation et utilisation comme medicaments notamment comme anti- bacteriens
JP2002212182A (ja) * 2000-11-16 2002-07-31 Sankyo Co Ltd 1−メチルカルバペネム誘導体
ES2273902T3 (es) 2000-11-16 2007-05-16 Sankyo Company, Limited Derivados de 1-metilcarbapenem.
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
CN1845897A (zh) * 2003-07-09 2006-10-11 帕拉特克药品公司 取代的四环素化合物
US6984652B2 (en) 2003-09-05 2006-01-10 Warner-Lambert Company Llc Gyrase inhibitors
JP2008502583A (ja) 2003-10-01 2008-01-31 バイエル・ヘルスケア・アクチェンゲゼルシャフト 抗細菌性アミド大員環
WO2005082050A2 (fr) 2004-02-24 2005-09-09 Ssci, Inc. Analyse et criblage de formes solides au moyen de la fonction de distribution de paires atomiques
SI1965798T1 (sl) * 2005-12-07 2012-01-31 Basilea Pharmaceutica Ag Uporabni monobaktamski antibiotiki
US20100009957A1 (en) 2006-09-27 2010-01-14 Blizzard Timothy A Novel inhibitors of beta-lactamase
SI2231667T1 (sl) * 2008-01-18 2013-12-31 Merck Sharp & Dohme Corp. Beta laktamazni inhibitorji

Also Published As

Publication number Publication date
CY2020023I1 (el) 2020-11-25
UA101966C2 (en) 2013-05-27
NO2020024I1 (no) 2020-08-10
US20110294777A1 (en) 2011-12-01
FR20C1031I2 (fr) 2022-07-29
FR20C1032I2 (fr) 2022-07-29
NO2020022I1 (no) 2020-08-10
EP2231667A2 (fr) 2010-09-29
DK2231667T3 (da) 2013-12-16
NO2020023I1 (no) 2020-08-10
CN102827067B (zh) 2015-09-23
AU2009206119C1 (en) 2016-05-26
CA2712783C (fr) 2013-03-19
CY2020024I2 (el) 2020-11-25
CY2020023I2 (el) 2020-11-25
IL206395A (en) 2015-04-30
CN102827067A (zh) 2012-12-19
KR20160099117A (ko) 2016-08-19
LTPA2020517I1 (lt) 2020-07-27
ES2433744T3 (es) 2013-12-12
KR20100130176A (ko) 2010-12-10
JP2011510012A (ja) 2011-03-31
EP2231667B1 (fr) 2013-09-04
MX2010007823A (es) 2010-08-10
WO2009091856A2 (fr) 2009-07-23
DK2666774T3 (en) 2015-03-23
IL206395A0 (en) 2010-12-30
CY2020025I2 (el) 2020-11-25
ECSP10010568A (es) 2010-11-30
HN2010001395A (es) 2012-11-12
KR101800610B1 (ko) 2017-11-23
KR101648728B1 (ko) 2016-08-17
LTPA2020516I1 (lt) 2020-07-27
AU2009206119B2 (en) 2012-06-07
EP2666774A1 (fr) 2013-11-27
LTPA2020518I1 (lt) 2020-07-27
JP2011207900A (ja) 2011-10-20
HUS2000024I1 (hu) 2021-03-29
WO2009091856A3 (fr) 2009-12-03
LTC2666774I2 (lt) 2022-01-25
PL2231667T3 (pl) 2014-01-31
FR20C1030I1 (fr) 2020-02-10
FR20C1032I1 (fr) 2020-02-10
RU2445314C1 (ru) 2012-03-20
CY1116243T1 (el) 2017-03-15
CY2020024I1 (el) 2020-11-25
ME02089B (fr) 2014-04-30
HRP20131123T1 (hr) 2013-12-20
MY162532A (en) 2017-06-15
BRPI0906871A2 (pt) 2020-07-28
CN101918407A (zh) 2010-12-15
LUC00165I2 (fr) 2021-08-16
JP2012214475A (ja) 2012-11-08
JP5597164B2 (ja) 2014-10-01
RS53862B1 (sr) 2015-08-31
US8487093B2 (en) 2013-07-16
PL2666774T3 (pl) 2015-06-30
RU2445314C9 (ru) 2013-04-10
US20130274475A1 (en) 2013-10-17
NL301051I2 (nl) 2020-09-03
NI201000115A (es) 2011-07-08
HK1186180A1 (en) 2014-03-07
CA2712783A1 (fr) 2009-07-23
HUS000504I2 (hu) 2021-03-29
CY1114900T1 (el) 2016-12-14
FR20C1031I1 (fr) 2020-02-10
MA32025B1 (fr) 2011-01-03
NL301050I2 (nl) 2020-09-03
EP2666774B1 (fr) 2015-01-07
PT2231667E (pt) 2013-12-13
SI2231667T1 (sl) 2013-12-31
CO6331438A2 (es) 2011-10-20
HUS2000023I1 (hu) 2021-03-29
CY2020025I1 (el) 2020-11-25
HUS000513I2 (hu) 2021-03-29
DOP2010000218A (es) 2010-08-31
PT2666774E (pt) 2015-04-13
ECSP10010345A (es) 2010-08-31
SI2666774T1 (sl) 2015-04-30
JP5038509B2 (ja) 2012-10-03
LTC2231667I2 (lt) 2021-07-26
HK1143809A1 (en) 2011-01-14
HRP20150269T1 (hr) 2015-04-24
RS53052B (sr) 2014-04-30
CN101918407B (zh) 2014-02-26
ZA201005333B (en) 2011-04-28
CR11626A (es) 2010-09-13
NZ586861A (en) 2011-12-22
ES2533826T3 (es) 2015-04-15
JP5422020B2 (ja) 2014-02-19
AU2009206119A1 (en) 2009-07-23
BRPI0906871B1 (pt) 2021-09-28

Similar Documents

Publication Publication Date Title
FR20C1030I2 (fr) Inhibiteurs de beta-lactamase
CY2017016I1 (el) Αναστολεις πρωτεασωματος
BRPI0917808A2 (pt) inibidores de cmet
CR10831A (es) INHIBIDORES ESPIRO CETONA DE ACETIL-CoA CARBOXILASA
BRPI0807547A2 (pt) Inibidores de aspartil protease hetercíclicos
BRPI0918564A2 (pt) inibidores
BRPI0810365A2 (pt) Inibidores de mlc-1 de indol 7-substituído
DK2041138T3 (da) Pyrroltriazinkinase-inhibitorer
DK2024375T3 (da) Cyclopropyl-kondenserede indolobenzazepin-HCV-NS5B-hæmmere
DK2340021T3 (da) Substituerede pyrrolidin-2-carboxamider
BRPI0806898A2 (pt) Inibidores de mek
BRPI0814797A2 (pt) Inibidores dna-pk
EP2374802A4 (fr) Inhibiteur de production de kynurénine
EP2467382A4 (fr) Inhibiteurs de pde10 d amino-tétrahydro-pyridopyrimidine
DK2066662T3 (da) Serinhydrolaseinhibitorer
EP2435048A4 (fr) Inhibiteurs de pde10 radio-marqués
DK2240506T3 (da) IAP inhibitorer
BRPI0918966A2 (pt) inibidores de protease
BRPI0912564A2 (pt) inibidores de jnk
ATE522533T1 (de) Pyrazolopyrimidinonkinaseinhibitor
BRPI0919073A2 (pt) inibidores de protease
FI20075320A0 (fi) Uusia käyttökelpoisia inhibiittoreita
FI20080062A0 (fi) Työkalu
ATE529422T1 (de) 3-indazolyl-4-pyridylisothiazole
AT10428U3 (de) Sport-stock