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)
  • 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)

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) KR101800610B1 (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) ES2533826T3 (fr)
FR (3) FR20C1032I2 (fr)
HN (1) HN2010001395A (fr)
HR (2) HRP20131123T1 (fr)
HU (2) HUS000504I2 (fr)
IL (1) IL206395A (fr)
LT (3) LTPA2020517I1 (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) NO2020022I1 (fr)
NZ (1) NZ586861A (fr)
PL (2) PL2231667T3 (fr)
PT (2) PT2666774E (fr)
RS (2) RS53862B1 (fr)
RU (1) RU2445314C9 (fr)
SI (2) SI2666774T1 (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
ES2533826T3 (es) * 2008-01-18 2015-04-15 Merck Sharp & Dohme Corp. Inhibidores de beta-lactamasa
RS60310B1 (sr) 2010-08-10 2020-07-31 Rempex Pharmaceuticals Inc Ciklični derivati estra boronske kiseline, postupak za pripremu injihove terapeutske upotrebe
SI2657234T1 (sl) 2010-12-22 2017-06-30 Meiji Seika Pharma Co., Ltd. Derivat optično-aktivnega diazabiciklooktana in metoda za njegovo izdelavo
US8772490B2 (en) * 2010-12-22 2014-07-08 Meiji Seika Pharma Co., Ltd. Optically active diazabicyclooctane derivatives and process for preparing the same
KR102143660B1 (ko) * 2011-06-17 2020-08-11 화이자 안티-인펙티브스 에이비 트랜스-7-옥소-6-(술포옥시)-1,6-디아자비시클로[3,2,1]옥탄-2-카르복스아미드 및 그의 염을 포함하는 헤테로시클릭 화합물의 제조 방법
RU2578370C2 (ru) * 2011-08-27 2016-03-27 Вокхардт Лимитед Производные 1,6- диазабицикло [3,2,1] октан-7-она и их применение при лечении бактериальных инфекционных болезней
MX340533B (es) * 2011-08-30 2016-07-13 Wockhardt Ltd Derivados de 1,6- diazabiciclo [3,2,1] octan-7-ona y su uso en el tratamiento de infecciones bacterianas.
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
CN104159587A (zh) * 2012-01-06 2014-11-19 南佛罗里达大学 组合物、使用方法、以及治疗方法
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
KR20150003777A (ko) 2012-03-30 2015-01-09 큐비스트 파마슈티컬즈 인코포레이티드 이속사졸 β-락타마제 억제제
TW201343645A (zh) 2012-03-30 2013-11-01 Cubist Pharm Inc 1,3,4-□二唑及1,3,4-噻二唑β-內醯胺酶抑制劑
AR090539A1 (es) * 2012-04-02 2014-11-19 Astrazeneca Ab COMPUESTOS INHIBIDORES DE b LACTAMASA
SG11201407295YA (en) 2012-05-08 2014-12-30 Codexis Inc Biocatalysts and methods for hydroxylation of chemical compounds
US9156858B2 (en) 2012-05-23 2015-10-13 Rempex Pharmaceuticals, Inc. Boronic acid derivatives and therapeutic uses thereof
RU2693898C2 (ru) 2012-05-30 2019-07-05 Мейдзи Сейка Фарма Ко., Лтд. НОВЫЙ ИНГИБИТОР бета-ЛАКТАМАЗЫ И СПОСОБ ЕГО ПОЛУЧЕНИЯ
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
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
CN105026407B (zh) 2012-12-07 2017-09-08 维纳拓尔斯制药公司 β‑内酰胺酶抑制剂
UA111925C2 (uk) * 2012-12-11 2016-06-24 Федора Фармасьютікалз Інк. БІЦИКЛІЧНІ СПОЛУКИ ТА ЇХ ВИКОРИСТАННЯ ЯК АНТИБАКТЕРІАЛЬНИХ АГЕНТІВ ТА ІНГІБІТОРІВ β-ЛАКТАМАЗИ
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
KR20150103269A (ko) 2013-01-04 2015-09-09 렘펙스 파머수티클스 인코퍼레이티드 보론산 유도체 및 그의 치료적 용도
KR20150103270A (ko) 2013-01-04 2015-09-09 렘펙스 파머수티클스 인코퍼레이티드 보론산 유도체 및 그의 치료적 용도
EP2943204B1 (fr) 2013-01-10 2019-03-13 Venatorx Pharmaceuticals Inc Inhibiteurs de bêta-lactamase
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
BR112015021186A2 (pt) 2013-03-08 2017-07-18 Wockhardt Ltd processo para a preparação de (2s,5r)-7-oxo-6-sulfóxi-2-[((3r)-pirrolidina-3-carbonil)-hidrazino carbonil]-1,6-diaza-biciclo[3.2.1]octano
AU2013399862B2 (en) * 2013-03-08 2016-07-14 Wockhardt Limited 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
CN108191864A (zh) 2013-03-08 2018-06-22 沃克哈特有限公司 制备氧代磺酰氧基[(哌啶羰基)-肼基羰基]二氮杂-双环辛烷的方法
CA2904089C (fr) * 2013-03-08 2017-05-02 Wockhardt Limited Procede pour sel de sodium de (2s, 5r)-2-carboxamido -7-oxo-6-sulfooxy -1,6-diaza-bicyclo[3.2.1]octane
WO2014151958A1 (fr) 2013-03-14 2014-09-25 VenatoRx Pharmaceuticals, Inc. Inhibiteurs de bêta-lactamase
US9120795B2 (en) 2013-03-14 2015-09-01 Cubist Pharmaceuticals, Inc. Crystalline form of a β-lactamase inhibitor
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
DK3050883T3 (da) 2013-09-24 2020-05-25 Meiji Seika Pharma Co Ltd Fremgangsmåde til fremstilling af diazabicyclooctanderivater og mellemprodukter
US9120796B2 (en) 2013-10-02 2015-09-01 Cubist Pharmaceuticals, Inc. B-lactamase inhibitor picoline salt
EP3613740A1 (fr) * 2013-10-08 2020-02-26 Meiji Seika Pharma Co., Ltd. Procédé de production d'un dérivé de diazabicyclooctane
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
MX373444B (es) 2014-03-24 2020-04-30 Novartis Ag Compuestos organicos de monobactam para el tratamiento de infecciones bacterianas.
IN2014MU01196A (fr) * 2014-03-29 2015-10-02 Wockhardt Ltd
IN2014MU01195A (fr) * 2014-03-29 2015-10-02 Wockhardt Ltd
EP3139930B1 (fr) 2014-05-05 2024-08-14 Melinta Therapeutics, Inc. Sels et polymorphes de dérivés cycliques d'ester d'acide boronique, et leurs utilisations thérapeutiques
SI3140310T1 (sl) 2014-05-05 2020-01-31 Rempex Pharmaceuticals, Inc. Sinteza boronatnih soli in njihova uporaba
WO2015179308A1 (fr) 2014-05-19 2015-11-26 Rempex Pharmaceuticals, Inc. Dérivés d'acide boronique et leurs utilisations thérapeutiques
PT3154989T (pt) 2014-06-11 2021-05-18 Venatorx Pharmaceuticals Inc Inibidores de beta-lactamase
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
KR102542392B1 (ko) * 2014-11-17 2023-06-09 엔타시스 테라퓨틱스 리미티드 내성 박테리아 감염의 치료를 위한 배합물 치료제
WO2016081297A1 (fr) 2014-11-18 2016-05-26 Rempex Pharmaceuticals, Inc. Dérivés d'esters d'acide boronique cycliques et leurs utilisations thérapeutiques
ES2812848T3 (es) 2014-12-02 2021-03-18 Merck Sharp & Dohme Proceso para la preparación de 4-((2S,5R)-6-(benciloxi)-7-oxo-1,6-diazabiciclo[3.2.1]octano-2-carboxamido)piperidin-1-carboxilato de terc-butilo y análogos del mismo
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
TW201639853A (zh) * 2015-03-31 2016-11-16 木塔比利斯公司 雜環化合物及其於預防或治療細菌感染之用途
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
US10501464B2 (en) * 2015-12-11 2019-12-10 Wockhardt Limited 7-oxo-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide containing compounds and their use in treating bacterial infections
WO2017136254A1 (fr) 2016-02-04 2017-08-10 Merck Sharp & Dohme Corp. Procédés de préparation de dérivés d'hydroxylamine utiles dans la préparation d'agents anti-infectieux
WO2017167218A1 (fr) * 2016-03-31 2017-10-05 山东轩竹医药科技有限公司 Composition antibactérienne et son utilisation
WO2017213758A1 (fr) 2016-06-09 2017-12-14 Codexis, Inc. Biocatalyseurs et procédés d'hydroxylation de composés chimiques
ES2894251T3 (es) 2016-06-30 2022-02-14 Qpex Biopharma Inc Derivados de ácido borónico y usos terapéuticos de los mismos
EP3494121B1 (fr) 2016-08-04 2021-10-06 Venatorx Pharmaceuticals, Inc. Composés contenant du bore
CN114591223B (zh) * 2016-09-16 2025-01-24 恩塔西斯治疗有限公司 β-内酰胺酶抑制剂化合物
US10464937B2 (en) * 2016-09-19 2019-11-05 Merck Sharp & Dohme Corp. Process for preparing beta-lactamase inhibitor hydroxylurea intermediates
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
MA47743A (fr) 2017-03-06 2020-01-15 Venatorx Pharmaceuticals Inc Formes solides et compositions de combinaison comprenant un inhibiteur de bêta-lactamase et leurs utilisations
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
NZ758200A (en) 2017-05-08 2025-12-19 Entasis Therapeutics Inc Compounds and methods for treating bacterial infections
US10085999B1 (en) * 2017-05-10 2018-10-02 Arixa Pharmaceuticals, Inc. Beta-lactamase inhibitors and uses thereof
EP3630783A4 (fr) 2017-05-26 2021-03-03 Venatorx Pharmaceuticals, Inc. Inhibiteurs protéiques de liaison à la pénicilline
US11332485B2 (en) 2017-05-26 2022-05-17 VenatoRx Pharmaceuticals, Inc. Penicillin-binding protein inhibitors
ES2946917T3 (es) 2017-07-21 2023-07-27 Antabio Sas Compuestos químicos
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
MX2020003495A (es) 2017-10-11 2020-09-18 Qpex Biopharma Inc Derivados de acido boronico y sintesis de los mismos.
JP6974614B2 (ja) 2017-12-01 2021-12-01 チールー ファーマシューティカル カンパニー、リミテッド β−ラクタマーゼ阻害剤の結晶形およびその製造方法
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
KR102769880B1 (ko) * 2018-01-25 2025-02-20 쑤저우 시노벤트 파마슈티칼즈 씨오., 엘티디. β-락타마제 억제제 및 그 용도
US12016868B2 (en) 2018-04-20 2024-06-25 Qpex Biopharma, Inc. Boronic acid derivatives and therapeutic uses thereof
EP3572411A1 (fr) 2018-05-21 2019-11-27 Antabio SAS Dérivés de thiazole comme inhibiteurs de métallo-bêta-lactamases
EP3802551A4 (fr) 2018-05-25 2022-03-02 Venatorx Pharmaceuticals, Inc. Inhibiteurs de protéine de liaison à la pénicilline
SG11202101255UA (en) * 2018-08-09 2021-03-30 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
US11905286B2 (en) 2018-08-09 2024-02-20 Antabio Sas Diazabicyclooctanones as inhibitors of serine beta-lactamases
CN119707784A (zh) 2018-09-21 2025-03-28 株式会社Api 氨基酸衍生物的制备方法
ES2991492T3 (es) * 2018-10-01 2024-12-03 Arixa Pharmaceuticals Inc Derivados de relebactam y usos de los mismos
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
CN113382713A (zh) 2018-11-29 2021-09-10 维纳拓尔斯制药公司 包含β-内酰胺酶抑制剂的组合式组合物及其用途
AU2020237440B2 (en) 2019-03-12 2022-10-20 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
BR112022022367A2 (pt) 2020-05-05 2023-01-10 Qpex Biopharma Inc Derivados e síntese de ácido borônico, formas polimórficas e usos terapêuticos dos mesmos
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
US12410166B2 (en) 2021-05-07 2025-09-09 Ningxia Academy Of Agriculture And Forestry Sciences Sulfonylamidine substituted compounds and their use as beta-lactamase inhibitors
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
GB202306826D0 (en) 2023-05-09 2023-06-21 Adjutec Pharma As Therapy
GB202306833D0 (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
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
US4880793A (en) 1978-07-24 1989-11-14 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
DK0508234T3 (da) 1991-04-11 1996-10-28 Hoffmann La Roche Beta-lactamer
HUT74682A (en) 1993-12-29 1997-01-28 Pfizer Diazabicyclic neurokinin antagonists and pharmaceutical compositions containing them
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
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
EP0882728B1 (fr) 1995-12-21 2002-09-04 Sankyo Company Limited Derives de 1-methylcarbapenem
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.
MXPA02001394A (es) 1999-08-10 2002-08-12 British Biotech Pharm Agentes antibacterianos.
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
HUP0303204A3 (en) 2000-11-16 2010-04-28 Sankyo Co 1-methylcarbapenem derivatives and pharmaceutical compositions containing them
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
CA2531728A1 (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
CA2783572C (fr) * 2005-12-07 2016-08-09 Basilea Pharmaceutica Ag Associations utiles d'antibiotiques monobactames et d'inhibiteurs de la beta-lactamase
AU2007300531A1 (en) 2006-09-27 2008-04-03 Merck Sharp & Dohme Corp. Novel inhibitors of beta-lactamase
ES2533826T3 (es) * 2008-01-18 2015-04-15 Merck Sharp & Dohme Corp. Inhibidores de beta-lactamasa

Also Published As

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

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
JO3588B1 (ar) مشتقات 3-تترازوليل -بنزين- 1، 2-ثنائي سلفوناميد كمثبطات ميتالو -بيتا- لاكتاماز
ZA202309204B (en) Lactivicin compounds, their preparation and use as antibacterial agents
Paterson et al. Fatal Infection Due to Extended-Spectrum Beta-Lactamase--Producing Escherichia coli: Implications...
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
TW200716102A (en) Bicyclic 6-alkylidene-penems as class-D β -lactamases inhibitors
TW200716104A (en) Tricyclic 6-alkylidene-penems as class-D β -lactamases inhibitors
WO2008073142A8 (fr) Nouveaux inhibiteurs de la beta-lactamase
CO2024006324A2 (es) Antibióticos monobactámicos de amidina cromano
Ray et al. Imipenem-resistance among multi-drug resistant clinical strains in urinary infections from Kolkata
Thirunavukkarasu et al. Clinical evaluation of ceftriaxone and tazobactam in canine urinary tract infection
US20110172200A1 (en) Use of inhibitor of beta-lactamases and its combination with beta-lactam antibiotics
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
Sobia et al. Class B-Type Beta-Lactamases: Treatment Strategies
EA202191461A1 (ru) Комбинированные композиции, содержащие ингибитор -лактамазы, и пути их применения
MA53270B1 (fr) Diazabicyclooctanones comme inhibiteurs de sérine beta-lactamases