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SG11201901658PA - Beta-lactamase inhibitor compounds - Google Patents

Beta-lactamase inhibitor compounds

Info

Publication number
SG11201901658PA
SG11201901658PA SG11201901658PA SG11201901658PA SG11201901658PA SG 11201901658P A SG11201901658P A SG 11201901658PA SG 11201901658P A SG11201901658P A SG 11201901658PA SG 11201901658P A SG11201901658P A SG 11201901658PA SG 11201901658P A SG11201901658P A SG 11201901658PA
Authority
SG
Singapore
Prior art keywords
international
street
drive
beta
english
Prior art date
Application number
SG11201901658PA
Inventor
Janelle Comita-Prevoir
Thomas Durand-Reville
Lise Gauthier
John O'donnell
Jan Romero
Ruben Tommasi
Jeroen Verheijen
Frank Wu
Xiaoyun Wu
Jing Zhang
Gregory Basarab
Bill Moss
Original Assignee
Entasis Therapeutics Ltd
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 Entasis Therapeutics Ltd filed Critical Entasis Therapeutics Ltd
Publication of SG11201901658PA publication Critical patent/SG11201901658PA/en

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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/439Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • 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
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • A61K31/546Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine containing further heterocyclic rings, e.g. cephalothin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B43/00Formation or introduction of functional groups containing nitrogen
    • 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
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0834Compounds having one or more O-Si linkage
    • C07F7/0892Compounds with a Si-O-N linkage
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date 22 March 2018 (22.03.2018) WIP0 I PCT omit VIII °nolo III 011110110111 °num oimIE (10) International Publication Number WO 2018/053215 Al (51) International Patent Classification: C07D 471/08 (2006.01) A61K 31/439 (2006.01) CO7D 211/78 (2006.01) A61P 31/04 (2006.01) (21) International Application Number: PCT/US2017/051692 (22) International Filing Date: 15 September 2017 (15.09.2017) (25) Filing Language: English (26) Publication Language: English (30) Priority Data: 62/395,464 16 September 2016 (16.09.2016) US 62/456,423 08 February 2017 (08.02.2017) US (71) Applicant: ENTASIS THERAPEUTICS LIMITED [GB/GB]; Two Kingdom Street, London W2 6BD (GB). (72) Inventors; and (71) Applicants: BASARAB, Gregory, S. [US/US]; Enta- sis Therapeutics Limited, 35 Gatehouse Drive, Waltham, MA 02451 (US). MOSS, Bill [GB/GB]; Woodlands Wil- lowmead Drive, Prestbury, Cheshire SK10 4BU (GB). (72) Inventors: COMITA-PREVOIR, Janelle; 11 Prospect Street, Northborough, MA 01532 (US). DU- RAND-REVILLE, Thomas, Francois; 34 Birch Hill Road, Belmont, MA 02478 (US). GAUTHIER, Lise; En- tasis Therapeutics Limited, 35 Gateshouse Drive, Waltham, MA 02451 (US). O'DONNELL, John; 7 Beacon Street, Mattapoisett, MA 02739 (US). ROMERO, Jan; 8 Lang- ley Road, Arlington, MA 02474 (US). TOMMASI, Ruben; 16 Salamander Lane, Stow, MA 01775 (US). VERHEI- JEN, Jeroen, Cunera; 5 Stratton Drive, Westborough, MA 01581 (US). WU, Frank; 5 Aspen Way, Shrewsbury, MA 01545 (US). WU, Xiaoyun; 3 Hundreds Road, Westbor- ough, MA 01581 (US). ZHANG, Jing; 11 Run Brook Cir- cle, Subdruy, MA 01776 (US). (74) Agent: DAVIS, Steven, G. et al.; Mccarter & English, LLP, 265 Franklin Street, Boston, MA 02110 (US). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). Published: with international search report (Art. 21(3)) before the expiration of the time limit for amending the claims and to be republished in the event of receipt of amendments (Rule 48.2(h)) (54) Title: BETA-LACTAMASE INHIBITOR COMPOUNDS (57) : The present invention is directed to compounds which are be- ta-lactamase inhibitors. The compounds and their pharmaceutically acceptable salts are useful in combination with beta- lactam antibiotics, for the treatment of bacterial infections, including infections caused by drug resistant organisms, including multi-drug resistant organisms. The present invention includes com- pounds according to Formula (I): or a pharmaceutically acceptable salt thereof, wherein the values of R 1 , R , R 2 3 , R 4 , R s and R 6 are described herein. R 2 R 3
SG11201901658PA 2016-09-16 2017-09-15 Beta-lactamase inhibitor compounds SG11201901658PA (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662395464P 2016-09-16 2016-09-16
US201762456423P 2017-02-08 2017-02-08
PCT/US2017/051692 WO2018053215A1 (en) 2016-09-16 2017-09-15 Beta-lactamase inhibitor compounds

Publications (1)

Publication Number Publication Date
SG11201901658PA true SG11201901658PA (en) 2019-04-29

Family

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Application Number Title Priority Date Filing Date
SG11201901658PA SG11201901658PA (en) 2016-09-16 2017-09-15 Beta-lactamase inhibitor compounds

Country Status (24)

Country Link
US (1) US10800778B2 (en)
EP (1) EP3512851B1 (en)
JP (2) JP6997178B2 (en)
KR (2) KR102667828B1 (en)
CN (2) CN109715630B (en)
AU (1) AU2017325863B2 (en)
CA (1) CA3036557A1 (en)
DK (1) DK3512851T3 (en)
ES (1) ES2927986T3 (en)
HR (1) HRP20221217T1 (en)
HU (1) HUE060282T2 (en)
IL (2) IL289686B2 (en)
LT (1) LT3512851T (en)
MA (1) MA46242A (en)
MX (2) MX392515B (en)
NZ (1) NZ751016A (en)
PH (1) PH12019500558B1 (en)
PL (1) PL3512851T3 (en)
PT (1) PT3512851T (en)
SG (1) SG11201901658PA (en)
SI (1) SI3512851T1 (en)
SM (1) SMT202200397T1 (en)
TW (1) TWI773687B (en)
WO (1) WO2018053215A1 (en)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10294249B2 (en) 2016-06-30 2019-05-21 Qpex Biopharma, Inc. Boronic acid derivatives and therapeutic uses thereof
SI3512851T1 (en) * 2016-09-16 2022-11-30 Entasis Therapeutics Limited Beta-lactamase inhibitor compounds
DK3630111T3 (en) 2017-05-08 2022-03-14 Entasis Therapeutics Inc Compounds and methods for treating bacterial infections
JP7329260B2 (en) 2018-04-20 2023-08-18 キューペックス バイオファーマ, インコーポレイテッド Boronic acid derivatives and their therapeutic use
US11905286B2 (en) 2018-08-09 2024-02-20 Antabio Sas Diazabicyclooctanones as inhibitors of serine beta-lactamases
CN112209928B (en) * 2019-07-10 2023-02-17 华东理工大学 Covalent bond labeled serine beta-lactamase reagent and preparation and application thereof
CN110898999A (en) * 2019-11-26 2020-03-24 中国矿业大学 A kind of coal tar-based slime flotation agent and preparation method thereof
CN111790439B (en) * 2020-07-29 2022-12-27 成都能特科技发展有限公司 Chiral secondary amine diphenylphosphine arylformamide bifunctional catalyst and preparation method and application thereof
WO2022047603A1 (en) 2020-09-01 2022-03-10 Ningxia Academy Of Agriculture And Forestry Sciences Beta-lactamase inhibitors and their preparation
JP2024512793A (en) * 2021-04-05 2024-03-19 キューペックス バイオファーマ, インコーポレイテッド Ceftibuten dosing regimen
CN115605480B (en) 2021-05-07 2024-04-05 宁夏农林科学院 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
WO2023206580A1 (en) 2022-04-29 2023-11-02 Entasis Therapeutics Limited Durlobactam crystalline forms
US20230398101A1 (en) * 2022-06-09 2023-12-14 Fleurir Abx Llc Co-agents as Therapy Against Anaerobic Pathogens
CN118271319B (en) * 2022-12-30 2025-02-28 成都四面体药物研究有限公司 A β-lactamase inhibitor containing urea bicyclic compound, preparation method and use thereof
CN116693531A (en) * 2023-06-09 2023-09-05 河南师范大学 A kind of synthetic method of bridged polycyclic lactam compound
WO2025106662A1 (en) * 2023-11-15 2025-05-22 Entasis Therapeutics, Inc. Preparation of boronic acid intermediates useful for the preparation of compounds for treating bacterial infections

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4607041A (en) * 1983-04-27 1986-08-19 Fisons Plc Antihypertensive 2-phenyl Hantzsch dihydropyridines
ATE177099T1 (en) 1993-12-29 1999-03-15 Pfizer DIAZABICYCLIC NEUROKININ ANTAGONISTS
FR2812635B1 (en) 2000-08-01 2002-10-11 Aventis Pharma Sa NOVEL HETEROCYCLIC COMPOUNDS, PREPARATION AND USE AS MEDICAMENTS IN PARTICULAR AS ANTI-BACTERIALS
FR2825705B1 (en) 2001-06-08 2005-05-20 Aventis Pharma Sa NOVEL HETEROCYCLIC COMPOUNDS, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS, IN PARTICULAR AS ANTI-BACTERIANS
FR2835186B1 (en) 2002-01-28 2006-10-20 Aventis Pharma Sa NOVEL HETEROCYCLIC COMPOUNDS ACTIVE AS BETA-LACTAMASES INHIBITORS
FR2848210B1 (en) 2002-12-06 2007-10-19 Aventis Pharma Sa NOVEL HETEROCYCLIC COMPOUNDS, PREPARATION THEREOF AND THEIR USE AS MEDICAMENTS, IN PARTICULAR AS ANTI-BACTERIALS AND INHIBITORS OF BETA-LACTAMASES
US7439253B2 (en) 2002-12-06 2008-10-21 Novexel Heterocyclic compounds, their preparation and their use as medicaments, in particular as antibacterials and beta-lactamase inhibitors
FR2914923B1 (en) 2007-04-12 2013-06-14 Novexel NOVEL HETEROCYCLIC NITROGEN COMPOUNDS, THEIR PREPARATION AND THEIR USE AS ANTIBACTERIAL MEDICINES.
JP5038509B2 (en) * 2008-01-18 2012-10-03 メルク・シャープ・エンド・ドーム・コーポレイション β-lactamase inhibitor
FR2930553B1 (en) 2008-04-29 2010-05-21 Novexel AZABICYCLIC COMPOUNDS, THEIR PREPARATION AND THEIR USE AS MEDICAMENTS, IN PARTICULAR BETA-LACTAMASES INHIBITORS
EP2921559A1 (en) 2008-06-19 2015-09-23 Astra Zeneca Holding France Use of (1r,2s,5r) 1,6-diazabicyclo [3.2.1]octane-2-carboxamide, 7-oxo-6-(sulfooxy)-, monosodium salt as a diagnostic reagent for detecting serine beta-lactamases
FR2936798B1 (en) 2008-10-03 2012-09-28 Novexel NOVEL HETEROCYCLIC NITROGEN COMPOUNDS, THEIR PREPARATION AND THEIR USE AS ANTIBACTERIAL MEDICINES.
FR2936951B1 (en) 2008-10-10 2010-12-03 Novexel NOVEL COMBINATIONS OF ANTIBACTERIAL NITROGENIC HETEROCYCLIC COMPOUNDS WITH OTHER ANTIBACTERIAL COMPOUNDS AND THEIR USE AS MEDICAMENTS
FR2937034B1 (en) 2008-10-10 2012-11-23 Novexel NOVEL HETEROCYCLIC NITROGEN COMPOUNDS, THEIR PREPARATION AND THEIR USE AS ANTIBACTERIAL MEDICINES
FR2951171A1 (en) 2009-10-09 2011-04-15 Novexel NOVEL SODIUM SALT OF A CRYSTALLIZED ENANTIOMER AZABICYCLIC COMPOUND AND NOVEL POLYMORPHIC AND PSEUDOPOLYMORPHIC FORMS AND THEIR PREPARATION
ES2738148T3 (en) * 2010-04-20 2020-01-20 Taisho Pharmaceutical Co Ltd Hydroxamic acid derivative
RU2560846C1 (en) 2011-07-26 2015-08-20 Вокхардт Лимитед Pharmaceutical compositions, containing sulbactam and beta-lactamase inhibitor
MX362683B (en) 2011-07-26 2019-01-31 Wockhardt Ltd Pharmaceutical compositions comprising beta-lactam antibiotic, sulbactam and beta-lactamase inhibitor.
RU2578370C2 (en) * 2011-08-27 2016-03-27 Вокхардт Лимитед 1,6-diazabicyclo[3,2,1]octan-7-one derivatives and using them for treating bacterial infections
WO2013030735A1 (en) 2011-08-30 2013-03-07 Wockhardt Limited 1,6- diazabicyclo [3,2,1] octan- 7 - one derivatives and their use in the treatment of bacterial infections
RU2569307C1 (en) 2011-09-13 2015-11-20 Вокхардт Лимитед Nitrogen-containing compounds and application thereof
US8796257B2 (en) 2011-12-02 2014-08-05 Naeja Pharmaceutical Inc. Bicyclic compounds and their use as antibacterial agents and β-lactamase inhibitors
EP2814483A2 (en) 2012-02-15 2014-12-24 Rempex Pharmaceuticals, Inc. Methods of treating bacterial infections
US8916709B2 (en) 2012-03-30 2014-12-23 Cubist Pharmaceuticals, Inc. 1,2,4-oxadiazole and 1,2,4-thiadiazole β-lactamase inhibitors
RU2014143821A (en) 2012-03-30 2016-05-27 Кьюбист Фармасьютикалз, Инк. 1, 3, 4-oxadiazole and 1, 3, 4-thiadiazole β-lactamase inhibitors
US8969570B2 (en) 2012-03-30 2015-03-03 Cubist Pharmaceuticals, Inc. Beta-lactamase inhibitors
KR20150003777A (en) 2012-03-30 2015-01-09 큐비스트 파마슈티컬즈 인코포레이티드 ISOXAZOLE β-LACTAMASE INHIBITORS
AR090539A1 (en) * 2012-04-02 2014-11-19 Astrazeneca Ab INHIBITING COMPOUNDS OF B LACTAMASA
US9181250B2 (en) 2012-05-30 2015-11-10 Meiji Seika Pharma Co., Ltd. Beta-lactamase inhibitor and process for preparing the same
CA2881169C (en) 2012-08-25 2020-06-16 Wockhardt Limited 1,6-diazabicyclo [3,2,1]octan - 7 - one derivatives and their use in the treatment of bacterial infections
AU2013308128B2 (en) 2012-09-03 2017-11-02 Wockhardt Limited Antibacterial compositions
MX2015010077A (en) 2013-02-06 2016-01-25 Astrazeneca Ab Combination therapy for the treatment of nosocomial pneumonia.
WO2014141132A1 (en) * 2013-03-14 2014-09-18 Naeja Pharmaceutical Inc. NEW HETEROCYCLIC COMPOUNDS AND THEIR USE AS ANTIBACTERIAL AGENTS AND β-LACTAMASE INHIBITORS
MX2017006383A (en) 2014-11-17 2017-08-21 Entasis Therapeutics Ltd Combination therapy for treatment of resistant bacterial infections.
EP3277686B1 (en) * 2015-03-31 2020-07-22 Mutabilis Novel heterocyclic compounds and their use in preventing or treating bacterial infections
SI3512851T1 (en) * 2016-09-16 2022-11-30 Entasis Therapeutics Limited Beta-lactamase inhibitor compounds
KR20230007830A (en) * 2021-07-06 2023-01-13 현대자동차주식회사 Thermoplastic resin composition and molded article comprising the same

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CN114591223A (en) 2022-06-07
EP3512851A1 (en) 2019-07-24
KR102537340B1 (en) 2023-05-26
HRP20221217T1 (en) 2022-12-23
IL265276B (en) 2022-02-01
TWI773687B (en) 2022-08-11
SMT202200397T1 (en) 2022-11-18
TW201823207A (en) 2018-07-01
JP6997178B2 (en) 2022-02-03
MX385507B (en) 2025-03-18
AU2017325863A1 (en) 2019-03-14
US20190202832A1 (en) 2019-07-04
WO2018053215A1 (en) 2018-03-22
JP7281527B2 (en) 2023-05-25
JP2019532928A (en) 2019-11-14
BR112019005053A2 (en) 2019-06-18
KR20190043630A (en) 2019-04-26
NZ751016A (en) 2025-02-28
US10800778B2 (en) 2020-10-13
PH12019500558A1 (en) 2019-07-29
JP2022046563A (en) 2022-03-23
CA3036557A1 (en) 2018-03-22
PH12019500558B1 (en) 2023-09-08
IL289686B2 (en) 2023-03-01
AU2017325863B2 (en) 2021-08-19
CN114591223B (en) 2025-01-24
IL289686B (en) 2022-11-01
MX2021010077A (en) 2022-05-23
ES2927986T3 (en) 2022-11-14
PL3512851T3 (en) 2022-11-14
IL289686A (en) 2022-03-01
KR20230078830A (en) 2023-06-02
KR102667828B1 (en) 2024-05-20
SI3512851T1 (en) 2022-11-30
HUE060282T2 (en) 2023-02-28
DK3512851T3 (en) 2022-10-17
CN109715630B (en) 2022-02-22
LT3512851T (en) 2022-10-25
IL265276A (en) 2019-05-30
MA46242A (en) 2019-07-24
MX2019003060A (en) 2019-07-08
CN109715630A (en) 2019-05-03
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EP3512851B1 (en) 2022-07-06

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