MX2022006109A - Derivados 1-aminosulfonil-2-carboxipirrol como inhibidores de metalo-beta-lactamasa. - Google Patents

Derivados 1-aminosulfonil-2-carboxipirrol como inhibidores de metalo-beta-lactamasa.

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Publication number
MX2022006109A
MX2022006109A MX2022006109A MX2022006109A MX2022006109A MX 2022006109 A MX2022006109 A MX 2022006109A MX 2022006109 A MX2022006109 A MX 2022006109A MX 2022006109 A MX2022006109 A MX 2022006109A MX 2022006109 A MX2022006109 A MX 2022006109A
Authority
MX
Mexico
Prior art keywords
metallo
compounds
carboxypyrrole
aminosulfonyl
beta
Prior art date
Application number
MX2022006109A
Other languages
English (en)
Inventor
Ian Cooper
David Orr
James Kirkham
Andrew Wilkinson
Jonathan Finlayson
Adam Bunt
Pia Appelqvist
Hans Wallberg
Fredrik Wångsell
Original Assignee
Infex 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 Infex Therapeutics Ltd filed Critical Infex Therapeutics Ltd
Publication of MX2022006109A publication Critical patent/MX2022006109A/es

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    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/46Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
    • C07D207/48Sulfur atoms
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    • 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
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    • 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
    • A61K31/4025Heterocyclic 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 not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • A61K31/403Heterocyclic 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 carbocyclic rings, e.g. carbazole
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    • 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
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    • A61K31/429Thiazoles condensed with heterocyclic ring systems
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    • A61K31/431Compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula, e.g. penicillins, penems containing further heterocyclic rings, e.g. ticarcillin, azlocillin, oxacillin
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    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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    • A61K31/53751,4-Oxazines, e.g. morpholine
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Abstract

Esta invención se refiere a compuestos de la fórmula (I) y método de tratamiento de uso de compuestos; los compuestos de la invención se pueden usar en combinación con agentes antibacterianos para tratar infecciones bacterianas; más específicamente, los compuestos de fórmula (I) se pueden utilizar en combinación con una clase de agentes antibacterianos conocidos como carbapenémicos; los compuestos novedosos de la presente invención son inhibidores de enzimas y más particularmente son inhibidores de metalo-ß-lactamasa. (ver Fórmula).
MX2022006109A 2019-11-20 2020-11-19 Derivados 1-aminosulfonil-2-carboxipirrol como inhibidores de metalo-beta-lactamasa. MX2022006109A (es)

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GBGB1916915.0A GB201916915D0 (en) 2019-11-20 2019-11-20 Compounds
PCT/GB2020/052961 WO2021099793A1 (en) 2019-11-20 2020-11-19 1-aminosulfonyl-2-carboxypyrrole derivatives as metallo-beta-lactamase inhibitors

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MX2022006109A true MX2022006109A (es) 2022-06-14

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US (1) US20230018460A1 (es)
EP (1) EP4061800A1 (es)
JP (1) JP2023502415A (es)
KR (1) KR20220103978A (es)
CN (1) CN114728902A (es)
AU (1) AU2020385668A1 (es)
BR (1) BR112022008938A2 (es)
CA (1) CA3156194A1 (es)
GB (1) GB201916915D0 (es)
IL (1) IL293015A (es)
MX (1) MX2022006109A (es)
WO (1) WO2021099793A1 (es)

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EP3793990B1 (en) * 2018-05-16 2023-07-19 Infex Therapeutics Limited Antibacterial compounds
GB202015885D0 (en) * 2020-10-07 2020-11-18 Infex Therapeutics Ltd Synthesis of pyrrole acid derivatives
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