MX2020009000A - Agonistas de fenilpirrolidinona del receptor 2 de formil peptido. - Google Patents

Agonistas de fenilpirrolidinona del receptor 2 de formil peptido.

Info

Publication number
MX2020009000A
MX2020009000A MX2020009000A MX2020009000A MX2020009000A MX 2020009000 A MX2020009000 A MX 2020009000A MX 2020009000 A MX2020009000 A MX 2020009000A MX 2020009000 A MX2020009000 A MX 2020009000A MX 2020009000 A MX2020009000 A MX 2020009000A
Authority
MX
Mexico
Prior art keywords
receptor agonists
formyl peptide
phenylpyrrolidinone
compounds
disclosure
Prior art date
Application number
MX2020009000A
Other languages
English (en)
Inventor
Ellen K Kick
Nicholas R Wurtz
Pravin Sudhakar Shirude
Vishweshwaraiah Baligar
Balaji Seshadri
Amit Kumar Chattopadhyay
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of MX2020009000A publication Critical patent/MX2020009000A/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
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2732-Pyrrolidones 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 other ring carbon atoms
    • C07D207/277Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/14Nitrogen atoms not forming part of a nitro radical
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    • 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
    • A61K31/4015Heterocyclic 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 having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
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    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
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    • A61P9/00Drugs for disorders of the cardiovascular system
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    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07F9/65586Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system at least one of the hetero rings does not contain nitrogen as ring hetero atom

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  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • Cardiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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  • Pyrrole Compounds (AREA)
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Abstract

La descripción se refiere a compuestos de la Fórmula (II), que son agonistas del receptor 2 de formil péptido (FPR2) y/o agonistas del receptor 1 de formil péptido (FPR1). La descripción también proporciona composiciones y métodos de uso de los compuestos, por ejemplo, para el tratamiento de ateroesclerosis, insuficiencia cardíaca, enfermedad pulmonar obstructiva crónica (EPOC) y enfermedades relacionadas. Ver formula.
MX2020009000A 2018-03-05 2019-03-04 Agonistas de fenilpirrolidinona del receptor 2 de formil peptido. MX2020009000A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862638556P 2018-03-05 2018-03-05
PCT/US2019/020493 WO2019173182A1 (en) 2018-03-05 2019-03-04 Phenylpyrrolidinone formyl peptide 2 receptor agonists

Publications (1)

Publication Number Publication Date
MX2020009000A true MX2020009000A (es) 2020-10-05

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Family Applications (1)

Application Number Title Priority Date Filing Date
MX2020009000A MX2020009000A (es) 2018-03-05 2019-03-04 Agonistas de fenilpirrolidinona del receptor 2 de formil peptido.

Country Status (28)

Country Link
US (3) US10676431B2 (es)
EP (2) EP3981767A1 (es)
JP (1) JP7155276B2 (es)
KR (1) KR20200128709A (es)
CN (1) CN111868052B (es)
AR (1) AR114429A1 (es)
AU (1) AU2019232704B2 (es)
BR (1) BR112020017744A2 (es)
CA (1) CA3092927A1 (es)
CL (1) CL2020002224A1 (es)
CY (1) CY1124985T1 (es)
DK (1) DK3762380T3 (es)
EA (1) EA202092094A1 (es)
ES (1) ES2904483T3 (es)
HR (1) HRP20220118T1 (es)
HU (1) HUE058044T2 (es)
IL (1) IL277044B2 (es)
LT (1) LT3762380T (es)
MX (1) MX2020009000A (es)
PE (1) PE20210046A1 (es)
PL (1) PL3762380T3 (es)
PT (1) PT3762380T (es)
RS (1) RS62833B1 (es)
SG (1) SG11202008504SA (es)
SI (1) SI3762380T1 (es)
TW (1) TWI804585B (es)
WO (1) WO2019173182A1 (es)
ZA (1) ZA202006115B (es)

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ES2869129T3 (es) 2017-06-09 2021-10-25 Bristol Myers Squibb Co Agonistas de piperidinona del receptor 2 de péptidos formilados
WO2018227067A1 (en) 2017-06-09 2018-12-13 Bristol-Myers Squibb Company Cyclopropyl urea formyl peptide 2 receptor and formyl peptide 1 receptor agonists
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JP7155276B2 (ja) 2018-03-05 2022-10-18 ブリストル-マイヤーズ スクイブ カンパニー フェニルピロリジノンホルミルペプチド2受容体アゴニスト
JP2023533037A (ja) * 2020-07-09 2023-08-01 ブリストル-マイヤーズ スクイブ カンパニー オキソピロリジン fpr2アゴニスト
US20230303513A1 (en) * 2020-08-12 2023-09-28 Bristol-Myers Squibb Company Oxopyrrolidine urea fpr2 agonists
EP4281452A1 (en) * 2021-01-21 2023-11-29 Beijing Tiantan Hospital Modulators of fpr1 and methods of using the same
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