SI3762380T1 - Receptor agonisti fenilpirolidinon peptida 2 - Google Patents

Receptor agonisti fenilpirolidinon peptida 2

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Publication number
SI3762380T1
SI3762380T1 SI201930151T SI201930151T SI3762380T1 SI 3762380 T1 SI3762380 T1 SI 3762380T1 SI 201930151 T SI201930151 T SI 201930151T SI 201930151 T SI201930151 T SI 201930151T SI 3762380 T1 SI3762380 T1 SI 3762380T1
Authority
SI
Slovenia
Prior art keywords
phenylpyrrolidinone
receptor agonists
formyl peptide
formyl
peptide
Prior art date
Application number
SI201930151T
Other languages
English (en)
Slovenian (sl)
Inventor
Pravin Sudhakar Shirude
Vishweshwaraiah Baligar
Balaji Seshadri
Amit Kumar Chattopadhyay
Nicholas R. Wurtz
Ellen K. Kick
Original Assignee
Bristol-Myers Squibb Company
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 Company filed Critical Bristol-Myers Squibb Company
Publication of SI3762380T1 publication Critical patent/SI3762380T1/sl

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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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    • 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
    • A61K31/4015Heterocyclic 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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    • A61K31/33Heterocyclic 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
    • A61K31/44Non 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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    • A61K31/33Heterocyclic compounds
    • 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
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
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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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    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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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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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
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SI201930151T 2018-03-05 2019-03-04 Receptor agonisti fenilpirolidinon peptida 2 SI3762380T1 (sl)

Applications Claiming Priority (3)

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
EP19711769.0A EP3762380B1 (en) 2018-03-05 2019-03-04 Phenylpyrrolidinone formyl peptide 2 receptor agonists

Publications (1)

Publication Number Publication Date
SI3762380T1 true SI3762380T1 (sl) 2022-09-30

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SI201930151T SI3762380T1 (sl) 2018-03-05 2019-03-04 Receptor agonisti fenilpirolidinon peptida 2

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US (3) US10676431B2 (enExample)
EP (2) EP3981767A1 (enExample)
JP (1) JP7155276B2 (enExample)
KR (1) KR102803660B1 (enExample)
CN (1) CN111868052B (enExample)
AR (1) AR114429A1 (enExample)
AU (1) AU2019232704B2 (enExample)
BR (1) BR112020017744A2 (enExample)
CA (1) CA3092927A1 (enExample)
CL (1) CL2020002224A1 (enExample)
CY (1) CY1124985T1 (enExample)
DK (1) DK3762380T3 (enExample)
EA (1) EA202092094A1 (enExample)
ES (1) ES2904483T3 (enExample)
HR (1) HRP20220118T1 (enExample)
HU (1) HUE058044T2 (enExample)
IL (1) IL277044B2 (enExample)
LT (1) LT3762380T (enExample)
MX (1) MX2020009000A (enExample)
MY (1) MY204384A (enExample)
PE (1) PE20210046A1 (enExample)
PL (1) PL3762380T3 (enExample)
PT (1) PT3762380T (enExample)
RS (1) RS62833B1 (enExample)
SG (1) SG11202008504SA (enExample)
SI (1) SI3762380T1 (enExample)
SM (1) SMT202200067T1 (enExample)
TW (1) TWI804585B (enExample)
WO (1) WO2019173182A1 (enExample)
ZA (1) ZA202006115B (enExample)

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KR20220024551A (ko) * 2019-06-18 2022-03-03 브리스톨-마이어스 스큅 컴퍼니 비아릴 디알킬 포스핀 옥시드 fpr2 효능제
JP7771157B2 (ja) * 2020-07-09 2025-11-17 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
EP4196471A1 (en) * 2020-08-12 2023-06-21 Bristol-Myers Squibb Company Oxopyrrolidine urea fpr2 agonists
US20240300973A1 (en) * 2021-01-21 2024-09-12 Biofront Therapeutics (Beijing) Co., Ltd. Modulators of fpr1 and methods of using the same
WO2022155859A1 (en) * 2021-01-21 2022-07-28 Beijing Tiantan Hospital Modulators of fpr1 and methods of using the same
EP4074317A1 (en) 2021-04-14 2022-10-19 Bayer AG Phosphorus derivatives as novel sos1 inhibitors
EP4483714A3 (en) 2021-12-15 2025-04-23 Adama Agan Ltd. Compounds useful for the preparation of various agrochemicals and markers thereof
US20250205164A1 (en) 2022-05-27 2025-06-26 Asahi Group Holdings, Ltd. Fpr2 agonist containing outer membrane vesicles derived from lactic acid bacterium
EP4602049A1 (en) 2022-10-13 2025-08-20 Bayer Aktiengesellschaft Sos1 inhibitors
WO2024220453A1 (en) * 2023-04-18 2024-10-24 Bristol-Myers Squibb Company Pyrrolidinone urea fpr2 agonists
WO2024220487A1 (en) * 2023-04-18 2024-10-24 Bristol-Myers Squibb Company Carbocyclic phenylpyrrolidinone urea fpr2 agonists
CN121013837A (zh) * 2023-04-18 2025-11-25 百时美施贵宝公司 吡咯烷酮脲fpr2激动剂
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