LT4161927T - Spiro junginiai kaip melanokortino receptoriaus antagonistai ir jų panaudojimas - Google Patents

Spiro junginiai kaip melanokortino receptoriaus antagonistai ir jų panaudojimas

Info

Publication number
LT4161927T
LT4161927T LTEPPCT/IB2021/054970T LTIB2021054970T LT4161927T LT 4161927 T LT4161927 T LT 4161927T LT IB2021054970 T LTIB2021054970 T LT IB2021054970T LT 4161927 T LT4161927 T LT 4161927T
Authority
LT
Lithuania
Prior art keywords
melanocortin
receptor antagonists
spiro compounds
spiro
compounds
Prior art date
Application number
LTEPPCT/IB2021/054970T
Other languages
English (en)
Inventor
Christopher Ryan BUTLER
Michelle Renee GARNSEY
Kevin Alexander OGILVIE
Jana Polivkova
Matthew Forrest Sammons
Aaron Christopher Smith
Qingyi YANG
Original Assignee
Pfizer Inc.
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=76422026&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=LT4161927(T) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Inc. filed Critical Pfizer Inc.
Publication of LT4161927T publication Critical patent/LT4161927T/lt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/12—Heterocyclic 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 three hetero rings
    • C07D471/20—Spiro-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Epidemiology (AREA)
  • Neurology (AREA)
  • Obesity (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Otolaryngology (AREA)
  • Hospice & Palliative Care (AREA)
  • Nutrition Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
LTEPPCT/IB2021/054970T 2020-06-09 2021-06-07 Spiro junginiai kaip melanokortino receptoriaus antagonistai ir jų panaudojimas LT4161927T (lt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202063036798P 2020-06-09 2020-06-09
US202163167271P 2021-03-29 2021-03-29
PCT/IB2021/054970 WO2021250541A1 (en) 2020-06-09 2021-06-07 Spiro compounds as melanocortin 4 receptor antagonists and uses thereof

Publications (1)

Publication Number Publication Date
LT4161927T true LT4161927T (lt) 2024-09-25

Family

ID=76422026

Family Applications (1)

Application Number Title Priority Date Filing Date
LTEPPCT/IB2021/054970T LT4161927T (lt) 2020-06-09 2021-06-07 Spiro junginiai kaip melanokortino receptoriaus antagonistai ir jų panaudojimas

Country Status (34)

Country Link
US (3) US11643412B2 (lt)
EP (1) EP4161927B9 (lt)
JP (1) JP7288554B1 (lt)
KR (1) KR102838870B1 (lt)
CN (1) CN116113635B (lt)
AU (1) AU2021289169B2 (lt)
BR (1) BR112022024527A2 (lt)
CA (1) CA3186348A1 (lt)
CL (1) CL2022003503A1 (lt)
CO (1) CO2022017790A2 (lt)
CR (1) CR20220632A (lt)
DK (1) DK4161927T3 (lt)
DO (1) DOP2022000281A (lt)
EC (1) ECSP22093794A (lt)
ES (1) ES2994968T3 (lt)
FI (1) FI4161927T3 (lt)
HR (1) HRP20241177T1 (lt)
HU (1) HUE068344T2 (lt)
IL (1) IL298891B2 (lt)
LT (1) LT4161927T (lt)
MA (1) MA59895B1 (lt)
MD (1) MD4161927T3 (lt)
MX (1) MX2022015706A (lt)
PE (1) PE20231215A1 (lt)
PH (1) PH12022553296A1 (lt)
PL (1) PL4161927T3 (lt)
PT (1) PT4161927T (lt)
PY (1) PY2146664A (lt)
RS (1) RS65929B9 (lt)
SI (1) SI4161927T1 (lt)
TW (1) TWI843949B (lt)
UY (1) UY39260A (lt)
WO (1) WO2021250541A1 (lt)
ZA (1) ZA202213427B (lt)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11704494B2 (en) * 2019-05-31 2023-07-18 Ab Initio Technology Llc Discovering a semantic meaning of data fields from profile data of the data fields
JP7573009B2 (ja) 2021-12-06 2024-10-24 ファイザー・インク メラノコルチン4受容体アンタゴニストとしてのスピロ化合物およびそれらの使用
WO2024104452A1 (zh) 2022-11-17 2024-05-23 长春金赛药业有限责任公司 Mc4r拮抗剂化合物、药物组合物及其在医药上的应用
WO2024173905A1 (en) * 2023-02-17 2024-08-22 Endevica Bio, Inc. Methods of preventing and/or treating side effects associated with anti-cancer agents using non-naturally occurring melanocortin analogs with anti-gdf-15 antibodies
WO2024255412A1 (zh) * 2023-06-14 2024-12-19 广州必贝特医药股份有限公司 螺杂环化合物及其应用
AU2024312554A1 (en) 2023-06-19 2025-12-18 F. Hoffmann-La Roche Ag Process for the preparation of a chiral pyrrolo triazole alcohol

Family Cites Families (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3773919A (en) 1969-10-23 1973-11-20 Du Pont Polylactide-drug mixtures
CA1146866A (en) 1979-07-05 1983-05-24 Yamanouchi Pharmaceutical Co. Ltd. Process for the production of sustained release pharmaceutical composition of solid medical material
US4485045A (en) 1981-07-06 1984-11-27 Research Corporation Synthetic phosphatidyl cholines useful in forming liposomes
US4544545A (en) 1983-06-20 1985-10-01 Trustees University Of Massachusetts Liposomes containing modified cholesterol for organ targeting
DE3438830A1 (de) 1984-10-23 1986-04-30 Rentschler Arzneimittel Nifedipin enthaltende darreichungsform und verfahren zu ihrer herstellung
US5013556A (en) 1989-10-20 1991-05-07 Liposome Technology, Inc. Liposomes with enhanced circulation time
ES2111065T5 (es) 1991-04-16 2005-06-16 Nippon Shinyaku Company, Limited Procedimiento para producir una dispersion solida.
US5340591A (en) 1992-01-24 1994-08-23 Fujisawa Pharmaceutical Co., Ltd. Method of producing a solid dispersion of the sparingly water-soluble drug, nilvadipine
JP3265680B2 (ja) 1992-03-12 2002-03-11 大正製薬株式会社 経口製剤用組成物
US5612359A (en) 1994-08-26 1997-03-18 Bristol-Myers Squibb Company Substituted biphenyl isoxazole sulfonamides
DE19504832A1 (de) 1995-02-14 1996-08-22 Basf Ag Feste Wirkstoff-Zubereitungen
TW536540B (en) 1997-01-30 2003-06-11 Bristol Myers Squibb Co Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe
PT901786E (pt) 1997-08-11 2007-08-07 Pfizer Prod Inc Disperções farmacêuticas sólidas com biodisponibilidade melhorada
ID26984A (id) 1998-07-06 2001-02-22 Bristol Myers Squibb Co Senyawa-senyawa sulfonamida sebagai antagonis reseptor angiotensin endotelin ganda
WO2004081643A1 (en) 2002-12-20 2004-09-23 Kaiser Aerospace & Electronics Corp. Lenslet array with polarization conversion
EP1460073A1 (en) 2003-03-20 2004-09-22 MyoContract Ltd. Substituted piperidine and piperazine derivatives as melanocortin-4 receptor modulators
EA011086B9 (ru) 2004-05-12 2012-08-30 Пфайзер Продактс Инк. Производные пролина и их применение в качестве ингибиторов дипептидилпептидазы iv
KR20080048502A (ko) * 2005-09-29 2008-06-02 머크 앤드 캄파니 인코포레이티드 멜라노코르틴-4 수용체 조절제로서의 아실화스피로피페리딘 유도체
AU2007219236B2 (en) 2006-02-23 2012-06-21 Pfizer Limited Melanocortin type 4 receptor agonist piperidinoylpyrrolidines
EP2003131A4 (en) * 2006-04-04 2009-12-16 Taisho Pharmaceutical Co Ltd AMINOPYRROLIDINE COMPOUND
EP2010520B1 (en) 2006-04-20 2012-09-12 Pfizer Products Inc. Heterobicyclic amides for the prevention and treatment of glucokinase-mediated diseases
CA2729581A1 (en) 2008-07-29 2010-02-04 Pfizer Inc. Fluorinated heteroaryls
ES2380408T3 (es) 2008-08-28 2012-05-11 Pfizer Inc. Derivados de dioxa-biciclo[3.2.1]octano-2,3,4-triol
FR2937868B1 (fr) 2008-11-04 2010-11-05 Galderma Res & Dev Composes antagonistes des recepteurs de la melanocortine, leur procede de preparation et leur utilisation en medecine humaine ainsi qu'en cosmetique
EP2210885A1 (en) 2009-01-14 2010-07-28 Santhera Pharmaceuticals (Schweiz) AG Substituted heteroarylpiperidine derivatives as melanocortin-4 receptor modulators
WO2010096854A1 (en) 2009-02-27 2010-09-02 Mimetica Pty Ltd Methods of modulating the activity of the mc3 and/or mc4 receptors and treatment of conditions related to these receptors
EP2406230A1 (en) 2009-03-11 2012-01-18 Pfizer Inc. Substituted indazole amides and their use as glucokinase activators
WO2010103437A1 (en) 2009-03-11 2010-09-16 Pfizer Inc. Benzofuranyl derivatives used as glucokinase inhibitors
CA2754523A1 (en) 2009-03-20 2010-09-23 Pfizer Inc. 3-oxa-7-azabicyclo[3.3.1]nonanes
CA2759843A1 (en) 2009-05-08 2010-11-10 Pfizer Inc. Gpr 119 modulators
EP2427448A1 (en) 2009-05-08 2012-03-14 Pfizer Inc. Gpr 119 modulators
GEP20135907B (en) 2009-06-05 2013-08-12 Pfizer L-(piperidin-4-yl)-pyrazole derivatives as gpr 119 modulators
WO2011005611A1 (en) 2009-07-09 2011-01-13 Merck Sharp & Dohme Corp. Neuromedin u receptor agonists and uses thereof
WO2016168660A1 (en) 2015-04-17 2016-10-20 Forma Therapeutics, Inc. 3-spiro-7-hydroxamic acid tetralins as hdac inhibitors
AR109179A1 (es) 2016-08-19 2018-11-07 Pfizer Inhibidores de diacilglicerol aciltransferasa 2
TR201618240A2 (tr) 2016-12-09 2017-01-23 Ahmet Elibol Aort kapak koruyucu kök replasman ameli̇yatlarinda kullanilan ölçüm ve si̇mülasyon terti̇bati
WO2018109607A1 (en) 2016-12-16 2018-06-21 Pfizer Inc. Glp-1 receptor agonists and uses thereof
MX2019008626A (es) * 2017-01-20 2019-09-19 Pfizer Derivados de 1,1,1-trifluoro-3-hidroxipropan-2-ilcarbamato como inhibidores de monoacilglicerol lipasa (magl).
NL2019545B1 (en) 2017-09-14 2019-03-27 Univ Delft Tech Instrument for minimal invasive surgical operations, comprising a rod or catheter and a tip mounted on the rod or catheter with an elastically deformable element

Also Published As

Publication number Publication date
MD4161927T2 (ro) 2024-11-30
DK4161927T3 (da) 2024-08-26
CL2022003503A1 (es) 2023-09-01
WO2021250541A1 (en) 2021-12-16
TW202204357A (zh) 2022-02-01
JP7288554B1 (ja) 2023-06-07
ES2994968T3 (en) 2025-02-04
MX2022015706A (es) 2023-01-24
PY2146664A (es) 2022-10-12
US12187727B2 (en) 2025-01-07
DOP2022000281A (es) 2023-01-15
JP2023525394A (ja) 2023-06-15
ZA202213427B (en) 2023-07-26
US20230174532A1 (en) 2023-06-08
MA59895B1 (fr) 2024-10-31
KR20230011968A (ko) 2023-01-25
SI4161927T1 (sl) 2024-11-29
EP4161927A1 (en) 2023-04-12
IL298891B2 (en) 2026-07-01
CN116113635A (zh) 2023-05-12
UY39260A (es) 2022-01-31
HUE068344T2 (hu) 2024-12-28
CR20220632A (es) 2023-01-23
US20230019853A1 (en) 2023-01-19
EP4161927B9 (en) 2024-11-06
MD4161927T3 (ro) 2025-02-28
ECSP22093794A (es) 2023-01-31
CA3186348A1 (en) 2021-12-16
RS65929B9 (sr) 2025-02-28
PL4161927T3 (pl) 2024-11-18
EP4161927B1 (en) 2024-08-07
FI4161927T3 (fi) 2024-10-03
AU2021289169B2 (en) 2024-01-04
US20250084084A1 (en) 2025-03-13
AU2021289169A1 (en) 2023-01-19
IL298891A (en) 2023-02-01
HRP20241177T1 (hr) 2024-11-22
US11643412B2 (en) 2023-05-09
BR112022024527A2 (pt) 2022-12-27
CN116113635B (zh) 2025-03-18
CO2022017790A2 (es) 2022-12-20
PE20231215A1 (es) 2023-08-17
RS65929B1 (sr) 2024-10-31
IL298891B1 (en) 2026-03-01
TWI843949B (zh) 2024-06-01
PH12022553296A1 (en) 2024-06-24
PT4161927T (pt) 2024-10-08
KR102838870B1 (ko) 2025-07-24

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