MA54758A - Inhibiteurs de pcsk9 et leurs procédés d'utilisation - Google Patents

Inhibiteurs de pcsk9 et leurs procédés d'utilisation

Info

Publication number
MA54758A
MA54758A MA054758A MA54758A MA54758A MA 54758 A MA54758 A MA 54758A MA 054758 A MA054758 A MA 054758A MA 54758 A MA54758 A MA 54758A MA 54758 A MA54758 A MA 54758A
Authority
MA
Morocco
Prior art keywords
methods
pcsk9 inhibitors
pcsk9
inhibitors
Prior art date
Application number
MA054758A
Other languages
English (en)
Inventor
Doug Daniels
Brian K Hubbard
Virendar Kaushik
Michael H Serrano-Wu
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of MA54758A publication Critical patent/MA54758A/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
    • C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
    • C12N9/6424—Serine endopeptidases (3.4.21)
    • 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
    • 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
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61K31/54—Heterocyclic 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
    • A61K31/541—Non-condensed thiazines containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
    • C07D235/30—Nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/42—One nitrogen atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
    • C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
    • C07D253/06—1,2,4-Triazines
    • C07D253/065—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
    • C07D253/07—1,2,4-Triazines having three 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
    • C07D253/075—Two hetero atoms, in positions 3 and 5
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
    • C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
    • C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles 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 in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D471/02—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 two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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
    • C07D471/02—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 two hetero rings
    • C07D471/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10—Spiro-condensed systems
    • C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/0004—Oxidoreductases (1.)
    • C12N9/0012—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • Biomedical Technology (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
MA054758A 2019-01-18 2020-01-16 Inhibiteurs de pcsk9 et leurs procédés d'utilisation MA54758A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201962794239P 2019-01-18 2019-01-18

Publications (1)

Publication Number Publication Date
MA54758A true MA54758A (fr) 2022-04-27

Family

ID=71608564

Family Applications (1)

Application Number Title Priority Date Filing Date
MA054758A MA54758A (fr) 2019-01-18 2020-01-16 Inhibiteurs de pcsk9 et leurs procédés d'utilisation

Country Status (16)

Country Link
US (2) US11603523B2 (fr)
EP (2) EP3911640B1 (fr)
JP (2) JP2022518016A (fr)
KR (2) KR20210116549A (fr)
CN (1) CN113412258A (fr)
AU (3) AU2020209216A1 (fr)
BR (1) BR112021013924A2 (fr)
CA (1) CA3125767A1 (fr)
EA (1) EA202191890A1 (fr)
IL (1) IL284661A (fr)
MA (1) MA54758A (fr)
MX (2) MX2021008661A (fr)
MY (1) MY210469A (fr)
SG (1) SG11202107615TA (fr)
TW (1) TWI921300B (fr)
WO (1) WO2020150474A1 (fr)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112021013924A2 (pt) 2019-01-18 2021-09-21 Astrazeneca Ab Inibidores de pcsk9 e métodos de uso do mesmo
WO2020150473A2 (fr) * 2019-01-18 2020-07-23 Dogma Therapeutics, Inc. Inhibiteurs de pcsk9 et leurs procédés d'utilisation
CN113248501B (zh) * 2021-06-17 2021-10-08 南京韦尔优众医药有限公司 Cly系列化合物及其制备方法和制备药物的用途
CN113735846A (zh) * 2021-10-11 2021-12-03 河北师范大学 一种苯并噻唑衍生物及其医药用途
WO2023084449A1 (fr) * 2021-11-12 2023-05-19 Novartis Ag Dérivés diaminocyclopentylpyridines pour le traitement d'une maladie ou d'un trouble
TW202329937A (zh) 2021-12-03 2023-08-01 美商英塞特公司 雙環胺ck12抑制劑
US12084453B2 (en) 2021-12-10 2024-09-10 Incyte Corporation Bicyclic amines as CDK12 inhibitors
US20240217951A1 (en) * 2022-09-23 2024-07-04 Astrazeneca Ab Pcsk9 inhibitors and methods of use thereof
US20240228469A1 (en) 2022-09-23 2024-07-11 Astrazeneca Ab Pcsk9 inhibitors and methods of use thereof
CN121913991A (zh) * 2022-10-14 2026-04-24 上海翰森生物医药科技有限公司 含氮杂环类衍生物抑制剂、其制备方法和应用
CN119264042A (zh) * 2023-07-04 2025-01-07 上海翰森生物医药科技有限公司 含环戊烷类衍生物抑制剂、其制备方法和应用
CN121443616A (zh) 2023-07-27 2026-01-30 上海拓界生物医药科技有限公司 二氨基环戊基取代的杂芳基衍生物及其用途和制备方法
TW202547505A (zh) 2024-02-05 2025-12-16 瑞典商阿斯特捷利康公司 包含azd0780之醫藥組合物
TW202545529A (zh) 2024-02-05 2025-12-01 瑞典商阿斯特捷利康公司 組合療法
WO2025183455A1 (fr) * 2024-02-29 2025-09-04 재단법인 대구경북첨단의료산업진흥재단 Dérivés de benzoxazole utilisés en tant qu'inhibiteur de pcsk9
TW202539678A (zh) * 2024-03-20 2025-10-16 瑞典商阿斯特捷利康公司 Pcsk9抑制劑及其使用方法
WO2025214500A1 (fr) * 2024-04-12 2025-10-16 上海翰森生物医药科技有限公司 Forme cristalline de base libre d'un dérivé hétérocyclique contenant de l'azote, sel d'acide et forme cristalline de celui-ci, procédé de préparation correspondant et utilisation associée
TW202612699A (zh) 2024-05-16 2026-04-01 瑞典商阿斯特捷利康公司 組合療法
WO2026021380A1 (fr) * 2024-07-22 2026-01-29 深圳信立泰药业股份有限公司 Composé à double cible pcsk9 et hmg-coa et son utilisation
WO2026026878A1 (fr) * 2024-07-30 2026-02-05 成都施贝康生物医药科技有限公司 Inhibiteur dérivé hétérocyclique, sa préparation et son utilisation
WO2026086805A1 (fr) * 2024-10-23 2026-04-30 深圳信立泰药业股份有限公司 Composé bicyclique de pcsk9 et hmg-coa, sa préparation et son utilisation
WO2026092600A1 (fr) * 2024-10-31 2026-05-07 石药集团中奇制药技术(石家庄)有限公司 Composé hétérocyclique azoté et son utilisation
WO2026093543A1 (fr) 2024-11-01 2026-05-07 Astrazeneca Ab Traitement combiné par agoniste du glp1r et inhibiteur de pcsk9
WO2026092659A1 (fr) * 2024-11-01 2026-05-07 盛睿泽华医药科技(苏州)有限公司 Composé polycyclique, son procédé de préparation et son utilisation
WO2026131688A2 (fr) * 2024-12-16 2026-06-25 Astrazeneca Ab Formes cristallines et procédés de synthèse
WO2026145737A1 (fr) * 2025-01-03 2026-07-09 江苏豪森药业集团有限公司 Sel de classe de dérivés hétérocycliques contenant de l'azote et sa forme cristalline, procédé de préparation correspondant et utilisation associée
WO2026158426A1 (fr) * 2025-01-23 2026-07-30 江苏恒瑞医药股份有限公司 Formes cristallines d'un dérivé hétéroaryle substitué par diaminocyclopentyle et leur procédé de préparation
WO2026158425A1 (fr) * 2025-01-23 2026-07-30 江苏恒瑞医药股份有限公司 Sel pharmaceutiquement acceptable d'un dérivé hétéroaryle substitué par diaminocyclopentyle, forme cristalline de celui-ci et utilisation de celui-ci
WO2026158633A1 (fr) * 2025-01-27 2026-07-30 乐普(北京)医疗器械股份有限公司 Inhibiteur de petite molécule à composé hétérocyclique azoté et utilisation de celui-ci

Family Cites Families (197)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4172896A (en) 1978-06-05 1979-10-30 Dainippon Pharmaceutical Co., Ltd. Methane-sulfonamide derivatives, the preparation thereof and composition comprising the same
GB9217295D0 (en) 1992-08-14 1992-09-30 Wellcome Found Controlled released tablets
US5541231A (en) 1993-07-30 1996-07-30 Glaxo Wellcome Inc. Stabilized Pharmaceutical
US5358970A (en) 1993-08-12 1994-10-25 Burroughs Wellcome Co. Pharmaceutical composition containing bupropion hydrochloride and a stabilizer
GB9315856D0 (en) 1993-07-30 1993-09-15 Wellcome Found Stabilized pharmaceutical
CA2192203A1 (fr) 1994-06-17 1995-12-28 Werner Hofheinz Derives n,n'-bis(quinolin-4-yle)-diamine, leur preparation et leur utilisation en tant qu'antipaludeens
AU4515696A (en) 1994-12-12 1996-07-03 Merck & Co., Inc. Substituted 2-aminopyridines as inhibitors of nitric oxide synthase
GB9526546D0 (en) 1995-12-23 1996-02-28 Pfizer Ltd Compounds useful in therapy
SE9603285D0 (sv) 1996-09-10 1996-09-10 Astra Ab New compounds
US5874438A (en) 1996-10-11 1999-02-23 Bayer Aktiengesellschaft 2,2'-bridged bis-2,4-diaminoquinazolines
DE69818675T2 (de) 1997-07-29 2004-07-29 Alcon Laboratories, Inc., Fort Worth Galaktomannanpolymere und borat enthaltende augenarzneimittel
AU2483599A (en) 1998-01-29 1999-08-16 Sepracor, Inc. Pharmaceutical uses of optically pure (-)-bupropion
US8889112B2 (en) 1999-09-16 2014-11-18 Ocularis Pharma, Llc Ophthalmic formulations including selective alpha 1 antagonists
US20040138284A1 (en) 2000-02-11 2004-07-15 Matthias Wiesner Indol-3-yl derivatives
GB0014022D0 (en) 2000-06-08 2000-08-02 Novartis Ag Organic compounds
WO2002020500A2 (fr) 2000-09-01 2002-03-14 Icos Corporation Substances potentialisant un traitement anticancereux et methodes a cet effet
EP1217000A1 (fr) 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Inhibiteurs du factor Xa et factor VIIa
AU2002341693B2 (en) 2001-09-21 2008-05-29 Bristol-Myers Squibb Holdings Ireland Unlimited Company Lactam-containing compounds and derivatives thereof as factor Xa inhibitors
JP2005519895A (ja) 2002-01-18 2005-07-07 ファルマシア・コーポレーション P38阻害剤としての置換ピリダジノン
WO2003099276A1 (fr) 2002-05-10 2003-12-04 Bristol-Myers Squibb Company Derives cycloalkyles 1,1-disubstitues utilises en tant qu'inhibiteurs du facteur xa
WO2004017920A2 (fr) 2002-08-23 2004-03-04 University Of Connecticut Nouveaux cannabinoides biphenyle et de type biphenyle
US7262200B2 (en) 2002-10-25 2007-08-28 Vertex Pharmaceuticals Incorporated Indazolinone compositions useful as kinase inhibitors
CA2510793A1 (fr) 2002-12-20 2004-07-15 Bayer Pharmaceuticals Corporation Derives d'acide acetique d'indane et leur utilisation en tant qu'agents pharmaceutiques et intermediaires, et procede de preparation correspondant
US20050197350A1 (en) 2003-03-31 2005-09-08 Taisho Pharmaceutical Co., Ltd. Novel quinoline, tetrahydroquinazoline, and pyrimidine derivatives and methods of treatment related to the use thereof
WO2004094471A2 (fr) 2003-04-22 2004-11-04 Avanir Pharmaceuticals Mediateurs du transport inverse du cholesterol pour le traitement de l'hypercholesterolemie
US6933289B2 (en) 2003-07-01 2005-08-23 Allergan, Inc. Inhibition of irritating side effects associated with use of a topical ophthalmic medication
EP1654002B2 (fr) 2003-08-07 2014-01-29 Allergan, Inc. Compositions d'administration d'agents therapeutiques dans les yeux
US20050059744A1 (en) 2003-09-12 2005-03-17 Allergan, Inc. Methods and compositions for the treatment of pain and other alpha 2 adrenergic-mediated conditions
MXJL06000069A (es) * 2004-06-09 2007-04-10 Avanir Pharmaceuticals Derivados heterociclicos para el tratamiento de hiperlipidemia y enfermedades relacionadas.
EP2316458A1 (fr) 2004-09-20 2011-05-04 Xenon Pharmaceuticals Inc. Derives de pyridazine destines a l'inhibition du desaturase-coa-stearoyl de l'humain
JP2008514546A (ja) 2004-09-30 2008-05-08 大正製薬株式会社 ピリジン誘導体及びその使用に関連する治療法
US7381732B2 (en) 2004-10-26 2008-06-03 Bristol-Myers Squibb Company Pyrazolobenzamides and derivatives as factor Xa inhibitors
EP1814856A1 (fr) 2004-11-12 2007-08-08 Galapagos N.V. Composés hétéroaromatiques de l'azote qui se lient au site actif d'enzymes de type protéines kinases
GB0428082D0 (en) 2004-12-22 2005-01-26 Welcome Trust The Ltd Therapeutic compounds
CA2598043A1 (fr) 2005-02-25 2006-08-31 Rigel Pharmaceuticals, Inc. Benzisothiazoles utiles dans le traitement ou la prevention de l'infection a vhc
WO2006126081A2 (fr) 2005-05-24 2006-11-30 Pharmacia & Upjohn Company Llc Pyridine [2,3-b] pyrazinones
EA015890B1 (ru) 2005-06-14 2011-12-30 Тайджен Байотекнолоджи Ко. Лтд. Производные пиримидина
US20070203236A1 (en) 2006-01-11 2007-08-30 Smith Jeffrey W Novel antagonists of the human fatty acid synthase thioesterase
JP2007291087A (ja) 2006-03-29 2007-11-08 Taisho Pharmaceut Co Ltd ピリジン誘導体及びその使用に関連する治療法
EP2502918B1 (fr) 2006-07-25 2015-03-25 Cephalon, Inc. Dérivés de pyridazinone
WO2008046216A1 (fr) 2006-10-18 2008-04-24 Methylgene, Inc. Inhibiteurs de kinase et leurs utilisations
EP2121619A2 (fr) 2006-11-24 2009-11-25 AC Immune S.A. Nouveaux composés destinés au traitement de maladies associés à des protéines amyloïdes ou de type amyloïde
WO2008072963A1 (fr) 2006-12-13 2008-06-19 Givaudan Nederland Services B.V. Dérivé de modulation de saveur d'acide carboxylique et de purine, de pyrimidine, de nucléoside ou de nucléotide
CN102232088A (zh) * 2007-10-26 2011-11-02 先灵公司 用于治疗脂类和胆固醇疾病的抗pcsk9及方法
US7803809B2 (en) 2008-11-12 2010-09-28 Amgen Inc. Substituted pyrano [2,3-b] pyridinamine compounds as beta-secretase modulators and methods of use
EP2296653B1 (fr) 2008-06-03 2016-01-27 Intermune, Inc. Composés et procédés de traitement des troubles inflammatoires et fibrotiques
WO2010048149A2 (fr) 2008-10-20 2010-04-29 Kalypsys, Inc. Modulateurs hétérocycliques de gpr119 pour le traitement d'une maladie
CN107233337A (zh) 2009-04-29 2017-10-10 阿马里纳药物爱尔兰有限公司 含有epa和心血管剂的药物组合物以及使用其的方法
WO2011008931A2 (fr) 2009-07-15 2011-01-20 Cystic Fibrosis Foundation Therapeutics, Inc. Composés arylpyrimidines et thérapie de combinaison comprenant ceux-ci pour traiter une mucoviscidose et des troubles apparentés
RU2012104214A (ru) 2009-08-05 2013-09-10 Верситек Лимитед Противовирусные соединения и способы их получения и применения
US8952037B2 (en) 2010-05-13 2015-02-10 Amgen Inc. Heteroaryloxycarbocyclyl compounds as PDE10 inhibitors
WO2011147199A1 (fr) 2010-05-28 2011-12-01 Versitech Limited Composés et procédés pour le traitement d'infections virales
KR20130111512A (ko) 2010-06-04 2013-10-10 코와 가부시키가이샤 광학 활성 디벤질아민 유도체 및 그의 제조 방법
CA2802952A1 (fr) 2010-06-24 2011-12-29 Arisaph Pharmaceuticals, Inc. Mimetiques de niacine et leurs procedes d'utilisation
AU2011270719B2 (en) 2010-06-24 2015-09-24 Arisaph Pharmaceuticals, Inc. Niacin mimetics, and methods of use thereof
WO2012009649A1 (fr) 2010-07-16 2012-01-19 Anderson Gaweco Inhibiteurs mif et leurs utilisations
WO2012016133A2 (fr) 2010-07-29 2012-02-02 President And Fellows Of Harvard College Inhibiteurs de la ros1 kinase pour le traitement de glioblastome et d'autres cancers déficients en p53
EP2655334B1 (fr) 2010-12-22 2018-10-03 Eutropics Pharmaceuticals, Inc. Compositions et méthodes utilisables en vue du traitement de maladies
WO2012101062A1 (fr) 2011-01-28 2012-08-02 Novartis Ag Composés bi-hétéroaryles substitués en tant qu'inhibiteurs de cdk9 et leurs utilisations
US9133164B2 (en) 2011-04-13 2015-09-15 Innov88 Llc MIF inhibitors and their uses
AU2012258618B2 (en) 2011-05-26 2017-05-25 Sunovion Pharmaceuticals Inc. Metabotropic glutamate receptors 5 modulators and methods of use thereof
US8815909B2 (en) 2011-07-18 2014-08-26 Bristol-Myers Squibb Company Diaminocyclohexane compounds and uses thereof
JP5741850B2 (ja) 2011-09-13 2015-07-01 コニカミノルタ株式会社 光学フィルム、それを含む偏光板および液晶表示装置
JP6295205B2 (ja) 2012-01-06 2018-03-14 ジェムファイア セラピューティクス インクGemphire Therapeutics Inc. 心血管疾患のリスクを低減する方法
TW201348231A (zh) 2012-02-29 2013-12-01 Amgen Inc 雜雙環化合物
US9567316B2 (en) 2012-03-07 2017-02-14 The Mclean Hospital Corporation Aminoquinoline derivatives and uses thereof
WO2013137371A1 (fr) 2012-03-15 2013-09-19 興和株式会社 Nouveau composé pyrimidine et médicament comprenant celui-ci
US9658211B2 (en) 2012-04-18 2017-05-23 Hemoshear, Llc In vitro model for pathological or physiologic conditions
US9255154B2 (en) 2012-05-08 2016-02-09 Alderbio Holdings, Llc Anti-PCSK9 antibodies and use thereof
WO2013177536A2 (fr) 2012-05-25 2013-11-28 Catabasis Pharmaceuticals, Inc. Méthodes de diminution de la proprotéine convertase subtilisine/kexine de type 9 (pcsk9)
US9434695B2 (en) 2012-07-18 2016-09-06 Sunshine Lake Pharma Co., Ltd Nitrogenous heterocyclic derivatives and their application in drugs
UA116217C2 (uk) 2012-10-09 2018-02-26 Санофі Пептидна сполука як подвійний агоніст рецепторів glp1-1 та глюкагону
AR092924A1 (es) 2012-10-09 2015-05-06 Sanofi Sa Derivados de pirrolidinona como moduladores de gpr119 para el tratamiento de diabetes, obesidad, dislipidemia y trastornos relacionados
HUE035803T2 (en) 2012-12-21 2018-05-28 Sanofi Sa Dual GLP1 / GIP or trigonal GLP1 / GIP / glucagon agonists
US10059671B2 (en) 2013-02-04 2018-08-28 Prexton Therapeutics Sa Positive allosteric modulators of mGluR3
TWI644899B (zh) 2013-02-04 2018-12-21 健生藥品公司 Flap調節劑
RS62649B1 (sr) 2013-03-12 2021-12-31 Vertex Pharma Inhibitori dnk-pk
CN105143203A (zh) 2013-04-17 2015-12-09 辉瑞大药厂 用于治疗心血管疾病的n-哌啶-3-基苯甲酰胺衍生物
TWI682780B (zh) 2013-05-30 2020-01-21 美商再生元醫藥公司 醫藥組成物用於製造治療與pcsk9功能獲得性突變有關之體染色體顯性高膽固醇血症的藥物之用途
TW201534324A (zh) 2013-06-07 2015-09-16 Sanofi Sa 藉由投與pcsk9抑制劑抑制動脈粥狀硬化的方法
US9212182B2 (en) 2013-06-12 2015-12-15 Amgen Inc. Bicyclic sulfonamide compounds as sodium channel inhibitors
AR092240A1 (es) 2013-08-26 2015-04-08 Sunshine Lake Pharma Co Ltd Derivados heterociclicos nitrogenados y su aplicacion en farmacos
US10010588B2 (en) 2013-08-30 2018-07-03 Armo Biosciences, Inc. Methods of using pegylated interleukin-10 for treating hyperlipidemia
MX373298B (es) 2013-10-11 2020-05-20 Sanofi Biotechnology Uso de un inhibidor de pcsk9 para tratar la hiperlipidemia.
CN104558685B (zh) 2013-10-24 2017-09-29 中国石油化工股份有限公司 一种磷氮膨胀型阻燃剂及其合成方法
JP2017019724A (ja) 2013-10-25 2017-01-26 第一三共株式会社 置換ピリジン化合物および他の医薬の組み合わせ
WO2015086723A2 (fr) 2013-12-11 2015-06-18 Glycotope Gmbh Peptides de glycophorine glycosylés
TW201609798A (zh) 2013-12-13 2016-03-16 賽諾菲公司 Exendin-4胜肽類似物
WO2015086731A1 (fr) 2013-12-13 2015-06-18 Sanofi Analogues peptidiques de l'exendine-4 en tant qu'agonistes mixtes des récepteurs glp-1/glucagon
WO2015086728A1 (fr) 2013-12-13 2015-06-18 Sanofi Analogues peptidiques de l'exendine 4 en tant qu'agonistes mixtes des récepteurs glp-1/gip
EP3080154B1 (fr) 2013-12-13 2018-02-07 Sanofi Agonistes doubles du récepteur glp-1/gip
TW201609797A (zh) 2013-12-13 2016-03-16 賽諾菲公司 雙重glp-1/升糖素受體促效劑
WO2015086730A1 (fr) 2013-12-13 2015-06-18 Sanofi Analogues peptidiques de l'exendine 4 non acylés
CU24395B1 (es) 2014-03-17 2019-04-04 Pfizer Inhibidores de diacilglicerol aciltransferasa 2
AR099937A1 (es) 2014-04-04 2016-08-31 Sanofi Sa Compuestos de isoindolinona como moduladores de gpr119 para el tratamiento de diabetes, obesidad, dislipidemia y trastornos relacionados
RU2016143092A (ru) 2014-04-04 2018-05-08 Санофи Замещенные соединения инданона в качестве модуляторов gpr119 для лечения диабета, ожирения, дислипидемии и связанных с ними нарушений
AR099936A1 (es) 2014-04-04 2016-08-31 Sanofi Sa Heterociclos condensados sustituidos como moduladores de gpr119 para el tratamiento de la diabetes, obesidad, dislipidemia y trastornos relacionados
TW201625669A (zh) 2014-04-07 2016-07-16 賽諾菲公司 衍生自艾塞那肽-4(Exendin-4)之肽類雙重GLP-1/升糖素受體促效劑
TW201625668A (zh) 2014-04-07 2016-07-16 賽諾菲公司 作為胜肽性雙重glp-1/昇糖素受體激動劑之艾塞那肽-4衍生物
TW201625670A (zh) 2014-04-07 2016-07-16 賽諾菲公司 衍生自exendin-4之雙重glp-1/升糖素受體促效劑
EP3148537B1 (fr) 2014-05-30 2018-09-26 Université Paris Descartes Composés cycliques présentant une fonctionnalité 1,3 diamino pour utilisation dans le traitement de l'infection par le vih
WO2015187295A2 (fr) 2014-06-02 2015-12-10 Armo Biosciences, Inc. Méthodes permettant de faire baisser le cholestérol sérique
US9932381B2 (en) 2014-06-18 2018-04-03 Sanofi Exendin-4 derivatives as selective glucagon receptor agonists
TWI744723B (zh) 2014-06-20 2021-11-01 美商基利科學股份有限公司 多環型胺甲醯基吡啶酮化合物之合成
AU2015289617B2 (en) 2014-07-16 2021-04-15 Regeneron Pharmaceuticals, Inc. Methods for treating high cardiovascular risk patients with hypercholesterolemia
US9862701B2 (en) 2014-09-25 2018-01-09 Araxes Pharma Llc Inhibitors of KRAS G12C mutant proteins
WO2016054388A1 (fr) 2014-10-03 2016-04-07 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Inhibiteurs de glutaminase
ES2907461T3 (es) 2015-01-20 2022-04-25 Boehringer Ingelheim Animal Health Usa Inc Compuestos antihelmínticos, composiciones y procedimientos de uso de los mismos
US20180000793A1 (en) 2015-02-06 2018-01-04 Ernesto Abel-Santos Inhibiting Germination of Clostridium Perfringens Spores to Reduce Necrotic Enteritis
AR103954A1 (es) 2015-03-18 2017-06-14 Zealand Pharma As Análogos de amilina
EP3271405A1 (fr) 2015-03-20 2018-01-24 Aarhus Universitet Inhibiteurs de pcsk9 pour le traitement de troubles du métabolisme des lipoprotéines
PL3283507T3 (pl) 2015-04-16 2020-05-18 Zealand Pharma A/S Acylowany analog glukagonu
MX2018005096A (es) 2015-11-06 2018-08-15 Gemphire Therapeutics Inc Combinaciones de gemcabeno para el tratamiento de enfermedad cardiovascular.
TW201731867A (zh) 2015-12-02 2017-09-16 賽諾菲公司 Fgf21變異體
EP4085934A1 (fr) 2015-12-11 2022-11-09 The Trustees of The University of Pennsylvania Thérapie génique pour traiter l'hypercholestérolémie familiale
BR112018014794A2 (pt) 2016-01-20 2018-12-11 Janssen Sciences Ireland Uc pirimidinas substituídas com arila para uso em infecção pelo vírus influenza
SG10201912756XA (en) 2016-02-26 2020-02-27 Gemphire Therapeutics Inc Treatment of patients with homozygous familial hypercholesterolemia on lipid lowering therapy
WO2017161028A1 (fr) 2016-03-16 2017-09-21 Kura Oncology, Inc. Inhibiteurs substitués de ménine-mll et méthodes d'utilisation
CA3020087A1 (fr) 2016-04-14 2017-10-19 Michael LUCEY Compositions combinatoires et leurs methodes d'utilisation
TW201808888A (zh) 2016-05-05 2018-03-16 嘉來克生命科學有限責任公司 整合應激途徑之調節劑
WO2018007999A1 (fr) 2016-07-08 2018-01-11 Staten Biotechnology B.V. Anticorps anti-apoc3 et leurs méthodes d'utilisation
US10960020B2 (en) 2016-09-15 2021-03-30 The Brigham And Women's Hospital, Inc. Modulation of PCSK9 and LDLR through DRP1 inhibition
HRP20240930T1 (hr) 2016-10-18 2024-10-11 Novartis Ag Postupci za prevenciju kardiovaskularnih događaja smanjenjem proteina proproteinske konvertaze suptilizin/keksin tipa 9 (pcsk9)
KR20240044543A (ko) 2016-11-10 2024-04-04 시에스엘 리미티드 심근경색의 재구성된 고밀도 지질단백질 치료
JOP20190112A1 (ar) 2016-11-14 2019-05-14 Amgen Inc علاجات مدمجة لتصلب الشرايين، شاملة مرض قلبي وعائي تصلبي
WO2018106818A1 (fr) 2016-12-07 2018-06-14 Kura Oncology, Inc. Procédés de promotion de la prolifération de cellules bêta
WO2018106820A1 (fr) 2016-12-07 2018-06-14 Kura Oncology, Inc. Procédés de promotion de la prolifération de cellules bêta
MA48602A (fr) 2016-12-13 2020-03-18 Bristol Myers Squibb Co Composés hétéroaryle substitués par un amide alkyle d'oxyde de phosphine en tant que modulateurs des réponses il-12, il-23 et/ou ifn alpha
EP3579782B1 (fr) 2017-02-08 2024-05-01 Brooke Schumm Capsule de radiothérapie peropératoire avec système d'obturateur de confinement de rayonnement à enveloppe cylindrique
SG10201912034UA (en) 2017-02-08 2020-02-27 Bristol Myers Squibb Co Modified relaxin polypeptides comprising a pharmacokinetic enhancer and uses thereof
AR110988A1 (es) 2017-02-21 2019-05-22 Sanofi Sa Compuestos de azetidina como moduladores de gpr119 para el tratamiento de la diabetes, la obesidad, la dislipidemia y trastornos relacionados
EP3609882B1 (fr) 2017-03-17 2022-07-13 Cardio Therapeutics Pty Ltd Inhibiteurs hétérocycliques de pcsk9
CN110691779B (zh) 2017-03-24 2023-10-10 库拉肿瘤学公司 治疗血液系统恶性肿瘤和尤因肉瘤的方法
WO2018193427A1 (fr) 2017-04-21 2018-10-25 Staten Biotechnology B.V. Anticorps anti-apoc3 et leurs méthodes d'utilisation
CN110831593A (zh) 2017-06-14 2020-02-21 特维娜有限公司 用于调节s1p1活性的化合物及其使用方法
JP6928986B2 (ja) 2017-06-26 2021-09-01 深▲チェン▼市塔吉瑞生物医薬有限公司Shenzhen TargetRx, Inc. キナーゼ活性を阻害するためのインダゾール系化合物、その組成物および使用
CN109384712B (zh) 2017-08-14 2021-05-07 北京宽厚医药科技有限公司 靶向nk1受体拮抗剂及其在化疗所致恶心、呕吐治疗中的应用
EP3676268A1 (fr) 2017-10-20 2020-07-08 Dana-Farber Cancer Institute, Inc. Composés hétérobifonctionnels présentant une spécificité améliorée pour le bromodomaine de brd4
US11400082B2 (en) 2017-10-30 2022-08-02 Montréal Heart Institute Methods of treating elevated plasma cholesterol
CN111315772A (zh) 2017-10-31 2020-06-19 斯塔顿生物技术有限公司 抗apoc3抗体及其使用方法
UY37957A (es) 2017-11-02 2019-05-31 Abbvie Inc Moduladores de la vía de estrés integrada
MY202167A (en) 2017-11-21 2024-04-12 Bristol Myers Squibb Co Sulfone pyridine alkyl amide-substituted heteroaryl compounds
WO2019111225A1 (fr) 2017-12-08 2019-06-13 Avaliv Therapeutics Composés et procédés destinés au traitement de la stéatohépatite non alcoolique
SG11202005146VA (en) 2017-12-18 2020-06-29 Regeneron Pharma Bispecific antigen binding molecules that bind leptin receptor and/or gp130, and methods of use thereof
BR112020014140A2 (pt) * 2018-01-17 2020-12-01 Vertex Pharmaceuticals Incorporated inibidores de dna-pk
US11513131B2 (en) 2018-01-22 2022-11-29 Global Genomics Group, LLC Low density lipoprotein triglycerides (LDL-TG) as a biomarker of cardiovascular disease and uses thereof
US11911445B2 (en) 2018-01-23 2024-02-27 Gila Therapeutics, Inc. Peptide YY pharmaceutical formulations, compositions, and methods
US20210324067A9 (en) 2018-03-09 2021-10-21 The Brigham And Women's Hospital, Inc. Combination therapy for cardiovascular diseases
JP7485609B2 (ja) 2018-03-22 2024-05-16 ブリストル-マイヤーズ スクイブ カンパニー IL-12、IL-23および/またはIFNα応答のモジュレーターとして有用なピリジン含有ヘテロ環式化合物
CN110384801B (zh) 2018-04-20 2021-09-14 中国科学院上海药物研究所 miRNA552簇的微小RNA在治疗LDLC相关代谢性疾病中的应用
EP3784669B1 (fr) 2018-04-24 2023-10-25 Vertex Pharmaceuticals Incorporated Composés de ptéridinone et leurs utilisations
US20190374526A1 (en) 2018-06-06 2019-12-12 Merck Sharp & Dohme Corp. Substituted Heterocyclic Compounds as Inhibitors of PRDM9
US11442072B2 (en) 2018-07-10 2022-09-13 Jenny and Antti Wihuri Foundation Method for measuring LDL aggregation
JP7161605B2 (ja) 2018-08-31 2022-10-26 ファイザー・インク Nash/nafldおよび関連疾患の治療のための組合せ
JP2022504287A (ja) 2018-10-03 2022-01-13 スターテン・バイオテクノロジー・ベー・フェー ヒト及びカニクイザルapoc3に特異的な抗体、並びにその使用の方法
RS66346B1 (sr) 2018-10-22 2025-01-31 Alumis Inc Inhibitori tyk2 i njihova upotreba
JP2022512911A (ja) 2018-11-09 2022-02-07 ノバルティス アーゲー apo(a)を標的化するコンジュゲートアンチセンス化合物を用いて心血管事象のリスクを低減する方法
WO2020115288A1 (fr) 2018-12-06 2020-06-11 Zora Biosciences Oy Marqueurs biologiques pour événements cardiovasculaires
BR112021013924A2 (pt) 2019-01-18 2021-09-21 Astrazeneca Ab Inibidores de pcsk9 e métodos de uso do mesmo
WO2020150473A2 (fr) * 2019-01-18 2020-07-23 Dogma Therapeutics, Inc. Inhibiteurs de pcsk9 et leurs procédés d'utilisation
CN111484480B (zh) 2019-01-29 2023-08-11 上海翰森生物医药科技有限公司 一种多环类衍生物抑制剂、其制备方法和应用
CA3128368A1 (fr) 2019-02-01 2020-08-06 Memorial Sloan Kettering Cancer Center Cellules car-t antisenescence ciblant upar, surface cellulaire et biomarqueur de senescence secrete
AU2020260110A1 (en) 2019-04-17 2021-11-11 Ngm Biopharmaceuticals, Inc. Combination therapy for modulating bile acid homeostasis and treatment of bile acid disorders and diseases
CA3140972C (fr) 2019-05-20 2024-06-18 Pfizer Inc. Combinaisons comprenant du benzodioxol en tant qu'agonistes de glp-1r destinees a etre utilisees dans le traitement de la nash/nafld et de maladies associees
JP2023506732A (ja) 2019-12-10 2023-02-20 リジェネロン・ファーマシューティカルズ・インコーポレイテッド ホモ接合型家族性高コレステロール血症を処置するためのpcsk9阻害剤の使用
WO2021209808A1 (fr) 2020-04-16 2021-10-21 Abionyx Pharma Sa Thérapie avec cer-001 pour le traitement d'une maladie rénale
CN113713107B (zh) 2020-05-26 2022-09-23 中国科学院上海药物研究所 miRNA552簇的微小RNA在治疗糖脂代谢病中的应用
WO2021243002A1 (fr) 2020-05-29 2021-12-02 Amgen Inc. Inhibiteurs de la pcsk9 et méthodes d'utilisation de ceux-ci pour traiter des troubles liées au cholestérol
MX2022015517A (es) 2020-06-10 2023-01-16 Ferring Bv Compuesto farmaceutico para el tratamiento de la enfermedad cardiovascular aterosclerotica.
US20240002354A1 (en) 2020-08-05 2024-01-04 Rezubio Pharmaceuticals Co., Ltd Antidiabetic compounds and compositions
WO2022029334A1 (fr) 2020-08-07 2022-02-10 Gbiotech S.À.R.L. Polythérapies pour le traitement d'une infection à coronavirus
JP7824930B2 (ja) 2020-08-19 2026-03-05 バイオジェン・エムエイ・インコーポレイテッド 高コレステロール血症の治療方法
BR112023004716A2 (pt) 2020-09-15 2023-05-09 Regeneron Pharma Uso de agonistas de lepr para dor
US20240158382A1 (en) 2020-10-20 2024-05-16 Gbiotech S. A. R. L. Agonists Of Free Fatty Acid Receptor 1 And Their Use In Diseases Associated With Said Receptor
KR20230104200A (ko) 2020-11-05 2023-07-07 암젠 인크 LPA-표적화된 RNAi 작제물을 이용하여 죽상경화성 심혈관질환을 치료하는 방법
IL303130A (en) 2020-12-11 2023-07-01 Helsingin Yliopisto A method for determining a patient's chance of response to lipid-lowering treatment
EP4011877A3 (fr) 2020-12-11 2023-01-11 Institut de Cardiologie de Montréal Méthodes de traitement du cholestérol plasmatique élevé
JP2024512255A (ja) 2021-02-22 2024-03-19 リジェネロン・ファーマシューティカルズ・インコーポレイテッド 部分性脂肪萎縮症を診断および処置するための方法
US20250281495A1 (en) 2021-02-25 2025-09-11 Icahn School Of Medicine At Mount Sinai Methods for inhibiting inflammation and progression of atherosclerotic plaques and cardiovascular events in patients with cerebro- and cardio-vascular disease
AU2022248850A1 (en) 2021-03-27 2023-11-09 TRx Biosciences Limited Compositions having improved bioavailability of therapeutics
US12612626B2 (en) 2021-06-24 2026-04-28 Sirnaomics, Inc. siRNA compound that inhibits expression of APOC3
MX2023015442A (es) 2021-06-25 2024-03-12 Amgen Inc Tratamiento de la enfermedad cardiovascular con proteínas de unión a antígeno trem-1.
WO2023285583A1 (fr) 2021-07-14 2023-01-19 Eternygen Uk Ltd. Dérivés de 5,6,7,8-tétrahydro-2,6- et 2,7-naphtyridine destinés à être utilisés dans le traitement de maladies sensibles à la modulation du transporteur de citrate
WO2023052783A1 (fr) 2021-09-30 2023-04-06 Sitryx Therapeutics Limited Nouveaux composés
TW202325288A (zh) 2021-11-05 2023-07-01 英商喜翠克斯治療有限公司 新穎化合物
EP4446307A4 (fr) 2021-11-12 2025-12-10 Shenzhen Jingtai Tech Co Ltd Dérivé d'acide aspartique et son utilisation dans le traitement de maladies métaboliques telles que la fibrose hépatique et l'hépatite non alcoolique
CN114277032A (zh) 2021-12-31 2022-04-05 华中科技大学同济医学院附属协和医院 一种低密度脂蛋白受体基因突变体及其应用
KR20240134933A (ko) 2022-01-14 2024-09-10 레주바이오 파마슈티칼스 컴퍼니 리미티드 항당뇨병 화합물 및 조성물
TW202345865A (zh) 2022-01-24 2023-12-01 大陸商上海舶望製藥有限公司 抑制LPA(Apo(a))蛋白表達的組合物和方法
CN116617390A (zh) 2022-02-11 2023-08-22 武汉大学 Asgr1抑制剂在促进胆固醇外排和治疗非酒精性脂肪性肝病中的应用
WO2023173004A2 (fr) 2022-03-11 2023-09-14 University Of Florida Research Foundation, Incorporated Ciblage de ptchd1 et de cholestérol neuronal pour améliorer la sécurité d'analgésiques opioïdes
US20230338419A1 (en) 2022-03-21 2023-10-26 The Trustees Of The University Of Pennsylvania Methods and apparatus for diagnosis and detection of cardiac allograft vasculopathy
CN116948030B (zh) 2022-04-25 2024-11-19 武汉大学 抗asgr1单克隆抗体及其应用
CN117045715B (zh) 2022-05-13 2025-06-06 浙江养生堂天然药物研究所有限公司 红肉苹果和樱桃李组合物及其在抗动脉粥样硬化方面的应用
CN115581694A (zh) 2022-11-10 2023-01-10 正大青春宝药业有限公司 洋川芎内脂i在制备治疗高血脂症药物中的应用
CN117180404A (zh) 2023-10-24 2023-12-08 清华大学 Cholesin在调节胆固醇稳态中的用途
CN117482076A (zh) 2023-11-24 2024-02-02 中国人民解放军陆军军医大学第二附属医院 甲硫氨酸类化合物在制备pcsk9抑制剂中的应用

Also Published As

Publication number Publication date
CA3125767A1 (fr) 2020-07-23
US20230407285A1 (en) 2023-12-21
EP3911640A4 (fr) 2022-10-26
JP2025106240A (ja) 2025-07-15
BR112021013924A2 (pt) 2021-09-21
SG11202107615TA (en) 2021-08-30
AU2020209216A1 (en) 2021-08-26
CN113412258A (zh) 2021-09-17
WO2020150474A1 (fr) 2020-07-23
US20200231584A1 (en) 2020-07-23
JP2022518016A (ja) 2022-03-11
US12584120B2 (en) 2026-03-24
MY210469A (en) 2025-09-24
KR20260035207A (ko) 2026-03-12
MX2021008661A (es) 2021-08-19
US11603523B2 (en) 2023-03-14
EP3911640B1 (fr) 2026-05-13
AU2023201972A1 (en) 2023-05-04
EP3911640A1 (fr) 2021-11-24
TW202042817A (zh) 2020-12-01
AU2023201972C1 (en) 2025-10-23
TWI921300B (zh) 2026-04-11
IL284661A (en) 2021-08-31
EP4790054A2 (fr) 2026-08-12
AU2023201972B2 (en) 2025-02-13
AU2025202886A1 (en) 2025-05-15
KR20210116549A (ko) 2021-09-27
MX2024009001A (es) 2024-07-31
EA202191890A1 (ru) 2022-02-03

Similar Documents

Publication Publication Date Title
EP3911648A4 (fr) Inhibiteurs de pcsk9 et leurs procédés d'utilisation
EP3911640A4 (fr) Inhibiteurs de pcsk9 et leurs procédés d'utilisation
EP3968999A4 (fr) Inhibiteurs de fgfr et leurs procédés d'utilisation
MA55136A (fr) Inhibiteurs de kras g12c et leurs procédés d'utilisation
MA54538A (fr) Inhibiteurs d'apol1 et leurs procédés d'utilisation
EP3962479A4 (fr) Inhibiteurs de kcnt1 et procédés d'utilisation
EP3962481A4 (fr) Inhibiteurs de kcnt1 et procédés d'utilisation
MA55301A (fr) Inhibiteurs de protéine tyrosine phosphatase et leurs procédés d'utilisation
MA55890A (fr) Modulateurs de thr-beta et leurs procédés d'utilisation
MA51837A (fr) Inhibiteurs de l'arginase et leurs procédés d'utilisation
EP3946329A4 (fr) Agonistes bêta-adrénergique et leurs procédés d'utilisation
EP3846808A4 (fr) Inhibiteurs de papd5 et leurs procédés d'utilisation
MA51848A (fr) Inhibiteurs de kras g12c et leurs procédés d'utilisation
MA52765A (fr) Inhibiteurs de kras g12c et leurs procédés d'utilisation
MA52501A (fr) Inhibiteurs de kras g12c et leurs procédés d'utilisation
MA52496A (fr) Inhibiteurs de kras g12c et leurs procédés d'utilisation
EP3810615A4 (fr) Inhibiteurs d'arginase et procédés d'utilisation
EP3765006A4 (fr) Inhibiteurs d'arginase et procédés d'utilisation
EP4284365A4 (fr) Inhibiteurs de cdk2 et leurs procédés d'utilisation
EP3510040A4 (fr) Inhibiteurs d'éctonucléotidase et leurs procédés d'utilisation
MA55025A (fr) Anticorps anti-trem2 et leurs procédés d'utilisation
MA56457A (fr) Modulateurs de hsd17b13 et leurs procédés d'utilisation
EP3802489A4 (fr) Inhibiteurs de masp -2 et procédés d'utilisation
EP4125831A4 (fr) Inhibiteurs de kcnt1 et procédés d'utilisation
MA55381A (fr) Pyridazinones et leurs procédés d'utilisation