NI202000101A - Compuestos antagonistas de pcsk9 - Google Patents

Compuestos antagonistas de pcsk9

Info

Publication number
NI202000101A
NI202000101A NI202000101A NI202000101A NI202000101A NI 202000101 A NI202000101 A NI 202000101A NI 202000101 A NI202000101 A NI 202000101A NI 202000101 A NI202000101 A NI 202000101A NI 202000101 A NI202000101 A NI 202000101A
Authority
NI
Nicaragua
Prior art keywords
compounds
antagonist compounds
pcsk9 antagonist
pcsk9
formula
Prior art date
Application number
NI202000101A
Other languages
English (en)
Spanish (es)
Inventor
B Wood Harold
B Josien Hubert
Joseph Tucker Thomas
Dawn Kerekes Angela
Tong Ling
M Walji Abbas
G Nair Anikumar
Ding Fa-Xiang
Bianchi Elisabetta
Branca Danila
Wu Chengwei
Xiong Yusheng
Nicole Ha Sookhee
Liu Jian
Babu Boga Sobhana
Original Assignee
Merck Sharp & Dohme
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 Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of NI202000101A publication Critical patent/NI202000101A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • 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
    • A61P9/10—Drugs 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/64—Cyclic peptides containing only normal peptide links
    • 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)
    • C12N9/6454—Dibasic site splicing serine proteases, e.g. kexin (3.4.21.61); furin (3.4.21.75) and other proprotein convertases
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
    • C12Y304/21—Serine endopeptidases (3.4.21)
    • C12Y304/21061—Kexin (3.4.21.61), i.e. proprotein convertase subtilisin/kexin type 9
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biophysics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (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)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
NI202000101A 2018-06-21 2020-12-14 Compuestos antagonistas de pcsk9 NI202000101A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201862687913P 2018-06-21 2018-06-21

Publications (1)

Publication Number Publication Date
NI202000101A true NI202000101A (es) 2021-05-28

Family

ID=67263083

Family Applications (1)

Application Number Title Priority Date Filing Date
NI202000101A NI202000101A (es) 2018-06-21 2020-12-14 Compuestos antagonistas de pcsk9

Country Status (38)

Country Link
US (3) US11427616B2 (enExample)
EP (2) EP4660303A3 (enExample)
JP (3) JP7112531B2 (enExample)
KR (2) KR20250161677A (enExample)
CN (2) CN112313243B (enExample)
AR (1) AR115597A1 (enExample)
AU (2) AU2019290163C1 (enExample)
BR (1) BR112020025274A8 (enExample)
CA (1) CA3102629A1 (enExample)
CL (2) CL2020003257A1 (enExample)
CO (1) CO2021000456A2 (enExample)
CR (1) CR20210031A (enExample)
DK (1) DK3810626T3 (enExample)
DO (1) DOP2020000250A (enExample)
EA (1) EA202190086A1 (enExample)
EC (1) ECSP21003643A (enExample)
ES (1) ES3047399T3 (enExample)
FI (1) FI3810626T3 (enExample)
GE (2) GEP20237506B (enExample)
HR (1) HRP20251302T1 (enExample)
HU (1) HUE073367T2 (enExample)
IL (2) IL279363B2 (enExample)
JO (1) JOP20190150A1 (enExample)
LT (1) LT3810626T (enExample)
MA (1) MA52967B1 (enExample)
MD (1) MD3810626T2 (enExample)
MX (1) MX2020013726A (enExample)
NI (1) NI202000101A (enExample)
PE (1) PE20211584A1 (enExample)
PH (1) PH12020552187A1 (enExample)
PL (1) PL3810626T3 (enExample)
PT (1) PT3810626T (enExample)
RS (1) RS67338B1 (enExample)
SG (1) SG11202012451WA (enExample)
SI (1) SI3810626T1 (enExample)
TW (1) TWI840376B (enExample)
UA (1) UA129467C2 (enExample)
WO (1) WO2019246349A1 (enExample)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100558932B1 (ko) * 2005-04-21 2006-03-10 주식회사 엠제이스마트 테크놀러지 다공성 세라믹 분리막 제조방법과, 이에 의해 제조되어진 다공성 세라믹 분리막
EP4091624A1 (en) 2013-03-15 2022-11-23 Protagonist Therapeutics, Inc. Hepcidin analogues and uses thereof
CA2949215C (en) 2014-05-16 2023-03-14 Protagonist Therapeutics, Inc. .alpha.4.beta.7 integrin thioether peptide antagonists
SG10201810154WA (en) 2014-07-17 2018-12-28 Protagonist Therapeutics Inc Oral peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory bowel diseases
WO2018022937A1 (en) 2016-07-27 2018-02-01 Protagonist Therapeutics, Inc. Peptide inhibitors of interleukin-23 and their use to treat inflammatory diseases
WO2019157268A1 (en) 2018-02-08 2019-08-15 Protagonist Therapeutics, Inc. Conjugated hepcidin mimetics
US11814444B2 (en) 2018-06-21 2023-11-14 Ra Pharmaceuticals, Inc. Cyclic polypeptides for PCSK9 inhibition
KR20250161677A (ko) 2018-06-21 2025-11-17 머크 샤프 앤드 돔 엘엘씨 Pcsk9 길항제 화합물
EP3810129B1 (en) 2018-06-21 2023-08-16 Merck Sharp & Dohme LLC Pcsk9 antagonist bicyclo-compounds
EP3810178A4 (en) 2018-06-21 2022-05-04 Merck Sharp & Dohme Corp. CYCLIC POLYPEPTIDES TO INHIBIT PCSK9
WO2019246405A1 (en) 2018-06-21 2019-12-26 Merck Sharp & Dohme Corp. Cyclic polypeptides for pcsk9 inhibition
ES3015132T3 (en) 2018-06-21 2025-04-29 Ucb Holdings Inc Cyclic polypeptides for pcsk9 inhibition
EP4021919A1 (en) 2019-08-30 2022-07-06 Merck Sharp & Dohme Corp. Pcsk9 antagonist compounds
US12577259B2 (en) 2019-12-20 2026-03-17 Merck Sharp & Dohme Llc PCSK9 antagonist compounds
SMT202500254T1 (it) 2020-01-15 2025-09-12 Janssen Biotech Inc Inibitori peptidici del recettore dell'interleuchina-23 e loro uso per trattare malattie infiammatorie
MX2022008740A (es) 2020-01-15 2022-09-23 Janssen Biotech Inc Peptidos inhibidores del receptor de interleucina-23 y su uso para tratar enfermedades inflamatorias.
AU2021383828A1 (en) 2020-11-20 2023-07-06 Janssen Pharmaceutica Nv Compositions of peptide inhibitors of interleukin-23 receptor
US11932705B2 (en) 2020-12-18 2024-03-19 Merck Sharp & Dohme Llc Cyclic polypeptides for PCSK9 inhibition
KR20240034224A (ko) 2021-07-14 2024-03-13 얀센 바이오테크 인코포레이티드 인터류킨-23 수용체의 지질화된 펩티드 억제제
MX2024002146A (es) * 2021-08-19 2024-03-08 Merck Sharp & Dohme Llc Compuestos para el tratamiento de afecciones relacionadas con la actividad de pcsk9.
SI4540267T1 (sl) 2022-06-15 2026-07-31 Merck Sharp & Dohme Llc Ciklični peptidi za ujetje interlevkina-1 beta
JP7866141B2 (ja) * 2022-08-17 2026-05-26 メルク・シャープ・アンド・ドーム・エルエルシー Pcsk9阻害薬の結晶形態、組成物及び使用
WO2024259310A2 (en) * 2023-06-15 2024-12-19 Merck Sharp & Dohme Llc Passive permeable pcsk9 antagonist compounds
IL328311A (en) 2023-11-14 2026-07-01 Merck Sharp & Dohme Llc Cyclic peptide for capturing Interleukin-1 Beta
AU2024401721A1 (en) 2023-12-15 2026-07-16 Merck Sharp & Dohme Llc A cyclic peptide il-1beta trap for the treatment of atherosclerosis and inflammatory disorders
WO2025242221A1 (zh) * 2024-05-24 2025-11-27 上海翰森生物医药科技有限公司 新型修饰侧链、其制备方法和应用
WO2025264781A1 (en) * 2024-06-18 2025-12-26 Kemira Oy J Cationizing agents for saccharides and methods
WO2026019622A1 (en) * 2024-07-15 2026-01-22 Merck Sharp & Dohme Llc Crystal forms of a cyclictetrapeptide and processes for preparing
WO2026019624A1 (en) * 2024-07-15 2026-01-22 Merck Sharp & Dohme Llc Synthesis of cyclic oligopeptides
WO2026032253A1 (zh) * 2024-08-06 2026-02-12 石药集团中奇制药技术(石家庄)有限公司 环肽类似物及其制备方法和用途
WO2026034639A1 (ja) * 2024-08-09 2026-02-12 株式会社Spin Wave ペプチド合成用可溶性担体およびこれを用いた合成方法
CN119930471A (zh) * 2024-12-31 2025-05-06 苏州默迪夫生物科技有限公司 Mk-a的制备方法、所用的中间体及其合成方法
CN122464947A (zh) * 2025-01-25 2026-07-28 深圳市祥根生物有限公司 一种环肽类pcsk9抑制剂和用途

Family Cites Families (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4393046A (en) 1981-01-30 1983-07-12 Merck & Co., Inc. Combination of thiopeptin and other related sulfur-containing cyclic polypeptide antibiotics with rumen-active diimides to improve ruminant feed efficiency
US4656269A (en) 1986-04-15 1987-04-07 Kissei Pharmaceutical Co., Ltd. Histidine derivatives
DE3841520A1 (de) 1988-12-09 1990-06-13 Hoechst Ag Enzymhemmende harnstoffderivate von dipeptiden, verfahren zu ihrer herstellung, diese enthaltende mittel und ihre verwendung
US5104869A (en) 1989-10-11 1992-04-14 American Cyanamid Company Renin inhibitors
US5114937A (en) 1989-11-28 1992-05-19 Warner-Lambert Company Renin inhibiting nonpeptides
US5095119A (en) 1990-03-08 1992-03-10 American Home Products Corporation Renin inhibitors
DE69819311T2 (de) 1997-03-07 2004-07-29 Metabasis Therapeutics Inc., San Diego Neue benzimidazol inhibitoren der fructose-1,6-bisphosphatase
AU6691798A (en) 1997-03-07 1998-09-22 Metabasis Therapeutics, Inc. Novel indole and azaindole inhibitors of fructose-1,6-bisphosphatase
WO1998039344A1 (en) 1997-03-07 1998-09-11 Metabasis Therapeutics, Inc. Novel purine inhibitors of fructose-1,6-bisphosphatase
CZ297264B6 (cs) 1998-09-09 2006-10-11 Metabasis Therapeutics, Inc. Nové heteroaromatické inhibitory fruktóza-1,6-bisfosfatázy
CA2415742A1 (en) 2000-07-25 2002-01-31 Merck & Co., Inc. N-substituted indoles useful in the treatment of diabetes
US6852738B2 (en) 2001-01-30 2005-02-08 Merck & Co., Inc. Acyl sulfamides for treatment of obesity, diabetes and lipid disorders
AR040241A1 (es) 2002-06-10 2005-03-23 Merck & Co Inc Inhibidores de la 11-beta-hidroxiesteroide deshidrogrenasa 1 para el tratamiento de la diabetes obesidad y dislipidemia
WO2004019869A2 (en) 2002-08-29 2004-03-11 Merck & Co., Inc. Indoles having anti-diabetic activity
CA2495943C (en) 2002-08-29 2009-07-21 Merck & Co., Inc. Indoles having anti-diabetic activity
CA2512879A1 (en) 2003-01-17 2004-08-12 Soumya P. Sahoo N-cyclohexylaminocarbonyl benzenesulfonamide derivatives
CA2667894A1 (en) 2006-11-07 2008-05-15 Merck & Co., Inc. Antagonists of pcsk9
EP2174343A1 (en) 2007-06-28 2010-04-14 Semiconductor Energy Laboratory Co, Ltd. Manufacturing method of semiconductor device
US20100179173A1 (en) 2007-06-28 2010-07-15 Daniel Guay Substituted fused pyrimidines as antagonists of gpr105 activity
US20110301079A1 (en) 2007-09-21 2011-12-08 Instituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. Neuromedin u receptor agonists and uses thereof
AR070316A1 (es) * 2008-02-07 2010-03-31 Merck & Co Inc Antagonistas de pcsk9 (proproteina subtilisina-kexina tipo 9)
US7928189B2 (en) 2008-05-05 2011-04-19 Ottawa Health Research Institute PCSK9 polypeptide fragment
WO2009148605A2 (en) 2008-06-04 2009-12-10 Isis Pharmaceuticals, Inc. Methods for treating hypercholesterolemia
UY32690A (es) 2009-06-08 2011-01-31 Astrazeneca Ab Péptidos específicos para receptores de melanocortina
US20120219558A1 (en) 2009-09-25 2012-08-30 Yan Ni Antagonists of pcsk9
CA2813049A1 (en) 2010-09-23 2012-03-29 The Trustees Of The University Of Pennsylvania Modified compstatin with improved stability and binding properties
NZ612544A (en) 2010-12-28 2015-04-24 Cadila Healthcare Ltd Heterocyclic compounds suitable for the treatment of dyslipidemia
MX2013009258A (es) * 2011-02-11 2013-10-17 Novartis Ag Antagonistas de pcsk9.
WO2012131504A1 (en) 2011-03-02 2012-10-04 Pfizer Inc. Pcsk9 vaccine
WO2012168491A1 (en) * 2011-06-10 2012-12-13 Novartis Ag Pharmaceutical formulations of pcsk9 antagonists
KR20140041747A (ko) 2011-06-20 2014-04-04 제넨테크, 인크. Pcsk9-결합 폴리펩티드 및 사용 방법
MX354705B (es) 2011-09-23 2018-03-16 Novo Nordisk As Analogos de glucagon novedosos.
US9512073B2 (en) 2011-10-27 2016-12-06 Massachusetts Institute Of Technology Amino acid-, peptide-and polypeptide-lipids, isomers, compositions, and uses thereof
EP2814501A4 (en) 2012-03-13 2016-03-02 Tensive Controls Inc MELANOCORTINANALOGA WITH INCREASED EFFECTIVENESS AND TRANSPORTATION OF THEREOF
US9238676B2 (en) 2012-05-17 2016-01-19 Ra Pharmaceuticals, Inc. Peptide and peptidomimetic inhibitors
EP2684865A1 (en) 2012-07-13 2014-01-15 Heidelberg Pharma GmbH Methods for synthesizing amatoxin building block and amatoxins
WO2014140210A1 (en) 2013-03-14 2014-09-18 Pieris Ag Novel binding proteins for pcsk9
JP2016512825A (ja) 2013-03-15 2016-05-09 シファ・バイオメディカル・コーポレイションShifa Biomedical Corporation 抗プロタンパク質転換酵素サブチリシン/ケキシン9型(抗pcsk9)化合物および心血管疾患の治療および/または予防におけるその使用方法
MX373298B (es) 2013-10-11 2020-05-20 Sanofi Biotechnology Uso de un inhibidor de pcsk9 para tratar la hiperlipidemia.
BR122021025449B1 (pt) 2014-06-12 2024-02-15 Ra Pharmaceuticals, Inc Composto, polipeptídeo e composição compreendendo o mesmo
WO2016119067A1 (en) 2015-01-30 2016-08-04 Pronasci Inc. Peptides derived from human pcsk9 catalytic domain and uses there of for promoting ldl-r activity
RU2747877C2 (ru) 2016-01-13 2021-05-17 Ново Нордиск А/С Аналоги эфр(а) с заместителями - жирными кислотами
CN107286158A (zh) 2016-03-30 2017-10-24 中国科学院上海药物研究所 苯基[a]吲哚[2,3-g]并喹嗪类化合物、其制备方法、药物组合物及其应用
EP3442991A4 (en) 2016-04-15 2019-11-20 RA Pharmaceuticals, Inc. RAS-BINDING PEPTIDES AND METHODS OF USE
AU2017281332A1 (en) 2016-06-24 2018-12-20 F. Hoffmann-La Roche Ag Compositions and methods for treating cardiovascular disease
US10577357B2 (en) 2016-09-19 2020-03-03 The Texas A&M University System Inhibitors of LDLR-PCSK9 protein-protein interaction and methods of their use
CN109284823B (zh) 2017-04-20 2020-08-04 上海寒武纪信息科技有限公司 一种运算装置及相关产品
CN107158002B (zh) * 2017-07-01 2020-06-16 维亚生物科技(上海)有限公司 苄撑巴比妥类化合物在作为pcsk9拮抗剂和降低低密度脂蛋白中的应用
WO2019246405A1 (en) 2018-06-21 2019-12-26 Merck Sharp & Dohme Corp. Cyclic polypeptides for pcsk9 inhibition
ES3015132T3 (en) 2018-06-21 2025-04-29 Ucb Holdings Inc Cyclic polypeptides for pcsk9 inhibition
KR20250161677A (ko) 2018-06-21 2025-11-17 머크 샤프 앤드 돔 엘엘씨 Pcsk9 길항제 화합물
US11814444B2 (en) 2018-06-21 2023-11-14 Ra Pharmaceuticals, Inc. Cyclic polypeptides for PCSK9 inhibition
EP3810178A4 (en) 2018-06-21 2022-05-04 Merck Sharp & Dohme Corp. CYCLIC POLYPEPTIDES TO INHIBIT PCSK9
EP3810129B1 (en) 2018-06-21 2023-08-16 Merck Sharp & Dohme LLC Pcsk9 antagonist bicyclo-compounds
EP4021919A1 (en) 2019-08-30 2022-07-06 Merck Sharp & Dohme Corp. Pcsk9 antagonist compounds
US12577259B2 (en) 2019-12-20 2026-03-17 Merck Sharp & Dohme Llc PCSK9 antagonist compounds

Also Published As

Publication number Publication date
SI3810626T1 (sl) 2025-12-31
JP2022141879A (ja) 2022-09-29
JP7112531B2 (ja) 2022-08-03
BR112020025274A2 (pt) 2021-03-09
HRP20251302T1 (hr) 2025-12-19
AU2022259744B2 (en) 2024-07-11
US12209145B2 (en) 2025-01-28
ECSP21003643A (es) 2021-02-26
ES3047399T3 (en) 2025-12-03
US20190389909A1 (en) 2019-12-26
MA52967A (fr) 2021-04-28
IL279363B1 (en) 2025-08-01
WO2019246349A1 (en) 2019-12-26
SG11202012451WA (en) 2021-01-28
EA202190086A1 (ru) 2021-05-18
EP4660303A2 (en) 2025-12-10
PL3810626T3 (pl) 2025-12-22
IL321719A (en) 2025-08-01
AU2022259744A1 (en) 2022-12-01
CR20210031A (es) 2021-02-11
PT3810626T (pt) 2025-10-15
DK3810626T3 (da) 2025-08-18
EP3810626A1 (en) 2021-04-28
US20250206781A1 (en) 2025-06-26
AU2019290163A1 (en) 2021-01-07
CN112313243A (zh) 2021-02-02
US11427616B2 (en) 2022-08-30
KR20250161677A (ko) 2025-11-17
EP3810626B1 (en) 2025-07-23
MX2020013726A (es) 2021-03-02
CL2020003257A1 (es) 2021-07-23
MD3810626T2 (ro) 2025-12-31
MA52967B1 (fr) 2025-09-30
RS67338B1 (sr) 2025-11-28
PH12020552187A1 (en) 2021-07-26
CN112313243B (zh) 2025-09-02
CL2022000027A1 (es) 2022-08-19
TW202019950A (zh) 2020-06-01
JP2025041712A (ja) 2025-03-26
BR112020025274A8 (pt) 2023-02-14
CN121130044A (zh) 2025-12-16
JP7855670B2 (ja) 2026-05-08
AU2019290163B2 (en) 2022-08-04
JP2021522311A (ja) 2021-08-30
CO2021000456A2 (es) 2021-01-29
KR20210024035A (ko) 2021-03-04
DOP2020000250A (es) 2021-02-28
AR115597A1 (es) 2021-02-03
KR102884527B1 (ko) 2025-11-13
HUE073367T2 (hu) 2026-01-28
US20230159592A1 (en) 2023-05-25
CA3102629A1 (en) 2019-12-26
GEP20237506B (en) 2023-05-25
EP4660303A3 (en) 2026-02-25
PE20211584A1 (es) 2021-08-18
FI3810626T3 (fi) 2025-10-21
TWI840376B (zh) 2024-05-01
UA129467C2 (uk) 2025-05-07
JP7607615B2 (ja) 2024-12-27
LT3810626T (lt) 2025-11-10
WO2019246349A8 (en) 2021-02-04
JOP20190150A1 (ar) 2019-12-21
IL279363B2 (en) 2025-12-01
IL279363A (en) 2021-01-31
AU2019290163C1 (en) 2022-11-03
GEAP202215540A (en) 2022-12-12

Similar Documents

Publication Publication Date Title
CO2021000456A2 (es) Compuestos antagonistas de pcsk9 referencia recíproca a solicitudes relacionadas
CY1123476T1 (el) Τροποποιητες πυρηνικης μεταφορας και χρησεις αυτων
CY1122821T1 (el) Παραγωγα 1,3-βενζοδιοξολιου ως αναστολεις εζη1 ή/και εζη2
CY1122730T1 (el) 1,2,4-τριαζολες ως διαμορφωτες πυρηνικης μεταφορας και χρησεις αυτων
ECSP20001149A (es) Compuestos antiproliferativos y métodos para utilizarlos
CY1121071T1 (el) Παραγωγα ναφθυριδινης ως ανταγωνιστες ιντεγκρινης αλφα v βητα 6 για τη θεραπεια π.χ. ινωτικων νοσων
CY1123093T1 (el) Φαρμακοφορο για την επαγωγη του trail
CO6531452A2 (es) Piperidinas sustituidas que aumentan la actividad de p53 y sus usos
CY1116405T1 (el) Ν1/ν2-λακταμικοι αναστολεις ακετυλο-coa καρβοξυλασης
UY37160A (es) COMPUESTOS DERIVADOS DE PIRROLIDINA CON ACTIVIDAD ANTAGONISTA DE INTEGRINA avß6
ECSP13012611A (es) Derivados de pirazol-aminopirimidina como moduladores de la lrrk2
CU20170026A7 (es) Compuestos derivados de 2-(benzamido/picolinamido/nicotinamido/isonicotinamido)-(2-metil-6-morfolino-(fenil/ (3,4´-bipiridin))-2-il)oxi)etil dihidrógeno fosfato como inhibidores de quinasa raf
CY1124933T1 (el) Κυτταροτοξικες και αντι-μιτωτικες ενωσεις και μεθοδοι χρησης αυτων
ECSP18024565A (es) Benzamidas sustituidas con isoxazolinas y análalogos como insecticidas
CY1125285T1 (el) Θεραπεια για τη νοσο του παρκινσον
CR20150419A (es) Derivados sustituidos del ácido bisfenil butanóico fosfónico como inhibidores de la nep
CY1123880T1 (el) Καινοτομοι 5-ητ2 ανταγωνιστες
CL2019001041A1 (es) Compuestos terapéuticos y métodos para utilizarlos.
MX2015016971A (es) Formulacion que comprende un agente hipolipidemico.
EP3480186A4 (en) NEW ARYLETE HAND DERIVATIVE AND PHARMACEUTICAL COMPOSITION THEREFORE AS AN ACTIVE SUBSTANCE
CO2017009989A2 (es) Piridopirimidinonas y utilización de las mismas como moduladores de receptores de nmda
NI201600091A (es) UREAS ASIMÉTRICAS p-SUSTITUIDAS Y USOS MÉDICOS DE LAS MISMAS
DOP2022000037A (es) Agentes antipalúdicos
AR082507A1 (es) Compuestos de tetrahidrofuranilo, medicamento en base al compuesto y un procedimiento para la fabricacion del medicamento
EA201990238A1 (ru) ФОСФОРСОДЕРЖАЩИЕ ПРОЛЕКАРСТВА СТИМУЛЯТОРОВ sGC