[go: up one dir, main page]

MA52063B1 - Composés de n-((hét)arylméthyl)hétéroaryle-carboxamides en tant qu'inhibiteurs de la kallicréine plasmatique - Google Patents

Composés de n-((hét)arylméthyl)hétéroaryle-carboxamides en tant qu'inhibiteurs de la kallicréine plasmatique

Info

Publication number
MA52063B1
MA52063B1 MA52063A MA52063A MA52063B1 MA 52063 B1 MA52063 B1 MA 52063B1 MA 52063 A MA52063 A MA 52063A MA 52063 A MA52063 A MA 52063A MA 52063 B1 MA52063 B1 MA 52063B1
Authority
MA
Morocco
Prior art keywords
compounds
plasma
kallicrein
arylmethyl
het
Prior art date
Application number
MA52063A
Other languages
English (en)
Other versions
MA52063A (fr
Inventor
Rebecca Louise Davie
Hannah Joy Edwards
David Michael Evans
Simon Teanby Hodgson
Original Assignee
Kalvista Pharmaceuticals Ltd
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=52349552&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA52063(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Kalvista Pharmaceuticals Ltd filed Critical Kalvista Pharmaceuticals Ltd
Publication of MA52063A publication Critical patent/MA52063A/fr
Publication of MA52063B1 publication Critical patent/MA52063B1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/435Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/495Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10Antioedematous agents; Diuretics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/02Non-specific cardiovascular stimulants, e.g. drugs for syncope, antihypotensives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/10Heterocyclic 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 carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/10Heterocyclic 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 carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Emergency Medicine (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Immunology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention propose des composés de formule (i) : compositions <img file="imga0001.Tif" frnum="0001" he="53" id="ia01" img-content="chem" img-format="tif" inline="no" orientation="portrait" pgnum="0001" wi="52"/> comprenant de tels composés ; l'utilisation de tels composés en thérapie (par exemple dans le traitement ou la prévention d'une maladie ou d'un état dans lequel l'activité de la kallikréine plasmatique est impliquée) ; et des procédés de traitement de patients avec de tels composés ; dans laquelle r5, r6, r7, a, b, w, x, y et z sont tels que définis ici.
MA52063A 2014-11-27 2015-11-26 Composés de n-((hét)arylméthyl)hétéroaryle-carboxamides en tant qu'inhibiteurs de la kallicréine plasmatique MA52063B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1421083.5A GB201421083D0 (en) 2014-11-27 2014-11-27 Enzyme inhibitors
PCT/GB2015/053615 WO2016083820A1 (fr) 2014-11-27 2015-11-26 Composés n-((het)arylméthyl)-hétéroaryl-carboxamides comme inhibiteurs de la kallikréine plasmatique

Publications (2)

Publication Number Publication Date
MA52063A MA52063A (fr) 2021-05-26
MA52063B1 true MA52063B1 (fr) 2022-01-31

Family

ID=52349552

Family Applications (3)

Application Number Title Priority Date Filing Date
MA47217A MA47217B1 (fr) 2014-11-27 2015-11-26 Composés de n-((hét)arylméthyl)hétéroaryle-carboxamides en tant qu'inhibiteurs de la kallicréine plasmatique
MA41014A MA41014B1 (fr) 2014-11-27 2015-11-26 Composés n-((het)arylméthyl)-hétéroaryl-carboxamides comme inhibiteurs de la kallikréine plasmatique
MA52063A MA52063B1 (fr) 2014-11-27 2015-11-26 Composés de n-((hét)arylméthyl)hétéroaryle-carboxamides en tant qu'inhibiteurs de la kallicréine plasmatique

Family Applications Before (2)

Application Number Title Priority Date Filing Date
MA47217A MA47217B1 (fr) 2014-11-27 2015-11-26 Composés de n-((hét)arylméthyl)hétéroaryle-carboxamides en tant qu'inhibiteurs de la kallicréine plasmatique
MA41014A MA41014B1 (fr) 2014-11-27 2015-11-26 Composés n-((het)arylméthyl)-hétéroaryl-carboxamides comme inhibiteurs de la kallikréine plasmatique

Country Status (39)

Country Link
US (7) US10364238B2 (fr)
EP (4) EP4039681A1 (fr)
JP (5) JP6653702B2 (fr)
KR (2) KR102267623B1 (fr)
CN (2) CN110577519A (fr)
AR (2) AR102850A1 (fr)
AU (2) AU2015352193B2 (fr)
BR (1) BR112017010882B8 (fr)
CA (1) CA2967894C (fr)
CL (1) CL2017001362A1 (fr)
CO (1) CO2017006230A2 (fr)
CY (3) CY1122255T1 (fr)
DK (3) DK3567037T3 (fr)
EC (1) ECSP17039127A (fr)
ES (3) ES2745815T3 (fr)
GB (1) GB201421083D0 (fr)
HK (1) HK1244268A1 (fr)
HR (3) HRP20220314T1 (fr)
HU (3) HUE053317T2 (fr)
IL (2) IL278182B (fr)
LT (3) LT3224256T (fr)
MA (3) MA47217B1 (fr)
MD (3) MD3567037T2 (fr)
ME (1) ME03514B (fr)
MX (2) MX378283B (fr)
MY (1) MY176853A (fr)
NZ (1) NZ731945A (fr)
PH (1) PH12017500901B1 (fr)
PL (3) PL3567037T3 (fr)
PT (3) PT3556752T (fr)
RS (3) RS59395B1 (fr)
RU (1) RU2707870C2 (fr)
SG (2) SG11201703988PA (fr)
SI (3) SI3556752T1 (fr)
SM (3) SMT202100112T1 (fr)
TW (2) TWI686383B (fr)
UA (1) UA123087C2 (fr)
WO (1) WO2016083820A1 (fr)
ZA (1) ZA201907052B (fr)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI636047B (zh) 2013-08-14 2018-09-21 英商卡爾維斯塔製藥有限公司 雜環衍生物
GB201421083D0 (en) 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd Enzyme inhibitors
GB201421085D0 (en) 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd New enzyme inhibitors
WO2017059178A1 (fr) 2015-10-01 2017-04-06 Biocryst Pharmaceuticals, Inc. Inhibiteurs de la kallicréine plasmatique humaine
SG11201809922YA (en) * 2016-05-31 2018-12-28 Kalvista Pharmaceuticals Ltd Pyrazole derivatives as plasma kallikrein inhibitors
GB201609519D0 (en) * 2016-05-31 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of n-[(2,6-difluoro-3-methoxyphenyl)methyl]-3-(methoxymethyl)-1-({4-[(2-oxopyr idin-1-yl)methyl]phenyl}methyl)pyrazole-4-carboxamide
GB201609607D0 (en) 2016-06-01 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of N-(3-Fluoro-4-methoxypyridin-2-yl)methyl)-3-(methoxymethyl)-1-({4-((2-oxopy ridin-1-yl)methyl)phenyl}methyl)pyrazole-4-carboxamide and salts
GB201609603D0 (en) * 2016-06-01 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of N-[(6-cyano-2-fluoro-3-methoxyphenyl)Methyl]-3-(methoxymethyl)-1-({4-[(2-ox opyridin-1-YL)Methyl]phenyl}methyl)pyrazole-4-carboxamide
US11168080B2 (en) 2017-04-26 2021-11-09 Mitobridge, Inc. Dynamin-1-like protein inhibitors
TW201925188A (zh) * 2017-11-29 2019-07-01 英商卡爾維斯塔製藥有限公司 酶抑制劑
GB201719881D0 (en) 2017-11-29 2018-01-10 Kalvista Pharmaceuticals Ltd Solid forms of plasma kallikrein inhibitor and salts thereof
GB201719882D0 (en) * 2017-11-29 2018-01-10 Kalvista Pharmaceuticals Ltd Solid forms of a plasma kallikrein inhibitor and salts thereof
GB201721515D0 (en) * 2017-12-21 2018-02-07 Kalvista Pharmaceuticals Ltd Dosage forms comprising a plasma kallikrein inhibtor
IL312036A (en) 2017-11-29 2024-06-01 Kalvista Pharmaceuticals Ltd Dosage forms comprising a plasma kallikrein inhibitor
CA3093802A1 (fr) 2018-03-13 2019-09-19 Shire Human Genetic Therapies, Inc. Imidazopyridines substituees en tant qu'inhibiteurs de la kallicreine plasmatique et leurs utilisations
EP3886854A4 (fr) 2018-11-30 2022-07-06 Nuvation Bio Inc. Composés pyrrole et pyrazole et leurs procédés d'utilisation
GB201910125D0 (en) * 2019-07-15 2019-08-28 Kalvista Pharmaceuticals Ltd Treatments of angioedema
GB201910116D0 (en) 2019-07-15 2019-08-28 Kalvista Pharmaceuticals Ltd Treatments of hereditary angioedema
EP4010333A1 (fr) 2019-08-09 2022-06-15 Kalvista Pharmaceuticals Limited Inhibiteurs de la kallicréine plasmatique
JP2022549601A (ja) 2019-09-18 2022-11-28 武田薬品工業株式会社 ヘテロアリール血漿カリクレインインヒビター
PL4031547T3 (pl) 2019-09-18 2024-10-07 Takeda Pharmaceutical Company Limited Inhibitory kalikreiny osoczowej i ich zastosowania
CN113004286B (zh) * 2019-12-20 2022-08-12 成都康弘药业集团股份有限公司 作为血浆激肽释放酶抑制剂的三环类化合物及其用途
TW202144331A (zh) * 2020-02-13 2021-12-01 德商百靈佳殷格翰國際股份有限公司 作為血漿激肽釋放酶抑制劑之雜芳族甲醯胺衍生物
CN115210230A (zh) * 2020-03-04 2022-10-18 南京明德新药研发有限公司 杂环类化合物
WO2022079446A1 (fr) 2020-10-15 2022-04-21 Kalvista Pharmaceuticals Limited Traitements de l'œdème de quincke
EP4232031A1 (fr) 2020-10-23 2023-08-30 Kalvista Pharmaceuticals Limited Traitements de l'oedème de quincke
US20240122909A1 (en) 2021-02-09 2024-04-18 Kalvista Pharmaceuticals Limited Treatments of hereditary angioedema
WO2023002219A1 (fr) 2021-07-23 2023-01-26 Kalvista Pharmaceuticals Limited Traitements de l'angio-oedème héréditaire
WO2023185634A1 (fr) * 2022-03-30 2023-10-05 南京明德新药研发有限公司 Composé hétérocyclique utilisé comme inhibiteur de la kallicréine plasmatique
KR20250002615A (ko) 2022-04-27 2025-01-07 칼비스타 파마슈티컬즈 리미티드 혈장 칼리크레인 저해제의 제형
WO2024025907A1 (fr) * 2022-07-29 2024-02-01 Rezolute, Inc. Inhibiteurs de la kallicréine plasmatique
WO2024180100A1 (fr) 2023-02-27 2024-09-06 Kalvista Pharmaceuticals Limited Nouvelle forme solide d'un inhibiteur de la kallicréine plasmatique

Family Cites Families (98)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5187157A (en) 1987-06-05 1993-02-16 Du Pont Merck Pharmaceutical Company Peptide boronic acid inhibitors of trypsin-like proteases
GB9019558D0 (en) 1990-09-07 1990-10-24 Szelke Michael Enzyme inhibitors
SE9301911D0 (sv) 1993-06-03 1993-06-03 Ab Astra New peptide derivatives
US5589467A (en) 1993-09-17 1996-12-31 Novo Nordisk A/S 2,5',N6-trisubstituted adenosine derivatives
US5786328A (en) 1995-06-05 1998-07-28 Genentech, Inc. Use of kunitz type plasma kallikrein inhibitors
US7101878B1 (en) 1998-08-20 2006-09-05 Agouron Pharmaceuticals, Inc. Non-peptide GNRH agents, methods and intermediates for their preparation
IL144910A0 (en) 1999-04-15 2002-06-30 Bristol Myers Squibb Co Cyclic compounds and pharmaceutical compositions containing the same
JP4351053B2 (ja) 2001-10-26 2009-10-28 イステイチユート・デイ・リチエルケ・デイ・ビオロジア・モレコラーレ・ピ・アンジエレツテイ・エツセ・ピー・アー ジヒドロキシピリミジンカルボキサミド系hivインテグラーゼ阻害薬
ATE455104T1 (de) 2001-11-01 2010-01-15 Icagen Inc Pyrazolamide zur anwendung in der behandlung von schmerz
GB0205527D0 (en) 2002-03-08 2002-04-24 Ferring Bv Inhibitors
AU2003230829B8 (en) 2002-04-26 2008-12-11 Eli Lilly And Company Triazole derivatives as tachykinin receptor antagonists
EP1426364A1 (fr) 2002-12-04 2004-06-09 Aventis Pharma Deutschland GmbH Dérivés d'imidazole comme inhibiteurs du facteur Xa
DE10301300B4 (de) 2003-01-15 2009-07-16 Curacyte Chemistry Gmbh Verwendung von acylierten 4-Amidino- und 4-Guanidinobenzylaminen zur Inhibierung von Plasmakallikrein
EP1603883B1 (fr) 2003-02-03 2012-03-28 Janssen Pharmaceutica NV Amides derives quinoliniques modulant le recepteur vr1 vanilloide
PT1660057E (pt) 2003-08-27 2012-08-02 Ophthotech Corp Terapia de associação para o tratamento de distúrbios neovasculares oculares
TW200526588A (en) * 2003-11-17 2005-08-16 Smithkline Beecham Corp Chemical compounds
GB0403155D0 (en) 2004-02-12 2004-03-17 Vernalis Res Ltd Chemical compounds
EP1568698A1 (fr) 2004-02-27 2005-08-31 Aventis Pharma Deutschland GmbH Dérivés de pyrrole en tant qu'inhibiteurs du facteur xa
US7429604B2 (en) 2004-06-15 2008-09-30 Bristol Myers Squibb Company Six-membered heterocycles useful as serine protease inhibitors
ATE518858T1 (de) 2004-09-03 2011-08-15 Yuhan Corp Pyrroloä3,2-cüpyridinderivate und herstellungsverfahren dafür
EP1858542A4 (fr) 2005-02-24 2009-08-19 Joslin Diabetes Center Inc Compositions et methodes permettant de traiter la permeabilite vasculaire
GB0508472D0 (en) 2005-04-26 2005-06-01 Glaxo Group Ltd Compounds
KR101142363B1 (ko) 2005-06-27 2012-05-21 주식회사유한양행 피롤로피리딘 유도체를 포함하는 항암제 조성물
KR20080032188A (ko) 2005-07-14 2008-04-14 다케다 샌디에고, 인코포레이티드 히스톤 탈아세틸화 효소 억제제
WO2007011328A1 (fr) * 2005-07-14 2007-01-25 Jackson Kenneth A Procédé d’inhibition d’aiguille hypodermique après utilisation
US20070254894A1 (en) 2006-01-10 2007-11-01 Kane John L Jr Novel small molecules with selective cytotoxicity against human microvascular endothelial cell proliferation
GB0606876D0 (en) 2006-04-05 2006-05-17 Glaxo Group Ltd Compounds
US20070258976A1 (en) 2006-05-04 2007-11-08 Ward Keith W Combination Therapy for Diseases Involving Angiogenesis
WO2008003697A1 (fr) 2006-07-06 2008-01-10 Glaxo Group Limited N-phenylmethyl -5-oxo-proline-2-amides substitués tenant lieu d'antagonistes du récepteur p2x7 et procédés d'utilisation
CA2658523C (fr) 2006-07-31 2012-06-12 Activesite Pharmaceuticals, Inc. Inhibiteurs de kallicreine plasmatique
DE102006050672A1 (de) 2006-10-24 2008-04-30 Curacyte Discovery Gmbh Hemmstoffe des Plasmins und des Plasmakallikreins
ES2381879T3 (es) 2006-12-29 2012-06-01 Abbott Gmbh & Co. Kg Compuestos de carboxamida y su uso como inhibidores de calpaína
WO2008091692A2 (fr) 2007-01-25 2008-07-31 Joslin Diabetes Center, Inc. Procédés de diagnostic, de traitement et de prévention de la perméabilité vasculaire accrue
CA2680173A1 (fr) 2007-03-07 2008-09-12 Alantos Pharmaceuticals Holding, Inc. Inhibiteurs de metalloprotease contenant une fraction heterocyclique
MY154895A (en) 2007-03-30 2015-08-14 Sanofi Aventis Pyrimidine hydrazide compounds as pgds inhibitors
EA200970912A1 (ru) 2007-04-03 2010-02-26 Глэксо Груп Лимитед Карбоксамидные производные имидазолидина в качестве модуляторов p2x7
CL2008002172A1 (es) 2007-07-26 2008-11-21 Syngenta Participations Ag Compuestos derivados de pirazol-etiloxiamidas; compuestos intermediarios; metodo para controlar o prevenir la infestacion de plantas utiles por parte de microorganismos fitopatogenos; y composicion para controlar y proteger contra microorganismos fitopatogenos.
JP2010536871A (ja) 2007-08-22 2010-12-02 アラーガン、インコーポレイテッド スフィンゴシン−1−リン酸受容体アゴニストまたはアンタゴニスト生物学的活性を有するピロール化合物
EP2219646A4 (fr) 2007-12-21 2010-12-22 Univ Rochester Procédé permettant de modifier la durée de vie d'organismes eucaryotes
WO2009083553A1 (fr) 2007-12-31 2009-07-09 Rheoscience A/S Composés azines en tant qu'activateurs de glucokinase
EP2259679A4 (fr) 2008-01-31 2011-09-14 Joslin Diabetes Ct Méthodes de traitement de troubles associés à la kallikréine
WO2009106980A2 (fr) 2008-02-29 2009-09-03 Pfizer Inc. Dérivés d'indazole
CN102026996B (zh) 2008-03-13 2015-01-07 百时美施贵宝公司 作为凝血因子xia抑制剂的哒嗪衍生物
WO2010004972A1 (fr) 2008-07-08 2010-01-14 第一三共株式会社 Composé à hétérocycle aromatique contenant de l'azote
US8324385B2 (en) 2008-10-30 2012-12-04 Madrigal Pharmaceuticals, Inc. Diacylglycerol acyltransferase inhibitors
GB0910003D0 (en) 2009-06-11 2009-07-22 Univ Leuven Kath Novel compounds for the treatment of neurodegenerative diseases
KR20120120237A (ko) 2009-12-18 2012-11-01 액티브사이트 파마슈티칼즈, 인크. 혈장 칼리크레인 억제제의 전구약물
JP2011157349A (ja) 2010-01-07 2011-08-18 Daiichi Sankyo Co Ltd 含窒素芳香族ヘテロシクリル化合物を含有する医薬組成物
MX345259B (es) 2010-01-28 2017-01-23 The Medicines Company (Leipzig) Gmbh Inhibidores de serina proteasas similares a tripsina, y su preparación y uso.
JP2013121919A (ja) 2010-03-25 2013-06-20 Astellas Pharma Inc 血漿カリクレイン阻害剤
EP2590945B1 (fr) 2010-07-07 2014-04-30 The Medicines Company (Leipzig) GmbH Inhibiteurs de la sérine protéase
WO2012009009A2 (fr) 2010-07-14 2012-01-19 Addex Pharma S.A. Nouveaux dérivés de 2-amino-4-pyrazolyl-thiazole et leur utilisation en tant que modulateurs allostériques des récepteurs métabotropiques du glutamate
US9290485B2 (en) * 2010-08-04 2016-03-22 Novartis Ag N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides
EP2458315B1 (fr) 2010-11-25 2017-01-04 Balcke-Dürr GmbH Echangeur thermique régénératif doté d'un joint de rotor forcé
EP2697196A1 (fr) 2011-04-13 2014-02-19 Activesite Pharmaceuticals, Inc. Promédicaments d'inhibiteurs de la kallicréine plasmatique
US9133128B2 (en) 2011-06-17 2015-09-15 Research Triangle Institute Pyrazole derivatives as cannabinoid receptor 1 antagonists
GB2494851A (en) 2011-07-07 2013-03-27 Kalvista Pharmaceuticals Ltd Plasma kallikrein inhibitors
US8952180B2 (en) 2011-09-27 2015-02-10 Bristol-Myers Squibb Company Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors
EP2760828B1 (fr) 2011-09-27 2015-10-21 Bristol-Myers Squibb Company Composés de pyrrolinone-carboxamide utiles en tant qu'inhibiteurs de lipase endothéliale
US20140378474A1 (en) * 2012-01-27 2014-12-25 Novartis Ag 5-membered heteroarylcarboxamide derivatives as plasma kallikrein inhibitors
WO2013111107A1 (fr) 2012-01-27 2013-08-01 Novartis Ag Dérivés d'aminopyridine utilisés en tant qu'inhibiteurs de la kallicréine plasmatique
CA2862289C (fr) 2012-02-10 2019-11-26 Constellation Pharmaceuticals, Inc. Modulateurs d'enzymes de modification par methylation, leurs compositions et utilisations
WO2013130603A1 (fr) 2012-02-27 2013-09-06 Board Of Regents, The University Of Texas System Ganglioside gd2 en tant que marqueur et cible sur des cellules souches cancéreuses
GB201212081D0 (en) 2012-07-06 2012-08-22 Kalvista Pharmaceuticals Ltd New polymorph
MX2015008293A (es) 2013-01-08 2016-06-02 Savira Pharmaceuticals Gmbh Derivados de pirimidona y su uso en el tratamiento, mejora o prevencion de una enfermedad viral.
GB201300304D0 (en) 2013-01-08 2013-02-20 Kalvista Pharmaceuticals Ltd Benzylamine derivatives
GB2510407A (en) 2013-02-04 2014-08-06 Kalvista Pharmaceuticals Ltd Aqueous suspensions of kallikrein inhibitors for parenteral administration
US11156612B2 (en) 2013-01-20 2021-10-26 Takeda Pharmaceutical Company Limited Methods of determining levels of cleaved and/or intact kininogen
EP2968297B1 (fr) 2013-03-15 2018-09-26 Verseon Corporation Composés aromatiques multisubstitués en tant qu'inhibiteurs de sérine protéase
ES2626968T3 (es) 2013-05-23 2017-07-26 Kalvista Pharmaceuticals Limited Derivados heterocíclicos
GB2517908A (en) 2013-08-14 2015-03-11 Kalvista Pharmaceuticals Ltd Bicyclic inhibitors
CA2920815C (fr) 2013-08-14 2021-09-21 Kalvista Pharmaceuticals Limited Inhibiteurs de la kallicreine plasmatique
US9611252B2 (en) 2013-12-30 2017-04-04 Lifesci Pharmaceuticals, Inc. Therapeutic inhibitory compounds
US10266515B2 (en) 2013-12-30 2019-04-23 Lifesci Pharmaceuticals, Inc. Therapeutic inhibitory compounds
NZ762034A (en) 2014-03-07 2022-02-25 Biocryst Pharm Inc Human plasma kallikrein inhibitors
WO2015171527A1 (fr) 2014-05-05 2015-11-12 Global Blood Therapeutics, Inc. Pyrazolopyridine, pyrazolopyrimidine et composés apparentés
WO2015171526A2 (fr) 2014-05-05 2015-11-12 Global Blood Therapeutics, Inc. Composés de pyrazolopyridine tricycliques
WO2016011209A1 (fr) 2014-07-16 2016-01-21 Lifesci Pharmaceuticals, Inc. Composés inhibiteurs thérapeutiques
AU2015305214B2 (en) 2014-08-22 2020-04-23 Biocryst Pharmaceuticals, Inc. Compositions and uses of amidine derivatives
JP2017528486A (ja) 2014-09-17 2017-09-28 ヴァーセオン コーポレイション セリンプロテアーゼ阻害剤としてのピラゾリル置換ピリドン化合物
GB201421088D0 (en) 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd New enzyme inhibitors
GB201421083D0 (en) * 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd Enzyme inhibitors
GB201421085D0 (en) 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd New enzyme inhibitors
PL3261639T3 (pl) 2015-02-27 2022-12-19 Verseon International Corporation Podstawione związki pirazolowe jako inhibitory proteazy serynowej
EP3317241A4 (fr) 2015-07-01 2019-01-23 Lifesci Pharmaceuticals, Inc. Composés inhibiteurs thérapeutiques
CA2991171A1 (fr) 2015-07-01 2017-01-05 Lifesci Pharmaceuticals, Inc. Composes inhibiteurs therapeutiques
WO2017072020A1 (fr) 2015-10-27 2017-05-04 Boehringer Ingelheim International Gmbh Utilisation de dérivés hétéroarylcarboxamides comme inhibiteurs de la kallicréine plasmatique
US10640486B2 (en) 2015-10-27 2020-05-05 Boehringer Ingelheim International Gmbh Heteroarylcarboxamide derivatives as plasma kallikrein inhibitors
SG11201809922YA (en) 2016-05-31 2018-12-28 Kalvista Pharmaceuticals Ltd Pyrazole derivatives as plasma kallikrein inhibitors
GB201609519D0 (en) 2016-05-31 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of n-[(2,6-difluoro-3-methoxyphenyl)methyl]-3-(methoxymethyl)-1-({4-[(2-oxopyr idin-1-yl)methyl]phenyl}methyl)pyrazole-4-carboxamide
GB201609603D0 (en) 2016-06-01 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of N-[(6-cyano-2-fluoro-3-methoxyphenyl)Methyl]-3-(methoxymethyl)-1-({4-[(2-ox opyridin-1-YL)Methyl]phenyl}methyl)pyrazole-4-carboxamide
GB201609601D0 (en) 2016-06-01 2016-07-13 Nucana Biomed Ltd Phosphoramidate compounds
GB201609607D0 (en) 2016-06-01 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of N-(3-Fluoro-4-methoxypyridin-2-yl)methyl)-3-(methoxymethyl)-1-({4-((2-oxopy ridin-1-yl)methyl)phenyl}methyl)pyrazole-4-carboxamide and salts
GB201609602D0 (en) 2016-06-01 2016-07-13 Nucuna Biomed Ltd Chemical compounds
EP3481391A4 (fr) 2016-07-11 2020-03-11 Lifesci Pharmaceuticals, Inc. Composés inhibiteurs thérapeutiques
TW201925188A (zh) 2017-11-29 2019-07-01 英商卡爾維斯塔製藥有限公司 酶抑制劑
GB201719881D0 (en) 2017-11-29 2018-01-10 Kalvista Pharmaceuticals Ltd Solid forms of plasma kallikrein inhibitor and salts thereof
GB201719882D0 (en) 2017-11-29 2018-01-10 Kalvista Pharmaceuticals Ltd Solid forms of a plasma kallikrein inhibitor and salts thereof

Also Published As

Publication number Publication date
PH12017500901A1 (en) 2017-12-18
NZ731945A (en) 2021-07-30
IL278182A (en) 2020-11-30
EP3567037A1 (fr) 2019-11-13
BR112017010882A2 (pt) 2017-12-26
US11084809B2 (en) 2021-08-10
US20200361923A1 (en) 2020-11-19
US20190330200A1 (en) 2019-10-31
US20250074903A1 (en) 2025-03-06
ES2745815T3 (es) 2020-03-03
CY1125214T1 (el) 2023-06-09
RS61497B1 (sr) 2021-03-31
PL3556752T3 (pl) 2022-05-02
MY176853A (en) 2020-08-24
CN107108576B (zh) 2020-03-10
AR121273A2 (es) 2022-05-04
US11198691B2 (en) 2021-12-14
MA47217A (fr) 2019-11-13
EP3556752A1 (fr) 2019-10-23
JP2021185138A (ja) 2021-12-09
ES2908303T3 (es) 2022-04-28
JP2022180520A (ja) 2022-12-06
MX2020013038A (es) 2022-12-09
LT3556752T (lt) 2022-03-10
DK3224256T3 (da) 2019-09-23
IL278182B (en) 2022-09-01
CO2017006230A2 (es) 2017-09-11
JP2020033357A (ja) 2020-03-05
NZ770256A (en) 2021-11-26
MD3556752T2 (ro) 2022-07-31
RU2019131174A (ru) 2019-10-10
SMT201900497T1 (it) 2019-11-13
EP3224256B1 (fr) 2019-07-03
RU2017122364A (ru) 2018-12-27
SG10201907819WA (en) 2019-09-27
HUE057647T2 (hu) 2022-05-28
CA2967894C (fr) 2024-01-30
LT3224256T (lt) 2019-09-25
TW201625548A (zh) 2016-07-16
PT3567037T (pt) 2021-02-23
MD3567037T2 (ro) 2021-05-31
SMT202100112T1 (it) 2021-05-07
TWI741377B (zh) 2021-10-01
KR20210075227A (ko) 2021-06-22
HRP20210350T1 (hr) 2021-04-16
US20180319782A1 (en) 2018-11-08
MX2017006823A (es) 2017-09-27
AU2019240616A1 (en) 2019-10-17
LT3567037T (lt) 2021-02-25
PL3224256T3 (pl) 2020-01-31
PT3556752T (pt) 2022-04-14
US20220289729A1 (en) 2022-09-15
PH12017500901B1 (en) 2022-04-27
CA2967894A1 (fr) 2016-06-02
ZA201907052B (en) 2025-01-29
US10364238B2 (en) 2019-07-30
KR102496404B1 (ko) 2023-02-06
PL3567037T3 (pl) 2021-06-14
SI3556752T1 (sl) 2022-05-31
HRP20191524T1 (hr) 2019-11-29
MD3224256T2 (ro) 2019-12-31
CL2017001362A1 (es) 2018-02-09
DK3567037T3 (da) 2021-02-08
MA41014B1 (fr) 2019-09-30
RS59395B1 (sr) 2019-11-29
RS63155B1 (sr) 2022-05-31
EP3567037B1 (fr) 2020-12-23
CN110577519A (zh) 2019-12-17
CN107108576A (zh) 2017-08-29
SI3224256T1 (sl) 2019-12-31
UA123087C2 (uk) 2021-02-17
MA52063A (fr) 2021-05-26
KR102267623B1 (ko) 2021-06-18
US11001578B2 (en) 2021-05-11
AR102850A1 (es) 2017-03-29
CY1124046T1 (el) 2022-05-27
AU2015352193B2 (en) 2019-10-10
KR20170090451A (ko) 2017-08-07
GB201421083D0 (en) 2015-01-14
HUE053317T2 (hu) 2021-06-28
BR112017010882B1 (pt) 2023-10-31
PT3224256T (pt) 2019-09-23
ECSP17039127A (es) 2017-12-01
US20200199116A1 (en) 2020-06-25
SI3567037T1 (sl) 2021-04-30
SMT202200107T1 (it) 2022-05-12
CY1122255T1 (el) 2020-11-25
ES2858082T3 (es) 2021-09-29
TWI686383B (zh) 2020-03-01
RU2017122364A3 (fr) 2019-06-19
TW202026285A (zh) 2020-07-16
RU2707870C2 (ru) 2019-12-02
JP2025000918A (ja) 2025-01-07
SG11201703988PA (en) 2017-06-29
IL252287B (en) 2020-11-30
HUE047425T2 (hu) 2020-04-28
US10611758B2 (en) 2020-04-07
JP6995101B2 (ja) 2022-01-14
JP7148683B2 (ja) 2022-10-05
WO2016083820A1 (fr) 2016-06-02
AU2015352193A1 (en) 2017-06-08
DK3556752T3 (da) 2022-03-07
HK1244268A1 (zh) 2018-08-03
MA41014A (fr) 2017-10-04
EP3224256A1 (fr) 2017-10-04
HRP20220314T1 (hr) 2022-05-13
MX378283B (es) 2025-03-10
MA47217B1 (fr) 2021-04-30
AU2019240616B2 (en) 2021-07-29
EP4039681A1 (fr) 2022-08-10
JP6653702B2 (ja) 2020-02-26
ME03514B (fr) 2020-04-20
BR112017010882B8 (pt) 2023-11-14
JP2017535568A (ja) 2017-11-30
EP3556752B1 (fr) 2022-01-05
US20190300517A1 (en) 2019-10-03
IL252287A0 (en) 2017-07-31

Similar Documents

Publication Publication Date Title
MA52063B1 (fr) Composés de n-((hét)arylméthyl)hétéroaryle-carboxamides en tant qu&#39;inhibiteurs de la kallicréine plasmatique
PH12021552497A1 (en) Enzyme inhibitors
MA39721A (fr) Nouvelles héteroaryldihydropyrimidines condensées en position 6 pour le traitement et la prophylaxie d&#39;une infection à virus de l&#39;hépatite b
MA45920A (fr) Inhibiteurs de pyridopyrimidinone cdk2/4/6
MA47043B1 (fr) Composés indole carboxamides utiles comme inhibiteurs de kinase
MA39219B1 (fr) Nouveaux composés inhibiteurs de la kinase lrrk2 utilisés pour le traitement du parkinson, de l’alzheimer et de la sclérose latérale amyotrophique
MA42795A (fr) Composés thérapeutiques utiles pour le traitement prophylactique ou thérapeutique d&#39;une infection par le virus du vih
MA40290A1 (fr) Agents immunorégulateurs
MA43335A (fr) Compositions d&#39;arni de transthyrétine (ttr) et procédés pour les utiliser pour le traitement ou la prévention de maladies associées à ttr
MA39984B1 (fr) Traitement d&#39;affections malignes par lymphocytes b par un inhibiteur jak et pi3k combiné
MA53399B1 (fr) Pyrazoles substitués en tant qu`inhibiteurs de la kallicréine plasmatique humaine
MA40225A (fr) Composés dihydroisoquinolinone substitués
MA41562A1 (fr) Agonistes d&#39;apj 4-hydroxy-3-(heteroaryl)pyridine-2-one a utiliser dans le traitement de troubles cardio-vasculaires
MA34002B1 (fr) Thérapie antivirale
MA40221A (fr) Dérivés d&#39;isoindoline à utiliser dans le traitement d&#39;une infection virale
MA50013B1 (fr) Analogues de benzoazépine utilisés en tant qu&#39;agents inhibiteurs de la tyrosine kinase de bruton
MA38986B1 (fr) Inhibiteurs marqués de l&#39;antigène membranaire spécifique de la prostate (psma), leur utilisation comme agents d&#39;imagerie et agents pharmaceutiques pour le traitement du cancer de la prostate
MA40955B1 (fr) 2-amino-6-(difluorométhyl)-5,5-difluoro-6-phényl-3,4,5,6-tétrahydropyridines comme inhibiteurs de bace1
EP2091328A4 (fr) Composés de spiropipéridine inhibiteurs de la bêta-sécrétase pour le traitement de la maladie d&#39;alzheimer
MA44948A1 (fr) Inhibiteurs de bace 1
MA34815B1 (fr) Compositions comprenant un inhibiteur de pi3k et un inhibiteur de mek et leur utilisation pour le traitement du cancer
MX2022000545A (es) Inhibidores de enzimas.
CO2017007691A2 (es) Inhibidores de la β-secretasa derivados de la 5-amino-3-(5-(3-isoxazol-5-il)-3-(fluorometil)-6,6-dimetil-1-(metilimino)-3,6-dihidro-2h-1,4-tiazina o 5-amino-3-(5-(1h-1,2,3-triazol-4-il)-2-fluorofenil)-6,6-dimetil-1-(metilimino)-3,6-dihidro-2h-1,4-tiazina composiciones que los comprenden y métodos de elaboración
MA41975B1 (fr) Derives d&#39;aminohydrothiazine fusionnee contenant du tetrahydrofurane utiles dans le traitement de la maladie d&#39;alzheimer
MA37849A1 (fr) Dérivés de diazépinone à utiliser pour le traitement du syndrome de l&#39;x fragile, de la maladie de parkinson ou de la maladie du reflux