MA54538A - Inhibiteurs d'apol1 et leurs procédés d'utilisation - Google Patents

Inhibiteurs d'apol1 et leurs procédés d'utilisation

Info

Publication number
MA54538A
MA54538A MA054538A MA54538A MA54538A MA 54538 A MA54538 A MA 54538A MA 054538 A MA054538 A MA 054538A MA 54538 A MA54538 A MA 54538A MA 54538 A MA54538 A MA 54538A
Authority
MA
Morocco
Prior art keywords
apol1
inhibitors
methods
apol1 inhibitors
Prior art date
Application number
MA054538A
Other languages
English (en)
Inventor
Michael Brodney
Jingrong Cao
Jon H Come
Leslie A Dakin
Francois Denis
Warren A Dorsch
Anne Fortier
Kevin Gagnon
Martine Hamel
Kan-Nian Hu
Elaine B Krueger
Brian Ledford
Ales Medek
Suganthini S Nanthakumar
Olivier Nicolas
Peter Rose
Camil Sayegh
Timothy J Senter
Yi Shi
Muna Shrestha
Tiansheng Wang
Faith Witkos
Original Assignee
Vertex Pharma
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 Vertex Pharma filed Critical Vertex Pharma
Publication of MA54538A publication Critical patent/MA54538A/fr

Links

Classifications

    • 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
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • 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
    • A61K31/66—Phosphorus compounds
    • A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • 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
    • A61K31/69—Boron compounds
    • 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
    • A61K31/695—Silicon compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02—Boron compounds
    • C07F5/025—Boronic and borinic acid compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • C07F7/0814—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • C07F7/0816—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring comprising Si as a ring atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/46—Phosphinous acids [R2POH], [R2P(= O)H]: Thiophosphinous acids including[R2PSH]; [R2P(=S)H]; Aminophosphines [R2PNH2]; Derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
    • C07F9/6584—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms having one phosphorus atom as ring hetero atom
    • C07F9/65842—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/05—Isotopically modified compounds, e.g. labelled
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
MA054538A 2018-12-17 2019-12-17 Inhibiteurs d'apol1 et leurs procédés d'utilisation MA54538A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201862780667P 2018-12-17 2018-12-17

Publications (1)

Publication Number Publication Date
MA54538A true MA54538A (fr) 2021-10-27

Family

ID=69182627

Family Applications (1)

Application Number Title Priority Date Filing Date
MA054538A MA54538A (fr) 2018-12-17 2019-12-17 Inhibiteurs d'apol1 et leurs procédés d'utilisation

Country Status (24)

Country Link
US (2) US11618746B2 (fr)
EP (1) EP3897833A1 (fr)
KR (1) KR20210116483A (fr)
CN (1) CN113453760B (fr)
AR (1) AR116913A1 (fr)
AU (1) AU2019405477A1 (fr)
BR (1) BR112021011564A2 (fr)
CA (1) CA3121910A1 (fr)
CL (1) CL2021001561A1 (fr)
CO (1) CO2021009053A2 (fr)
CR (1) CR20210383A (fr)
DO (1) DOP2021000116A (fr)
EC (1) ECSP21052184A (fr)
IL (1) IL283592A (fr)
JO (3) JOP20210130A1 (fr)
MA (1) MA54538A (fr)
MX (1) MX2021007152A (fr)
PE (1) PE20212302A1 (fr)
SA (1) SA521422270B1 (fr)
SG (1) SG11202105769XA (fr)
TW (1) TWI848031B (fr)
UA (1) UA128375C2 (fr)
UY (1) UY38514A (fr)
WO (1) WO2020131807A1 (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11202105769XA (en) 2018-12-17 2021-07-29 Vertex Pharma Inhibitors of apol1 and methods of using same
CN116348447A (zh) 2020-01-29 2023-06-27 弗特克斯药品有限公司 Apol1的抑制剂及其使用其的方法
TW202140459A (zh) * 2020-02-04 2021-11-01 美商維泰克斯製藥公司 Ａｐｏｌ１抑制劑之固體形式及其使用方法
WO2021178768A1 (fr) * 2020-03-06 2021-09-10 Vertex Pharmaceuticals Incorporated Méthodes de traitement de la glomérulosclérose segmentaire et focale dépendante de l'apol -1
EP4165036A1 (fr) * 2020-06-12 2023-04-19 Vertex Pharmaceuticals Incorporated Formes solides d'un inhibiteur d'apol1 et utilisation de celles-ci
MX2023002269A (es) 2020-08-26 2023-05-16 Vertex Pharma Inhibidores de apol1 y metodos para usar los mismos.
EP4392426A1 (fr) * 2021-08-26 2024-07-03 Vertex Pharmaceuticals Incorporated Formes à l'état solide d'inhibiteurs d'apol1 spirotricycliques et leurs procédés d'utilisation
WO2023101981A1 (fr) * 2021-11-30 2023-06-08 Vertex Pharmaceuticals Incorporated Inhibiteurs spirocycliques d'apol1 et procédés d'utilisationde ceux-ci
AU2023208684A1 (en) 2022-01-18 2024-09-05 Maze Therapeutics, Inc. Apol1 inhibitors and methods of use
AU2023218994A1 (en) * 2022-02-08 2024-08-22 Vertex Pharmaceuticals Incorporated 2-methyl-4',5'-dihydrospiro[piperidine-4,7'-thieno[2,3-c]pyran] derivatives as inhibitors of apol1 and methods of using same
WO2023194895A1 (fr) 2022-04-06 2023-10-12 Glaxosmithkline Intellectual Property Development Limited Dérivés pyrroliques utilisés en tant qu'inhibiteurs de l'apolipoprotéine l-1
WO2024040235A1 (fr) * 2022-08-19 2024-02-22 Maze Therapeutics, Inc. Inhibiteurs d'apol1 et procédés d'utilisation

Family Cites Families (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4039676A (en) 1975-06-23 1977-08-02 Ciba-Geigy Corporation 2-piperidinoalkyl-1,4-benzodioxans
AU3784997A (en) 1996-08-09 1998-03-06 Eisai Co. Ltd. Benzopiperidine derivatives
AU2201699A (en) 1997-12-19 1999-07-12 Eli Lilly And Company Hypoglycemic imidazoline compounds
GB9905010D0 (en) 1999-03-04 1999-04-28 Merck Sharp & Dohme Therapeutic agents
WO2001017965A2 (fr) 1999-09-07 2001-03-15 Syngenta Participations Ag Cyanopiperidines
FR2801585B1 (fr) 1999-11-25 2002-02-15 Fournier Ind & Sante Nouveaux antagonistes des recepteurs de l'ii-8
GB0003397D0 (en) 2000-02-14 2000-04-05 Merck Sharp & Dohme Therapeutic agents
EP1324985A4 (fr) 2000-10-02 2004-10-06 Merck & Co Inc Inhibiteurs de la prenyl-proteine transferase
FR2824827B1 (fr) 2001-05-17 2004-02-13 Fournier Lab Sa Nouveaux derives de 5-phenyl-1h-indole antagoniste des recepteurs de l'interleukine-8
FR2824826B1 (fr) 2001-05-17 2003-11-07 Fournier Lab Sa Nouveaux derives de 5-cyano-1h-indole antagonistes des recepteurs de l'interleukine-8
WO2003048135A1 (fr) 2001-11-14 2003-06-12 Teva Pharmaceutical Industries Ltd. Formes cristallines amorphes de losartan potassique et leur procede de preparation
WO2003104180A1 (fr) * 2002-06-05 2003-12-18 Natco Pharma Limited Procede de preparation d'acide 4-(4-fluorobenzoyl) butyrique
EP1572660B1 (fr) 2002-12-20 2011-01-26 X-Ceptor Therapeutics, Inc. Dérives d'isoquinolinone et leur utilisation comme agents thérapeutiques
EP1663972A1 (fr) 2003-09-03 2006-06-07 Galapagos N.V. Nouveau 4-piperidine-carboxamide et leur utilisation pour preparer des medicaments contre des troubles lies au recepteur de la 5-ht2a
CA2557745A1 (fr) 2004-03-03 2005-10-06 Eli Lilly And Company Modulateurs de recepteur nucleaire d'hormones steroides a base de derives indole substitues bicycliques
AR048523A1 (es) 2004-04-07 2006-05-03 Kalypsys Inc Compuestos con estructura de aril sulfonamida y sulfonilo como moduladores de ppar y metodos para tratar trastornos metabolicos
EP1954276A2 (fr) 2005-11-22 2008-08-13 Merck & Co., Inc. Antagonistes des recepteurs de l'indole orexine
US8222288B2 (en) 2006-08-30 2012-07-17 The Regents Of The University Of Michigan Small molecule inhibitors of MDM2 and the uses thereof
EP2086935A1 (fr) 2006-10-16 2009-08-12 Grünenthal GmbH Derives de sulfonamide substitues en tant que modulateurs du recepteur de bradykinine-1
WO2008077810A2 (fr) 2006-12-22 2008-07-03 F. Hoffmann-La Roche Ag Dérivés de spiropipéridine
DK2118074T3 (en) 2007-02-01 2014-03-10 Resverlogix Corp Compounds for the prevention and treatment of cardiovascular diseases
EP2020414A1 (fr) 2007-06-20 2009-02-04 Laboratorios del Dr. Esteve S.A. Derivés spiro[piperidine-4,4'-thieno[3,2-c]pyran] et composés similaires en tant que inhibiteurs du recepteur sigma pour le traitement de pyschose
RU2437883C1 (ru) 2007-08-17 2011-12-27 Эл Джи Лайф Сайенсиз Лтд. Соединения индола и индазола в качестве ингибитора некроза клетки
CA2761639C (fr) 2009-05-29 2016-06-07 Raqualia Pharma Inc. Derives de carboxamide substitues par aryle comme inhibiteurs des canaux calciques ou sodiques
SI2501704T1 (sl) 2009-11-16 2013-11-29 Eli Lilly Company Spojine spiropiperidina kot antagonisti oral-1 receptorja
UA107943C2 (en) 2009-11-16 2015-03-10 Lilly Co Eli Compounds of spiropiperidines as antagonists of the orl-1 receptors
WO2012025155A1 (fr) 2010-08-26 2012-03-01 Novartis Ag Composés à base d'hydroxamate en tant qu'inhibiteurs des désacétylases
BR102012024778A2 (pt) 2012-09-28 2014-08-19 Cristalia Prod Quimicos Farm Compostos heteroaromáticos; processo para preparar os compostos, composições farmacêuticas, usos e método de tratamento para as dores aguda e crônica
US10130632B2 (en) 2012-11-27 2018-11-20 Beth Israel Deaconess Medical Center, Inc. Methods for treating renal disease
US9850203B2 (en) 2013-09-26 2017-12-26 Pharmakea, Inc. Autotaxin inhibitor compounds
ES2687843T3 (es) 2014-03-27 2018-10-29 Academisch Medisch Centrum Iminoazúcares N-(5-((aril o heteroril)metiloxi)pentil)-sustituidos como inhibidores de glucosilceramida sintasa
EP3186225A4 (fr) 2014-08-27 2018-02-28 The Governing Council of the University of Toronto Modulateurs du récepteur cannabinoïde de type 1
BR112017007178A2 (pt) 2014-10-08 2017-12-19 Ass Francaise Contre Les Myopathies compostos de aminopiridina úteis como inibidores de prenilação de proteína
EP3221314B1 (fr) 2014-11-21 2019-07-03 Esteve Pharmaceuticals, S.A. Composés de spiro-isoquinoline-1,4'-pipéridine présentant une activité plurimodale contre la douleur
CA2996389C (fr) 2015-08-27 2020-04-07 Pfizer Inc. Composes heteroaryle ou aryle bicycliques fusionnes en tant que modulateurs d'irak 4
WO2017137334A1 (fr) 2016-02-08 2017-08-17 F. Hoffmann-La Roche Ag Spiroindolinones utilisés en tant qu'inhibiteurs de ddr1
EP3787669A4 (fr) 2018-04-30 2022-03-30 The Trustees of Indiana University Composés destinés à moduler les niveaux de ddah et d'adma, ainsi que leurs méthodes d'utilisation pour traiter une maladie
JOP20200291A1 (ar) 2018-05-22 2020-11-15 Ionis Pharmaceuticals Inc معدلات التعبير عن apol1
SG11202105769XA (en) 2018-12-17 2021-07-29 Vertex Pharma Inhibitors of apol1 and methods of using same
WO2020186220A1 (fr) 2019-03-13 2020-09-17 Immunophage Biomedical Co., Ltd. Composés en tant qu'inhibiteurs du facteur inhibiteur de la migration des macrophages
TW202136219A (zh) 2019-12-19 2021-10-01 美商卡司馬療法公司 Trpml調節劑
CN116348447A (zh) 2020-01-29 2023-06-27 弗特克斯药品有限公司 Apol1的抑制剂及其使用其的方法
TW202140459A (zh) 2020-02-04 2021-11-01 美商維泰克斯製藥公司 Ａｐｏｌ１抑制劑之固體形式及其使用方法
WO2021178768A1 (fr) 2020-03-06 2021-09-10 Vertex Pharmaceuticals Incorporated Méthodes de traitement de la glomérulosclérose segmentaire et focale dépendante de l'apol -1
CN115427404A (zh) 2020-04-22 2022-12-02 艾尼莫生物科技公司 胶原蛋白1翻译抑制剂和其使用方法
WO2021220178A1 (fr) 2020-04-29 2021-11-04 Cominnex Zrt. Antagonistes d'iap et leurs applications thérapeutiques
AU2021268129A1 (en) 2020-05-07 2022-12-08 Rambam Med-Tech Ltd. Composition for use in the treatment of ApoL1-associated disease
JP2023529216A (ja) 2020-06-12 2023-07-07 バーテックス ファーマシューティカルズ インコーポレイテッド Ａｐｏｌ１の阻害剤及びその使用
JP2023530271A (ja) 2020-06-12 2023-07-14 バーテックス ファーマシューティカルズ インコーポレイテッド Ａｐｏｌ１の阻害剤及びこれを使用する方法
EP4165036A1 (fr) 2020-06-12 2023-04-19 Vertex Pharmaceuticals Incorporated Formes solides d'un inhibiteur d'apol1 et utilisation de celles-ci
MX2023002269A (es) 2020-08-26 2023-05-16 Vertex Pharma Inhibidores de apol1 y metodos para usar los mismos.
EP4392426A1 (fr) 2021-08-26 2024-07-03 Vertex Pharmaceuticals Incorporated Formes à l'état solide d'inhibiteurs d'apol1 spirotricycliques et leurs procédés d'utilisation
WO2023101981A1 (fr) 2021-11-30 2023-06-08 Vertex Pharmaceuticals Incorporated Inhibiteurs spirocycliques d'apol1 et procédés d'utilisationde ceux-ci
US20230203000A1 (en) 2021-11-30 2023-06-29 Vertex Pharmaceuticals Incorporated Inhibitors of apol1 and methods of using same
WO2023154314A1 (fr) 2022-02-08 2023-08-17 Vertex Pharmaceuticals Incorporated Dérivés de spiro pipéridine utilisés en tant qu'inhibiteurs de apol1 et leurs procédés d'utilisation
AU2023219516A1 (en) 2022-02-08 2024-08-22 Vertex Pharmaceuticals Incorporated 2-methyl-4-phenylpiperidin-4-ol derivatives as inhibitors of apol1 and methods of using same
AU2023218939A1 (en) 2022-02-08 2024-08-22 Vertex Pharmaceuticals Incorporated 4',5'-dihydrospiro[piperidine-4,7'-thieno[2,3-c]pyran] derivatives as inhibitors of apol1 and methods of using same
AU2023218994A1 (en) 2022-02-08 2024-08-22 Vertex Pharmaceuticals Incorporated 2-methyl-4',5'-dihydrospiro[piperidine-4,7'-thieno[2,3-c]pyran] derivatives as inhibitors of apol1 and methods of using same

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Publication number Publication date
CA3121910A1 (fr) 2020-06-25
MX2021007152A (es) 2021-11-03
AR116913A1 (es) 2021-06-23
UY38514A (es) 2020-07-31
JOP20210130A1 (ar) 2023-01-30
ECSP21052184A (es) 2021-08-31
WO2020131807A1 (fr) 2020-06-25
SA521422270B1 (ar) 2024-02-18
TW202039471A (zh) 2020-11-01
TWI848031B (zh) 2024-07-11
CR20210383A (es) 2021-09-22
KR20210116483A (ko) 2021-09-27
PE20212302A1 (es) 2021-12-10
US11618746B2 (en) 2023-04-04
CN113453760B (zh) 2024-05-24
CO2021009053A2 (es) 2021-08-09
JOP20210131A1 (ar) 2023-01-30
UA128375C2 (uk) 2024-06-26
US20200377479A1 (en) 2020-12-03
CL2021001561A1 (es) 2021-11-26
AU2019405477A1 (en) 2021-06-24
IL283592A (en) 2021-07-29
EP3897833A1 (fr) 2021-10-27
SG11202105769XA (en) 2021-07-29
US12060346B2 (en) 2024-08-13
JP2022515369A (ja) 2022-02-18
BR112021011564A2 (pt) 2021-08-31
JOP20210129A1 (ar) 2023-01-30
DOP2021000116A (es) 2021-09-30
US20230271945A1 (en) 2023-08-31
CN113453760A (zh) 2021-09-28

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