CL2024000239A1 - Derivados de piridina sustituida como inhibidores de sarm1 - Google Patents

Derivados de piridina sustituida como inhibidores de sarm1

Info

Publication number
CL2024000239A1
CL2024000239A1 CL2024000239A CL2024000239A CL2024000239A1 CL 2024000239 A1 CL2024000239 A1 CL 2024000239A1 CL 2024000239 A CL2024000239 A CL 2024000239A CL 2024000239 A CL2024000239 A CL 2024000239A CL 2024000239 A1 CL2024000239 A1 CL 2024000239A1
Authority
CL
Chile
Prior art keywords
pyridine derivatives
substituted pyridine
sarm1 inhibitors
sarm1
inhibitors
Prior art date
Application number
CL2024000239A
Other languages
English (en)
Spanish (es)
Inventor
Kolluri Rao
Michael Tegley Christopher
Zhu Liusheng
Pomeroy Brown Sean
Stewart Tasker Andrew
A Grice Cheryl
Howard Reynolds Charles
Original Assignee
Nura Bio Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nura Bio Inc filed Critical Nura Bio Inc
Publication of CL2024000239A1 publication Critical patent/CL2024000239A1/es

Links

Classifications

    • 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
    • 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
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • 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
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/14Heterocyclic 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)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
CL2024000239A 2021-07-28 2024-01-26 Derivados de piridina sustituida como inhibidores de sarm1 CL2024000239A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202163226557P 2021-07-28 2021-07-28
US202263305103P 2022-01-31 2022-01-31
US202263368034P 2022-07-08 2022-07-08

Publications (1)

Publication Number Publication Date
CL2024000239A1 true CL2024000239A1 (es) 2024-06-07

Family

ID=85087993

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2024000239A CL2024000239A1 (es) 2021-07-28 2024-01-26 Derivados de piridina sustituida como inhibidores de sarm1

Country Status (12)

Country Link
US (2) US11629136B1 (enExample)
EP (1) EP4376840A4 (enExample)
JP (1) JP2024528036A (enExample)
KR (1) KR20240041987A (enExample)
AU (1) AU2022320699A1 (enExample)
CA (1) CA3226869A1 (enExample)
CL (1) CL2024000239A1 (enExample)
CO (1) CO2024001716A2 (enExample)
IL (1) IL310403A (enExample)
MX (1) MX2024001322A (enExample)
TW (1) TW202313009A (enExample)
WO (1) WO2023009663A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12404265B2 (en) 2020-08-04 2025-09-02 Nura Bio, Inc. Substituted pyridine derivatives as SARM1 inhibitors
CN116438171A (zh) 2020-09-16 2023-07-14 努拉生物公司 作为sarm1抑制剂的取代的吡啶衍生物
EP4304586A4 (en) 2021-03-10 2025-04-02 Jnana Therapeutics Inc. SMALL MOLECULE INHIBITORS OF MAMMALIAN SLC6A19 FUNCTION
EP4376840A4 (en) * 2021-07-28 2025-05-21 Nura Bio, Inc. SUBSTITUTED PYRIDINE DERIVATIVES AS SARM1 INHIBITORS
CN113655155A (zh) * 2021-07-28 2021-11-16 任贤金 一种测定sph3127有关物质的方法
EP4562001A1 (en) * 2022-07-27 2025-06-04 Nura Bio, Inc. Substituted pyridine derivatives as sarm1 inhibitors
CN120424050A (zh) * 2024-02-05 2025-08-05 科辉智药(深圳)新药研究中心有限公司 作为sarm1酶活性抑制剂的吡啶类化合物及其应用
WO2025179205A1 (en) * 2024-02-23 2025-08-28 Nura Bio, Inc. Methods for the treatment of neurological disorders
WO2026080488A1 (en) 2024-10-09 2026-04-16 Genentech, Inc. Heterocyclic compounds for the treatment of neurodegenerative diseases

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU9781098A (en) * 1997-10-02 1999-04-27 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
CA2460345A1 (en) * 2001-09-13 2003-03-20 Synta Pharmaceuticals Corp. 2-aroylimidazole compounds for treating cancer
DE102004009933A1 (de) 2004-02-26 2005-09-15 Merck Patent Gmbh Verwendung von Thiadiazolharnstoffderivaten
WO2005105780A2 (en) 2004-04-28 2005-11-10 Vertex Pharmaceuticals Incorporated Compositions useful as inhibitors of rock and other protein kinases
PE20060426A1 (es) * 2004-06-02 2006-06-28 Schering Corp DERIVADOS DE ACIDO TARTARICO COMO INHIBIDORES DE MMPs, ADAMs, TACE Y TNF-alfa
US8236824B2 (en) 2007-10-09 2012-08-07 MERCK Patent Gesellschaft mit beschränkter Haftung N-(pyrazole-3-yl)-benzamide derivatives as glucokinase activators
WO2009114552A1 (en) 2008-03-10 2009-09-17 The Board Of Trustees Of The Leland Stanford Junior University Heteroaryl compounds, compositions, and methods of use in cancer treatment
US8785468B2 (en) 2009-02-13 2014-07-22 Amgen Inc. Phenylalanine amide derivatives useful for treating insulin-related diseases and conditions
WO2012049161A1 (en) 2010-10-13 2012-04-19 Glaxo Group Limited 3 -amino- pyrazole derivatives useful against tuberculosis
WO2012050141A1 (ja) 2010-10-14 2012-04-19 住友化学株式会社 ヘテロ芳香環化合物およびその有害生物防除用途
JP6282721B2 (ja) 2013-03-14 2018-02-21 ダート・ニューロサイエンス・(ケイマン)・リミテッド Pde4阻害剤としての置換ピリジン及びピラジン化合物
AR096393A1 (es) 2013-05-23 2015-12-30 Bayer Cropscience Ag Compuestos heterocíclicos pesticidas
WO2015140130A1 (en) 2014-03-17 2015-09-24 Remynd Nv Oxadiazole compounds
WO2015175704A1 (en) * 2014-05-14 2015-11-19 The Regents Of The University Of California Inhibitors of bacterial dna gyrase with efficacy against gram-negative bacteria
CA2955872A1 (en) 2014-07-24 2016-01-28 Bayer Pharma Aktiengesellschaft Glucose transport inhibitors
JP2018515623A (ja) 2015-05-18 2018-06-14 トランスレイショナル・ドラッグ・ディベロップメント・エルエルシー キナーゼ阻害剤としての複素環式化合物
US20170355708A1 (en) 2016-06-09 2017-12-14 Cadent Therapeutics, Inc. Potassium channel modulators
EP3541806A4 (en) 2016-11-21 2020-07-01 Translational Drug Development, LLC HETEROCYCLIC COMPOUNDS FOR USE AS KINASE INHIBITORS
CA3108669A1 (en) 2018-06-07 2019-12-12 Disarm Therapeutics, Inc. Inhibitors of sarm1
KR20210143783A (ko) * 2019-02-28 2021-11-29 케자르 라이프 사이언스 단백질 분비 저해제로서 티아졸 유도체
JP7289375B2 (ja) * 2019-06-06 2023-06-09 ディスアーム セラピューティクス, インコーポレイテッド Sarm1の阻害剤
US12595252B2 (en) 2019-06-14 2026-04-07 Disarm Therapeutics, Inc. Inhibitors of SARM1
CA3150878A1 (en) * 2019-09-12 2021-03-18 Jonathan Bentley Inhibitors of sarm1
WO2021142006A1 (en) * 2020-01-07 2021-07-15 Disarm Therapeutics, Inc. Inhibitors of sarm1
US12435084B2 (en) 2020-04-09 2025-10-07 Eli Lilly And Company Indazole derivatives as inhibitors of SARM1
US12404265B2 (en) 2020-08-04 2025-09-02 Nura Bio, Inc. Substituted pyridine derivatives as SARM1 inhibitors
TWI904906B (zh) 2020-08-24 2025-11-11 美商達薩瑪治療公司 Sarm1之抑制劑
CN116438171A (zh) 2020-09-16 2023-07-14 努拉生物公司 作为sarm1抑制剂的取代的吡啶衍生物
EP4376840A4 (en) 2021-07-28 2025-05-21 Nura Bio, Inc. SUBSTITUTED PYRIDINE DERIVATIVES AS SARM1 INHIBITORS
EP4562001A1 (en) 2022-07-27 2025-06-04 Nura Bio, Inc. Substituted pyridine derivatives as sarm1 inhibitors

Also Published As

Publication number Publication date
US11629136B1 (en) 2023-04-18
JP2024528036A (ja) 2024-07-26
KR20240041987A (ko) 2024-04-01
US20230105696A1 (en) 2023-04-06
US12110285B2 (en) 2024-10-08
WO2023009663A1 (en) 2023-02-02
CO2024001716A2 (es) 2024-03-07
US20230286941A1 (en) 2023-09-14
EP4376840A1 (en) 2024-06-05
IL310403A (en) 2024-03-01
CA3226869A1 (en) 2023-02-02
TW202313009A (zh) 2023-04-01
MX2024001322A (es) 2024-04-30
EP4376840A4 (en) 2025-05-21
AU2022320699A1 (en) 2024-02-29

Similar Documents

Publication Publication Date Title
CL2024000239A1 (es) Derivados de piridina sustituida como inhibidores de sarm1
CL2022000751A1 (es) Inhibidores de la fosfatasa shp2 y métodos para su uso (divisional de la solicitud no. 202002419)
CL2020001576A1 (es) Componentes heterocíclicos bicíclicos sustituidos como inhibidores de prmt5.
ECSP22087539A (es) Inhibidores de kras tricíclicos fusionados
JOP20210097B1 (ar) مركبات 2-أمينو-n-أريل غير متجانس-نيكوتيناميد كمثبطات nav1.8
CL2020002146A1 (es) Derivados de n-(fenil)-2-(fenil)pirimidina-4-carboxamida y compuestos relacionados como inhibidores hpki para tratar el cáncer.
DOP2021000234A (es) Pirroles triciclicos condensados como moduladores de alfa-1 antitripsina
MX2020007265A (es) Derivados de rapamicina.
MX2021013146A (es) Inhibidores de receptores del factor de crecimiento de fibroblastos (fgfr) y metodos de uso de los mismos.
CO2019014455A2 (es) Amidas heterocíclicas de 5 miembros y bicíclicas como inhibidores de rock
CO2021001219A2 (es) Benzimidazoles sustituidos como inhibidores de pad4
WO2020104648A3 (en) TGFβ INHIBITOR AND PRODRUGS
CO2021008018A2 (es) Composiciones y métodos para modular la actividad de deshidrogenasas de cadena corta
UY37073A (es) Salicilamidas espiroheptanos y compuestos relacionados como inhibidores de rock, y las composiciones que los contienen
CL2023002223A1 (es) Inhibidores de cdk2 y métodos de uso de los mismos
MX2023006002A (es) Derivados de heterociclo para tratar trastornos mediados por potencial de receptor transitorio melastatina (trpm3).
CL2022001887A1 (es) Pirazolo-pirimidinas sustituidas y usos de las mismas
MX2016016530A (es) Inhibidores de fosfatidilinositol 3-quinasa.
CL2022000758A1 (es) Tienopirimidonas como inhibidores de trpa1
MX2022004270A (es) Inhibidores de aldosa reductasa para el tratamiento de la deficiencia de fosfomannomutasa 2.
MX2022002443A (es) Compuestos inhibidores de perk.
JOP20250149A1 (ar) مثبطات malt1
CL2019003107A1 (es) Compuestos heterocíclicos bicíclicos sustituidos utilizados como inhibidores de nadph oxidasa.
CO2017000011A2 (es) Derivados de quinolizinona como inhibidores de pi3k
CO2025003090A2 (es) Compuestos de piridinona sustituida como inhibidores de cbl-b