[go: up one dir, main page]

AR123089A2 - Compuesto de piridinona - Google Patents

Compuesto de piridinona

Info

Publication number
AR123089A2
AR123089A2 ARP210102120A ARP210102120A AR123089A2 AR 123089 A2 AR123089 A2 AR 123089A2 AR P210102120 A ARP210102120 A AR P210102120A AR P210102120 A ARP210102120 A AR P210102120A AR 123089 A2 AR123089 A2 AR 123089A2
Authority
AR
Argentina
Prior art keywords
optionally substituted
group
alkyl
aryl
alkynyl
Prior art date
Application number
ARP210102120A
Other languages
English (en)
Inventor
Brad Buckman
John B Nicholas
Johnnie Y Ramphal
Kumaraswamy Emayan
Scott D Seiwert
Original Assignee
Intermune 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 Intermune Inc filed Critical Intermune Inc
Publication of AR123089A2 publication Critical patent/AR123089A2/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/64One oxygen atom attached in position 2 or 6
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/04Drugs for skeletal disorders for non-specific disorders of the connective tissue
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/69Two or more oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/22Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
    • C07D217/24Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/04Ortho- or peri-condensed ring systems
    • C07D221/06Ring systems of three rings
    • C07D221/16Ring systems of three rings containing carbocyclic rings other than six-membered
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/04Ortho- or peri-condensed ring systems
    • C07D221/18Ring systems of four or more 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Dermatology (AREA)
  • Pulmonology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Un compuesto de piridinona que presenta la estructura de fórmula (1) o una de sus sales farmacéuticamente aceptables, en la cual: R¹ se selecciona entre el grupo que comprende halógeno, -CN, -C(O)R⁸, -SO₂R¹⁶, alquilo-C₁₋₆ opcionalmente sustituido por uno o más R⁴, alquenilo-C₂₋₆ opcionalmente sustituido por uno o más R⁴, alquinilo-C₂₋₆ opcionalmente sustituido por uno o más R⁴, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R⁴, un heteroarilo de 5 - 10 miembros opcionalmente sustituido por uno o más R⁴, carbociclilo-C₃₋₁₀ opcionalmente sustituido por uno o más R⁴, y heterociclilo de 3 - 10 miembros opcionalmente sustituido por uno o más R⁴; R² se selecciona entre el grupo que comprende halógeno, -CN, -OR⁵, -SR⁵, -NR⁶R⁷, y -C(O)R⁸; R³ se selecciona entre el grupo que comprende hidrógeno, -(CH₂)ₙ-(arilo-C₆₋₁₀), -(CH₂)ₙ-(heteroarilo de 5 - 10 miembros), -(CH₂)ₙ-(carbociclilo-C₃₋₁₀), y -(CH₂)ₙ-(heterociclilo de 3 - 10 miembros), cada uno opcionalmente sustituido por uno o más R⁹; cada R⁴ se selecciona independientemente entre el grupo que comprende halógeno, -CN, -OH, -C(O)R⁸, -SO₂R¹⁶, alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, alcoxi-C₁₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R¹¹, aralquilo-C₇₋₁₄ opcionalmente sustituido por uno o más R¹¹, heteroarilo de 5 - 10 miembros opcionalmente sustituido por uno o más R¹¹, o independientemente dos R⁴ geminales juntos son oxo; cada R⁵ se selecciona independientemente entre el grupo que comprende hidrógeno, alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, alcoxialquilo-C₂₋₈ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R¹¹, aralquilo-C₇₋₁₄ opcionalmente sustituido por uno o más R¹¹, y -(CH₂)ₙ-(heterociclilo de 3 - 10 miembros) opcionalmente sustituido por uno o más R¹⁰; R⁶ se selecciona entre el grupo que comprende hidrógeno, alquilo-C₁₋₆ opcionalmente sustituido, alqueniloC₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R¹¹, aralquilo-C₇₋₁₄ opcionalmente sustituido por uno o más R¹¹, y alquilo-(heteroarilo de 5 - 10 miembros) opcionalmente sustituido por uno o más R¹¹, -C(O)R⁸, y -C(O)OR⁵; R⁷ se selecciona entre el grupo que comprende hidrógeno, alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R¹¹, aralquilo-C₇₋₁₄ opcionalmente sustituido por uno o más R¹¹, y alquilo-(heteroarilo de 5 - 10 miembros) opcionalmente sustituido por uno o más R¹¹, -C(O)R⁸, y -C(O)OR⁵; o R⁶ y R⁷ junto con el nitrógeno al que están unidos forman un heterociclilo de 3 - 10 miembros opcionalmente sustituido por uno o más R¹⁰; cada R⁸ se selecciona independientemente entre el grupo que comprende hidrógeno, alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R¹¹, aralquilo-C₇₋₁₄ opcionalmente sustituido por uno o más R¹¹, -NR¹²R¹³, y -OR⁵; cada R⁹ se selecciona independientemente entre el grupo que comprende hidroxi, halógeno, alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, alquiltio-C₁₋₆ opcionalmente sustituido, alcoxialquilo-C₂₋₈ opcionalmente sustituido, carbociclilo-C₃₋₁₀ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido, -OR⁵, -NR¹⁴R¹⁵, -C(O)R⁸, -CN, -SO₂R¹⁶, y -NO₂; cada R¹⁰ se selecciona independientemente entre el grupo que comprende alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, y alquinilo-C₂₋₆ opcionalmente sustituido, o independientemente dos R¹⁰ geminales juntos son oxo; cada R¹¹ se selecciona independientemente entre el grupo que comprende halógeno, -CN, alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, -O-(CH₂)ₙ-alcoxi-C₁₋₈, -C(O)R⁸, y alcoxi-C₁₋₆ opcionalmente sustituido; cada R¹² se selecciona independientemente entre el grupo que comprende hidrógeno, alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R¹¹, aralquilo-C₇₋₁₄ opcionalmente sustituido por uno o más R¹¹; cada R¹³ se selecciona independientemente entre el grupo que comprende hidrógeno, alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R¹¹, aralquilo-C₇₋₁₄ opcionalmente sustituido por uno o más R¹¹; R¹⁴ se selecciona entre el grupo que comprende hidrógeno, alquilo-C₁₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido, y -C(O)R⁸; R¹⁵ se selecciona entre el grupo que comprende hidrógeno, alquilo-C₁₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido, y -C(O)R⁸; cada R¹⁶ se selecciona independientemente entre el grupo que comprende alquilo-C₁₋₆ opcionalmente sustituido, alquenilo-C₂₋₆ opcionalmente sustituido, alquinilo-C₂₋₆ opcionalmente sustituido, arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R¹¹, aralquilo-C₇₋₁₄ opcionalmente sustituido por uno o más R¹¹, -NR¹²R¹³, y -OR⁵; Z se selecciona entre oxígeno y azufre; cada n es, independientemente, un entero que oscila entre 0 y 4; y los enlaces representados por una línea continua y de guiones se seleccionan independientemente entre el grupo que comprende un enlace simple y un enlace doble, siempre que: cuando R³ es H, entonces R¹ se selecciona entre arilo-C₆₋₁₀ opcionalmente sustituido por uno o más R⁴, o heteroarilo de 5 - 10 miembros opcionalmente sustituido por uno o más R⁴; cuando R² es -NH-(2-fluoro-4-bromo-fenilo) y R¹ es C(O)OH, entonces R³ no puede ser fenilo-CH₂; cuando R² es metoxi, R¹ es 4-metoxifenilo, y Z es O, entonces R³ no es 2-fluoro-4-cloro-fenilo-(CH₂); cuando R³ es un fenilo; R² es OR⁵ o NR⁶R⁷; entonces R¹ no es triazolilo; cuando R³ es 4-metil fenilo, R² es morfolinilo, y Z es O; entonces R¹ no es metilo; y cuando R³ es 4-metil fenilo, R² es -N(CH₃)₂, Z es O; entonces R¹ no es metilo. Se proveen entonces el compuesto de piridinona descrito, un método para preparar este compuesto y métodos para tratar trastornos fibróticos.
ARP210102120A 2012-10-02 2021-07-26 Compuesto de piridinona AR123089A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201261709075P 2012-10-02 2012-10-02

Publications (1)

Publication Number Publication Date
AR123089A2 true AR123089A2 (es) 2022-10-26

Family

ID=50385786

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP210102120A AR123089A2 (es) 2012-10-02 2021-07-26 Compuesto de piridinona

Country Status (3)

Country Link
US (1) US20140094456A1 (es)
AR (1) AR123089A2 (es)
MA (1) MA38054A1 (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR092742A1 (es) 2012-10-02 2015-04-29 Intermune Inc Piridinonas antifibroticas
NZ722927A (en) 2014-01-10 2022-07-29 Avalyn Pharma Inc Aerosol pirfenidone and pyridone analog compounds and uses thereof
CA2943363A1 (en) 2014-04-02 2015-10-08 Intermune, Inc. Anti-fibrotic pyridinones
CN104031044A (zh) * 2014-06-06 2014-09-10 江西科技师范大学 电子受体吡啶并杂环化合物的制备方法
MA40940A (fr) * 2014-11-10 2017-09-19 Constellation Pharmaceuticals Inc Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines
WO2016077375A1 (en) 2014-11-10 2016-05-19 Genentech, Inc. Bromodomain inhibitors and uses thereof
MA40943A (fr) * 2014-11-10 2017-09-19 Constellation Pharmaceuticals Inc Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines
JP6709792B2 (ja) 2015-01-29 2020-06-17 ジェネンテック, インコーポレイテッド 治療用化合物およびその使用
US10836742B2 (en) 2015-08-11 2020-11-17 Neomed Institute N-substituted bicyclic lactams, their preparation and their use as pharmaceuticals
CN108290856A (zh) 2015-08-11 2018-07-17 尼奥迈德研究所 芳基-取代的二氢喹诺酮、它们的制备和它们作为药物的用途
KR102784592B1 (ko) 2015-08-12 2025-03-19 에피제네틱스, 인크. 치환된 벤즈이미다졸, 그의 제조법 및 제약으로서의 그의 용도
US10501459B2 (en) 2015-10-21 2019-12-10 Neomed Institute Substituted imidazo[1,2-a]pyridines as bromodomain inhibitors
WO2017127930A1 (en) 2016-01-28 2017-08-03 Neomed Institute Substituted [1,2,4]triazolo[4,3-a]pyridines, their preparation and their use as pharmaceuticals
CN109311859B (zh) * 2016-04-14 2022-01-21 广州嘉越医药科技有限公司 用于治疗纤维化和炎性疾病的含杂原子环丁烷取代基的吡啶酮衍生物
MX379459B (es) 2016-04-15 2025-03-10 Abbvie Inc Inhibidores de bromodominios.
CA3108048A1 (en) 2017-07-31 2019-02-07 Washington University Pirfenidone derivatives for modulation of b lymphocyte activity and organ protection
GB201801128D0 (en) 2018-01-24 2018-03-07 Univ Oxford Innovation Ltd Compounds
BR112020015759A2 (pt) * 2018-02-02 2020-12-08 Genentech, Inc. Composto farmacêutico, sais do mesmo, formulações do mesmo e métodos para produzir e usar o mesmo

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3034994A1 (en) * 2008-06-03 2009-12-10 Intermune, Inc. Substituted aryl-2 pyridone compounds and use thereof for treating inflammatory and fibrotic disorders

Also Published As

Publication number Publication date
US20140094456A1 (en) 2014-04-03
MA38054A1 (fr) 2016-11-30

Similar Documents

Publication Publication Date Title
AR123089A2 (es) Compuesto de piridinona
AR092742A1 (es) Piridinonas antifibroticas
AR099363A1 (es) Pirrolo[2,3-d]pirimidinil, pirrolo[2,3-b]pirazinil y pirrolo[2,3-d]piridinil acrilamidas
AR105392A1 (es) Inhibidores del receptor del factor estimulador de colonias 1 (csf-1r)
AR116666A1 (es) Compuestos heterocíclicos
AR089285A1 (es) Derivados de betulina
PE20171240A1 (es) Derivados de 4h-pirrol[3,2-c]piridin-4-ona
AR095326A1 (es) Heterociclos tricíclicos como inhibidores de la proteína bet
AR100418A1 (es) Compuestos y composiciones para inducir condrogénesis
AR097571A1 (es) Compuestos espirocíclicos como inhibidores de la triptofano hidroxilasa
AR099228A1 (es) Inhibidores macrocíclicos de fxia que tienen grupos heterocíclicos
AR088760A1 (es) Derivados de pirrolopirimidina y purina
AR063318A1 (es) Pirazoliltienopiridinas terapeuticas
AR103969A1 (es) Inmunomoduladores
AR107032A1 (es) Inhibidores bicíclicos de pad4
AR091424A1 (es) Compuestos triciclicos sustituidos como inhibidores de receptores del factor de crecimiento del fibroplasto (fgfr)
AR087328A1 (es) Derivados de imidazo[1,2-b]piridazina e imidazo[4,5-b]piridina como inhibidores de jak
AR087102A1 (es) Derivados de bencilamina como inhibidores de la calicreina plasmatica
AR096837A1 (es) Heterociclos tricíclicos como inhibidores de proteínas bet
AR106865A1 (es) Piridinas sustituidas y métodos de uso
AR104461A1 (es) Pirrolo[2,3-d]pirimidinil, pirrolo[2,3-b]pirazinil, pirrolo[2,3-b]piridinil acrilamidas y epóxidos de estas
AR098492A1 (es) Derivados de purina
AR103232A1 (es) ANTAGONISTAS DE TGFbR
AR090572A1 (es) Derivados de tienopirimidina, procesos para su preparacion y sus usos terapeuticos
AR111271A1 (es) Inhibidores dobles de magl y faah

Legal Events

Date Code Title Description
FB Suspension of granting procedure