AR090203A1 - Compuestos heterobiciclicos como inhibidores de pde10 - Google Patents
Compuestos heterobiciclicos como inhibidores de pde10Info
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- AR090203A1 AR090203A1 ARP130100649A ARP130100649A AR090203A1 AR 090203 A1 AR090203 A1 AR 090203A1 AR P130100649 A ARP130100649 A AR P130100649A AR P130100649 A ARP130100649 A AR P130100649A AR 090203 A1 AR090203 A1 AR 090203A1
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic 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
- C07D417/02—Heterocyclic 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
- C07D417/12—Heterocyclic 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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/28—Oxygen atom
- C07D473/30—Oxygen atom attached in position 6, e.g. hypoxanthine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic 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
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic 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
- C07D513/02—Heterocyclic 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
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Addiction (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Composiciones que los contienen, y procesos para preparar dichos compuestos. En la presente se proveen también métodos para tratar trastornos o enfermedades que se pueden tratar mediante la inhibición de PDE10, tal como obesidad, diabetes no dependiente de insulina, esquizofrenia, trastorno bipolar, trastorno obsesivo compulsivo, enfermedad de Huntington, y similares. Reivindicación 1: Un compuesto caracterizado porque es de fórmula (1) o una sal farmacéuticamente aceptable, tautómero, o estereoisómero del mismo, donde: cada p y q es en forma independiente 0, 1, 2, 3, 4, 5 ó 6; donde la suma de p y q es 1, 2, 3, 4, 5 ó 6; m es 0, 1, 2, 3 ó 4; A es un anillo heterocíclico de 9 ó 10 miembros de la fórmula (2), donde el grupo -W-T-D< se selecciona del grupo que consiste en: -N=CR⁵-N<; NR⁷-N=C<; -NR⁷-(C=O)-N<; NR⁷-CR⁶R⁷-(C=O)-N<; -NR⁷-(SO₂)-N<; -CR⁵=CR⁵-N<; -CR⁸=N-N<; -CR⁶R⁷-(C=O)-N<; -CR⁶R⁷-NR⁷-(C=O)-N<; -CR⁶R⁷-O-(C=O)-N<; -CR⁶R⁷-(SO₂)-N<; -O-(C=O)-N<; y -O-CR⁶R⁷-(C=O)-N<; J es en forma independiente N o CR³ᶜ; donde cada E, X, Y, y Z son en forma independiente N o CR⁴; donde 0, 1, 2 ó 3 de E, X, Y, y Z son N; (a) cuando J es N, luego G es R¹ o (C=O)R¹; donde R¹ se une a través de carbono; (b) cuando J es CR³ᶜ; luego G es R¹, -NR¹R²; -NH(C=O)R¹; -OR¹, -(C=O)R¹; o -CHR¹R²; donde R¹ se une a través de carbono o nitrógeno; y el anillo que contiene a p y q contiene 0, 1 ó 2 átomos de N y 0, 1 ó 2 átomos de O ó S; R¹ es un anillo monocíclico saturado, parcialmente saturado o insaturado de 5 ó 6 miembros, o un anillo bicíclico saturado, parcialmente saturado o insaturado de 9 ó 10 miembros, unido por carbono o unido por nitrógeno, donde cada uno de dichos anillos contiene 0, 1, 2, 3 ó 4 átomos de N y 0, 1 ó 2 átomos de O ó S; donde cada R¹ en forma independiente está sustituido con 0, 1, 2 ó 3 grupos R⁹; R² es en forma independiente H, OH, alq C₁₋₄, un anillo monocíclico saturado, parcialmente saturado o insaturado de 5 ó 6 miembros unido por carbono o unido por nitrógeno, donde cada uno de dichos anillos contiene 0, 1, 2, 3 ó 4 átomos de N y 0, 1 ó 2 átomos de O ó S; donde cada R² alq C₁₋₄ o anillo monocíclico en forma independiente está sustituido con 0, 1, 2 ó 3 grupos R⁹; cada R³ᵃ y R³ᶜ es en forma independiente H, F, OH, alq C₁₋₄, o haloalq C₁₋₄; R³ᵇ es en forma independiente F, Cl, Br, CN, OH, O-alq C₁₋₄, alq C₁₋₄, haloalq C₁₋₄, o oxo; R⁴ es halo, R⁴ᵃ, -SR⁴ᵃ, -OR⁴ᵃ, -NHR⁴ᵃ, o -N(alq C₁₋₄)R⁴ᵃ, donde -R⁴ᵃ es H, alq C₁₋₄, un anillo monocíclico saturado, parcialmente saturado o insaturado de 3, 4, 5 ó 6 miembros, donde cada uno de dichos anillos contiene 0, 1, 2, 3 ó 4 átomos de N y 0, 1 ó 2 átomos de O ó S; donde cada R⁴ alq C₁₋₄ o anillo monocíclico en forma independiente está sustituido con 0, 1, 2 ó 3 grupos R⁹; cada R⁵ es en forma independiente R⁵ᵃ, -OR⁵ᵇ, -NHR⁵ᵃ, o -N(alq C₁₋₄)R⁵ᵃ, donde R⁵ᵃ es H, alq C₁₋₄, un anillo monocíclico saturado, parcialmente saturado o insaturado de 3, 4, 5 ó 6 miembros, donde cada uno de dichos anillos contiene 0, 1, 2, 3, o 4 átomos de N y 0, 1 ó 2 átomos de O ó S; R⁵ᵇ es alq C₁₋₄, un anillo monocíclico saturado, parcialmente saturado o insaturado de 3, 4, 5 ó 6 miembros, donde cada uno de dichos anillos contiene 0, 1, 2, 3 ó 4 átomos de N y 0, 1 ó 2 átomos de O ó S; donde cada R⁵ alq C₁₋₄ o anillo monocíclico en forma independiente está sustituido con 0, 1, 2 ó 3 grupos R⁹; cada R⁶ y R⁷ es en forma independiente H, halo, OH, alq C₁₋₄, O-alq C₁₋₄, un anillo monocíclico saturado, parcialmente saturado o insaturado de 3, 4, 5 ó 6 miembros, donde cada uno de dichos anillos contiene 0, 1, 2, 3, o 4 átomos de N y 0, 1 ó 2 átomos de O ó S; donde cada R⁶ y R⁷ alq C₁₋₄ o anillo monocíclico en forma independiente está sustituido con 0, 1, 2 ó 3 grupos R⁹; o R⁶ y R⁷ opcionalmente pueden formar un anillo monocíclico saturado o parcialmente saturado de 3, 4, 5 ó 6 miembros, donde cada uno de dichos anillos contiene 0, 1, 2, 3 ó 4 átomos de N y 0, 1 ó 2 átomos de O ó S; donde dicho anillo monocíclico en forma independiente está sustituido con 0, 1, 2 ó 3 grupos R⁹; R⁸ es R⁸ᵃ, -O-R⁸ᵃ, -NHR⁸ᵃ, o -N(alq C₁₋₄)R⁸ᵃ, donde R⁸ᵃ es H, alq C₁₋₄, un anillo monocíclico saturado, parcialmente saturado o insaturado de 3, 4, 5 ó 6 miembros, donde cada uno de dichos anillos contiene 0, 1, 2, 3 ó 4 átomos de N y 0, 1 ó 2 átomos de O ó S; donde cada R⁸ alq C₁₋₄ o anillo monocíclico en forma independiente está sustituido con 0, 1, 2 ó 3 grupos R⁹; R⁹ es en forma independiente F, Cl, Br, alq C₁₋₆, haloalq C₁₋₄, -ORᵃ, ORᶜ, -O-haloalq C₁₋₄, CN, Rᵇ, Rᶜ, -C(=O)Rᵇ, -C(=O)Rᶜ, -C(=O)ORᵃ, -C(=O)NRᵃRᵃ, -C(=O)NRᵃRᶜ, -C(=NRᵃ)NRᵃRᵃ, -OC(=O)Rᵇ, -OC(=O)NRᵃRᵃ, -O-alq C₁₋₆NRᵃRᵃ, -O-alq C₁₋₆ORᵃ, -SRᵃ, -S(=O)Rᵇ, -S(=O)₂Rᵇ, -S(=O)₂NRᵃRᵃ, -NRᵃRᵃ, -N(Rᵃ)C(=O)Rᵇ, -N(Rᵃ)C(=O)ORᵇ, -N(Rᵃ)C(=O)NRᵃRᵃ, -N(Rᵃ)C(=NRᵃ)NRᵃRᵃ, -N(Rᵃ)S(=O)₂Rᵇ, -N(Rᵃ)S(=O)₂NRᵃRᵃ, -NRᵃalq C₁₋₆NRᵃRᵃ, -NRᵃalq C₁₋₆ORᵃ, -alq C₁₋₆NRᵃRᵃ, -alq C₁₋₆ORᵃ, -alq C₁₋₆N(Rᵃ)C(=O)Rᵇ, -alq C₁₋₆OC(=O)Rᵇ, -alq C₁₋₆C₍₌O₎NRᵃRᵃ, -alq C₁₋₆C₍₌O₎ORᵃ, o oxo; R¹⁰ es halo, alq C₁₋₆, haloalq C₁₋₄, -ORᵃ, -O-haloalq C₁₋₄, CN, -C(=O)Rᵇ, -C(=O)ORᵃ, -C(=O)NRᵃRᵃ, -C(=NRᵃ)NRᵃRᵃ, -OC(=O)Rᵇ, -OC(=O)NRᵃRᵃ, -Oalq C₁₋₆NRᵃRᵃ, -O-alq C₁₋₆ORᵃ, -SRᵃ, -S(=O)Rᵇ, -S(=O)₂Rᵇ, -S(=O)₂NRᵃRᵃ, -NRᵃRᵃ, -N(Rᵃ)C(=O)Rᵇ, -N(Rᵃ)C(=O)ORᵇ, -N(Rᵃ)C(=O)NRᵃRᵃ, -N(Rᵃ)C(=NRᵃ)NRᵃRᵃ, -N(Rᵃ)S(=O)₂Rᵇ, -N(Rᵃ)S(=O)₂NRᵃRᵃ, -NRᵃalq C₁₋₆NRᵃRᵃ, -NRᵃalq C₁₋₆ORᵃ, -alq C₁₋₆NRᵃRᵃ, -alq C₁₋₆ORᵃ, -alq C₁₋₆N(Rᵃ)C(=O)Rᵇ, -alq C₁₋₆OC(=O)Rᵇ, -alq C₁₋₆C₍₌O₎NRᵃRᵃ, -alq C₁₋₆C₍₌O₎ORᵃ, o oxo; Rᵃ es en forma independiente H o Rᵇ; Rᵇ es en forma independiente fenilo, bencilo, o alq C₁₋₆, donde dichos fenilo, bencilo, y alq C₁₋₆ están sustituidos con 0, 1, 2 ó 3 sustituyentes que son alq C₁₋₄, haloalq C₁₋₃, -OH, -O-alq C₁₋₄, -NH₂, -NH-alq C₁₋₄, -OC(=O)alq C₁₋₄, o -N(alq C₁₋₄)alq C₁₋₄; y Rᶜ es en forma independiente un anillo monocíclico saturado, parcialmente saturado o insaturado de 3, 4, 5, 6 ó 7 miembros o un anillo bicíclico saturado, parcialmente saturado o insaturado de 6, 7, 8, 9, 10, 11 ó 12 miembros unido por carbono o unido por nitrógeno, donde dicho anillo contiene 0, 1, 2, 3 ó 4 átomos de N y 0, 1 ó 2 átomos de O ó S; Rᶜ en forma independiente está sustituido con 0, 1, 2 ó 3 grupos R¹⁰.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261605148P | 2012-02-29 | 2012-02-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR090203A1 true AR090203A1 (es) | 2014-10-29 |
Family
ID=47846219
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP130100649A AR090203A1 (es) | 2012-02-29 | 2013-02-28 | Compuestos heterobiciclicos como inhibidores de pde10 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9174992B2 (es) |
| EP (1) | EP2820014A1 (es) |
| JP (1) | JP2015508826A (es) |
| AR (1) | AR090203A1 (es) |
| AU (1) | AU2013225838A1 (es) |
| CA (1) | CA2865980A1 (es) |
| MX (1) | MX2014010377A (es) |
| TW (1) | TW201348231A (es) |
| UY (1) | UY34649A (es) |
| WO (1) | WO2013130890A1 (es) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014106238A1 (en) * | 2012-12-31 | 2014-07-03 | Fang, Qun, Kevin | Heterocyclic compounds and methods of use thereof |
| CA2949511A1 (en) | 2014-05-19 | 2015-11-26 | Merial, Inc. | Anthelmintic compounds |
| US10221172B2 (en) | 2015-01-13 | 2019-03-05 | Vanderbilt University | Benzothiazole and benzisothiazole-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
| KR20170016754A (ko) * | 2015-08-04 | 2017-02-14 | 씨제이헬스케어 주식회사 | 크로마논 유도체의 신규한 제조방법 |
| CN108430986B (zh) | 2015-10-26 | 2021-08-31 | 拜耳作物科学股份公司 | 作为有害生物控制剂的稠合双环杂环衍生物 |
| US10112924B2 (en) | 2015-12-02 | 2018-10-30 | Astraea Therapeutics, Inc. | Piperdinyl nociceptin receptor compounds |
| JP7011596B2 (ja) | 2015-12-02 | 2022-02-10 | アストライア セラピューティクス, エルエルシー | ピペリジニルノシセプチン受容体化合物 |
| MA46191A (fr) | 2016-09-09 | 2021-04-21 | Incyte Corp | Dérivés de pyrazolopyridine comme modulateurs de hpk1 et leurs utilisations pour le traitement du cancer |
| TW201811799A (zh) | 2016-09-09 | 2018-04-01 | 美商英塞特公司 | 吡唑并嘧啶化合物及其用途 |
| US20180072718A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyridine compounds and uses thereof |
| WO2018049191A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyridone derivatives as hpk1 modulators and uses thereof for the treatment of cancer |
| GB201617630D0 (en) | 2016-10-18 | 2016-11-30 | Cellcentric Ltd | Pharmaceutical compounds |
| WO2018152220A1 (en) | 2017-02-15 | 2018-08-23 | Incyte Corporation | Pyrazolopyridine compounds and uses thereof |
| CN111051308A (zh) | 2017-06-08 | 2020-04-21 | 默沙东公司 | 吡唑并嘧啶pde9抑制剂 |
| US10722495B2 (en) | 2017-09-08 | 2020-07-28 | Incyte Corporation | Cyanoindazole compounds and uses thereof |
| KR102717600B1 (ko) | 2017-10-06 | 2024-10-15 | 포르마 세라퓨틱스 인크. | 유비퀴틴 특이적 펩티다제 30의 억제 |
| JP2021501785A (ja) | 2017-11-02 | 2021-01-21 | カリコ ライフ サイエンシーズ エルエルシー | 統合的ストレス経路の調節剤 |
| CA3080959A1 (en) * | 2017-11-02 | 2019-05-09 | Calico Life Sciences Llc | Modulators of the integrated stress pathway |
| BR112020016466A2 (pt) | 2018-02-13 | 2020-12-15 | Gilead Sciences, Inc. | Composto, composição farmacêutica, métodos para inibir pd-1, pd-l1 e/ou a interação de pd-1/pd-l1, para tratar câncer e para aprimorar a função de células-t em pacientes com hepatite b crônica (chb), e, kit para tratar ou prevenir câncer ou uma doença ou condição. |
| US10752635B2 (en) | 2018-02-20 | 2020-08-25 | Incyte Corporation | Indazole compounds and uses thereof |
| LT3755703T (lt) | 2018-02-20 | 2022-10-10 | Incyte Corporation | N-(fenil)-2-(fenil)pirimidin-4-karboksamido dariniai ir susiję junginiai, kaip hpk1 inhibitoriai, skirti vėžio gydymui |
| US10745388B2 (en) | 2018-02-20 | 2020-08-18 | Incyte Corporation | Indazole compounds and uses thereof |
| US11299473B2 (en) | 2018-04-13 | 2022-04-12 | Incyte Corporation | Benzimidazole and indole compounds and uses thereof |
| GB201806320D0 (en) | 2018-04-18 | 2018-05-30 | Cellcentric Ltd | Process |
| IL278291B2 (en) | 2018-05-17 | 2023-10-01 | Forma Therapeutics Inc | Fused bicyclic compounds useful as ubiquitin-specific peptidase 30 inhibitors |
| AU2019301811B2 (en) | 2018-07-13 | 2022-05-26 | Gilead Sciences, Inc. | PD-1/PD-L1 inhibitors |
| US10899755B2 (en) | 2018-08-08 | 2021-01-26 | Incyte Corporation | Benzothiazole compounds and uses thereof |
| ES2973117T3 (es) | 2018-09-25 | 2024-06-18 | Incyte Corp | Compuestos de pirazolo[4,3-d]pirimidina como moduladores de ALK2 y/o FGFR |
| CA3110113A1 (en) | 2018-10-05 | 2020-04-09 | Forma Therapeutics, Inc. | Fused pyrrolines which act as ubiquitin-specific protease 30 (usp30) inhibitors |
| US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
| FI3911648T3 (fi) * | 2019-01-18 | 2025-01-10 | Astrazeneca Ab | 6'-[[[(1s,3s)-3-[[5-(difluorometoksi)-2-pyrimidinyyli]amino]syklopentyyli]amino][1(2h),3'-bipyridin]-2-oni pcsk9:n estäjänä ja menetelmät sen käyttöön |
| US11384083B2 (en) | 2019-02-15 | 2022-07-12 | Incyte Corporation | Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors |
| EP3696175A1 (en) | 2019-02-18 | 2020-08-19 | Syngenta Crop Protection AG | Pesticidally active azole-amide compounds |
| TW202100520A (zh) | 2019-03-05 | 2021-01-01 | 美商英塞特公司 | 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物 |
| ES2953140T3 (es) | 2019-03-08 | 2023-11-08 | Syngenta Crop Protection Ag | Compuestos de azol-amida activos de manera plaguicida |
| US20220183294A1 (en) | 2019-03-20 | 2022-06-16 | Syngenta Crop Protection Ag | Pesticidally active azole amide compounds |
| US20220306599A1 (en) | 2019-03-20 | 2022-09-29 | Syngenta Crop Protection Ag | Pesticidally active azole amide compounds |
| BR112021018822A2 (pt) | 2019-03-22 | 2021-11-23 | Syngenta Crop Protection Ag | Derivados de n-[1-(5-bromo-2-pirimidin-2-il-1,2,4-triazol-3-il)etil]-2-ciclopropil-6-(trifluorometil)piridina-4-carboxamida e compostos relacionados como inseticidas |
| WO2020205560A1 (en) | 2019-03-29 | 2020-10-08 | Incyte Corporation | Sulfonylamide compounds as cdk2 inhibitors |
| TWI853009B (zh) | 2019-03-29 | 2024-08-21 | 瑞士商先正達農作物保護公司 | 殺有害生物活性之二-醯胺化合物 |
| EP3953343A1 (en) | 2019-04-11 | 2022-02-16 | Syngenta Crop Protection AG | Pesticidally active diazine-amide compounds |
| US11447494B2 (en) | 2019-05-01 | 2022-09-20 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| WO2020223469A1 (en) | 2019-05-01 | 2020-11-05 | Incyte Corporation | N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer |
| CR20220097A (es) | 2019-08-06 | 2022-06-01 | Incyte Corp | Formas sólidas de un inhibidor de hpk1 |
| AU2020328025A1 (en) | 2019-08-14 | 2022-03-03 | Incyte Corporation | Imidazolyl pyrimidinylamine compounds as CDK2 inhibitors |
| CN119930611A (zh) | 2019-10-11 | 2025-05-06 | 因赛特公司 | 作为cdk2抑制剂的双环胺 |
| CA3195127A1 (en) * | 2020-10-16 | 2022-05-05 | John K. Walker | Rev-erb agonists |
| KR20230157981A (ko) * | 2021-02-19 | 2023-11-17 | 칼비스타 파마슈티컬즈 리미티드 | 인자 xiia 저해제 |
| EP4074712A1 (en) | 2021-04-13 | 2022-10-19 | Siegfried AG | Process for the synthesis of 1,3-dihydro-imidazo[4,5-b]pyridin-2-one and/or derivatives thereof |
| US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
| WO2023107705A1 (en) | 2021-12-10 | 2023-06-15 | Incyte Corporation | Bicyclic amines as cdk12 inhibitors |
| US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| CN118239959A (zh) * | 2022-12-23 | 2024-06-25 | 上海深势唯思科技有限责任公司 | 环丙烷类tlr7和8抑制剂及其制备方法和用途 |
| WO2025132870A1 (en) | 2023-12-21 | 2025-06-26 | Glaxosmithkline Intellectual Property (No.4) Limited | Chemical compounds and uses thereof |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4107288A (en) | 1974-09-18 | 1978-08-15 | Pharmaceutical Society Of Victoria | Injectable compositions, nanoparticles useful therein, and process of manufacturing same |
| PT72878B (en) | 1980-04-24 | 1983-03-29 | Merck & Co Inc | Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents |
| US5145684A (en) | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
| AU701127B2 (en) | 1994-10-27 | 1999-01-21 | Merck & Co., Inc. | Muscarine antagonists |
| ES2223588T3 (es) * | 1999-10-13 | 2005-03-01 | Banyu Pharmaceutical Co., Ltd. | Derivados de imidazolidinona sustituidos. |
| ES2322158T3 (es) * | 2001-04-18 | 2009-06-17 | Euro-Celtique S.A. | Derivados 1-(4-piperidinil)-1,3-dihidro-2h-indol-2-ona y compuestos afines como analogos de la nociceptina y ligandos del orl-1 para el tratamiento del dolor. |
| SE0300456D0 (sv) * | 2003-02-19 | 2003-02-19 | Astrazeneca Ab | Novel compounds |
| EP1651251A4 (en) | 2003-07-31 | 2008-06-18 | Bayer Pharmaceuticals Corp | METHOD FOR THE TREATMENT OF DIABETES AND RELATED DISEASES USING PDE 10A INHIBITORS |
| US20060019975A1 (en) | 2004-07-23 | 2006-01-26 | Pfizer Inc | Novel piperidyl derivatives of quinazoline and isoquinoline |
| CA2605899C (en) * | 2005-04-26 | 2011-02-08 | Pfizer Limited | Triazole derivatives as vasopressin antagonists |
| BRPI0707223A2 (pt) | 2006-01-27 | 2011-04-26 | Pfizer Prod Inc | compostos de derivados de aminoftalazina |
| CA2643044A1 (en) | 2006-02-28 | 2007-09-07 | Amgen Inc. | Cinnoline and quinazoline derivates as phosphodiesterase 10 inhibitors |
| EP1849781A1 (en) | 2006-04-28 | 2007-10-31 | Laboratorios del Dr. Esteve S.A. | Substituted 3-Amino-4-hydroxy pyrrolidines compounds, their preparation and use as medicaments |
| US8093257B2 (en) | 2007-05-04 | 2012-01-10 | Bristol-Myers Squibb Company | [6,5]-bicyclic GPR119 G protein-coupled receptor agonists |
| US20110118286A1 (en) | 2008-07-16 | 2011-05-19 | Santhosh Francis Neelamkavil | Bicyclic heterocycle derivatives and their use as gpcr modulators |
| US20120016119A1 (en) * | 2009-01-22 | 2012-01-19 | Yasunori Tsuboi | NOVEL PYRROLO(2,3-d)PYRIMIDINE COMPOUND |
| AU2010294209A1 (en) * | 2009-09-10 | 2012-03-29 | Irm Llc | Ether derivatives of bicyclic heteroaryls |
| AU2011253143A1 (en) | 2010-05-13 | 2012-12-06 | Amgen Inc. | Nitrogen- heterocyclic compounds as phosphodiesterase 10 inhibitors |
| MX2012013130A (es) * | 2010-05-13 | 2013-04-11 | Amgen Inc | Compuestos heterociclicos de nitrogeno utiles como inhibidores de pde10. |
| WO2011145718A1 (ja) * | 2010-05-21 | 2011-11-24 | 田辺三菱製薬株式会社 | 新規ピロロ[2,3-d]ピリミジン化合物 |
| JP2012020973A (ja) * | 2010-07-15 | 2012-02-02 | Mitsubishi Tanabe Pharma Corp | 医薬組成物 |
| WO2012022045A1 (en) | 2010-08-20 | 2012-02-23 | Hutchison Medipharma Limited | Pyrrolopyrimidine compounds and uses thereof |
| CN102617548A (zh) | 2011-01-31 | 2012-08-01 | 北京赛林泰医药技术有限公司 | 作为gpr受体激动剂的双环杂芳基化合物及其组合物和应用 |
-
2013
- 2013-02-27 TW TW102107090A patent/TW201348231A/zh unknown
- 2013-02-28 WO PCT/US2013/028436 patent/WO2013130890A1/en not_active Ceased
- 2013-02-28 US US13/780,557 patent/US9174992B2/en active Active
- 2013-02-28 UY UY0001034649A patent/UY34649A/es not_active Application Discontinuation
- 2013-02-28 EP EP13709033.8A patent/EP2820014A1/en not_active Withdrawn
- 2013-02-28 AU AU2013225838A patent/AU2013225838A1/en not_active Abandoned
- 2013-02-28 MX MX2014010377A patent/MX2014010377A/es not_active Application Discontinuation
- 2013-02-28 AR ARP130100649A patent/AR090203A1/es unknown
- 2013-02-28 JP JP2014560058A patent/JP2015508826A/ja active Pending
- 2013-02-28 CA CA2865980A patent/CA2865980A1/en not_active Abandoned
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| US9174992B2 (en) | 2015-11-03 |
| TW201348231A (zh) | 2013-12-01 |
| AU2013225838A1 (en) | 2014-09-11 |
| JP2015508826A (ja) | 2015-03-23 |
| WO2013130890A1 (en) | 2013-09-06 |
| CA2865980A1 (en) | 2013-09-06 |
| UY34649A (es) | 2013-09-30 |
| MX2014010377A (es) | 2014-10-23 |
| US20130225552A1 (en) | 2013-08-29 |
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