AR093740A1 - Amidas como inhibidores de pim - Google Patents
Amidas como inhibidores de pimInfo
- Publication number
- AR093740A1 AR093740A1 ARP130100648A ARP130100648A AR093740A1 AR 093740 A1 AR093740 A1 AR 093740A1 AR P130100648 A ARP130100648 A AR P130100648A AR P130100648 A ARP130100648 A AR P130100648A AR 093740 A1 AR093740 A1 AR 093740A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- unsubstituted
- alkyl
- heterocyclyl
- cycloalkyl
- Prior art date
Links
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/04—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Composición farmacéutica y usos para la prevención y tratamiento del cáncer. Reivindicación 1: Un compuesto de la fórmula (1) en donde el enlace g es un enlace simple o un enlace doble; disponiéndose que g es un enlace simple si Y es C=O o C(Rᵃ)₂ o X es C=O o CH₂; el anillo a es un anillo que junto con los 2 átomos de carbono a los cuales se une, forma un anillo fenilo o un anillo heterocíclico de 5 - 6 miembros; X es N, NRᵇ, C=O, CH o CH₂; Y es N, NRᵇ, C=O, CRᵃ o C(Rᵃ)₂; R es una amida bicíclica opcionalmente sustituida, una tioamida bicíclica opcionalmente sustituida, una oxima bicíclica opcionalmente sustituida, o un compuesto del grupo de fórmulas (2); R¹ es H, halo, alquilo, amino, alquilamino, alquenilamino, haloalquilamino, alquilsulfonilalquilamino, aminocarbonilalquilamino, aminoalquilamino, hidroxialquilamino, alquilsulfonilamino, carboxialquilamino, alcoxicarbonilalquilamino, alcoxialquilamino, alcoxicarbonilaminoalquilamino, alcoxialcoxialquilamino, alcoxialquilaminoalquilamino, alquilsulfonilalquilaminoalquilamino, cicloalquilamino sustituido o no sustituido, cicloalquilalquilamino sustituido o no sustituido, arilamino sustituido o no sustituido, arilalquilamino sustituido o no sustituido, heterociclilamino sustituido o no sustituido, heterociclil-alquil C₁₋₆amino sustituido o no sustituido, guanidinilo, -CONHRᵇ, -NHC=ORᵇ, -ORᵇ, -S(=O)ₙRᵇ, -CORᶜ, arilo sustituido o no sustituido, arilalquilo sustituido o no sustituido, arilalquenilo sustituido o no sustituido, cicloalquilo sustituido o no sustituido, cicloalquilalquilo sustituido o no sustituido, heterociclilalquilo sustituido o no sustituido o heterociclilo sustituido o no sustituido; R² es H, o halo; Rᵃ es H, halo, haloalquilo, hidroxialquilo, alquilo, alquinilalcoxi, amino, alquilamino, ciano, HC(=O)-, HC(=NOH)-, carboxi, alcoxicarbonilo, o heterociclilo sustituido o no sustituido; Rᵇ es H, alquilo, haloalquilo, aminoalquilo, alcoxialquilo, cicloalquilo sustituido o no sustituido, arilo sustituido o no sustituido, arilalquilo sustituido o no sustituido o heterociclilo sustituido o no sustituido; Rᶜ es H, alquilo, alcoxi, alcoxialquilo, cicloalquilo sustituido o no sustituido, arilo sustituido o no sustituido, arilalquilo sustituido o no sustituido o heterociclilo sustituido o no sustituido; Rʰ es alquilo; Rᵐ es H, alquilo, cicloalquilo o aminoalquilo; y una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261604444P | 2012-02-28 | 2012-02-28 | |
US201261720936P | 2012-10-31 | 2012-10-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR093740A1 true AR093740A1 (es) | 2015-06-24 |
Family
ID=47827485
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP130100648A AR093740A1 (es) | 2012-02-28 | 2013-02-28 | Amidas como inhibidores de pim |
Country Status (5)
Country | Link |
---|---|
US (1) | US9394297B2 (es) |
AR (1) | AR093740A1 (es) |
TW (1) | TW201348226A (es) |
UY (1) | UY34648A (es) |
WO (1) | WO2013130660A1 (es) |
Families Citing this family (45)
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JP6437452B2 (ja) | 2013-01-14 | 2018-12-12 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Pimキナーゼ阻害剤として有用な二環式芳香族カルボキサミド化合物 |
MX2015009057A (es) | 2013-01-15 | 2015-10-05 | Incyte Corp | Compuestos de tiazolcarboxamidas y piridinacarboxamida utiles como inhibidores de cinasa pim. |
WO2014165127A1 (en) * | 2013-03-12 | 2014-10-09 | Abbvie Inc. | Pyrrole amide inhibitors |
CA2918530C (en) | 2013-07-19 | 2023-10-03 | Onyx Therapeutics, Inc. | Peptide epoxyketone proteasome inhibitors in combination with pim kinase inhibitors for treatment of cancers |
TW201605866A (zh) | 2013-08-23 | 2016-02-16 | 英塞特公司 | 可用作pim激酶抑制劑之呋喃并-及噻吩并-吡啶甲醯胺化合物 |
EP3035936B1 (en) * | 2013-08-23 | 2019-03-13 | NeuPharma, Inc. | Certain chemical entities, compositions, and methods |
FR3019819B1 (fr) * | 2014-04-09 | 2018-03-23 | Centre National De La Recherche Scientifique (Cnrs) | Composes cytotoxiques inhibiteurs de la polymerisation de la tubuline |
CN104262268B (zh) * | 2014-07-10 | 2016-03-02 | 浙江工业大学 | 一种2-腈基喹喔啉类化合物的合成方法 |
US9822124B2 (en) | 2014-07-14 | 2017-11-21 | Incyte Corporation | Bicyclic heteroaromatic carboxamide compounds useful as Pim kinase inhibitors |
US9580418B2 (en) | 2014-07-14 | 2017-02-28 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors |
MA41291A (fr) | 2014-12-30 | 2017-11-07 | Forma Therapeutics Inc | Dérivés de la pyrrolotriazinone et de l'imidazotriazinone en tant qu'inhibiteurs de la protéase spécifique de l'ubiquitine n° 7 (usp7) pour le traitement d'un cancer |
TWI770525B (zh) | 2014-12-30 | 2022-07-11 | 美商瓦洛健康公司 | 作為泛素特異性蛋白酶7抑制劑之吡咯并及吡唑并嘧啶 |
WO2016126926A1 (en) | 2015-02-05 | 2016-08-11 | Forma Therapeutics, Inc. | Quinazolinones and azaquinazolinones as ubiquitin-specific protease 7 inhibitors |
JP2018504432A (ja) | 2015-02-05 | 2018-02-15 | フォーマ セラピューティクス,インコーポレイテッド | ユビキチン特異的プロテアーゼ7阻害物質としてのイソチアゾロピリミジノン、ピラゾロピリミジノン及びピロロピリミジノン |
WO2016126929A1 (en) | 2015-02-05 | 2016-08-11 | Forma Therapeutics, Inc. | Thienopyrimidinones as ubiquitin-specific protease 7 inhibitors |
CA2976227C (en) | 2015-02-17 | 2023-10-24 | Neupharma, Inc. | Quinazoline derivatives and their use in treatment of cancer |
US9540347B2 (en) | 2015-05-29 | 2017-01-10 | Incyte Corporation | Pyridineamine compounds useful as Pim kinase inhibitors |
CN107849046B (zh) * | 2015-06-03 | 2020-06-12 | 常州捷凯医药科技有限公司 | 作为erk抑制剂的杂环化合物 |
CN106536522B (zh) * | 2015-06-03 | 2020-08-28 | 捷思英达医药技术(上海)有限公司 | 用于治疗银屑病的杂环化合物 |
CN105418440B (zh) * | 2015-07-24 | 2017-08-25 | 张家港吉慕特化工科技有限公司 | 一种由异丙胺合成2‑氨基‑2‑甲基‑1‑丙醇的方法 |
AR105967A1 (es) | 2015-09-09 | 2017-11-29 | Incyte Corp | Sales de un inhibidor de pim quinasa |
WO2017059251A1 (en) | 2015-10-02 | 2017-04-06 | Incyte Corporation | Heterocyclic compounds useful as pim kinase inhibitors |
US10525047B2 (en) | 2016-03-25 | 2020-01-07 | University Of Maryland, Baltimore County | PIM kinase inhibitors in combination with RNA splicing modulators/inhibitors for treatment of cancers |
EP3484881B1 (en) | 2016-07-14 | 2020-04-29 | Bristol-Myers Squibb Company | Bicyclic heteroaryl substituted compounds |
EP3484894B1 (en) | 2016-07-14 | 2020-08-19 | Bristol-Myers Squibb Company | Tricyclic heteroaryl-substituted quinoline and azaquinoline compounds as par4 inhibitors |
KR102492715B1 (ko) | 2016-07-14 | 2023-01-26 | 브리스톨-마이어스 스큅 컴퍼니 | 모노시클릭 헤테로아릴 치환된 화합물 |
CA3033370A1 (en) | 2016-08-15 | 2018-02-22 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
US11040958B2 (en) | 2017-02-17 | 2021-06-22 | Wuhan Ll Science And Technology Development Co., Ltd. | Triazole antimicrobial derivative, pharmaceutical composition and use thereof |
TWI782056B (zh) * | 2017-07-14 | 2022-11-01 | 日商鹽野義製藥股份有限公司 | 具有mgat2抑制活性的縮合環衍生物 |
AR113922A1 (es) | 2017-12-08 | 2020-07-01 | Incyte Corp | Terapia de combinación de dosis baja para el tratamiento de neoplasias mieloproliferativas |
MA52183A (fr) | 2018-04-06 | 2021-02-17 | H Lundbeck As | Procédé de préparation de 2,2-diméthylpipérazine |
KR20210034554A (ko) * | 2018-07-23 | 2021-03-30 | 스미또모 가가꾸 가부시키가이샤 | 화합물 및 그 제조 방법 |
EP3846904B1 (en) | 2018-09-07 | 2023-05-31 | Merck Patent GmbH | 5-morpholin-4-yl-pyrazolo[4,3-b]pyridine derivatives |
TW202028207A (zh) | 2018-09-25 | 2020-08-01 | 美商英塞特公司 | 吡唑并嘧啶化合物及其用途 |
LT3873903T (lt) | 2018-10-31 | 2024-05-10 | Gilead Sciences, Inc. | Pakeistieji 6-azabenzimidazolo junginiai, kaip hpk1 inhibitoriai |
US11071730B2 (en) | 2018-10-31 | 2021-07-27 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds |
TW202102505A (zh) * | 2019-03-29 | 2021-01-16 | 大陸商江蘇恆瑞醫藥股份有限公司 | 吡咯并雜環類衍生物、其製備方法及其在醫藥上的應用 |
CN109824675A (zh) * | 2019-04-09 | 2019-05-31 | 唐山师范学院 | 一种4-氯吡咯并嘧啶的合成方法 |
CN110078674B (zh) * | 2019-04-10 | 2022-11-01 | 昆明理工大学 | 一种2-烃基胺基嘧啶酮的制备方法 |
EP3725788A1 (en) * | 2019-04-15 | 2020-10-21 | Bayer AG | Novel heteroaryl-substituted aminoalkyl azole compounds as pesticides |
EP3972695A1 (en) | 2019-05-23 | 2022-03-30 | Gilead Sciences, Inc. | Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors |
AU2020288273A1 (en) * | 2019-06-06 | 2022-01-06 | Hutchison Medipharma Limited | Tricyclic compounds and their use |
CA3194077A1 (en) * | 2020-09-29 | 2022-04-07 | Xianqiang ZHOU | Crystal form of pyrrolo heterocyclic derivative and preparation method therefor |
CN114315837B (zh) * | 2020-09-29 | 2023-06-16 | 江苏恒瑞医药股份有限公司 | 一种erk抑制剂的结晶形式及其制备方法 |
WO2023078401A1 (en) * | 2021-11-05 | 2023-05-11 | Fochon Biosciences, Ltd. | Compounds as protein kinase inhibitors |
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US4107288A (en) | 1974-09-18 | 1978-08-15 | Pharmaceutical Society Of Victoria | Injectable compositions, nanoparticles useful therein, and process of manufacturing same |
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KR101616388B1 (ko) | 2006-03-27 | 2016-04-29 | 네르비아노 메디칼 사이언시스 에스.알.엘. | 키나제 억제제로서의 피리딜- 및 피리미디닐-치환된 피롤-, 티오펜- 및 푸란-유도체 |
EP2217601A1 (en) * | 2007-11-08 | 2010-08-18 | Centro Nacional de Investigaciones Oncológicas (CNIO) | Imidazopyridazines for use as protein kinase inhibitors |
CA2790176A1 (en) | 2010-02-18 | 2011-08-25 | Centro Nacional De Investigaciones Oncologicas (Cnio) | Triazolo [4, 5 - b] pyridin derivatives |
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-
2013
- 2013-02-27 TW TW102107123A patent/TW201348226A/zh unknown
- 2013-02-27 WO PCT/US2013/028087 patent/WO2013130660A1/en active Application Filing
- 2013-02-27 US US14/380,918 patent/US9394297B2/en active Active
- 2013-02-28 UY UY0001034648A patent/UY34648A/es not_active Application Discontinuation
- 2013-02-28 AR ARP130100648A patent/AR093740A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
US9394297B2 (en) | 2016-07-19 |
WO2013130660A1 (en) | 2013-09-06 |
US20150329538A1 (en) | 2015-11-19 |
TW201348226A (zh) | 2013-12-01 |
UY34648A (es) | 2013-09-02 |
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