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AR084370A1 - Derivados de aminopirazol - Google Patents

Derivados de aminopirazol

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Publication number
AR084370A1
AR084370A1 ARP100102875A ARP100102875A AR084370A1 AR 084370 A1 AR084370 A1 AR 084370A1 AR P100102875 A ARP100102875 A AR P100102875A AR P100102875 A ARP100102875 A AR P100102875A AR 084370 A1 AR084370 A1 AR 084370A1
Authority
AR
Argentina
Prior art keywords
alkyl
aryl
haloalkyl
membered
membered heteroaryl
Prior art date
Application number
ARP100102875A
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English (en)
Original Assignee
Chugai Pharmaceutical Co Ltd
Hoffmann La Roche
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43544423&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR084370(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Chugai Pharmaceutical Co Ltd, Hoffmann La Roche filed Critical Chugai Pharmaceutical Co Ltd
Publication of AR084370A1 publication Critical patent/AR084370A1/es

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    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0803Compounds with Si-C or Si-Si linkages
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
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    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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Abstract

Composiciones farmacéuticas y usos de los mismos. Reivindicación 1: Un compuesto representado por la formula (1), o una sal farmacéuticamente aceptable del mismo, en donde R1, R2, R3, y R4 cada uno representa independientemente el grupo que se lista más abajo: R1 representa hidrógeno, hidroxi, halógeno, ciano, nitro, haloalquilo C1-4, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, arilo C6-10 alquilo C1-4, -OR5, -NR6R7, -(CR8R9)nZ1, -C(O)NR12R13, -SR14, -SOR15, -SO2R16, -NR17SO2R18, COOH, arilo C6-10 que está opcionalmente sustituido con uno o más grupos seleccionados independientemente a partir del grupo P, heteroarilo de 5 a 10 miembros o heterociclilo de 3 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q, -COR19, -COOR20, -OC(O)R21, -NR22C(O)R23, -NR24C(S)R25, -C(S)NR26R27, -SO2NR28R29, -OSO2R30, -SO3R31, o -Si(R32)3; R2 representa hidrógeno, hidroxi, halógeno, ciano, nitro, haloalquilo C1-4, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-7, aril C6-10 alquilo C1-4, -OR5, -NR6R7, -(CR8R9)nZ1, -C(O)NR12R13, -SR14, -SOR15, -SO2R16, -NR17SO2R18, COOH, arilo C6-10 que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo P, heteroarilo de 5 a 10 miembros o heterociclilo de 3 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q, -COR19, -COOR20, -OC(O)R21, -NR22C(O)R23, -NR24C(S)R25, -C(S)NR26R27, -SO2NR28R29, -OSO2R30, -SO3R31, o -Si(R32)3; o R1 y R2, junto con un átomo al cual están unidos, forman heterociclilo de 3 a 10 miembros o heteroarilo de 5 a 10 miembros, en donde el heterociclilo o heteroarilo está opcionalmente sustituido con halógeno; R3 representa hidrógeno, alquilo C1-5, aril C6-10 alquilo C1-6 o haloalquilo C1-4; R4 representa hidrógeno, halógeno, alquilo C1-3, haloalquilo C1-4, hidroxi, ciano, nitro, alcoxi C1-4, -(CH2)nZ1, -NR6R7, -OR5, -C(O)NR12R13, -SR14, -SOR15, -SO2R16, NR17SO2R18, COOH, -COR19, -COOR20, -OC(O)R21, -NR22C(O)R23, -NR24C(S)R25, -C(S)NR26R27, -SO2NR28R29, -OSO2R30, -SO3R31, o -Si(R32)3; A representa un anillo heteroarilo de 5 a 10 miembros o anillo arilo C6-10; R5 representa alquilo C1-5, cicloalquilo C3-7, cicloalquilo C3-7 alquilo C1-3, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, alcoxi C1-3 alquilo C1-4, alcoxi C1-3alquilo C1-4, aminoalquilo C1-4, alquil C1-4amino-alquilo C1-4, di(alquil C1-4)amino-alquilo C1-4, arilo C6-10, aril C6-10alquilo C1-3, o heterociclil de 3 a 10 miembros-alquilo C1-3, heterociclilo de 3 a 10 miembros, heteroarilo de 5 a 10 miembros, heteroaril de 5 a 10 miembros-alquilo C1-3, monohidroxialquilo C1-6, dihidroxialquilo C1-6, o trihidroxialquilo C1-6 que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q; R6 y R7, que son iguales o diferentes, cada uno representa hidrógeno, alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, alcoxi C1-3alquilo C1-4, aril C6-10alquilo C1-3, heterociclil de 3 a 10 miembros-alquilo C1-3, heteroarilo de 5 a 10 miembros-alquilo C1-3, monohidroxialquilo C1-6, dihidroxialquilo C1-6, trihidroxialquilo C1-6, heterociclil de 3 a 10 miembros, aminoalquilo C1-4, alquil C1-4amino-alquilo C1-4, di(alquil C1-4)amino-alquilo C1-4, o ciano(alquilo C1-3); o R6 y R7, junto con un átomo de nitrógeno al cual están unidos, forman heterociclilo de 3 a 10 miembros o heteroarilo de 5 a 10 miembros; n representa 1 a 3; R8 y R9, que son iguales o diferentes, cada uno representa hidrógeno, alquilo C1-4, o halógeno; o alternativamente, R8 y R9, junto con un átomo de carbono al cual están unidos, forman un anillo cicloalifático; Z1 representa hidrógeno, NR10R11, -OH, o heterociclilo de 3 a 10 miembros o heteroarilo de 5 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q; R10 y R11, que son iguales o diferentes, cada uno representa alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, alcoxi C1-3alquilo C1-4, ciano(alquilo C1-3), o alquil C1-3sulfonil-alquilo C1-4 o alternativamente, R10 y R11, junto con un átomo de nitrógeno al cual están unidos, forman heterociclilo de 3 a 10 miembros o heteroarilo de 5 a 10 miembros; R12 y R13, que son iguales o diferentes, cada uno representa hidrógeno, alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, alcoxi C1-3alquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, heterociclilo de 3 a 10 miembros, aril C6-10alquilo C1-4, heterociclil de 3 a 10 miembros-alquilo C1-3, heteroarilo de 5 a 10 miembros-alquilo C1-3, ciano(alquilo C1-3), alquil C1-3sulfonilo-alquilo C1-4, anillo cicloalifático de 3 a 10 miembros, heteroarilo de 5 a 10 miembros, o heterociclilo de 3 a 10 miembros; o alternativamente, R12 y R13, junto con un átomo de nitrógeno al cual están unidos, forman heterociclilo de 3 a 10 miembros o heteroarilo de 5 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q; R14 representa alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, arilo C6-10 que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo P, o heteroarilo de 5 a 10 miembros o heterociclilo de 3 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q; R15 representa alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, arilo C6-10 que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo P, o heteroarilo de 5 a 10 miembros o heterociclilo de 3 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q; R16 representa alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, arilo C6-10 que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo P, o heteroarilo de 5 a 10 miembros o heterociclilo de 3 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q; R17 representa hidrógeno o alquilo C1-4; R18 representa alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, arilo C6-10 que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo P, o heteroarilo de 5 a 10 miembros o heterociclilo de 3 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q; R19 representa hidrógeno, alquilo C1-4, cicloalquilo C3-7, haloalquilo C1-4, arilo C6-10, o heteroarilo de 5 a 10 miembros o heterociclilo de 3 a 10 miembros que está opcionalmente sustituido con uno o más grupos independientemente seleccionados a partir del grupo Q; R20 representa alquilo C1-4, cicloalquilo C3-7, haloalquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, o heterociclilo de 3 a 10 miembros; R21 representa alquilo C1-4, cicloalquilo C3-7, haloalquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, o heterociclilo de 3 a 10 miembros; R22 representa hidrógeno, alquilo C1-4, o haloalquilo C1-4; R23 representa hidrógeno, alquilo C1-4, cicloalquilo C3-7, haloalquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, o heterociclilo de 3 a 10 miembros; R24 representa hidrógeno, alquilo C1-4, o haloalquilo C1-4; R25 representa alquilo C1-4, cicloalquilo C3-7, haloalquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, o heterociclilo de 3 a 10 miembros; R26 y R27, que son iguales o diferentes, cada uno representa hidrógeno, alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, alcoxi C1-3alquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, heterociclilo de 3 a 10 miembros, aril C6-10alquilo C1-4, heterociclilo de 3 a 10 miembros-alquilo C1-3, heteroarilo de 5 a 10 miembros-alquilo C1-3, ciano(alquilo C1-3), alquilo C1-3sulfonilo-alquilo C1-4, o un anillo cicloalifático de 3 a 10 miembros; o alternativamente, R26 y R27, junto con un átomo de nitrógeno al cual están unidos, forman heterociclilo de 3 a 10 miembros o heteroarilo de 5 a 10 miembros; R28 y R29, que son iguales o diferentes, cada uno representa hidrógeno, alquilo C1-4, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-4, alcoxi C1-3, alquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, heterociclilo de 3 a 10 miembros, aril C6-10alquilo C1-4, heterociclil de 3 a 10 miembros-alquilo C1-3, heteroaril de 5 a 10 miembros-alquilo C1-3, ciano(alquilo C1-3), alquil C1-3sulfonil-alquilo C1-4, o un anillo cicloalifático de 3 a 10 miembros; o alternativamente, R28 y R29, junto con un átomo de nitrógeno al cual están unidos, forman heterociclilo de 3 a 10 miembros o heteroarilo de 5 a 10 miembros; R30 representa alquilo C1-4, cicloalquilo C3-7, haloalquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, o heterociclilo de 3 a 10 miembros; R31 representa alquilo C1-4, cicloalquilo C3-7, haloalquilo C1-4, arilo C6-10, heteroarilo de 5 a 10 miembros, o heterociclilo de 3 a 10 miembros; R32 representa alquilo C1-4 o arilo C6-10;
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Families Citing this family (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH12012500252A1 (en) 2009-08-07 2015-06-26 Chugai Pharmaceutical Co Ltd Aminopyrazole derivative
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
CN104487424A (zh) * 2012-02-20 2015-04-01 罗地亚经营管理公司 用于生产dfmb衍生物的方法
CN107652289B (zh) 2012-06-13 2020-07-21 因塞特控股公司 作为fgfr抑制剂的取代的三环化合物
HUE055502T2 (hu) 2012-07-11 2021-11-29 Blueprint Medicines Corp Fibroblaszt növekedési faktor receptor gátlók
US9388185B2 (en) 2012-08-10 2016-07-12 Incyte Holdings Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
CN107501413A (zh) * 2012-09-27 2017-12-22 中外制药株式会社 Fgfr3融合基因和以其作为标靶的药物
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
AR094812A1 (es) 2013-02-20 2015-08-26 Eisai R&D Man Co Ltd Derivado de piridina monocíclico como inhibidor del fgfr
KR102269032B1 (ko) 2013-04-19 2021-06-24 인사이트 홀딩스 코포레이션 Fgfr 저해제로서 이환식 헤테로사이클
CN103224479B (zh) * 2013-04-26 2014-10-15 温州大学 一种2-芳基苯并呋喃类化合物的合成方法
US9814776B2 (en) 2013-07-31 2017-11-14 Chugai Seiyaku Kabushiki Kaisha Pharmaceutical preparation comprising aminopyrazole derivative
CA2928042C (en) 2013-10-25 2022-05-10 Blueprint Medicines Corporation Inhibitors of the fibroblast growth factor receptor
BR112016013541B1 (pt) 2013-12-13 2021-03-02 F. Hoffmann-La Roche Ag inibidores de quinase tirosina de bruton
RU2648236C2 (ru) * 2013-12-13 2018-03-23 Ф. Хоффманн-Ля Рош Аг Ингибиторы тирозинкиназы брутона
CN105814035B (zh) * 2013-12-13 2018-02-02 豪夫迈·罗氏有限公司 布鲁顿氏酪氨酸激酶抑制剂
JP6514645B2 (ja) * 2013-12-27 2019-05-15 中外製薬株式会社 Fgfrゲートキーパー変異遺伝子およびそれを標的とする医薬
US9695165B2 (en) 2014-01-15 2017-07-04 Blueprint Medicines Corporation Inhibitors of the fibroblast growth factor receptor
KR20160138494A (ko) 2014-03-31 2016-12-05 데비오팜 인터네셔날 에스 에이 Fgfr 융합물
JP6515175B2 (ja) * 2014-07-08 2019-05-15 サンシャイン・レイク・ファーマ・カンパニー・リミテッドSunshine Lake Pharma Co.,Ltd. 芳香族ヘテロ環誘導体及びその医薬的適用
ES2914072T3 (es) 2014-08-18 2022-06-07 Eisai R&D Man Co Ltd Sal de derivado de piridina monocíclico y su cristal
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
WO2016134294A1 (en) 2015-02-20 2016-08-25 Incyte Corporation Bicyclic heterocycles as fgfr4 inhibitors
PE20171514A1 (es) 2015-02-20 2017-10-20 Incyte Corp Heterociclos biciclicos como inhibidores de fgfr
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
JP6503450B2 (ja) 2015-03-25 2019-04-17 国立研究開発法人国立がん研究センター 胆管癌治療剤
US10479780B2 (en) 2015-06-17 2019-11-19 Chugai Seiyaku Kabushiki Kaisha Aminopyrazole derivatives
JP2018524010A (ja) 2015-07-24 2018-08-30 デバイオファーム インターナショナル エスエイ Fgfr発現とfgfr阻害剤に対する感受性
JP6549311B2 (ja) * 2015-08-20 2019-07-24 浙江海正薬業股▲ふん▼有限公司Zhejiang Hisun Pharmaceutical CO.,LTD. インドール誘導体、その調製方法および医薬におけるその使用
MX384034B (es) 2015-12-17 2025-03-14 Eisai R&D Man Co Ltd Agente terapeutico para cancer de mama.
WO2017157332A1 (zh) * 2016-03-18 2017-09-21 江苏恒瑞医药股份有限公司 芳香酰胺类衍生物、其制备方法及其在医药上的应用
US20190192522A1 (en) 2016-09-08 2019-06-27 Blueprint Medicines Corporation Inhibitors of the fibroblast growth factor receptor 4 in combination with cyclin-dependent kinase inhibitors
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
BR112020017922A2 (pt) 2018-03-28 2020-12-22 Eisai R&D Management Co., Ltd. Agente terapêutico para carcinoma hepatocelular
BR112020022373A2 (pt) 2018-05-04 2021-02-02 Incyte Corporation sais de um inibidor de fgfr
SG11202010636VA (en) 2018-05-04 2020-11-27 Incyte Corp Solid forms of an fgfr inhibitor and processes for preparing the same
GB201810092D0 (en) 2018-06-20 2018-08-08 Ctxt Pty Ltd Compounds
CN110950848B (zh) * 2018-09-27 2024-03-26 徐诺药业 新型氨基吡唑类衍生物的合成与应用
WO2020072580A1 (en) * 2018-10-02 2020-04-09 Disc Medicine, Inc. Matriptase 2 inhibitors and uses thereof
WO2020185532A1 (en) 2019-03-08 2020-09-17 Incyte Corporation Methods of treating cancer with an fgfr inhibitor
CN110092791B (zh) * 2019-05-17 2020-04-03 河南大学 5,6-吲哚并二恶烷类衍生物及其制备方法和应用
AU2020296361A1 (en) 2019-06-18 2022-01-06 Ctxt Pty Ltd Benzisoxazole sulfonamide derivatives
WO2021007269A1 (en) 2019-07-09 2021-01-14 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
WO2021067374A1 (en) 2019-10-01 2021-04-08 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
CN112358435B (zh) * 2019-10-12 2023-01-10 中国医学科学院医药生物技术研究所 取代芳并杂环类化合物、制备方法和抑制ulk1及抗肿瘤用途
WO2021076602A1 (en) 2019-10-14 2021-04-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
WO2021076728A1 (en) 2019-10-16 2021-04-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
CN115151539A (zh) 2019-12-04 2022-10-04 因赛特公司 Fgfr抑制剂的衍生物
JP7720840B2 (ja) 2019-12-04 2025-08-08 インサイト・コーポレイション Fgfr阻害剤としての三環式複素環
WO2021146424A1 (en) 2020-01-15 2021-07-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
KR20230035031A (ko) 2020-06-05 2023-03-10 킨네이트 바이오파마 인크. 섬유아세포 성장 인자 수용체 키나아제의 억제제
US12065494B2 (en) 2021-04-12 2024-08-20 Incyte Corporation Combination therapy comprising an FGFR inhibitor and a Nectin-4 targeting agent
AR126102A1 (es) 2021-06-09 2023-09-13 Incyte Corp Heterociclos tricíclicos como inhibidores de fgfr
CA3220155A1 (en) 2021-06-09 2022-12-15 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
CA3240059A1 (en) * 2021-12-08 2023-06-15 Kinnate Biopharma Inc. Treatment of cancer with an fgfr kinase inhibitor
EP4450494A1 (en) 2023-04-20 2024-10-23 Consejo Superior De Investigaciones Científicas Indole derivatives as histone deacetylase (hdac) inhibitors for the treatment of cancer

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL175831B1 (pl) 1992-12-17 1999-02-26 Pfizer Pochodna pirazolu
US6316466B1 (en) 1998-05-05 2001-11-13 Syntex (U.S.A.) Llc Pyrazole derivatives P-38 MAP kinase inhibitors
YU67600A (sh) 1998-05-05 2003-07-07 F.Hofmann - La Roche Ag. Derivati pirazola kao inhibitori p-38 map kinaze
US6534535B1 (en) * 1999-08-12 2003-03-18 Millennium Pharmaceuticals, Inc. Inhibitors of factor Xa
JP2003050945A (ja) 2001-08-06 2003-02-21 Takashi Hashimoto 連動型広告配信システム及び広告配信サーバの動作方法
FR2831537B1 (fr) * 2001-10-26 2008-02-29 Aventis Pharma Sa Nouveaux derives de benzimidazoles, leur procede de preparation, leur application a titre de medicament, compositions pharmaceutiques et nouvelle utilisation
IL161576A0 (en) 2001-10-26 2004-09-27 Aventis Pharma Inc Benzimidazoles and analogues and their use as protein kinases inhibitors
FR2854159B1 (fr) 2003-04-25 2008-01-11 Aventis Pharma Sa Nouveaux derives de l'indole, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de kdr
PL1641764T3 (pl) * 2003-06-26 2011-12-30 Novartis Ag Inhibitory kinazy P38 na bazie 5-członowych heterocykli
JP2008545776A (ja) 2005-06-11 2008-12-18 ヴァーナリス アールアンドディー リミテッド 癌および自己免疫疾患の治療における使用のためのピラゾール−置換ベンズイミダゾール誘導体
US8399442B2 (en) 2005-12-30 2013-03-19 Astex Therapeutics Limited Pharmaceutical compounds
FR2903406B1 (fr) 2006-07-04 2012-08-10 Aventis Pharma Sa Derives de pyrazolylbenzimidazole,compositions les contenant et utilisation
RU2011106357A (ru) * 2008-07-23 2012-08-27 Ф.Хоффманн-Ля Рош Аг (Ch) Гетероциклические антивирусные соединения
CA2730517A1 (en) 2008-07-23 2010-01-28 F. Hoffmann-La Roche Ag Heterocyclic antiviral compounds
PH12012500252A1 (en) 2009-08-07 2015-06-26 Chugai Pharmaceutical Co Ltd Aminopyrazole derivative

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