AR055273A1 - Pi3-quinasas, sus usos y composiciones farmaceuticas que los contienen - Google Patents
Pi3-quinasas, sus usos y composiciones farmaceuticas que los contienenInfo
- Publication number
- AR055273A1 AR055273A1 ARP050104225A ARP050104225A AR055273A1 AR 055273 A1 AR055273 A1 AR 055273A1 AR P050104225 A ARP050104225 A AR P050104225A AR P050104225 A ARP050104225 A AR P050104225A AR 055273 A1 AR055273 A1 AR 055273A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- het
- alkenyl
- aryl
- nitrogen
- Prior art date
Links
Classifications
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/84—Naphthothiazoles
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Immunology (AREA)
- Communicable Diseases (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Virology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Debido a su accion farmacéutica como moduladores de la PI3-quinasa pueden utilizarse en el área terapéutica para el tratamiento de enfermedades inflamatorias o alérgicas. A modo de ejemplo, se mencionan enfermedades inflamatorias o alérgicas de las vías respiratorias, enfermedades inflamatorias del tracto gastro-intestinal, artritis reumatoidea, patologías dérmicas inflamatorias y alérgicas, patologías oftálmicas inflamatorias, patologías de la mucosa nasal, estados patologicas inflamatorios o alérgicos, en los cuales inciden reacciones autoinmunes o inflamaciones renales. Reivindicacion 1: Compuestos de formula (1), con la condicion, que la línea circular identificada con A significa un sistema aromático; donde Y significa carbono, átomo de nitrogeno, azufre; de preferencial carbono, nitrogeno; Z significa carbono, nitrogeno, azufre; de preferencia carbono, nitrogeno; j 1, 2 o 3; k 0 o 1; Ra es H, COR8, NR9R10, NO2, OR8, SR11, SOR11, SO2R11, NHCO-alquiloC1-6-NH2, o un radical seleccionado del grupo que incluye alquilo C1-6, alquenilo C2-6, cicloalquilo C3-8, cicloalquenilo C3-8, haloalquilo C1-6, arilo, aralquilo C7-11, espiro, Het, heteroarilo y CH2-O-arilo, que en su caso puede estar sustituido; R8 significa alquilo C1- 6, cicloalquilo C3-6, NH2, hetarilo o arilo, en su caso sustituido con uno o varios halogenos o alquilo C1-4; R9 significa H, COOR12, CONR12 o alquilo C1-6, en su caso sustituido con uno o varios COOH, N(alquilo C1-6)2 o Het, en su caso sustituido con uno o varios alquilo C1-6; o R9 significa Het, en su caso sustituido con uno o varios alquilo C1-4; R10 significa H, alquilo C1-6, CO-alquiloC1-6 o alquinilo C2-6; R11 significa alquilo C1-6, en su caso sustituido con uno o varios N(alquilo C1- 4)2; Rb es R4, OR4, -CH2OR4, COR4, COOR4, CONR4R5, NR4R5, NR5COR4, NR5COOR4, NR5CONR4R5, NR5SOR4 o NR5SO2R4; R4, R5 significan H, alquilo C1-6, haloalquilo C1-6, alquileno C1-6-OH, alquenilo C2-6, aralquilo C7-11, alqueniloC2-4-arilo, alquiniloC2-4- arilo, alquiloC1-4-hetarilo, alqueniloC2-4-hetarilo, alquiniloC2-4-hetarilo, alquinilo C2-6, en su caso sustituido con Si(alquilo C1-4)3, o R4 significa un radical seleccionado del grupo que incluye arilo, Het, Hetarilo y en su caso alquilo C1-4; o R4 y R5 forman conjuntamente un anillo de cinco, seis o siete miembros que se compone de átomo de carbono y en su caso un heteroátomo seleccionado del grupo que se compone de oxígeno, nitrogeno y azufre; Rc significa NHR6 o un radical seleccionado del grupo que incluye la formula (2) donde: B significa un enlace, alquilo C1-6, alquenilo C2-6 o alquinilo C2-6; R6 es H o un radical seleccionado del grupo alquilo C1-4, alquenilo C2-4, alquinilo C2-4, cicloalquilo C3-6, cicloalquenilo C3-6, Het, arilo, hetarilo en su caso sustituido con uno o varios radicales R6,1; R6,1 es halogeno, CF3, OH, CN, OMe, SO2(alquilo C1-4); R7 significa H, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, cicloalquilo C3-6, NR7,1R7,2, OR7,2, SR7,2, hetarilo, Het, en su caso sustituido con alquilo C1-4 o CONH2; R7,1 significa H, alquilo C1-6, (CH2)2-4R7,1,1 o COO-butilo; R7,2 significa H, alquilo C1-6, en su caso sustituido con uno o varios OH; R7,1,1NR7,1,1,1R7,1,1,2, Het o 1-imidazolilo, 2-(N-etilpirrolidina); R7,1,1,1 es H o alquilo C1-6; R7,1,1,2 es H o alquilo C1-6; así como sales aceptables para uso farmacéuticos, diaesteromeros, enantiomeros, racematos, hidratos o solvatos de éstos, con la condicion, que Ra no puede ser H o Me, cuando significan Y = nitrogeno; Z = nitrogeno; j = 2; k = 0; Rb= H y Rc = NHCONH-Et.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004048877A DE102004048877A1 (de) | 2004-10-07 | 2004-10-07 | PI3-Kinasen |
| DE102005005813A DE102005005813A1 (de) | 2005-02-09 | 2005-02-09 | PI3-Kinasen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR055273A1 true AR055273A1 (es) | 2007-08-15 |
Family
ID=35583390
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050104225A AR055273A1 (es) | 2004-10-07 | 2005-10-07 | Pi3-quinasas, sus usos y composiciones farmaceuticas que los contienen |
Country Status (14)
| Country | Link |
|---|---|
| US (4) | US20060106013A1 (es) |
| EP (2) | EP1802636B1 (es) |
| JP (1) | JP5122287B2 (es) |
| KR (1) | KR20070064660A (es) |
| CN (1) | CN101048418A (es) |
| AR (1) | AR055273A1 (es) |
| AU (1) | AU2005293607A1 (es) |
| BR (1) | BRPI0516557A (es) |
| CA (1) | CA2579279C (es) |
| IL (1) | IL182398A0 (es) |
| MX (1) | MX2007004051A (es) |
| RU (2) | RU2403258C2 (es) |
| TW (1) | TW200628475A (es) |
| WO (1) | WO2006040279A1 (es) |
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| RU2403258C2 (ru) * | 2004-10-07 | 2010-11-10 | Бёрингер Ингельхайм Интернациональ Гмбх | Тиазолилдигидроиндазолы |
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| US20070238718A1 (en) * | 2006-04-06 | 2007-10-11 | Matthias Grauert | Thiazolyl-dihydro-indazole |
| US7691868B2 (en) * | 2006-04-06 | 2010-04-06 | Boehringer Ingelheim International Gmbh | Thiazolyl-dihydro-quinazoline |
| BRPI0710843A2 (pt) * | 2006-04-06 | 2011-08-23 | Boehringer Ingelheim Int | tiazolil-di-hidro-indazóis |
| US20070259855A1 (en) * | 2006-04-06 | 2007-11-08 | Udo Maier | Thiazolyl-dihydro-indazole |
| US7517995B2 (en) * | 2006-04-06 | 2009-04-14 | Boehringer Ingelheim International Gmbh | Thiazolyl-dihydro-cyclopentapyrazole |
| DE602006002385D1 (de) * | 2006-06-26 | 2008-10-02 | Helm Ag | Verfahren zur Herstellung von Pramipexole |
| EP2045253A4 (en) * | 2006-06-29 | 2013-01-23 | Nissan Chemical Ind Ltd | alpha-amino acid derivative and pharmaceutical agent containing it as an active ingredient |
| US8779154B2 (en) * | 2006-09-26 | 2014-07-15 | Qinglin Che | Fused ring compounds for inflammation and immune-related uses |
| GB0619611D0 (en) | 2006-10-04 | 2006-11-15 | Ark Therapeutics Ltd | Compounds and their use |
| US20100204222A1 (en) * | 2007-09-17 | 2010-08-12 | GlaxoSmithKline, LLC | Pyridopyrimidine derivatives as p13 kinase inhibitors |
| CA2711644A1 (en) * | 2008-01-07 | 2009-07-16 | Synta Pharmaceuticals Corp. | Compounds for inflammation and immune-related uses |
| UY31700A (es) * | 2008-03-13 | 2009-11-10 | Boehringer Ingelheim Int | Tiazolil-dihidro-indazoles |
| WO2009120826A1 (en) * | 2008-03-27 | 2009-10-01 | Wyeth | 2-aryl- and 2-heteroarylthiazolyl compounds, methods for their preparation and use thereof |
| EP2276767B1 (en) * | 2008-03-31 | 2014-05-07 | Genentech, Inc. | Benzopyran and benzoxepin pi3k inhibitor compounds and methods of use |
| CA2728095A1 (en) * | 2008-07-17 | 2010-01-21 | Asahi Kasei Pharma Corporation | Pyrazole-containing tricyclic compounds as antagonists of an ep1 receptor |
| EP2327704A4 (en) * | 2008-08-29 | 2012-05-09 | Shionogi & Co | RING-CONDENSED AZOL DERIVATIVE WITH PI3K-INHIBITING EFFECT |
| EP2350084B1 (en) | 2008-10-17 | 2015-06-24 | Boehringer Ingelheim International GmbH | Tetra-aza-heterocycles as phosphatidylinositol-3-kinases (pi3-kinases) inhibitor |
| GB0900404D0 (en) | 2009-01-12 | 2009-02-11 | Addex Pharmaceuticals Sa | New compounds 4 |
| US8278302B2 (en) | 2009-04-08 | 2012-10-02 | Boehringer Ingelheim International Gmbh | Substituted piperidines as CCR3 antagonists |
| US9243000B2 (en) | 2009-04-22 | 2016-01-26 | Boehringer Ingelheim International Gmbh | Thia-triaza-indacenes |
| US8288379B2 (en) * | 2009-04-22 | 2012-10-16 | Boehringer Ingelheim International Gmbh | Thia-triaza-cyclopentazulenes |
| MX2012000178A (es) * | 2009-07-02 | 2012-02-28 | Novartis Ag | 2-carboxamida-cicloamino-ureas utiles como inhibidores de pi3k. |
| PE20170003A1 (es) | 2009-08-17 | 2017-03-15 | Intellikine Llc | Compuestos heterociclicos y usos de los mismos |
| SI2483278T1 (sl) | 2009-09-28 | 2014-03-31 | F. Hoffmann-La Roche Ag | Inhibitorske spojine benzoksazepina pi3k in njihova uporaba pri zdravljenju raka |
| SG10201407781SA (en) * | 2009-09-28 | 2015-01-29 | Hoffmann La Roche | Benzoxepin PI3K Inhibitor Compounds And Methods Of Use |
| JP5735526B2 (ja) * | 2009-11-13 | 2015-06-17 | メルク セローノ ソシエテ アノニム | 三環式ピラゾールアミン誘導体 |
| CN103153062B (zh) | 2010-05-24 | 2015-07-15 | 因特利凯有限责任公司 | 杂环化合物及其用途 |
| WO2012009000A2 (en) * | 2010-07-14 | 2012-01-19 | Addex Pharma S.A. | Novel fused pyrazole derivatives and their use as allosteric modulators of metabotropic glutamate receptors |
| GB201011831D0 (en) | 2010-07-14 | 2010-09-01 | Addex Pharmaceuticals Sa | New compounds 5 |
| TW201245176A (en) | 2011-01-26 | 2012-11-16 | Boehringer Ingelheim Int | New 5-alkynyl-pyridines |
| EP2546249A1 (en) | 2011-07-15 | 2013-01-16 | Boehringer Ingelheim International Gmbh | 5-Alkynyl-pyridines |
| US8466162B2 (en) | 2011-01-26 | 2013-06-18 | Boehringer Ingelheim International Gmbh | 5-alkynyl-pyridines |
| EP2678018A4 (en) | 2011-02-23 | 2015-09-30 | Intellikine Llc | COMBINATION OF CHINESE HEMMER AND USES THEREOF |
| WO2012116237A2 (en) | 2011-02-23 | 2012-08-30 | Intellikine, Llc | Heterocyclic compounds and uses thereof |
| WO2012126901A1 (en) | 2011-03-21 | 2012-09-27 | F. Hoffmann-La Roche Ag | Benzoxazepin compounds selective for pi3k p110 delta and methods of use |
| KR20140129120A (ko) * | 2012-02-06 | 2014-11-06 | 글락소스미스클라인 인털렉츄얼 프로퍼티 (넘버 2) 리미티드 | 기침 치료용 pi3k 저해제 |
| US10722484B2 (en) | 2016-03-09 | 2020-07-28 | K-Gen, Inc. | Methods of cancer treatment |
| CA3102279A1 (en) | 2018-06-01 | 2019-12-05 | Cornell University | Combination therapy for pi3k-associated disease or disorder |
| WO2020142557A1 (en) | 2018-12-31 | 2020-07-09 | Biomea Fusion, Llc | Irreversible inhibitors of menin-mll interaction |
| TW202043205A (zh) | 2018-12-31 | 2020-12-01 | 美商拜歐米富士恩有限公司 | Menin-mll相互作用之抑制劑 |
| EP4384179A1 (en) | 2021-08-11 | 2024-06-19 | Biomea Fusion, Inc. | Covalent inhibitors of menin-mll interaction for diabetes mellitus |
| CN119816500A (zh) | 2021-08-20 | 2025-04-11 | 拜欧米富士恩公司 | 用于治疗癌症的不可逆menin-MLL抑制剂N-[4-[4-(4-吗啉基)-7H-吡咯并[2,3-d]嘧啶-6-基]苯基]-4-[[3(R)-[(1-氧代-2-丙烯-1-基)氨基]-1-哌啶基]甲基]-2-吡啶甲酰胺的结晶形式 |
| WO2024155710A1 (en) | 2023-01-18 | 2024-07-25 | Biomea Fusion, Inc. | Crystalline forms of n-[4-[4-(4-morpholinyl)-7h-pyrrolo[2,3-d]pyrimidin-6- yl]phenyl]-4-[[3(r)-[(l-oxo-2-propen-l-yl)amino]-l-piperidinyl]methyl]-2-pyridinecarboxamide as a covalent inhibitor of menin-mll interaction |
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| IL113112A (en) * | 1994-03-28 | 2000-06-01 | Nissan Chemical Ind Ltd | Pyridine substituted thiazolidinediones and pharmaceutical compositions comprising them |
| AU727654B2 (en) * | 1997-06-13 | 2000-12-21 | Yamanouchi Pharmaceutical Co., Ltd. | Tricyclic pyrazole derivative |
| JP2003521543A (ja) * | 2000-02-07 | 2003-07-15 | アボット ゲーエムベーハー ウント カンパニー カーゲー | 2−ベンゾチアゾリル尿素誘導体およびそのプロテインキナーゼ阻害剤としての使用 |
| CA2401748A1 (en) * | 2000-03-29 | 2001-10-04 | Cyclacel Limited | 2-substituted 4-heteroaryl-pyrimidines and their use in the treatment of proliferative disorders |
| US6608053B2 (en) * | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| KR100423899B1 (ko) * | 2000-05-10 | 2004-03-24 | 주식회사 엘지생명과학 | 세포 증식 억제제로 유용한 1,1-디옥소이소티아졸리딘을갖는 인다졸 |
| AU2002349912A1 (en) | 2001-10-24 | 2003-05-06 | Iconix Pharmaceuticals, Inc. | Modulators of phosphoinositide 3-kinase |
| TWI314928B (en) * | 2002-02-28 | 2009-09-21 | Novartis A | 5-phenylthiazole derivatives and use as pi3 kinase inhibitors |
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| HRP20131159B1 (hr) | 2002-09-30 | 2019-11-01 | Bayer Ip Gmbh | Taljeni azol-pirimidin derivati |
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-
2005
- 2005-10-05 RU RU2007116858/04A patent/RU2403258C2/ru not_active IP Right Cessation
- 2005-10-05 RU RU2007116861/04A patent/RU2007116861A/ru not_active Application Discontinuation
- 2005-10-05 EP EP05805652A patent/EP1802636B1/de not_active Expired - Lifetime
- 2005-10-05 EP EP11158787A patent/EP2343303A1/de not_active Withdrawn
- 2005-10-05 CA CA2579279A patent/CA2579279C/en not_active Expired - Lifetime
- 2005-10-05 CN CNA2005800344060A patent/CN101048418A/zh active Pending
- 2005-10-05 KR KR1020077010387A patent/KR20070064660A/ko not_active Withdrawn
- 2005-10-05 WO PCT/EP2005/055015 patent/WO2006040279A1/de not_active Ceased
- 2005-10-05 US US11/244,299 patent/US20060106013A1/en not_active Abandoned
- 2005-10-05 BR BRPI0516557-1A patent/BRPI0516557A/pt not_active IP Right Cessation
- 2005-10-05 MX MX2007004051A patent/MX2007004051A/es not_active Application Discontinuation
- 2005-10-05 US US11/243,796 patent/US7691888B2/en not_active Expired - Lifetime
- 2005-10-05 AU AU2005293607A patent/AU2005293607A1/en not_active Abandoned
- 2005-10-05 JP JP2007535159A patent/JP5122287B2/ja not_active Expired - Lifetime
- 2005-10-06 TW TW094134899A patent/TW200628475A/zh unknown
- 2005-10-07 AR ARP050104225A patent/AR055273A1/es unknown
-
2007
- 2007-04-10 IL IL182398A patent/IL182398A0/en unknown
-
2009
- 2009-02-05 US US12/366,248 patent/US8232286B2/en active Active
-
2010
- 2010-01-11 US US12/685,213 patent/US8207349B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP2343303A1 (de) | 2011-07-13 |
| US8207349B2 (en) | 2012-06-26 |
| TW200628475A (en) | 2006-08-16 |
| US20090156554A1 (en) | 2009-06-18 |
| CA2579279A1 (en) | 2006-04-20 |
| KR20070064660A (ko) | 2007-06-21 |
| US7691888B2 (en) | 2010-04-06 |
| JP2008515852A (ja) | 2008-05-15 |
| AU2005293607A1 (en) | 2006-04-20 |
| MX2007004051A (es) | 2007-05-24 |
| WO2006040279A1 (de) | 2006-04-20 |
| CN101048418A (zh) | 2007-10-03 |
| RU2403258C2 (ru) | 2010-11-10 |
| BRPI0516557A (pt) | 2008-09-09 |
| JP5122287B2 (ja) | 2013-01-16 |
| EP1802636B1 (de) | 2013-03-27 |
| US20100113414A1 (en) | 2010-05-06 |
| EP1802636A1 (de) | 2007-07-04 |
| CA2579279C (en) | 2013-10-01 |
| RU2007116861A (ru) | 2009-03-20 |
| US20060106013A1 (en) | 2006-05-18 |
| US8232286B2 (en) | 2012-07-31 |
| RU2007116858A (ru) | 2008-12-27 |
| US20060100254A1 (en) | 2006-05-11 |
| IL182398A0 (en) | 2007-07-24 |
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