PE20090596A1 - Imidazoles biciclicos fusionados - Google Patents
Imidazoles biciclicos fusionadosInfo
- Publication number
- PE20090596A1 PE20090596A1 PE2008001379A PE2008001379A PE20090596A1 PE 20090596 A1 PE20090596 A1 PE 20090596A1 PE 2008001379 A PE2008001379 A PE 2008001379A PE 2008001379 A PE2008001379 A PE 2008001379A PE 20090596 A1 PE20090596 A1 PE 20090596A1
- Authority
- PE
- Peru
- Prior art keywords
- phenyl
- alkyl
- imidazo
- triazol
- piperidin
- Prior art date
Links
- 150000002460 imidazoles Chemical class 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 3
- -1 AMINO Chemical class 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 abstract 2
- 206010060999 Benign neoplasm Diseases 0.000 abstract 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 abstract 1
- FIULGFJIHJJXMT-UHFFFAOYSA-N [C]1[N]C=CC=C1 Chemical class [C]1[N]C=CC=C1 FIULGFJIHJJXMT-UHFFFAOYSA-N 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000003463 hyperproliferative effect Effects 0.000 abstract 1
- UTCSSFWDNNEEBH-UHFFFAOYSA-N imidazo[1,2-a]pyridine Chemical compound C1=CC=CC2=NC=CN21 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 abstract 1
- INSWZAQOISIYDT-UHFFFAOYSA-N imidazo[1,2-a]pyrimidine Chemical compound C1=CC=NC2=NC=CN21 INSWZAQOISIYDT-UHFFFAOYSA-N 0.000 abstract 1
- SYLTXFOKMOCILU-UHFFFAOYSA-N imidazo[1,2-b][1,2,4]triazine Chemical compound N1=CC=NC2=NC=CN21 SYLTXFOKMOCILU-UHFFFAOYSA-N 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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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
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non 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
-
- 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
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D401/10—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 linked by a carbon chain containing aromatic rings
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
REFERIDA A COMPUESTOS DERIVADOS DE IMIDAZOLES BICICLICOS FUSIONADOS DE FORMULA (I) DONDE EL ANILLO B Y EL IMIDAZOL AL CUAL ESTA FUSIONADO FORMAN (a), (b), (c), ENTRE OTROS, EN DONDE R1 ES H, ALQUILO(C1-C4), HALOGENO, AMINO, -CF3, -CN, ENTRE OTROS; R3 ES H, ALQUILO(C1-C4) O HALOGENO; R4 ES FENILO NO SUSTITUIDO, PIRIDINILO, OXAZOLILO, ENTRE OTROS; R6 ES H O ALQUILO(C1-C4); R7 ES -W-Y, DONDE W ES HETEROARILENO MONOCICLICO DE 5 MIEMBROS OPCIONALMENTE SUSTITUIDO CON R8, EN DONDE R8 ES ALQUILO(C1-C4) O CICLOALQUILO(C3-C7); Y ES FENILO O HETEROARILO MONOCICLICO DE 5 O 6 MIEMBROS OPCIONALMENTE SUSTITUIDO CON R9, EN DONDE R9 ES ALQUILO(C1-C4), ALCOXI(C1-C4) O HALOGENO. SON COMPUESTOS PREFERIDOS: 3-FENIL-2-(4-{[4-(5-PIRIDIN-2-IL-1,2,4-TRIAZOL-3-IL)PIPERIDIN-1-IL]METIL}FENIL)IMIDAZO[1,2-a]PIRIMIDINA, 3-FENIL-2-(4-{[4-(5-PIRIDIN-2-IL-1H-1,2,4-TRIAZOL-3-IL)PIPERIDIN-1-IL]METIL}FENIL)IMIDAZO[1,2-a]PIRIDINA, 7-FENIL-6-(4-{[4-(5-PIRIDIN-2-IL-1H-1,2,4-TRIAZOL-3-IL)PIPERIDIN-1-IL]METIL}FENIL)IMIDAZO[1,2-b][1,2,4]TRIAZINA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA QUINASA AKt SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDADES HIPERPROLIFERATIVAS TALES COMO NEOPLASIAS BENIGNAS O MALIGNAS
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN1573MU2007 | 2007-08-14 | ||
| EP07118733A EP2062893A1 (en) | 2007-10-18 | 2007-10-18 | Fused imidazoles for cancer treatment |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20090596A1 true PE20090596A1 (es) | 2009-06-07 |
Family
ID=39876840
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008001379A PE20090596A1 (es) | 2007-08-14 | 2008-08-14 | Imidazoles biciclicos fusionados |
Country Status (24)
| Country | Link |
|---|---|
| US (2) | US8592591B2 (es) |
| EP (1) | EP2176259B1 (es) |
| JP (1) | JP5327652B2 (es) |
| KR (1) | KR20100049589A (es) |
| CN (1) | CN101835776A (es) |
| AR (1) | AR067946A1 (es) |
| AT (1) | ATE503757T1 (es) |
| AU (1) | AU2008288390A1 (es) |
| CA (1) | CA2695251C (es) |
| CL (1) | CL2008002397A1 (es) |
| CR (1) | CR11271A (es) |
| DE (1) | DE602008005894D1 (es) |
| DO (1) | DOP2010000057A (es) |
| EA (1) | EA201000297A1 (es) |
| EC (1) | ECSP109965A (es) |
| MA (1) | MA31609B1 (es) |
| MX (1) | MX2010001745A (es) |
| PA (1) | PA8793301A1 (es) |
| PE (1) | PE20090596A1 (es) |
| SV (1) | SV2010003482A (es) |
| TN (1) | TN2010000071A1 (es) |
| TW (1) | TW200924761A (es) |
| UY (1) | UY31292A1 (es) |
| WO (1) | WO2009021990A1 (es) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101573357B (zh) * | 2006-10-19 | 2013-01-23 | 武田药品工业株式会社 | 吲哚化合物 |
| PE20090596A1 (es) * | 2007-08-14 | 2009-06-07 | Bayer Schering Pharma Ag | Imidazoles biciclicos fusionados |
| GB2467670B (en) | 2007-10-04 | 2012-08-01 | Intellikine Inc | Chemical entities and therapeutic uses thereof |
| US7868001B2 (en) * | 2007-11-02 | 2011-01-11 | Hutchison Medipharma Enterprises Limited | Cytokine inhibitors |
| EP2252293B1 (en) | 2008-03-14 | 2018-06-27 | Intellikine, LLC | Kinase inhibitors and methods of use |
| US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
| AU2009268611B2 (en) | 2008-07-08 | 2015-04-09 | Intellikine, Llc | Kinase inhibitors and methods of use |
| US8476431B2 (en) | 2008-11-03 | 2013-07-02 | Itellikine LLC | Benzoxazole kinase inhibitors and methods of use |
| JP5667085B2 (ja) * | 2009-02-13 | 2015-02-12 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | Aktインヒビターとしての融合されたピリミジン |
| AU2010226490A1 (en) | 2009-03-20 | 2011-10-06 | Amgen Inc. | Inhibitors of PI3 kinase |
| WO2010125799A1 (ja) | 2009-04-27 | 2010-11-04 | 塩野義製薬株式会社 | Pi3k阻害活性を有するウレア誘導体 |
| AU2010284254B2 (en) | 2009-08-17 | 2015-09-17 | Intellikine, Llc | Heterocyclic compounds and uses thereof |
| CA2778949C (en) | 2009-10-30 | 2018-02-27 | Janssen Pharmaceutica Nv | Imidazo[1,2-b]pyridazine derivatives and their use as pde10 inhibitors |
| CA2778265A1 (en) * | 2009-11-02 | 2011-05-05 | Abbott Laboratories | Imidazopyridines as a novel scaffold for multi-targeted kinase inhibition |
| US9073927B2 (en) | 2010-01-22 | 2015-07-07 | Fundacion Centro Nacional De Investigaciones Oncologicas Carlos Iii | Inhibitors of PI3 kinase |
| UY33213A (es) | 2010-02-18 | 2011-09-30 | Almirall Sa | Derivados de pirazol como inhibidores de jak |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| EP2593451B1 (en) * | 2010-07-12 | 2015-08-19 | Bayer Intellectual Property GmbH | Substituted imidazo[1,2-a]pyrimidines and -pyridines |
| CA2806655A1 (en) | 2010-07-28 | 2012-02-02 | Bayer Intellectual Property Gmbh | Substituted imidazo[1,2-b]pyridazines |
| EP2463289A1 (en) | 2010-11-26 | 2012-06-13 | Almirall, S.A. | Imidazo[1,2-b]pyridazine derivatives as JAK inhibitors |
| DE102011008352A1 (de) * | 2011-01-12 | 2012-07-12 | Merck Patent Gmbh | 5-([1,2,3]Triazol-4-yl)-7H-pyrrolo-[2,3-d]pyrimidinderivate |
| CA2828483A1 (en) | 2011-02-23 | 2012-11-01 | Intellikine, Llc | Combination of kinase inhibitors and uses thereof |
| US8772283B2 (en) | 2011-04-06 | 2014-07-08 | Taiho Pharmaceutical Co., Ltd. | Imidazo-oxazine compound or salt thereof |
| US9206185B2 (en) * | 2011-04-07 | 2015-12-08 | Bayer Intellectual Property Gmbh | Imidazopyridazines as Akt kinase inhibitors |
| AU2012277912B2 (en) | 2011-06-27 | 2017-03-23 | Janssen Pharmaceutica Nv | 1-aryl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline derivatives |
| EP2554544A1 (en) | 2011-08-01 | 2013-02-06 | Almirall, S.A. | Pyridin-2(1h)-one derivatives as jak inhibitors |
| CA2860724A1 (en) | 2012-01-10 | 2013-07-18 | Bayer Intellectual Property Gmbh | Substituted pyrazolopyrimidines as akt kinase inhibitors |
| CA2860723A1 (en) * | 2012-01-10 | 2013-07-18 | Bayer Intellectual Property Gmbh | Substituted imidazopyrazines as akt kinase inhibitors |
| CA2872216C (en) | 2012-06-26 | 2021-07-20 | Janssen Pharmaceutica Nv | Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl-[1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders |
| ES2660215T3 (es) * | 2012-07-02 | 2018-03-21 | Taiho Pharmaceutical Co., Ltd. | Potenciador de efecto antitumoral que comprende un compuesto de imidazooxazina |
| CN104411314B (zh) | 2012-07-09 | 2017-10-20 | 詹森药业有限公司 | 磷酸二酯酶10的抑制剂 |
| JP6360881B2 (ja) | 2013-03-22 | 2018-07-18 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | 触媒的mtorc1/2阻害薬及びオーロラaキナーゼの選択的阻害薬の組合せ |
| GB201321732D0 (en) * | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic agents |
| CN107428779A (zh) | 2015-02-27 | 2017-12-01 | 大鹏药品工业株式会社 | 咪唑并噁嗪晶体、含有所述晶体的药物组合物和制备所述晶体的方法 |
| US11883404B2 (en) | 2016-03-04 | 2024-01-30 | Taiho Pharmaceuticals Co., Ltd. | Preparation and composition for treatment of malignant tumors |
| CN110099898B (zh) * | 2016-10-24 | 2023-07-25 | 优曼尼蒂治疗公司 | 化合物及其用途 |
| WO2018129403A1 (en) | 2017-01-06 | 2018-07-12 | Yumanity Therapeutics | Methods for the treatment of neurological disorders |
| EP3700934A4 (en) | 2017-10-24 | 2021-10-27 | Yumanity Therapeutics, Inc. | COMPOUNDS AND USES THEREOF |
| CN112312913B (zh) | 2018-03-23 | 2024-03-08 | 詹森药业有限公司 | 化合物和其用途 |
| CA3102279A1 (en) | 2018-06-01 | 2019-12-05 | Cornell University | Combination therapy for pi3k-associated disease or disorder |
| AU2020212034A1 (en) | 2019-01-24 | 2021-09-16 | Janssen Pharmaceutica Nv | Compounds and uses thereof |
| EA202192047A1 (ru) | 2019-11-13 | 2021-12-08 | Юманити Терапьютикс, Инк. | Соединения и их применение |
| CN118812530A (zh) * | 2023-04-18 | 2024-10-22 | 中国科学院大连化学物理研究所 | 一种Pd/C双组分体系催化木质素及模型化合物制备咪唑吡啶类化合物的方法 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2001249679A1 (en) * | 2000-03-31 | 2001-10-15 | Ortho-Mcneil Pharmaceutical, Inc. | Phenyl-substituted imidazopyridines |
| CA2407573C (en) * | 2000-04-27 | 2011-09-13 | Yamanouchi Pharmaceutical Co. Ltd. | Imidazopyridine derivatives |
| AU2004233828B2 (en) | 2003-04-24 | 2009-05-28 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| DE602004010680T2 (de) * | 2003-07-30 | 2009-01-02 | Laboratorios S.A.L.V.A.T., S.A., Esplugues De Llobregat | Substituierte imidazopyrimidine zur prävention und behandlung von krebs |
| US7655649B2 (en) | 2004-04-09 | 2010-02-02 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| EP1784175A4 (en) * | 2004-08-23 | 2009-07-22 | Merck & Co Inc | INHIBITORS OF ACT ACTIVITY |
| AU2005316826A1 (en) * | 2004-12-15 | 2006-06-22 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| WO2006125101A2 (en) | 2005-05-20 | 2006-11-23 | Array Biopharma Inc. | Raf inhibitor compounds and methods of use thereof |
| US20070049591A1 (en) | 2005-08-25 | 2007-03-01 | Kalypsys, Inc. | Inhibitors of MAPK/Erk Kinase |
| WO2007028051A2 (en) * | 2005-09-02 | 2007-03-08 | Abbott Laboratories | Novel imidazo based heterocycles |
| PE20070978A1 (es) * | 2006-02-14 | 2007-11-15 | Novartis Ag | COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks) |
| US7530313B2 (en) | 2006-05-12 | 2009-05-12 | Day & Zimmerman, Inc. | Self-destruct fuze delay mechanism |
| PE20090596A1 (es) * | 2007-08-14 | 2009-06-07 | Bayer Schering Pharma Ag | Imidazoles biciclicos fusionados |
-
2008
- 2008-08-14 PE PE2008001379A patent/PE20090596A1/es not_active Application Discontinuation
- 2008-08-14 AU AU2008288390A patent/AU2008288390A1/en not_active Abandoned
- 2008-08-14 DE DE602008005894T patent/DE602008005894D1/de active Active
- 2008-08-14 EP EP08787222A patent/EP2176259B1/en active Active
- 2008-08-14 CL CL2008002397A patent/CL2008002397A1/es unknown
- 2008-08-14 CA CA2695251A patent/CA2695251C/en not_active Expired - Fee Related
- 2008-08-14 JP JP2010520584A patent/JP5327652B2/ja not_active Expired - Fee Related
- 2008-08-14 WO PCT/EP2008/060686 patent/WO2009021990A1/en not_active Ceased
- 2008-08-14 AT AT08787222T patent/ATE503757T1/de not_active IP Right Cessation
- 2008-08-14 MX MX2010001745A patent/MX2010001745A/es not_active Application Discontinuation
- 2008-08-14 CN CN200880103578A patent/CN101835776A/zh active Pending
- 2008-08-14 KR KR1020107003250A patent/KR20100049589A/ko not_active Withdrawn
- 2008-08-14 UY UY31292A patent/UY31292A1/es not_active Application Discontinuation
- 2008-08-14 US US12/191,706 patent/US8592591B2/en not_active Expired - Fee Related
- 2008-08-14 EA EA201000297A patent/EA201000297A1/ru unknown
- 2008-08-14 PA PA20088793301A patent/PA8793301A1/es unknown
- 2008-08-14 TW TW097131067A patent/TW200924761A/zh unknown
- 2008-08-15 AR ARP080103563A patent/AR067946A1/es unknown
-
2010
- 2010-02-12 DO DO2010000057A patent/DOP2010000057A/es unknown
- 2010-02-12 MA MA32618A patent/MA31609B1/fr unknown
- 2010-02-12 TN TNP2010000071A patent/TN2010000071A1/fr unknown
- 2010-02-12 SV SV2010003482A patent/SV2010003482A/es not_active Application Discontinuation
- 2010-02-12 CR CR11271A patent/CR11271A/es not_active Application Discontinuation
- 2010-02-12 EC EC2010009965A patent/ECSP109965A/es unknown
-
2013
- 2013-11-26 US US14/090,367 patent/US9387204B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| MA31609B1 (fr) | 2010-08-02 |
| CR11271A (es) | 2010-05-19 |
| EP2176259B1 (en) | 2011-03-30 |
| EA201000297A1 (ru) | 2010-08-30 |
| WO2009021990A1 (en) | 2009-02-19 |
| AR067946A1 (es) | 2009-10-28 |
| US8592591B2 (en) | 2013-11-26 |
| PA8793301A1 (es) | 2009-04-23 |
| US9387204B2 (en) | 2016-07-12 |
| UY31292A1 (es) | 2009-03-31 |
| TW200924761A (en) | 2009-06-16 |
| MX2010001745A (es) | 2010-03-10 |
| US20140088110A1 (en) | 2014-03-27 |
| SV2010003482A (es) | 2010-07-06 |
| KR20100049589A (ko) | 2010-05-12 |
| AU2008288390A1 (en) | 2009-02-19 |
| CL2008002397A1 (es) | 2009-09-25 |
| DOP2010000057A (es) | 2010-04-15 |
| EP2176259A1 (en) | 2010-04-21 |
| DE602008005894D1 (de) | 2011-05-12 |
| CA2695251A1 (en) | 2009-02-19 |
| US20090156604A1 (en) | 2009-06-18 |
| JP5327652B2 (ja) | 2013-10-30 |
| ECSP109965A (es) | 2010-03-31 |
| CN101835776A (zh) | 2010-09-15 |
| TN2010000071A1 (en) | 2011-09-26 |
| CA2695251C (en) | 2016-06-21 |
| JP2010535847A (ja) | 2010-11-25 |
| ATE503757T1 (de) | 2011-04-15 |
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