WO2013136254A1 - Heterocyclyl compounds - Google Patents
Heterocyclyl compounds Download PDFInfo
- Publication number
- WO2013136254A1 WO2013136254A1 PCT/IB2013/051915 IB2013051915W WO2013136254A1 WO 2013136254 A1 WO2013136254 A1 WO 2013136254A1 IB 2013051915 W IB2013051915 W IB 2013051915W WO 2013136254 A1 WO2013136254 A1 WO 2013136254A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkyl
- group
- substituted
- cycloalkyl
- unsubstituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
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- 0 *C(C(N(*)C(Nc1ccccc1)=C1C(N2*)=O)=O)=C1N(c1ccccc1)C2=O Chemical compound *C(C(N(*)C(Nc1ccccc1)=C1C(N2*)=O)=O)=C1N(c1ccccc1)C2=O 0.000 description 1
Classifications
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- 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
- 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
- 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
- A61K31/535—Heterocyclic 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
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further 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
- A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
- A61N5/00—Radiation therapy
- A61N5/10—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
-
- 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
- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61P31/04—Antibacterial agents
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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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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
- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Definitions
- R 1 is selected from the group consisting of hydrogen, substituted- or unsubstituted-alkyl, substituted- or unsubstituted- cycloalkyl, and substituted- or unsubstituted- heterocyclyl;
- alkenyl as used herein, means an 'alkyl' group as defined hereinabove containing 2 to 20 carbon atoms and containing at least one double bond.
- alkenyl include, but are not limited to, pent-2-enyl, hex-3-enyl, allyl, vinyl, and the like.
- Step-1 Synthesis of 3-(3-bromophenyl) oxetan-3-ol
- Azetidin-3-ol hydrochloride (1.0 g, 9.13 mmol) was taken in DMSO and l-fluoro-3- nitrobenzene (1.0 g, 7.09 mmol) was added followed by K 2 C0 3 (2.449 g, 17.72 mmol).
- the reaction mixture was heated to 100 °C for 16 hrs. After completion of the reaction, the reaction mixture was cooled and poured into water which was then extracted with ethyl acetate (3 x 8ml). The organic layers were combined, washed with water and brine, dried over sodium sulfate, and concentrated under vacuum.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Radiology & Medical Imaging (AREA)
- Pathology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Psychiatry (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
Priority Applications (25)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| UAA201411011A UA114906C2 (uk) | 2012-03-14 | 2013-03-11 | Гетероциклільні сполуки як інгібітори мек |
| EA201491671A EA029768B1 (ru) | 2012-03-14 | 2013-03-11 | Гетероциклильные соединения |
| CA2865167A CA2865167C (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| IN1754MUN2014 IN2014MN01754A (2) | 2012-03-14 | 2013-03-11 | |
| CUP2014000109A CU24335B1 (es) | 2012-03-14 | 2013-03-11 | Piridopirimidinas sustituidas como inhibidores de la quinasa mek y útiles para el tratamiento del cáncer |
| JP2014561567A JP6093384B2 (ja) | 2012-03-14 | 2013-03-11 | ヘテロシクリル化合物 |
| US14/385,106 US9573944B2 (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| MA37405A MA37405A1 (fr) | 2012-03-14 | 2013-03-11 | Composés hétérocyclyle |
| HK15106571.7A HK1206020B (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| ES13711973T ES2741896T3 (es) | 2012-03-14 | 2013-03-11 | Compuestos de heterociclilo |
| NZ629442A NZ629442A (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds as mek inhibitors |
| AP2014008008A AP3834A (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| SG11201405007QA SG11201405007QA (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| DK13711973.1T DK2834236T3 (da) | 2012-03-14 | 2013-03-11 | Heterocyclylforbindelser |
| MX2014010925A MX355526B (es) | 2012-03-14 | 2013-03-11 | Compuesto de heterociclilo. |
| KR1020147028556A KR20140138910A (ko) | 2012-03-14 | 2013-03-11 | 헤테로사이클릴 화합물 |
| AU2013234014A AU2013234014B2 (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| EP13711973.1A EP2834236B1 (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| KR1020197017334A KR102240101B1 (ko) | 2012-03-14 | 2013-03-11 | 헤테로사이클릴 화합물 |
| CN201380014210.XA CN104203947A (zh) | 2012-03-14 | 2013-03-11 | 杂环基化合物 |
| TNP2014000357A TN2014000357A1 (en) | 2012-03-14 | 2014-08-18 | Heterocyclyl compounds |
| IL234559A IL234559A (en) | 2012-03-14 | 2014-09-09 | Heterocyclic compounds |
| PH12014502040A PH12014502040B1 (en) | 2012-03-14 | 2014-09-12 | Heterocyclyl compounds |
| CR20140464A CR20140464A (es) | 2012-03-14 | 2014-10-06 | Compuestos de heterociclilo |
| US15/400,627 US9827247B2 (en) | 2012-03-14 | 2017-01-06 | Heterocyclyl compounds |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN288/KOL/2012 | 2012-03-14 | ||
| IN288KO2012 | 2012-03-14 |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US14/385,106 A-371-Of-International US9573944B2 (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| US15/400,627 Continuation US9827247B2 (en) | 2012-03-14 | 2017-01-06 | Heterocyclyl compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2013136254A1 true WO2013136254A1 (en) | 2013-09-19 |
Family
ID=47997632
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IB2013/051915 Ceased WO2013136254A1 (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds |
| PCT/IB2013/051908 Ceased WO2013136249A1 (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds as mek inhibitors |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IB2013/051908 Ceased WO2013136249A1 (en) | 2012-03-14 | 2013-03-11 | Heterocyclyl compounds as mek inhibitors |
Country Status (35)
| Country | Link |
|---|---|
| US (5) | US9428499B2 (2) |
| EP (2) | EP2834236B1 (2) |
| JP (3) | JP6093384B2 (2) |
| KR (4) | KR102241111B1 (2) |
| CN (4) | CN108383836B (2) |
| AP (2) | AP3859A (2) |
| AU (4) | AU2013234009B2 (2) |
| BR (1) | BR112014022713B1 (2) |
| CA (2) | CA2865167C (2) |
| CL (2) | CL2014002412A1 (2) |
| CO (2) | CO7160029A2 (2) |
| CR (2) | CR20140464A (2) |
| CU (2) | CU24335B1 (2) |
| DK (2) | DK2834236T3 (2) |
| DO (2) | DOP2014000204A (2) |
| EA (2) | EA029768B1 (2) |
| ES (2) | ES2741896T3 (2) |
| GE (2) | GEP201706774B (2) |
| GT (2) | GT201400195A (2) |
| IL (2) | IL234559A (2) |
| IN (2) | IN2014MN01754A (2) |
| MA (2) | MA37405A1 (2) |
| MX (3) | MX355474B (2) |
| MY (2) | MY174188A (2) |
| NI (2) | NI201400107A (2) |
| NZ (2) | NZ629432A (2) |
| PE (2) | PE20141974A1 (2) |
| PH (2) | PH12014502040B1 (2) |
| PL (1) | PL2834237T3 (2) |
| SG (2) | SG11201405006PA (2) |
| TN (2) | TN2014000357A1 (2) |
| TR (1) | TR201811976T4 (2) |
| UA (2) | UA114907C2 (2) |
| WO (2) | WO2013136254A1 (2) |
| ZA (1) | ZA201406186B (2) |
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| WO2016009306A1 (en) * | 2014-07-15 | 2016-01-21 | Lupin Limited | Heterocyclyl compounds as mek inhibitors |
| WO2016035008A1 (en) * | 2014-09-04 | 2016-03-10 | Lupin Limited | Pyridopyrimidine derivatives as mek inhibitors |
| WO2020188015A1 (en) | 2019-03-21 | 2020-09-24 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
| WO2020254451A1 (en) | 2019-06-19 | 2020-12-24 | Boehringer Ingelheim International Gmbh | Anticancer combination therapy |
| WO2021089791A1 (en) | 2019-11-08 | 2021-05-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| WO2021245051A1 (en) | 2020-06-02 | 2021-12-09 | Boehringer Ingelheim International Gmbh | Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer |
| WO2022214594A1 (en) | 2021-04-09 | 2022-10-13 | Boehringer Ingelheim International Gmbh | Anticancer therapy |
| WO2023099620A1 (en) | 2021-12-01 | 2023-06-08 | Boehringer Ingelheim International Gmbh | Kras degrading compounds comprising annulated 2-amino-3-cyano thiophenes |
| WO2023099592A1 (en) | 2021-12-01 | 2023-06-08 | Boehringer Ingelheim International Gmbh | Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer |
| WO2023099624A1 (en) | 2021-12-01 | 2023-06-08 | Boehringer Ingelheim International Gmbh | Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer |
| WO2023099608A1 (en) | 2021-12-01 | 2023-06-08 | Boehringer Ingelheim International Gmbh | Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer |
| WO2023099623A1 (en) | 2021-12-01 | 2023-06-08 | Boehringer Ingelheim International Gmbh | Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer |
| US11814380B2 (en) | 2017-12-21 | 2023-11-14 | Boehringer Ingelheim International Gmbh | Benzylamino substituted pyridopyrimidinones and derivatives as SOS1 inhibitors |
| US12053473B2 (en) | 2016-12-22 | 2024-08-06 | Boehringer Ingelheim International Gmbh | Benzylamino substituted quinazolines and derivatives as SOS1 inhibitors |
| WO2024246099A1 (en) | 2023-05-30 | 2024-12-05 | Boehringer Ingelheim International Gmbh | Spirocyclic annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer |
| WO2025073765A1 (en) | 2023-10-03 | 2025-04-10 | Institut National de la Santé et de la Recherche Médicale | Methods of prognosis and treatment of patients suffering from melanoma |
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| NZ629432A (en) | 2012-03-14 | 2017-01-27 | Lupin Ltd | Heterocyclyl compounds as mek inhibitors |
| RS58514B1 (sr) | 2012-06-13 | 2019-04-30 | Incyte Holdings Corp | Supstituisana triciklična jedinjenja kao inhibitori fgfr |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
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| JP6403172B2 (ja) * | 2013-10-25 | 2018-10-10 | シャンハイ ヘンルイ ファーマスーティカル カンパニー リミテッドShanghai Hengrui Pharmaceutical Co., Ltd. | ピリジンのケトン誘導体、それらの製造方法、およびそれらの医薬適用 |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| TWI712601B (zh) | 2015-02-20 | 2020-12-11 | 美商英塞特公司 | 作為fgfr抑制劑之雙環雜環 |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
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| HRP20241288T1 (hr) | 2018-05-04 | 2024-12-06 | Incyte Corporation | Čvrsti oblici fgfr inhibitora i postupci za njihovu proizvodnju |
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| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
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