AU2015236855B2 - Pyridyl piperidines - Google Patents
Pyridyl piperidines Download PDFInfo
- Publication number
- AU2015236855B2 AU2015236855B2 AU2015236855A AU2015236855A AU2015236855B2 AU 2015236855 B2 AU2015236855 B2 AU 2015236855B2 AU 2015236855 A AU2015236855 A AU 2015236855A AU 2015236855 A AU2015236855 A AU 2015236855A AU 2015236855 B2 AU2015236855 B2 AU 2015236855B2
- Authority
- AU
- Australia
- Prior art keywords
- methyl
- spiro
- dihydro
- mmol
- pyrazol
- 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
Links
- CTEQBPXLNRNFRC-UHFFFAOYSA-N C[n]1ncc2c1ccc(-c(cncc1Cl)c1N(CC1)CCC1(C(CN1)O)C1=O)c2 Chemical compound C[n]1ncc2c1ccc(-c(cncc1Cl)c1N(CC1)CCC1(C(CN1)O)C1=O)c2 CTEQBPXLNRNFRC-UHFFFAOYSA-N 0.000 description 2
- YPRODAZVOKKURG-UHFFFAOYSA-N Clc(cncc1Br)c1Cl Chemical compound Clc(cncc1Br)c1Cl YPRODAZVOKKURG-UHFFFAOYSA-N 0.000 description 2
- 0 O=C1NC*C1(CC1)CCN1c(c(Br)cnc1)c1Cl Chemical compound O=C1NC*C1(CC1)CCN1c(c(Br)cnc1)c1Cl 0.000 description 2
- REYFNZOBKWUTGR-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(C(N)=O)N)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(C(N)=O)N)=O REYFNZOBKWUTGR-UHFFFAOYSA-N 0.000 description 1
- VRRWOCAEBNMKJH-NSHDSACASA-N CC(C)(C)OC(N([C@@H](CC1(CC=C)CC=C)C(F)(F)F)C1=O)=O Chemical compound CC(C)(C)OC(N([C@@H](CC1(CC=C)CC=C)C(F)(F)F)C1=O)=O VRRWOCAEBNMKJH-NSHDSACASA-N 0.000 description 1
- LHZLRWWPERDCOB-UHFFFAOYSA-N CC(C)(NC1(CC2)CCN2c(c(-c(cc2)cc3c2[nH]nc3)cnc2)c2Cl)NC1=O Chemical compound CC(C)(NC1(CC2)CCN2c(c(-c(cc2)cc3c2[nH]nc3)cnc2)c2Cl)NC1=O LHZLRWWPERDCOB-UHFFFAOYSA-N 0.000 description 1
- FACCNKUBBPNFCK-UHFFFAOYSA-N CC(C)(NC1(CC2)CCN2c(c(-c(cc2)cc3c2[n](C)nc3)cnc2)c2Cl)NC1=O Chemical compound CC(C)(NC1(CC2)CCN2c(c(-c(cc2)cc3c2[n](C)nc3)cnc2)c2Cl)NC1=O FACCNKUBBPNFCK-UHFFFAOYSA-N 0.000 description 1
- KORCJQHIJVZNSC-UHFFFAOYSA-N CC(C)(NC1(CC2)CCN2c(c(Cl)cnc2)c2Br)NC1=O Chemical compound CC(C)(NC1(CC2)CCN2c(c(Cl)cnc2)c2Br)NC1=O KORCJQHIJVZNSC-UHFFFAOYSA-N 0.000 description 1
- SYGOECWEWQKERP-UHFFFAOYSA-N CC(C)(NC12CCN(Cc3ccccc3)CC1)NC2=O Chemical compound CC(C)(NC12CCN(Cc3ccccc3)CC1)NC2=O SYGOECWEWQKERP-UHFFFAOYSA-N 0.000 description 1
- XTMIYXUZRQBOBU-UHFFFAOYSA-N CC(C)(NC12CCNCC1)NC2=O Chemical compound CC(C)(NC12CCNCC1)NC2=O XTMIYXUZRQBOBU-UHFFFAOYSA-N 0.000 description 1
- JDXCSIRVKISGTF-UHFFFAOYSA-N CC(C)[n]1ncc(-c2ccc(B3OC(C)(C)C(C)(C)O3)cc2)c1 Chemical compound CC(C)[n]1ncc(-c2ccc(B3OC(C)(C)C(C)(C)O3)cc2)c1 JDXCSIRVKISGTF-UHFFFAOYSA-N 0.000 description 1
- YMGZVEUZXPFHPA-YMTSCGQJSA-N CC/C=N\N(C)C([C@@H]1C2)=CC[C@@H]1N=CC(Cl)=C2N(CC1)CCC11NCNC1=O Chemical compound CC/C=N\N(C)C([C@@H]1C2)=CC[C@@H]1N=CC(Cl)=C2N(CC1)CCC11NCNC1=O YMGZVEUZXPFHPA-YMTSCGQJSA-N 0.000 description 1
- UXRSZFUAPMDVPA-ZVAWYAOSSA-N CC1(C)OB(c(cc2)ccc2-c2c[n](C(CCC3)[C@H]3O)nc2)OC1(C)C Chemical compound CC1(C)OB(c(cc2)ccc2-c2c[n](C(CCC3)[C@H]3O)nc2)OC1(C)C UXRSZFUAPMDVPA-ZVAWYAOSSA-N 0.000 description 1
- MFDMZBYMEOBNNL-UHFFFAOYSA-N CCOC(CC(C(N)(N)N)=O)=O Chemical compound CCOC(CC(C(N)(N)N)=O)=O MFDMZBYMEOBNNL-UHFFFAOYSA-N 0.000 description 1
- CDCHDSMJPBCYFA-UHFFFAOYSA-N CN(c(cc1)c(C2)cc1-c(cncc1Cl)c1N(CC1)CCC1(CCO)C#N)S2(=O)=O Chemical compound CN(c(cc1)c(C2)cc1-c(cncc1Cl)c1N(CC1)CCC1(CCO)C#N)S2(=O)=O CDCHDSMJPBCYFA-UHFFFAOYSA-N 0.000 description 1
- BJVCNXHQFWYWDD-UHFFFAOYSA-N CN1c2cc(-c3cncc(Cl)c3N(CC3)CCC33NCNC3=O)ccc2CC1=C Chemical compound CN1c2cc(-c3cncc(Cl)c3N(CC3)CCC33NCNC3=O)ccc2CC1=C BJVCNXHQFWYWDD-UHFFFAOYSA-N 0.000 description 1
- HOFCDHUGGVZPCY-UHFFFAOYSA-N C[n]1ncc(-c(cc2)ccc2-c(cncc2C(F)(F)F)c2N(CC2)CCC2(CCN2)C2=O)c1 Chemical compound C[n]1ncc(-c(cc2)ccc2-c(cncc2C(F)(F)F)c2N(CC2)CCC2(CCN2)C2=O)c1 HOFCDHUGGVZPCY-UHFFFAOYSA-N 0.000 description 1
- SOGOUJPVOZWDFQ-UHFFFAOYSA-N C[n]1ncc(-c(cc2)ccc2-c(cncc2Cl)c2N(CC2)CCC2(C(NC2)=O)NC2=O)c1 Chemical compound C[n]1ncc(-c(cc2)ccc2-c(cncc2Cl)c2N(CC2)CCC2(C(NC2)=O)NC2=O)c1 SOGOUJPVOZWDFQ-UHFFFAOYSA-N 0.000 description 1
- LBFYQISQYCGDDW-UHFFFAOYSA-N C[n]1ncc(-c(cc2)ccc2-c2cncc(Cl)c2N(CC2)CCC2(CCN2)C2=O)c1 Chemical compound C[n]1ncc(-c(cc2)ccc2-c2cncc(Cl)c2N(CC2)CCC2(CCN2)C2=O)c1 LBFYQISQYCGDDW-UHFFFAOYSA-N 0.000 description 1
- NEFSLCFEEMICGS-UHFFFAOYSA-N C[n]1ncc2c1ccc(-c(cncc1Cl)c1N(CC1)CCC1(C(N)O)N)c2 Chemical compound C[n]1ncc2c1ccc(-c(cncc1Cl)c1N(CC1)CCC1(C(N)O)N)c2 NEFSLCFEEMICGS-UHFFFAOYSA-N 0.000 description 1
- XIDFIEVUDNVHJZ-UHFFFAOYSA-N Cc(cc1)ccc1-c1c[n](CCO)nc1 Chemical compound Cc(cc1)ccc1-c1c[n](CCO)nc1 XIDFIEVUDNVHJZ-UHFFFAOYSA-N 0.000 description 1
- NBDSMJAPOOUCBK-UHFFFAOYSA-N NC(CC1)(CCN1c(c(Cl)cnc1)c1Br)C(N)=O Chemical compound NC(CC1)(CCN1c(c(Cl)cnc1)c1Br)C(N)=O NBDSMJAPOOUCBK-UHFFFAOYSA-N 0.000 description 1
- YITYNCSQCPGDGO-UHFFFAOYSA-N NC1(CCN(Cc2ccccc2)CC1)C(N)=O Chemical compound NC1(CCN(Cc2ccccc2)CC1)C(N)=O YITYNCSQCPGDGO-UHFFFAOYSA-N 0.000 description 1
- OGGPDXYGVLXFIT-UHFFFAOYSA-O O=C(NC1)OC1(CC1)CCN1c(c(C(F)(F)F)cnc1)c1-c(cc1)ccc1C1=C[NH2+]N=C1 Chemical compound O=C(NC1)OC1(CC1)CCN1c(c(C(F)(F)F)cnc1)c1-c(cc1)ccc1C1=C[NH2+]N=C1 OGGPDXYGVLXFIT-UHFFFAOYSA-O 0.000 description 1
- MJTKLZHVCWYYON-UHFFFAOYSA-N O=C1NC=NC1(CC1)CCN1c(c(Cl)cnc1)c1Br Chemical compound O=C1NC=NC1(CC1)CCN1c(c(Cl)cnc1)c1Br MJTKLZHVCWYYON-UHFFFAOYSA-N 0.000 description 1
- IAGUOXYCEHJLAO-KZUDCZAMSA-N O[C@@H](CCC1)C1[n]1ncc(-c(cc2)ccc2Br)c1 Chemical compound O[C@@H](CCC1)C1[n]1ncc(-c(cc2)ccc2Br)c1 IAGUOXYCEHJLAO-KZUDCZAMSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further 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
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further 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
- A61K31/495—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
- A61K31/499—Spiro-condensed pyrazines or piperazines
-
- 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
-
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- 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
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- 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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- 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
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- 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
- C07D401/14—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 three or more hetero 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
- C07D417/14—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 three or more hetero rings
-
- 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
- C07D471/10—Spiro-condensed systems
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/20—Spiro-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
- C07D498/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14001145 | 2014-03-27 | ||
| EP14001145.3 | 2014-03-27 | ||
| PCT/EP2015/000528 WO2015144290A1 (en) | 2014-03-27 | 2015-03-10 | Pyridyl piperidines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2015236855A1 AU2015236855A1 (en) | 2016-11-10 |
| AU2015236855B2 true AU2015236855B2 (en) | 2018-11-01 |
Family
ID=50389770
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2015236855A Ceased AU2015236855B2 (en) | 2014-03-27 | 2015-03-10 | Pyridyl piperidines |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9926319B2 (enExample) |
| EP (1) | EP3122739B1 (enExample) |
| JP (1) | JP6434989B2 (enExample) |
| CN (1) | CN106458992B (enExample) |
| AU (1) | AU2015236855B2 (enExample) |
| CA (1) | CA2943659C (enExample) |
| ES (1) | ES2720324T3 (enExample) |
| IL (1) | IL247728B (enExample) |
| WO (1) | WO2015144290A1 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6447304B2 (ja) * | 2015-03-27 | 2019-01-09 | Jsr株式会社 | 液晶配向剤、液晶配向膜及びその製造方法、液晶表示素子、位相差フィルム及びその製造方法、重合体並びに化合物 |
| JP6707630B2 (ja) | 2015-06-01 | 2020-06-10 | バンタム、ファーマシューティカル、リミテッド、ライアビリティー、カンパニーBantam Pharmaceutical, Llc | 置換ピラゾールおよびピロール化合物、および翻訳開始の阻害およびこれらに関連する疾患および障害の治療のためにこれらを用いる方法 |
| CN108348509A (zh) * | 2015-11-03 | 2018-07-31 | Lu许可公司 | 用于治疗增殖减少性病症的化合物 |
| JP2020513403A (ja) | 2016-11-30 | 2020-05-14 | バンタム、ファーマシューティカル、リミテッド、ライアビリティー、カンパニーBantam Pharmaceutical, Llc | 置換ピラゾールおよびピロール化合物の使用する方法ならびに過剰増殖性疾患の治療のための方法 |
| CN110603254B (zh) * | 2016-11-30 | 2024-04-12 | 班塔姆制药有限责任公司 | 被取代的吡唑化合物以及使用其治疗过度增生性疾病的方法 |
| WO2018139660A1 (ja) | 2017-01-30 | 2018-08-02 | 国立大学法人京都大学 | 新規化合物及び制御性t細胞の製造方法 |
| EP3691642B1 (en) | 2017-10-02 | 2024-03-06 | Boehringer Ingelheim International GmbH | [1,6]naphthyridine compounds and derivatives as cdk8/cdk19 inhibitors |
| EP4076443B1 (en) * | 2019-12-17 | 2025-09-10 | Merck Sharp & Dohme LLC | Substituted 1,3,8-triazaspiro[4,5]decane-2,4-dione compound as indoleamine 2,3-dioxygenase (ido) and/or tryptophan 2,3-dioxygenase (tdo) inhibitors |
| EP4410965A4 (en) | 2021-09-27 | 2025-09-24 | Univ Kyoto | T LYMPHOCYTE PRODUCTION PROCESS |
| EP4438048A4 (en) | 2021-11-24 | 2025-10-22 | Regcell Co Ltd | PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OR PREVENTION OF DISORDERS RELATED TO T LYMPHOCYTES |
| CA3239019A1 (en) | 2021-11-24 | 2023-06-01 | Regcell Co., Ltd. | Human inducibility controllable t-cell and method for preparing same |
| EP4497822A1 (en) | 2022-03-23 | 2025-01-29 | Kyoto University | Method for producing regulatory t cells |
| TW202421780A (zh) | 2022-09-26 | 2024-06-01 | 國立大學法人京都大學 | T細胞的製造方法 |
| WO2024071039A1 (ja) | 2022-09-26 | 2024-04-04 | レグセル株式会社 | キメラ抗原受容体(car)を含む誘導性制御性t細胞 |
| WO2024166969A1 (ja) | 2023-02-08 | 2024-08-15 | レグセル株式会社 | 天疱瘡を治療または予防するための医薬組成物 |
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| NZ629282A (en) * | 2012-05-04 | 2017-04-28 | Samumed Llc | 1h-pyrazolo[3,4-b]pyridines and therapeutic uses thereof |
| AU2013337086B2 (en) * | 2012-10-08 | 2017-06-15 | Cancer Research Technology Limited | 2-aminopyridine compounds |
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| EP3122739A1 (en) | 2017-02-01 |
| CN106458992B (zh) | 2019-03-15 |
| JP6434989B2 (ja) | 2018-12-05 |
| IL247728A0 (en) | 2016-11-30 |
| CA2943659C (en) | 2023-04-25 |
| AU2015236855A1 (en) | 2016-11-10 |
| CA2943659A1 (en) | 2015-10-01 |
| US9926319B2 (en) | 2018-03-27 |
| WO2015144290A8 (en) | 2015-12-23 |
| IL247728B (en) | 2019-12-31 |
| US20170107222A1 (en) | 2017-04-20 |
| ES2720324T3 (es) | 2019-07-19 |
| JP2017510590A (ja) | 2017-04-13 |
| EP3122739B1 (en) | 2019-01-16 |
| WO2015144290A1 (en) | 2015-10-01 |
| CN106458992A (zh) | 2017-02-22 |
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