KR101964479B1 - 신규 푸라논 유도체 - Google Patents
신규 푸라논 유도체 Download PDFInfo
- Publication number
- KR101964479B1 KR101964479B1 KR1020137028226A KR20137028226A KR101964479B1 KR 101964479 B1 KR101964479 B1 KR 101964479B1 KR 1020137028226 A KR1020137028226 A KR 1020137028226A KR 20137028226 A KR20137028226 A KR 20137028226A KR 101964479 B1 KR101964479 B1 KR 101964479B1
- Authority
- KR
- South Korea
- Prior art keywords
- mmol
- yield
- oxo
- carboxylate
- solid
- 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.)
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- 0 CCCCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCO)O*1=Cc1c[n]c2c1cccn2)=O Chemical compound CCCCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCO)O*1=Cc1c[n]c2c1cccn2)=O 0.000 description 1
- XFNOBFSTABEODO-VBKFSLOCSA-N CCN(CCCN(C)CCO)C(O/C1=C\c2c[nH]c3c2cccn3)=C(C(O)=O)C1=O Chemical compound CCN(CCCN(C)CCO)C(O/C1=C\c2c[nH]c3c2cccn3)=C(C(O)=O)C1=O XFNOBFSTABEODO-VBKFSLOCSA-N 0.000 description 1
- FKEBEPKKNMVZFC-WJDWOHSUSA-N CCOC(C(C1=O)=C(N2CCC(C)CC2)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(N2CCC(C)CC2)O/C1=C\c1c[nH]c2ncccc12)=O FKEBEPKKNMVZFC-WJDWOHSUSA-N 0.000 description 1
- LUPMYBRJNMJYJT-PDGQHHTCSA-N CCOC(C(C1=O)=C(NC(C)c2ccccc2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(NC(C)c2ccccc2)O/C1=C\c1c[nH]c2c1cccn2)=O LUPMYBRJNMJYJT-PDGQHHTCSA-N 0.000 description 1
- HPSIVLOJRIXIKB-VYQXCNRSSA-N CCOC(C(C1=O)=C(NC[C@H](C2)C2c2ccccc2)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(NC[C@H](C2)C2c2ccccc2)O/C1=C\c1c[nH]c2ncccc12)=O HPSIVLOJRIXIKB-VYQXCNRSSA-N 0.000 description 1
- CSKNOBGKYACPRG-KQWNVCNZSA-N CCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCN2CCCC2)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCN2CCCC2)O/C1=C\c1c[nH]c2ncccc12)=O CSKNOBGKYACPRG-KQWNVCNZSA-N 0.000 description 1
- KENLUACKRNMYPI-SXGWCWSVSA-N CCOC(C(C1=O)=C(Nc2c(C)cncc2)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(Nc2c(C)cncc2)O/C1=C\c1c[nH]c2ncccc12)=O KENLUACKRNMYPI-SXGWCWSVSA-N 0.000 description 1
- CUNBLKGSVPNPST-GDNBJRDFSA-N CCOC(C(C1=O)=C(Nc2ccncc2)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(Nc2ccncc2)O/C1=C\c1c[nH]c2ncccc12)=O CUNBLKGSVPNPST-GDNBJRDFSA-N 0.000 description 1
- LFRPDQZGCSUIMG-UHFFFAOYSA-O CCOC(C1=C(Nc(cc2)c(C)cc2OCCO)OC(Cc2c[nH]c3c2CCC=[NH+]3)C1=O)=O Chemical compound CCOC(C1=C(Nc(cc2)c(C)cc2OCCO)OC(Cc2c[nH]c3c2CCC=[NH+]3)C1=O)=O LFRPDQZGCSUIMG-UHFFFAOYSA-O 0.000 description 1
- SOKAQFYYMNVLAX-UHFFFAOYSA-N CCOC(C1=C(Nc2ccc(C)cc2O)OC(Cc2c[nH]c3ncccc23)C1=O)=O Chemical compound CCOC(C1=C(Nc2ccc(C)cc2O)OC(Cc2c[nH]c3ncccc23)C1=O)=O SOKAQFYYMNVLAX-UHFFFAOYSA-N 0.000 description 1
- MTUZBINVNZFNOC-STZFKDTASA-N CCO[IH](C(C1=O)=C(Nc(c(C)c2)ccc2OCCOCCO)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCO[IH](C(C1=O)=C(Nc(c(C)c2)ccc2OCCOCCO)O/C1=C\c1c[nH]c2c1cccn2)=O MTUZBINVNZFNOC-STZFKDTASA-N 0.000 description 1
- XBJOGFOFDGSEMZ-MOSHPQCFSA-N CN(CC1)CCC1OC(NC(C1=O)=C(Nc(cc2)ccc2F)O/C1=C\c1c[nH]c2ncccc12)O Chemical compound CN(CC1)CCC1OC(NC(C1=O)=C(Nc(cc2)ccc2F)O/C1=C\c1c[nH]c2ncccc12)O XBJOGFOFDGSEMZ-MOSHPQCFSA-N 0.000 description 1
- JQNHNPVOLVBKPT-YBEGLDIGSA-N CN(Cc1ccc[s]1)C(O/C1=C\c2c[nH]c3ncccc23)=C(C(OCCO)=O)C1=O Chemical compound CN(Cc1ccc[s]1)C(O/C1=C\c2c[nH]c3ncccc23)=C(C(OCCO)=O)C1=O JQNHNPVOLVBKPT-YBEGLDIGSA-N 0.000 description 1
- XJRGEAUNMRFFTM-YVLHZVERSA-N CN(Cc1ccccc1)C(O/C1=C\c2c[nH]c3ncccc23)=C(C(OCI)=O)C1=O Chemical compound CN(Cc1ccccc1)C(O/C1=C\c2c[nH]c3ncccc23)=C(C(OCI)=O)C1=O XJRGEAUNMRFFTM-YVLHZVERSA-N 0.000 description 1
- DYLIOUFQYKOMNL-ZDLGFXPLSA-O O=C(C(C1=O)=C(Nc(cc2)ccc2F)O/C1=C\c1c[nH]c2c1CCC=[NH+]2)OCC1CC1 Chemical compound O=C(C(C1=O)=C(Nc(cc2)ccc2F)O/C1=C\c1c[nH]c2c1CCC=[NH+]2)OCC1CC1 DYLIOUFQYKOMNL-ZDLGFXPLSA-O 0.000 description 1
- SWOMCSZKSHIOFY-YVLHZVERSA-O O=C(C=C(NC1CCCCCC1)O1)/C1=C/c1c[nH]c2[nH+]cccc12 Chemical compound O=C(C=C(NC1CCCCCC1)O1)/C1=C/c1c[nH]c2[nH+]cccc12 SWOMCSZKSHIOFY-YVLHZVERSA-O 0.000 description 1
- UGMMGVZUPDFBQF-UHFFFAOYSA-N OCCOC(C(C1=O)=C(Nc2ccccc2Cl)[O-]/C1=C\C1=CNC2N=CC=CC12)=O Chemical compound OCCOC(C(C1=O)=C(Nc2ccccc2Cl)[O-]/C1=C\C1=CNC2N=CC=CC12)=O UGMMGVZUPDFBQF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/435—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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- A61K31/44—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
- A61K31/435—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
- A61K31/495—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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed 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
- A61K31/535—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
- A61K31/5355—Non-condensed oxazines 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
- A61K31/54—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
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JPJP-P-2011-080185 | 2011-03-31 | ||
| JP2011080185 | 2011-03-31 | ||
| PCT/JP2012/058636 WO2012133802A1 (ja) | 2011-03-31 | 2012-03-30 | 新規フラノン誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20140056164A KR20140056164A (ko) | 2014-05-09 |
| KR101964479B1 true KR101964479B1 (ko) | 2019-04-01 |
Family
ID=46931496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137028226A Active KR101964479B1 (ko) | 2011-03-31 | 2012-03-30 | 신규 푸라논 유도체 |
Country Status (12)
| Country | Link |
|---|---|
| US (3) | USRE48140E1 (https=) |
| EP (1) | EP2692728B1 (https=) |
| JP (3) | JP5659356B2 (https=) |
| KR (1) | KR101964479B1 (https=) |
| CN (1) | CN103459388B (https=) |
| AU (3) | AU2012233246B2 (https=) |
| BR (1) | BR112013024957A2 (https=) |
| CA (1) | CA2830148C (https=) |
| DK (1) | DK2692728T3 (https=) |
| ES (1) | ES2687450T3 (https=) |
| MX (1) | MX344474B (https=) |
| WO (1) | WO2012133802A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2687450T3 (es) | 2011-03-31 | 2018-10-25 | Carna Biosciences, Inc. | Nuevo derivado de furanona |
| JP6569908B2 (ja) * | 2014-01-31 | 2019-09-04 | カルナバイオサイエンス株式会社 | 抗がん剤組成物 |
| CN104744353B (zh) * | 2015-03-31 | 2017-11-24 | 山东友帮生化科技有限公司 | 2‑氨基‑3‑碘‑5‑氯吡啶的合成方法 |
| CA3042849A1 (en) * | 2016-11-04 | 2018-05-11 | Carna Biosciences, Inc. | Furanone derivates and methods of use thereof |
| GB201807147D0 (en) | 2018-05-01 | 2018-06-13 | Oncologica Uk Ltd | Therapeutic combination |
| AU2019350581B2 (en) * | 2018-09-24 | 2025-07-10 | Carna Biosciences, Inc. | Methods of treatment of cancer comprising Cdc7 inhibitors |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001098299A1 (en) | 2000-06-19 | 2001-12-27 | Pharmacia Italia S.P.A. | Azaindole derivatives, process for their preparation, and their use as antitumor agents |
| WO2007054508A1 (en) | 2005-11-11 | 2007-05-18 | Pfizer Italia Srl | Pyrrolopyridines as kinase inhibitors |
| FR2907120A1 (fr) | 2006-10-12 | 2008-04-18 | Sanofi Aventis Sa | Nouveaux derives imidazolones,leur preparation a titre de medicaments,compositions pharmaceutiques,utilisation comme inhibiteurs de proteines kinases notamment cdc7 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6987113B2 (en) * | 1997-06-11 | 2006-01-17 | Sugen, Inc. | Tyrosine kinase inhibitors |
| BR0312722A (pt) | 2002-07-17 | 2005-05-10 | Pharmacia Italia Spa | Derivados de pirazol heterobicìclico como inibidores de qinase |
| US20050137220A1 (en) | 2003-07-23 | 2005-06-23 | Pharmacia Corporation | Beta-carboline compounds and analogues thereof as mitogen-activated protein kinase-activated protein kinase-2 inhibitors |
| US20050043346A1 (en) | 2003-08-08 | 2005-02-24 | Pharmacia Italia S.P.A. | Pyridylpyrrole derivatives active as kinase inhibitors |
| JP2007501827A (ja) | 2003-08-08 | 2007-02-01 | ファルマシア・イタリア・エス・ピー・エー | キナーゼ阻害剤として活性なピリミジルピロール誘導体 |
| FR2876103B1 (fr) | 2004-10-01 | 2008-02-22 | Aventis Pharma Sa | Nouveaux derives bis-azaindoles, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases |
| KR100875870B1 (ko) * | 2004-10-14 | 2008-12-26 | 에프. 호프만-라 로슈 아게 | 항암제로서의 신규 아자인돌 티아졸리논 |
| US20060122232A1 (en) * | 2004-12-06 | 2006-06-08 | Development Center For Biotechnology | 4-Hydroxyfuroic acid derivatives |
| BRPI0709680B8 (pt) | 2006-03-27 | 2021-05-25 | Nerviano Medical Sciences Srl | derivados de pirrol, tiofeno e furano substituídos por piridil e piridimil como inibidores de quinase |
| WO2008109443A2 (en) | 2007-03-02 | 2008-09-12 | Mdrna, Inc. | Nucleic acid compounds for inhibiting cdk2 gene expression and uses thereof |
| WO2009155052A1 (en) | 2008-05-28 | 2009-12-23 | Wyeth | 3-substituted-1h-pyrrolo[2,3-b]pyridine and 3-substituted-1h-pyrrolo[3,2-b]pyridine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses |
| WO2010030727A1 (en) | 2008-09-10 | 2010-03-18 | Wyeth Llc | 3-substituted-1h-indole, 3-substituted-1h-pyrrolo[2,3-b]pyridine and 3-substituted-1h-pyrrolo[3,2-b]pyridine compounds, their use as mtor kinase and pi3 kinase inhibitors, and their syntheses |
| CN102471339A (zh) | 2009-07-15 | 2012-05-23 | 雅培制药有限公司 | 激酶的吡咯并吡啶抑制剂 |
| TW201127384A (en) | 2009-11-18 | 2011-08-16 | Nerviano Medical Sciences Srl | Therapeutic combination comprising a Cdc7 inhibitor and an antineoplastic agent |
| US20120135989A1 (en) | 2010-06-29 | 2012-05-31 | Crystalgenomics, Inc. | Azaindole derivative |
| ES2687450T3 (es) | 2011-03-31 | 2018-10-25 | Carna Biosciences, Inc. | Nuevo derivado de furanona |
| JP6569908B2 (ja) | 2014-01-31 | 2019-09-04 | カルナバイオサイエンス株式会社 | 抗がん剤組成物 |
-
2012
- 2012-03-30 ES ES12763979.7T patent/ES2687450T3/es active Active
- 2012-03-30 US US15/967,323 patent/USRE48140E1/en active Active
- 2012-03-30 DK DK12763979.7T patent/DK2692728T3/en active
- 2012-03-30 BR BR112013024957A patent/BR112013024957A2/pt not_active IP Right Cessation
- 2012-03-30 US US15/172,021 patent/USRE46815E1/en active Active
- 2012-03-30 WO PCT/JP2012/058636 patent/WO2012133802A1/ja not_active Ceased
- 2012-03-30 MX MX2013010962A patent/MX344474B/es active IP Right Grant
- 2012-03-30 CA CA2830148A patent/CA2830148C/en active Active
- 2012-03-30 AU AU2012233246A patent/AU2012233246B2/en active Active
- 2012-03-30 KR KR1020137028226A patent/KR101964479B1/ko active Active
- 2012-03-30 JP JP2013507805A patent/JP5659356B2/ja active Active
- 2012-03-30 US US14/008,488 patent/US8742113B2/en not_active Ceased
- 2012-03-30 CN CN201280015870.5A patent/CN103459388B/zh active Active
- 2012-03-30 EP EP12763979.7A patent/EP2692728B1/en active Active
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001098299A1 (en) | 2000-06-19 | 2001-12-27 | Pharmacia Italia S.P.A. | Azaindole derivatives, process for their preparation, and their use as antitumor agents |
| WO2007054508A1 (en) | 2005-11-11 | 2007-05-18 | Pfizer Italia Srl | Pyrrolopyridines as kinase inhibitors |
| FR2907120A1 (fr) | 2006-10-12 | 2008-04-18 | Sanofi Aventis Sa | Nouveaux derives imidazolones,leur preparation a titre de medicaments,compositions pharmaceutiques,utilisation comme inhibiteurs de proteines kinases notamment cdc7 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2830148C (en) | 2020-07-28 |
| CN103459388A (zh) | 2013-12-18 |
| WO2012133802A1 (ja) | 2012-10-04 |
| AU2019203483A1 (en) | 2019-06-06 |
| JP5891576B2 (ja) | 2016-03-23 |
| MX344474B (es) | 2016-12-16 |
| USRE46815E1 (en) | 2018-05-01 |
| AU2017203986B2 (en) | 2019-02-28 |
| EP2692728A1 (en) | 2014-02-05 |
| BR112013024957A2 (pt) | 2016-12-20 |
| JP2016084363A (ja) | 2016-05-19 |
| EP2692728A4 (en) | 2014-08-20 |
| CA2830148A1 (en) | 2012-10-04 |
| AU2012233246B2 (en) | 2017-03-30 |
| JPWO2012133802A1 (ja) | 2014-07-28 |
| JP5659356B2 (ja) | 2015-01-28 |
| DK2692728T3 (en) | 2018-10-08 |
| ES2687450T3 (es) | 2018-10-25 |
| USRE48140E1 (en) | 2020-08-04 |
| AU2017203986A1 (en) | 2017-07-06 |
| US20140018533A1 (en) | 2014-01-16 |
| CN103459388B (zh) | 2015-11-25 |
| JP6256927B2 (ja) | 2018-01-10 |
| MX2013010962A (es) | 2014-04-25 |
| US8742113B2 (en) | 2014-06-03 |
| JP2015042663A (ja) | 2015-03-05 |
| EP2692728B1 (en) | 2018-07-04 |
| AU2012233246A1 (en) | 2013-10-10 |
| KR20140056164A (ko) | 2014-05-09 |
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