CN103459388B - 新型呋喃酮衍生物 - Google Patents
新型呋喃酮衍生物 Download PDFInfo
- Publication number
- CN103459388B CN103459388B CN201280015870.5A CN201280015870A CN103459388B CN 103459388 B CN103459388 B CN 103459388B CN 201280015870 A CN201280015870 A CN 201280015870A CN 103459388 B CN103459388 B CN 103459388B
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- China
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- mmol
- oxo
- amino
- dihydrofuran
- ppm
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- 0 *[N+]C(*C1)=C(C(C=O)O*)C1=O Chemical compound *[N+]C(*C1)=C(C(C=O)O*)C1=O 0.000 description 5
- OJTGVMYIYHSITP-ZRLZFEMFSA-N C/C=C\C=C(\CCNC(O/C1=C\c2c[nH]cc2/C=C\C=N)=C(C(OC)=O)C1=O)/C#C Chemical compound C/C=C\C=C(\CCNC(O/C1=C\c2c[nH]cc2/C=C\C=N)=C(C(OC)=O)C1=O)/C#C OJTGVMYIYHSITP-ZRLZFEMFSA-N 0.000 description 1
- SPKIUIHOKJOLOS-ZDLGFXPLSA-N CC(C)COC(C(C1=O)=C(Nc(cc2)ccc2F)O/C1=C\C1=CNC2[N-]CC=CC12)=O Chemical compound CC(C)COC(C(C1=O)=C(Nc(cc2)ccc2F)O/C1=C\C1=CNC2[N-]CC=CC12)=O SPKIUIHOKJOLOS-ZDLGFXPLSA-N 0.000 description 1
- HIAJIDYNKJSCKM-UHFFFAOYSA-O CC(C)OC(C1=C(NC2CCCCC2)OC(CC2=C[NH2+]c3ncccc23)C1=O)=O Chemical compound CC(C)OC(C1=C(NC2CCCCC2)OC(CC2=C[NH2+]c3ncccc23)C1=O)=O HIAJIDYNKJSCKM-UHFFFAOYSA-O 0.000 description 1
- YAQLWVSTZGURGE-UHFFFAOYSA-O CCOC(C(C(C(C1)=Cc2c[nH]c3ncccc23)=O)=C1[NH+](C)CCO)=O Chemical compound CCOC(C(C(C(C1)=Cc2c[nH]c3ncccc23)=O)=C1[NH+](C)CCO)=O YAQLWVSTZGURGE-UHFFFAOYSA-O 0.000 description 1
- NCJWQEXGNRZCFG-YBEGLDIGSA-N CCOC(C(C1=O)=C(N(C)Cc2ccc[s]2)O/C1=C\c1c[nH]c2c1cccn2)=[O-] Chemical compound CCOC(C(C1=O)=C(N(C)Cc2ccc[s]2)O/C1=C\c1c[nH]c2c1cccn2)=[O-] NCJWQEXGNRZCFG-YBEGLDIGSA-N 0.000 description 1
- LDYNTRAZACAOLI-ZDLGFXPLSA-N CCOC(C(C1=O)=C(N2CC3C=CC=CC3C2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(N2CC3C=CC=CC3C2)O/C1=C\c1c[nH]c2c1cccn2)=O LDYNTRAZACAOLI-ZDLGFXPLSA-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
- MLNIIHLLRPURBY-BEEBJDIISA-N CCOC(C(C1=O)=C(NC/C(/C=C(C)C)=C/C)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(NC/C(/C=C(C)C)=C/C)O/C1=C\c1c[nH]c2c1cccn2)=O MLNIIHLLRPURBY-BEEBJDIISA-N 0.000 description 1
- LAVJAQWOFCEFJY-UHFFFAOYSA-O CCOC(C(C1=O)=C(NN(C)C2=CCCC(C)=C2)OC1=CC1=C2[NH2+]c3ncccc3C12)=O Chemical compound CCOC(C(C1=O)=C(NN(C)C2=CCCC(C)=C2)OC1=CC1=C2[NH2+]c3ncccc3C12)=O LAVJAQWOFCEFJY-UHFFFAOYSA-O 0.000 description 1
- LLEZBRGVMLLJPS-KQWNVCNZSA-N CCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCN2CCOCC2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCN2CCOCC2)O/C1=C\c1c[nH]c2c1cccn2)=O LLEZBRGVMLLJPS-KQWNVCNZSA-N 0.000 description 1
- AJAKPJCLCWVBFB-ODLFYWEKSA-O CCOC(C(C1=O)=C(Nc(c(F)c2)ccc2[OH+]CCOC)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(Nc(c(F)c2)ccc2[OH+]CCOC)O/C1=C\c1c[nH]c2c1cccn2)=O AJAKPJCLCWVBFB-ODLFYWEKSA-O 0.000 description 1
- JZJQKWVEYCTBTI-UNOMPAQXSA-N CCOC(C(C1=O)=C(Nc(cc2)c(C)cc2OCCO)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(Nc(cc2)c(C)cc2OCCO)O/C1=C\c1c[nH]c2c1cccn2)=O JZJQKWVEYCTBTI-UNOMPAQXSA-N 0.000 description 1
- QBWWTXZXJZXREP-BKUYFWCQSA-N CCOC(C(C1=O)=C(Nc(cc2)c(C)cc2OCc2ncccn2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(Nc(cc2)c(C)cc2OCc2ncccn2)O/C1=C\c1c[nH]c2c1cccn2)=O QBWWTXZXJZXREP-BKUYFWCQSA-N 0.000 description 1
- BNRXOZGYCGMTNM-WQRHYEAKSA-N CCOC(C(C1=O)=C(Nc2ccc(C)cc2C)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(Nc2ccc(C)cc2C)O/C1=C\c1c[nH]c2c1cccn2)=O BNRXOZGYCGMTNM-WQRHYEAKSA-N 0.000 description 1
- CSQRWELQUCCCLJ-WGEAQBOBSA-N CCOC(CC(C(/C(/C1)=C/c2c[nH]c(N=C)c2/C=C\C)=O)=C1N(CC1)CCC1O)=O Chemical compound CCOC(CC(C(/C(/C1)=C/c2c[nH]c(N=C)c2/C=C\C)=O)=C1N(CC1)CCC1O)=O CSQRWELQUCCCLJ-WGEAQBOBSA-N 0.000 description 1
- KWSIPBSCPDVJKH-KSWICFSLSA-N Cc1c(/C=C\C=N)c(/C=C2\OC(Nc(cc3)ccc3F)=C(C(OC3CCN(C)CC3)=O)C2=O)c[nH]1 Chemical compound Cc1c(/C=C\C=N)c(/C=C2\OC(Nc(cc3)ccc3F)=C(C(OC3CCN(C)CC3)=O)C2=O)c[nH]1 KWSIPBSCPDVJKH-KSWICFSLSA-N 0.000 description 1
- AXWHDSXTDRBUIJ-SSDOTTSWSA-N Cc1c[nH]c(N=C2)c1[C@H]1C2=C1 Chemical compound Cc1c[nH]c(N=C2)c1[C@H]1C2=C1 AXWHDSXTDRBUIJ-SSDOTTSWSA-N 0.000 description 1
- IGTWOMQOFJWKKR-ZDLGFXPLSA-P O/C(/C(/C(/C([OH+]CC1CC1)=O)=[I]/Nc(cc1)ccc1F)=O)=C\c1c[nH]c2[nH+]cccc12 Chemical compound O/C(/C(/C(/C([OH+]CC1CC1)=O)=[I]/Nc(cc1)ccc1F)=O)=C\c1c[nH]c2[nH+]cccc12 IGTWOMQOFJWKKR-ZDLGFXPLSA-P 0.000 description 1
- KAIWRKYDYWYFIT-UHFFFAOYSA-N O=Cc1c[nH]c2c1cccn2 Chemical compound O=Cc1c[nH]c2c1cccn2 KAIWRKYDYWYFIT-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)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (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 |
|---|---|---|---|
| JP2011080185 | 2011-03-31 | ||
| JP2011-080185 | 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 |
|---|---|
| CN103459388A CN103459388A (zh) | 2013-12-18 |
| CN103459388B true CN103459388B (zh) | 2015-11-25 |
Family
ID=46931496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201280015870.5A Active CN103459388B (zh) | 2011-03-31 | 2012-03-30 | 新型呋喃酮衍生物 |
Country Status (12)
| Country | Link |
|---|---|
| US (3) | USRE46815E1 (enExample) |
| EP (1) | EP2692728B1 (enExample) |
| JP (3) | JP5659356B2 (enExample) |
| KR (1) | KR101964479B1 (enExample) |
| CN (1) | CN103459388B (enExample) |
| AU (3) | AU2012233246B2 (enExample) |
| BR (1) | BR112013024957A2 (enExample) |
| CA (1) | CA2830148C (enExample) |
| DK (1) | DK2692728T3 (enExample) |
| ES (1) | ES2687450T3 (enExample) |
| MX (1) | MX344474B (enExample) |
| WO (1) | WO2012133802A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE46815E1 (en) | 2011-03-31 | 2018-05-01 | Carna Biosciences, Inc. | Furanone derivative |
| WO2015115355A1 (ja) * | 2014-01-31 | 2015-08-06 | 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 |
| US20200055848A1 (en) * | 2016-11-04 | 2020-02-20 | Carna Biosciences, Inc. | Furanone derivates and methods of use thereof |
| GB201807147D0 (en) | 2018-05-01 | 2018-06-13 | Oncologica Uk Ltd | Therapeutic combination |
| US20210393620A1 (en) * | 2018-09-24 | 2021-12-23 | Sierra Oncology, 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 |
| WO2008046982A2 (fr) * | 2006-10-12 | 2008-04-24 | Sanofi-Aventis | 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 |
| DE60320560T2 (de) | 2002-07-17 | 2008-12-11 | Pfizer Italia S.R.L. | Heterobicyclische pyrazolderivate als kinaseinhibitoren |
| US20050143371A1 (en) | 2003-07-23 | 2005-06-30 | 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 |
| BRPI0413438A (pt) | 2003-08-08 | 2006-10-17 | Pharmacia Italia Spa | derivados de pirimidilpirrol ativos como inibidores de cinase |
| 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 |
| PL1805175T3 (pl) * | 2004-10-14 | 2008-08-29 | Hoffmann La Roche | Nowe azaindolotiazolinony jako środki przeciwrakowe |
| US20060122232A1 (en) * | 2004-12-06 | 2006-06-08 | Development Center For Biotechnology | 4-Hydroxyfuroic acid derivatives |
| UA94097C2 (ru) | 2006-03-27 | 2011-04-11 | НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. | Пиридил- и пиримидинилзамещенные производной пиррола, тиофена и фурана как ингибиторы киназ |
| 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 |
| WO2011008915A1 (en) | 2009-07-15 | 2011-01-20 | Abbott Laboratories | Pyrrolopyridine inhibitors of kinases |
| TW201127384A (en) | 2009-11-18 | 2011-08-16 | Nerviano Medical Sciences Srl | Therapeutic combination comprising a Cdc7 inhibitor and an antineoplastic agent |
| KR20140009106A (ko) | 2010-06-29 | 2014-01-22 | 에스비아이 바이오테크 가부시키가이샤 | 아자인돌 유도체 |
| USRE46815E1 (en) * | 2011-03-31 | 2018-05-01 | Carna Biosciences, Inc. | Furanone derivative |
| WO2015115355A1 (ja) | 2014-01-31 | 2015-08-06 | カルナバイオサイエンス株式会社 | 抗がん剤組成物 |
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2012
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- 2012-03-30 KR KR1020137028226A patent/KR101964479B1/ko active Active
- 2012-03-30 JP JP2013507805A patent/JP5659356B2/ja active Active
- 2012-03-30 MX MX2013010962A patent/MX344474B/es active IP Right Grant
- 2012-03-30 CN CN201280015870.5A patent/CN103459388B/zh active Active
- 2012-03-30 US US14/008,488 patent/US8742113B2/en not_active Ceased
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2014
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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 |
| WO2008046982A2 (fr) * | 2006-10-12 | 2008-04-24 | Sanofi-Aventis | Nouveaux derives imidazolones, leur preparation a titre de medicaments, compositions pharmaceutiques, utilisation comme inhibiteurs de proteines kinases notamment cdc7 |
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| Title |
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| "4-Substituted-7-azaindoles bearing a ureidobenzofuranone moiety as potent and selective, ATP-competitive inhibitors of the mammalian target of rapamycin (mTOR)";Hwei-Ru Tsou et al;《Bioorganic & Medicinal Chemistry Letters》;20100206;第20卷(第7期);第2259-2263页 * |
Also Published As
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| WO2012133802A1 (ja) | 2012-10-04 |
| AU2017203986A1 (en) | 2017-07-06 |
| US8742113B2 (en) | 2014-06-03 |
| BR112013024957A2 (pt) | 2016-12-20 |
| CA2830148A1 (en) | 2012-10-04 |
| AU2012233246B2 (en) | 2017-03-30 |
| MX344474B (es) | 2016-12-16 |
| JP6256927B2 (ja) | 2018-01-10 |
| AU2012233246A1 (en) | 2013-10-10 |
| JP5891576B2 (ja) | 2016-03-23 |
| KR101964479B1 (ko) | 2019-04-01 |
| JP2015042663A (ja) | 2015-03-05 |
| USRE48140E1 (en) | 2020-08-04 |
| DK2692728T3 (en) | 2018-10-08 |
| AU2017203986B2 (en) | 2019-02-28 |
| EP2692728A1 (en) | 2014-02-05 |
| USRE46815E1 (en) | 2018-05-01 |
| JPWO2012133802A1 (ja) | 2014-07-28 |
| EP2692728B1 (en) | 2018-07-04 |
| US20140018533A1 (en) | 2014-01-16 |
| CA2830148C (en) | 2020-07-28 |
| KR20140056164A (ko) | 2014-05-09 |
| JP2016084363A (ja) | 2016-05-19 |
| CN103459388A (zh) | 2013-12-18 |
| ES2687450T3 (es) | 2018-10-25 |
| JP5659356B2 (ja) | 2015-01-28 |
| AU2019203483A1 (en) | 2019-06-06 |
| EP2692728A4 (en) | 2014-08-20 |
| MX2013010962A (es) | 2014-04-25 |
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