JP5659356B2 - 新規フラノン誘導体 - Google Patents
新規フラノン誘導体 Download PDFInfo
- Publication number
- JP5659356B2 JP5659356B2 JP2013507805A JP2013507805A JP5659356B2 JP 5659356 B2 JP5659356 B2 JP 5659356B2 JP 2013507805 A JP2013507805 A JP 2013507805A JP 2013507805 A JP2013507805 A JP 2013507805A JP 5659356 B2 JP5659356 B2 JP 5659356B2
- Authority
- JP
- Japan
- Prior art keywords
- mmol
- oxo
- dihydrofuran
- yield
- carboxylate
- 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.)
- Active
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- 0 *N(*)C(OC1=C[C@@]2c3cccnc3NC2)=C(C(O*)=O)C1=O Chemical compound *N(*)C(OC1=C[C@@]2c3cccnc3NC2)=C(C(O*)=O)C1=O 0.000 description 6
- GKDFYJDRBNATEA-WQRHYEAKSA-N CC(C)(c1ccccc1)NC(O/C1=C\c2c[nH]c3ncccc23)=CC1=O Chemical compound CC(C)(c1ccccc1)NC(O/C1=C\c2c[nH]c3ncccc23)=CC1=O GKDFYJDRBNATEA-WQRHYEAKSA-N 0.000 description 1
- VSYRFYZXANWBTR-YVLHZVERSA-N CC(C)OC(C(C1=O)=C(Nc(cc2)ccc2F)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CC(C)OC(C(C1=O)=C(Nc(cc2)ccc2F)O/C1=C\c1c[nH]c2c1cccn2)=O VSYRFYZXANWBTR-YVLHZVERSA-N 0.000 description 1
- UKNSDRUWZAASLO-GRSHGNNSSA-N CC(C)c(cc1)ccc1NC(O/C1=C\c2c[nH]c3c2cccn3)=CC1=O Chemical compound CC(C)c(cc1)ccc1NC(O/C1=C\c2c[nH]c3c2cccn3)=CC1=O UKNSDRUWZAASLO-GRSHGNNSSA-N 0.000 description 1
- HZUCQTJMDZYJFP-KQWNVCNZSA-N CCCCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCN(C)C)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCCCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCN(C)C)O/C1=C\c1c[nH]c2c1cccn2)=O HZUCQTJMDZYJFP-KQWNVCNZSA-N 0.000 description 1
- LVAJHQWZVYRGFJ-LCYFTJDESA-N CCOC(C(C1=O)=C(N(C)CCO)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(N(C)CCO)O/C1=C\c1c[nH]c2ncccc12)=O LVAJHQWZVYRGFJ-LCYFTJDESA-N 0.000 description 1
- SITIFCMIPLYBRT-WQRHYEAKSA-N CCOC(C(C1=O)=C(N(CC2)Cc3c2cccn3)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(N(CC2)Cc3c2cccn3)O/C1=C\c1c[nH]c2c1cccn2)=O SITIFCMIPLYBRT-WQRHYEAKSA-N 0.000 description 1
- UDJVLYNGILAAIH-WQRHYEAKSA-N CCOC(C(C1=O)=C(N(CC2)Cc3c2nccc3)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(N(CC2)Cc3c2nccc3)O/C1=C\c1c[nH]c2c1cccn2)=O UDJVLYNGILAAIH-WQRHYEAKSA-N 0.000 description 1
- CZSOHNKWYXDPSI-DHDCSXOGSA-N CCOC(C(C1=O)=C(N(CCC2)CC2C(N)=O)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(N(CCC2)CC2C(N)=O)O/C1=C\c1c[nH]c2ncccc12)=O CZSOHNKWYXDPSI-DHDCSXOGSA-N 0.000 description 1
- VJGJCWJLDRNURJ-ATVHPVEESA-N CCOC(C(C1=O)=C(N(CCC2)CCN2C(C)=O)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(N(CCC2)CCN2C(C)=O)O/C1=C\c1c[nH]c2ncccc12)=O VJGJCWJLDRNURJ-ATVHPVEESA-N 0.000 description 1
- PBKVOMXAISHYCT-JYRVWZFOSA-N CCOC(C(C1=O)=C(NC2CC2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(NC2CC2)O/C1=C\c1c[nH]c2c1cccn2)=O PBKVOMXAISHYCT-JYRVWZFOSA-N 0.000 description 1
- FQQOQWUUMVOMEV-UVTDQMKNSA-N CCOC(C(C1=O)=C(NCCN(C)C)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(NCCN(C)C)O/C1=C\c1c[nH]c2c1cccn2)=O FQQOQWUUMVOMEV-UVTDQMKNSA-N 0.000 description 1
- XUYBCVIWMGTAFB-VWKMBWMVSA-N CCOC(C(C1=O)=C(N[C@H](CC2)CC[C@H]2O)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(N[C@H](CC2)CC[C@H]2O)O/C1=C\c1c[nH]c2c1cccn2)=O XUYBCVIWMGTAFB-VWKMBWMVSA-N 0.000 description 1
- JZHBMODROBRDLG-STZFKDTASA-N CCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCOCCO)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(Nc(c(C)c2)ccc2OCCOCCO)O/C1=C\c1c[nH]c2ncccc12)=O JZHBMODROBRDLG-STZFKDTASA-N 0.000 description 1
- YXUIWKJEAKYYCN-JMIUGGIZSA-N CCOC(C(C1=O)=C(Nc(cc2)c(C)cc2OCC(CO)O)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(Nc(cc2)c(C)cc2OCC(CO)O)O/C1=C\c1c[nH]c2c1cccn2)=O YXUIWKJEAKYYCN-JMIUGGIZSA-N 0.000 description 1
- DHFQSDYDROYOAS-QRVIBDJDSA-N CCOC(C(C1=O)=C(Nc(cc2)c(C)cc2OCc2cccnc2)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(Nc(cc2)c(C)cc2OCc2cccnc2)O/C1=C\c1c[nH]c2ncccc12)=O DHFQSDYDROYOAS-QRVIBDJDSA-N 0.000 description 1
- QPAXZIZGWCIBJI-SXGWCWSVSA-N CCOC(C(C1=O)=C(Nc2cc(Cl)ccc2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(Nc2cc(Cl)ccc2)O/C1=C\c1c[nH]c2c1cccn2)=O QPAXZIZGWCIBJI-SXGWCWSVSA-N 0.000 description 1
- BNRXOZGYCGMTNM-WQRHYEAKSA-N CCOC(C(C1=O)=C(Nc2ccc(C)cc2C)O/C1=C\c1c[nH]c2ncccc12)=O Chemical compound CCOC(C(C1=O)=C(Nc2ccc(C)cc2C)O/C1=C\c1c[nH]c2ncccc12)=O BNRXOZGYCGMTNM-WQRHYEAKSA-N 0.000 description 1
- MNGIMRBHILIORK-PXNMLYILSA-N CCOC(C(C1=O)=C(Nc2ccccc2)O/C1=C\c1c[nH]c(nc2)c1cc2Cl)=O Chemical compound CCOC(C(C1=O)=C(Nc2ccccc2)O/C1=C\c1c[nH]c(nc2)c1cc2Cl)=O MNGIMRBHILIORK-PXNMLYILSA-N 0.000 description 1
- KGMJZRVANPEFFP-WJDWOHSUSA-N CCOC(C(C1=O)=C(Nc2ccccc2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound CCOC(C(C1=O)=C(Nc2ccccc2)O/C1=C\c1c[nH]c2c1cccn2)=O KGMJZRVANPEFFP-WJDWOHSUSA-N 0.000 description 1
- NPTDGZSLLHZCBJ-BOPFTXTBSA-N CN(Cc1ccc[s]1)C(O/C1=C\c2c[nH]c3ncccc23)=C(C(OCCOC)=O)C1=O Chemical compound CN(Cc1ccc[s]1)C(O/C1=C\c2c[nH]c3ncccc23)=C(C(OCCOC)=O)C1=O NPTDGZSLLHZCBJ-BOPFTXTBSA-N 0.000 description 1
- RFDVLWWDHNJUJR-BKUYFWCQSA-N CN1C(COC(C(C2=O)=C(Nc(cc3)ccc3F)O/C2=C\c2c[nH]c3ncccc23)=O)CCCC1 Chemical compound CN1C(COC(C(C2=O)=C(Nc(cc3)ccc3F)O/C2=C\c2c[nH]c3ncccc23)=O)CCCC1 RFDVLWWDHNJUJR-BKUYFWCQSA-N 0.000 description 1
- HZNPECADQYLKMC-LGMDPLHJSA-N COCCOC(C(C1=O)=C(N2CCCCCC2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound COCCOC(C(C1=O)=C(N2CCCCCC2)O/C1=C\c1c[nH]c2c1cccn2)=O HZNPECADQYLKMC-LGMDPLHJSA-N 0.000 description 1
- IOVPUSDTYBXUJK-NVMNQCDNSA-N Cc(cc1)cc(C)c1NC(O/C1=C\c2c[nH]c3c2cccn3)=CC1=O Chemical compound Cc(cc1)cc(C)c1NC(O/C1=C\c2c[nH]c3c2cccn3)=CC1=O IOVPUSDTYBXUJK-NVMNQCDNSA-N 0.000 description 1
- SWOMCSZKSHIOFY-YVLHZVERSA-N O=C(C=C(NC1CCCCCC1)O1)/C1=C/c1c[nH]c2ncccc12 Chemical compound O=C(C=C(NC1CCCCCC1)O1)/C1=C/c1c[nH]c2ncccc12 SWOMCSZKSHIOFY-YVLHZVERSA-N 0.000 description 1
- SASWFXQWNYXTJT-IDUWFGFVSA-N O=C(C=C(Nc1ccc2[nH]ncc2c1)O1)/C1=C/c1c[nH]c2c1cccn2 Chemical compound O=C(C=C(Nc1ccc2[nH]ncc2c1)O1)/C1=C/c1c[nH]c2c1cccn2 SASWFXQWNYXTJT-IDUWFGFVSA-N 0.000 description 1
- ZCXOLOPSZIKQTP-ZROIWOOFSA-N OC(C(C1=O)=C(Nc2ccccc2)O/C1=C\c1c[nH]c2c1cccn2)=O Chemical compound OC(C(C1=O)=C(Nc2ccccc2)O/C1=C\c1c[nH]c2c1cccn2)=O ZCXOLOPSZIKQTP-ZROIWOOFSA-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)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (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)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013507805A JP5659356B2 (ja) | 2011-03-31 | 2012-03-30 | 新規フラノン誘導体 |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011080185 | 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 |
| JP2013507805A JP5659356B2 (ja) | 2011-03-31 | 2012-03-30 | 新規フラノン誘導体 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014219074A Division JP5891576B2 (ja) | 2011-03-31 | 2014-10-28 | 新規フラノン誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPWO2012133802A1 JPWO2012133802A1 (ja) | 2014-07-28 |
| JP5659356B2 true JP5659356B2 (ja) | 2015-01-28 |
Family
ID=46931496
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013507805A Active JP5659356B2 (ja) | 2011-03-31 | 2012-03-30 | 新規フラノン誘導体 |
| JP2014219074A Active JP5891576B2 (ja) | 2011-03-31 | 2014-10-28 | 新規フラノン誘導体 |
| JP2016020407A Active JP6256927B2 (ja) | 2011-03-31 | 2016-02-05 | 新規フラノン誘導体 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014219074A Active JP5891576B2 (ja) | 2011-03-31 | 2014-10-28 | 新規フラノン誘導体 |
| JP2016020407A Active JP6256927B2 (ja) | 2011-03-31 | 2016-02-05 | 新規フラノン誘導体 |
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=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016084363A (ja) * | 2011-03-31 | 2016-05-19 | カルナバイオサイエンス株式会社 | 新規フラノン誘導体 |
| US9974795B2 (en) | 2014-01-31 | 2018-05-22 | Carna Biosciences, Inc. | Anticancer agent composition |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
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| 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 |
| EP3856352A4 (en) * | 2018-09-24 | 2022-06-29 | Sierra Oncology, Inc. | Methods of treatment of cancer comprising cdc7 inhibitors |
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| JP2016084363A (ja) * | 2011-03-31 | 2016-05-19 | カルナバイオサイエンス株式会社 | 新規フラノン誘導体 |
| US9974795B2 (en) | 2014-01-31 | 2018-05-22 | Carna Biosciences, Inc. | Anticancer agent composition |
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| CA2830148C (en) | 2020-07-28 |
| CN103459388A (zh) | 2013-12-18 |
| EP2692728A1 (en) | 2014-02-05 |
| AU2017203986A1 (en) | 2017-07-06 |
| KR101964479B1 (ko) | 2019-04-01 |
| AU2012233246A1 (en) | 2013-10-10 |
| CN103459388B (zh) | 2015-11-25 |
| JP2015042663A (ja) | 2015-03-05 |
| US20140018533A1 (en) | 2014-01-16 |
| JP5891576B2 (ja) | 2016-03-23 |
| DK2692728T3 (en) | 2018-10-08 |
| EP2692728A4 (en) | 2014-08-20 |
| USRE48140E1 (en) | 2020-08-04 |
| EP2692728B1 (en) | 2018-07-04 |
| AU2017203986B2 (en) | 2019-02-28 |
| WO2012133802A1 (ja) | 2012-10-04 |
| CA2830148A1 (en) | 2012-10-04 |
| JP2016084363A (ja) | 2016-05-19 |
| JP6256927B2 (ja) | 2018-01-10 |
| MX344474B (es) | 2016-12-16 |
| BR112013024957A2 (pt) | 2016-12-20 |
| KR20140056164A (ko) | 2014-05-09 |
| MX2013010962A (es) | 2014-04-25 |
| AU2012233246B2 (en) | 2017-03-30 |
| ES2687450T3 (es) | 2018-10-25 |
| US8742113B2 (en) | 2014-06-03 |
| JPWO2012133802A1 (ja) | 2014-07-28 |
| AU2019203483A1 (en) | 2019-06-06 |
| USRE46815E1 (en) | 2018-05-01 |
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