JP6027610B2 - 複素環式化合物及びその使用 - Google Patents
複素環式化合物及びその使用 Download PDFInfo
- Publication number
- JP6027610B2 JP6027610B2 JP2014521730A JP2014521730A JP6027610B2 JP 6027610 B2 JP6027610 B2 JP 6027610B2 JP 2014521730 A JP2014521730 A JP 2014521730A JP 2014521730 A JP2014521730 A JP 2014521730A JP 6027610 B2 JP6027610 B2 JP 6027610B2
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- JP
- Japan
- Prior art keywords
- substituted
- alkyl
- cancer
- heteroaryl
- compound
- 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.)
- Expired - Fee Related
Links
- 0 BN(C(***)C(*)c1cccc(*)c11)C1=O Chemical compound BN(C(***)C(*)c1cccc(*)c11)C1=O 0.000 description 42
- MZINZXIFJMLTOK-NSHDSACASA-N C[C@@H](C(N1c2ccccc2)=Cc2cccc(Cl)c2C1=O)N Chemical compound C[C@@H](C(N1c2ccccc2)=Cc2cccc(Cl)c2C1=O)N MZINZXIFJMLTOK-NSHDSACASA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N C1CCCCC1 Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- RCRXYJOKNXNDAC-HBHSWBPBSA-N CC(/C=N/C1N=C(N)N=C2C=CC=NC12)C(N1c2ccccc2)=Nc2cccc(-c3cnc(C)nc3)c2C1=O Chemical compound CC(/C=N/C1N=C(N)N=C2C=CC=NC12)C(N1c2ccccc2)=Nc2cccc(-c3cnc(C)nc3)c2C1=O RCRXYJOKNXNDAC-HBHSWBPBSA-N 0.000 description 1
- VMKDGGAESMWIHI-UHFFFAOYSA-N CC(C(N(c1ccccc1)C1=O)=CC(CC=C2)C1=C2Cl)[NH+2]C1(C)NC(N)=Nc2c1nccc2 Chemical compound CC(C(N(c1ccccc1)C1=O)=CC(CC=C2)C1=C2Cl)[NH+2]C1(C)NC(N)=Nc2c1nccc2 VMKDGGAESMWIHI-UHFFFAOYSA-N 0.000 description 1
- TVNVFCFROWWXJQ-KRWDZBQOSA-N CC(C)N(C([C@H](C)Nc1ncnc2c1nccc2)=Cc1cccc(C(C=C2)=CN(C)C2=O)c11)C1=O Chemical compound CC(C)N(C([C@H](C)Nc1ncnc2c1nccc2)=Cc1cccc(C(C=C2)=CN(C)C2=O)c11)C1=O TVNVFCFROWWXJQ-KRWDZBQOSA-N 0.000 description 1
- TTYBVMKQNQJIJE-UHFFFAOYSA-N CC(C)NCC(CC1)CCN1C(C)=O Chemical compound CC(C)NCC(CC1)CCN1C(C)=O TTYBVMKQNQJIJE-UHFFFAOYSA-N 0.000 description 1
- DWPMJTVAEDBIES-UHFFFAOYSA-N CC(CC1)CCN1C(C)=O Chemical compound CC(CC1)CCN1C(C)=O DWPMJTVAEDBIES-UHFFFAOYSA-N 0.000 description 1
- OJOWBMWDFLWCGE-UHFFFAOYSA-N CC(N1CCN(CCI)CC1)=O Chemical compound CC(N1CCN(CCI)CC1)=O OJOWBMWDFLWCGE-UHFFFAOYSA-N 0.000 description 1
- QOGNDJLSYMJGPP-UHFFFAOYSA-N CC1(C)OB(c(cn2)ccc2OC)OC1(C)C Chemical compound CC1(C)OB(c(cn2)ccc2OC)OC1(C)C QOGNDJLSYMJGPP-UHFFFAOYSA-N 0.000 description 1
- TVSMLBGFGKLKOO-UHFFFAOYSA-N CC1CCN(C)CC1 Chemical compound CC1CCN(C)CC1 TVSMLBGFGKLKOO-UHFFFAOYSA-N 0.000 description 1
- OVRKATYHWPCGPZ-UHFFFAOYSA-N CC1CCOCC1 Chemical compound CC1CCOCC1 OVRKATYHWPCGPZ-UHFFFAOYSA-N 0.000 description 1
- KPMAAWSUWBPRKZ-UHFFFAOYSA-N CCC(N1Cc(cc2)ccc2OC)=Cc2cccc(Cl)c2C1=O Chemical compound CCC(N1Cc(cc2)ccc2OC)=Cc2cccc(Cl)c2C1=O KPMAAWSUWBPRKZ-UHFFFAOYSA-N 0.000 description 1
- JHZLCGGZBRKJNV-UHFFFAOYSA-N CCC(N1c2ccccc2)=Nc2cccc(-c3ccnc(C)c3)c2C1=O Chemical compound CCC(N1c2ccccc2)=Nc2cccc(-c3ccnc(C)c3)c2C1=O JHZLCGGZBRKJNV-UHFFFAOYSA-N 0.000 description 1
- XYXPOBONPWKSEZ-UHFFFAOYSA-N CCC(N=C1Cl)=CC(C)(CC=C2)C1=C2Cl Chemical compound CCC(N=C1Cl)=CC(C)(CC=C2)C1=C2Cl XYXPOBONPWKSEZ-UHFFFAOYSA-N 0.000 description 1
- FDLPYXZDNRULKJ-UHFFFAOYSA-N CCCN(CC1)CCN1S(C)(=O)=O Chemical compound CCCN(CC1)CCN1S(C)(=O)=O FDLPYXZDNRULKJ-UHFFFAOYSA-N 0.000 description 1
- NSZKMHUXDXFLAZ-UHFFFAOYSA-N CCc1cc2cccc(Cl)c2c(C(N2CCOCC2)=O)n1 Chemical compound CCc1cc2cccc(Cl)c2c(C(N2CCOCC2)=O)n1 NSZKMHUXDXFLAZ-UHFFFAOYSA-N 0.000 description 1
- WPCSHVNGXOKEQD-UHFFFAOYSA-N CCc1cc2cccc(Cl)c2c(C=O)n1 Chemical compound CCc1cc2cccc(Cl)c2c(C=O)n1 WPCSHVNGXOKEQD-UHFFFAOYSA-N 0.000 description 1
- MSUDDBPZPQWAMS-UHFFFAOYSA-N CCc1nc(C(Cl)=O)c2c(Cl)cccc2c1 Chemical compound CCc1nc(C(Cl)=O)c2c(Cl)cccc2c1 MSUDDBPZPQWAMS-UHFFFAOYSA-N 0.000 description 1
- QDPPTBPKAKUPNZ-UHFFFAOYSA-N CCc1nc(C=C)c2c(Cl)cccc2c1 Chemical compound CCc1nc(C=C)c2c(Cl)cccc2c1 QDPPTBPKAKUPNZ-UHFFFAOYSA-N 0.000 description 1
- WMBCUXKYKVTJRF-UHFFFAOYSA-N CNCC1CCOCC1 Chemical compound CNCC1CCOCC1 WMBCUXKYKVTJRF-UHFFFAOYSA-N 0.000 description 1
- WWXPJKGWWPWBTB-UHFFFAOYSA-N CNCCN1CCOCC1 Chemical compound CNCCN1CCOCC1 WWXPJKGWWPWBTB-UHFFFAOYSA-N 0.000 description 1
- CQKKNUZLUVTPTE-UHFFFAOYSA-N COCCN(CC1)CCN1S(C)(=O)=O Chemical compound COCCN(CC1)CCN1S(C)(=O)=O CQKKNUZLUVTPTE-UHFFFAOYSA-N 0.000 description 1
- DHADXDMPEUWEAS-UHFFFAOYSA-N COc1ccc(B(O)O)cn1 Chemical compound COc1ccc(B(O)O)cn1 DHADXDMPEUWEAS-UHFFFAOYSA-N 0.000 description 1
- POEOXZQLWUIFQW-UHFFFAOYSA-N CS(NC1CC1)(=O)=O Chemical compound CS(NC1CC1)(=O)=O POEOXZQLWUIFQW-UHFFFAOYSA-N 0.000 description 1
- JAZVFUIINCFLED-OIGLVOGNSA-N C[C@@H](C(N(C1O)c2ccccc2)=Cc2c1c(-c1ccnnc1)ccc2)Nc1nc(N)nc2c1nccc2 Chemical compound C[C@@H](C(N(C1O)c2ccccc2)=Cc2c1c(-c1ccnnc1)ccc2)Nc1nc(N)nc2c1nccc2 JAZVFUIINCFLED-OIGLVOGNSA-N 0.000 description 1
- YDNSGJTVFSSLIL-INIZCTEOSA-N C[C@@H](C(N1C2=CC=CC=CC2)=Cc2cccc(C3=CNN(C)C=C3)c2C1=O)N Chemical compound C[C@@H](C(N1C2=CC=CC=CC2)=Cc2cccc(C3=CNN(C)C=C3)c2C1=O)N YDNSGJTVFSSLIL-INIZCTEOSA-N 0.000 description 1
- BIAVXOOUJFEMLT-QMMMGPOBSA-N C[C@@H](C(N1C2CC2)=Cc2cccc(Cl)c2C1=O)N Chemical compound C[C@@H](C(N1C2CC2)=Cc2cccc(Cl)c2C1=O)N BIAVXOOUJFEMLT-QMMMGPOBSA-N 0.000 description 1
- CKGZVEIKWKUPCY-LBPRGKRZSA-N C[C@@H](C(N1C2CC2)=Cc2cccc(Cl)c2C1=O)Nc1ccnc2ccn[n]12 Chemical compound C[C@@H](C(N1C2CC2)=Cc2cccc(Cl)c2C1=O)Nc1ccnc2ccn[n]12 CKGZVEIKWKUPCY-LBPRGKRZSA-N 0.000 description 1
- YHYLOQLVVMJZOM-LBPRGKRZSA-N C[C@@H](C(N1Cc(cc2)ccc2OC)=Cc2cccc(Cl)c2C1=O)N Chemical compound C[C@@H](C(N1Cc(cc2)ccc2OC)=Cc2cccc(Cl)c2C1=O)N YHYLOQLVVMJZOM-LBPRGKRZSA-N 0.000 description 1
- VPIZZTJCQPVZKR-ZDUSSCGKSA-N C[C@@H](C(N1c(cc2)ccc2F)=Cc2cccc(Cl)c2C1=O)Nc1c2ncccc2nc(N)n1 Chemical compound C[C@@H](C(N1c(cc2)ccc2F)=Cc2cccc(Cl)c2C1=O)Nc1c2ncccc2nc(N)n1 VPIZZTJCQPVZKR-ZDUSSCGKSA-N 0.000 description 1
- NGWSVJVXAWMNOQ-ZDUSSCGKSA-N C[C@@H](C(N1c2cccc(F)c2)=Cc(cccc2-c(cn3)cnc3OC)c2C1=O)N Chemical compound C[C@@H](C(N1c2cccc(F)c2)=Cc(cccc2-c(cn3)cnc3OC)c2C1=O)N NGWSVJVXAWMNOQ-ZDUSSCGKSA-N 0.000 description 1
- HOQJCBWEYZOEPJ-IBGZPJMESA-N C[C@@H](C(N1c2ccccc2)=CCc2cccc(-c3cnc(C)nc3)c2C1=O)Nc1nc(NC)nc2c1nccc2 Chemical compound C[C@@H](C(N1c2ccccc2)=CCc2cccc(-c3cnc(C)nc3)c2C1=O)Nc1nc(NC)nc2c1nccc2 HOQJCBWEYZOEPJ-IBGZPJMESA-N 0.000 description 1
- JMQNQSBGFNGVJL-TUAJMSPBSA-N C[C@@H](C(N1c2ccccc2)=Cc2cccc(-c(cn3)cnc3OC)c2C1=O)NC1=CC(O)=NC2C=CC=NC12 Chemical compound C[C@@H](C(N1c2ccccc2)=Cc2cccc(-c(cn3)cnc3OC)c2C1=O)NC1=CC(O)=NC2C=CC=NC12 JMQNQSBGFNGVJL-TUAJMSPBSA-N 0.000 description 1
- ADPSSFTXFZPSOW-IBGZPJMESA-N C[C@@H](C(N1c2ccccc2)=Cc2cccc(-c3c[n](C)nc3)c2C1=O)Nc(c(nccc1)c1nc1)c1C#N Chemical compound C[C@@H](C(N1c2ccccc2)=Cc2cccc(-c3c[n](C)nc3)c2C1=O)Nc(c(nccc1)c1nc1)c1C#N ADPSSFTXFZPSOW-IBGZPJMESA-N 0.000 description 1
- WDYDSZZBZGTFEP-IBGZPJMESA-N C[C@@H](C(N1c2ccccc2)=Cc2cccc(C(C=C3)=CN(C)C3=O)c2C1=O)Nc1ncnc2c1nccc2 Chemical compound C[C@@H](C(N1c2ccccc2)=Cc2cccc(C(C=C3)=CN(C)C3=O)c2C1=O)Nc1ncnc2c1nccc2 WDYDSZZBZGTFEP-IBGZPJMESA-N 0.000 description 1
- BMXVCDVGHIZYTN-HNNXBMFYSA-N C[C@@H](C(N1c2ccccc2)=Cc2cccc(Cl)c2C1=O)Nc1c(ccnc2)c2ncn1 Chemical compound C[C@@H](C(N1c2ccccc2)=Cc2cccc(Cl)c2C1=O)Nc1c(ccnc2)c2ncn1 BMXVCDVGHIZYTN-HNNXBMFYSA-N 0.000 description 1
- HBDGMXBEDSNTCX-HNNXBMFYSA-N C[C@@H](C(N1c2ccccc2)=Cc2cccc(Cl)c2C1=O)Nc1cc(O)nc2c1nccc2 Chemical compound C[C@@H](C(N1c2ccccc2)=Cc2cccc(Cl)c2C1=O)Nc1cc(O)nc2c1nccc2 HBDGMXBEDSNTCX-HNNXBMFYSA-N 0.000 description 1
- LJEYBBQHCDNBJW-INIZCTEOSA-N C[C@@H](C(N1c2ccccc2)=Nc2cccc(-c3c[n](C)nc3)c2C1=O)Nc1c2ncccc2nc(N)n1 Chemical compound C[C@@H](C(N1c2ccccc2)=Nc2cccc(-c3c[n](C)nc3)c2C1=O)Nc1c2ncccc2nc(N)n1 LJEYBBQHCDNBJW-INIZCTEOSA-N 0.000 description 1
- VTZNOQULKKVHPI-JTQLQIEISA-N C[C@@H](c1cc2cccc(Cl)c2c(C(N2CCOCC2)=O)n1)N Chemical compound C[C@@H](c1cc2cccc(Cl)c2c(C(N2CCOCC2)=O)n1)N VTZNOQULKKVHPI-JTQLQIEISA-N 0.000 description 1
- OOIGRSVFUGYGNB-UHFFFAOYSA-N Cc1c[n]2nccc(C)c2n1 Chemical compound Cc1c[n]2nccc(C)c2n1 OOIGRSVFUGYGNB-UHFFFAOYSA-N 0.000 description 1
- XULKFQGSMHRNLF-UHFFFAOYSA-N Cc1ccnc2ccn[n]12 Chemical compound Cc1ccnc2ccn[n]12 XULKFQGSMHRNLF-UHFFFAOYSA-N 0.000 description 1
- ZMENDMAMYVBZMD-UHFFFAOYSA-N Cc1ncnc2c1nccc2 Chemical compound Cc1ncnc2c1nccc2 ZMENDMAMYVBZMD-UHFFFAOYSA-N 0.000 description 1
- UKTHPAHJCQLABU-UHFFFAOYSA-N Clc1ncnc2c1ccnc2 Chemical compound Clc1ncnc2c1ccnc2 UKTHPAHJCQLABU-UHFFFAOYSA-N 0.000 description 1
- LBJBQKHZRGKNME-UHFFFAOYSA-N N#Cc(cnc1cccnc11)c1Cl Chemical compound N#Cc(cnc1cccnc11)c1Cl LBJBQKHZRGKNME-UHFFFAOYSA-N 0.000 description 1
- YCHZKMHRQVLCRR-UHFFFAOYSA-N N#Cc(cnc1cccnc11)c1O Chemical compound N#Cc(cnc1cccnc11)c1O YCHZKMHRQVLCRR-UHFFFAOYSA-N 0.000 description 1
- BOOMHTFCWOJWFO-UHFFFAOYSA-N Nc1c(C(O)=O)nccc1 Chemical compound Nc1c(C(O)=O)nccc1 BOOMHTFCWOJWFO-UHFFFAOYSA-N 0.000 description 1
- CUYKNJBYIJFRCU-UHFFFAOYSA-N Nc1cnccc1 Chemical compound Nc1cnccc1 CUYKNJBYIJFRCU-UHFFFAOYSA-N 0.000 description 1
- FSKYZRCACCHDGR-UHFFFAOYSA-N Oc1ncnc2cccnc12 Chemical compound Oc1ncnc2cccnc12 FSKYZRCACCHDGR-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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161509458P | 2011-07-19 | 2011-07-19 | |
| US201161509409P | 2011-07-19 | 2011-07-19 | |
| US201161509474P | 2011-07-19 | 2011-07-19 | |
| US61/509,458 | 2011-07-19 | ||
| US61/509,409 | 2011-07-19 | ||
| US61/509,474 | 2011-07-19 | ||
| US201161562247P | 2011-11-21 | 2011-11-21 | |
| US61/562,247 | 2011-11-21 | ||
| PCT/US2012/047186 WO2013012915A1 (en) | 2011-07-19 | 2012-07-18 | Heterocyclic compounds and uses thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014520887A JP2014520887A (ja) | 2014-08-25 |
| JP2014520887A5 JP2014520887A5 (https=) | 2015-09-10 |
| JP6027610B2 true JP6027610B2 (ja) | 2016-11-16 |
Family
ID=46598987
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014521730A Expired - Fee Related JP6027610B2 (ja) | 2011-07-19 | 2012-07-18 | 複素環式化合物及びその使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US8969363B2 (https=) |
| EP (1) | EP2734520B1 (https=) |
| JP (1) | JP6027610B2 (https=) |
| CN (1) | CN103930422A (https=) |
| AU (1) | AU2012284088B2 (https=) |
| HK (1) | HK1198443A1 (https=) |
| WO (1) | WO2013012915A1 (https=) |
Families Citing this family (104)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0406647A (pt) | 2003-01-06 | 2005-12-06 | Angiochem Inc | Método para transportar um composto através da barreira sanguìnea do cérebro |
| EP3219705B1 (en) | 2005-12-28 | 2020-03-11 | Vertex Pharmaceuticals Incorporated | Pharmaceutical compositions of the amorphous form of n-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide |
| US9365634B2 (en) * | 2007-05-29 | 2016-06-14 | Angiochem Inc. | Aprotinin-like polypeptides for delivering agents conjugated thereto to tissues |
| EP3613743B1 (en) | 2008-01-04 | 2022-03-16 | Intellikine, LLC | Processes for the preparation of 1h-pyrazolo[3,4-d]pyrimidin-4-amine derivatives |
| US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
| TR201905480T4 (tr) | 2008-04-18 | 2019-05-21 | Angiochem Inc | Paklitaksel, paklitaksel analogları veya paklitaksel konjugatlarının farmasötik bileşimleri ve ilgili preparasyon ve kullanım yöntemleri. |
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| WO2013012915A9 (en) | 2013-03-28 |
| HK1198443A1 (en) | 2015-04-24 |
| JP2014520887A (ja) | 2014-08-25 |
| US20130029982A1 (en) | 2013-01-31 |
| EP2734520A1 (en) | 2014-05-28 |
| AU2012284088A1 (en) | 2013-03-21 |
| US9718815B2 (en) | 2017-08-01 |
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| R250 | Receipt of annual fees |
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