JP6475158B2 - Mnk1およびmnk2調節剤としての二環式ヘテロアリール誘導体、およびその使用 - Google Patents
Mnk1およびmnk2調節剤としての二環式ヘテロアリール誘導体、およびその使用 Download PDFInfo
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- JP6475158B2 JP6475158B2 JP2015503165A JP2015503165A JP6475158B2 JP 6475158 B2 JP6475158 B2 JP 6475158B2 JP 2015503165 A JP2015503165 A JP 2015503165A JP 2015503165 A JP2015503165 A JP 2015503165A JP 6475158 B2 JP6475158 B2 JP 6475158B2
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- certain embodiments
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- pyrazin
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- 0 CCCC(C)(C*c(cc1C)ccc1I)**(C=*C(C(**C(N)=C1*)=C1[U])=*1)*1=I Chemical compound CCCC(C)(C*c(cc1C)ccc1I)**(C=*C(C(**C(N)=C1*)=C1[U])=*1)*1=I 0.000 description 12
- IYBFVRUXEKUNNQ-UHFFFAOYSA-N BrC1=CCCC=C1 Chemical compound BrC1=CCCC=C1 IYBFVRUXEKUNNQ-UHFFFAOYSA-N 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N C1NCCOC1 Chemical compound C1NCCOC1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- NNCRPGCQBWRZRT-UHFFFAOYSA-N CC(C)N(CC1)CCN1C(c(cc1)ccc1-c(nc1)c[n]2c1ncc2-c(cc1)ccc1C#N)=O Chemical compound CC(C)N(CC1)CCN1C(c(cc1)ccc1-c(nc1)c[n]2c1ncc2-c(cc1)ccc1C#N)=O NNCRPGCQBWRZRT-UHFFFAOYSA-N 0.000 description 1
- MMLFTVNOTKOBQP-UHFFFAOYSA-N CN(C)C(CC1)CCN1C(c(cc1)ccc1-c(cc[n]1nc2)nc1c2-c(cc1)ccc1C#N)=O Chemical compound CN(C)C(CC1)CCN1C(c(cc1)ccc1-c(cc[n]1nc2)nc1c2-c(cc1)ccc1C#N)=O MMLFTVNOTKOBQP-UHFFFAOYSA-N 0.000 description 1
- MZZHWIKSBQQXPM-UHFFFAOYSA-N CN(CC1)CCN1C(c(ccc(-c(cc1)c[n]2c1ncc2-c(cc1)ccc1C#N)c1)c1Cl)=O Chemical compound CN(CC1)CCN1C(c(ccc(-c(cc1)c[n]2c1ncc2-c(cc1)ccc1C#N)c1)c1Cl)=O MZZHWIKSBQQXPM-UHFFFAOYSA-N 0.000 description 1
- LYTGYBKKCRNLRM-UHFFFAOYSA-N CN(CCC1)CCN1C(C(CC1)=CC=C1c(cc1)c[n]2c1ncc2-c(cc1)ccc1C#N)=O Chemical compound CN(CCC1)CCN1C(C(CC1)=CC=C1c(cc1)c[n]2c1ncc2-c(cc1)ccc1C#N)=O LYTGYBKKCRNLRM-UHFFFAOYSA-N 0.000 description 1
- RHHZMNYARSYVAH-UHFFFAOYSA-N CNc(cc(cc1)-c2c[n]3s(C(CSC4)=CC=C4C#N)cnc3cc2)c1C(N1CCN(C)CC1)=O Chemical compound CNc(cc(cc1)-c2c[n]3s(C(CSC4)=CC=C4C#N)cnc3cc2)c1C(N1CCN(C)CC1)=O RHHZMNYARSYVAH-UHFFFAOYSA-N 0.000 description 1
- KDMIMSVULGCVRU-UHFFFAOYSA-N CS(NC(CC1)CCN1C(c(cc1)ccc1-c(cc1)c[n]2c1ncc2-c(cc1)ccc1C#N)=O)(=O)=O Chemical compound CS(NC(CC1)CCN1C(c(cc1)ccc1-c(cc1)c[n]2c1ncc2-c(cc1)ccc1C#N)=O)(=O)=O KDMIMSVULGCVRU-UHFFFAOYSA-N 0.000 description 1
- XBKLZTRLWNSRBO-UHFFFAOYSA-N N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)cc(CN(C(c2ccccc22)=O)C2=O)c1C(N1CCOCC1)=O Chemical compound N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)cc(CN(C(c2ccccc22)=O)C2=O)c1C(N1CCOCC1)=O XBKLZTRLWNSRBO-UHFFFAOYSA-N 0.000 description 1
- BSPHAHZHXYDNOR-UHFFFAOYSA-N N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)ccc1C(N(CC1)CCC1N1CCNCC1)=O Chemical compound N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)ccc1C(N(CC1)CCC1N1CCNCC1)=O BSPHAHZHXYDNOR-UHFFFAOYSA-N 0.000 description 1
- JMEPKLCDLMXURZ-UHFFFAOYSA-N N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)ccc1C(N(CC1)CCC1NC(C(F)(F)F)=O)=O Chemical compound N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)ccc1C(N(CC1)CCC1NC(C(F)(F)F)=O)=O JMEPKLCDLMXURZ-UHFFFAOYSA-N 0.000 description 1
- OMLINGDSSXAOLB-UHFFFAOYSA-N N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)ccc1C(N1CCN(Cc2ccccc2)CC1)=O Chemical compound N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)ccc1C(N1CCN(Cc2ccccc2)CC1)=O OMLINGDSSXAOLB-UHFFFAOYSA-N 0.000 description 1
- XIQUTCDRLNPPCT-UHFFFAOYSA-N N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)ccc1C(NCCN1CCOCC1)=O Chemical compound N#Cc(cc1)ccc1-c1cnc(cc2)[n]1cc2-c(cc1)ccc1C(NCCN1CCOCC1)=O XIQUTCDRLNPPCT-UHFFFAOYSA-N 0.000 description 1
- FWEWVNHDCXMKLM-UHFFFAOYSA-N N#Cc(cc1)ccc1-c1cnc(cc2)[n]1nc2-c(cc1)ccc1C(N1CCOCCC1)=O Chemical compound N#Cc(cc1)ccc1-c1cnc(cc2)[n]1nc2-c(cc1)ccc1C(N1CCOCCC1)=O FWEWVNHDCXMKLM-UHFFFAOYSA-N 0.000 description 1
- ZGBQVYAZQQXVGT-UHFFFAOYSA-N O=C(c(cc1)ccc1-c(cc1)n[n]2c1ncc2-c(cc1)cc(C2)c1NC2=O)N1CCNCC1 Chemical compound O=C(c(cc1)ccc1-c(cc1)n[n]2c1ncc2-c(cc1)cc(C2)c1NC2=O)N1CCNCC1 ZGBQVYAZQQXVGT-UHFFFAOYSA-N 0.000 description 1
- QTNFZHRNSIPSLB-UHFFFAOYSA-N O=C(c(cc1)ccc1-c(cc1)n[n]2c1ncc2C(CC1)=CC(C2)=C1NC2=O)N(CC1)CCC11NCCCC1 Chemical compound O=C(c(cc1)ccc1-c(cc1)n[n]2c1ncc2C(CC1)=CC(C2)=C1NC2=O)N(CC1)CCC11NCCCC1 QTNFZHRNSIPSLB-UHFFFAOYSA-N 0.000 description 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N O=C(c1ccccc11)NC1=O Chemical compound O=C(c1ccccc11)NC1=O XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
- IUSPXLCLQIZFHL-UHFFFAOYSA-N O=C1OCc2cc(Br)ccc12 Chemical compound O=C1OCc2cc(Br)ccc12 IUSPXLCLQIZFHL-UHFFFAOYSA-N 0.000 description 1
- BGFLONLHLQLSPF-UHFFFAOYSA-N OC(N1CCOCC1)O Chemical compound OC(N1CCOCC1)O BGFLONLHLQLSPF-UHFFFAOYSA-N 0.000 description 1
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- 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
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- 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
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- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- 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
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
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- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- 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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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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- A—HUMAN NECESSITIES
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- 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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- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1205669.3 | 2012-03-30 | ||
| GBGB1205669.3A GB201205669D0 (en) | 2012-03-30 | 2012-03-30 | Bicyclic heterocyclic derivatives as mnk2 and mnk2 modulators and uses thereof |
| PCT/SG2013/000126 WO2013147711A1 (en) | 2012-03-30 | 2013-04-01 | Bicyclic heterocyclic derivatives as mnk1 and mnk2 modulators and uses thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018206109A Division JP6662984B2 (ja) | 2012-03-30 | 2018-10-31 | Mnk1およびmnk2調節剤としての二環式ヘテロアリール誘導体、およびその使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015511638A JP2015511638A (ja) | 2015-04-20 |
| JP2015511638A5 JP2015511638A5 (enExample) | 2016-06-09 |
| JP6475158B2 true JP6475158B2 (ja) | 2019-02-27 |
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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015503165A Active JP6475158B2 (ja) | 2012-03-30 | 2013-04-01 | Mnk1およびmnk2調節剤としての二環式ヘテロアリール誘導体、およびその使用 |
| JP2018206109A Active JP6662984B2 (ja) | 2012-03-30 | 2018-10-31 | Mnk1およびmnk2調節剤としての二環式ヘテロアリール誘導体、およびその使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018206109A Active JP6662984B2 (ja) | 2012-03-30 | 2018-10-31 | Mnk1およびmnk2調節剤としての二環式ヘテロアリール誘導体、およびその使用 |
Country Status (14)
| Country | Link |
|---|---|
| US (3) | US9908886B2 (enExample) |
| EP (2) | EP2831079B1 (enExample) |
| JP (2) | JP6475158B2 (enExample) |
| KR (1) | KR102153320B1 (enExample) |
| CN (1) | CN104350055B (enExample) |
| AU (2) | AU2013240612B2 (enExample) |
| BR (1) | BR112014024255B1 (enExample) |
| DK (1) | DK2831079T3 (enExample) |
| ES (2) | ES3034431T3 (enExample) |
| GB (1) | GB201205669D0 (enExample) |
| NO (1) | NO2831079T3 (enExample) |
| PL (2) | PL3321268T3 (enExample) |
| SG (2) | SG10201706594PA (enExample) |
| WO (1) | WO2013147711A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2019031560A (ja) * | 2012-03-30 | 2019-02-28 | エージェンシー フォー サイエンス,テクノロジー アンド リサーチ | Mnk1およびmnk2調節剤としての二環式ヘテロアリール誘導体、およびその使用 |
Families Citing this family (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013142817A2 (en) | 2012-03-23 | 2013-09-26 | Dennis Brown | Compositions and methods to improve the therapeutic benefit of indirubin and analogs thereof, including meisoindigo |
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| JP2019031560A (ja) * | 2012-03-30 | 2019-02-28 | エージェンシー フォー サイエンス,テクノロジー アンド リサーチ | Mnk1およびmnk2調節剤としての二環式ヘテロアリール誘導体、およびその使用 |
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