JP6896715B2 - セピアプテリン還元酵素としてのヘテロアリール誘導体 - Google Patents
セピアプテリン還元酵素としてのヘテロアリール誘導体 Download PDFInfo
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- JP6896715B2 JP6896715B2 JP2018517345A JP2018517345A JP6896715B2 JP 6896715 B2 JP6896715 B2 JP 6896715B2 JP 2018517345 A JP2018517345 A JP 2018517345A JP 2018517345 A JP2018517345 A JP 2018517345A JP 6896715 B2 JP6896715 B2 JP 6896715B2
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- Prior art keywords
- mmol
- alkylene
- methyl
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- 0 CC([C-]=*)(OC(N(C(CC1)C2)C1C=C2c1ccccc1)=O)I=N Chemical compound CC([C-]=*)(OC(N(C(CC1)C2)C1C=C2c1ccccc1)=O)I=N 0.000 description 23
- VFBNJJZKAXQVRU-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCN1C(C(C1)(C2)CC12C(OC)=O)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CCN1C(C(C1)(C2)CC12C(OC)=O)=O)=O VFBNJJZKAXQVRU-UHFFFAOYSA-N 0.000 description 1
- GPHGETSVSBZRQC-UHFFFAOYSA-N CC(N1)=NC(CCC2)=C2C1=O Chemical compound CC(N1)=NC(CCC2)=C2C1=O GPHGETSVSBZRQC-UHFFFAOYSA-N 0.000 description 1
- HALUNHIFIXLLOE-UHFFFAOYSA-N CCOC(c1ncc(C(N(CC2)CCC2C(F)(F)F)=O)[s]1)=O Chemical compound CCOC(c1ncc(C(N(CC2)CCC2C(F)(F)F)=O)[s]1)=O HALUNHIFIXLLOE-UHFFFAOYSA-N 0.000 description 1
- RUYVPGSLDVENCT-UHFFFAOYSA-N CCOc1ccc(COc2nc(Cl)nc(C)c2)cc1 Chemical compound CCOc1ccc(COc2nc(Cl)nc(C)c2)cc1 RUYVPGSLDVENCT-UHFFFAOYSA-N 0.000 description 1
- CJEBYTJVBNWEHA-UHFFFAOYSA-N CCc1nc(OCC[IH]CC)nc(-c2c[n](CCC(N(CC3)Cc4c3cccc4)=O)nc2)c1 Chemical compound CCc1nc(OCC[IH]CC)nc(-c2c[n](CCC(N(CC3)Cc4c3cccc4)=O)nc2)c1 CJEBYTJVBNWEHA-UHFFFAOYSA-N 0.000 description 1
- KKHFCYJOZSYPBJ-UHFFFAOYSA-N CN1C(c(cc2)ncc2C(OC)=O)=NC(CCC2)=C2C1=O Chemical compound CN1C(c(cc2)ncc2C(OC)=O)=NC(CCC2)=C2C1=O KKHFCYJOZSYPBJ-UHFFFAOYSA-N 0.000 description 1
- YQLLVJWZYPCFGE-UHFFFAOYSA-N CN1CCC(CC(F)(F)F)CC1 Chemical compound CN1CCC(CC(F)(F)F)CC1 YQLLVJWZYPCFGE-UHFFFAOYSA-N 0.000 description 1
- VVYWSEKJVXXTQL-UHFFFAOYSA-N COC(CN(CC=C)Cc1ccccc1)=O Chemical compound COC(CN(CC=C)Cc1ccccc1)=O VVYWSEKJVXXTQL-UHFFFAOYSA-N 0.000 description 1
- UAWVZBDVSNLPDT-UHFFFAOYSA-N COC(CNCc1ccccc1)=O Chemical compound COC(CNCc1ccccc1)=O UAWVZBDVSNLPDT-UHFFFAOYSA-N 0.000 description 1
- SKTCDJAMAYNROS-UHFFFAOYSA-N COC1CCCC1 Chemical compound COC1CCCC1 SKTCDJAMAYNROS-UHFFFAOYSA-N 0.000 description 1
- MSHFRERJPWKJFX-UHFFFAOYSA-N COc1ccc(CO)cc1 Chemical compound COc1ccc(CO)cc1 MSHFRERJPWKJFX-UHFFFAOYSA-N 0.000 description 1
- ZKISZUHEMYJWLL-UHFFFAOYSA-N COc1ccc(COc2c(CCC3)c3nc(Cl)n2)cc1 Chemical compound COc1ccc(COc2c(CCC3)c3nc(Cl)n2)cc1 ZKISZUHEMYJWLL-UHFFFAOYSA-N 0.000 description 1
- NLJMATZRBFTTED-UHFFFAOYSA-N CSC(NC1=O)=N[n]2c1cc(F)c2 Chemical compound CSC(NC1=O)=N[n]2c1cc(F)c2 NLJMATZRBFTTED-UHFFFAOYSA-N 0.000 description 1
- AVQWHVUSEVULRH-UHFFFAOYSA-N C[ClH]c1nc(Cl)c(CCC2)c2n1 Chemical compound C[ClH]c1nc(Cl)c(CCC2)c2n1 AVQWHVUSEVULRH-UHFFFAOYSA-N 0.000 description 1
- XRIXMJIDGDXUGR-UHFFFAOYSA-N Cc([n](-c1nc(Cl)cc(C(F)(F)F)c1)nc1)c1C(OC)=O Chemical compound Cc([n](-c1nc(Cl)cc(C(F)(F)F)c1)nc1)c1C(OC)=O XRIXMJIDGDXUGR-UHFFFAOYSA-N 0.000 description 1
- DNBXGOZMZFHGGA-UHFFFAOYSA-N Cc([n](-c1nc(OCc2ccccc2)cc(C)c1)nc1)c1C(N(CC1)CCC1C(F)(F)I)=O Chemical compound Cc([n](-c1nc(OCc2ccccc2)cc(C)c1)nc1)c1C(N(CC1)CCC1C(F)(F)I)=O DNBXGOZMZFHGGA-UHFFFAOYSA-N 0.000 description 1
- BQSZGJDWGLSGSW-UHFFFAOYSA-N Cc([n](C(N1)=NC(CCC2)=C2C1=O)nc1)c1C(N(CC1)CC11NCCCC1)=O Chemical compound Cc([n](C(N1)=NC(CCC2)=C2C1=O)nc1)c1C(N(CC1)CC11NCCCC1)=O BQSZGJDWGLSGSW-UHFFFAOYSA-N 0.000 description 1
- GZUTVXROFWKPMA-UHFFFAOYSA-N Cc([n](C(N1)=NC(CCC2)=C2C1=O)nc1)c1C(N(CC1)CCN1C(C(C1)(C2)CC12C(OC)=O)=O)=O Chemical compound Cc([n](C(N1)=NC(CCC2)=C2C1=O)nc1)c1C(N(CC1)CCN1C(C(C1)(C2)CC12C(OC)=O)=O)=O GZUTVXROFWKPMA-UHFFFAOYSA-N 0.000 description 1
- FOVMFFNMVBGMPX-UHFFFAOYSA-N Cc([n](CCC(N(CC1)Cc2c1cccc2)=O)nc1C)c1C(N1)=NC(C)=CC1=O Chemical compound Cc([n](CCC(N(CC1)Cc2c1cccc2)=O)nc1C)c1C(N1)=NC(C)=CC1=O FOVMFFNMVBGMPX-UHFFFAOYSA-N 0.000 description 1
- CHEJMOJRCXKTCT-UHFFFAOYSA-N Cc(c(C(N(CC1)CCC1C(F)(F)F)=O)c1)n[n]1C(N1)=NC(C)=CC1=O Chemical compound Cc(c(C(N(CC1)CCC1C(F)(F)F)=O)c1)n[n]1C(N1)=NC(C)=CC1=O CHEJMOJRCXKTCT-UHFFFAOYSA-N 0.000 description 1
- UCESXSXUTBAJHN-UHFFFAOYSA-N Cc(c(C(N(CC1)CCC1C(F)(F)I)=O)c1)n[n]1-c1nc(OCc2ccccc2)cc(C)c1 Chemical compound Cc(c(C(N(CC1)CCC1C(F)(F)I)=O)c1)n[n]1-c1nc(OCc2ccccc2)cc(C)c1 UCESXSXUTBAJHN-UHFFFAOYSA-N 0.000 description 1
- XFWMFDQQOXFBNP-UHFFFAOYSA-N Cc(c(C(O)=O)c1)n[n]1C(N1)=NC(C)=CC1=O Chemical compound Cc(c(C(O)=O)c1)n[n]1C(N1)=NC(C)=CC1=O XFWMFDQQOXFBNP-UHFFFAOYSA-N 0.000 description 1
- GLMMFDNBWVECMO-UHFFFAOYSA-N Cc1c(C(N(CC2)CCC2C(F)(F)F)=O)c(C(N)=O)n[n]1C(N1)=NC(CCC2)=C2C1=O Chemical compound Cc1c(C(N(CC2)CCC2C(F)(F)F)=O)c(C(N)=O)n[n]1C(N1)=NC(CCC2)=C2C1=O GLMMFDNBWVECMO-UHFFFAOYSA-N 0.000 description 1
- QILMJBQZJMBKEF-UHFFFAOYSA-N Cc1c(C(O)=O)c(C(N)=O)n[n]1C(N1)=NC(CCC2)=C2C1=O Chemical compound Cc1c(C(O)=O)c(C(N)=O)n[n]1C(N1)=NC(CCC2)=C2C1=O QILMJBQZJMBKEF-UHFFFAOYSA-N 0.000 description 1
- SZQCPPRPWDXLMM-UHFFFAOYSA-N Cc1c[n](C)nc1 Chemical compound Cc1c[n](C)nc1 SZQCPPRPWDXLMM-UHFFFAOYSA-N 0.000 description 1
- XBNQFSRYSDCLQZ-UHFFFAOYSA-N Clc1nc([nH]nc2)c2c(OCc2ccccc2)n1 Chemical compound Clc1nc([nH]nc2)c2c(OCc2ccccc2)n1 XBNQFSRYSDCLQZ-UHFFFAOYSA-N 0.000 description 1
- IDQGJZBQOYSDJH-UHFFFAOYSA-N N#CC(CC1)(CCN1C(c1c[n](C(NC2=O)=Nc3c2[s]cc3)nc1)=O)c1ccccc1 Chemical compound N#CC(CC1)(CCN1C(c1c[n](C(NC2=O)=Nc3c2[s]cc3)nc1)=O)c1ccccc1 IDQGJZBQOYSDJH-UHFFFAOYSA-N 0.000 description 1
- YNGWGJGOTQQSOU-UHFFFAOYSA-N N#Cc1nccc(C(Oc2ccccc2)=O)c1 Chemical compound N#Cc1nccc(C(Oc2ccccc2)=O)c1 YNGWGJGOTQQSOU-UHFFFAOYSA-N 0.000 description 1
- GQGHNHXCLCHVIH-UHFFFAOYSA-N O=C(c1ccc(C(N2)=NC(CCC3)=C3C2=O)[s]1)N(CC1)CCC1C(F)(F)F Chemical compound O=C(c1ccc(C(N2)=NC(CCC3)=C3C2=O)[s]1)N(CC1)CCC1C(F)(F)F GQGHNHXCLCHVIH-UHFFFAOYSA-N 0.000 description 1
- MJCTXWDVTKYWRE-UHFFFAOYSA-N O=C1NC(Cl)=NC2=C1CCC2 Chemical compound O=C1NC(Cl)=NC2=C1CCC2 MJCTXWDVTKYWRE-UHFFFAOYSA-N 0.000 description 1
- HUMNYLRZRPPJDN-UHFFFAOYSA-N O=Cc1ccccc1 Chemical compound O=Cc1ccccc1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 1
- COIVMDCJOCXENS-UHFFFAOYSA-N OC(c1ccc(C(N2)=NC(CCC3)=C3C2=O)[s]1)=O Chemical compound OC(c1ccc(C(N2)=NC(CCC3)=C3C2=O)[s]1)=O COIVMDCJOCXENS-UHFFFAOYSA-N 0.000 description 1
- ROZUZZWOTMMUTR-UHFFFAOYSA-N OC1(CC(CC2)NC2C1)c1ccccc1 Chemical compound OC1(CC(CC2)NC2C1)c1ccccc1 ROZUZZWOTMMUTR-UHFFFAOYSA-N 0.000 description 1
- WAYNFUALTYDWRJ-RYUDHWBXSA-N O[C@]1(C2)[C@@H]2CN(Cc2ccccc2)C1 Chemical compound O[C@]1(C2)[C@@H]2CN(Cc2ccccc2)C1 WAYNFUALTYDWRJ-RYUDHWBXSA-N 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
-
- 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
-
- 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
- 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
- C07D487/08—Bridged systems
-
- 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
- C07D487/10—Spiro-condensed systems
-
- 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
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
-
- 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
-
- 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)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (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 |
|---|---|---|---|
| US201562235191P | 2015-09-30 | 2015-09-30 | |
| US62/235,191 | 2015-09-30 | ||
| PCT/US2016/054657 WO2017059191A1 (en) | 2015-09-30 | 2016-09-30 | Heteroaryl derivatives as sepiapterin reductase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018529739A JP2018529739A (ja) | 2018-10-11 |
| JP2018529739A5 JP2018529739A5 (enExample) | 2019-11-14 |
| JP6896715B2 true JP6896715B2 (ja) | 2021-06-30 |
Family
ID=57133442
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018517345A Active JP6896715B2 (ja) | 2015-09-30 | 2016-09-30 | セピアプテリン還元酵素としてのヘテロアリール誘導体 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9963462B2 (enExample) |
| EP (1) | EP3356345B1 (enExample) |
| JP (1) | JP6896715B2 (enExample) |
| CA (1) | CA3038280A1 (enExample) |
| DK (1) | DK3356345T3 (enExample) |
| ES (1) | ES2969565T3 (enExample) |
| WO (1) | WO2017059191A1 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG11201804901WA (en) | 2015-12-22 | 2018-07-30 | SHY Therapeutics LLC | Compounds for the treatment of cancer and inflammatory disease |
| CA3066939A1 (en) | 2017-06-21 | 2018-12-27 | SHY Therapeutics LLC | Compounds that interact with the ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease |
| CN107312011A (zh) * | 2017-06-29 | 2017-11-03 | 上海药明康德新药开发有限公司 | 外消旋‑7‑叔丁氧基羰基‑1‑氧亚基‑2,7‑二氮杂螺壬烷‑4‑羧酸的合成方法 |
| CN107817307B (zh) * | 2017-11-01 | 2020-12-25 | 重庆华邦制药有限公司 | Hplc法分离测定帕司烟肼及其相关杂质的方法 |
| WO2019145174A1 (en) | 2018-01-23 | 2019-08-01 | Basf Se | Preparation of optionally substituted 5-substituted pyridine |
| CN111630033A (zh) | 2018-01-23 | 2020-09-04 | 巴斯夫欧洲公司 | 任选取代的二氢异喹啉的制备 |
| US11591312B2 (en) | 2018-01-23 | 2023-02-28 | Basf Se | Halogenation of pyridine derivatives |
| WO2019145177A1 (en) | 2018-01-23 | 2019-08-01 | Basf Se | Bromination of pyridine derivatives |
| WO2019175332A1 (en) | 2018-03-14 | 2019-09-19 | Imba - Institut Für Molekulare Biotechnologie Gmbh | Bh4 pathway inhibition and use thereof for treating t-cell mediated autoimmune diseases or hypersensitivity |
| TWI803696B (zh) * | 2018-09-14 | 2023-06-01 | 日商橘生藥品工業股份有限公司 | 次黃嘌呤化合物 |
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| EP3356345A1 (en) | 2018-08-08 |
| EP3356345B1 (en) | 2023-11-08 |
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| US9963462B2 (en) | 2018-05-08 |
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