JP2018505207A - 置換モノおよびポリアザナフタレン誘導体およびその使用 - Google Patents
置換モノおよびポリアザナフタレン誘導体およびその使用 Download PDFInfo
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- JP2018505207A JP2018505207A JP2017542888A JP2017542888A JP2018505207A JP 2018505207 A JP2018505207 A JP 2018505207A JP 2017542888 A JP2017542888 A JP 2017542888A JP 2017542888 A JP2017542888 A JP 2017542888A JP 2018505207 A JP2018505207 A JP 2018505207A
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- MWUOYZRNHSFVEW-UHFFFAOYSA-N NC1CCN(Cc(cc2)cc3c2cncc3-c2cc3cccnc3[o]2)CC1 Chemical compound NC1CCN(Cc(cc2)cc3c2cncc3-c2cc3cccnc3[o]2)CC1 MWUOYZRNHSFVEW-UHFFFAOYSA-N 0.000 description 1
- UJBKDUWYORYGON-UHFFFAOYSA-N NC1CCN(Cc2cc(c(-c3cc4ccccc4[o]3)cnc3)c3c(Cl)c2)CC1 Chemical compound NC1CCN(Cc2cc(c(-c3cc4ccccc4[o]3)cnc3)c3c(Cl)c2)CC1 UJBKDUWYORYGON-UHFFFAOYSA-N 0.000 description 1
- JVBMDNLMFTZWGD-UHFFFAOYSA-N NCCCOCc(ccc1cnc2)cc1c2-c1cc(cccc2)c2[o]1 Chemical compound NCCCOCc(ccc1cnc2)cc1c2-c1cc(cccc2)c2[o]1 JVBMDNLMFTZWGD-UHFFFAOYSA-N 0.000 description 1
- IJHIRCMYZWJUCD-RZDIXWSQSA-N N[C@H](CC1)CC[C@@H]1C(Nc(cc1)cc2c1cncc2-c1cc2ccccc2[o]1)=O Chemical compound N[C@H](CC1)CC[C@@H]1C(Nc(cc1)cc2c1cncc2-c1cc2ccccc2[o]1)=O IJHIRCMYZWJUCD-RZDIXWSQSA-N 0.000 description 1
- SFKFTULNIAEYML-NHCUHLMSSA-N N[C@H](CCN(Cc(cc1)cc2c1cncc2-c1cc(cccc2)c2[o]1)C1)[C@@H]1O Chemical compound N[C@H](CCN(Cc(cc1)cc2c1cncc2-c1cc(cccc2)c2[o]1)C1)[C@@H]1O SFKFTULNIAEYML-NHCUHLMSSA-N 0.000 description 1
- MWYDJLJRXTUMFG-UHFFFAOYSA-N Nc(ncc1c2CC(CNc3ccnc4c3cccc4)C=C1)c2Br Chemical compound Nc(ncc1c2CC(CNc3ccnc4c3cccc4)C=C1)c2Br MWYDJLJRXTUMFG-UHFFFAOYSA-N 0.000 description 1
- BLJNIQDOJJBXIN-UHFFFAOYSA-N Nc1cc(NC(c(cc2)cc3c2nncc3-c2cc3ccccc3[o]2)=O)ccn1 Chemical compound Nc1cc(NC(c(cc2)cc3c2nncc3-c2cc3ccccc3[o]2)=O)ccn1 BLJNIQDOJJBXIN-UHFFFAOYSA-N 0.000 description 1
- CSBAIBZWNJNZSI-UHFFFAOYSA-N Nc1cc(NCc(cc2)cc3c2cncc3-c2cc(cccc3)c3[o]2)ccn1 Chemical compound Nc1cc(NCc(cc2)cc3c2cncc3-c2cc(cccc3)c3[o]2)ccn1 CSBAIBZWNJNZSI-UHFFFAOYSA-N 0.000 description 1
- LNSXSJJODLSNDR-UHFFFAOYSA-N Nc1cc(NCc(cc2)cc3c2nncc3-c2cc3ccccc3[o]2)ccn1 Chemical compound Nc1cc(NCc(cc2)cc3c2nncc3-c2cc3ccccc3[o]2)ccn1 LNSXSJJODLSNDR-UHFFFAOYSA-N 0.000 description 1
- PBYQZNMIZCHOHA-UHFFFAOYSA-N Nc1cc(NCc2ccc3NNCC(c4cc5ccccc5[o]4)c3c2)ccn1 Chemical compound Nc1cc(NCc2ccc3NNCC(c4cc5ccccc5[o]4)c3c2)ccn1 PBYQZNMIZCHOHA-UHFFFAOYSA-N 0.000 description 1
- ILNJKYJEWVVTIK-UHFFFAOYSA-N Nc1ncc(-c2cc(cccc3)c3[o]2)c2c1ccc(NCc1ccncc1)c2 Chemical compound Nc1ncc(-c2cc(cccc3)c3[o]2)c2c1ccc(NCc1ccncc1)c2 ILNJKYJEWVVTIK-UHFFFAOYSA-N 0.000 description 1
- JKOGJIUTDIMESI-UHFFFAOYSA-N Nc1ncc(-c2ccccc2)c2c1ccc(NCC1CCCCC1)c2 Chemical compound Nc1ncc(-c2ccccc2)c2c1ccc(NCC1CCCCC1)c2 JKOGJIUTDIMESI-UHFFFAOYSA-N 0.000 description 1
- XFDYLZVFLLHJGB-UHFFFAOYSA-N Nc1ncc(C2=CC=CCC2)c2c1c(Cl)cc(NC1CCCCC1)c2 Chemical compound Nc1ncc(C2=CC=CCC2)c2c1c(Cl)cc(NC1CCCCC1)c2 XFDYLZVFLLHJGB-UHFFFAOYSA-N 0.000 description 1
- YAMMKKPDFJQLOS-UHFFFAOYSA-N O=C(c1c2cccc1)N(CCCOCc(cc1)cc3c1cncc3-c1cc(cccc3)c3[o]1)C2=O Chemical compound O=C(c1c2cccc1)N(CCCOCc(cc1)cc3c1cncc3-c1cc(cccc3)c3[o]1)C2=O YAMMKKPDFJQLOS-UHFFFAOYSA-N 0.000 description 1
- KXOCXDDVIWYCNY-UHFFFAOYSA-N O=Cc(cc1)nc2c1cncc2-c1cc(cccc2)c2[o]1 Chemical compound O=Cc(cc1)nc2c1cncc2-c1cc(cccc2)c2[o]1 KXOCXDDVIWYCNY-UHFFFAOYSA-N 0.000 description 1
- COIQUVGFTILYGA-UHFFFAOYSA-N OB(c(cc1)ccc1O)O Chemical compound OB(c(cc1)ccc1O)O COIQUVGFTILYGA-UHFFFAOYSA-N 0.000 description 1
- PKRRNTJIHGOMRC-UHFFFAOYSA-N OB(c1cc2ccccc2[o]1)O Chemical compound OB(c1cc2ccccc2[o]1)O PKRRNTJIHGOMRC-UHFFFAOYSA-N 0.000 description 1
- UDIUXGQYPTZDSM-UHFFFAOYSA-N OC(c(cc1)cc2c1cncc2-c(cc1)ccc1OCc1ccccc1)=O Chemical compound OC(c(cc1)cc2c1cncc2-c(cc1)ccc1OCc1ccccc1)=O UDIUXGQYPTZDSM-UHFFFAOYSA-N 0.000 description 1
- BCNQTHDKDMYAPU-UHFFFAOYSA-N OC(c(cc1)cc2c1nncc2-c1cc(cccc2)c2[o]1)=O Chemical compound OC(c(cc1)cc2c1nncc2-c1cc(cccc2)c2[o]1)=O BCNQTHDKDMYAPU-UHFFFAOYSA-N 0.000 description 1
- OZZMWXQJCJUCEJ-UHFFFAOYSA-N OC(c(cc1)nc2c1cncc2)=O Chemical compound OC(c(cc1)nc2c1cncc2)=O OZZMWXQJCJUCEJ-UHFFFAOYSA-N 0.000 description 1
- ISJKXVUODLFGIU-UHFFFAOYSA-N OC(c(cc1)nc2c1cncc2Br)=O Chemical compound OC(c(cc1)nc2c1cncc2Br)=O ISJKXVUODLFGIU-UHFFFAOYSA-N 0.000 description 1
- SGKANYYYKALPHW-UHFFFAOYSA-N OCc(cc(c1cnc2)Cl)cc1c2Br Chemical compound OCc(cc(c1cnc2)Cl)cc1c2Br SGKANYYYKALPHW-UHFFFAOYSA-N 0.000 description 1
- WUHWDJHEXXOMSF-UHFFFAOYSA-N O[N+](c1cc2cccc(Br)c2cc1CBr)=O Chemical compound O[N+](c1cc2cccc(Br)c2cc1CBr)=O WUHWDJHEXXOMSF-UHFFFAOYSA-N 0.000 description 1
- RWBNRWZCKKATBH-UHFFFAOYSA-N [O-][N+](c1cc2cncc(Br)c2cc1CBr)=O Chemical compound [O-][N+](c1cc2cncc(Br)c2cc1CBr)=O RWBNRWZCKKATBH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero 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
- A61K31/435—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
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- 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
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/04—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
- C07D215/06—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms having only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
- C07D217/04—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/28—Cinnolines
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D401/10—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 carbon chain containing aromatic rings
-
- 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
- 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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- 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
- 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
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
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- Chemical & Material Sciences (AREA)
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- Life Sciences & Earth Sciences (AREA)
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- Public Health (AREA)
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- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
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| EP15197976.2 | 2015-12-04 | ||
| PCT/EP2016/052828 WO2016128465A1 (en) | 2015-02-11 | 2016-02-10 | Substituted mono- and polyazanaphthalene derivatives and their use |
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| JP2018505207A true JP2018505207A (ja) | 2018-02-22 |
| JP2018505207A5 JP2018505207A5 (enExample) | 2019-03-14 |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2023535096A (ja) * | 2020-07-23 | 2023-08-15 | シトシンラボ セラピューティクス カンパニー, リミテッド | キナーゼ阻害活性を有する化合物 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014100719A2 (en) | 2012-12-21 | 2014-06-26 | Epizyme, Inc. | Prmt5 inhibitors and uses thereof |
| CN106674085B (zh) * | 2016-12-20 | 2020-06-23 | 苏州汉德创宏生化科技有限公司 | N-1,3-二氟异丙基-4-氨基哌啶类化合物的合成方法 |
| CN108033909A (zh) * | 2017-12-20 | 2018-05-15 | 北京六合宁远科技有限公司 | 一种6-甲基-4-溴-异喹啉的制备方法 |
| CN108373443A (zh) * | 2018-05-25 | 2018-08-07 | 陈海鹏 | 一种含金刚烷取代基的吡啶类化合物及其在制备抗肿瘤药物中的用途 |
| CN108484489A (zh) * | 2018-05-25 | 2018-09-04 | 陈海鹏 | 一种含金刚烷取代基的吡啶类化合物及其在制备抗肿瘤药物中的用途 |
| CN108774167A (zh) * | 2018-05-25 | 2018-11-09 | 陈海鹏 | 一种含金刚烷取代基的吡啶类化合物及其在制备抗肿瘤药物中的用途 |
| CN110903286B (zh) * | 2019-12-16 | 2021-09-24 | 沈阳药科大学 | 4,6-双取代吡啶[3,2-d]嘧啶类化合物及其制备和应用 |
| US11753413B2 (en) | 2020-06-19 | 2023-09-12 | Incyte Corporation | Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors |
| US11691971B2 (en) | 2020-06-19 | 2023-07-04 | Incyte Corporation | Naphthyridinone compounds as JAK2 V617F inhibitors |
| SI4175719T1 (sl) | 2020-07-02 | 2025-07-31 | Incyte Corporation | Triciklične sečninske spojine kot zaviralci jak2 v617f |
| US11767323B2 (en) | 2020-07-02 | 2023-09-26 | Incyte Corporation | Tricyclic pyridone compounds as JAK2 V617F inhibitors |
| WO2022026380A1 (en) * | 2020-07-29 | 2022-02-03 | Board Of Regents, The University Of Texas System | Urea inhibitors of micro-rna |
| US11661422B2 (en) | 2020-08-27 | 2023-05-30 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
| WO2022140231A1 (en) | 2020-12-21 | 2022-06-30 | Incyte Corporation | Deazaguaine compounds as jak2 v617f inhibitors |
| CN112876412B (zh) * | 2021-01-21 | 2022-05-24 | 温州大学 | 掺杂发光材料及其制备方法和应用 |
| US11958861B2 (en) | 2021-02-25 | 2024-04-16 | Incyte Corporation | Spirocyclic lactams as JAK2 V617F inhibitors |
| WO2023143344A1 (zh) * | 2022-01-30 | 2023-08-03 | 微境生物医药科技(上海)有限公司 | 新型egfr抑制剂 |
| US12084430B2 (en) | 2022-03-17 | 2024-09-10 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
| WO2024079733A1 (en) * | 2022-10-12 | 2024-04-18 | Adama Makhteshim Ltd. | Process for the preparation of aminopyridazine derivatives |
| AR131541A1 (es) | 2023-01-07 | 2025-04-09 | Syngenta Crop Protection Ag | Compuestos de carboxamida novedosos |
| WO2025109114A1 (en) | 2023-11-24 | 2025-05-30 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| WO2025149637A1 (en) | 2024-01-12 | 2025-07-17 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
| WO2025149629A1 (en) | 2024-01-12 | 2025-07-17 | Syngenta Crop Protection Ag | Novel carboxamide compounds |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008509151A (ja) * | 2004-08-03 | 2008-03-27 | セレネックス, インコーポレイテッド | 2,8−二置換ナフチリジン誘導体 |
| JP2012519211A (ja) * | 2009-03-02 | 2012-08-23 | サートリス ファーマシューティカルズ, インコーポレイテッド | サーチュイン調節化合物としての8−置換キノリンおよび関連類似体 |
| WO2014079787A1 (en) * | 2012-11-20 | 2014-05-30 | F. Hoffmann-La Roche Ag | Substituted 1,6-naphthyridines |
| WO2014177596A1 (en) * | 2013-05-03 | 2014-11-06 | F. Hoffmann-La Roche Ag | Neurogenesis-stimulating isoquinoline derivatives |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK0584222T3 (da) | 1991-05-10 | 1998-02-23 | Rhone Poulenc Rorer Int | Bis-mono- og bicycliske aryl- og heteroarylforbindelser, som inhiberer EGF- og/eller PDGF-receptor-tyrosinkinase |
| US5451596A (en) | 1992-12-29 | 1995-09-19 | Rhone Poulenc Rorer Pharmaceuticals Inc. | Cycloalkyl amine bis-aryl squalene synthase inhibitors |
| MX226123B (es) | 1999-09-17 | 2005-02-07 | Millennium Pharm Inc | Benzamidas e inhibidores del factor xa relacionadas. |
| EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
| WO2004087153A2 (en) | 2003-03-28 | 2004-10-14 | Chiron Corporation | Use of organic compounds for immunopotentiation |
| PE20050952A1 (es) | 2003-09-24 | 2005-12-19 | Novartis Ag | Derivados de isoquinolina como inhibidores de b-raf |
| JP2009528365A (ja) * | 2006-02-28 | 2009-08-06 | アムゲン インコーポレイティッド | ホスホジエステラーゼ10阻害剤としてのシンノリン及びキナゾリン誘導体 |
| US20090099175A1 (en) * | 2006-03-01 | 2009-04-16 | Arrington Mark P | Phosphodiesterase 10 inhibitors |
| MX2008011257A (es) | 2006-03-08 | 2008-09-25 | Amgen Inc | Derivados de quinolina e isoquinolina como inhibidores de fosfodiesterasa 10. |
| WO2009025823A1 (en) * | 2007-08-21 | 2009-02-26 | Amgen Inc. | Phosphodiesterase 10 inhibitors |
| GB0905441D0 (en) | 2009-03-30 | 2009-05-13 | Syngenta Ltd | Herbicidal compounds |
| BRPI1013988A2 (pt) * | 2009-04-06 | 2016-04-05 | Daiichi Sankyo Co Ltd | composto, composição farmacêutica , e, uso de um composto ou um sal farmacologicamente aceitável do mesmo |
| TW201116281A (en) * | 2009-08-06 | 2011-05-16 | Astellas Pharma Inc | N atom containing ring acylguanidine derivatives |
| TW201311149A (zh) * | 2011-06-24 | 2013-03-16 | Ishihara Sangyo Kaisha | 有害生物防治劑 |
| WO2013142390A1 (en) * | 2012-03-21 | 2013-09-26 | Gtx, Inc. | Aldo-keto reductase subfamily 1c3 (akr1c3) inhibitors |
| TWI647220B (zh) | 2013-03-15 | 2019-01-11 | 美商西建卡爾有限責任公司 | 雜芳基化合物及其用途 |
| RU2685234C1 (ru) | 2013-12-09 | 2019-04-17 | Юсб Байофарма Спрл | Конденсированные бициклические гетероароматические производные в качестве модуляторов активности tnf |
| EP3169678A1 (en) | 2014-07-17 | 2017-05-24 | Merck Patent GmbH | Novel naphthryidines and isoquinolines and their use as cdk8/19 inhibitors |
| WO2018119263A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Heterocyclic compounds derivatives as pd-l1 internalization inducers |
-
2016
- 2016-02-10 EP EP16703791.0A patent/EP3256217A1/en not_active Withdrawn
- 2016-02-10 US US15/545,149 patent/US10487075B2/en not_active Expired - Fee Related
- 2016-02-10 WO PCT/EP2016/052828 patent/WO2016128465A1/en not_active Ceased
- 2016-02-10 BR BR112017017032A patent/BR112017017032A2/pt not_active Application Discontinuation
- 2016-02-10 MX MX2017010230A patent/MX2017010230A/es unknown
- 2016-02-10 CN CN201680009637.4A patent/CN107428692A/zh active Pending
- 2016-02-10 KR KR1020177025452A patent/KR20170117479A/ko not_active Withdrawn
- 2016-02-10 EA EA201791781A patent/EA201791781A1/ru unknown
- 2016-02-10 AU AU2016217874A patent/AU2016217874A1/en not_active Abandoned
- 2016-02-10 CA CA2974874A patent/CA2974874A1/en not_active Abandoned
- 2016-02-10 JP JP2017542888A patent/JP2018505207A/ja not_active Ceased
- 2016-02-15 TW TW105104357A patent/TW201636327A/zh unknown
-
2017
- 2017-07-25 IL IL253656A patent/IL253656A0/en unknown
-
2019
- 2019-10-04 US US16/593,231 patent/US20200031811A1/en not_active Abandoned
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008509151A (ja) * | 2004-08-03 | 2008-03-27 | セレネックス, インコーポレイテッド | 2,8−二置換ナフチリジン誘導体 |
| JP2012519211A (ja) * | 2009-03-02 | 2012-08-23 | サートリス ファーマシューティカルズ, インコーポレイテッド | サーチュイン調節化合物としての8−置換キノリンおよび関連類似体 |
| WO2014079787A1 (en) * | 2012-11-20 | 2014-05-30 | F. Hoffmann-La Roche Ag | Substituted 1,6-naphthyridines |
| WO2014177596A1 (en) * | 2013-05-03 | 2014-11-06 | F. Hoffmann-La Roche Ag | Neurogenesis-stimulating isoquinoline derivatives |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2023535096A (ja) * | 2020-07-23 | 2023-08-15 | シトシンラボ セラピューティクス カンパニー, リミテッド | キナーゼ阻害活性を有する化合物 |
| JP7584623B2 (ja) | 2020-07-23 | 2024-11-15 | シトシンラボ セラピューティクス カンパニー, リミテッド | キナーゼ阻害活性を有する化合物 |
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| BR112017017032A2 (pt) | 2018-04-10 |
| TW201636327A (zh) | 2016-10-16 |
| CN107428692A (zh) | 2017-12-01 |
| MX2017010230A (es) | 2017-12-04 |
| US10487075B2 (en) | 2019-11-26 |
| IL253656A0 (en) | 2017-09-28 |
| US20200031811A1 (en) | 2020-01-30 |
| AU2016217874A1 (en) | 2017-08-10 |
| EA201791781A1 (ru) | 2018-02-28 |
| EP3256217A1 (en) | 2017-12-20 |
| WO2016128465A1 (en) | 2016-08-18 |
| US20180002321A1 (en) | 2018-01-04 |
| CA2974874A1 (en) | 2016-08-18 |
| KR20170117479A (ko) | 2017-10-23 |
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