JP6855379B2 - 癌の処置のためのヒストンデメチラーゼkdm2bのインヒビターとしての(ピペリジン−3−イル)(ナフタレン−2−イル)メタノン誘導体および関連化合物 - Google Patents
癌の処置のためのヒストンデメチラーゼkdm2bのインヒビターとしての(ピペリジン−3−イル)(ナフタレン−2−イル)メタノン誘導体および関連化合物 Download PDFInfo
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- JP6855379B2 JP6855379B2 JP2017536302A JP2017536302A JP6855379B2 JP 6855379 B2 JP6855379 B2 JP 6855379B2 JP 2017536302 A JP2017536302 A JP 2017536302A JP 2017536302 A JP2017536302 A JP 2017536302A JP 6855379 B2 JP6855379 B2 JP 6855379B2
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- UPGOXMUQOUACMG-UHFFFAOYSA-N Ic1ccc(CCCC2)c2c1 Chemical compound Ic1ccc(CCCC2)c2c1 UPGOXMUQOUACMG-UHFFFAOYSA-N 0.000 description 1
- IWIBDSGNVAVVCF-UHFFFAOYSA-N N#CCN(CCC1)CC1I Chemical compound N#CCN(CCC1)CC1I IWIBDSGNVAVVCF-UHFFFAOYSA-N 0.000 description 1
- RKVZCWLRCCFODE-UHFFFAOYSA-N NC(CCC1)CN1C(C1)CC1(F)F Chemical compound NC(CCC1)CN1C(C1)CC1(F)F RKVZCWLRCCFODE-UHFFFAOYSA-N 0.000 description 1
- BPEXQYURTRYAMW-UHFFFAOYSA-N NC(CCC1)CN1C1CCCC1 Chemical compound NC(CCC1)CN1C1CCCC1 BPEXQYURTRYAMW-UHFFFAOYSA-N 0.000 description 1
- CWVITUDPTUTLBV-UHFFFAOYSA-N NC(CCC1)CN1C1COCC1 Chemical compound NC(CCC1)CN1C1COCC1 CWVITUDPTUTLBV-UHFFFAOYSA-N 0.000 description 1
- HLNMNVVYUUGBJN-UHFFFAOYSA-N NC1CN(CCC#N)CCC1 Chemical compound NC1CN(CCC#N)CCC1 HLNMNVVYUUGBJN-UHFFFAOYSA-N 0.000 description 1
- SMXGNHQOYUEWSE-UHFFFAOYSA-N NCC1=C(C=CC=C2)C2=C[I]=C1 Chemical compound NCC1=C(C=CC=C2)C2=C[I]=C1 SMXGNHQOYUEWSE-UHFFFAOYSA-N 0.000 description 1
- OTQROCNBFDQPQA-UHFFFAOYSA-N Nc(c1c2cccc1)ccc2[IH]I Chemical compound Nc(c1c2cccc1)ccc2[IH]I OTQROCNBFDQPQA-UHFFFAOYSA-N 0.000 description 1
- BDPTUIIYKNMWIR-UHFFFAOYSA-N O=C(C(CCC1)CN1C1CCC1)c1cc2ccncc2cc1 Chemical compound O=C(C(CCC1)CN1C1CCC1)c1cc2ccncc2cc1 BDPTUIIYKNMWIR-UHFFFAOYSA-N 0.000 description 1
- JEHDQSLDGUXOLU-UHFFFAOYSA-N O=C(C(CCC1)CN1C1CCC1)c1ccc(CCCC2)c2c1 Chemical compound O=C(C(CCC1)CN1C1CCC1)c1ccc(CCCC2)c2c1 JEHDQSLDGUXOLU-UHFFFAOYSA-N 0.000 description 1
- MYYHWQJQNCTUIY-UHFFFAOYSA-N O=C(C(CCC1)CN1C1CCC1)c1ccc(CCCCC2)c2c1 Chemical compound O=C(C(CCC1)CN1C1CCC1)c1ccc(CCCCC2)c2c1 MYYHWQJQNCTUIY-UHFFFAOYSA-N 0.000 description 1
- RJZUIWNAWGHYLY-UHFFFAOYSA-N O=C(C(CCC1)CN1C1CCCC1)c1cc(Cl)ccc1 Chemical compound O=C(C(CCC1)CN1C1CCCC1)c1cc(Cl)ccc1 RJZUIWNAWGHYLY-UHFFFAOYSA-N 0.000 description 1
- XNJGAPZVEJULOZ-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c(cc1)c(cccc2)c2c1F Chemical compound O=C(C1CN(CC2CC2)CCC1)c(cc1)c(cccc2)c2c1F XNJGAPZVEJULOZ-UHFFFAOYSA-N 0.000 description 1
- SINLODAAPXHAPY-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c(cc1)cc2c1c(OCc1ccccc1)ccc2 Chemical compound O=C(C1CN(CC2CC2)CCC1)c(cc1)cc2c1c(OCc1ccccc1)ccc2 SINLODAAPXHAPY-UHFFFAOYSA-N 0.000 description 1
- UBYKJFFYSFOUIJ-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c(cc1)ccc1Oc1ccccc1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c(cc1)ccc1Oc1ccccc1 UBYKJFFYSFOUIJ-UHFFFAOYSA-N 0.000 description 1
- AXUUDIOSRNDXDS-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c(ccc1c2cccc1)c2F Chemical compound O=C(C1CN(CC2CC2)CCC1)c(ccc1c2cccc1)c2F AXUUDIOSRNDXDS-UHFFFAOYSA-N 0.000 description 1
- AJTQSUWGAMKKNQ-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1c(cccc2)c2ccc1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1c(cccc2)c2ccc1 AJTQSUWGAMKKNQ-UHFFFAOYSA-N 0.000 description 1
- XOIDLSKXTNAWBW-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1c[n](-c2ccccc2)nc1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1c[n](-c2ccccc2)nc1 XOIDLSKXTNAWBW-UHFFFAOYSA-N 0.000 description 1
- ZYOZTMOQLFECSW-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1cc(-c2ccccc2)ccc1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1cc(-c2ccccc2)ccc1 ZYOZTMOQLFECSW-UHFFFAOYSA-N 0.000 description 1
- RYJFCIWDGHWSHT-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1cc(Oc(cc2)ccc2F)ccc1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1cc(Oc(cc2)ccc2F)ccc1 RYJFCIWDGHWSHT-UHFFFAOYSA-N 0.000 description 1
- WRTOKCDDGCGMII-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1cc(cccc2)c2c(F)c1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1cc(cccc2)c2c(F)c1 WRTOKCDDGCGMII-UHFFFAOYSA-N 0.000 description 1
- BQLHOXBXFSKKTD-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1cc2ccccc2[s]1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1cc2ccccc2[s]1 BQLHOXBXFSKKTD-UHFFFAOYSA-N 0.000 description 1
- SEYGZEITJAZXBO-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1cc2ccccc2nc1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1cc2ccccc2nc1 SEYGZEITJAZXBO-UHFFFAOYSA-N 0.000 description 1
- QQXIHZPBERETOJ-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1ccc(C(F)(F)F)cc1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1ccc(C(F)(F)F)cc1 QQXIHZPBERETOJ-UHFFFAOYSA-N 0.000 description 1
- PCFOMCRBYJFUHA-UHFFFAOYSA-N O=C(C1CN(CC2CC2)CCC1)c1nc(cccc2)c2cc1 Chemical compound O=C(C1CN(CC2CC2)CCC1)c1nc(cccc2)c2cc1 PCFOMCRBYJFUHA-UHFFFAOYSA-N 0.000 description 1
- SRNPMFKSBZEHEX-UHFFFAOYSA-N O=C(C1CN(CC2CCC2)CCC1)c(cc1)ccc1-c1ccccc1 Chemical compound O=C(C1CN(CC2CCC2)CCC1)c(cc1)ccc1-c1ccccc1 SRNPMFKSBZEHEX-UHFFFAOYSA-N 0.000 description 1
- VDXRJKMDSWTORW-AWEZNQCLSA-N O=C([C@@H]1CN(CC2CC2)CCC1)c1cc(Cl)ccc1 Chemical compound O=C([C@@H]1CN(CC2CC2)CCC1)c1cc(Cl)ccc1 VDXRJKMDSWTORW-AWEZNQCLSA-N 0.000 description 1
- KGFUFBDYJBZAGT-XPWCNEFFSA-N O=C([C@H]1CN(CC2CC2)CCC1)c(cc1)ccc1Oc1ccc(C2C(CN(CCC3)C[C@@H]3C(c3cc(Oc4cccc([C@H]5C(CN(CCC6)C[C@H]6C(c6cc(Oc7ccccc7)ccc6)=O)C5)c4)ccc3)=O)C2)cc1 Chemical compound O=C([C@H]1CN(CC2CC2)CCC1)c(cc1)ccc1Oc1ccc(C2C(CN(CCC3)C[C@@H]3C(c3cc(Oc4cccc([C@H]5C(CN(CCC6)C[C@H]6C(c6cc(Oc7ccccc7)ccc6)=O)C5)c4)ccc3)=O)C2)cc1 KGFUFBDYJBZAGT-XPWCNEFFSA-N 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/30—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562101927P | 2015-01-09 | 2015-01-09 | |
| US62/101,927 | 2015-01-09 | ||
| PCT/US2016/012638 WO2016112284A1 (en) | 2015-01-09 | 2016-01-08 | (piperidin-3-yl)(naphthalen-2-yl)methanone derivatives and related compounds as inhibitors of the histone demethylase kdm2b for the treatment of cancer |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018501288A JP2018501288A (ja) | 2018-01-18 |
| JP2018501288A5 JP2018501288A5 (enExample) | 2019-02-14 |
| JP6855379B2 true JP6855379B2 (ja) | 2021-04-07 |
Family
ID=55299746
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017536302A Expired - Fee Related JP6855379B2 (ja) | 2015-01-09 | 2016-01-08 | 癌の処置のためのヒストンデメチラーゼkdm2bのインヒビターとしての(ピペリジン−3−イル)(ナフタレン−2−イル)メタノン誘導体および関連化合物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US10280149B2 (enExample) |
| EP (1) | EP3242872B1 (enExample) |
| JP (1) | JP6855379B2 (enExample) |
| CN (1) | CN107406414B (enExample) |
| WO (1) | WO2016112284A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7788208B2 (ja) * | 2017-03-29 | 2025-12-18 | パデュー リサーチ ファウンデイション | キナーゼネットワークの阻害剤およびその使用 |
| MA52005A (fr) * | 2018-03-14 | 2021-01-20 | Prelude Therapeutics Inc | Inhibiteurs sélectifs de la protéine arginine méthyltransférase 5 (prmt5) |
| EP4149917B1 (en) * | 2020-05-12 | 2025-07-30 | Merck Sharp & Dohme LLC | Factor xi activation inhibitors |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CU22545A1 (es) | 1994-11-18 | 1999-03-31 | Centro Inmunologia Molecular | Obtención de un anticuerpo quimérico y humanizado contra el receptor del factor de crecimiento epidérmico para uso diagnóstico y terapéutico |
| LU77659A1 (de) * | 1977-06-30 | 1979-03-26 | Byk Gulden Lomberg Chem Fab | Piperidinoadamantane,verfahren zu ihrer herstellung und sie enthaltende arzneimittel |
| US4943533A (en) | 1984-03-01 | 1990-07-24 | The Regents Of The University Of California | Hybrid cell lines that produce monoclonal antibodies to epidermal growth factor receptor |
| CA2066428C (en) | 1989-09-08 | 2000-11-28 | Bert Vogelstein | Structural alterations of the egf receptor gene in human gliomas |
| GB9300059D0 (en) | 1992-01-20 | 1993-03-03 | Zeneca Ltd | Quinazoline derivatives |
| GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
| DK0659439T3 (da) | 1993-12-24 | 2002-01-14 | Merck Patent Gmbh | Immunkonjugater |
| IL112249A (en) | 1994-01-25 | 2001-11-25 | Warner Lambert Co | Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds |
| US5654307A (en) | 1994-01-25 | 1997-08-05 | Warner-Lambert Company | Bicyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| HU216142B (hu) | 1994-07-21 | 1999-04-28 | Akzo Nobel N.V. | Ciklusos keton-peroxidokat tartalmazó kompozíciók, és azok alkalmazása (ko)polimerek módosítására |
| US5804396A (en) | 1994-10-12 | 1998-09-08 | Sugen, Inc. | Assay for agents active in proliferative disorders |
| DE69536015D1 (de) | 1995-03-30 | 2009-12-10 | Pfizer Prod Inc | Chinazolinone Derivate |
| GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| GB9508565D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quiazoline derivative |
| US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
| JPH11507535A (ja) | 1995-06-07 | 1999-07-06 | イムクローン システムズ インコーポレイテッド | 腫瘍の成長を抑制する抗体および抗体フラグメント類 |
| EP0836605B1 (en) | 1995-07-06 | 2002-02-06 | Novartis AG | Pyrrolopyrimidines and processes for the preparation thereof |
| US5760041A (en) | 1996-02-05 | 1998-06-02 | American Cyanamid Company | 4-aminoquinazoline EGFR Inhibitors |
| GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
| JP3370340B2 (ja) | 1996-04-12 | 2003-01-27 | ワーナー―ランバート・コンパニー | チロシンキナーゼの不可逆的阻害剤 |
| DE69716916T2 (de) | 1996-07-13 | 2003-07-03 | Glaxo Group Ltd., Greenford | Kondensierte heterozyklische verbindungen als protein kinase inhibitoren |
| ID18494A (id) | 1996-10-02 | 1998-04-16 | Novartis Ag | Turunan pirazola leburan dan proses pembuatannya |
| UA73073C2 (uk) | 1997-04-03 | 2005-06-15 | Уайт Холдінгз Корпорейшн | Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція |
| US6002008A (en) | 1997-04-03 | 1999-12-14 | American Cyanamid Company | Substituted 3-cyano quinolines |
| US6235883B1 (en) | 1997-05-05 | 2001-05-22 | Abgenix, Inc. | Human monoclonal antibodies to epidermal growth factor receptor |
| ES2201484T3 (es) | 1997-05-06 | 2004-03-16 | Wyeth Holdings Corporation | Utilizacion de compuestos de quinazolina para el tratamiento de la enfermedad de la poliquistosis renal. |
| ZA986732B (en) | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitiors of tyrosine kinases |
| ZA986729B (en) | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitors of tyrosine kinases |
| TW436485B (en) | 1997-08-01 | 2001-05-28 | American Cyanamid Co | Substituted quinazoline derivatives |
| NZ503991A (en) | 1997-11-06 | 2001-11-30 | American Cyanamid Co | Use of quinazoline derivatives as tyrosine kinase inhibitors for treating colonic polyps |
| ES2188254T3 (es) | 1998-11-19 | 2003-06-16 | Warner Lambert Co | N-(4-(3-chloro-4-fluoro-fenilamino)-7-(3-morfolin-4-il-propoxi)-quin azolin-6-il)-acrilamada, un inhibidor irreversible de tirosina quinasas. |
| CA2389049A1 (en) * | 1999-09-27 | 2001-04-05 | Georgetown University | Dopamine transporter inhibitors and their use |
| PE20071079A1 (es) * | 2005-11-15 | 2007-12-16 | Cytokinetics Inc | Compuestos de piperidina como inhibidores de la proliferacion celular |
| US8541572B2 (en) * | 2008-11-10 | 2013-09-24 | Merck Sharp & Dohme Corp. | Compounds for the treatment of inflammatory disorders |
| WO2012071469A2 (en) * | 2010-11-23 | 2012-05-31 | Nevada Cancer Institute | Histone demethylase inhibitors and uses thereof for treatment o f cancer |
| WO2013123411A1 (en) * | 2012-02-17 | 2013-08-22 | Board Of Regents, The University Of Texas System | Methods for diagnosing and treating cancer |
| RS56561B1 (sr) * | 2013-03-15 | 2018-02-28 | Quanticel Pharmaceuticals Inc | Inhibitori histon demetilaze |
-
2016
- 2016-01-08 WO PCT/US2016/012638 patent/WO2016112284A1/en not_active Ceased
- 2016-01-08 EP EP16702830.7A patent/EP3242872B1/en active Active
- 2016-01-08 JP JP2017536302A patent/JP6855379B2/ja not_active Expired - Fee Related
- 2016-01-08 CN CN201680014364.2A patent/CN107406414B/zh not_active Expired - Fee Related
-
2017
- 2017-07-07 US US15/643,808 patent/US10280149B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP3242872B1 (en) | 2019-07-03 |
| CN107406414B (zh) | 2022-04-19 |
| US10280149B2 (en) | 2019-05-07 |
| CN107406414A (zh) | 2017-11-28 |
| JP2018501288A (ja) | 2018-01-18 |
| EP3242872A1 (en) | 2017-11-15 |
| WO2016112284A1 (en) | 2016-07-14 |
| HK1247198A1 (zh) | 2018-09-21 |
| US20180022727A1 (en) | 2018-01-25 |
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