CN104271132B - 靶向Ral GTP酶的抗癌化合物及使用其的方法 - Google Patents
靶向Ral GTP酶的抗癌化合物及使用其的方法 Download PDFInfo
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- CN104271132B CN104271132B CN201280070263.9A CN201280070263A CN104271132B CN 104271132 B CN104271132 B CN 104271132B CN 201280070263 A CN201280070263 A CN 201280070263A CN 104271132 B CN104271132 B CN 104271132B
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- 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
- A61K31/41—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
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring 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
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/351—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
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- 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
- A61K31/41—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
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
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- 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
- A61K31/4353—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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/33—Heterocyclic compounds
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- 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
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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- A—HUMAN NECESSITIES
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- 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
- A61K31/495—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
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- 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
- A61K31/55—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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K31/55—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
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
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- 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
- A61P37/04—Immunostimulants
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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
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161578869P | 2011-12-21 | 2011-12-21 | |
| US61/578,869 | 2011-12-21 | ||
| PCT/US2012/071341 WO2013096820A1 (en) | 2011-12-21 | 2012-12-21 | Anti-cancer compounds targeting ral gtpases and methods of using the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN104271132A CN104271132A (zh) | 2015-01-07 |
| CN104271132B true CN104271132B (zh) | 2018-01-12 |
Family
ID=48669550
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201280070263.9A Expired - Fee Related CN104271132B (zh) | 2011-12-21 | 2012-12-21 | 靶向Ral GTP酶的抗癌化合物及使用其的方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (3) | US9353121B2 (enExample) |
| EP (1) | EP2793881B1 (enExample) |
| JP (1) | JP6473330B2 (enExample) |
| KR (1) | KR102097343B1 (enExample) |
| CN (1) | CN104271132B (enExample) |
| AU (1) | AU2012358317B2 (enExample) |
| CA (1) | CA2859985C (enExample) |
| WO (1) | WO2013096820A1 (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104271132B (zh) | 2011-12-21 | 2018-01-12 | 科罗拉多大学董事会法人团体 | 靶向Ral GTP酶的抗癌化合物及使用其的方法 |
| EP3166609B1 (en) * | 2014-07-10 | 2020-03-11 | The Regents of The University of Colorado, A Body Corporate | 6-amino-1,3-dimethyl-4-(4-(trifluoromethyl)phenyl)-1,4-dihydropyrano [2,3-c]pyrazole-5-carbonitrile and related compounds as ral gtpase inhibitors for treating cancer metastasis |
| SI3447050T1 (sl) | 2014-09-19 | 2020-08-31 | Forma Therapeutics, Inc. | Derivati piridin-2(1H)-on kinolinona kot inhibitorji mutirane izocitratne dehidrogenaze |
| CA2961793C (en) | 2014-09-19 | 2021-03-16 | Forma Therapeutics, Inc. | Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors |
| US10934291B2 (en) | 2014-09-25 | 2021-03-02 | Duke University | Kinase inhibitors and related methods of use |
| US10646475B2 (en) * | 2015-03-10 | 2020-05-12 | The Trustees Of Princeton University | SHMT inhibitors |
| WO2016205460A1 (en) * | 2015-06-16 | 2016-12-22 | Nantbioscience, Inc. | Polycyclic derivatives targeting ral gtpases and their therapeutical applications |
| GEP20207167B (en) | 2016-06-22 | 2020-10-12 | Univ Vanderbilt | Positive allosteric modulators of the muscarinic acetylcholine receptor m4 |
| US10077273B2 (en) | 2016-09-14 | 2018-09-18 | The Trustees Of Princeton University | SHMT inhibitors |
| KR102507847B1 (ko) | 2016-10-28 | 2023-03-08 | 서울대학교병원 | 페닐 프탈라진 유도체, 이의 제조 방법 및 이를 포함하는 약학적 조성물 |
| CN109863139B (zh) | 2016-11-07 | 2023-02-17 | 范德比尔特大学 | 毒蕈碱型乙酰胆碱受体m4的正向别构调节剂 |
| CN109862893B (zh) | 2016-11-07 | 2023-02-17 | 范德比尔特大学 | 毒蕈碱型乙酰胆碱受体m4的正向别构调节剂 |
| US11008335B2 (en) | 2016-11-07 | 2021-05-18 | Vanderbilt University | Positive allosteric modulators of the muscarinic acetylcholine receptor M4 |
| CN112397076A (zh) | 2016-11-23 | 2021-02-23 | 瑞典爱立信有限公司 | 用于自适应控制去相关滤波器的方法和装置 |
| TW201930311A (zh) | 2017-12-05 | 2019-08-01 | 泛德比爾特大學 | 蕈毒鹼型乙醯膽鹼受體m4之正向別構調節劑 |
| MA51036A (fr) | 2017-12-05 | 2021-03-17 | Univ Vanderbilt | Modulateurs allostériques positifs du récepteur muscarinique de l'acétylcholine m4 |
| WO2019142191A1 (en) * | 2018-01-17 | 2019-07-25 | Gavish-Galilee Bio Applications Ltd. | New methionine metabolic pathway inhibitors |
| BR112020014559A2 (pt) | 2018-01-17 | 2020-12-08 | Migal - Galilee Research Institute Ltd. | Inibidores inovadores da via metabólica da metionina |
| US11013734B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation |
| US11013733B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1) |
| US11311527B2 (en) | 2018-05-16 | 2022-04-26 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1) |
| US10532047B2 (en) | 2018-05-16 | 2020-01-14 | Forma Therapeutics, Inc. | Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile |
| US11576906B2 (en) | 2018-05-16 | 2023-02-14 | Forma Therapeutics, Inc. | Inhibiting mutant IDH-1 |
| CN109305972B (zh) * | 2018-09-27 | 2021-07-09 | 广州医科大学 | 一种二氢吡喃并吡唑类化合物及其制备方法和应用 |
| CN109734676B (zh) * | 2019-01-16 | 2021-01-29 | 四川大学 | 苯并二氮杂卓类衍生物及其制备方法和应用 |
| EP4076416A4 (en) * | 2019-12-19 | 2024-04-10 | The Trustees of Indiana University | Small-molecule covalent inhibition of ral gtpases |
| CN111406752B (zh) * | 2020-04-23 | 2021-07-23 | 中国农业科学院植物保护研究所 | 二氢吡咯并吡唑酮类衍生物作为几丁质酶抑制剂或杀线虫剂的应用 |
| US20230293490A1 (en) * | 2020-08-17 | 2023-09-21 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Profilin1:actin inhibitor as an anti-angiogenic compound |
| US20230414610A1 (en) * | 2020-11-18 | 2023-12-28 | Texas Tech University System | Therapies for cancer using small molecules that bind to and inhibit rail interacting proteins |
| US20240325374A1 (en) * | 2021-07-23 | 2024-10-03 | The Research Institute At Nationwide Children's Hospital | Inhibiting intracellular pathogens |
| US20250134888A1 (en) * | 2022-02-07 | 2025-05-01 | Cornell University | Inhibitors of malic enzyme 1 |
| CN120168481B (zh) * | 2025-05-14 | 2025-08-19 | 天津医科大学 | 一种抑制REXO4消解R-loop酶活性的小分子及其在制备肿瘤药物中的应用 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008143894A2 (en) * | 2007-05-14 | 2008-11-27 | Dana-Farber Cancer Institute, Inc. | Phosphorylated rala |
| US20090163545A1 (en) * | 2007-12-21 | 2009-06-25 | University Of Rochester | Method For Altering The Lifespan Of Eukaryotic Organisms |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US362503A (en) * | 1887-05-10 | Sectional boat | ||
| US361185A (en) * | 1887-04-12 | Poueths to john h | ||
| US4555396A (en) | 1982-12-22 | 1985-11-26 | Eastman Kodak Company | Use of pyrylium and thiapyrylium compounds as biological stains |
| US5750550A (en) * | 1995-09-15 | 1998-05-12 | Sanofi | 2-(pyrazol-5-yl-oxymethyl)-1,2-benzisothiazol-3 (2H)-One 1, 1-dioxides and compositions and method of use thereof |
| JPH10279480A (ja) * | 1997-04-07 | 1998-10-20 | Mitsubishi Chem Corp | 皮膚組織障害の予防・治療剤 |
| US6143471A (en) * | 1998-03-10 | 2000-11-07 | Mitsubishi Paper Mills Limited | Positive type photosensitive composition |
| AU1853600A (en) | 1999-01-06 | 2000-07-24 | Choong-Chin Liew | Method for the detection of gene transcripts in blood and uses thereof |
| US20070105105A1 (en) | 2003-05-23 | 2007-05-10 | Mount Sinai School Of Medicine Of New York University | Surrogate cell gene expression signatures for evaluating the physical state of a subject |
| CA2533803A1 (en) | 2003-07-29 | 2005-02-10 | Bristol-Myers Squibb Company | Biomarkers of cyclin-dependent kinase modulation |
| WO2006126625A1 (ja) * | 2005-05-25 | 2006-11-30 | Mitsubishi Tanabe Pharma Corporation | ピラゾロン誘導体を含む医薬 |
| EP1920048A4 (en) * | 2005-07-29 | 2009-12-09 | Childrens Hosp Medical Center | GTASE INHIBITORS AND USE METHOD AND CRYSTAL STRUCTURE OF RAC-1 GTASE |
| KR20080040032A (ko) | 2005-09-02 | 2008-05-07 | 티보텍 파마슈티칼즈 리미티드 | Hcv 저해제로서의 벤조디아제핀 |
| EP1957474A4 (en) | 2005-11-04 | 2011-08-24 | Harvard College | SYNTHESIS OF FTSZ HEMMERN |
| WO2007081966A2 (en) | 2006-01-09 | 2007-07-19 | University Of Southern California | Small molecules for treating cancer and abnormal cell proliferation disorders |
| WO2011010715A1 (ja) | 2009-07-24 | 2011-01-27 | 国立大学法人 東京大学 | Pr-Set7阻害剤 |
| WO2011035143A2 (en) | 2009-09-17 | 2011-03-24 | The Regents Of The University Of Michigan | Methods and compositions for inhibiting rho-mediated diseases and conditions |
| US8673913B2 (en) | 2009-11-13 | 2014-03-18 | Case Western Reserve University | SHP-2 phosphatase inhibitor |
| US20120214824A1 (en) | 2010-12-08 | 2012-08-23 | Bradley Tait | Proteostasis regulators |
| CN104271132B (zh) | 2011-12-21 | 2018-01-12 | 科罗拉多大学董事会法人团体 | 靶向Ral GTP酶的抗癌化合物及使用其的方法 |
| WO2013096852A1 (en) | 2011-12-21 | 2013-06-27 | The Regents Of The University Of Colorado | Biomarkers of cancer |
| WO2013152313A1 (en) * | 2012-04-05 | 2013-10-10 | The Regents Of The University Of California | Compositions and methods for treating cancer and diseases and conditions responsive to growth factor inhibition |
| EP2858981A1 (en) | 2012-06-06 | 2015-04-15 | Basf Se | Pyrazolopyrans having herbicidal and pharmaceutical properties |
| CN103910737B (zh) | 2014-03-25 | 2016-08-17 | 浙江师范大学 | 手性的1,4-二氢吡喃(2,3-c)吡唑衍生物及其合成方法和应用 |
-
2012
- 2012-12-21 CN CN201280070263.9A patent/CN104271132B/zh not_active Expired - Fee Related
- 2012-12-21 EP EP12859252.4A patent/EP2793881B1/en active Active
- 2012-12-21 AU AU2012358317A patent/AU2012358317B2/en not_active Ceased
- 2012-12-21 JP JP2014548963A patent/JP6473330B2/ja not_active Expired - Fee Related
- 2012-12-21 WO PCT/US2012/071341 patent/WO2013096820A1/en not_active Ceased
- 2012-12-21 US US14/366,035 patent/US9353121B2/en not_active Expired - Fee Related
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2016
- 2016-04-29 US US15/142,011 patent/US10689392B2/en not_active Expired - Fee Related
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2020
- 2020-05-12 US US15/930,188 patent/US11964985B2/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008143894A2 (en) * | 2007-05-14 | 2008-11-27 | Dana-Farber Cancer Institute, Inc. | Phosphorylated rala |
| US20090163545A1 (en) * | 2007-12-21 | 2009-06-25 | University Of Rochester | Method For Altering The Lifespan Of Eukaryotic Organisms |
Non-Patent Citations (2)
| Title |
|---|
| Activation of RalA is critical for Ras-induced tumorigenesis of human cells;Kian-Huat Lim等;《CANCER CELL》;20050630;第7卷;第533-545页 * |
| The Metastasis-Associated Gene CD24 Is Regulated by Ral GTPase and Is a Mediator of Cell Proliferation and Survival in Human Cancer;Steven C. Smith等;《Cancer Res》;20060215;第66卷(第4期);第1917-1922页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2793881B1 (en) | 2018-10-31 |
| US11964985B2 (en) | 2024-04-23 |
| US20160280715A1 (en) | 2016-09-29 |
| AU2012358317B2 (en) | 2017-12-14 |
| CA2859985A1 (en) | 2013-06-27 |
| EP2793881A1 (en) | 2014-10-29 |
| CN104271132A (zh) | 2015-01-07 |
| KR20150010696A (ko) | 2015-01-28 |
| AU2012358317A1 (en) | 2014-07-17 |
| US9353121B2 (en) | 2016-05-31 |
| JP2015503507A (ja) | 2015-02-02 |
| WO2013096820A1 (en) | 2013-06-27 |
| CA2859985C (en) | 2020-11-03 |
| JP6473330B2 (ja) | 2019-02-20 |
| EP2793881A4 (en) | 2015-05-20 |
| US10689392B2 (en) | 2020-06-23 |
| US20140315894A1 (en) | 2014-10-23 |
| KR102097343B1 (ko) | 2020-04-07 |
| US20200270263A1 (en) | 2020-08-27 |
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