KR101485645B1 - p53 활성을 증가시키는 치환된 피페리딘 및 그의 용도 - Google Patents
p53 활성을 증가시키는 치환된 피페리딘 및 그의 용도 Download PDFInfo
- Publication number
- KR101485645B1 KR101485645B1 KR1020127012244A KR20127012244A KR101485645B1 KR 101485645 B1 KR101485645 B1 KR 101485645B1 KR 1020127012244 A KR1020127012244 A KR 1020127012244A KR 20127012244 A KR20127012244 A KR 20127012244A KR 101485645 B1 KR101485645 B1 KR 101485645B1
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- cycloalkyl
- cancer
- compound
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 C*(C)N(CC1)C[C@@](C2)C1C2(*)c(c(I)c1I)c(**)c(C)c1I Chemical compound C*(C)N(CC1)C[C@@](C2)C1C2(*)c(c(I)c1I)c(**)c(C)c1I 0.000 description 15
- UPVAIJPDWVTFKT-UHFFFAOYSA-N CC(C)(CCO1)C1=O Chemical compound CC(C)(CCO1)C1=O UPVAIJPDWVTFKT-UHFFFAOYSA-N 0.000 description 1
- GEIOAUWKXCTXLT-UHFFFAOYSA-N CC(C)(CCOCc(cccc1)c1Br)C(O)=O Chemical compound CC(C)(CCOCc(cccc1)c1Br)C(O)=O GEIOAUWKXCTXLT-UHFFFAOYSA-N 0.000 description 1
- XXRZYQDSKSKLCK-UHFFFAOYSA-N CC(C)(CCOCc(cccc1)c1Br)C(OC)=O Chemical compound CC(C)(CCOCc(cccc1)c1Br)C(OC)=O XXRZYQDSKSKLCK-UHFFFAOYSA-N 0.000 description 1
- UWQNXPIEFRYWSJ-UHFFFAOYSA-N CC(C)(CCOCc1ccccc1CC#N)C(OC)=O Chemical compound CC(C)(CCOCc1ccccc1CC#N)C(OC)=O UWQNXPIEFRYWSJ-UHFFFAOYSA-N 0.000 description 1
- WMDNWWWVQKAFDR-UHFFFAOYSA-N CCC(C(C)N)NC Chemical compound CCC(C(C)N)NC WMDNWWWVQKAFDR-UHFFFAOYSA-N 0.000 description 1
- AHMHBKPNKPDLEV-UHFFFAOYSA-N CCC1(C(C)C)OCCC1 Chemical compound CCC1(C(C)C)OCCC1 AHMHBKPNKPDLEV-UHFFFAOYSA-N 0.000 description 1
- IAELBZKZVBXUHW-WXJLAGGASA-N CCC[C@H]([C@@](CCC1)(C(N(CC2)CCC2(C(CC(C)C=C2)=C2O[C@@H](CC2)C[C@H]2C(O)=O)C#N)=O)OC(C2)=CSC2(C)C(F)(F)F)N1C(c1c(C(F)(F)F)cccn1)=O Chemical compound CCC[C@H]([C@@](CCC1)(C(N(CC2)CCC2(C(CC(C)C=C2)=C2O[C@@H](CC2)C[C@H]2C(O)=O)C#N)=O)OC(C2)=CSC2(C)C(F)(F)F)N1C(c1c(C(F)(F)F)cccn1)=O IAELBZKZVBXUHW-WXJLAGGASA-N 0.000 description 1
- UZTIQPNXMZSPCL-DVECYGJZSA-N CCC[C@H]([C@@](CCC1)(C(N(CC2)CCC2=O)=O)Oc2c[s]c(C(F)(F)F)c2)N1C(c1ncccc1C(F)(F)F)=O Chemical compound CCC[C@H]([C@@](CCC1)(C(N(CC2)CCC2=O)=O)Oc2c[s]c(C(F)(F)F)c2)N1C(c1ncccc1C(F)(F)F)=O UZTIQPNXMZSPCL-DVECYGJZSA-N 0.000 description 1
- NIULOVGPRAJIJM-UHFFFAOYSA-N COC(CCc1ccccc1Br)=O Chemical compound COC(CCc1ccccc1Br)=O NIULOVGPRAJIJM-UHFFFAOYSA-N 0.000 description 1
- ASZRODBLMORHAR-NTSWFWBYSA-N COC([C@@H](CC1)C[C@@H]1O)=O Chemical compound COC([C@@H](CC1)C[C@@H]1O)=O ASZRODBLMORHAR-NTSWFWBYSA-N 0.000 description 1
- ARFJCWHOIQOWBM-NKWVEPMBSA-N COC([C@@H](CC1)C[C@@H]1OS(C)(=O)=O)=O Chemical compound COC([C@@H](CC1)C[C@@H]1OS(C)(=O)=O)=O ARFJCWHOIQOWBM-NKWVEPMBSA-N 0.000 description 1
- VRJHQPZVIGNGMX-UHFFFAOYSA-N O=C1CCNCC1 Chemical compound O=C1CCNCC1 VRJHQPZVIGNGMX-UHFFFAOYSA-N 0.000 description 1
- YUQUNWNSQDULTI-UHFFFAOYSA-N Sc(cccc1)c1Br Chemical compound Sc(cccc1)c1Br YUQUNWNSQDULTI-UHFFFAOYSA-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
- C07D401/14—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
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4436—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
-
- 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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Communicable Diseases (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Transplantation (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25160309P | 2009-10-14 | 2009-10-14 | |
| US61/251,603 | 2009-10-14 | ||
| US25246809P | 2009-10-16 | 2009-10-16 | |
| US61/252,468 | 2009-10-16 | ||
| PCT/US2010/051403 WO2011046771A1 (en) | 2009-10-14 | 2010-10-05 | SUBSTITUTED PIPERIDINES THAT INCREASE p53 ACTIVITY AND THE USES THEREOF |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20120110097A KR20120110097A (ko) | 2012-10-09 |
| KR101485645B1 true KR101485645B1 (ko) | 2015-01-22 |
Family
ID=43876442
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127012244A Expired - Fee Related KR101485645B1 (ko) | 2009-10-14 | 2010-10-05 | p53 활성을 증가시키는 치환된 피페리딘 및 그의 용도 |
Country Status (28)
| Country | Link |
|---|---|
| US (2) | US8859776B2 (enExample) |
| EP (1) | EP2488028B1 (enExample) |
| JP (2) | JP5099731B1 (enExample) |
| KR (1) | KR101485645B1 (enExample) |
| CN (2) | CN104945382B (enExample) |
| AR (1) | AR078622A1 (enExample) |
| AU (1) | AU2010307198B9 (enExample) |
| BR (1) | BR112012008849A2 (enExample) |
| CA (1) | CA2777043C (enExample) |
| CL (1) | CL2012000949A1 (enExample) |
| CO (1) | CO6531452A2 (enExample) |
| CR (1) | CR20120183A (enExample) |
| EA (1) | EA023838B1 (enExample) |
| GT (1) | GT201200111A (enExample) |
| IL (1) | IL219125A0 (enExample) |
| IN (1) | IN2012DN03085A (enExample) |
| MA (1) | MA33745B1 (enExample) |
| MX (1) | MX2012004377A (enExample) |
| MY (1) | MY174452A (enExample) |
| NI (1) | NI201200059A (enExample) |
| NZ (1) | NZ599343A (enExample) |
| PE (1) | PE20121172A1 (enExample) |
| PH (1) | PH12012500713A1 (enExample) |
| TN (1) | TN2012000129A1 (enExample) |
| TW (1) | TWI507405B (enExample) |
| UA (1) | UA109417C2 (enExample) |
| WO (1) | WO2011046771A1 (enExample) |
| ZA (2) | ZA201202667B (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2732806A1 (en) | 2008-08-04 | 2010-02-11 | John Wityak | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| US7718662B1 (en) | 2009-10-12 | 2010-05-18 | Pharmacyclics, Inc. | Pyrazolo-pyrimidine inhibitors of bruton's tyrosine kinase |
| PH12012501480A1 (en) | 2010-01-25 | 2012-10-22 | Chdi Foundation Inc | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| EA031737B1 (ru) | 2010-06-03 | 2019-02-28 | Фармасайкликс, Инк. | Применение ингибиторов тирозинкиназы брутона (btk) для лечения лейкоза и лимфомы |
| WO2013033068A1 (en) | 2011-08-30 | 2013-03-07 | Stephen Martin Courtney | Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
| SI2750677T1 (sl) | 2011-08-30 | 2017-10-30 | Chdi Foundation, Inc. | Inhibitorji kinurenin-3-monooksigenaze, farmacevtski sestavki in postopki njihove uporabe |
| EP2771008A4 (en) | 2011-10-28 | 2015-04-08 | Merck Sharp & Dohme | MACROCYCLES FOR INCREASING P53 ACTIVITY AND USES THEREOF |
| EP2793890B1 (en) * | 2011-12-21 | 2016-09-07 | Merck Sharp & Dohme Corp. | Substituted piperidines as hdm2 inhibitors |
| BR112014032346A2 (pt) * | 2012-06-26 | 2017-06-27 | Del Mar Pharmaceuticals | métodos para tratamento de malignidades resistentes ao inibidor de tirosina-quinase em pacientes com polimorfismos genéticos ou desregulações de ahi1 mutações empregando dianidrogalactitol, diacetildianidrogalactitol, dibromodulcitol, ou análogos ou derivados destes |
| EP3550031A1 (en) | 2012-07-24 | 2019-10-09 | Pharmacyclics, LLC | Mutations associated with resistance to inhibitors of bruton's tyrosine kinase (btk) |
| BR112015013611A2 (pt) | 2012-12-20 | 2017-11-14 | Merck Sharp & Dohme | composto, e, composição farmacêutica |
| US9169214B2 (en) | 2012-12-21 | 2015-10-27 | The Board Of Trustees Of The Leland Stanford Junior University | Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions |
| US9993472B2 (en) | 2014-01-28 | 2018-06-12 | Unity Biotechnology, Inc. | Treatment for osteoarthritis in a joint by administering a means for inhibiting MDM2 |
| EP3119910A4 (en) | 2014-03-20 | 2018-02-21 | Pharmacyclics LLC | Phospholipase c gamma 2 and resistance associated mutations |
| US10258621B2 (en) | 2014-07-17 | 2019-04-16 | Chdi Foundation, Inc. | Methods and compositions for treating HIV-related disorders |
| AU2018222739C1 (en) | 2017-02-17 | 2024-10-03 | Eidos Therapeutics, Inc. | Processes for preparing AG-10, its intermediates, and salts thereof |
| US10085999B1 (en) | 2017-05-10 | 2018-10-02 | Arixa Pharmaceuticals, Inc. | Beta-lactamase inhibitors and uses thereof |
| US12233073B2 (en) | 2017-06-09 | 2025-02-25 | Regents Of The University Of Minnesota | Skin care formulations and skin cancer treatment |
| SG11202002300QA (en) | 2017-10-02 | 2020-04-29 | Arixa Pharmaceuticals Inc | Aztreonam derivatives and uses thereof |
| KR20200135996A (ko) | 2018-03-23 | 2020-12-04 | 에이도스 테라퓨틱스, 인코포레이티드 | Ag10을 사용하여 ttr 아밀로이드증을 치료하는 방법 |
| WO2019204354A1 (en) | 2018-04-16 | 2019-10-24 | C4 Therapeutics, Inc. | Spirocyclic compounds |
| CA3104695A1 (en) | 2018-08-17 | 2020-02-20 | Eidos Therapeutics, Inc. | Formulations of ag10 |
| WO2020072442A1 (en) | 2018-10-01 | 2020-04-09 | Arixa Pharmaceuticals, Inc. | Derivatives of relebactam and uses thereof |
| MX2021011026A (es) | 2019-03-12 | 2021-10-13 | Arixa Pharmaceuticals Inc | Forma cristalina de un derivado de avibactam. |
| US11565999B2 (en) | 2019-04-25 | 2023-01-31 | Arixa Pharmaceuticals, Inc. | Methods of synthesizing aztreonam derivatives |
| CN111072475A (zh) * | 2019-12-20 | 2020-04-28 | 牡丹江恒远药业股份有限公司 | 1-羟甲基环丙基乙酸的合成方法及应用 |
| US11944604B1 (en) | 2023-03-10 | 2024-04-02 | King Saud University | Nanoformulation of spriooxindole and methods for treating hepatocellular carcinoma |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080004287A1 (en) * | 2006-06-30 | 2008-01-03 | Schering Corporation | Substituted Piperidines that Increase P53 Activity and the Uses Thereof |
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| US8354444B2 (en) | 2008-09-18 | 2013-01-15 | Hoffmann-La Roche Inc. | Substituted pyrrolidine-2-carboxamides |
| KR20120050492A (ko) | 2009-08-26 | 2012-05-18 | 노파르티스 아게 | 테트라-치환된 헤테로아릴 화합물 및 mdm2 및/또는 mdm4 조절제로서의 그의 용도 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080004287A1 (en) * | 2006-06-30 | 2008-01-03 | Schering Corporation | Substituted Piperidines that Increase P53 Activity and the Uses Thereof |
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