JO3170B1 - مركبات و تراكيب لتثبيت parp و طرق استعمالها - Google Patents
مركبات و تراكيب لتثبيت parp و طرق استعمالهاInfo
- Publication number
- JO3170B1 JO3170B1 JOP/2008/0433A JOP20080433A JO3170B1 JO 3170 B1 JO3170 B1 JO 3170B1 JO P20080433 A JOP20080433 A JO P20080433A JO 3170 B1 JO3170 B1 JO 3170B1
- Authority
- JO
- Jordan
- Prior art keywords
- inhibitor compounds
- relates
- parp inhibitor
- compounds
- disclosed
- Prior art date
Links
- 239000012661 PARP inhibitor Substances 0.000 title abstract 4
- 229940121906 Poly ADP ribose polymerase inhibitor Drugs 0.000 title abstract 4
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000000203 mixture Substances 0.000 title 1
- 102000012338 Poly(ADP-ribose) Polymerases Human genes 0.000 abstract 2
- 108010061844 Poly(ADP-ribose) Polymerases Proteins 0.000 abstract 2
- 229920000776 Poly(Adenosine diphosphate-ribose) polymerase Polymers 0.000 abstract 2
- 238000002512 chemotherapy Methods 0.000 abstract 2
- 208000033808 peripheral neuropathy Diseases 0.000 abstract 2
- 230000033616 DNA repair Effects 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- BPEGJWRSRHCHSN-UHFFFAOYSA-N Temozolomide Chemical compound O=C1N(C)N=NC2=C(C(N)=O)N=CN21 BPEGJWRSRHCHSN-UHFFFAOYSA-N 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 239000012830 cancer therapeutic Substances 0.000 abstract 1
- 230000003034 chemosensitisation Effects 0.000 abstract 1
- 229940127089 cytotoxic agent Drugs 0.000 abstract 1
- 230000007547 defect Effects 0.000 abstract 1
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 230000006698 induction Effects 0.000 abstract 1
- 230000005865 ionizing radiation Effects 0.000 abstract 1
- 201000001119 neuropathy Diseases 0.000 abstract 1
- 230000007823 neuropathy Effects 0.000 abstract 1
- WWBGWPHHLRSTFI-UHFFFAOYSA-N phenalen-1-one Chemical class C1=CC(C(=O)C=C2)=C3C2=CC=CC3=C1 WWBGWPHHLRSTFI-UHFFFAOYSA-N 0.000 abstract 1
- 229960004964 temozolomide Drugs 0.000 abstract 1
- 210000004881 tumor cell Anatomy 0.000 abstract 1
Classifications
-
- 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
- A61K31/495—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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
- 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
- C07D487/06—Peri-condensed systems
-
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
يتعلق الاختراع الراهن بمركبات رابع ازاز فنالين -3- ون تثبط انزيم بولي( ADP- ribose) بوليميراز ( PARP) وهي مفيدة في ا لاحساس الكيميائي لعقاقير علاج السرطان، يعتبر حث المرض العصبي المحيطي من التاثيرات الجانبية الشائعه في العددي من عقاقير العلاج الكيميائي التقليدية والجديدة، والاختراع الراهن يكفل وسائل لمنع او علاج المرض العصبي المحفز بالعلاج الكيميائي بكفاءه، ويتعلق الاختراع كذلك باستعمال مركبات تثبيط PARP موضوع الاختراع في تعزيز كفاءه عوامل العلاج الكيميائي مثل تيموزواوميد، ويتعلق الاختراع كذلك باستعمال مركبات تثبيط PARP موضوع الاختراع في الخلايا الحساسة للاشعاع وذلك لتاين الاشعاع، ويتعلق الاختراع كذلك باستعمال مركبات تثبيط PARP موضوع الاختراع في علاج السرطان الذي يتميز بعيوب اصلاح DNA .
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97711507P | 2007-10-03 | 2007-10-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JO3170B1 true JO3170B1 (ar) | 2017-09-20 |
Family
ID=40526672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JOP/2008/0433A JO3170B1 (ar) | 2007-10-03 | 2008-10-05 | مركبات و تراكيب لتثبيت parp و طرق استعمالها |
Country Status (27)
| Country | Link |
|---|---|
| US (3) | US8236802B2 (ar) |
| EP (2) | EP2209375B1 (ar) |
| JP (1) | JP5439380B2 (ar) |
| KR (1) | KR101596526B1 (ar) |
| CN (1) | CN102083314B (ar) |
| AU (1) | AU2008308664B2 (ar) |
| BR (1) | BRPI0820518B1 (ar) |
| CA (1) | CA2700903C (ar) |
| CL (1) | CL2010000320A1 (ar) |
| CY (1) | CY1115747T1 (ar) |
| DK (1) | DK2209375T3 (ar) |
| ES (1) | ES2504690T3 (ar) |
| HR (1) | HRP20140853T1 (ar) |
| IL (1) | IL204776A (ar) |
| JO (1) | JO3170B1 (ar) |
| MX (1) | MX2010003564A (ar) |
| MY (1) | MY155237A (ar) |
| NZ (1) | NZ585012A (ar) |
| PL (1) | PL2209375T3 (ar) |
| PT (1) | PT2209375E (ar) |
| RU (1) | RU2485122C2 (ar) |
| SG (1) | SG185272A1 (ar) |
| SI (1) | SI2209375T1 (ar) |
| TW (1) | TWI426912B (ar) |
| UA (1) | UA99483C2 (ar) |
| WO (1) | WO2009046205A1 (ar) |
| ZA (1) | ZA201002317B (ar) |
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| US7820668B2 (en) | 2005-01-19 | 2010-10-26 | Eisai Inc. | Diazabenzo[de]anthracen-3-one compounds and methods for inhibiting PARP |
| ES2504690T3 (es) | 2007-10-03 | 2014-10-08 | Eisai Inc. | Compuestos inhibidores de PARP, composiciones y métodos de uso |
| CN104478875B (zh) * | 2008-08-06 | 2017-04-12 | 麦迪韦逊科技有限公司 | 聚(adp‑核糖)聚合酶(parp)的二氢吡啶并酞嗪酮抑制剂 |
| EP2322658A1 (en) | 2009-11-13 | 2011-05-18 | Centre National de la Recherche Scientifique (CNRS) | Signature for the diagnosis of breast cancer aggressiveness and genetic instability |
| KR101826652B1 (ko) * | 2010-02-08 | 2018-02-07 | 메디베이션 테크놀로지즈, 인크. | 디히드로피리도프탈라지논 유도체의 합성 방법 |
| EP3012329B1 (en) | 2010-06-18 | 2017-10-25 | Myriad Genetics, Inc. | Methods and materials for assessing loss of heterozygosity |
| WO2012074840A2 (en) | 2010-11-22 | 2012-06-07 | The General Hospital Corporation | Compositions and methods for in vivo imaging |
| US9359605B2 (en) * | 2011-03-11 | 2016-06-07 | Sarissa Inc. | Method of treating cancer by inhibition of DNA repair proteins |
| SG2014014294A (en) * | 2011-04-11 | 2014-06-27 | Abbvie Inc | Parp inhibitors for the treatment of cipn |
| EP2710142B1 (en) | 2011-05-18 | 2017-04-26 | Centre National de la Recherche Scientifique (CNRS) | Signature for the diagnosis of cancer aggressiveness and genetic instability |
| EP2731942B1 (en) * | 2011-07-13 | 2015-09-23 | Novartis AG | Novel 2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors |
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| BR112014015152A2 (pt) * | 2011-12-21 | 2017-07-04 | Myriad Genetics Inc | métodos e materiais para a avaliação da perda de heterozigosidade |
| EP2800821B1 (en) | 2012-01-05 | 2016-11-16 | Centre National de la Recherche Scientifique (CNRS) | Signature for the diagnosis of lung cancer aggressiveness |
| KR20160061911A (ko) | 2013-04-08 | 2016-06-01 | 데니스 엠. 브라운 | 최적하 투여된 화학 화합물의 치료 효과 |
| CN112472699A (zh) | 2013-07-26 | 2021-03-12 | 种族肿瘤学公司 | 改善比生群及衍生物的治疗益处的组合方法 |
| SG11201608303QA (en) | 2014-04-04 | 2016-11-29 | Del Mar Pharmaceuticals | Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer |
| WO2015184145A1 (en) * | 2014-05-28 | 2015-12-03 | Eisai R&D Management Co., Ltd. | Use of eribulin and poly (adp ribose) polymerase (parp) inhibitors as combination therapy for the treatment of cancer |
| TW201702218A (zh) | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法 |
| EP3265560B1 (en) | 2015-03-02 | 2021-12-08 | Sinai Health System | Homologous recombination factors |
| CN104945406B (zh) * | 2015-05-25 | 2017-10-10 | 苏州康润医药有限公司 | 氮杂非那烯‑3‑酮的衍生物、其制备方法及其作为parp抑制剂的应用 |
| AU2016296905B2 (en) | 2015-07-23 | 2018-07-05 | Centre National De La Recherche Scientifique | Use of a combination of Dbait molecule and parp inhibitors to treat cancer |
| WO2018162439A1 (en) | 2017-03-08 | 2018-09-13 | Onxeo | New predictive biomarker for the sensitivity to a treatment of cancer with a dbait molecule |
| WO2018165615A1 (en) * | 2017-03-09 | 2018-09-13 | The Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Parp-1 and methods of use thereof |
| US12121518B2 (en) * | 2017-03-09 | 2024-10-22 | The Board Of Supervisors Of Louisiana State Universi And Agricultural And Mechanical College | PARP-1 and methods of use thereof |
| MY206158A (en) | 2017-05-24 | 2024-12-02 | Novartis Ag | Antibody-cytokine engrafted proteins and methods of use in the treatment of cancer |
| CA3092779A1 (en) | 2018-03-13 | 2019-09-19 | Onxeo | A dbait molecule against acquired resistance in the treatment of cancer |
| AU2019373416A1 (en) | 2018-10-30 | 2021-06-10 | Repare Therapeutics Inc. | Compounds, pharmaceutical compositions, and methods of preparing compounds and of their use as ATR kinase inhibitors |
| US12479830B2 (en) * | 2019-10-10 | 2025-11-25 | Esteve Pharmaceuticals, S.A. | Homopiperazinyl and homopiperidinyl quinazolin-4(3H)-one derivatives having multimodal activity against pain |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| WO2021249996A1 (en) | 2020-06-08 | 2021-12-16 | Oncology Venture ApS | Compositions comprising 2x-121 and methods for treating coronavirus infection |
| CN114053276B (zh) * | 2020-07-30 | 2024-05-07 | 江苏天士力帝益药业有限公司 | 一种parp抑制剂tsl-1502中间体tsl-1502m的用途 |
| TW202508595A (zh) | 2023-05-04 | 2025-03-01 | 美商銳新醫藥公司 | 用於ras相關疾病或病症之組合療法 |
| CN121398822A (zh) | 2023-06-21 | 2026-01-23 | 四方生物科学有限公司 | 用于在治疗hr功能正常的癌症的方法中的用途的包含脱氧胞苷衍生物和parp抑制剂的组合 |
| US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| AU2024360465A1 (en) | 2023-10-12 | 2026-04-09 | Revolution Medicines, Inc. | Macrocyclic ras inhibitors |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025217307A1 (en) | 2024-04-09 | 2025-10-16 | Revolution Medicines, Inc. | Methods for predicting response to a ras(on) inhibitor and combination therapies |
| TW202547461A (zh) | 2024-05-17 | 2025-12-16 | 美商銳新醫藥公司 | Ras抑制劑 |
| WO2025255438A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| WO2025265060A1 (en) | 2024-06-21 | 2025-12-26 | Revolution Medicines, Inc. | Therapeutic compositions and methods for managing treatment-related effects |
| WO2026006747A1 (en) | 2024-06-28 | 2026-01-02 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026015790A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015796A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015801A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Methods of treating a ras related disease or disorder |
| WO2026015825A1 (en) | 2024-07-12 | 2026-01-15 | Revolution Medicines, Inc. | Use of ras inhibitor for treating pancreatic cancer |
| WO2026050446A1 (en) | 2024-08-29 | 2026-03-05 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2026072904A2 (en) | 2024-09-26 | 2026-04-02 | Revolution Medicines, Inc. | Compositions and methods for treating lung cancer |
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2008
- 2008-10-02 ES ES08836018.5T patent/ES2504690T3/es active Active
- 2008-10-02 CN CN200880118681.4A patent/CN102083314B/zh active Active
- 2008-10-02 KR KR1020107009588A patent/KR101596526B1/ko active Active
- 2008-10-02 HR HRP20140853AT patent/HRP20140853T1/hr unknown
- 2008-10-02 WO PCT/US2008/078606 patent/WO2009046205A1/en not_active Ceased
- 2008-10-02 MX MX2010003564A patent/MX2010003564A/es active IP Right Grant
- 2008-10-02 UA UAA201005117A patent/UA99483C2/ru unknown
- 2008-10-02 EP EP08836018.5A patent/EP2209375B1/en active Active
- 2008-10-02 SG SG2012073482A patent/SG185272A1/en unknown
- 2008-10-02 RU RU2010117397/04A patent/RU2485122C2/ru active
- 2008-10-02 MY MYPI2010001496A patent/MY155237A/en unknown
- 2008-10-02 DK DK08836018.5T patent/DK2209375T3/da active
- 2008-10-02 SI SI200831302T patent/SI2209375T1/sl unknown
- 2008-10-02 CA CA2700903A patent/CA2700903C/en active Active
- 2008-10-02 JP JP2010528132A patent/JP5439380B2/ja active Active
- 2008-10-02 NZ NZ585012A patent/NZ585012A/en not_active IP Right Cessation
- 2008-10-02 EP EP14179976.7A patent/EP2842956A1/en not_active Withdrawn
- 2008-10-02 PT PT88360185T patent/PT2209375E/pt unknown
- 2008-10-02 AU AU2008308664A patent/AU2008308664B2/en active Active
- 2008-10-02 PL PL08836018T patent/PL2209375T3/pl unknown
- 2008-10-02 US US12/244,399 patent/US8236802B2/en active Active
- 2008-10-02 BR BRPI0820518-3A patent/BRPI0820518B1/pt active IP Right Grant
- 2008-10-03 TW TW097138166A patent/TWI426912B/zh active
- 2008-10-05 JO JOP/2008/0433A patent/JO3170B1/ar active
-
2010
- 2010-03-28 IL IL204776A patent/IL204776A/en active IP Right Grant
- 2010-03-31 ZA ZA2010/02317A patent/ZA201002317B/en unknown
- 2010-04-05 CL CL2010000320A patent/CL2010000320A1/es unknown
-
2012
- 2012-06-19 US US13/527,158 patent/US8894989B2/en active Active
-
2014
- 2014-09-25 CY CY20141100783T patent/CY1115747T1/el unknown
- 2014-11-11 US US14/538,447 patent/US20150141429A1/en not_active Abandoned
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