RU2010113569A - Производное бензохинона е3330 в комбинации с химиотерапевтическими агентами для лечения рака и ангиогенеза - Google Patents
Производное бензохинона е3330 в комбинации с химиотерапевтическими агентами для лечения рака и ангиогенеза Download PDFInfo
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- 206010028980 Neoplasm Diseases 0.000 title claims abstract 11
- 201000011510 cancer Diseases 0.000 title claims abstract 9
- 230000033115 angiogenesis Effects 0.000 title claims abstract 3
- 239000002246 antineoplastic agent Substances 0.000 title 1
- 229940127089 cytotoxic agent Drugs 0.000 title 1
- 239000003795 chemical substances by application Substances 0.000 claims abstract 11
- 239000003814 drug Substances 0.000 claims abstract 8
- 229940124597 therapeutic agent Drugs 0.000 claims abstract 8
- 150000003839 salts Chemical class 0.000 claims abstract 7
- 101100452003 Caenorhabditis elegans ape-1 gene Proteins 0.000 claims abstract 4
- 230000000694 effects Effects 0.000 claims abstract 4
- UEJJHQNACJXSKW-UHFFFAOYSA-N 2-(2,6-dioxopiperidin-3-yl)-1H-isoindole-1,3(2H)-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1C1CCC(=O)NC1=O UEJJHQNACJXSKW-UHFFFAOYSA-N 0.000 claims abstract 3
- SHGAZHPCJJPHSC-YCNIQYBTSA-N all-trans-retinoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C SHGAZHPCJJPHSC-YCNIQYBTSA-N 0.000 claims abstract 3
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims abstract 3
- 229960004316 cisplatin Drugs 0.000 claims abstract 3
- SDUQYLNIPVEERB-QPPQHZFASA-N gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 claims abstract 3
- 229960005277 gemcitabine Drugs 0.000 claims abstract 3
- SGDBTWWWUNNDEQ-LBPRGKRZSA-N melphalan Chemical group OC(=O)[C@@H](N)CC1=CC=C(N(CCCl)CCCl)C=C1 SGDBTWWWUNNDEQ-LBPRGKRZSA-N 0.000 claims abstract 3
- 229960001924 melphalan Drugs 0.000 claims abstract 3
- 229930002330 retinoic acid Natural products 0.000 claims abstract 3
- 229960003433 thalidomide Drugs 0.000 claims abstract 3
- 229960001727 tretinoin Drugs 0.000 claims abstract 3
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims abstract 2
- 208000024172 Cardiovascular disease Diseases 0.000 claims abstract 2
- 206010012689 Diabetic retinopathy Diseases 0.000 claims abstract 2
- 201000009273 Endometriosis Diseases 0.000 claims abstract 2
- 201000009794 Idiopathic Pulmonary Fibrosis Diseases 0.000 claims abstract 2
- 208000002260 Keloid Diseases 0.000 claims abstract 2
- 201000004681 Psoriasis Diseases 0.000 claims abstract 2
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims abstract 2
- 206010038933 Retinopathy of prematurity Diseases 0.000 claims abstract 2
- 201000009594 Systemic Scleroderma Diseases 0.000 claims abstract 2
- 206010042953 Systemic sclerosis Diseases 0.000 claims abstract 2
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims abstract 2
- 208000006673 asthma Diseases 0.000 claims abstract 2
- 210000000481 breast Anatomy 0.000 claims abstract 2
- 208000037976 chronic inflammation Diseases 0.000 claims abstract 2
- 208000037893 chronic inflammatory disorder Diseases 0.000 claims abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract 2
- 208000035475 disorder Diseases 0.000 claims abstract 2
- 230000002401 inhibitory effect Effects 0.000 claims abstract 2
- 208000036971 interstitial lung disease 2 Diseases 0.000 claims abstract 2
- 210000001117 keloid Anatomy 0.000 claims abstract 2
- 208000002780 macular degeneration Diseases 0.000 claims abstract 2
- 210000000496 pancreas Anatomy 0.000 claims abstract 2
- 210000002307 prostate Anatomy 0.000 claims abstract 2
- 206010039073 rheumatoid arthritis Diseases 0.000 claims abstract 2
- 206010018338 Glioma Diseases 0.000 claims 1
- 208000034578 Multiple myelomas Diseases 0.000 claims 1
- 208000034176 Neoplasms, Germ Cell and Embryonal Diseases 0.000 claims 1
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 1
- 229960000397 bevacizumab Drugs 0.000 claims 1
- 210000003679 cervix uteri Anatomy 0.000 claims 1
- 210000001072 colon Anatomy 0.000 claims 1
- 208000032839 leukemia Diseases 0.000 claims 1
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims 1
- 201000008968 osteosarcoma Diseases 0.000 claims 1
- 201000009410 rhabdomyosarcoma Diseases 0.000 claims 1
- 239000012453 solvate Substances 0.000 claims 1
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims 1
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- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- A61K31/201—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having one or two double bonds, e.g. oleic, linoleic acids
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- A61K31/122—Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
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- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
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- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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Abstract
1. Способ подавления физиологических нарушений, связанных с измененным ангиогенезом, включающий введение нуждающемуся субъекту эффективного количества агента, селективно ингибирующего окислительно-восстановительную активность Ape1/Ref-1. ! 2. Способ по п.1, где указанным агентом является Е3330 или его фармацевтически приемлемая соль. ! 3. Способ по п.1, где указанное нарушение выбрано из онкологического заболевания, сердечно-сосудистого заболевания, хронического воспалительного заболевания, ревматоидного артрита, диабетической ретинопатии, макулярной дегенерации, ретролентальной фиброплазии, идиопатического фиброза легких, острого респираторного дистресс-синдрома взрослых, астмы, эндометриоза, псориаза, келоидов и системного склероза. ! 4. Способ по п.3, где указанным нарушением является рак. ! 5. Способ по п.4, где указанным агентом является Е3330, или его фармацевтически приемлемая соль, или сольват. ! 6. Способ по п.5, где указанному субъекту вводится по меньшей мере один дополнительный терапевтический агент. ! 7. Способ по п.6, где указанный дополнительный терапевтический агент выбран из мелфалана, гемцитабина, цисплатина, метосиамина, талидомида и его производных и ретиноевой кислоты. !8. Способ подавления онкологического заболевания, включающий введение нуждающемуся субъекту эффективного количества агента, который селективно ингибирует окислительно-восстановительную активность Ape1/Ref-1. ! 9. Способ по п.8, где указанным агентом является Е3330 или его фармацевтически приемлемая соль. ! 10. Способ по п.8, где указанное онкологическое заболевание выбрано из опухолей молочной железы, простаты, поджелудочной железы, толсто�
Claims (15)
1. Способ подавления физиологических нарушений, связанных с измененным ангиогенезом, включающий введение нуждающемуся субъекту эффективного количества агента, селективно ингибирующего окислительно-восстановительную активность Ape1/Ref-1.
2. Способ по п.1, где указанным агентом является Е3330 или его фармацевтически приемлемая соль.
3. Способ по п.1, где указанное нарушение выбрано из онкологического заболевания, сердечно-сосудистого заболевания, хронического воспалительного заболевания, ревматоидного артрита, диабетической ретинопатии, макулярной дегенерации, ретролентальной фиброплазии, идиопатического фиброза легких, острого респираторного дистресс-синдрома взрослых, астмы, эндометриоза, псориаза, келоидов и системного склероза.
4. Способ по п.3, где указанным нарушением является рак.
5. Способ по п.4, где указанным агентом является Е3330, или его фармацевтически приемлемая соль, или сольват.
6. Способ по п.5, где указанному субъекту вводится по меньшей мере один дополнительный терапевтический агент.
7. Способ по п.6, где указанный дополнительный терапевтический агент выбран из мелфалана, гемцитабина, цисплатина, метосиамина, талидомида и его производных и ретиноевой кислоты.
8. Способ подавления онкологического заболевания, включающий введение нуждающемуся субъекту эффективного количества агента, который селективно ингибирует окислительно-восстановительную активность Ape1/Ref-1.
9. Способ по п.8, где указанным агентом является Е3330 или его фармацевтически приемлемая соль.
10. Способ по п.8, где указанное онкологическое заболевание выбрано из опухолей молочной железы, простаты, поджелудочной железы, толстого кишечника, шейки матки, герминогенных опухолей, глиомы взрослых и детей, остеосаркомы, рабдомиосаркомы, немелкоклеточного рака легких, лейкоза и множественной миеломы.
11. Способ по п.10, где указанным агентом является Е3330, или его фармацевтически приемлемая соль, или сольват.
12. Способ по п.11, где указанному субъекту вводят по меньшей мере один дополнительный терапевтический агент.
13. Способ по п.12, где указанный дополнительный терапевтический агент выбран из мелфалана, гемцитабина, цисплатина, талидомида и его производных и ретиноевой кислоты.
14. Способ по п.2, где указанному субъекту вводят по меньшей мере один дополнительный терапевтический агент.
15. Способ по п.14, где указанным дополнительным терапевтическим агентом является бевацизумаб.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US97539607P | 2007-09-26 | 2007-09-26 | |
| US60/975,396 | 2007-09-26 | ||
| US98956607P | 2007-11-21 | 2007-11-21 | |
| US60/989,566 | 2007-11-21 | ||
| PCT/US2008/077210 WO2009042542A1 (en) | 2007-09-26 | 2008-09-22 | Benzoquinone derivative e3330 in combination with chemotherapeutic agents for the treatment of cancer and angiogenesis |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2010113569A true RU2010113569A (ru) | 2011-11-10 |
| RU2510270C2 RU2510270C2 (ru) | 2014-03-27 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2010113569/15A RU2510270C2 (ru) | 2007-09-26 | 2008-09-22 | Производное бензохинона е3330 в комбинации с химиотерапевтическими агентами для лечения рака и ангиогенеза |
Country Status (13)
| Country | Link |
|---|---|
| US (6) | US9089605B2 (ru) |
| EP (4) | EP2203161B1 (ru) |
| JP (4) | JP5628674B2 (ru) |
| KR (2) | KR101572688B1 (ru) |
| AU (5) | AU2008304619C1 (ru) |
| BR (1) | BRPI0817293A2 (ru) |
| CA (2) | CA2700365C (ru) |
| ES (2) | ES2675951T3 (ru) |
| IL (1) | IL204675A0 (ru) |
| MX (1) | MX2010003315A (ru) |
| RU (1) | RU2510270C2 (ru) |
| WO (2) | WO2009042542A1 (ru) |
| ZA (1) | ZA201002246B (ru) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2203161B1 (en) * | 2007-09-26 | 2018-05-09 | Indiana University Research and Technology Corporation | Quinone derivatives, pharmaceutical compositions, and uses thereof |
| US11331294B2 (en) | 2007-09-26 | 2022-05-17 | Indiana University Research And Technology Corporation | Benzoquinone derivative E3330 in combination with chemotherapeutic agents for the treatment of bladder cancer |
| US9567346B2 (en) * | 2010-10-29 | 2017-02-14 | Life Technologies Corporation | Biotin derivatives |
| US9517244B2 (en) | 2011-04-22 | 2016-12-13 | University Of Florida Research Foundation, Inc. | Therapeutic combinations for use in neoplasia |
| JP6109821B2 (ja) * | 2011-05-26 | 2017-04-05 | インディアナ ユニバーシティー リサーチ アンド テクノロジー コーポレーションIndiana University Research And Technology Corporation | Ape1媒介疾患を処置するためのキノン化合物 |
| WO2012167122A1 (en) | 2011-06-03 | 2012-12-06 | Indiana University Research And Technology Corporation | Compounds, compositions and methods for treating oxidative dna damage disorders |
| WO2013021953A1 (ja) * | 2011-08-05 | 2013-02-14 | 帝人株式会社 | 縮合多環芳香族化合物、芳香族重合体、及び芳香族化合物の合成方法 |
| US9624235B2 (en) * | 2012-01-31 | 2017-04-18 | University of Pittsburgh—of the Commonwealth System of Higher Education | Compounds and methods for inhibition of AP endonuclease-1/redox factor-1 (HAPE1) activity |
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