RU2008138534A - Фармацевтическая комбинация для лечения и/или хемосенсебилизации опухолей, устойчивых к противораковым средствам - Google Patents
Фармацевтическая комбинация для лечения и/или хемосенсебилизации опухолей, устойчивых к противораковым средствам Download PDFInfo
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- cytostatic substance
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- 206010028980 Neoplasm Diseases 0.000 title claims abstract 5
- 239000000126 substance Substances 0.000 claims abstract 25
- 239000000824 cytostatic agent Substances 0.000 claims abstract 23
- 230000001085 cytostatic effect Effects 0.000 claims abstract 23
- 239000003112 inhibitor Substances 0.000 claims abstract 8
- 230000026731 phosphorylation Effects 0.000 claims abstract 8
- 238000006366 phosphorylation reaction Methods 0.000 claims abstract 8
- 239000000758 substrate Substances 0.000 claims abstract 8
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 claims abstract 4
- NWIBSHFKIJFRCO-WUDYKRTCSA-N Mytomycin Chemical group C1N2C(C(C(C)=C(N)C3=O)=O)=C3[C@@H](COC(N)=O)[C@@]2(OC)[C@@H]2[C@H]1N2 NWIBSHFKIJFRCO-WUDYKRTCSA-N 0.000 claims abstract 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract 4
- 150000001875 compounds Chemical class 0.000 claims abstract 3
- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical group ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims abstract 2
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000005517 L01XE01 - Imatinib Substances 0.000 claims abstract 2
- 239000005411 L01XE02 - Gefitinib Substances 0.000 claims abstract 2
- 229940122803 Vinca alkaloid Drugs 0.000 claims abstract 2
- 229960004562 carboplatin Drugs 0.000 claims abstract 2
- 190000008236 carboplatin Chemical compound 0.000 claims abstract 2
- 239000000969 carrier Substances 0.000 claims abstract 2
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims abstract 2
- 229960004316 cisplatin Drugs 0.000 claims abstract 2
- 229960004397 cyclophosphamide Drugs 0.000 claims abstract 2
- 229960004679 doxorubicin Drugs 0.000 claims abstract 2
- 229960002949 fluorouracil Drugs 0.000 claims abstract 2
- XGALLCVXEZPNRQ-UHFFFAOYSA-N gefitinib Chemical group C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 claims abstract 2
- 201000005787 hematologic cancer Diseases 0.000 claims abstract 2
- 208000024200 hematopoietic and lymphoid system neoplasm Diseases 0.000 claims abstract 2
- KTUFNOKKBVMGRW-UHFFFAOYSA-N imatinib Chemical compound C1CN(C)CCN1CC1=CC=C(C(=O)NC=2C=C(NC=3N=C(C=CN=3)C=3C=NC=CC=3)C(C)=CC=2)C=C1 KTUFNOKKBVMGRW-UHFFFAOYSA-N 0.000 claims abstract 2
- 229960002411 imatinib Drugs 0.000 claims abstract 2
- 239000004615 ingredient Substances 0.000 claims abstract 2
- 229940084651 iressa Drugs 0.000 claims abstract 2
- 229960004857 mitomycin Drugs 0.000 claims abstract 2
- 229910052697 platinum Inorganic materials 0.000 claims abstract 2
- 239000007787 solid Substances 0.000 claims abstract 2
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 claims abstract 2
- 229960004528 vincristine Drugs 0.000 claims abstract 2
- OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000003814 drug Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 1
- 108090000765 processed proteins & peptides Proteins 0.000 claims 1
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Abstract
1. Фармацевтическая комбинация для одновременного, раздельного или последовательного введения, которая содержит ингибитор сайта фосфорилирования на субстратах СК2 наряду с цитостатическим веществом, фармацевтически приемлемо смешанным с соответствующими переносчиками. ! 2. Фармацевтическая комбинация по п.1, в которой ингибитор сайта фосфорилирования на субстратах СК2 включает пептид Р15 (CWMSPRHLGTC). ! 3. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является химическим соединением, которое принадлежит к платинам (карбоплатин и цисплатин), таксолам (пакситаксел и досетаксел) и алкалоидам Vinca (винкристин и винблатин). ! 4. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является 5-фторурацилом. ! 5. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является доксорубицином. ! 6. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является циклофосфамидом. ! 7. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является Митомицином С. ! 8. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является Велкадом (вортезомибом). ! 9. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является Ирессой. ! 10. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является Иматинибом. ! 11. Применение фармацевтических комбинаций по пп.1-10 для обхода химической устойчивости солидных и гематопоэтических опухолей к фармацевтически приемлемым цитостатическим веществом и, где ингредиенты фармацевтической комбинации вводятся одновременно, разд
Claims (15)
1. Фармацевтическая комбинация для одновременного, раздельного или последовательного введения, которая содержит ингибитор сайта фосфорилирования на субстратах СК2 наряду с цитостатическим веществом, фармацевтически приемлемо смешанным с соответствующими переносчиками.
2. Фармацевтическая комбинация по п.1, в которой ингибитор сайта фосфорилирования на субстратах СК2 включает пептид Р15 (CWMSPRHLGTC).
3. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является химическим соединением, которое принадлежит к платинам (карбоплатин и цисплатин), таксолам (пакситаксел и досетаксел) и алкалоидам Vinca (винкристин и винблатин).
4. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является 5-фторурацилом.
5. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является доксорубицином.
6. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является циклофосфамидом.
7. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является Митомицином С.
8. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является Велкадом (вортезомибом).
9. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является Ирессой.
10. Фармацевтическая комбинация по пп.1 и 2, в которой цитостатическое вещество является Иматинибом.
11. Применение фармацевтических комбинаций по пп.1-10 для обхода химической устойчивости солидных и гематопоэтических опухолей к фармацевтически приемлемым цитостатическим веществом и, где ингредиенты фармацевтической комбинации вводятся одновременно, раздельно или последовательно.
12. Применение фармацевтических комбинаций по пп.1-10, где ингибитор сайта фосфорилирования на субстратах СК2 является химическим соединением или пептидом.
13. Применение фармацевтических комбинаций по пп.1-10, где ингибитор сайта фосфорилирования на субстратах СК2 экспрессируется в ДНК векторе.
14. Применение ингибитора сайта фосфорилирования на субстратах СК2 наряду с фармацевтически приемлемым цитостатическим веществом для получения лекарственного средства для лечения рака.
15. Применение ингибитора сайта фосфорилирования на субстратах СК2 наряду с фармацевтически приемлемым цитостатическим веществом для получения лекарственного средства для лечения химически устойчивых опухолей к цитостатическим веществам.
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| CU2006-0049 | 2006-02-28 | ||
| CU20060049A CU23511B6 (es) | 2006-02-28 | 2006-02-28 | Combinación farmacéutica para el tratamiento y/o quimiosensibilización de tumores refractarios a drogas anticancerígenas |
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| RU2008138534A true RU2008138534A (ru) | 2010-04-10 |
| RU2396974C2 RU2396974C2 (ru) | 2010-08-20 |
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| RU2008138534/15A RU2396974C2 (ru) | 2006-02-28 | 2007-02-28 | Фармацевтическая комбинация для лечения и/или хемосенсибилизации опухолей, устойчивых к противораковым средствам |
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| EP (1) | EP1997506B8 (ru) |
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| BR (1) | BRPI0708307B1 (ru) |
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| UY (1) | UY30175A1 (ru) |
| WO (1) | WO2007098719A1 (ru) |
| ZA (1) | ZA200807323B (ru) |
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| CU23511B6 (es) * | 2006-02-28 | 2010-04-13 | Biorec B V | Combinación farmacéutica para el tratamiento y/o quimiosensibilización de tumores refractarios a drogas anticancerígenas |
| GB0803352D0 (en) | 2008-02-22 | 2008-04-02 | Ntnu Technology Transfer As | Oligopeptidic compounds and uses thereof |
| US20100173013A1 (en) * | 2009-01-08 | 2010-07-08 | Denis Drygin | Treatment of neoplastic disorders using combination therapies |
| EP3866804A4 (en) | 2018-10-19 | 2022-08-03 | Senhwa Biosciences, Inc. | Combinations for immune-modulation in cancer treatment |
| CN109875998B (zh) * | 2019-01-24 | 2021-09-03 | 武汉大学 | 酰胺类生物碱在制备肿瘤化疗药物增敏剂中的应用及抗肿瘤药物组合物 |
| CN110448699B (zh) * | 2019-06-12 | 2022-03-11 | 天津医科大学 | 包含功能性多肽修饰七甲川花菁素类染料的肿瘤细胞核靶向载药纳米粒子及制备方法 |
| CU20200103A7 (es) * | 2020-12-18 | 2022-07-08 | Ct Ingenieria Genetica Biotecnologia | Péptido sintético para la inducción de inmunidad antitumoral y antiviral |
| CN114712377B (zh) * | 2022-04-26 | 2023-08-15 | 江苏师范大学 | 断血流皂苷a在制造药物中的用途 |
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| DE69738815D1 (de) * | 1996-10-15 | 2008-08-14 | Searle Llc | Verwendung von Cyclooxygenase-2 Inhibitoren zur Behandlung und Vorbeugung von Neoplasia |
| CU23225A1 (es) * | 2001-12-20 | 2007-08-30 | Ct Ingenieria Genetica Biotech | PéPTIDOS PARA EL TRATAMIENTO DEL CáNCER ASOCIADO AL VIRUS PAPILOMA HUMANO (VPH) Y DE OTROS TUMORES EPITELIALES |
| JP2005533748A (ja) * | 2002-03-08 | 2005-11-10 | シグナル ファーマシューティカルズ,インコーポレイテッド | 増殖性障害および癌を治療、予防、または管理するための併用療法 |
| US20060014987A1 (en) * | 2003-07-07 | 2006-01-19 | Lan Huang | Synthesis of beta-elemene, intermediates thereto, analogues and uses thereof |
| WO2005049030A1 (en) * | 2003-11-14 | 2005-06-02 | Pharma Mar, S.A. | Combination therapy comprising the use of et-743 and paclitaxel for treating cancer |
| CA2546920A1 (en) * | 2003-12-09 | 2005-06-23 | Joel Moss | Methods for suppressing an immune response or treating a proliferative disorder |
| TW200538149A (en) * | 2004-05-20 | 2005-12-01 | Telik Inc | Sensitization to another anticancer therapy and/or amelioration of a side effect of another anticancer therapy by treatment with a GST-activated anticancer compound |
| CU23511B6 (es) * | 2006-02-28 | 2010-04-13 | Biorec B V | Combinación farmacéutica para el tratamiento y/o quimiosensibilización de tumores refractarios a drogas anticancerígenas |
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