UA82753C2 - Производные пролина, которые используются в качестве фармацевтических активных ингредиентов для лечения опухолей - Google Patents
Производные пролина, которые используются в качестве фармацевтических активных ингредиентов для лечения опухолей Download PDFInfo
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- UA82753C2 UA82753C2 UAA200608086A UAA200608086A UA82753C2 UA 82753 C2 UA82753 C2 UA 82753C2 UA A200608086 A UAA200608086 A UA A200608086A UA A200608086 A UAA200608086 A UA A200608086A UA 82753 C2 UA82753 C2 UA 82753C2
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- XFCLJVABOIYOMF-QPLCGJKRSA-N toremifene Chemical compound C1=CC(OCCN(C)C)=CC=C1C(\C=1C=CC=CC=1)=C(\CCCl)C1=CC=CC=C1 XFCLJVABOIYOMF-QPLCGJKRSA-N 0.000 description 1
- 229960005026 toremifene Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 229960000575 trastuzumab Drugs 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 1
- NOYPYLRCIDNJJB-UHFFFAOYSA-N trimetrexate Chemical compound COC1=C(OC)C(OC)=CC(NCC=2C(=C3C(N)=NC(N)=NC3=CC=2)C)=C1 NOYPYLRCIDNJJB-UHFFFAOYSA-N 0.000 description 1
- 229960001099 trimetrexate Drugs 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 230000001573 trophoblastic effect Effects 0.000 description 1
- 102000003390 tumor necrosis factor Human genes 0.000 description 1
- 230000001173 tumoral effect Effects 0.000 description 1
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
- 210000000626 ureter Anatomy 0.000 description 1
- 210000003708 urethra Anatomy 0.000 description 1
- 210000003932 urinary bladder Anatomy 0.000 description 1
- 210000002229 urogenital system Anatomy 0.000 description 1
- 206010046766 uterine cancer Diseases 0.000 description 1
- 238000002255 vaccination Methods 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 210000001215 vagina Anatomy 0.000 description 1
- 208000019553 vascular disease Diseases 0.000 description 1
- 230000024883 vasodilation Effects 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229960003048 vinblastine Drugs 0.000 description 1
- JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-N 0.000 description 1
- 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 description 1
- 229960004528 vincristine Drugs 0.000 description 1
- 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 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 210000003905 vulva Anatomy 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 235000021119 whey protein Nutrition 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Изобретение относится к производным пролина и их солей, к фармацевтическим средствам, которые содержат указанные производные, и к использованию указанных средств для лечения опухолей. Изобретение относится также к способам получения указанных соединений и фармацевтических средств.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/DE2003/004211 WO2005058816A1 (de) | 2003-12-18 | 2003-12-18 | Prolinderivate als pharmazeutische wirkstoffe in der tumortherapie |
Publications (1)
Publication Number | Publication Date |
---|---|
UA82753C2 true UA82753C2 (ru) | 2008-05-12 |
Family
ID=34683207
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UAA200608086A UA82753C2 (ru) | 2003-12-18 | 2003-12-18 | Производные пролина, которые используются в качестве фармацевтических активных ингредиентов для лечения опухолей |
Country Status (10)
Country | Link |
---|---|
US (1) | US20080176923A1 (ru) |
EP (1) | EP1711462A1 (ru) |
JP (1) | JP2007523829A (ru) |
CN (1) | CN1942438A (ru) |
AU (1) | AU2003298077A1 (ru) |
BR (1) | BR0318659A (ru) |
CA (1) | CA2548391A1 (ru) |
MX (1) | MXPA06007007A (ru) |
UA (1) | UA82753C2 (ru) |
WO (1) | WO2005058816A1 (ru) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005120495A1 (en) | 2004-06-14 | 2005-12-22 | Salama Zoser B | Anti-cancer composition comprising proline or its derivatives and an anti-tumour antibody |
CN100396666C (zh) * | 2005-12-14 | 2008-06-25 | 郑州大学 | (4s)-1-叔丁氧羰基-4-氨基-l-脯氨酸乙酯及其合成工艺 |
WO2012024367A2 (en) * | 2010-08-18 | 2012-02-23 | Del Mar Pharmaceuticals | Compositions and methods to improve the therapeutic benefit of suboptimally administered chemical compounds including substituted hexitols such as dianhydrogalactitol and diacetyldianhydrogalactitol |
US10201521B2 (en) * | 2012-01-20 | 2019-02-12 | Del Mar Pharmaceuticals (Bc) Ltd. | Use of substituted hexitols including dianhydrogalactitol and analogs to treat neoplastic disease and cancer stem and cancer stem cells including glioblastoma multiforme and medulloblastoma |
WO2013169600A1 (en) | 2012-05-09 | 2013-11-14 | Delmar Pharmaceuticals | Veterinary use of dianhydrogalactitol, diacetyldianhydrogalactitol, and dibromodulcitol to treat malignancies |
EA030611B1 (ru) * | 2013-03-15 | 2018-08-31 | Кэнсер Рисерч Текнолоджи, Ллк | Способы и композиции для модуляции гамма-глутамилового цикла |
US10328051B2 (en) * | 2014-09-22 | 2019-06-25 | Zoser B. Salama | Proline or proline derivatives for the treatment of dementia |
CN105061282A (zh) * | 2015-07-28 | 2015-11-18 | 黑龙江省科学院石油化学研究院 | 氢解合成α,α-二苯基-2-吡咯烷甲醇的方法 |
AU2020349967A1 (en) * | 2019-09-20 | 2022-05-12 | Michiko Koga | Peptide, and cell fusion agent and pharmaceutical composition for cancer therapy containing said peptide |
CN113968808B (zh) * | 2021-11-26 | 2024-04-09 | 河南中医药大学 | 一类水苏碱衍生物的制备方法及其应用 |
CN114028388B (zh) * | 2021-12-16 | 2023-05-12 | 郑州大学第一附属医院 | 脯氨酸在制备肺癌治疗药物中的应用 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4499287A (en) * | 1981-02-02 | 1985-02-12 | E. R. Squibb & Sons, Inc. | Certain-4-hydroxy-proline derivatives |
CA1281288C (en) * | 1984-11-05 | 1991-03-12 | Wilhelm Hoerrmann | Tumor therapy |
DE3518078A1 (de) * | 1985-05-20 | 1986-11-20 | Wilhelm Dr. 8127 Iffeldorf Hoerrmann | Arzneimittel, die derivate des prolin oder hydroxyprolin enthalten |
JPH05213957A (ja) * | 1992-02-07 | 1993-08-24 | Tsumura & Co | 新規なスピロピロリジンイミダゾリン誘導体および新規なアミノピロリジンカルボン酸誘導体並びに該化合物を有効成分とする鎮けい剤 |
WO1997033578A1 (de) * | 1996-03-11 | 1997-09-18 | Wilhelm Hoerrmann | Kombination aus cis-4-hydroxy-l-prolin und n-methyl-cis-4-hydroxy-l-prolin zur anwendung als therapeutischer wirkstoff insbesondere für die krebstherapie |
AU2002227020A1 (en) * | 2001-01-05 | 2002-07-16 | Eli Lilly And Company | Pyrrolidinylmethyl- and piperidinyl substituted decahydroisoquinolines as excitatory amino acid receptor antagonists |
-
2003
- 2003-12-18 CA CA002548391A patent/CA2548391A1/en not_active Abandoned
- 2003-12-18 US US10/596,636 patent/US20080176923A1/en not_active Abandoned
- 2003-12-18 AU AU2003298077A patent/AU2003298077A1/en not_active Abandoned
- 2003-12-18 UA UAA200608086A patent/UA82753C2/ru unknown
- 2003-12-18 MX MXPA06007007A patent/MXPA06007007A/es not_active Application Discontinuation
- 2003-12-18 EP EP03795774A patent/EP1711462A1/de not_active Withdrawn
- 2003-12-18 WO PCT/DE2003/004211 patent/WO2005058816A1/de active Application Filing
- 2003-12-18 JP JP2005512148A patent/JP2007523829A/ja not_active Withdrawn
- 2003-12-18 BR BRPI0318659-8A patent/BR0318659A/pt not_active IP Right Cessation
- 2003-12-18 CN CNA200380110862XA patent/CN1942438A/zh active Pending
Also Published As
Publication number | Publication date |
---|---|
CN1942438A (zh) | 2007-04-04 |
EP1711462A1 (de) | 2006-10-18 |
JP2007523829A (ja) | 2007-08-23 |
AU2003298077A1 (en) | 2005-07-05 |
BR0318659A (pt) | 2006-11-28 |
CA2548391A1 (en) | 2005-06-30 |
US20080176923A1 (en) | 2008-07-24 |
WO2005058816A1 (de) | 2005-06-30 |
AU2003298077A2 (en) | 2005-07-05 |
MXPA06007007A (es) | 2007-06-08 |
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