MXPA06011886A - Derivados de (poli)aminoacetamida de epipodofilotoxina, sus procedimientos de preparacion y sus aplicaciones en terapeutica como agentes anticancerigenos. - Google Patents
Derivados de (poli)aminoacetamida de epipodofilotoxina, sus procedimientos de preparacion y sus aplicaciones en terapeutica como agentes anticancerigenos.Info
- Publication number
- MXPA06011886A MXPA06011886A MXPA06011886A MXPA06011886A MXPA06011886A MX PA06011886 A MXPA06011886 A MX PA06011886A MX PA06011886 A MXPA06011886 A MX PA06011886A MX PA06011886 A MXPA06011886 A MX PA06011886A MX PA06011886 A MXPA06011886 A MX PA06011886A
- Authority
- MX
- Mexico
- Prior art keywords
- oxo
- hydroxy
- dioxol
- acetamide
- dimethoxyphenyl
- Prior art date
Links
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- 238000000034 method Methods 0.000 title claims abstract description 43
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- NJAPCAIWQRPQPY-UHFFFAOYSA-N benzyl hydrogen carbonate Chemical compound OC(=O)OCC1=CC=CC=C1 NJAPCAIWQRPQPY-UHFFFAOYSA-N 0.000 description 1
- QMMFTRJQCCVPCE-UHFFFAOYSA-N benzyl n-(2-aminoethyl)carbamate Chemical compound NCCNC(=O)OCC1=CC=CC=C1 QMMFTRJQCCVPCE-UHFFFAOYSA-N 0.000 description 1
- ZZRXQSABHQZWCC-UHFFFAOYSA-N benzyl n-(5-aminopentyl)carbamate Chemical compound NCCCCCNC(=O)OCC1=CC=CC=C1 ZZRXQSABHQZWCC-UHFFFAOYSA-N 0.000 description 1
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000006037 cell lysis Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- JCKYGMPEJWAADB-UHFFFAOYSA-N chlorambucil Chemical compound OC(=O)CCCC1=CC=C(N(CCCl)CCCl)C=C1 JCKYGMPEJWAADB-UHFFFAOYSA-N 0.000 description 1
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- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
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- SYHPANJAVIEQQL-UHFFFAOYSA-N dicarboxy carbonate Chemical class OC(=O)OC(=O)OC(O)=O SYHPANJAVIEQQL-UHFFFAOYSA-N 0.000 description 1
- XHFGWHUWQXTGAT-UHFFFAOYSA-N dimethylamine hydrochloride Natural products CNC(C)C XHFGWHUWQXTGAT-UHFFFAOYSA-N 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 description 1
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- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
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- 238000009472 formulation Methods 0.000 description 1
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- 125000005842 heteroatom Chemical group 0.000 description 1
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- 239000007928 intraperitoneal injection Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- RWIVICVCHVMHMU-UHFFFAOYSA-N n-aminoethylmorpholine Chemical compound NCCN1CCOCC1 RWIVICVCHVMHMU-UHFFFAOYSA-N 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- 230000017095 negative regulation of cell growth Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 208000002154 non-small cell lung carcinoma Diseases 0.000 description 1
- 229940127084 other anti-cancer agent Drugs 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
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- 238000012552 review Methods 0.000 description 1
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- 238000000926 separation method Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000011806 swiss nude mouse Methods 0.000 description 1
- 229960001278 teniposide Drugs 0.000 description 1
- NRUKOCRGYNPUPR-QBPJDGROSA-N teniposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@@H](OC[C@H]4O3)C=3SC=CC=3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 NRUKOCRGYNPUPR-QBPJDGROSA-N 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 210000004881 tumor cell Anatomy 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 description 1
- GBABOYUKABKIAF-GHYRFKGUSA-N vinorelbine Chemical compound C1N(CC=2C3=CC=CC=C3NC=22)CC(CC)=C[C@H]1C[C@]2(C(=O)OC)C1=CC([C@]23[C@H]([C@]([C@H](OC(C)=O)[C@]4(CC)C=CCN([C@H]34)CC2)(O)C(=O)OC)N2C)=C2C=C1OC GBABOYUKABKIAF-GHYRFKGUSA-N 0.000 description 1
- 229960002066 vinorelbine Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0404053A FR2869035B1 (fr) | 2004-04-16 | 2004-04-16 | Derives (poly)aminoalkylaminoacetamide d'epipodophyllotoxine leur procede de preparation et leurs applications en therapeutique comme agent anticancereux |
| PCT/IB2005/001268 WO2005100363A1 (en) | 2004-04-16 | 2005-04-14 | (poly) aminoacetamide derivatives of epipodophyllotoxin their process of preparation and their applications in therapeutics as anticancer agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA06011886A true MXPA06011886A (es) | 2006-12-14 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA06011886A MXPA06011886A (es) | 2004-04-16 | 2005-04-14 | Derivados de (poli)aminoacetamida de epipodofilotoxina, sus procedimientos de preparacion y sus aplicaciones en terapeutica como agentes anticancerigenos. |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US7846926B2 (enExample) |
| EP (1) | EP1742952B1 (enExample) |
| JP (1) | JP4876070B2 (enExample) |
| CN (1) | CN1946727B (enExample) |
| AR (1) | AR048607A1 (enExample) |
| AT (1) | ATE402938T1 (enExample) |
| AU (1) | AU2005233382C1 (enExample) |
| BR (1) | BRPI0509912B8 (enExample) |
| CA (1) | CA2562617C (enExample) |
| CY (1) | CY1108444T1 (enExample) |
| DE (1) | DE602005008578D1 (enExample) |
| DK (1) | DK1742952T3 (enExample) |
| ES (1) | ES2311985T3 (enExample) |
| FR (1) | FR2869035B1 (enExample) |
| HR (1) | HRP20080542T3 (enExample) |
| MX (1) | MXPA06011886A (enExample) |
| MY (1) | MY137712A (enExample) |
| PL (1) | PL1742952T3 (enExample) |
| PT (1) | PT1742952E (enExample) |
| RS (1) | RS50628B (enExample) |
| SI (1) | SI1742952T1 (enExample) |
| TW (1) | TWI350288B (enExample) |
| WO (1) | WO2005100363A1 (enExample) |
| ZA (1) | ZA200609055B (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2888849B1 (fr) * | 2005-07-19 | 2007-10-05 | Pierre Fabre Medicament Sa | Procede de preparation de la 4b-amino-4'-demethyl-4-desoxypodophyllotoxine |
| FR2919287B1 (fr) * | 2007-07-26 | 2012-10-12 | Pf Medicament | Nouveaux derives fluorescents de polyamines, leur procede de preparation et leurs applications en tant qu'outils de diagnostic dans le traitement des tumeurs cancereuses. |
| FR2921369B1 (fr) * | 2007-09-25 | 2014-07-11 | Pf Medicament | Nouveau procede de preparation de derives (poly) aminoalkylaminoacetamide d'epipodophyllotoxine,utiles pour leurs applications en therapeutique comme agent anticancereux. |
| FR2921368B1 (fr) * | 2007-09-25 | 2012-10-12 | Pf Medicament | Nouveau procede de synthese de derives anticancereux de (poly) aminoalkylaminoacetamide d'epipodophyllotoxine. |
| FR2935143B1 (fr) * | 2008-08-19 | 2010-12-03 | Pf Medicament | Nouveaus derives (poly)aminoalkylaminoalkylamides, alkyl-urees, ou alkyl-sulfonamides d'epipodophyllotoxine, leur procede de preparation et leur application en therapeuthique comme agent cancereux |
| US8288585B2 (en) | 2008-12-31 | 2012-10-16 | Dow Global Technologies Llc | Procatalyst composition with substitute 1,2-phenylene aromatic diester internal donor and method |
| CN102741341B (zh) | 2008-12-31 | 2015-08-05 | 陶氏环球技术有限责任公司 | 丙烯抗冲共聚物和方法 |
| US8263520B2 (en) | 2009-12-02 | 2012-09-11 | Dow Global Technologies Llc | Two atom bridged dicarbonate compounds as internal donors in catalysts for polypropylene manufacture |
| CN102712704B (zh) | 2009-12-02 | 2015-01-07 | 陶氏环球技术有限责任公司 | 作为用于聚丙烯制造的催化剂中的内部给体的三个和四个原子桥接的二碳酸酯化合物 |
| CN102234283B (zh) | 2010-04-23 | 2013-06-12 | 湖北工业大学 | 4′-去甲基表鬼臼毒素衍生物及其合成方法和应用 |
| US8673969B2 (en) * | 2010-11-11 | 2014-03-18 | Council Of Scientific & Industrial Research | Substituted 4-β-acrylamidopodophyllotoxin congeners as antitumour antibiotics and the process for preparation thereof |
| FR2967675B1 (fr) | 2010-11-24 | 2015-02-27 | Pf Medicament | Derives fluorescents de cyanines polyamines en tant que sonde de diagnostic |
| WO2015161745A1 (zh) * | 2014-04-25 | 2015-10-29 | 中国医药工业研究总院 | 鬼臼毒素衍生物、其制备方法、药物组合物及应用 |
| CN104926841A (zh) * | 2015-06-30 | 2015-09-23 | 遵义医学院 | 青蒿琥酯与鬼臼毒素偶联物在抗白血病药物中的应用及制备方法 |
| WO2018234574A1 (en) | 2017-06-22 | 2018-12-27 | Ygm Consult Sas | Combination therapy for the treatment of cancer |
| CN113801129A (zh) * | 2021-09-30 | 2021-12-17 | 大连民族大学 | 一种鬼臼毒素脂质衍生物、纳米载体及其制备方法和在肿瘤治疗中的应用 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6323884A (ja) * | 1986-07-17 | 1988-02-01 | Nippon Kayaku Co Ltd | 新規ポドフイロトキシン誘導体 |
| US5300500A (en) * | 1989-02-23 | 1994-04-05 | The University Of North Carolina At Chapel Hill | 4 beta-amino podophyllotoxin analog compounds and methods |
| US5332811A (en) * | 1989-09-12 | 1994-07-26 | The University Of North Carolina At Chapel Hill | Etopside analogs |
| CN1068330A (zh) * | 1991-07-03 | 1993-01-27 | 国家医药管理局上海医药工业研究院 | 4-氮取代-4-脱氧-4′-去甲表鬼臼毒素衍生物及其合成方法 |
| FR2725990B1 (fr) * | 1994-10-21 | 1997-01-10 | Pf Medicament | Derives hydrosolubles d'epipodophyllotoxine, leur procede de preparation, leur utilisation a titre de medicament, et leur utilisation destinee aux traitements anticancereux |
| FR2742439B1 (fr) | 1995-12-14 | 1998-03-06 | Pf Medicament | Procede de preparation de la 4'-demethylepipodophyllotoxine a partir de la podophyllotoxine |
| FR2810321B1 (fr) | 2000-06-20 | 2002-07-26 | Adir | Nouveaux derives de podophyllotoxine carbamate et thiocarbamate, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| AU2002249559A1 (en) | 2002-03-28 | 2003-10-13 | Council Of Scientific And Industrial Research | 4-beta-1''-`(2''-(substituted benzoyl)anilino! podophyllotoxin analogues useful as anticancer agents |
| US6566393B1 (en) | 2002-06-21 | 2003-05-20 | The University Of North Carolina At Chapel Hill | Etoposide analogs and methods of use thereof |
| WO2004073752A2 (en) | 2003-02-14 | 2004-09-02 | The Board Of Trustees Of The Leland Stanford Junior University | Electrosurgical system with uniformly enhanced electric field and minimal collateral damage |
| US20070066837A1 (en) | 2003-02-18 | 2007-03-22 | Ahmed Kamal | Podophyllotoxin derivatives as antitumor agents |
-
2004
- 2004-04-16 FR FR0404053A patent/FR2869035B1/fr not_active Expired - Fee Related
-
2005
- 2005-04-09 MY MYPI20051581A patent/MY137712A/en unknown
- 2005-04-14 HR HR20080542T patent/HRP20080542T3/xx unknown
- 2005-04-14 DK DK05734896T patent/DK1742952T3/da active
- 2005-04-14 AU AU2005233382A patent/AU2005233382C1/en not_active Ceased
- 2005-04-14 AT AT05734896T patent/ATE402938T1/de active
- 2005-04-14 CN CN2005800123034A patent/CN1946727B/zh not_active Expired - Fee Related
- 2005-04-14 MX MXPA06011886A patent/MXPA06011886A/es active IP Right Grant
- 2005-04-14 US US11/578,266 patent/US7846926B2/en not_active Expired - Fee Related
- 2005-04-14 CA CA2562617A patent/CA2562617C/en not_active Expired - Fee Related
- 2005-04-14 WO PCT/IB2005/001268 patent/WO2005100363A1/en not_active Ceased
- 2005-04-14 PT PT05734896T patent/PT1742952E/pt unknown
- 2005-04-14 BR BRPI0509912A patent/BRPI0509912B8/pt not_active IP Right Cessation
- 2005-04-14 PL PL05734896T patent/PL1742952T3/pl unknown
- 2005-04-14 JP JP2007507869A patent/JP4876070B2/ja not_active Expired - Fee Related
- 2005-04-14 DE DE602005008578T patent/DE602005008578D1/de not_active Expired - Lifetime
- 2005-04-14 ES ES05734896T patent/ES2311985T3/es not_active Expired - Lifetime
- 2005-04-14 EP EP05734896A patent/EP1742952B1/en not_active Expired - Lifetime
- 2005-04-14 RS RSP-2008/0494A patent/RS50628B/sr unknown
- 2005-04-14 SI SI200530369T patent/SI1742952T1/sl unknown
- 2005-04-15 TW TW094111918A patent/TWI350288B/zh not_active IP Right Cessation
- 2005-04-15 AR ARP050101486A patent/AR048607A1/es active IP Right Grant
-
2006
- 2006-10-31 ZA ZA200609055A patent/ZA200609055B/en unknown
-
2008
- 2008-10-20 CY CY20081101164T patent/CY1108444T1/el unknown
-
2010
- 2010-11-10 US US12/943,804 patent/US9216989B2/en not_active Expired - Fee Related
-
2015
- 2015-09-01 US US14/842,068 patent/US9403840B2/en not_active Expired - Fee Related
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