DE2329485C3 - Platinkoordinationsverbindungen und ein diese Verbindungen enthaltendes Antitumormittel - Google Patents
Platinkoordinationsverbindungen und ein diese Verbindungen enthaltendes AntitumormittelInfo
- Publication number
- DE2329485C3 DE2329485C3 DE2329485A DE2329485A DE2329485C3 DE 2329485 C3 DE2329485 C3 DE 2329485C3 DE 2329485 A DE2329485 A DE 2329485A DE 2329485 A DE2329485 A DE 2329485A DE 2329485 C3 DE2329485 C3 DE 2329485C3
- Authority
- DE
- Germany
- Prior art keywords
- platinum
- compounds
- tumor
- malonato
- dose
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 title claims description 64
- 150000001875 compounds Chemical class 0.000 title claims description 31
- 229910052697 platinum Inorganic materials 0.000 title claims description 26
- 239000002246 antineoplastic agent Substances 0.000 title claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 claims description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- 150000003973 alkyl amines Chemical class 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 description 24
- 241001465754 Metazoa Species 0.000 description 21
- 238000012360 testing method Methods 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 238000002347 injection Methods 0.000 description 13
- 239000007924 injection Substances 0.000 description 13
- 241000699666 Mus <mouse, genus> Species 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 239000003446 ligand Substances 0.000 description 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 7
- 241000699670 Mus sp. Species 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 230000034994 death Effects 0.000 description 6
- 231100000517 death Toxicity 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- 230000000259 anti-tumor effect Effects 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- HRGDZIGMBDGFTC-UHFFFAOYSA-N platinum(2+) Chemical compound [Pt+2] HRGDZIGMBDGFTC-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000004696 coordination complex Chemical class 0.000 description 4
- 150000004985 diamines Chemical class 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 239000012452 mother liquor Substances 0.000 description 4
- 229910021607 Silver chloride Inorganic materials 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 208000006268 Sarcoma 180 Diseases 0.000 description 2
- DQVUZTMWSYWINI-UHFFFAOYSA-N azanide;platinum(2+);propanedioic acid Chemical compound [NH2-].[NH2-].[Pt+2].OC(=O)CC(O)=O DQVUZTMWSYWINI-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 201000011510 cancer Diseases 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- -1 ion compounds Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- NHBKXEKEPDILRR-UHFFFAOYSA-N 2,3-bis(butanoylsulfanyl)propyl butanoate Chemical compound CCCC(=O)OCC(SC(=O)CCC)CSC(=O)CCC NHBKXEKEPDILRR-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 206010039491 Sarcoma Diseases 0.000 description 1
- 240000003834 Triticum spelta Species 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 229920005556 chlorobutyl Polymers 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000002354 daily effect Effects 0.000 description 1
- HCDITHVDEPPNIL-UHFFFAOYSA-L dipotassium;propanedioate Chemical compound [K+].[K+].[O-]C(=O)CC([O-])=O HCDITHVDEPPNIL-UHFFFAOYSA-L 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000011038 discontinuous diafiltration by volume reduction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 238000002265 electronic spectrum Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 150000002171 ethylene diamines Chemical class 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- ZIYVHBGGAOATLY-UHFFFAOYSA-N methylmalonic acid Chemical compound OC(=O)C(C)C(O)=O ZIYVHBGGAOATLY-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000003891 oxalate salts Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000009295 sperm incapacitation Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- 230000004614 tumor growth Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0086—Platinum compounds
- C07F15/0093—Platinum compounds without a metal-carbon linkage
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26098972A | 1972-06-08 | 1972-06-08 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2329485A1 DE2329485A1 (de) | 1973-12-20 |
| DE2329485B2 DE2329485B2 (de) | 1979-11-22 |
| DE2329485C3 true DE2329485C3 (de) | 1980-07-31 |
Family
ID=22991508
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2329485A Expired DE2329485C3 (de) | 1972-06-08 | 1973-06-08 | Platinkoordinationsverbindungen und ein diese Verbindungen enthaltendes Antitumormittel |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4140707A (enExample) |
| JP (1) | JPS5629676B2 (enExample) |
| CA (1) | CA1023759A (enExample) |
| CH (2) | CH588505A5 (enExample) |
| DE (1) | DE2329485C3 (enExample) |
| FR (1) | FR2187345B1 (enExample) |
| GB (1) | GB1380228A (enExample) |
| NL (2) | NL183724C (enExample) |
| SE (2) | SE415182B (enExample) |
Families Citing this family (101)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4258051A (en) * | 1975-01-10 | 1981-03-24 | Research Corporation | Method of treating viral infections |
| JPS6041077B2 (ja) * | 1976-09-06 | 1985-09-13 | 喜徳 喜谷 | １，２‐ジアミノシクロヘキサン異性体のシス白金（２）錯体 |
| US4440782A (en) * | 1977-03-01 | 1984-04-03 | Research Corporation | Method of treating viral infections |
| NL7810433A (nl) * | 1977-10-19 | 1979-04-23 | Johnson Matthey Co Ltd | Nieuwe platinaverbindingen. |
| US4225529A (en) * | 1977-10-19 | 1980-09-30 | Johnson, Matthey & Co., Limited | Compositions containing platinum |
| US4230631A (en) * | 1977-10-19 | 1980-10-28 | Johnson, Matthey & Co., Limited | Platinum coordination compounds |
| SE7903361L (sv) * | 1978-04-20 | 1979-10-21 | Johnson Matthey Co Ltd | Kompositioner innehallande platina |
| SE7903360L (sv) * | 1978-04-20 | 1979-10-21 | Johnson Matthey Co Ltd | Kompositioner innehallande platina |
| SE7903359L (sv) * | 1978-04-20 | 1979-10-21 | Johnson Matthey Co Ltd | Kompositioner innehallande platina |
| NL7807334A (nl) * | 1978-07-06 | 1980-01-08 | Tno | Platina-diaminecomplexen, werkwijze voor het bereiden daarvan, werkwijze voor het bereiden van een genees- middel met toepassing van een dergelijk platina-dia- minecomplex voor de behandeling van kanker, alsmede al- dus verkregen gevormd geneesmiddel. |
| JPS6034958B2 (ja) * | 1978-09-02 | 1985-08-12 | 喜徳 喜谷 | 新規白金錯体 |
| US4291027A (en) * | 1979-03-07 | 1981-09-22 | Engelhard Minerals & Chemicals Corp. | Method for treating tumors with ethylenediamine platinum (II) and 1,2-diaminocyclohexane-platinum (II) pyrophosphate complexes |
| US4234500A (en) * | 1979-03-07 | 1980-11-18 | Engelhard Minerals & Chemicals Corporation | Ethylenediamine platinum(II) and 1,2-diamino-cyclohexane platinum(II) pyrophosphate complexes |
| US4462998A (en) * | 1979-06-20 | 1984-07-31 | Engelhard Corporation | Method of using a cis-platinum(II) amine ascorbate |
| US4505928A (en) * | 1979-06-20 | 1985-03-19 | Engelhard Corporation | Pharmaceutical composition containing cis-platinum (II) amine lactate and a method of using same |
| US4271085A (en) * | 1979-06-20 | 1981-06-02 | Engelhard Minerals & Chemicals Corporation | Cis-platinum (II) amine lactate complexes |
| US4457926A (en) * | 1979-06-20 | 1984-07-03 | Engelhard Corporation | Cis-Platinum(II) amine ascorbate complexes |
| US4284579A (en) * | 1979-07-17 | 1981-08-18 | The United States Of America As Represented By The Of The Department Of Health & Human Services | (N-Phosphonacetyl-L-aspartato)(1,2-diaminocyclchexane)platinum(II) or alkali metal salt |
| GB2060615B (en) * | 1979-08-23 | 1983-06-22 | Johnson Matthey Co Ltd | Platinum-amine complexes |
| NL181434C (nl) * | 1980-01-03 | 1987-08-17 | Tno | Platina(iv)-diamine-complexen, alsmede hun bereiding en toepassing. |
| GR75598B (enExample) * | 1980-04-29 | 1984-08-01 | Sanofi Sa | |
| JPS56154493A (en) * | 1980-04-30 | 1981-11-30 | Shionogi & Co Ltd | Novel platinum complex |
| US4322362A (en) * | 1980-07-28 | 1982-03-30 | Bristol-Myers Company | Salts of 2-hydroxymalonate platinum complexes |
| NZ197104A (en) * | 1980-05-27 | 1984-05-31 | Bristol Myers Co | Soluble ammonium and sodium salts of 2-hydroxymalonato platinum ii derivatives |
| US4428943A (en) | 1980-06-09 | 1984-01-31 | The United States Of America As Represented By The Department Of Health And Human Services | (N-Phosphonacetyl-L-aspartato) (1,2-diaminocyclohexane)platinum(II) or alkali metal salt |
| JPS5851959B2 (ja) * | 1980-06-11 | 1983-11-19 | 呉羽化学工業株式会社 | プラチナ化合物とその医薬組成物 |
| JPS5716895A (en) * | 1980-07-05 | 1982-01-28 | Otsuka Chem Co Ltd | Platinum 2 complex and antitumor agent containing the same as active principle |
| JPS57123198A (en) * | 1981-01-23 | 1982-07-31 | Shionogi & Co Ltd | Novel platinum complex |
| JPS5896024A (ja) * | 1981-10-16 | 1983-06-07 | リチヤ−ド・エフ・ストツケル | 白金毒解毒剤 |
| US4500465A (en) * | 1982-06-28 | 1985-02-19 | Engelhard Corporation | Solubilized platinum (II) complexes |
| US4584392A (en) * | 1982-11-10 | 1986-04-22 | Inco Alloys International, Inc. | Platinum and palladium complexes |
| US4560782A (en) * | 1982-11-19 | 1985-12-24 | Research Corporation | Anti-tumor diplatinum coordination compounds |
| IL67789A (en) * | 1983-01-31 | 1986-09-30 | Yissum Res Dev Co | Amino-substituted malonato platinum(ii)complexes and method for their preparation |
| US4533502A (en) * | 1983-02-22 | 1985-08-06 | Rochon Fernande D | Platinum (II) compounds and their preparation |
| US4906646A (en) * | 1983-03-31 | 1990-03-06 | Board Of Governors Of Wayne State University | Method and composition for the treatment of tumors by administering a platinum coordination compound and a calcium channel blocker compound of the dihydropyridine class |
| US4617189A (en) * | 1983-04-14 | 1986-10-14 | Stockel Richard F | Use of selenium-containing compounds for negating the toxic effects of platinum compounds used in chemotherapy, and a novel selenium-containing platinum compound and use thereof as an anti-cancer medicine |
| JPS59222498A (ja) * | 1983-06-01 | 1984-12-14 | Shionogi & Co Ltd | 新規グリコ−ル酸系白金錯体および抗悪性腫瘍剤 |
| US4758588A (en) * | 1983-06-20 | 1988-07-19 | Research Corporation Technologies | Diaminocyclohexane platinum complexes |
| US4661516A (en) * | 1983-06-20 | 1987-04-28 | Research Corporation | Diaminocyclohexane platinum complexes |
| DK301684A (da) * | 1983-06-20 | 1984-12-21 | Research Corp | Diaminocyklohexanplatinkomplekser |
| US4710577A (en) * | 1983-08-05 | 1987-12-01 | Yoshinori Kidani | Cytostatic platinum organic complexes |
| GB8328218D0 (en) * | 1983-10-21 | 1983-11-23 | Johnson Matthey Plc | Oral compositions |
| WO1985003296A1 (fr) * | 1984-01-23 | 1985-08-01 | Institut Obschei I Neorganicheskoi Khimii Imeni N. | Complexes carboxyles de platine melanges |
| US4843161A (en) * | 1984-06-01 | 1989-06-27 | Massachusetts Institute Of Technology | Platinum-intercalative complexes for the treatment of cancer |
| GB8416048D0 (en) * | 1984-06-22 | 1984-07-25 | Johnson Matthey Plc | Anti-tumour compounds of platinum |
| EP0169645A1 (en) * | 1984-06-27 | 1986-01-29 | Johnson Matthey Public Limited Company | Platinum co-ordination compounds |
| US4645661A (en) * | 1984-06-29 | 1987-02-24 | St. Jude Children's Research Hospital | Method for alleviating cisplatin-induced nephrotoxicity and dithiocarbamate compounds for effecting same |
| IL76889A0 (en) * | 1984-11-02 | 1986-02-28 | Johnson Matthey Plc | Solubilised platinum compound,method for the production thereof and pharmaceutical compositions containing the same |
| US4588831A (en) * | 1984-11-09 | 1986-05-13 | Natec | Platinum complex compounds of substituted 5,8-dihydroxyl-1,4-naphthoquinone, and process for their production and use |
| US4665210A (en) * | 1984-12-17 | 1987-05-12 | American Cyanamid Company | Platinum complexes of aliphatic tricarboxylic acids |
| ZA86704B (en) * | 1985-02-23 | 1986-10-29 | Asta Werke Ag Chem Fab | Tumor retarding(1-benzyl-ethylenediamine9-platin(ii)-complexes |
| CA1274529A (en) * | 1985-09-05 | 1990-09-25 | Federico Sampedro | Platinum(ii) complexes of 1,1-cyclobutane- dicarboxylate and process for their production |
| US4658047A (en) * | 1985-09-27 | 1987-04-14 | The United States Of America As Represented By The Department Of Health And Human Services | Method of preparing 1,2-diaminocyclohexane tetrachloro platinum (IV) isomers |
| US5041581A (en) * | 1985-10-18 | 1991-08-20 | The University Of Texas System Board Of Regents | Hydrophobic cis-platinum complexes efficiently incorporated into liposomes |
| US5384127A (en) * | 1985-10-18 | 1995-01-24 | Board Of Regents, The University Of Texas System | Stable liposomal formulations of lipophilic platinum compounds |
| US5117022A (en) * | 1985-10-18 | 1992-05-26 | The Board Of Regents, The University Of Texas System | Hydrophobic cis-platinum complexes efficiently incorporated into liposomes |
| US4670458A (en) * | 1986-01-31 | 1987-06-02 | American Cyanamid Company | Hydroxylated 1,2-diaminocyclohexane platinum complexes |
| US4760157A (en) * | 1986-01-31 | 1988-07-26 | American Cyanamid Company | (2,2,-bis(aminomethyl)-1,3-propanediol-N,N')platinum complexes |
| CS269719B1 (en) * | 1986-12-29 | 1990-05-14 | Kiss Frantisek | Platinum cytostatic |
| US5393909A (en) * | 1988-11-22 | 1995-02-28 | Board Of Regents, The University Of Texas System | Diamine platinum complexes as antitumor agents |
| US5434256A (en) * | 1988-11-22 | 1995-07-18 | Board Of Regents, The University Of Texas System | Diamine platinum complexes as antitumor agents |
| US5041578A (en) * | 1988-11-22 | 1991-08-20 | Board Of Regents, The University Of Texas System | Water soluble 1,2-diaminocyclohexane platinum (IV) complexes as antitumor agents |
| US6884418B1 (en) | 1989-08-04 | 2005-04-26 | Berlex Laboratories, Inc. | Use of ligand-mimicking agents and anti-neoplastic drugs in cancer therapy |
| US5455270A (en) * | 1993-08-11 | 1995-10-03 | Bristol-Myers Squibb Co. | Stabilized solutions of platinum(II) antitumor agents |
| DE69427595T2 (de) * | 1994-02-07 | 2002-04-25 | Pliva Pharmaceutical Industry | Antitumormittel auf basis von carboplatin und herstellung desselben |
| JP3154399B2 (ja) * | 1996-07-04 | 2001-04-09 | デビオファーム エス．アー． | 白金化合物の製造方法 |
| US5922689A (en) * | 1995-09-11 | 1999-07-13 | Unitech Pharmaceuticals, Inc. | Cisplatin analogs for cancer treatment |
| US20040072889A1 (en) * | 1997-04-21 | 2004-04-15 | Pharmacia Corporation | Method of using a COX-2 inhibitor and an alkylating-type antineoplastic agent as a combination therapy in the treatment of neoplasia |
| CN1068002C (zh) * | 1997-04-30 | 2001-07-04 | 中国科学院大连化学物理研究所 | 铂抗癌药物及合成 |
| HUP0102521A3 (en) * | 1998-04-03 | 2003-08-28 | Ajinomoto Kk | Antitumor agents comprising a stilbene derivative and a platinum coordination compound |
| US6858598B1 (en) | 1998-12-23 | 2005-02-22 | G. D. Searle & Co. | Method of using a matrix metalloproteinase inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
| US6833373B1 (en) | 1998-12-23 | 2004-12-21 | G.D. Searle & Co. | Method of using an integrin antagonist and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
| HK1049787B (en) | 1999-10-01 | 2014-07-25 | Immunogen, Inc. | Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents |
| AU1608801A (en) | 1999-11-15 | 2001-05-30 | Parker Hughes Institute | Diamino platinum (ii) antitumor complexes |
| US6545010B2 (en) * | 2000-03-17 | 2003-04-08 | Aventis Pharma S.A. | Composition comprising camptothecin or a camptothecin derivative and a platin derivative for the treatment of cancer |
| US7053065B2 (en) * | 2000-06-30 | 2006-05-30 | Eli Lilly And Company | Vitamin B12 and pemetrexed disodium combination therapies |
| DE10032256C2 (de) * | 2000-07-03 | 2003-06-05 | Infineon Technologies Ag | Chip-ID-Register-Anordnung |
| TWI315982B (en) | 2001-07-19 | 2009-10-21 | Novartis Ag | Combinations comprising epothilones and pharmaceutical uses thereof |
| AU2002337713A1 (en) * | 2001-09-26 | 2003-04-07 | Intermune, Inc. | Pharmaceutical compositions and methods for treating cancer |
| US7038071B2 (en) * | 2002-07-16 | 2006-05-02 | Sonus Pharmaceuticals, Inc. | Platinum compounds |
| US7160908B2 (en) * | 2003-03-04 | 2007-01-09 | Unitech Pharmaceuticals, Inc. | Dynamic anticancer platinum compounds |
| WO2005090372A2 (en) * | 2004-03-15 | 2005-09-29 | Sonus Pharmaceuticals, Inc. | Platinum carboxylate anticancer compounds |
| WO2006077424A1 (en) | 2005-01-21 | 2006-07-27 | Astex Therapeutics Limited | Pharmaceutical compounds |
| WO2006103691A1 (en) * | 2005-03-28 | 2006-10-05 | Dabur Pharma Ltd. | Stable pharmaceutical compositions of platinum (ii) antitumour agents |
| WO2007128820A1 (en) | 2006-05-09 | 2007-11-15 | Novartis Ag | Combination comprising an iron chelator and an anti-neoplastic agent and use thereof |
| JP5528807B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
| US8916552B2 (en) | 2006-10-12 | 2014-12-23 | Astex Therapeutics Limited | Pharmaceutical combinations |
| MX2009003938A (es) * | 2006-10-27 | 2009-04-24 | Genentech Inc | Anticuerpos e inmunoconjugados y sus usos. |
| JP5809415B2 (ja) | 2007-11-09 | 2015-11-10 | ペレグリン ファーマシューティカルズ，インコーポレーテッド | 抗ｖｅｇｆ抗体の組成物および方法 |
| KR102449659B1 (ko) | 2008-03-18 | 2022-09-29 | 제넨테크, 인크. | 항-ｈｅｒ２ 항체-약물 접합체와 화학요법제의 병용물, 및 사용 방법 |
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| CN107773556B (zh) * | 2016-08-26 | 2020-08-18 | 广州安好医药科技有限公司 | 一种具有抗肿瘤药物功效的联合用药物 |
| KR102667951B1 (ko) | 2017-04-03 | 2024-05-22 | 에프. 호프만-라 로슈 아게 | Steap-1에 결합하는 항체 |
-
1973
- 1973-06-04 CH CH799973A patent/CH588505A5/xx not_active IP Right Cessation
- 1973-06-04 CH CH203677A patent/CH605550A5/xx not_active IP Right Cessation
- 1973-06-05 CA CA173,182A patent/CA1023759A/en not_active Expired
- 1973-06-06 NL NLAANVRAGE7307863,A patent/NL183724C/xx active Protection Beyond IP Right Term
- 1973-06-07 GB GB2730473A patent/GB1380228A/en not_active Expired
- 1973-06-07 FR FR7320788A patent/FR2187345B1/fr not_active Expired
- 1973-06-07 SE SE7308050A patent/SE415182B/xx active Protection Beyond IP Right Term
- 1973-06-08 DE DE2329485A patent/DE2329485C3/de not_active Expired
- 1973-06-08 JP JP6463673A patent/JPS5629676B2/ja not_active Expired
-
1977
- 1977-03-18 US US05/778,955 patent/US4140707A/en not_active Expired - Lifetime
-
1978
- 1978-10-10 SE SE7810577A patent/SE7810577L/xx unknown
-
1993
- 1993-06-03 NL NL930049C patent/NL930049I2/nl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH605550A5 (enExample) | 1978-09-29 |
| CA1023759A (en) | 1978-01-03 |
| FR2187345A1 (enExample) | 1974-01-18 |
| NL7307863A (enExample) | 1973-12-11 |
| GB1380228A (en) | 1975-01-08 |
| FR2187345B1 (enExample) | 1976-12-31 |
| NL930049I2 (nl) | 1993-11-16 |
| NL930049I1 (nl) | 1993-09-01 |
| DE2329485B2 (de) | 1979-11-22 |
| CH588505A5 (enExample) | 1977-06-15 |
| JPS4948621A (enExample) | 1974-05-11 |
| JPS5629676B2 (enExample) | 1981-07-09 |
| SE7810577L (sv) | 1978-10-10 |
| US4140707A (en) | 1979-02-20 |
| SE415182B (sv) | 1980-09-15 |
| US4140707B1 (enExample) | 1989-12-19 |
| NL183724C (nl) | 1989-01-02 |
| DE2329485A1 (de) | 1973-12-20 |
| NL183724B (nl) | 1988-08-01 |
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Legal Events
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| OD | Request for examination | ||
| C3 | Grant after two publication steps (3rd publication) | ||
| 8328 | Change in the person/name/address of the agent |
Free format text: VON FUENER, A., DIPL.-CHEM. DR.RER.NAT. EBBINGHAUS, D., DIPL.-ING., PAT.-ANW., 8000 MUENCHEN |