DD156909A5 - Verfahren zur herstellung von platin(iv)-diaminkomplexen - Google Patents
Verfahren zur herstellung von platin(iv)-diaminkomplexen Download PDFInfo
- Publication number
- DD156909A5 DD156909A5 DD81226806A DD22680681A DD156909A5 DD 156909 A5 DD156909 A5 DD 156909A5 DD 81226806 A DD81226806 A DD 81226806A DD 22680681 A DD22680681 A DD 22680681A DD 156909 A5 DD156909 A5 DD 156909A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- platinum
- formula
- cis
- bis
- aminomethyl
- Prior art date
Links
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 title claims description 45
- 238000004519 manufacturing process Methods 0.000 title description 2
- OETHQSJEHLVLGH-UHFFFAOYSA-N metformin hydrochloride Chemical class Cl.CN(C)C(=N)N=C(N)N OETHQSJEHLVLGH-UHFFFAOYSA-N 0.000 title description 2
- 238000000034 method Methods 0.000 claims abstract description 17
- NDBYXKQCPYUOMI-UHFFFAOYSA-N platinum(4+) Chemical compound [Pt+4] NDBYXKQCPYUOMI-UHFFFAOYSA-N 0.000 claims abstract description 17
- 238000002360 preparation method Methods 0.000 claims abstract description 7
- 229910003460 diamond Inorganic materials 0.000 claims abstract description 4
- 239000010432 diamond Substances 0.000 claims abstract description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 18
- 101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 13
- 125000000129 anionic group Chemical group 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- VZHILEBJJVLVFT-UHFFFAOYSA-N cyclohexylmethanamine platinum(4+) Chemical compound [Pt+4].NCC1CCCCC1 VZHILEBJJVLVFT-UHFFFAOYSA-N 0.000 claims description 3
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims 1
- DTXIBGOOQOFXLX-UHFFFAOYSA-N cyclobutane platinum(4+) Chemical compound [Pt+4].C1CCC1 DTXIBGOOQOFXLX-UHFFFAOYSA-N 0.000 claims 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 abstract description 16
- 201000011510 cancer Diseases 0.000 abstract description 15
- 239000003814 drug Substances 0.000 abstract description 4
- 239000000460 chlorine Substances 0.000 description 40
- 150000001875 compounds Chemical class 0.000 description 23
- 231100000417 nephrotoxicity Toxicity 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000000725 suspension Substances 0.000 description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
- 229910052801 chlorine Inorganic materials 0.000 description 8
- 238000002329 infrared spectrum Methods 0.000 description 8
- 238000000921 elemental analysis Methods 0.000 description 7
- 239000003446 ligand Substances 0.000 description 7
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 description 6
- 238000009738 saturating Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 150000003057 platinum Chemical class 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 241000699670 Mus sp. Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000259 anti-tumor effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- -1 platinum platinum diamine Chemical class 0.000 description 3
- HRGDZIGMBDGFTC-UHFFFAOYSA-N platinum(2+) Chemical compound [Pt+2] HRGDZIGMBDGFTC-UHFFFAOYSA-N 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 description 2
- OTIBCCGEIHPIDI-UHFFFAOYSA-N [Pt].NCC1CCCC1 Chemical compound [Pt].NCC1CCCC1 OTIBCCGEIHPIDI-UHFFFAOYSA-N 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- VWSMIDHPVBAZHE-UHFFFAOYSA-N cyclopentylmethanamine platinum(4+) Chemical compound [Pt+4].NCC1CCCC1 VWSMIDHPVBAZHE-UHFFFAOYSA-N 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 231100000053 low toxicity Toxicity 0.000 description 2
- 231100001095 no nephrotoxicity Toxicity 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 208000028018 Lymphocytic leukaemia Diseases 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical class [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical class OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- CHKXDMWKXWDMPF-UHFFFAOYSA-N [Pt+2].NCC1CCC1 Chemical compound [Pt+2].NCC1CCC1 CHKXDMWKXWDMPF-UHFFFAOYSA-N 0.000 description 1
- ZOMQMEPCANLMJZ-UHFFFAOYSA-N [Pt+4].NCC1CCC1 Chemical compound [Pt+4].NCC1CCC1 ZOMQMEPCANLMJZ-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 208000003747 lymphoid leukemia Diseases 0.000 description 1
- 150000002690 malonic acid derivatives Chemical class 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate group Chemical group [N+](=O)([O-])[O-] NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-M oxidooxomethyl Chemical class [O-][C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-M 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- GGHDAUPFEBTORZ-UHFFFAOYSA-N propane-1,1-diamine Chemical class CCC(N)N GGHDAUPFEBTORZ-UHFFFAOYSA-N 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 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 |
|---|---|---|---|
| NLAANVRAGE8000032,A NL181434C (nl) | 1980-01-03 | 1980-01-03 | Platina(iv)-diamine-complexen, alsmede hun bereiding en toepassing. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD156909A5 true DD156909A5 (de) | 1982-09-29 |
Family
ID=19834620
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD81226806A DD156909A5 (de) | 1980-01-03 | 1981-01-02 | Verfahren zur herstellung von platin(iv)-diaminkomplexen |
Country Status (31)
| Country | Link |
|---|---|
| US (2) | US4431666A (it) |
| JP (1) | JPS56100796A (it) |
| AR (1) | AR227903A1 (it) |
| AT (1) | AT377242B (it) |
| AU (1) | AU542600B2 (it) |
| BE (1) | BE886929A (it) |
| CA (1) | CA1154030A (it) |
| CH (1) | CH650003A5 (it) |
| CS (1) | CS239911B2 (it) |
| DD (1) | DD156909A5 (it) |
| DE (1) | DE3100017A1 (it) |
| DK (1) | DK153468C (it) |
| ES (2) | ES8205231A1 (it) |
| FI (1) | FI72321C (it) |
| FR (1) | FR2473046A1 (it) |
| GB (1) | GB2066819B (it) |
| GR (1) | GR72849B (it) |
| HU (1) | HU184922B (it) |
| IE (1) | IE50653B1 (it) |
| IL (1) | IL61708A (it) |
| IT (1) | IT1193395B (it) |
| LU (1) | LU83046A1 (it) |
| NL (1) | NL181434C (it) |
| NO (1) | NO810004L (it) |
| NZ (1) | NZ195926A (it) |
| PH (1) | PH21998A (it) |
| PT (1) | PT72298B (it) |
| SE (1) | SE439921B (it) |
| SU (1) | SU1083911A3 (it) |
| YU (1) | YU41754B (it) |
| ZA (1) | ZA8114B (it) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4415263C1 (de) * | 1994-04-15 | 1995-11-30 | Asta Medica Ag | Cis-[trans-1,2-Cyclobutanbis(methylamin)-N,N']-[(2S)-lactato-O·1·, O·2·]-platin(II)-trihydrat (Lobaplatin-Trihydrat), seine Herstellung und arzneiliche Verwendung |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL8101026A (nl) * | 1981-03-03 | 1982-10-01 | Tno | Platinadiamine-complexen, werkwijze voor het bereiden daarvan, werkwijze voor het bereiden van een geneesmiddel met toepassing van een dergelijk platinadiamine-complex voor de behandeling van kanker alsmede aldus verkregen gevormd geneesmiddel. |
| US4786725A (en) * | 1982-06-28 | 1988-11-22 | Engelhard Corporation | Solubilized platinum (II) complexes |
| US4598091A (en) * | 1983-02-18 | 1986-07-01 | Degussa Aktiengesellschaft | (1,2-diphenyl)-ethylenediamine)-platinum (II) complex compounds |
| JPS6087295A (ja) * | 1983-10-19 | 1985-05-16 | Nippon Kayaku Co Ltd | 新規白金錯体 |
| US4599352A (en) * | 1984-03-01 | 1986-07-08 | The United States Of America As Represented By The Department Of Health And Human Services | Antineoplastic platinum (IV) complexes and compositions |
| US4550187A (en) * | 1984-04-12 | 1985-10-29 | The Research Foundation Of State University Of New York | Synthesis of platinum (IV) antineoplastic agents |
| HU193809B (en) * | 1984-09-12 | 1987-12-28 | Chugai Pharmaceutical Co Ltd | Process for producing new platinum complexes |
| US4737589A (en) * | 1985-08-27 | 1988-04-12 | Nippon Kayaku Kabushiki Kaisha | Platinum Complexes |
| 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 |
| 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 |
| US5384127A (en) * | 1985-10-18 | 1995-01-24 | Board Of Regents, The University Of Texas System | Stable liposomal formulations of lipophilic platinum compounds |
| US5041581A (en) * | 1985-10-18 | 1991-08-20 | The University Of Texas System Board Of Regents | Hydrophobic cis-platinum complexes efficiently incorporated into liposomes |
| US4760157A (en) * | 1986-01-31 | 1988-07-26 | American Cyanamid Company | (2,2,-bis(aminomethyl)-1,3-propanediol-N,N')platinum complexes |
| JPS63203692A (ja) * | 1987-02-19 | 1988-08-23 | Nippon Kayaku Co Ltd | 新規白金錯体 |
| ATE86967T1 (de) * | 1988-01-09 | 1993-04-15 | Asta Medica Ag | 1,2-bis(aminomethyl)cyclobutan-platin-komplexe. |
| NL8802150A (nl) * | 1988-08-31 | 1990-03-16 | Tno | Platina-(ii)-diaminecomplex, werkwijze voor het bereiden van deze verbinding, preparaat met anti-tumor werking, dat deze verbinding bevat, alsmede gevormde preparaten met anti-tumor werking. |
| NL8802149A (nl) * | 1988-08-31 | 1990-03-16 | Tno | Platina-(iv)diaminecomplex, werkwijze voor het bereiden van deze verbinding, preparaat met anti-tumor werking, dat ten minste een platinaverbinding bevat, alsmede gevormde preparaten met anti-tumor werking. |
| US5393909A (en) * | 1988-11-22 | 1995-02-28 | 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 |
| US5434256A (en) * | 1988-11-22 | 1995-07-18 | Board Of Regents, The University Of Texas System | Diamine platinum complexes as antitumor agents |
| US4994591A (en) * | 1989-06-02 | 1991-02-19 | The Research Foundation Of State University Of Ny | Platinum complexes derived from b-silyamines |
| FI905018A0 (fi) * | 1989-10-17 | 1990-10-12 | Bristol Myers Squibb Co | I vatten och loesningsmedel loesliga axiala hydroxi-och mono- och dikarboxylsyraderivat med stor tumoeraktivitet. |
| US5196555A (en) * | 1989-10-17 | 1993-03-23 | Bristol-Myers Squibb Company | Water and solvent soluble axial hydroxy and mono- and di- carboxylic acid derivatives having high tumor activity |
| US5130450A (en) * | 1990-04-25 | 1992-07-14 | Nippon Kayaku Kabushiki Kaisha | Platinum complexes |
| GB9211291D0 (en) * | 1992-05-28 | 1992-07-15 | British Tech Group | Antifungal compounds |
| US5843475A (en) * | 1996-12-06 | 1998-12-01 | Board Of Regents, The University Of Texas System | Delivery and activation through liposome incorporation of diaminocyclohexane platinum (II) complexes |
| US6264891B1 (en) * | 1998-12-22 | 2001-07-24 | Eos Biotechnology, Inc. | Apparatus and method for concurrent chemical synthesis |
| CA2385528C (en) | 1999-10-01 | 2013-12-10 | Immunogen, Inc. | Compositions and methods for treating cancer using immunoconjugates and chemotherapeutic agents |
| CN105198933B (zh) * | 2014-06-20 | 2018-08-14 | 贵州益佰制药股份有限公司 | 一种洛铂晶体、制备方法及药物应用 |
| AU2016284156B2 (en) | 2015-06-24 | 2020-01-30 | Nippon Kayaku Kabushiki Kaisha | Novel platinum (IV) complex |
| RU2715048C2 (ru) | 2015-09-14 | 2020-02-25 | Ниппон Каяку Кабусики Каися | Полимерный конъюгат гексакоординированного комплекса платины |
| CN105713046B (zh) * | 2016-02-01 | 2018-10-26 | 复旦大学 | 一种铂类抗肿瘤前体药物，其纳米水凝胶药物及其制备方法 |
| CN106946946A (zh) * | 2017-03-29 | 2017-07-14 | 昆明贵研药业有限公司 | 一种铂类抗肿瘤药物米铂氧化物的制备方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH605550A5 (it) * | 1972-06-08 | 1978-09-29 | Research Corp | |
| US4053587A (en) * | 1973-04-13 | 1977-10-11 | Research Corporation | Method of treating viral infections |
| GB1578323A (en) * | 1976-02-26 | 1980-11-05 | Rustenburg Platinum Mines Ltd | Compositions containing platinum |
| SE7810798L (sv) * | 1977-10-19 | 1979-04-20 | Johnson Matthey Co Ltd | Kompositioner, innehallande platina |
| 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 |
| JPS6034958B2 (ja) * | 1978-09-02 | 1985-08-12 | 喜徳 喜谷 | 新規白金錯体 |
-
1980
- 1980-01-03 NL NLAANVRAGE8000032,A patent/NL181434C/xx not_active IP Right Cessation
- 1980-12-03 IE IE2744/80A patent/IE50653B1/en not_active IP Right Cessation
- 1980-12-04 CH CH8972/80A patent/CH650003A5/de not_active IP Right Cessation
- 1980-12-15 IL IL61708A patent/IL61708A/xx unknown
- 1980-12-19 AR AR283721A patent/AR227903A1/es active
- 1980-12-23 SU SU803217401A patent/SU1083911A3/ru active
- 1980-12-23 NZ NZ195926A patent/NZ195926A/xx unknown
- 1980-12-30 JP JP18945180A patent/JPS56100796A/ja active Granted
- 1980-12-30 GR GR63769A patent/GR72849B/el unknown
- 1980-12-30 HU HU803161A patent/HU184922B/hu not_active IP Right Cessation
- 1980-12-30 ES ES498240A patent/ES8205231A1/es not_active Expired
- 1980-12-31 CS CS809611A patent/CS239911B2/cs unknown
- 1980-12-31 IT IT27029/80A patent/IT1193395B/it active
- 1980-12-31 YU YU3363/80A patent/YU41754B/xx unknown
- 1980-12-31 CA CA000367793A patent/CA1154030A/en not_active Expired
- 1980-12-31 BE BE0/203372A patent/BE886929A/nl not_active IP Right Cessation
- 1980-12-31 PT PT72298A patent/PT72298B/pt not_active IP Right Cessation
-
1981
- 1981-01-02 DK DK001681A patent/DK153468C/da not_active IP Right Cessation
- 1981-01-02 LU LU83046A patent/LU83046A1/de unknown
- 1981-01-02 DD DD81226806A patent/DD156909A5/de not_active IP Right Cessation
- 1981-01-02 SE SE8100006A patent/SE439921B/sv not_active IP Right Cessation
- 1981-01-02 ZA ZA00810014A patent/ZA8114B/xx unknown
- 1981-01-02 FI FI810002A patent/FI72321C/fi not_active IP Right Cessation
- 1981-01-02 AU AU65949/81A patent/AU542600B2/en not_active Ceased
- 1981-01-02 NO NO810004A patent/NO810004L/no unknown
- 1981-01-02 AT AT0000381A patent/AT377242B/de not_active IP Right Cessation
- 1981-01-02 GB GB8100027A patent/GB2066819B/en not_active Expired
- 1981-01-02 DE DE19813100017 patent/DE3100017A1/de not_active Ceased
- 1981-01-02 PH PH25046A patent/PH21998A/en unknown
- 1981-01-05 FR FR8100058A patent/FR2473046A1/fr active Granted
- 1981-02-06 US US06/232,298 patent/US4431666A/en not_active Expired - Fee Related
- 1981-11-26 ES ES507474A patent/ES8207119A1/es not_active Expired
-
1983
- 1983-01-18 US US06/458,979 patent/US4482569A/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4415263C1 (de) * | 1994-04-15 | 1995-11-30 | Asta Medica Ag | Cis-[trans-1,2-Cyclobutanbis(methylamin)-N,N']-[(2S)-lactato-O·1·, O·2·]-platin(II)-trihydrat (Lobaplatin-Trihydrat), seine Herstellung und arzneiliche Verwendung |
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