ZA200409061B - Platinum complexes having antitumor activity. - Google Patents
Platinum complexes having antitumor activity. Download PDFInfo
- Publication number
- ZA200409061B ZA200409061B ZA200409061A ZA200409061A ZA200409061B ZA 200409061 B ZA200409061 B ZA 200409061B ZA 200409061 A ZA200409061 A ZA 200409061A ZA 200409061 A ZA200409061 A ZA 200409061A ZA 200409061 B ZA200409061 B ZA 200409061B
- Authority
- ZA
- South Africa
- Prior art keywords
- cis
- mmoles
- antitumor activity
- pph
- compound
- Prior art date
Links
- 230000000259 anti-tumor effect Effects 0.000 title description 8
- 150000003057 platinum Chemical class 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims description 13
- 239000008194 pharmaceutical composition Substances 0.000 claims description 9
- 238000012790 confirmation Methods 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 6
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 13
- OHXPGWPVLFPUSM-KLRNGDHRSA-N 3,7,12-trioxo-5beta-cholanic acid Chemical compound C1CC(=O)C[C@H]2CC(=O)[C@H]3[C@@H]4CC[C@H]([C@@H](CCC(O)=O)C)[C@@]4(C)C(=O)C[C@@H]3[C@]21C OHXPGWPVLFPUSM-KLRNGDHRSA-N 0.000 description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical class [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000007787 solid Substances 0.000 description 8
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 8
- 206010028980 Neoplasm Diseases 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 229960002997 dehydrocholic acid Drugs 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 6
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 description 5
- 229960004316 cisplatin Drugs 0.000 description 5
- 229940009979 dehydrocholate Drugs 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 4
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 3
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 229910001923 silver oxide Inorganic materials 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 230000008034 disappearance Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000007911 parenteral administration Methods 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- HRGDZIGMBDGFTC-UHFFFAOYSA-N platinum(2+) Chemical class [Pt+2] HRGDZIGMBDGFTC-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical group C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 description 1
- VYXHVRARDIDEHS-QGTKBVGQSA-N (1z,5z)-cycloocta-1,5-diene Chemical compound C\1C\C=C/CC\C=C/1 VYXHVRARDIDEHS-QGTKBVGQSA-N 0.000 description 1
- 101710134784 Agnoprotein Proteins 0.000 description 1
- 101100522123 Caenorhabditis elegans ptc-1 gene Proteins 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 108010024636 Glutathione Proteins 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 206010029155 Nephropathy toxic Diseases 0.000 description 1
- 101100113485 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) chs-3 gene Proteins 0.000 description 1
- 101100030361 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pph-3 gene Proteins 0.000 description 1
- 206010033109 Ototoxicity Diseases 0.000 description 1
- -1 Platinum Metals Chemical class 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 239000012050 conventional carrier Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 230000002601 intratumoral effect Effects 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- 231100000417 nephrotoxicity Toxicity 0.000 description 1
- 230000007694 nephrotoxicity Effects 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 231100000262 ototoxicity Toxicity 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 210000001550 testis Anatomy 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 1
- 210000004881 tumor cell Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J75/00—Processes for the preparation of steroids in general
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2002MI000993A ITMI20020993A1 (it) | 2002-05-10 | 2002-05-10 | Complessi di platino ad attivita' antitumorale |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200409061B true ZA200409061B (en) | 2005-11-10 |
Family
ID=11449869
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200409061A ZA200409061B (en) | 2002-05-10 | 2003-05-08 | Platinum complexes having antitumor activity. |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US7205287B2 (zh) |
| EP (1) | EP1504019B1 (zh) |
| JP (1) | JP2005533763A (zh) |
| CN (1) | CN1653082A (zh) |
| AT (1) | ATE302791T1 (zh) |
| AU (1) | AU2003236633B2 (zh) |
| CA (1) | CA2485431A1 (zh) |
| DE (1) | DE60301404T2 (zh) |
| DK (1) | DK1504019T3 (zh) |
| EA (1) | EA200401316A1 (zh) |
| ES (1) | ES2247544T3 (zh) |
| HR (1) | HRP20041016A2 (zh) |
| IL (1) | IL165123A (zh) |
| IS (1) | IS7522A (zh) |
| IT (1) | ITMI20020993A1 (zh) |
| MX (1) | MXPA04011056A (zh) |
| NO (1) | NO20044876L (zh) |
| NZ (1) | NZ536457A (zh) |
| PL (1) | PL372553A1 (zh) |
| PT (1) | PT1504019E (zh) |
| WO (1) | WO2003095470A1 (zh) |
| ZA (1) | ZA200409061B (zh) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2706420C (en) * | 2007-12-07 | 2016-04-19 | Prana Biotechnology Ltd | Organometallic ligands for therapy and diagnosis |
| CN102030784A (zh) * | 2010-11-26 | 2011-04-27 | 金川集团有限公司 | 一种顺-二(三苯基膦)二氯化铂(ii)的制备方法 |
| CN102653548A (zh) * | 2011-03-02 | 2012-09-05 | 陈建华 | 一种靶向性抗肿瘤的化合物及其制备方法和用途 |
| RU2667128C2 (ru) | 2016-12-29 | 2018-09-14 | Герман Петрович Беккер | Композиция для приготовления противоопухолевого средства и способ приготовления противоопухолевого средства на ее основе |
-
2002
- 2002-05-10 IT IT2002MI000993A patent/ITMI20020993A1/it unknown
-
2003
- 2003-05-08 PL PL03372553A patent/PL372553A1/xx unknown
- 2003-05-08 EP EP03735368A patent/EP1504019B1/en not_active Expired - Lifetime
- 2003-05-08 EA EA200401316A patent/EA200401316A1/ru unknown
- 2003-05-08 MX MXPA04011056A patent/MXPA04011056A/es active IP Right Grant
- 2003-05-08 CN CNA038105314A patent/CN1653082A/zh active Pending
- 2003-05-08 ZA ZA200409061A patent/ZA200409061B/en unknown
- 2003-05-08 AT AT03735368T patent/ATE302791T1/de not_active IP Right Cessation
- 2003-05-08 DK DK03735368T patent/DK1504019T3/da active
- 2003-05-08 NZ NZ536457A patent/NZ536457A/en unknown
- 2003-05-08 PT PT03735368T patent/PT1504019E/pt unknown
- 2003-05-08 DE DE60301404T patent/DE60301404T2/de not_active Expired - Fee Related
- 2003-05-08 CA CA002485431A patent/CA2485431A1/en not_active Abandoned
- 2003-05-08 AU AU2003236633A patent/AU2003236633B2/en not_active Ceased
- 2003-05-08 JP JP2004503484A patent/JP2005533763A/ja active Pending
- 2003-05-08 WO PCT/EP2003/004828 patent/WO2003095470A1/en active IP Right Grant
- 2003-05-08 ES ES03735368T patent/ES2247544T3/es not_active Expired - Lifetime
-
2004
- 2004-10-22 US US10/971,900 patent/US7205287B2/en not_active Expired - Fee Related
- 2004-10-29 HR HR20041016A patent/HRP20041016A2/hr not_active Application Discontinuation
- 2004-11-09 IL IL165123A patent/IL165123A/en not_active IP Right Cessation
- 2004-11-09 IS IS7522A patent/IS7522A/is unknown
- 2004-11-09 NO NO20044876A patent/NO20044876L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| CA2485431A1 (en) | 2003-11-20 |
| ITMI20020993A0 (it) | 2002-05-10 |
| NO20044876L (no) | 2004-11-09 |
| IL165123A (en) | 2009-09-01 |
| IL165123A0 (en) | 2005-12-18 |
| AU2003236633B2 (en) | 2008-02-28 |
| EP1504019A1 (en) | 2005-02-09 |
| JP2005533763A (ja) | 2005-11-10 |
| ATE302791T1 (de) | 2005-09-15 |
| DE60301404T2 (de) | 2006-03-09 |
| DE60301404D1 (de) | 2005-09-29 |
| EP1504019B1 (en) | 2005-08-24 |
| CN1653082A (zh) | 2005-08-10 |
| AU2003236633A1 (en) | 2003-11-11 |
| HRP20041016A2 (en) | 2005-02-28 |
| DK1504019T3 (da) | 2005-12-19 |
| NZ536457A (en) | 2006-07-28 |
| WO2003095470A1 (en) | 2003-11-20 |
| US20050107337A1 (en) | 2005-05-19 |
| ITMI20020993A1 (it) | 2003-11-10 |
| US7205287B2 (en) | 2007-04-17 |
| EA200401316A1 (ru) | 2005-04-28 |
| PL372553A1 (en) | 2005-07-25 |
| PT1504019E (pt) | 2005-10-31 |
| MXPA04011056A (es) | 2005-02-14 |
| ES2247544T3 (es) | 2006-03-01 |
| IS7522A (is) | 2004-11-09 |
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