NO862006L - Cytostatisk virksomme titanocen-komplekser og fremgangsmaate for deres fremstilling. - Google Patents
Cytostatisk virksomme titanocen-komplekser og fremgangsmaate for deres fremstilling.Info
- Publication number
- NO862006L NO862006L NO862006A NO862006A NO862006L NO 862006 L NO862006 L NO 862006L NO 862006 A NO862006 A NO 862006A NO 862006 A NO862006 A NO 862006A NO 862006 L NO862006 L NO 862006L
- Authority
- NO
- Norway
- Prior art keywords
- general formula
- titanocene
- preparation
- halide
- complexes
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 12
- 238000002360 preparation method Methods 0.000 title claims description 10
- KOMDZQSPRDYARS-UHFFFAOYSA-N cyclopenta-1,3-diene titanium Chemical class [Ti].C1C=CC=C1.C1C=CC=C1 KOMDZQSPRDYARS-UHFFFAOYSA-N 0.000 claims abstract description 19
- 150000004820 halides Chemical class 0.000 claims abstract description 7
- 229910052717 sulfur Chemical group 0.000 claims abstract description 5
- 125000004434 sulfur atom Chemical group 0.000 claims abstract description 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000005843 halogen group Chemical group 0.000 claims abstract 2
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- -1 aminothiophenol compound Chemical class 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- AEOPMIMUXJFTBN-UHFFFAOYSA-M lithium;2-aminobenzenethiolate Chemical compound [Li+].NC1=CC=CC=C1[S-] AEOPMIMUXJFTBN-UHFFFAOYSA-M 0.000 claims description 2
- UUEIWXVUDZHBLX-UHFFFAOYSA-M lithium;2-aminophenolate Chemical compound [Li+].NC1=CC=CC=C1[O-] UUEIWXVUDZHBLX-UHFFFAOYSA-M 0.000 claims description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims 1
- 150000002366 halogen compounds Chemical class 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 229910052719 titanium Inorganic materials 0.000 description 6
- 239000010936 titanium Substances 0.000 description 6
- WCDSVWRUXWCYFN-UHFFFAOYSA-N 4-aminobenzenethiol Chemical compound NC1=CC=C(S)C=C1 WCDSVWRUXWCYFN-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- LCKIEQZJEYYRIY-UHFFFAOYSA-N Titanium ion Chemical compound [Ti+4] LCKIEQZJEYYRIY-UHFFFAOYSA-N 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940125782 compound 2 Drugs 0.000 description 2
- MKNXBRLZBFVUPV-UHFFFAOYSA-L cyclopenta-1,3-diene;dichlorotitanium Chemical compound Cl[Ti]Cl.C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 MKNXBRLZBFVUPV-UHFFFAOYSA-L 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 101150041968 CDC13 gene Proteins 0.000 description 1
- VSEOIQRHQSIHRZ-UHFFFAOYSA-N Cl.Cl.[Ti+4] Chemical compound Cl.Cl.[Ti+4] VSEOIQRHQSIHRZ-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 241000394605 Viola striata Species 0.000 description 1
- 201000008275 breast carcinoma Diseases 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 230000001085 cytostatic effect Effects 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 201000005296 lung carcinoma Diseases 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- C07F17/00—Metallocenes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19853518447 DE3518447A1 (de) | 1985-05-22 | 1985-05-22 | Titanocen-komplexe und deren verwendung als cytostatica bei der krebsbekaempfung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO862006L true NO862006L (no) | 1986-11-24 |
Family
ID=6271383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO862006A NO862006L (no) | 1985-05-22 | 1986-05-21 | Cytostatisk virksomme titanocen-komplekser og fremgangsmaate for deres fremstilling. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5002969A (da) |
| EP (1) | EP0202673B1 (da) |
| JP (1) | JPS61271294A (da) |
| AT (1) | ATE56018T1 (da) |
| DE (2) | DE3518447A1 (da) |
| DK (1) | DK237086A (da) |
| FI (1) | FI82941C (da) |
| IE (1) | IE59017B1 (da) |
| NO (1) | NO862006L (da) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3800760A1 (de) * | 1988-01-13 | 1989-07-27 | Koepf Maier Petra | Cytostatisch wirksame titanocen-derivate und diese enthaltende arzneimittel |
| DE3923270A1 (de) * | 1989-07-14 | 1991-01-17 | Medac Klinische Spezialpraep | Wasserloesliche pharmazeutische metallocen-komplex-zusammensetzung |
| DE4135291A1 (de) * | 1991-10-25 | 1993-04-29 | Koepf Maier Petra | Cytostatisch wirksame ionische metallocen-komplexe und diese komplexe enthaltende arzneimittel |
| US5496854A (en) * | 1992-08-19 | 1996-03-05 | Technion Research & Development Foundation Ltd. | Metallocenes as anti-tumor drugs |
| IL102866A (en) * | 1992-08-19 | 1998-08-16 | Technion Res & Dev Foundation | Metallocenes as anti-tumor drugs |
| HU212105B (en) * | 1993-03-19 | 1996-02-28 | Nitrokemia Ipartelepek | Process for producing titanium compounds of antitumor activiti and pharmaceutical compositions containing them |
| US6051603A (en) * | 1998-01-20 | 2000-04-18 | Wayne Hughes Institute | Vanadium (IV) metallocene complexes having sperm motility inhibiting activity |
| GB9929353D0 (en) | 1999-12-13 | 2000-02-02 | Univ Leeds | Metallocene synthesis |
| GB0215593D0 (en) * | 2002-07-05 | 2002-08-14 | Univ Leeds | New anticancer drugs |
| DE102006054690A1 (de) * | 2006-11-17 | 2008-05-21 | Charité - Universitätsmedizin Berlin | Carbonyl-substituierte Titanocene |
| EP2717884A1 (en) | 2011-06-06 | 2014-04-16 | Chevron Phillips Chemical Company LP | Use of metallocene compounds for cancer treatment |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2923334C2 (de) * | 1979-06-08 | 1985-03-07 | Hartmut Prof. Dipl.-Chem. Dr. Köpf | Verwendung von Cyclopentadienylmetall-Acido-Komplexen bei der Krebsbekämpfung und diese Komplexe enthaltende Arzneipräparate |
-
1985
- 1985-05-22 DE DE19853518447 patent/DE3518447A1/de not_active Withdrawn
-
1986
- 1986-05-21 EP EP86106912A patent/EP0202673B1/de not_active Expired - Lifetime
- 1986-05-21 AT AT86106912T patent/ATE56018T1/de not_active IP Right Cessation
- 1986-05-21 DK DK237086A patent/DK237086A/da not_active Application Discontinuation
- 1986-05-21 FI FI862132A patent/FI82941C/fi not_active IP Right Cessation
- 1986-05-21 IE IE135186A patent/IE59017B1/en not_active IP Right Cessation
- 1986-05-21 DE DE8686106912T patent/DE3673692D1/de not_active Expired - Fee Related
- 1986-05-21 NO NO862006A patent/NO862006L/no unknown
- 1986-05-22 JP JP61118381A patent/JPS61271294A/ja active Pending
- 1986-05-22 US US06/866,077 patent/US5002969A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| IE59017B1 (en) | 1993-12-15 |
| FI82941B (fi) | 1991-01-31 |
| DK237086A (da) | 1986-11-23 |
| FI82941C (fi) | 1991-05-10 |
| FI862132A (fi) | 1986-11-23 |
| ATE56018T1 (de) | 1990-09-15 |
| JPS61271294A (ja) | 1986-12-01 |
| EP0202673A3 (en) | 1987-03-25 |
| DK237086D0 (da) | 1986-05-21 |
| EP0202673A2 (de) | 1986-11-26 |
| IE861351L (en) | 1986-11-22 |
| FI862132A0 (fi) | 1986-05-21 |
| US5002969A (en) | 1991-03-26 |
| DE3518447A1 (de) | 1986-11-27 |
| DE3673692D1 (de) | 1990-10-04 |
| EP0202673B1 (de) | 1990-08-29 |
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