DE385517T1 - Arzneimittel zur behandlung von erbrechen. - Google Patents
Arzneimittel zur behandlung von erbrechen.Info
- Publication number
- DE385517T1 DE385517T1 DE199090107640T DE90107640T DE385517T1 DE 385517 T1 DE385517 T1 DE 385517T1 DE 199090107640 T DE199090107640 T DE 199090107640T DE 90107640 T DE90107640 T DE 90107640T DE 385517 T1 DE385517 T1 DE 385517T1
- Authority
- DE
- Germany
- Prior art keywords
- use according
- methyl
- cytotoxic agent
- alkyl
- formula
- 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.)
- Pending
Links
- 239000003814 drug Substances 0.000 title claims 5
- 229940127089 cytotoxic agent Drugs 0.000 claims 6
- 239000002254 cytotoxic agent Substances 0.000 claims 6
- 231100000599 cytotoxic agent Toxicity 0.000 claims 6
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 claims 4
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 claims 4
- 229960004316 cisplatin Drugs 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- -1 C3-6-alkenyl Chemical group 0.000 claims 3
- 206010047700 Vomiting Diseases 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 206010028813 Nausea Diseases 0.000 claims 2
- 229960004397 cyclophosphamide Drugs 0.000 claims 2
- 229960004679 doxorubicin Drugs 0.000 claims 2
- 150000002431 hydrogen Chemical group 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 201000003152 motion sickness Diseases 0.000 claims 2
- 230000008693 nausea Effects 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 230000005855 radiation Effects 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 230000008673 vomiting Effects 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/46—8-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Neurosurgery (AREA)
- Anesthesiology (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Otolaryngology (AREA)
- Biomedical Technology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Claims (11)
1. Die Verwendung einer Verbindung der Formel(II) oder eines
pharmazeutisch verträglichen Salzes davon:
(II)
in welcher Rio Wasserstoff, Ci-io-Alkyl, C3-7-Cycloalkyl, C3-6-Alkenyl,
Phenyl oder Phenyl-Ci-3-alkyl ist ; und eine der Gruppen,
dargestellt durch Rll,Ri2 und R13, Wasserstoff, C1-6-AI-kyl,
CS-y-Cycloalkyl, C2-6~Alkenyl oder Phenyl-Ci-3-alkyl ist
und jede der anderen Gruppen, welche gleich oder verschieden sein können, Wasserstoff oder Ci-6-Alkyl bedeutet; für die Herstellung
eines Medikaments zum Einsatz bei der Behandlung von durch einen zytotoxischen Wirkstoff oder Bestrahlung ausgelöster
Übelkeit und Erbrechen, oder von Reisekrankheit.
2. Verwendung nach Anspruch 1, wobei die Verbindung der Formel(II)
die Formel (HA) aufweist:
(HA)
in welcher RiO^- ein Wasserstoff atom oder eine Methyl-,Äthyl-,
Propyl-, Prop-2-yl, Prop-2-enyl oder Cyclopentylgruppe ist;
R12I ein Wasserstoffatom bedeutet; und entweder RnI eine
Methyl-,Äthyl-, Propyl- oder Prop-2-yl-gruppe ist und R13I ein
Wasserstoffatom ist; oder RnI ein Wasserstoffatom darstellt
und R13I eine Methyl- oder Äthylgruppe bedeutet.
3. Verwendung nach Anspruch 2, wobei Rio-*- Methyl ist und R12I
und R13I jeweils Wasserstoff darstellen.
4. Verwendung nach Anspruch 1, wobei die Verbindung der Formel(II)
l,2,3,9-Tetrahydro-9-methyl-3-/"(2-methyl-lH-imidazol-lyl)methyl7-4H-carbazol-4-on
oder ein pharmazeutisch verträgliches Salz davon ist.
5. Verwendung nach einem der Ansprüche 1 bis 4, wobei das Medikament
zur Verwendung bei der Behandlung von durch einen zytotoxischen Wirkstoff verursachte Übelkeit oder Erbrechen bestimmt
ist.
6. Verwendung nach Anspruch 5, wobei der zytotoxische Wirkstoff Cisplatin, Doxorubicin oder Cyclophosphamid ist.
7. Verwendung nach Anspruch 6, wobei der zytotoxische Wirkstoff Doxorubicin oder Cyclophosphamid ist.
8. Verwendung nach Anspruch 6, wobei der zytotoxische Wirkstoff Cisplatin ist und wobei die Verbindung der Formel(II) vor oder
nach der Verabreichung von Cisplatin verabreicht wird.
9. Verwendung nach Anspruch 6, wobei der zytotoxische Wirkstoff Cisplatin ist, das intravenös verabreicht wird.
- 10.Verwendung nach einem der Ansprüche 1 bis 4, wobei das Mediv
kament zur Verwendung bei der Behandlung von durch Bestrahlung verursachter Übelkeit oder Erbrechen bestimmt ist.
11.Verwendung nach einem der Ansprüche 1 bis 4, wobei das
Medikament zur Verwendung bei der Behandlung von Reisekrankheit bestimmt ist.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB858506642A GB8506642D0 (en) | 1985-03-14 | 1985-03-14 | Compounds |
GB858509039A GB8509039D0 (en) | 1985-04-09 | 1985-04-09 | Treatment |
GB858531614A GB8531614D0 (en) | 1985-12-23 | 1985-12-23 | Treatment |
Publications (1)
Publication Number | Publication Date |
---|---|
DE385517T1 true DE385517T1 (de) | 1991-07-25 |
Family
ID=27262620
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE199090107640T Pending DE385517T1 (de) | 1985-03-14 | 1986-03-10 | Arzneimittel zur behandlung von erbrechen. |
DE3689974T Expired - Lifetime DE3689974T2 (de) | 1985-03-14 | 1986-03-10 | Arzneimittel zur Behandlung von Emesis. |
DE198686301684T Pending DE201165T1 (de) | 1985-03-14 | 1986-03-10 | Arzneimittel zur behandlung von emesis, anxietas und "irritable bowel syndrome". |
DE90107640T Expired - Lifetime DE3688296T2 (de) | 1985-03-14 | 1986-03-10 | Arzneimittel zur behandlung von erbrechen. |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE3689974T Expired - Lifetime DE3689974T2 (de) | 1985-03-14 | 1986-03-10 | Arzneimittel zur Behandlung von Emesis. |
DE198686301684T Pending DE201165T1 (de) | 1985-03-14 | 1986-03-10 | Arzneimittel zur behandlung von emesis, anxietas und "irritable bowel syndrome". |
DE90107640T Expired - Lifetime DE3688296T2 (de) | 1985-03-14 | 1986-03-10 | Arzneimittel zur behandlung von erbrechen. |
Country Status (7)
Country | Link |
---|---|
US (3) | US4721720A (de) |
EP (3) | EP0405617A3 (de) |
JP (3) | JPS61212521A (de) |
CY (1) | CY1727A (de) |
DE (4) | DE385517T1 (de) |
HK (1) | HK77593A (de) |
SG (1) | SG61693G (de) |
Families Citing this family (90)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5122528A (en) * | 1983-12-22 | 1992-06-16 | Erbamont, Inc. | Analgesic use of benzobicyclic carboxamides |
US4820715A (en) * | 1984-06-28 | 1989-04-11 | Bristol-Myers Company | Anti-emetic quinuclidinyl benzamides |
EP0189002B1 (de) * | 1984-12-20 | 1993-03-03 | Sandoz Ag | Behandlung von Gastrointestinalkrankheiten durch Anwendung von 5-HT3-Antagonisten |
US5578628A (en) * | 1985-06-25 | 1996-11-26 | Glaxo Group Limited | Medicaments for the treatment of nausea and vomiting |
GB8516083D0 (en) * | 1985-06-25 | 1985-07-31 | Glaxo Group Ltd | Heterocyclic compounds |
US5204356A (en) * | 1985-07-24 | 1993-04-20 | Glaxo Group Limited | Treatment of anxiety |
GB8518658D0 (en) * | 1985-07-24 | 1985-08-29 | Glaxo Group Ltd | Medicaments |
GB8525844D0 (en) * | 1985-10-19 | 1985-11-20 | Beecham Group Plc | Compounds |
US4910193A (en) * | 1985-12-16 | 1990-03-20 | Sandoz Ltd. | Treatment of gastrointestinal disorders |
HU895334D0 (en) * | 1986-07-30 | 1990-01-28 | Sandoz Ag | Process for the preparation of nasal pharmaceutical compositions |
DE3777805D1 (de) * | 1986-11-21 | 1992-04-30 | Glaxo Group Ltd | Arzneimittel zur behandlung oder vorbeugung des entzugssyndromes. |
GB8627909D0 (en) * | 1986-11-21 | 1986-12-31 | Glaxo Group Ltd | Medicaments |
GB8628475D0 (en) * | 1986-11-28 | 1987-01-07 | Glaxo Group Ltd | Medicaments |
EP0272052B1 (de) * | 1986-12-16 | 1992-07-08 | A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) | Angstlösende N-(1-Azabicyclo[2.2.2)oct-3-yl)benzamide und -thiobenzamide |
US5244909A (en) * | 1986-12-17 | 1993-09-14 | Glaxo Group Limited | Methods for the treatment of cognitive disorders |
GB8630071D0 (en) * | 1986-12-17 | 1987-01-28 | Glaxo Group Ltd | Medicaments |
DE3752062T2 (de) * | 1986-12-17 | 1997-09-11 | Glaxo Group Ltd | Verwendung von heterozyklischen Derivaten zur Herstellung von Arzneimitteln |
US5330982A (en) * | 1986-12-17 | 1994-07-19 | Glaxo Group Limited | Pharmaceutical composition containing a 5-HT receptor antagonist and an H+ K+ Atpase inhibitor and a method of treating gastrointestingal disorders therewith |
DE3788057T2 (de) * | 1986-12-17 | 1994-03-03 | Glaxo Group Ltd | Verwendung von heterocyclischen Verbindungen zur Behandlung von Depressionen. |
AU618520B2 (en) * | 1986-12-17 | 1992-01-02 | Glaxo Group Limited | Medicaments |
GB8806990D0 (en) * | 1988-03-23 | 1988-04-27 | Beecham Group Plc | Novel compounds |
GB8701022D0 (en) * | 1987-01-19 | 1987-02-18 | Beecham Group Plc | Treatment |
US4943428A (en) * | 1987-07-10 | 1990-07-24 | Wright State University | Stimulation of serotonin-1A receptors in mammals to alleviate motion sickness and emesis induced by chemical agents |
DE3822792C2 (de) * | 1987-07-11 | 1997-11-27 | Sandoz Ag | Neue Verwendung von 5HT¶3¶-Antagonisten |
EP0307077A1 (de) * | 1987-07-21 | 1989-03-15 | Merck Frosst Canada Inc. | Tetrahydrocarbazole zur Verbesserung der Cyclosporintherapie |
CA1307790C (en) * | 1987-08-04 | 1992-09-22 | Ian Anthony Cliffe | Ethers |
GB8718445D0 (en) * | 1987-08-04 | 1987-09-09 | Wyeth John & Brother Ltd | Pyridyl-ethers |
GB8720805D0 (en) * | 1987-09-04 | 1987-10-14 | Naylor R J | 2-alkoxy-n-(1-azabicyclo(2 2 2)oct-3-yl)benzamides & thiobenzamides |
US4863919A (en) * | 1988-02-01 | 1989-09-05 | A. H. Robins Company, Incorporated | Method of enhancing memory or correcting memory deficiency with arylamido(and arylthiomido)-azabicycloalkanes |
EP0329932B1 (de) * | 1988-02-23 | 1995-10-18 | Merrell Pharmaceuticals Inc. | Verwendung von Chinolizin- und Chinolizinon-Derivaten zur Herstellung von Arzneimitteln |
GB8805269D0 (en) * | 1988-03-04 | 1988-04-07 | Glaxo Group Ltd | Medicaments |
GB8806224D0 (en) * | 1988-03-16 | 1988-04-13 | Johnson Matthey Plc | Platinum chemotherapeutic product |
GB8816187D0 (en) * | 1988-07-07 | 1988-08-10 | Glaxo Group Ltd | Medicaments |
IT1228288B (it) * | 1989-01-09 | 1991-06-07 | Zambon Spa | Composti ad attivita' antiserotoninica |
WO1990012569A1 (en) * | 1989-04-21 | 1990-11-01 | Sandoz Ag | Therapeutic use of 5-ht3 receptor antagonists |
AU5650890A (en) * | 1989-05-24 | 1990-12-18 | Nippon Shinyaku Co. Ltd. | Indole derivatives and medicine |
US5223613A (en) * | 1990-04-27 | 1993-06-29 | G. D. Searle & Co. | Azatetracycle compounds and process of preparing same |
US5140023A (en) * | 1990-04-27 | 1992-08-18 | G. D. Searle & Co. | Azatetracycle compounds |
WO1992004347A1 (fr) * | 1990-08-31 | 1992-03-19 | Nippon Shinyaku Co., Ltd. | Derive d'indole et medicament |
US5234921A (en) * | 1991-03-07 | 1993-08-10 | G. D. Searle & Co. | Meso-azacyclic amides of imidazopyridine carboxylic acids and analogs thereof as pharmaceuticals |
US5219850A (en) * | 1991-03-07 | 1993-06-15 | G. D. Searle & Co. | Pharmaceutically useful meso-azacyclic amides of imidazopyridine carboxylic acids and analogs thereof |
US5260303A (en) * | 1991-03-07 | 1993-11-09 | G. D. Searle & Co. | Imidazopyridines as serotonergic 5-HT3 antagonists |
US5516782A (en) * | 1991-03-07 | 1996-05-14 | G. D. Searle & Co. | New meso-azacyclic aromatic acid amides and esters as novel serotonergic agents |
US5196547A (en) * | 1991-03-07 | 1993-03-23 | G. D. Searle & Co. | Meso-azacyclic amides of imidazopyridine carboxylic acids and analogs thereof |
EP0528026A1 (de) * | 1991-03-07 | 1993-02-24 | G.D. Searle & Co. | Meso-azacyclische aromatisch Carbonsäureamide und ester serotonergische Mittel |
US5137893A (en) * | 1991-03-07 | 1992-08-11 | G. D. Searle & Co. | Pharmaceutically useful meso-azacyclic amides of imidazopyridine carboxylic acids and analogs thereof |
US5227377A (en) * | 1991-03-07 | 1993-07-13 | G. D. Searle & Co. | Meso-azacyclic amides of certain bicyclic carboxylic acids |
CA2112487C (en) * | 1991-06-26 | 2003-04-15 | James W. Young | Method and compositions for treating emesis, nausea and other disorders using optically pure r(+) ondansetron |
DE4126999A1 (de) * | 1991-08-16 | 1993-02-18 | Basf Ag | Herbizide mittel, enthaltend 3-aminobenzo(b)thiophene als antidots |
JP2699794B2 (ja) * | 1992-03-12 | 1998-01-19 | 三菱化学株式会社 | チエノ〔3,2−b〕ピリジン誘導体 |
DE4238553A1 (de) * | 1992-11-14 | 1994-05-19 | Kali Chemie Pharma Gmbh | Neue Imidazol-1-yl-Verbindungen enthaltende Arzneimittel |
CN1039623C (zh) * | 1993-10-22 | 1998-09-02 | 中国人民解放军军事医学科学院毒物药物研究所 | 一种防治运动病综合征的药物组合物及其制备方法 |
GB2290963A (en) * | 1994-06-28 | 1996-01-17 | Kenneth Francis Prendergast | Pharmaceutical uses of ondansetron |
JP2002538102A (ja) | 1999-03-01 | 2002-11-12 | セプラコア インコーポレーテッド | 光学的に純粋なr(+)オンダンセトロンを使用する無呼吸および無呼吸障害の治療方法 |
JP2004506735A (ja) | 2000-08-18 | 2004-03-04 | ファルマシア・アンド・アップジョン・カンパニー | 疾患治療用キヌクリジン置換アリール化合物 |
US6492385B2 (en) | 2000-08-18 | 2002-12-10 | Pharmacia & Upjohn Company | Quinuclidine-substituted heteroaryl moieties for treatment of disease |
AU2001282873A1 (en) | 2000-08-18 | 2002-03-04 | Pharmacia And Upjohn Company | Quinuclidine-substituted aryl compounds for treatment of disease |
WO2002017358A2 (en) | 2000-08-21 | 2002-02-28 | Pharmacia & Upjohn Company | Quinuclidine-substituted heteroaryl moieties for treatment of disease (nicotinic acetylcholine receptor antagonists) |
WO2002015662A2 (en) | 2000-08-21 | 2002-02-28 | Pharmacia & Upjohn Company | Quinuclidine-substituted heteroaryl moieties for treatment of disease (nicotinic acetylcholine receptor antagonists |
YU32003A (sh) * | 2000-10-30 | 2006-05-25 | Teva Pharmaceutical Industries Ltd. | Novi kristalni i solvatni oblici ondansteron hlorovodonika i postupci za njihovo pripremanje |
US20020115707A1 (en) * | 2001-01-11 | 2002-08-22 | Rami Lidor-Hadas | Process for preparing pure ondansetron hydrochloride dihydrate |
PE20021019A1 (es) | 2001-04-19 | 2002-11-13 | Upjohn Co | Grupos azabiciclicos sustituidos |
KR100434390B1 (ko) * | 2001-04-20 | 2004-06-04 | 안국약품 주식회사 | 1,2,3,9-테트라히드로-9-메틸-3-[(2-메틸-1h-이미다졸-1-일)메틸]-4h-카바졸-4-온을 유효성분으로 하는 비강분무용조성물 |
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GB8516083D0 (en) * | 1985-06-25 | 1985-07-31 | Glaxo Group Ltd | Heterocyclic compounds |
GB8518658D0 (en) * | 1985-07-24 | 1985-08-29 | Glaxo Group Ltd | Medicaments |
HU895334D0 (en) * | 1986-07-30 | 1990-01-28 | Sandoz Ag | Process for the preparation of nasal pharmaceutical compositions |
EP0272052B1 (de) * | 1986-12-16 | 1992-07-08 | A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) | Angstlösende N-(1-Azabicyclo[2.2.2)oct-3-yl)benzamide und -thiobenzamide |
GB8806224D0 (en) * | 1988-03-16 | 1988-04-13 | Johnson Matthey Plc | Platinum chemotherapeutic product |
-
1986
- 1986-03-10 EP EP19900115499 patent/EP0405617A3/en not_active Withdrawn
- 1986-03-10 DE DE199090107640T patent/DE385517T1/de active Pending
- 1986-03-10 EP EP90107640A patent/EP0385517B1/de not_active Expired - Lifetime
- 1986-03-10 DE DE3689974T patent/DE3689974T2/de not_active Expired - Lifetime
- 1986-03-10 DE DE198686301684T patent/DE201165T1/de active Pending
- 1986-03-10 EP EP86301684A patent/EP0201165B1/de not_active Expired - Lifetime
- 1986-03-10 DE DE90107640T patent/DE3688296T2/de not_active Expired - Lifetime
- 1986-03-12 US US06/838,904 patent/US4721720A/en not_active Expired - Lifetime
- 1986-03-13 JP JP61053809A patent/JPS61212521A/ja active Granted
-
1987
- 1987-07-09 US US07/071,424 patent/US4783478A/en not_active Expired - Lifetime
-
1988
- 1988-09-16 US US07/245,892 patent/US4851407A/en not_active Expired - Lifetime
-
1992
- 1992-06-02 JP JP4165493A patent/JPH0720863B2/ja not_active Expired - Lifetime
-
1993
- 1993-05-07 SG SG616/93A patent/SG61693G/en unknown
- 1993-07-29 HK HK775/93A patent/HK77593A/xx not_active IP Right Cessation
-
1994
- 1994-05-06 CY CY172794A patent/CY1727A/xx unknown
- 1994-06-06 JP JP6145767A patent/JPH0748372A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
JPH0720863B2 (ja) | 1995-03-08 |
EP0385517A2 (de) | 1990-09-05 |
HK77593A (en) | 1993-08-06 |
SG61693G (en) | 1993-07-09 |
DE3688296T2 (de) | 1993-11-04 |
JPS61212521A (ja) | 1986-09-20 |
DE3689974D1 (de) | 1994-08-25 |
EP0201165A2 (de) | 1986-11-12 |
DE201165T1 (de) | 1989-04-20 |
JPH05310734A (ja) | 1993-11-22 |
JPH0555484B2 (de) | 1993-08-17 |
EP0201165A3 (en) | 1990-08-16 |
EP0405617A2 (de) | 1991-01-02 |
EP0385517A3 (en) | 1990-10-31 |
EP0201165B1 (de) | 1994-07-20 |
EP0385517B1 (de) | 1993-04-14 |
CY1727A (en) | 1994-05-06 |
DE3688296D1 (de) | 1993-05-19 |
JPH0748372A (ja) | 1995-02-21 |
DE3689974T2 (de) | 1994-11-03 |
US4851407A (en) | 1989-07-25 |
US4721720B1 (de) | 1992-06-30 |
US4721720A (en) | 1988-01-26 |
US4783478A (en) | 1988-11-08 |
EP0405617A3 (en) | 1992-11-25 |
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