UY26852A1 - USE OF CONDENSED DIHYDROPIRIDINS FOR THE PREPARATION OF AGENTS INTENDED FOR THE TREATMENT OF CHRONIC PAIN - Google Patents
USE OF CONDENSED DIHYDROPIRIDINS FOR THE PREPARATION OF AGENTS INTENDED FOR THE TREATMENT OF CHRONIC PAINInfo
- Publication number
- UY26852A1 UY26852A1 UY26852A UY26852A UY26852A1 UY 26852 A1 UY26852 A1 UY 26852A1 UY 26852 A UY26852 A UY 26852A UY 26852 A UY26852 A UY 26852A UY 26852 A1 UY26852 A1 UY 26852A1
- Authority
- UY
- Uruguay
- Prior art keywords
- condensed
- preparation
- treatment
- chronic pain
- dihydropiridins
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- 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
- A61K31/47—Quinolines; Isoquinolines
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4747—Quinolines; Isoquinolines spiro-condensed
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
- C07D217/14—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
- C07D217/16—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals substituted by oxygen atoms
Abstract
El invento se refiere a la utilización de dihidropiridinas condensadas y sus sales con ácidos fisiológicamente compatibles para la preparación de agentes destinados al tratamiento de dolores crónicos, de la Fórmula general I, en la que A es benzo o tieno, y Z, R1, R2, R3, R4, R5 y R6 son como se han definido en la memoria descriptiva, así como nuevos compuestos de la Fórmula I.The invention relates to the use of condensed dihydropyridines and their salts with physiologically compatible acids for the preparation of agents for the treatment of chronic pain, of the general Formula I, in which A is benzo or thieno, and Z, R1, R2 , R3, R4, R5 and R6 are as defined in the specification, as well as new compounds of Formula I.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10035997A DE10035997A1 (en) | 2000-07-25 | 2000-07-25 | Use of fused dihydropyridines for the manufacture of agents for the treatment of chronic pain |
Publications (1)
Publication Number | Publication Date |
---|---|
UY26852A1 true UY26852A1 (en) | 2002-02-28 |
Family
ID=7650021
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY26852A UY26852A1 (en) | 2000-07-25 | 2001-07-25 | USE OF CONDENSED DIHYDROPIRIDINS FOR THE PREPARATION OF AGENTS INTENDED FOR THE TREATMENT OF CHRONIC PAIN |
Country Status (5)
Country | Link |
---|---|
AR (1) | AR029981A1 (en) |
AU (1) | AU2001289719A1 (en) |
DE (1) | DE10035997A1 (en) |
UY (1) | UY26852A1 (en) |
WO (1) | WO2002007714A2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003014089A1 (en) * | 2001-07-31 | 2003-02-20 | Virginia Commonwealth University | Aminotetrahydroisoquinoline derivatives as analgesics |
RU2711646C1 (en) * | 2019-04-08 | 2020-01-17 | Федеральное государственное бюджетное учреждение науки Институт молекулярной генетики Российской академии наук | Synthesis of tritium-labeled 6,7-dimethoxy-4,4-dimethyl-1-[4-(4-trifluoromethylphenoxy)phenyl]-3n-isoquinoline |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1386076A (en) * | 1971-06-03 | 1975-03-05 | Wyeth John & Brother Ltd | Isoquinoline derivatives |
CA1330560C (en) * | 1986-05-21 | 1994-07-05 | Maurits E. A. Vandewalle | Di- and tetrahydroisoquinoline derivatives |
GB8921304D0 (en) * | 1989-09-20 | 1989-11-08 | Wyeth John & Brother Ltd | New method of treatment and heterocyclic compounds used therein |
KR930703259A (en) * | 1990-12-17 | 1993-11-29 | 알베르투스 빌헬무스 요아네스 쩨스트라텐 | Disinfectant Isoquinoline Derivatives |
WO2000044725A1 (en) * | 1999-01-28 | 2000-08-03 | Boehringer Ingelheim Pharma Kg | Fused dihydropyridines and use of fused dihydropyridines in the preparation of agents for the treatment of epilepsy |
-
2000
- 2000-07-25 DE DE10035997A patent/DE10035997A1/en not_active Withdrawn
-
2001
- 2001-07-21 WO PCT/EP2001/008453 patent/WO2002007714A2/en active Application Filing
- 2001-07-21 AU AU2001289719A patent/AU2001289719A1/en not_active Abandoned
- 2001-07-25 UY UY26852A patent/UY26852A1/en not_active Application Discontinuation
- 2001-07-25 AR ARP010103543A patent/AR029981A1/en not_active Suspension/Interruption
Also Published As
Publication number | Publication date |
---|---|
AU2001289719A1 (en) | 2002-02-05 |
WO2002007714A2 (en) | 2002-01-31 |
AR029981A1 (en) | 2003-07-23 |
WO2002007714A3 (en) | 2002-09-06 |
DE10035997A1 (en) | 2002-02-07 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
109 | Application deemed to be withdrawn |
Effective date: 20140513 |