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antiasthmatic/zánět
Odkaz je uložen do schránky
Strana 1 z 113 Výsledek
Potentiation of the antireactive-antiasthmatic effect of inhaled loop diuretics by inhaled non-steroidal anti-inflammatory drugs
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The invention relates to the potentiation of the antireactive-antiasthmatic effect of inhaled loop diuretics by inhaled non-steroidal anti-inflammatory drugs.
Despite the fact that more refined drugs are available and that asthma care is better overall, nevertheless the mortality and morbidity of
Potentiation of the anti-reactive-antiasthmatic effect of inhaled loop diuretics by inhaled non-steroidal anti-inflammatory drugs
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The invention relates to the potentiation of the antireactive-antiasthmatic effect of inhaled loop diuretics by inhaled non-steroidal anti-inflammatory drugs.
Despite the fact that more refined drugs are available and that asthma care is better overall, nevertheless the mortality and morbidity of
Anti-asthmatic, anti-allergic, anti-cholinergic, bronchodilator and anti-inflammatory 1-[(benzoylphenyl)-lower-alkyl]piperidines and analogs thereof
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Přihlášení Registrace
BACKGROUND OF THE INVENTION
(a) Field of the Invention
This invention relates to 1-[(3- or 4-benzoylphenyl)-lower-alkyl]-[(CH.sub.2).sub.n --N.dbd.B]-substituted-piperidines and analogs thereof, useful as anti-asthmatic, anti-allergic, anti-cholinergic, bronchodilator and anti-inflammatory agents;
1,5- and 3-O-substituted 1H-indazoles having anti-asthmatic, anti-allergic, anti-inflammatory, immunomodulating and neuroprotective action, process for their preparation and their use as medicaments
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
TECHNICAL FIELD
The invention relates to the preparation and use of novel derivatives of indazol-3-ol as medicaments having anti-asthmatic, anti-allergic, anti-inflammatory, immuno-nodulating and neuroprotective properties.
PRIOR ART
Cyclosporin A (CsA) or FK 506 are immunosuppressant natural
Muscle-strengthening drugs and anti-inflammatory drugs
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
TECHNICAL FIELD
The present invention relates to a novel agent or composition for use as a muscle-strengthening drug, an anti-inflammatory drug, an antiasthmatic, an antidiarrheal, an antidepressant, or a drug for the treatment of secondary diseases following cerebral infarction (human stroke
Amorphous (quinolin-2-ylmethoxy)indole compounds useful for treating inflammatory diseases
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND OF THE INVENTION
EP 419,049, Prasit et al., Mar. 27, 1991, describes a series of quinolin-2-ylmethoxy indoles useful as inhibitors of leukotriene biosynthesis. Examples 1 and 1A therein teach the synthesis of 3-[N-(p-chlorobenzyl)-3-(t-butylthio)-5-(quinolin-2-ylmethoxy)indol-2-yl]-
Use of 3-(arylmethyleneamino)-1-aryl-2-pyrazolines in the prophylaxis and treatment of inflammation, pain, pyresis, and asthma
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
This invention relates to heterocyclic compounds and their preparation and to the use of such compounds of pharmaceutical formulations thereof in medicine in a mammal, including man, as e.g. anti-inflammatory or anti-allergic agents or as agents in the prevention of tissue rejection.
Accordingly,
Composition comprising an extract of Tiarella polyphylla and tiarellic acid isolated therefrom having antiinflammatory, antiallergic and antiasthmatic activity
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
TECHNICAL FIELD
The present invention relates to a composition comprising an extract of Tiarella polyphylla and tiarellic acid isolated therefrom having anti-inflammatory, anti-allergic and anti-asthmatic activity.
BACKGROUND ART
Asthma has been regarded as a complex syndrome occurring in the
Pharmaceutical composition comprising an extract of Pseudolysimachion longifolium and the catalpol derivatives isolated therefrom having antiinflammatory, antiallergic and antiasthmatic activity
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a 371 of PCT/KR2006/002092 filed on May 30, 2006, which claims the benefit of Korean Patent Application Nos. 10-2005-0045755 filed on May 30, 2005, 10-2005-0045756 filed on May 30, 2005, 10-2006-0048104 filed on May 29, 2006 and
Pharmaceutical composition comprising an extract of pseudolysimachion longifolium and the catalpol derivatives isolated therefrom having antiinflammatory, antiallergic and antiasthmatic activity
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
TECHNICAL FIELD
The present invention relates to a composition comprising an extract of Pseudolysimachion longifolium and the catalpol derivatives isolated therefrom having anti-inflammatory, anti-allergic and anti-asthmatic activity.
BACKGROUND ART
Asthma has been regarded as a complex syndrome
Pharmaceutical composition comprising an extract of Pseudolysimachion longifolium and the catalpol derivatives isolated therefrom having antiinflammatory, antiallergic and antiasthmatic activity
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
TECHNICAL FIELD
The present invention relates to a composition comprising an extract of Pseudolysimachion longifolium and the catalpol derivatives isolated therefrom having anti-inflammatory, anti-allergic and anti-asthmatic activity.
BACKGROUND ART
Asthma has been regarded as a complex syndrome
Metabolically inert anti-inflammatory and anti-tumor antifolates
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Přihlášení Registrace
FIELD OF INVENTION
This invention relates to folic acid antagonists that are metabolically inert exhibiting a high level of anti-inflammatory and anti-tumor activity. Metabolically inert classical antifolates are new and therefore they exhibit unexpected biological properties such as those recited
[3H,7H]thiazolo[3,4-a]pyridines with antiasthmatic and antiinflammatory actions on the respiratory tract
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Přihlášení Registrace
The present invention relates to [3H, 7H]thiazolo[3,4-a]-pyridines, a method for preparing them and pharmaceutical compositions which contain them.
More precisely the invention relates to compounds of formula (I) ##STR2## in which: R is (C.sub.1 -C.sub.4) alkyl;
R.sub.1 is a cyano, free or salified
N-hydroxyurea derivative and pharmaceutical composition containing the same
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
TECHNICAL FIELD
The present invention relates to novel N-hydroxyurea derivative having a lipoxygenase inhibitory activity and a thromboxane synthase inhibitory activity and pharmaceutical composition containing the same.
BACKGROUND ART
In recent years, the role of chemical mediators in asthma and
Indenyl hydroxamic acids and hydroxy ureas as inhibitors of 5-lipoxygenase
Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND OF THE INVENTION
The leukotrienes and their biological activities, especially their role in various disease states, have been extensively studied. Their properties are described in the book Leukotrienes and Lipoxygenases, Ed., J. Rokach, Elsevier, N.Y., 1989.
Inhibitors of the
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