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dementia/murtall

Sábháiltear an nasc chuig an gearrthaisce
Leathanach 1 ó 118 torthaí
FIELD OF INVENTION A product for use in the treatment of obesity, the metabolic syndrome, type 2 diabetes, cardiovascular diseases, dementia, alzheimers disease and inflammatory bowel disease comprising at least one isolated bacterial strain from the species Prevotellaceae, herein the strain is

Compositions and methods for utilization of algal compounds

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
BACKGROUND OF THE INVENTION Field of the Invention This invention relates to algal biochemistry, and more specifically, to algal compositions and methods of utilization. SUMMARY OF THE INVENTION Provided herein are exemplary products for mammalian consumption selected from any of a composition

Phenylpyrrole derivative

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
CROSS REFERENCE TO RELATED APPLICATIONS This application is a National Stage of International Application No. PCT/JP2012/081744 filed Dec. 7, 2012, claiming priority based on Japanese Patent Application No. 2011-268561 filed Dec. 8, 2011, the contents of all of which are incorporated herein by

Compound with agitation effect on peroxisome proliferator-activated receptor process for its preparation and use thereof

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
RELATED APPLICATIONS The instant application is the U.S. National Phase under 35 U.S.C. .sctn.371 of International Application No. PCT/CN2009/073140 entitled COMPOUND WITH AGITATION EFFECT ON PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR .delta., AND PREPARATION METHOD AND USE THEREOF, filed Aug. 7,

Nitrogen-containing bicyclic compounds and drugs containing the same as the active ingredient

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
TECHNICAL FIELD The present invention relates to a nitrogen-containing bicyclic compound or a pharmacologically acceptable salt thereof and a pharmaceutical composition comprising it as active ingredient. More specifically, the present invention relates to (1) a compound of formula (I) ##STR00002##

Substituted benzopyrans as selective estrogen receptor-beta agonists

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
BACKGROUND OF THE INVENTION The present invention relates to novel benzopyran ER-.beta. agonist compounds, pharmaceutical compositions thereof, and use of these compounds to treat a ER-.beta. mediated disease such as benign prostatic hypertrophy, obesity, dementia, hypertension, incontinence, colon

Treatment of male androgen deficiency symptoms or diseases with sex steroid precursor combined with SERM

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
FIELD OF THE INVENTION The present invention relates to a novel treatment of low total androgens accompanied by one or more symptoms classically attributed to male hypogonadism or low testosterone. The number of individuals over 65 years of age has increased more than 10-fold compared with the 1990s

Treatment of male androgen deficiency symptoms or diseases with sex steroid precursor combined with SERM

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
FIELD OF THE INVENTION The present invention relates to a novel treatment of low total androgens accompanied by one or more symptoms classically attributed to male hypogonadism or low testosterone. The number of individuals over 65 years of age has increased more than 10-fold compared with the 1990s

Piperidine derivative compounds and drugs containing the compounds as the active ingredient

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
TECHNICAL FIELD The present invention relates to a piperidine derivative. More specifically, the present invention relates to (1) a piperidine derivative of formula (I) ##STR00002## (2) a method for the preparation thereof, (3) a composition comprising it as an active ingredient, (4) a compound of

Amido-thiophene compounds and their use

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
TECHNICAL FIELD The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain amido-thiophene compounds that, inter alia, inhibit 11.beta.-hydroxysteroid dehydrogenase type 1 (11.beta.-HSD1). The present invention also

Amido-thiophene compounds and their use

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
TECHNICAL FIELD The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain amido-thiophene compounds that, inter alia, inhibit 11.beta.-hydroxysteroid dehydrogenase type 1 (11.beta.-HSD1). The present invention also

Amido-thiophene compounds and their use as 11-beta-HSD1 inhibitors

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
TECHNICAL FIELD The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain amido-thiophene compounds that, inter alia, inhibit 11.beta.-hydroxysteroid dehydrogenase type 1 (11.beta.-HSD1). The present invention also

25-hydroxyvitamin D3 24-hydroylase transgenic rats

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
TECHNICAL FIELD This invention relates to 25-hydroxyvitamin D.sub.3 24-hydroxylase transgenic animals. BACKGROUND ART The transgenic animal carries a gene introduced to its own or progenitor's germ cell line in an early stage of development (usually, single cells). Wagner et al. (1981, ProNAS, USA,

(4-phenyl-piperidin-1-yl)-[5-(1H-pyrazol-4-yl)-thiophen-3-yl]-methanone compounds and their use

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
TECHNICAL FIELD The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain (4-phenyl-piperidin-1-yl)-[5-(1H-pyrazol-4-yl)-thiophen-3-yl]-methanone compounds that, inter alfa, inhibit 11.beta.-hydroxysteroid

3,3-disubstituted-(8-aza-bicyclo[3.2.1]oct-8-yl)-[5-(1H-pyrazol-4-yl)-thio- phen-3-yl]-methanones as inhibitors of 11 (.beta.)-HSD1

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
TECHNICAL FIELD The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain 3,3-disubstituted-(8-aza-bicyclo[3.2.1]oct-8-yl)-[5-(1H-pyrazol-4-yl)-thi- ophen-3-yl]-methanone,
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