BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to pharmaceutical compositions containing (-)-hydroxycitric acid useful for reducing inflammation and regulating inflammatory responses and processes.
2. Description Of Prior Art
Chronic inflammation recently has received
BACKGROUND OF THE INVENTION
1. Field of the Invention (Technical Field)
The present invention relates to cyclic hexapeptides that are highly-specific antagonists for the melanocortin-4 receptor (MC4-R), and which may be used in the treatment of a variety of body weight disorders including cachexia,
FIELD OF THE INVENTION
The present invention relates to 17-acetamido-4-azasteroid derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators (SARMs) and are thereby useful
FIELD OF THE INVENTION
The present invention relates to fluorinated 4-azasteroid derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators (SARMs) and are thereby useful for
FIELD OF THE INVENTION
The present invention relates to N-(2-benzyl)-2-phenylbutanamide derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators (SARMs) and are thereby
FIELD OF THE INVENTION
The present invention relates to 3-4 fused-imidazolyl steroidal derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators (SARMs) and are thereby
FIELD OF THE INVENTION
The present invention relates to N-(2-benzyl)-2-phenylbutanamide derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators (SARMs) and are thereby
FIELD OF THE INVENTION
The present invention relates to 17-heterocyclic-4-azasteroid derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators (SARMs) and are thereby useful
FIELD OF THE INVENTION
The present invention relates to crystalline and amorphous forms and solvates of N-(3H-imidazo[4,5-B]pyridin-2-ylmethyl)-2-fluoro-4-methyl-3-oxo-4-aza-5-a- lpha-androst-1-en-17-beta-carboxamide, a tissue-selective androgen receptor modulator (SARM). This SARM is thereby useful
FIELD OF THE INVENTION
The present invention relates to N-(2-benzyl)-2-phenylbutanamide derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators (SARMs) and are thereby
FIELD OF THE INVENTION
The present invention relates to fluorinated 4-azasteroid derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators and are thereby useful for the
FIELD OF THE INVENTION
The present invention relates to 4-azasteroid derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators and are thereby useful for the treatment of
FIELD OF THE INVENTION
The present invention relates to fluorinated 4-azasteroid derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators and are thereby useful for the
FIELD OF THE INVENTION
The present invention relates to 21-benzimidazole-4-azasteroid and 21-azabenzimidazole-azasteroid derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor
FIELD OF THE INVENTION
The present invention relates to 17-acetamido-4-azasteroid derivatives, their synthesis, and their use as androgen receptor modulators. More particularly, the compounds of the present invention are tissue-selective androgen receptor modulators (SARMs) and are thereby useful
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