中文(简体)
Albanian
Arabic
Armenian
Azerbaijani
Belarusian
Bengali
Bosnian
Catalan
Czech
Danish
Deutsch
Dutch
English
Estonian
Finnish
Français
Greek
Haitian Creole
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Irish
Italian
Japanese
Korean
Latvian
Lithuanian
Macedonian
Mongolian
Norwegian
Persian
Polish
Portuguese
Romanian
Russian
Serbian
Slovak
Slovenian
Spanish
Swahili
Swedish
Turkish
Ukrainian
Vietnamese
Български
中文(简体)
中文(繁體)

suma/hypoxia

链接已保存到剪贴板
页 1 从 37 结果

Imidazole derivatives having anti-hypoxia properties

只有注册用户可以翻译文章
登陆注册
BACKGROUND OF THE INVENTION (1) Field of the Invention The present invention relates to a novel imidazole derivative, a salt thereof and a medicine comprising the derivative or salt as an active ingredient. More particularly, the present invention relates to a novel N-substituted imidazole
FIELD OF THE INVENTION Modifications to various proteins including, but not limited to, proteins involved in the tricarboxylic acid (TCA) cycle, oxidative phosphorylation (OxPhos) pathways, calcium (Ca.sup.2+) handling, and/or chaperoning, as well as proteins selected from aldehyde dehydrogenase,

Compositions and method of treating hypoxia-associated diseases

只有注册用户可以翻译文章
登陆注册
BACKGROUND OF THE INVENTION Hypoxia, a state of lower than normal tissue oxygen tension, has recently been implicated in a host of human diseases, including cancer, heart disease, and neurological disorders. An early response to tissue hypoxia is induction of hypoxia inducible factor (HIF), a basic

Treating cognition with, aminocyclopropanecarboxylic derivatives

只有注册用户可以翻译文章
登陆注册
BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to the field of neuropsychiatry and relates specifically to methods for memory enhancement and treatment of memory deficits consequent to neurological disorders. 2. Description of the Background Art The N-methyl-D-aspartate

Imidazole compounds and their use as calcium channel blockers

只有注册用户可以翻译文章
登陆注册
The present invention relates to therapeutically-active compounds and their use as well as to pharmaceutical preparations comprising the compounds. The compounds of the invention possess valuable activity as calcium channel blockers which make them useful in the treatment of anoxia, ischemia,

1,3-Disubstituted thiourea compounds and preparation thereof

只有注册用户可以翻译文章
登陆注册
The present invention relates to novel 1,3-disubstituted thiourea compounds and their pharmaceutically acceptable acid addition salts and process for the preparation thereof and composition containing the 1,3-disubstituted thiourea compounds and their salts. More particularly, it relates to

Optimization of cells for endogenous gene activation

只有注册用户可以翻译文章
登陆注册
The invention concerns a process for optimizing gene expression in cells. A first aspect concerns a process for changing the expression of a target gene that is present endogenously in a eukaryotic cell by introducing a heterologous expression control sequence or/and an amplification gene into the
BACKGROUND OF THE INVENTION Cardiovascular diseases are a leading cause of death resulting in almost 40% of deaths annually in the United States. Inadequate human myocardial regeneration poses a significant public health problem. It is estimated that 13 million Americans have coronary artery
FIELD OF THE INVENTION The present invention pertains to improved methods for using selegiline in therapeutic applications. In particular, the invention is directed to improved methods for treating certain selegiline-responsive diseases and conditions by administering selegiline either buccally or

Therapeutic intervention to mimic the effect of caloric restriction

只有注册用户可以翻译文章
登陆注册
BACKGROUND OF THE INVENTION 1. Field of the Invention This invention is directed to methods for increased longevity, delay of aging associated disorders, protection from acute physical stress and induction of regeneration and healing by administration of Long chain Free Fatty Acids (LFFA) and CoA

Benzimidazole compounds useful as calcium channel blockers

只有注册用户可以翻译文章
登陆注册
The present invention relates to therapeutical active compounds and their use as well as to pharmaceutical preparations comprising the compounds. The compounds of the invention possess valuable activity as calcium channel blockers which make them useful in the treatment of anoxia, ischemia,
FIELD OF THE INVENTION The present invention relates to 4-hydroxy-4-methyl-piperidine-1-carboxylic acid(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-amide, which is a compound of formula ##STR00002## and to pharmaceutically acceptable acid addition salts thereof. This compound is generically
TECHNICAL FIELD The present disclosure relates to novel crystalline acid salts of a tricyclic derivative or a hydrate thereof, and a production method thereof. BACKGROUND Drugs administered orally show medicinal effects through absorption, distribution, metabolism or elimination, and the intrinsic

Compositions and methods for neovascularization

只有注册用户可以翻译文章
登陆注册
BACKGROUND OF THE INVENTION Angiogenesis represents a major challenge in regenerative medicine and tissue engineering. Thus, a need exists for compositions and methods for inducing angiogenesis. SUMMARY OF THE INVENTION The invention relates to the fields which include tissue engineering, advanced

Piperidine compounds and their preparation and use

只有注册用户可以翻译文章
登陆注册
The present invention relate s to therapeutically active piperidine compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful in the treatment of anoxia, ischemia, migraine and epilepsy. It is well known that accumulation of
加入我们的脸书专页

科学支持的最完整的草药数据库

  • 支持55种语言
  • 科学支持的草药疗法
  • 通过图像识别草药
  • 交互式GPS地图-在位置标记草药(即将推出)
  • 阅读与您的搜索相关的科学出版物
  • 通过药效搜索药草
  • 组织您的兴趣并及时了解新闻研究,临床试验和专利

输入症状或疾病,并阅读可能有用的草药,输入草药并查看所使用的疾病和症状。
*所有信息均基于已发表的科学研究

Google Play badgeApp Store badge