نتایج جستجو برای: tacrine

تعداد نتایج: 1379  

Journal: :The Journal of Experimental Medicine 2003
Thomas M. Rivers Frederick L. Gates

Rabbit skin treated for a few minutes with ultra-violet light and then inoculated at once with vaccine virus is less susceptible to the action of the virus than is untreated skin. If 24, 48, or 72 hours elapse between the time of irradiation and inoculation, the treated skin appears to be more susceptible than is untreated skin. Skin repeatedly exposed to ultra-violet light is less susceptible ...

Journal: :International journal of pharmaceutics 2000
J Lee T G Park H Choi

80% except for acetaminophen, due to its lower solubility in water and higher solubility in corn oil. The release profile of the drug was pH dependent. In acidic medium, the release rate was much slower, however, the drug was released quickly at pH 7.4. Tacrine showed unexpected release profiles, probably due to ionic interaction with polymer matrix and the shell structure and the highest relea...

Journal: :Emergency medicine journal : EMJ 2006
S Sener M Ozsarac

Rivastigmine, which has been approved by the US Food and Drugs Administration for the treatment of Alzheimer's disease, is a non-competitive reversible inhibitor of acetylcholinesterase. We present a case of rivastigmine toxicity at a dose of 90 mg, with evidence of respiratory depression. To our knowledge, this case report provides evidence of the highest rivastigmine ingestion recorded (90 mg...

Journal: :Molecules 2016
Yingbo Fu Yu Mu Hui Lei Pu Wang Xin Li Qiao Leng Li Han Xiaodan Qu Zhanyou Wang Xueshi Huang

Five novel tacrine-ferulic acid hybrid compounds (8a-e) were synthesized and their structures were identified on the basis of a detailed spectroscopic analysis. The activities of inhibiting acetyl cholinesterase (AChE) and butyryl cholinesterase (BuChE), reducing self-induced β-amyloid (Aβ) aggregation and chelating Cu2+ were evaluated in vitro. Among them, 8c and 8d displayed the higher select...

Journal: :Molecules 2016
Houssem Boulebd Lhassane Ismaili Manuela Bartolini Abdelmalek Bouraiou Vincenza Andrisano Helene Martin Alexandre Bonet Ignacio Moraleda Isabel Iriepa Mourad Chioua Ali Belfaitah José Marco-Contelles

Herein we describe the synthesis and in vitro biological evaluation of thirteen new, racemic, diversely functionalized imidazo pyranotacrines as non-hepatotoxic, multipotent tacrine analogues. Among these compounds, 1-(5-amino-2-methyl-4-(1-methyl-1H-imidazol-2-yl)-6,7,8,9-tetrahydro-4H-pyrano[2,3-b]quinolin-3-yl)ethan-1-one (4) is non-hepatotoxic (cell viability assay on HepG2 cells), a select...

2008
Lijun Zhang Daxin Shi Jiarong Li Ling Zhang Yanqiu Fan

The title compound, C(17)H(18)N(4), contains a pyrazolopyridine system fused with a seven-membered carbocyclic ring. The pyrazole ring is coplanar with the pyridine ring, while the phenyl ring is twisted by a dihedral angle of 14.38 (14)° with respect to the pyridine ring. The seven-membered ring displays a chair conformation. The packing is stabilized by N-H⋯N hydrogen bonds and N-H⋯π(arene) i...

1989
Friedemann MATTERN

We present a new, yet very simple principle for global quiescence deteco tion. All active processes and all messages of the underlying computation have a share f a credit initially distributed by the environment. The sum of all credit shares is kept t n invariant. When the environment has recovered the whole credit, it can conclude tha o processes are active and no messages are in transit. We s...

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