نتایج جستجو برای: ec50

تعداد نتایج: 4357  

Journal: :World Journal Of Advanced Research and Reviews 2023

Background: Wild edible fruits are good source of phenolic compounds such as anthocyanins. Those known for their anti-inflammatory potential. They interact with many mediators the physiopathological pathway NF-kB which is at a central position in inflammatory response macrophages. This study aimed to determine and antioxidant potential ten wild aqueous extracts. Methods: The was evaluate throug...

Journal: :Anesthesiology 2011
Linda Groom Sheila M Muldoon Zhen Zhi Tang Barbara W Brandom Munkhuu Bayarsaikhan Saiid Bina Hee-Suk Lee Xing Qiu Nyamkhishig Sambuughin Robert T Dirksen

BACKGROUND Mutations in the type 1 ryanodine receptor gene (RYR1) result in malignant hyperthermia, a pharmacogenetic disorder typically triggered by administration of anesthetics. However, cases of sudden death during exertion, heat challenge, and febrile illness in the absence of triggering drugs have been reported. The underlying causes of such drug-free fatal "awake" episodes are unknown. ...

Journal: :Chemosphere 2007
Sébastien Haye Vera I Slaveykova Jérôme Payet

Life cycle impact assessment aims to translate the amounts of substance emitted during the life cycle of a product into a potential impact on the environment, which includes terrestrial ecosystems. This work suggests some possible improvements in assessing the toxicity of metals on soil ecosystems in life cycle assessment (LCA). The current available data on soil ecotoxicity allow one to calcul...

Journal: :British journal of pharmacology 1998
R J Vandenberg A D Mitrovic G A Johnston

1. Expression of the recombinant human excitatory amino aid transporters, EAAT1 and EAAT2, in Xenopus laevis oocytes allows electrogenic transport to be studied under voltage clamp conditions. 2. We have investigated the transport of the pharmacological substrate, L-serine-O-sulphate transport by EAAT1 and EAAT2. The EC50 values for L-serine-O-sulphate transport by EAAT2 showed a steep voltage-...

Journal: :The Journal of pharmacology and experimental therapeutics 1998
M Bencherif J D Schmitt B S Bhatti P Crooks W S Caldwell M E Lovette K Fowler L Reeves P M Lippiello

The present report describes in vitro studies demonstrating that the heterocyclic substituted pyridine compound (+/-)-2-(3-pyridinyl)-1-azabicyclo[2.2.2]octane (RJR-2429) is extremely potent in activating human muscle nicotine ACh receptor (nAChR) (EC50 = 59 +/- 17 nM; Emax = 110 +/- 09% vs. nicotine). RJR-2429 is markedly less potent in activating nAChRs in the clonal cell line PC12, with EC50...

Journal: :Chemical & pharmaceutical bulletin 2001
Y Fujinami A Tai I Yamamoto

The radical scavenging activity of the stable derivatives, which are O-substituted at the C-2 position of ascorbic acid (AA), against 1,1-diphenyl-2-picrylhydrazyl (DPPH) was evaluated in buffer under different pH conditions, and compared with those of AA and alpha-tocopherol. AA was shown to have 50% radical scavenging ability (EC50) at a concentration of 2.2 x 10(-5) M against 0.1 mM DPPH in ...

Journal: :The Journal of General Physiology 1995
B N Cohen A Figl M W Quick C Labarca N Davidson H A Lester

We constructed chimeras of the rat beta 2 and beta 4 neuronal nicotinic subunits to locate the regions that contribute to differences between the acetylcholine (ACh) dose-response relationships of the alpha 3 beta 2 and alpha 3 beta 4 receptors. Expressed in Xenopus oocytes, the alpha 3 beta 2 receptor displays an EC50 for ACh approximately 20-fold less than the EC50 of the alpha 3 beta 4 recep...

Journal: :Circulation research 1995
G L Stahl W R Reenstra G Frendl

Reperfusion of the ischemic myocardium results in the loss of endothelium-dependent relaxation. We have shown recently that the alternate complement pathway is activated immediately on reperfusion of the ischemic porcine myocardium. We hypothesized that complement activation directly attenuates endothelium-dependent relaxation of porcine coronary arteries. Bradykinin (BK) or substance P concent...

2016
Olesja M. Bondarenko Margit Heinlaan Mariliis Sihtmäe Angela Ivask Imbi Kurvet Elise Joonas Anita Jemec Marika Mannerström Tuula Heinonen Rohit Rekulapelly Shashi Singh Jing Zou Ilmari Pyykkö Damjana Drobne Anne Kahru

Within EU FP7 project NANOVALID, the (eco)toxicity of 7 well-characterized engineered nanomaterials (NMs) was evaluated by 15 bioassays in 4 laboratories. The highest tested nominal concentration of NMs was 100 mg/l. The panel of the bioassays yielded the following toxicity order: Ag > ZnO > CuO > TiO2 > MWCNTs > SiO2 > Au. Ag, ZnO and CuO proved very toxic in the majority of assays, assumingly...

Journal: :Antimicrobial agents and chemotherapy 2014
Ravikiran S Yedidi Harisha Garimella Manabu Aoki Hiromi Aoki-Ogata Darshan V Desai Simon B Chang David A Davis W Sean Fyvie Joshua D Kaufman David W Smith Debananda Das Paul T Wingfield Kenji Maeda Arun K Ghosh Hiroaki Mitsuya

In the present study, GRL008, a novel nonpeptidic human immunodeficiency virus type 1 (HIV-1) protease inhibitor (PI), and darunavir (DRV), both of which contain a P2-bis-tetrahydrofuranyl urethane (bis-THF) moiety, were found to exert potent antiviral activity (50% effective concentrations [EC50s], 0.029 and 0.002 μM, respectively) against a multidrug-resistant clinical isolate of HIV-1 (HIVA0...

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