نتایج جستجو برای: acid amide hydrolase

تعداد نتایج: 772887  

Journal: :Recent patents on CNS drug discovery 2012
Marion Feledziak Didier M Lambert Jacqueline Marchand-Brynaert Giulio G Muccioli

Endocannabinoids are lipid transmitters binding and activating the cannabinoid receptors. Both cannabinoid receptors and endocannabinoids, such as 2-arachidonoylglycerol and anandamide, have been shown to control numerous physiological and pathological processes, including in the central nervous system. Thus regulating endocannabinoid levels in-vivo represents an interesting therapeutic perspec...

2002
N. S. Waleh B. F. Cravatt A. Apte-Deshpande A. Terao T. S. Kilduff

Fatty acid amide hydrolase (FAAH) is a membrane-bound enzyme that inactivates a family of fatty acid amide molecules which are implicated in physiological processes such as pain and sleep. We cloned a 1.9 kb fragment of the 5 0-untranslated region of the mouse FAAH gene into the pGL3 basic luciferase reporter vector and showed that this sequence has promoter activity in vitro. By primer extensi...

Journal: :The Journal of biological chemistry 1985
C M Pickart I A Rose

Ubiquitin carboxyl-terminal hydrolase (formerly known as ubiquitin carboxyl-terminal esterase), from rabbit reticulocytes, has been shown to hydrolyze thiol esters formed between the ubiquitin carboxyl terminus and small thiols (e.g. glutathione), as well as free ubiquitin adenylate (Rose, I. A., and Warms, J. V. B. (1983) Biochemistry 22, 4234-4237). We now show that this enzyme hydrolyzes ami...

Journal: :iranian journal of pharmaceutical research 0
mahdi hedayati cellular & molecular research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, iran. laleh hoghughi rad cellular & molecular research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, iran. mehrdad faizi department of pharmacology and toxicology, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran sayyed abbas tabatabai a) department of pharmaceutical chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran

inhibitors of soluble epoxide hydrolase (seh) represent one of the novel pharmaceutical approaches for treating hypertension, vascular inflammation, pain and other cardiovascular related diseases. most of the potent seh inhibitors reported in literature often suffer from poor solubility and bioavailability. toward improving pharmacokinetic profile beside favorable potency, two series of 4-benza...

Journal: :The Journal of biological chemistry 2011
Aruna Kilaru Cornelia Herrfurth Jantana Keereetaweep Ellen Hornung Barney J Venables Ivo Feussner Kent D Chapman

N-acylethanolamines (NAEs) are bioactive fatty acid derivatives that occur in all eukaryotes. In plants, NAEs have potent negative growth-regulating properties, and fatty acid amide hydrolase (FAAH)-mediated hydrolysis is a primary catabolic pathway that operates during seedling establishment to deplete these compounds. Alternatively, polyunsaturated (PU)-NAEs may serve as substrates for lipid ...

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