Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Shrouq I, Farah"'
Publikováno v:
Biochemical and Biophysical Research Communications. 591:31-36
2-Arachidonoylglycerol (2-AG) is the most potent and abundant endocannabinoid that acts as a full agonist at the cannabinoid 1 (CB1) and 2 (CB2) receptors. It serves as a substrate for several serine hydrolases, including monoacylglycerol lipase (MGL
Autor:
Shakiru O. Alapafuja, Jodi Anne T. Wood, Dimitrios N. Pelekoudas, Christina Miyabe Shields, Alexandros Makriyannis, Girija Rajarshi, Nicholas Thomas Perry, Spiro Pavlopoulos, Honrao Chandrashekhar, Michael S. Malamas, Khadijah A. Mohammad, Alexander Zvonok, Jay A. A. West, Shrouq I. Farah
Publikováno v:
Journal of Medicinal Chemistry. 64:5956-5972
N-Acylethanolamines are signaling lipid molecules implicated in pathophysiological conditions associated with inflammation and pain. N-Acylethanolamine acid amidase (NAAA) favorably hydrolyzes lipid palmitoylethanolamide, which plays a key role in th
Autor:
Michael S, Malamas, Spiro, Pavlopoulos, Shakiru O, Alapafuja, Shrouq I, Farah, Alexander, Zvonok, Khadijah A, Mohammad, Jay, West, Nicholas Thomas, Perry, Dimitrios N, Pelekoudas, Girija, Rajarshi, Christina, Shields, Honrao, Chandrashekhar, Jodi, Wood, Alexandros, Makriyannis
Publikováno v:
Journal of medicinal chemistry. 64(9)
Autor:
Michael S. Malamas, Joseph Anderson, Karen L.G. Farizatto, JodiAnne T. Wood, Alexandros Makriyannis, Michael F. Almeida, Ben A. Bahr, Catherine M. Weerts, Shrouq I. Farah, Manjunath Lamani, Vidyanand G. Shukla
Publikováno v:
Bioorganicmedicinal chemistry. 27(23)
FAAH inhibitors offer safety advantages by augmenting the anandamide levels "on demand" to promote neuroprotective mechanisms without the adverse psychotropic effects usually seen with direct and chronic activation of the CB1 receptor. FAAH is an enz
Autor:
Alex Straiker, Shrouq I. Farah, Khadijah A. Mohammad, Alexandros Makriyannis, Catherine M. Weerts, Michael Speziale, Samantha Hilston, Nikolai Zvonok, Manjunath Lamani, Michael S. Malamas, Honrao Chandrashekhar, Christina Yume Miyabe, Maya Ploss
Publikováno v:
Bioorganic & Medicinal Chemistry. :116244
Autor:
Christina Yume Miyabe, Jay A. A. West, Michael S. Malamas, Girija Rajarshi, Dimitrios N. Pelekoudas, Nicholas Thomas Perry, Honrao Chandrashekhar, Manjunath Lamani, Spiro Pavlopoulos, Alexandros Makriyannis, Shrouq I. Farah
Publikováno v:
Bioorganic & Medicinal Chemistry. 28:115195
N-acylethanolamine acid amidase (NAAA) inhibition represents an exciting novel approach to treat inflammation and pain. NAAA is a cysteine amidase which preferentially hydrolyzes the endogenous biolipids palmitoylethanolamide (PEA) and oleoylethanola
Autor:
Evangelos Theodorou, Jonathan N. Glickman, Katharine A. Germansky, Alan C. Moss, Efi Kokkotou, Shrouq I. Farah, Alexandros Makriyannis, Michael S. Malamas
Publikováno v:
Gastroenterology. 156:S-65