Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Fenmei Yao"'
Autor:
Mark Gao, Nguyen Son H, Stephen P. Raillard, Wendy Luo, Juthamas Sukbuntherng, Ritu Lal, Quincey Q. Wu, Hui Yan, Jeanelle Zamora, Fenmei Yao, Randall A. Scheuerman, Ying Bao, Ge Peng, Tracy Dias, Thu Phan, Mark S. Warren, Mark A. Gallop, Ezra Tai, Shubhra Upadhyay, Kerry J. Koller, Maria J. Ludwikow, Lin Bu, Thamil Annamalai, Kenneth C. Cundy
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 330:911-921
Baclofen is a racemic GABA B receptor agonist that has a number of significant pharmacokinetic limitations, including a narrow window of absorption in the upper small intestine and rapid clearance from the blood. Arbaclofen placarbil is a novel trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a951efa7bfd8f716079a44ae1822a240
https://doi.org/10.1124/jpet.108.149773
https://doi.org/10.1124/jpet.108.149773
Autor:
Xiaoyu Tian, Sonya L. Palmer, Atmaram D. Khanolkar, Jianxin Guo, Alexandros Makriyannis, Fenmei Yao
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 46:115-129
Four isotopically labeled, metabolically stable analogs of arachidony-lethanolamide (anandamide), an endogenous cannabinoid ligand, were synthesized via a five-step reaction sequence starting from arachidonic acid. These stable methanandamide derivat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::144cb4ad61a1e2b95c37032532ad3a9a
https://doi.org/10.1002/jlcr.650
https://doi.org/10.1002/jlcr.650
Publikováno v:
Bioorganicmedicinal chemistry letters. 18(22)
To explore the hydrophobic groove subsite within the CB1 cannabinoid receptor we have designed and synthesized a group of tail-substituted anandamide analogs. Our design involves the introduction of aryl or heterocyclic ring as terminal substituents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dcdee7aba06f112113cfcf377e8af41
https://pubmed.ncbi.nlm.nih.gov/18723350
https://pubmed.ncbi.nlm.nih.gov/18723350
Publikováno v:
The Journal of biological chemistry. 280(33)
The endogenous cannabinoid ligand anandamide is biosynthesized from membrane phospholipid precursors and is believed to reach its sites of action on the CB1 and CB2 receptors through fast lateral diffusion within the cell membrane. To gain a better i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75fe20666d2fbd804c9337f497b2a6ad
https://pubmed.ncbi.nlm.nih.gov/15964843
https://pubmed.ncbi.nlm.nih.gov/15964843
Autor:
C, Cundy Kenneth, Thamil, Annamalai, Lin, Bu, Josephine, De Vera, Jenny, Estrela, Wendy, Luo, Payal, Shirsat, Allan, Torneros, Fenmei, Yao, Joan, Zou, W, Barrett Ronald, A, Gallop Mark
Publikováno v:
The Journal of Pharmacology and Experimental Therapeutics; October 2004, Vol. 311 Issue: 1 p324-33, 10p
Autor:
Xiaoyu Tian1, Jianxin Guo1, Fenmei Yao1, De-Ping Yang2, Makriyannis, Alexandros1 a.makriyannis@neu.edu
Publikováno v:
Journal of Biological Chemistry. 8/19/2005, Vol. 280 Issue 33, p29788-29795. 8p.