Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Jian-Nong Ma"'
Autor:
David, Malin, Mallori, Henceroth, Gadam Srinivas, Rao, Joseph, Campbell, Jian-Nong, Ma, Ping-Hsun, Tsai, Jordan C, Kishbaugh, Ethan S, Burstein
Publikováno v:
Neuroscience letters. 713
Previous work has shown that chronic nicotine administration causes adaptive changes in 5-HT
Autor:
Christian Ottmann, Anja Schäfer, Ethan S. Burstein, Marcus Malo, Luc Brunsveld, Henrik Sundén, Jian-Nong Ma, Seppe Leysen, Roger Olsson, Marcel Scheepstra
Publikováno v:
Journal of Medicinal Chemistry, 59(3), 1232-1238. American Chemical Society
The nuclear receptor Nurr1 can be activated by RXR via heterodimerization (RXR-Nurr1) and is a promising target for treating neurodegenerative diseases. We herein report the enantioselective synthesis and SAR of sterically constricted benzofurans at
Autor:
Marcel Scheepstra, Christian Ottmann, Jian-Nong Ma, Femke A. Meijer, Roger Olsson, Ethan S. Burstein, Rens M J M de Vries, Luc Brunsveld, Sebastian A. Andrei, Lech-Gustav Milroy
Publikováno v:
ACS Chemical Neuroscience
ACS Chemical Neuroscience, 8(9), 2065-2077. American Chemical Society
ACS chemical neuroscience 8(9), 2065-2077 (2017). doi:10.1021/acschemneuro.7b00216
ACS Chemical Neuroscience, 8(9), 2065-2077. American Chemical Society
ACS chemical neuroscience 8(9), 2065-2077 (2017). doi:10.1021/acschemneuro.7b00216
Retinoid X receptors (RXRs) play key roles in many physiological processes in both the periphery and central nervous system. In addition, RXRs form heterodimers with other nuclear receptors to exert their physiological effects. The nuclear receptor r
Autor:
Joseph R. Campbell, Ethan S. Burstein, Jian-Nong Ma, Mallori M. Henceroth, David H. Malin, Gadam Srinivas Rao, Ping-Hsun Tsai, Jordan C. Kishbaugh
Publikováno v:
Neuroscience Letters. 713:134524
Previous work has shown that chronic nicotine administration causes adaptive changes in 5-HT2A receptor expression. Based on this relationship, it was hypothesized that inactivating 5-HT2A receptors with the inverse agonists pimavanserin and volinans
Autor:
Weissman, Jacques T.1, Jian-Nong Ma, Jacques T.1, Essex, Anthony1, Yan Gao1, Burstein, Ethan S.1 eburstein@acadia-pharm.com
Publikováno v:
Oncogene. 1/8/2004, Vol. 23 Issue 1, p241-249. 9p. 2 Diagrams, 2 Charts, 8 Graphs.
Autor:
Tracy A. Spalding, Roger Olsson, David Hubbard, Jian-Nong Ma, Ethan S. Burstein, Krista McFarland
Publikováno v:
ACS Chemical Neuroscience. 4:1430-1438
Nurr1 is a nuclear hormone receptor (NucHR) strongly implicated in the growth, maintenance, and survival of dopaminergic neurons. Nurr1 may be unable to bind ligands directly, but it forms heterodimers with other NucHRs that do. Using bioluminescence
Autor:
Lars Kr. Hansen, Anna-Lena Gustavsson, Henrik Sundén, Roger Olsson, Jian-Nong Ma, Ethan S. Burstein
Publikováno v:
ChemMedChem. 8:1283-1294
Selective activation of the estrogen receptor β (ERβ) could be a safe approach to hormone replacement therapy for both women and men, in contrast to the estrogens currently used for women which activate both ERβ and ERα, occasionally causing seve
Publikováno v:
ACS chemical neuroscience. 7(9)
Chemotherapy-induced neuropathic pain (CINP) remains a major unmet medical need. Estrogen receptor beta (ERβ)-selective agonists represent a novel strategy for treating CINP because they are neuroprotective and may also have anticancer activity. We
Autor:
Ethan S. Burstein, Roger Olsson, Erika A. Currier, Sine Mandrup Bertozzi, Jacob Jensen, Jian Nong Ma, Magnus Gustafsson
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:5918-5921
1-(Benzothiazol-2-yl)-1-(4-chlorophenyl)ethanol (1) was identified as a positive allosteric modulator (PAM) of the CaSR in a functional cell-based assay. This compound belongs to a class of compounds that is structurally distinct from other known pos
Autor:
Roger Olsson, Erika A. Currier, Jian Nong Ma, Fredrik Lehmann, Ethan S. Burstein, Kristina Luthman, Uli Hacksell
Publikováno v:
Bioorganic & Medicinal Chemistry. 18:4844-4854
A series of novel isochromanone based urotensin II receptor agonists have been synthesized and evaluated for their activity using a functional cell based assay (R-SAT). Several potent and efficacious derivatives were identified with 3-(3,4-dichloroph