Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Adam, Hendricson"'
Autor:
Sateja Paradkar, Adam Hendricson, Mark Plummer, Ranjini K. Sundaram, James Herrington, Denton Hoyer, Ranjit S. Bindra, Yulia V. Surovtseva, Piyasena Hewawasam
Publikováno v:
Oncotarget
Glioblastoma (GBM) is the most common primary malignant tumor of the central nervous system with a dismal prognosis. Locoregional failure is common despite high doses of radiation therapy, which has prompted great interest in developing novel strateg
Autor:
Linda J Bristow, Amy E Easton, Yu-Wen Li, Digavalli V Sivarao, Regina Lidge, Kelli M Jones, Debra Post-Munson, Christopher Daly, Nicholas J Lodge, Lizbeth Gallagher, Thaddeus Molski, Richard Pieschl, Ping Chen, Adam Hendricson, Ryan Westphal, James Cook, Christiana Iwuagwu, Daniel Morgan, Yulia Benitex, Dalton King, John E Macor, Robert Zaczek, Richard Olson
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0159996 (2016)
The development of alpha7 nicotinic acetylcholine receptor agonists is considered a promising approach for the treatment of cognitive symptoms in schizophrenia patients. In the present studies we characterized the novel agent, (2R)-N-(6-(1H-imidazol-
Externí odkaz:
https://doaj.org/article/cb2d80cbb97446c297511d2d30823d16
Autor:
Valerie J. Whiterock, Amy Easton, Regina Miller, Lawrence R. Marcin, Meredith Ferrante, Bradley C. Pearce, John B. Hogan, Joanne J. Bronson, Clotilde Bourin, Mendi A. Higgins, Robert G. Gentles, F. Christopher Zusi, Walter Kostich, John E. Macor, Michael Gulianello, Min Ding, Linda J. Bristow, Adam Hendricson, Kim A. Johnson, Andrew Alt, Yanling Huang, Matthew A. Seager
Publikováno v:
Bioorganic & Medicinal Chemistry. 25:496-513
Triazolopyridine ethers with mGlu2 positive allosteric modulator (PAM) activity are disclosed. The synthesis, in vitro activity, and metabolic stability data for a series of analogs is provided. The effort resulted in the discovery of a potent, selec
Autor:
Mendi A, Higgins, Lawrence R, Marcin, F, Christopher Zusi, Robert, Gentles, Min, Ding, Bradley C, Pearce, Amy, Easton, Walter A, Kostich, Matthew A, Seager, Clotilde, Bourin, Linda J, Bristow, Kim A, Johnson, Regina, Miller, John, Hogan, Valerie, Whiterock, Michael, Gulianello, Meredith, Ferrante, Yanling, Huang, Adam, Hendricson, Andrew, Alt, John E, Macor, Joanne J, Bronson
Publikováno v:
Bioorganicmedicinal chemistry. 25(2)
Triazolopyridine ethers with mGlu
Autor:
Ronald J. Knox, Linda J. Bristow, Rick L. Pieschl, Ivar M. McDonald, Michael R. Weed, Thaddeus F. Molski, Michael K. Ahlijanian, James Herrington, Laszlo Kiss, Debra J. Post-Munson, Adam Hendricson, John E. Macor, Richard E. Olson, John D. Graef
Publikováno v:
European journal of pharmacology. 799
The alpha7 (α7) nicotinic acetylcholine receptor is a therapeutic target for cognitive disorders. Here we describe 3-(3,4-difluorophenyl)-N-(1-(6-(4-(pyridin-2-yl)piperazin-1-yl)pyrazin-2-yl)ethyl)propanamide (B-973), a novel piperazine-containing m
Autor:
Debra J. Post-Munson, Ping Chen, Linda J. Bristow, Daniel G. Morgan, Ryan Westphal, Kelli M. Jones, Adam Hendricson, Lizbeth Gallagher, Dalton King, Yulia Benitex, Richard Pieschl, Digavalli V. Sivarao, Christiana I. Iwuagwu, Robert Zaczek, Regina Lidge, Nicholas J. Lodge, John E. Macor, Amy Easton, James H. Cook, Yu-Wen Li, Thaddeus F. Molski, Richard E. Olson, Christopher Daly
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 7, p e0159996 (2016)
PLoS ONE, Vol 11, Iss 7, p e0159996 (2016)
The development of alpha7 nicotinic acetylcholine receptor agonists is considered a promising approach for the treatment of cognitive symptoms in schizophrenia patients. In the present studies we characterized the novel agent, (2R)-N-(6-(1H-imidazol-
Autor:
Diana Janke, Haiheng Dong, David Parker, Hassan Pajouhesh, Francesco Belardetti, Afsheen Khawaja, Stephen P. Arneric, Terrance P. Snutch, Cyrus Eduljee, Robert A. Fraser, Adam Hendricson, Elizabeth Tringham, Yoko Shimizu, Xinpo Jiang, Janette Mezeyova
Publikováno v:
ASSAY and Drug Development Technologies. 7:266-280
T-type voltage-gated Ca(2+) channels have been implicated in contributing to a broad variety of human disorders, including pain, epilepsy, sleep disturbances, cardiac arrhythmias, and certain types of cancer. However, potent and selective T-type Ca(2
Autor:
John J. Herbst, Meredith Ferrante, Annapurna Pendri, Kristin L. Rockwell, Jonathan O’Connell, Susan Jenkins, James Loy, Chi Shing Sum, Adam Hendricson, Martyn Banks, Robert G. Gentles, Yulia Benitex, Robert L. Bertekap, Neil T. Burford, Mary Ellen Cvijic, John E. Macor, Andrew Alt, Litao Zhang, Ryan Westphal, Jing Chen, Michelle Nophsker, Guo Li
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 356(2)
The muscarinic acetylcholine receptor subtype 1 (M1) receptors play an important role in cognition and memory, and are considered to be attractive targets for the development of novel medications to treat cognitive impairments seen in schizophrenia a
Autor:
Michael R. Weed, Jeffrey M. Brown, Brett R. Beno, Ryan S. Westphal, Robert G. Gentles, John Watson, Yan Kong, Lisa Hunihan, Martin A. Lewis, Mary Ellen Cvijic, John E. Macor, Joanne J. Bronson, Meredith Ferrante, Thaddeus F. Molski, Ronald J. Knox, Andrew Alt, Angela Cacace, Kristin L. Rockwell, Shuanghua Hu, Adam Hendricson, Yazhong Huang
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 354(3)
The present studies represent the first published report of a dopamine D1 positive allosteric modulator (PAM). D1 receptors have been proposed as a therapeutic target for the treatment of cognitive deficits associated with schizophrenia. However, the
Autor:
Joanne J. Bronson, Adam Hendricson, Ryan Westphal, John E. Macor, Lisa Hunihan, Margaret M. Prack, Jeffrey M. Brown, David G. Harden, Robert G. Gentles, Rudy Krause, Carolyn Diane Dzierba
Publikováno v:
Journal of neurochemistry. 129(2)
NMDA receptor hypofunction is hypothesized to contribute to cognitive deficits associated with schizophrenia. Since direct activation of NMDA receptors is associated with serious adverse effects, modulation of the NMDA co-agonists, glycine or D-serin