Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Barton H. Manning"'
Autor:
Eileen Johnson, Jerry Ryan Holder, Barton H. Manning, Licheng Shi, Kevin Salyers, Michael Stenkilsson, Colin V. Gegg, Marie E. Wright, George Doellgast, Kenneth D. Wild, Les P. Miranda
Publikováno v:
Biopolymers. 100:422-430
Antagonism of the calcitonin gene-related peptide (CGRP) receptor may be a useful approach for migraine treatment. Selective PEGylated peptide antagonists to the CGRP receptor are described, derived from CGRP(8-37) with polymer derivatization at an e
Autor:
Randall W. Hungate, Ming Huang, Gloria Biddlecome, Jason Brooks Human, Benny C. Askew, Jian J. Chen, Dianna Lester-Zeiner, Eileen Johnson, Wenyuan Qian, Barton H. Manning, Leyla Arik, Richard Loeloff, Toshihiro Aya, Kaustav Biswas, Hong Dong, Tanya Peterkin, Hong Sun, Gondi N. Kumar
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:4764-4769
We report the development of aryl sulfones as Bradykinin B1 receptor antagonists. Variation of the linker region identified diol 23 as a potent B1 antagonist, while modifications of the aryl moiety led to compound 26, both of which were efficacious i
Autor:
Mark H. Norman, Lana Klionsky, Maosheng Zhang, Jue Wang, Ella Magal, Sekhar Surapaneni, Rami Tamir, Judy Wang, John Rubino, Hong Deng, Jean-Claude Louis, Dawn Zhu, Doo Lee, Barton H. Manning, Tingrong Wang, Weiya Wang, April Le, Nuria A. Tamayo, Rongzhen Kuang, Narender R. Gavva, Sonya G. Lehto, Brad Youngblood
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 326:218-229
Antagonists of the vanilloid receptor TRPV1 (transient receptor potential vanilloid type 1) have been reported to produce antihyperalgesic effects in animal models of pain. These antagonists, however, also caused concomitant hyperthermia in rodents,
Autor:
Xiao Ding, Jian J. Chen, Eileen Johnson, Hong Dong, Hong Sun, Gondi N. Kumar, Barton H. Manning, Ella Magal
Publikováno v:
Journal of Neuroscience Methods. 168:76-87
The discovery of novel analgesic compounds that target some receptors can be challenging due to species differences in ligand pharmacology. If a putative analgesic compound has markedly lower affinity for rodent versus other mammalian orthologs of a
Autor:
Burgess Laurence E, Leyla Arik, Chester Chenguang Yuan, Nianhe Han, Randall W. Hungate, Derin C. D'amico, David A. Mareska, Feng-Yin Hsieh, Eileen Johnson, Hong Sun, Qingyian Liu, Barton H. Manning, Bobby Riahi, Christopher H. Fotsch, Gloria Biddlecome, Mark H. Norman, Augustus Kamassah, Ming Huang, Richard Loeloff, Gondi N. Kumar, Andras Toro, Jian J. Chen, Jason Brooks Human, Hideo Suzuki, Robert D. Groneberg, Benny C. Askew, Aiwen Li, Gordon Ng, James Zhan, Kaustav Biswas, Dianna Lester-Zeiner, Hong Dong, David E. Clarke
Publikováno v:
Journal of Medicinal Chemistry. 50:2200-2212
The bradykinin B1 receptor is induced following tissue injury and/or inflammation. Antagonists of this receptor have been studied as promising candidates for treatment of chronic pain. We have identified aryl sulfonamides containing a chiral chroman
Publikováno v:
Proceedings of the National Academy of Sciences. 98:8077-8082
Numerous human and animal studies indirectly implicate neurons in the anterior cingulate cortex (ACC) in the encoding of the affective consequences of nociceptor stimulation. No causal evidence, however, has been put forth linking the ACC specificall
Autor:
Les P, Miranda, Licheng, Shi, Jerry R, Holder, Marie, Wright, Colin V, Gegg, Eileen, Johnson, Kenneth, Wild, Michael, Stenkilsson, George, Doellgast, Barton H, Manning, Kevin, Salyers
Publikováno v:
Biopolymers. 100(4)
Antagonism of the calcitonin gene-related peptide (CGRP) receptor may be a useful approach for migraine treatment. Selective PEGylated peptide antagonists to the CGRP receptor are described, derived from CGRP(8-37) with polymer derivatization at an e
Publikováno v:
Pain. 67:79-88
N-Methyl-D-aspartate (NMDA) receptor antagonists have been repeatedly shown to attenuate the development of opiate tolerance and dependence in rodents. In the present experiments, continuous subcutaneous infusion of either MK-801 (0.01 mg/kg/h but no
Autor:
Sonya G, Lehto, Rami, Tamir, Hong, Deng, Lana, Klionsky, Rongzhen, Kuang, April, Le, Doo, Lee, Jean-Claude, Louis, Ella, Magal, Barton H, Manning, John, Rubino, Sekhar, Surapaneni, Nuria, Tamayo, Tingrong, Wang, Judy, Wang, Jue, Wang, Weiya, Wang, Brad, Youngblood, Maosheng, Zhang, Dawn, Zhu, Mark H, Norman, Narender R, Gavva
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 326(1)
Antagonists of the vanilloid receptor TRPV1 (transient receptor potential vanilloid type 1) have been reported to produce antihyperalgesic effects in animal models of pain. These antagonists, however, also caused concomitant hyperthermia in rodents,