Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Mark L. Richards"'
Substituted 2-phenyl-benzimidazole derivatives: novel compounds that suppress key markers of allergy
Autor:
Shirley Cruz Lio, Mark Tanji, Anjana Sinha, Jagadish C. Sircar, Major Michael W, Homayon Banie, Thomas Richard J, Mark L. Richards
Publikováno v:
European Journal of Medicinal Chemistry. 41:950-969
The pharmacotherapy of allergy and asthma has traditionally focused on the effecter molecules of the allergic cascade, while neglecting targets that play an early role in their development. Reasoning that IgE is central to the expansion of atopic dis
Publikováno v:
International Archives of Allergy and Immunology. 96:289-295
Multiple mRNA species encoding several predicted forms of the high-affinity IgE receptor alpha subunit (Fc epsilon RI-alpha) have been previously characterized from rat basophilic leukemia cells. Using the polymerase chain reaction procedure, we have
Autor:
Carlos Labat, Hirokazu Arakawa, C.S. Hosking, Toru Miura, R. Deppisch, R. Jäger, Xavier Norel, D.G. Klapper, X.J. Hong, D.M. Roberton, A.K. Nault, Tatsuo Sakamoto, A. Francker, Kristiina Turjanmaa, U. Rother, Hiroshi Tamura, Jacques Benveniste, Mark L. Richards, Martin D. Chapman, G.P. Pesce, G. Ciprandi, M. Schmitz-Schumann, K. Inoue, A.M. Collins, Michael W. Robertson, S. Buscaglia, Takayoshi Kuroume, Charles Brink, Masaki Kondo, F.F.M. Castro, B.L. Rogers, U. Schauer, Soili Mäkinen-Kiljunen, Harri Alenius, B. Albini, M. Schönermark, Hiroichi Nagai, G.R. Flannery, C.H.L. Rieger, N. Niesen, Moeness M. Alshishtawy, C. Leinhaas, Makoto Shigeta, G. Riedasch, I.J. Griffith, Lawrence E. Gelber, Naoki Inagaki, E. Marchesi, Hiroyuki Mochizuki, F. Milgrom, Timo Reunala, Timo Palosuo, Akihide Koda, G.M. Hänsch, G.W. Canonica, K. Rother, Isabelle Haye-Legrand, Aly M. Abdella, Virginia S. Mehl, Fu-Tong Liu, J. Pollock, B. Diamant, M. Kirschfink
Publikováno v:
International Archives of Allergy and Immunology. 96:I-V
Publikováno v:
Journal of medicinal chemistry. 50(24)
Drugs targeted to viral proteins are highly vulnerable to the development of resistant strains. We previously characterized a group of 2-phenylbenzimidazole compounds for their activity against allergy and asthma and more recently established the Gol
Autor:
Arka Chatterjee, Diane Millis, Shirley Cruz Lio, Jagadish C. Sircar, Anjana Sinha, Jessica Johnson, Jeffrey W. Ludwig, Mark L. Richards, Homayon Banie
Publikováno v:
Cancer chemotherapy and pharmacology. 61(6)
Cancer chemotherapy continues to be challenged by the emergence of resistant tumors, and one organelle entwined in the development of drug resistance is the Golgi apparatus. Recently, we discovered a group of 2-(substituted phenyl)-benzimidazole (2-P
Autor:
Mark L. Richards, Jeffrey W. Ludwig
Publikováno v:
Current topics in medicinal chemistry. 6(2)
Inflammatory diseases are a complex group of disorders involving multiple levels of the immune system and as such present a daunting challenge to understand and treat. Contemporary drug development targets individual cytokines, chemokines, and recept
Autor:
Carl, Bertrams, Mary Lee, DeCoster, Dennis G, Gooche, Mike, Englehart, Joanne B, Martucci, Mark L, Richards
Publikováno v:
Healthcare financial management : journal of the Healthcare Financial Management Association. 59(8)
Publikováno v:
Journal of medicinal chemistry. 47(26)
The effectiveness of the injectable anti-IgE antibody omalizumab has validated IgE as an important target for allergic diseases, thus spawning the development of small-molecule IgE inhibitors. Herein, a brief SAR is described for novel phenylbenzimid
Publikováno v:
Regulatory peptides. 60(2-3)
Neuropeptides exert a variety of putative immunomodulatory actions. Despite the molecular cloning of multiple forms of receptors for several neuropeptides with putative immunomodulatory effects, including vasoactive intestinal peptide (VIP), the rela
Differential expression of VIP/PACAP receptor genes in breast, intestinal, and pancreatic cell lines
Publikováno v:
Cancer letters. 92(2)
Vasoactive intestinal peptide (VIP) and pituitary adenylate cyclase-activating peptide (PACAP) are structurally-related neuropeptides that function as trophic factors in addition to their more classical roles as neurotransmitters. Binding and molecul