Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Karl J. Mathis"'
Autor:
Huey-Sheng Shieh, Grace E. Munie, Nicole Caspers, Alfredo G. Tomasselli, James R. Kiefer, Karl J. Mathis, Arthur J. Wittwer, Micky D. Tortorella, Scott S. Woodard, Mark E. Schnute, Jennifer M. Williams, Anne-Marie Malfait
Publikováno v:
Protein Science. 20:735-744
A ((1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl) succinamide derivative (here referred to as Compound 12) shows significant activity toward many matrix metalloproteinases (MMPs), including MMP-2, MMP-8, MMP-9, and MMP-13. Modeling studies had predicte
Autor:
Beverly A. Reitz, Joseph W. Leone, Michael J. Bienkowski, Daniel F. Curran, Karl J. Mathis, Thomas L. Emmons, Jacqueline E. Day, Mary E. Shuck, Mark C. Walker, Alfredo G. Tomasselli, H. David Fischer
Publikováno v:
Protein Expression and Purification. 65:133-139
Soluble guanylate cyclase (sGC) has been purified from 100 L cell culture infected by baculovirus using the newer and highly effective titerless infected-cells preservation and scale-up (TIPS) method. Successive passage of the enzyme through DEAE, Ni
Autor:
Beverly A. Reitz, Thomas L. Emmons, Alfredo G. Tomasselli, H. David Fischer, Michael J. Bienkowski, S. Edward Lee, David Wasilko, Karl J. Mathis, Kim Jonelle Stutzman-Engwall
Publikováno v:
Protein Expression and Purification. 65:122-132
Compounds capable of stimulating soluble guanylate cyclase (sGC) activity might become important new tools to treat hypertension. While rational design of these drugs would be aided by elucidation of the sGC three-dimensional structure and molecular
Autor:
Scott D. Hauser, Peter C. Isakson, Karl J. Mathis, Dean J. Welsch, David Paul Creely, Gwen G. Krivi
Publikováno v:
Proceedings of the National Academy of Sciences. 91:9745-9749
Leukotriene-C4 synthase (LTC4S; EC 2.5.1.37) catalyzes the committed step in the biosynthesis of the peptidoleukotrienes, which are important in the pathogenesis of asthma. Antibodies were generated to a synthetic peptide based on the partial amino a
Autor:
Karl J. Mathis, Madeleine H. Li, Alan M. Easton, Clara I. Villamil, Barta Thomas E, Grace E. Munie, Daniel P. Becker, Jennifer M. Williams, James R. Kiefer, Louis J. Bedell, Rico Joseph G, Susan L. Hockerman
Publikováno v:
Bioorganicmedicinal chemistry letters. 21(10)
Seeking compounds preferentially potent and selective for MMP-13, we reported in the preceding Letter on a series of hydroxamic acids with a flexible benzamide tail groups.(1a) Here, we replace the amide moiety with non-hydrolyzable heterocycles in a
Autor:
Chris P. Carron, Madeleine H. Li, Daniel P. Becker, T. Sunyer, John N. Freskos, Louis J. Bedell, Boehm Terri L, Chris L. Funckes-Shippy, Decrescenzo Gary A, Clara I. Villamil, Joseph J. McDonald, Grace E. Munie, Jeffery N. Carroll, Pramod P. Mehta, Jun Yao, Brian R. Bond, Craig Swearingen, Jennifer M. Williams, Barta Thomas E, Marcia I. Heron, Dean Welsch, Karl J. Mathis, Carol Pearcy Howard, James R. Kiefer, Susan L. Hockerman, Alan M. Easton, Ying Yu
Publikováno v:
Journal of medicinal chemistry. 53(18)
α-Sulfone-α-piperidine and α-tetrahydropyranyl hydroxamates were explored that are potent inhibitors of MMP's-2, -9, and -13 that spare MMP-1, with oral efficacy in inhibiting tumor growth in mice and left-ventricular hypertrophy in rats and in th
Autor:
Grace E. Munie, Nicole Caspers, Alfredo G. Tomasselli, Karl J. Mathis, Jennifer M. Williams, Mark E. Schnute, Anne-Marie Malfait, Arthur J. Wittwer, Micky D. Tortorella, Scott S. Woodard, Huey-Sheng Shieh
Publikováno v:
The Journal of biological chemistry. 284(36)
Several inhibitors of a series of cis-1(S)2(R)-amino-2-indanol-based compounds were reported to be selective for the aggrecanases, ADAMTS-4 and -5 over other metalloproteases. To understand the nature of this selectivity for aggrecanases, the inhibit
Autor:
Xiong Li, Jacqueline E. Day, James R. Kiefer, Wei Huang, John I. Trujillo, Robin A. Weinberg, Li Xing, Karl J. Mathis, Kuniko K. Kretzmer, Beverley A. Reitz, Nicole Caspers, Lori Christine, Robert P. Compton, Roderick A. Stegeman, Atli Thorarensen, Ann D. Wrightstone
Publikováno v:
Bioorganicmedicinal chemistry letters. 19(3)
The inhibition of PKC-zeta has been proposed to be a potential drug target for immune and inflammatory diseases. A series of 2-(6-phenyl-1H indazol-3-yl)-1H-benzo[d]imidazoles with initial high crossover to CDK-2 has been optimized to afford potent a
Publikováno v:
Protein expression and purification. 60(1)
Soluble guanylate cyclase (sGC), the main target of nitric oxide (NO), is a cytosolic, heme-containing, heterodimeric enzyme that catalyzes the conversion of guanosine 5'-triphosphate (GTP) to 3,5'-cyclic guanosine monophosphate (cGMP) and pyrophosph
Autor:
Alfredo G. Tomasselli, Margaret H. Marino, Timothy E. Benson, James R. Kiefer, Huey-Sheng Shieh, Jennifer M. Williams, Joseph W. Leone, Elizabeth C. Arner, Micky D. Tortorella, Anne-Marie Malfait, Joe F. Wiese, Jeffery N. Carroll, Robert L. Hills, Karl J. Mathis
Publikováno v:
The Journal of biological chemistry. 283(3)
Aggrecanase-2 (a disintegrin and metalloproteinase with thrombospondin motifs-5 (ADAMTS-5)), a member of the ADAMTS protein family, is critically involved in arthritic diseases because of its direct role in cleaving the cartilage component aggrecan.