Search Results - "Gonsiorek, W"

  • Showing 1 - 16 results of 16
Refine Results
  1. 1

    Expansion of SAR studies on triaryl bis sulfone cannabinoid CB2 receptor ligands by Tong, Ling, Shankar, B.B., Chen, Lei, Rizvi, Razia, Kelly, Joseph, Gilbert, Eric, Huang, Chunli, Yang, De-Yi, Kozlowski, Joseph A., Shih, N.-Y., Gonsiorek, W., Hipkin, R. William, Malikzay, Asra, Lunn, Charles A., Lundell, Daniel J.

    Published in Bioorganic & medicinal chemistry letters (15-11-2010)
    “…SAR exploration on triaryl bis sulfone A led us to structurally novel and diverse CB2 selective ligands B. We report further expansion of the structure…”
    Get full text
    Journal Article
  2. 2

    Human interferon-inducible 10-kDa protein and human interferon-inducible T cell alpha chemoattractant are allotopic ligands for human CXCR3: differential binding to receptor states by Cox, M A, Jenh, C H, Gonsiorek, W, Fine, J, Narula, S K, Zavodny, P J, Hipkin, R W

    Published in Molecular pharmacology (01-04-2001)
    “…The human CXC chemokines IP-10 (10-kDa interferon-inducible protein), MIG (monokine induced by human interferon-gamma), and I-TAC (interferon-inducible T cell…”
    Get more information
    Journal Article
  3. 3

    Sch35966 is a potent, selective agonist at the peripheral cannabinoid receptor (CB2) in rodents and primates by Gonsiorek, W, Lunn, C A, Fan, X, Deno, G, Kozlowski, J, Hipkin, R W

    Published in British journal of pharmacology (01-08-2007)
    “…Background and purpose: The peripheral cannabinoid receptor (CB2) is expressed on peripheral immune cells and is thought to have a role in the…”
    Get full text
    Journal Article
  4. 4
  5. 5
  6. 6

    Endocannabinoid 2-arachidonyl glycerol is a full agonist through human type 2 cannabinoid receptor: antagonism by anandamide by Gonsiorek, W, Lunn, C, Fan, X, Narula, S, Lundell, D, Hipkin, R W

    Published in Molecular pharmacology (01-05-2000)
    “…The endocannabinoids anandamide and 2-arachidonyl glycerol (2-AG) bind to G protein-coupled central and peripheral cannabinoid receptors CB1 and CB2,…”
    Get more information
    Journal Article
  7. 7
  8. 8

    Cloning and characterization of a novel human histamine receptor by Morse, K L, Behan, J, Laz, T M, West, Jr, R E, Greenfeder, S A, Anthes, J C, Umland, S, Wan, Y, Hipkin, R W, Gonsiorek, W, Shin, N, Gustafson, E L, Qiao, X, Wang, S, Hedrick, J A, Greene, J, Bayne, M, Monsma, Jr, F J

    “…Histamine exerts its numerous physiological functions through interaction with G protein-coupled receptors. Three such receptors have been defined at both the…”
    Get more information
    Journal Article
  9. 9

    Expansion of SAR studies on triaryl bis sulfone cannabinoid CB sub(2) receptor ligands by Tong, Ling, Shankar, B B, Chen, Lei, Rizvi, Razia, Kelly, Joseph, Gilbert, Eric, Huang, Chunli, Yang, De-Yi, Kozlowski, Joseph A, Shih, N-Y, Gonsiorek, W, Hipkin, RWilliam, Malikzay, Asra, Lunn, Charles A, Lundell, Daniel J

    Published in Bioorganic & medicinal chemistry letters (15-11-2010)
    “…We report further expansion of the structure activity relationship (SAR) on the triaryl bis sulfone class of compounds ( I), which are potent CB sub(2)…”
    Get full text
    Journal Article
  10. 10

    Triaryl bis-sulfones as a new class of cannabinoid CB2 receptor inhibitors: identification of a lead and initial SAR studies by Lavey, Brian J., Kozlowski, Joseph A., Hipkin, R. William, Gonsiorek, Waldemar, Lundell, Daniel J., Piwinski, John J., Narula, Satwant, Lunn, Charles A.

    Published in Bioorganic & medicinal chemistry letters (01-02-2005)
    “…A novel class of cannabinoid CB2 receptor ligands is described. The compounds are nanomolar inhibitors of the CB2 receptor and can show high selectivity over…”
    Get full text
    Journal Article
  11. 11

    Triaryl bis-sulfones as cannabinoid-2 receptor ligands: SAR studies by Shankar, Bandarpalle B., Lavey, Brian J., Zhou, Guowei, Spitler, James A., Tong, Ling, Rizvi, Razia, Yang, De-Yi, Wolin, Ronald, Kozlowski, Joseph A., Shih, Neng-Yang, Wu, Jie, Hipkin, R. William, Gonsiorek, Waldemar, Lunn, Charles A.

    Published in Bioorganic & medicinal chemistry letters (15-10-2005)
    “…SAR studies on recently reported triaryl bis-sulfone cannabinoid CB2 receptor ligands are described. Modification of aryl substitution and their respective…”
    Get full text
    Journal Article
  12. 12

    The study of CXCR3 and CCR7 pharmacology using [ 35S]GTPγS exchange assays in cell membranes and permeabilized peripheral blood lymphocytes by Gonsiorek, Waldemar, Zavodny, Paul, Hipkin, R.William

    Published in Journal of immunological methods (01-02-2003)
    “…The GTPγS exchange assay is a functional model corresponding to the first step of G protein-coupled receptor activation. We provide simple methodologies and…”
    Get full text
    Journal Article
  13. 13
  14. 14

    Cloning and pharmacological characterization of CXCR1 and CXCR2 from Macaca fascicularis by Hipkin, R William, Deno, Gregory, Fine, Jay, Sun, Yongliang, Wilburn, Brian, Fan, Xuedong, Gonsiorek, Waldemar, Wiekowski, Maria T

    “…Two genes with high sequence homology to human CXCR1 (hCXCR1) and CXCR2 (hCXCR2) were cloned from blood of cynomolgus monkey (Macaca fascicularis). Comparison…”
    Get more information
    Journal Article
  15. 15

    HUMAN B CELL-ATTRACTING CHEMOKINE 1 (BCA-1; CXCL13) IS AN AGONIST FOR THE HUMAN CXCR3 RECEPTOR by Jenh, Chung-Her, Cox, Mary Ann, Hipkin, William, Lu, Tianhong, Pugliese-Sivo, Catherine, Gonsiorek, Waldemar, Chou, Chuan-Chu, Narula, Satwant K., Zavodny, Paul J.

    Published in Cytokine (Philadelphia, Pa.) (07-08-2001)
    “…The CXC chemokine CXCL13, known as BCA-1 (B cell-attracting chemokine 1) or BLC (B-lymphocyte chemoattractant), has been identified as an efficacious…”
    Get full text
    Journal Article
  16. 16

    Kinetic studies of desensitization and resensitization of the relaxation response to beta-2 adrenoceptor agonists in isolated guinea pig trachea by Wachsman, D E, Kavaler, J P, Sugár, I P, Schachter, E N, Gonsiorek, W, Maayani, S

    “…Activation of beta-2 adrenoceptors (BAR) in smooth muscle preparations is associated with a rapid, reversible and incomplete receptor desensitization,…”
    Get more information
    Journal Article