Patented small molecules against psoriasis

被引:6
作者
Abdelnoor, Alexander M. [1 ]
机构
[1] Amer Univ Beirut, Dept Microbiol & Immunol, Fac Med, Beirut 11072020, Lebanon
关键词
angiogenesis; apoptosis; differentiation; keratinocyte; leukocyte trafficking; leukotrienes; psoriasis; super antigens; T lymphocytes; toll-like receptors; ANGIOGENESIS IN-VITRO; TOLL-LIKE-RECEPTORS; PEPTIDE-T; INNATE IMMUNITY; VALPROIC ACID; SKIN-LESIONS; INHIBITOR; CELLS; EXPRESSION; THERAPY;
D O I
10.1517/13543770903029201
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: It is hypothesized that psoriasis is an autoimmune disease. The most recent therapeutic approach that proved to be more effective than earlier methods of treatment is the use of mAb/fusion proteins. Efforts nowadays are focused on investigating the antipsoriatic affect of small molecules that can be administered orally, some of which are capable of entering cells, and being selective in targeting intracellular pathways. Objective: Preclinical patented small molecules that are recommended for the treatment of psoriasis are reviewed. Emphasis is placed on their mechanism of action. Methods: http://ep.espacenet.com/, Pubmed, Scopus and Google websites were the main sources used for the patented small molecule search. A number of patents were poorly described and difficulties were faced in trying to figure out the patentee(s) explanation. Moreover, most patents were recommended for the treatment of a number of autoimmune diseases and cancer, and not only for psoriasis. Results/conclusions: Small molecules that inhibit the activation of T lymphocytes, leukocyte trafficking, leukotriene activity/production and angiogenesis, and promote apoptosis have been patented. Small molecules that have been patented for the treatment of other autoimmune diseases and could be used for treating psoriasis are described. Moreover, other possible mechanistic approaches using small molecules are discussed.
引用
收藏
页码:1057 / 1071
页数:15
相关论文
共 130 条
[1]   Molecular characterization of CCR6: Involvement of multiple domains in ligand binding and receptor signaling [J].
Ai, LS ;
Lee, SF ;
Chen, SSL ;
Liao, F .
JOURNAL OF BIOMEDICAL SCIENCE, 2004, 11 (06) :818-828
[2]   HLA allele associations and V-beta T-lymphocyte expansions in patients with psoriasis, harboring toxin-producing Staphylococcus aureus [J].
Ajib, R ;
Janbazian, L ;
Rahal, E ;
Matar, GM ;
Zaynoun, S ;
Kibbi, AG ;
Abdelnoor, AM .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2005, (04) :310-315
[3]  
Alwawi Eihab A, 2008, Ther Clin Risk Manag, V4, P345
[4]   The phenotype of human Th17 cells and their precursors, the cytokines that mediate their differentiation and the role of Th17 cells in inflammation [J].
Annunziato, Francesco ;
Cosmi, Lorenzo ;
Liotta, Francesco ;
Maggi, Enrico ;
Romagnani, Sergio .
INTERNATIONAL IMMUNOLOGY, 2008, 20 (11) :1361-1368
[5]   Synthesis and evaluation of diverse analogs of amygdalin as potential peptidomimetics of peptide T [J].
Araya, E ;
Rodriguez, A ;
Rubio, J ;
Spada, A ;
Joglar, J ;
Llebaria, A ;
Lagunas, C ;
Fernandez, AG ;
Spisani, S ;
Perez, JJ .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (05) :1493-1496
[6]  
ARBISER J, 2008, Patent No. 1896035
[7]   Carbazole is a naturally occurring inhibitor of angiogenesis and inflammation isolated from antipsoriatic coal tar [J].
Arbiser, Jack L. ;
Govindarajan, Baskaran ;
Battle, Traci E. ;
Lynch, Rebecca ;
Frank, David A. ;
Ushio-Fukai, Masuko ;
Perry, Betsy N. ;
Stern, David F. ;
Bowden, G. Tim ;
Liu, Anquan ;
Klein, Eva ;
Kolodziejski, Pawel J. ;
Eissa, N. Tony ;
Hossain, Chowdhury F. ;
Nagle, Dale G. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (06) :1396-1402
[8]  
Arnold R, 1999, J IMMUNOL, V162, P7140
[9]  
Badger AM, 1996, J PHARMACOL EXP THER, V279, P1453
[10]  
BALACHANDRAN S, 2007, Patent No. 20070105020