Immunology Research

Immunology is a branch of science that studies all aspects of the immune system, ranging from normal physiological functioning through to malfunctions which can lead to immunological diseases. Disorders that result from aberrant activation of the immune system are termed autoimmune diseases.

Immunology Research Products Areas

Products for Immunology Research - Page 2

  1. Cat.No. Product Name Information/Activity
  2. BCC1509 D609 D609 is a selective competitive inhibitor of phosphatidyl choline-specific phospholipase C (PC-PLC), with Ki of 6.4 μM. D609 chemical structure
  3. BCC5909 DAPTA DAPTA is a synthetic peptide, functions as a viral entry inhibitor by targeting selectively CCR5, and shows potent anti-HIV activities. DAPTA chemical structure
  4. BCN4804 Deguelin Deguelin, a naturally occurring rotenoid, is a potent PI3K/AKT inhibitor. Deguelin chemical structure
  5. BCC4069 Delavirdine mesylate Delavirdine mesylate (U 90152 mesylate) is a potent non-nucleoside HIV-1 reverse transcriptase inhibitor (NNRTI) of HIV-1. Delavirdine mesylate chemical structure
  6. BCC3644 DMXAA (Vadimezan) Vadimezan (DMXAA; ASA-404), the tumor vascular disrupting agent (tumor-VDA), is a murine agonist of the stimulator of interferon genes (STING) and also a potent inducer of type I IFNs and other cytokines. Vadimezan has anti-influenza virus H1N1-PR8 activities. DMXAA (Vadimezan) chemical structure
  7. BCC7917 FC 131 606968-52-9 FC 131 chemical structure
  8. BCN5977 Hypericin Hypericin is a photosensitive antiviral with anticancer and antidepressant agent derived from Hypericum perforatum. Hypericin chemical structure
  9. BCC2492 Imiquimod Imiquimod (R 837) is an immune response modifier that acts as a toll-like receptor 7 agonist. Imiquimod chemical structure
  10. BCC6234 IT1t dihydrochloride IT1t dihydrochloride is a potent CXCR4 antagonist; inhibits CXCL12/CXCR4 interaction with an IC50 of 2.1 nM. IT1t dihydrochloride chemical structure
  11. BCC3706 K-252c K-252c, a staurosporine analog isolated from Nocardiopsis sp., is a cell-permeable PKC inhibitor, with an IC50 of 2.45 µM. K-252c induces apoptosis in human chronic myelogenous leukemia cancer cells. K-252c also inhibits β-lactamase, chymotrypsin, and malate dehydrogenase. K-252c chemical structure

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