CymitQuimica logo
Immunology and Inflammation

Immunology and Inflammation

Immunology and inflammation inhibitors are compounds that modulate the immune response and inflammatory processes. These inhibitors are crucial in studying the mechanisms of immune regulation, autoimmunity, and chronic inflammation, as well as in developing treatments for inflammatory diseases, allergies, and immune-related disorders. By targeting key pathways in the immune system, these inhibitors can help reduce excessive or inappropriate immune responses. At CymitQuimica, we provide a comprehensive selection of high-quality immunology and inflammation inhibitors to support your research in immunology, inflammation, and therapeutic development.

Subcategories of "Immunology and Inflammation"

Show 11 more subcategories

Found 3034 products of "Immunology and Inflammation"

Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
products per page.
  • AHR antagonist 5 hemimaleate


    <p>Potent oral AHR antagonist with IC50 &lt; 0.5 μM, hinders tumor growth with anti-PD-1.</p>
    Formula:C29H28FN7O4
    Color and Shape:Solid
    Molecular weight:499.55
  • CD73-IN-7

    CAS:
    <p>CD73-IN-7: potent inhibitor of CD73, blocks adenosine production to treat tumors.</p>
    Formula:C13H11ClN4O2
    Color and Shape:Solid
    Molecular weight:290.7
  • Heme Oxygenase-2-IN-1


    <p>Heme Oxygenase-2-IN-1 is a selective HO-2 inhibitor with IC50s: 14.9 μM (HO-1), 0.9 μM (HO-2).</p>
    Formula:C19H17N3O2
    Color and Shape:Solid
    Molecular weight:319.36
  • Hetrombopag olamine

    CAS:
    <p>Hetrombopag olamine is a non-peptide thrombopoietin (TPO) receptor agonist with oral activity.</p>
    Formula:C29H36N6O7
    Purity:98%
    Color and Shape:Solid
    Molecular weight:580.63
  • iNOs-IN-1


    <p>iNOs-IN-1 (YPW) is a strong iNOS inhibitor with dose-dependent anti-inflammatory properties, reducing IL-6, iNOS, and NO levels.</p>
    Formula:C25H30N4O5
    Color and Shape:Solid
    Molecular weight:466.53
  • RuDiOBn

    CAS:
    <p>RuDiOBn exhibits low antioxidant activity by scavenging DPPH and ABTS free radicals with scavenging rates of 13.2% and 5.9% at a concentration of 100 μg/mL. It inhibits collagen glycation and reduces the formation of advanced glycation end-products (AGE) with an IC50 of 2.45 μg/mL. RuDiOBn also enhances fibroblast proliferation and migration, stimulates collagen synthesis, and aids in skin repair and regeneration while inhibiting collagenase.</p>
    Formula:C29H22O7
    Color and Shape:Solid
    Molecular weight:482.481
  • NP3-146 sodium

    CAS:
    <p>NP3-146 sodium is an inhibitor of the NLRP3 inflammasome.</p>
    Formula:C20H26ClN2NaO5S
    Color and Shape:Solid
    Molecular weight:464.94
  • ODN 21158

    CAS:
    <p>ODN 21158 is a potent, non-cytotoxic inhibitor of G-modified TLR3 and TLR9. ODN 21158 dose-dependently inhibits IFN-α secretion.</p>
    Color and Shape:Solid
  • NLRP3-IN-58

    CAS:
    <p>NLRP3-IN-58 (Compound DS15) acts as an inhibitor of NLRP3 inflammasome activation, with an IC50 value of 3.85 μM, and is capable of inhibiting 33% of IL-1β release at a concentration of 10 μM.</p>
    Formula:C22H18ClN3O3S
    Color and Shape:Solid
    Molecular weight:439.92
  • IRAK4-IN-14

    CAS:
    <p>IRAK4-IN-14 is a selective, potent, orally active IRAK4 inhibitor (IC50: 0.003 μM) with favorable PK parameters in rats and mice. effect.</p>
    Formula:C25H28FN9O
    Color and Shape:Solid
    Molecular weight:489.55
  • C5aR-IN-3

    CAS:
    <p>C5aR-IN-3, a potent C5aR inhibitor, may treat autoimmune and inflammatory diseases.</p>
    Formula:C36H40FN5O3
    Color and Shape:Solid
    Molecular weight:609.73
  • IRAK4-IN-19


    <p>IRAK4-IN-19, an IRAK4 inhibitor (IC50: 4.3 nM), hampers IL23 synthesis and arthritis progression.</p>
    Formula:C25H26F2N8O
    Color and Shape:Solid
    Molecular weight:492.52
  • Ocadusertib

    CAS:
    <p>Ocadusertib is an effective inhibitor of the serine/threonine kinase receptor-interacting protein kinase 1 (RIPK1).</p>
    Formula:C25H25N5O4
    Color and Shape:Solid
    Molecular weight:459.50
  • NLRP3-IN-56

    CAS:
    <p>NLRP3-IN-56 (compound 062) is an inhibitor of NLRP3. It effectively suppresses the secretion of IL-1β in THP-1 cells, demonstrating an IC50 of 9.7 nM. NLRP3-IN-56 is useful for research into NLRP3-mediated symptoms and/or diseases.</p>
    Formula:C20H18ClN3O3
    Color and Shape:Solid
    Molecular weight:383.83
  • CD73-IN-13


    <p>CD73-IN-13, a potent CD73 inhibitor, may be developed for tumor-related disease treatment.</p>
    Formula:C13H11F3N4O2
    Color and Shape:Solid
    Molecular weight:312.25
  • RGT-068A

    CAS:
    <p>RGT-068A is a potent, selective and oral bioavailable MALT1 inhibitor .</p>
    Formula:C17H16ClN9O2
    Color and Shape:Solid
    Molecular weight:413.82
  • OP-5244 sodium


    <p>OP-5244 sodium: potent oral CD73 inhibitor (IC50: 0.25 nM), potential in cancer research by hindering adenosine, reversing immunosuppression.</p>
    Formula:C19H28ClN5NaO9P
    Color and Shape:Solid
    Molecular weight:559.87
  • oxLig-1

    CAS:
    <p>OxLig-1 (7-Ketocholesteryl-9-carboxynonanoate) constitutes a lipid component of oxidized low-density lipoprotein (oxLDL) and serves as a critical ligand for β-glycoprotein I (β(2)-GPI). It induces nuclear translocation by activating the NF-κB pathway. Additionally, oxLig-1 is utilized in the study of atherosclerosis (AS).</p>
    Formula:C36H58O5
    Color and Shape:Solid
    Molecular weight:570.84
  • TLR7/8 antagonist 1


    <p>Compound 16c, an imidazoquinoline, is a TLR7/8 agonist; IC50: 3.91 μM (TLR7), 2.19 μM (TLR8); targets TLR-2050 for disease treatment.</p>
    Formula:C24H27N5O2
    Color and Shape:Solid
    Molecular weight:417.5
  • STING agonist-20

    CAS:
    <p>STING agonist-20: potent, aids in XMT-2056 synthesis, used as a cancer vaccine adjuvant.</p>
    Formula:C36H39N11O8
    Color and Shape:Solid
    Molecular weight:753.76