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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"

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Found 3045 products of "Immunology and Inflammation"

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  • ACHP Hydrochloride
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    ACHP Hydrochloride

    CAS:
    <p>ACHP Hydrochloride (IKK-2 Inhibitor VIII) is a highly potent and selective IKK-β inhibitor with an IC50 of 8.5 nM.</p>
    Formula:C21H25ClN4O2
    Purity:99.83%
    Color and Shape:Solid
    Molecular weight:400.9

    Ref: TM-T10237

  • ML-090
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    ML-090

    CAS:
    <p>ML-090 is NOX1-specific inhibitor(IC50 = 90 nM) which is &gt;100 selectivity for NOX1 over NOX2, NOX3, NOX4 (all IC50s &gt;10 μM).</p>
    Formula:C14H10N4
    Purity:98.55%
    Color and Shape:Solid
    Molecular weight:234.26

    Ref: TM-T22990

  • CCT374705
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    CCT374705

    CAS:
    <p>CCT374705, an orally active BCL6 inhibitor, exhibits potent antiproliferative effects in vitro and effectively inhibits tumor growth in a lymphoma xenograft</p>
    Formula:C21H18ClF3N4O2
    Color and Shape:Solid
    Molecular weight:450.84

    Ref: TM-T78177

  • TLR7 agonist 23
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    TLR7 agonist 23

    CAS:
    <p>TLR7 agonist23 (compound 12b) is a potent agonist of Toll-like receptor-7 (TLR7), with an EC50 value of 0.15 uM. It is suitable for research in immune diseases.</p>
    Formula:C21H22N4O2
    Color and Shape:Solid
    Molecular weight:362.42

    Ref: TM-T88779

  • GBT1118
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    GBT1118

    CAS:
    <p>GBT1118 is an orally active allosteric modulator of haemoglobin oxygen affinity, enhancing tolerance to acute severe hypoxia and suitable for hypoxia research.</p>
    Formula:C19H20N2O4
    Purity:99.69%
    Color and Shape:Solid
    Molecular weight:340.37

    Ref: TM-T78075

  • MALT1-IN-6
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    MALT1-IN-6

    CAS:
    <p>MALT1-IN-6 is a MALT1 protease inhibitor (Ki: 9 nM) that exhibits anticancer activity.</p>
    Formula:C18H12Cl2F3N9O
    Color and Shape:Solid
    Molecular weight:498.25

    Ref: TM-T63372

  • (Rac)-BAY-985
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    (Rac)-BAY-985

    CAS:
    <p>(Rac)-BAY-985 is a potent, ATP-competitive and selective inhibitor of TBK1(IC50 of 1.5 nM),with antitumor efficacy.</p>
    Formula:C27H30F3N9O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:553.58

    Ref: TM-T12659

  • 3'-Azido-3'-deoxy-5-methylcytidine
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    3'-Azido-3'-deoxy-5-methylcytidine

    CAS:
    <p>3'-Azido-3'-deoxy-5-methylcytidine inhibits HIV-1 reverse transcriptase(EC50 = 0.06 μM) and is an effective inhibitor of xenotropic murine leukemia-related</p>
    Formula:C10H14N6O4
    Purity:99.55%
    Color and Shape:Solid
    Molecular weight:282.26

    Ref: TM-T10133

  • CD38 inhibitor 2
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    CD38 inhibitor 2

    CAS:
    <p>CD38 inhibitor 2 is a potent CD38 inhibitor ( IC 50 = 0.01 ~ 0.1 μΜ).</p>
    Formula:C19H24N6O3
    Color and Shape:Solid
    Molecular weight:384.43

    Ref: TM-T61681

  • h-NTPDase-IN-3
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    h-NTPDase-IN-3

    CAS:
    <p>h-NTPDase-IN-3 is an h-NTPDase inhibitor that inhibits h-NTPDase1, h-NTPDase2, h-NTPDase3 and h-NTPDase8.</p>
    Formula:C16H10N4S
    Purity:98.24%
    Color and Shape:Solid
    Molecular weight:290.34

    Ref: TM-T79622

  • Glabrescone C
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    Glabrescone C

    CAS:
    <p>Glabrescone C exhibits strong anti-inflammatory properties through direct binding to IKKα/β.</p>
    Formula:C19H22O7
    Color and Shape:Solid
    Molecular weight:362.37

    Ref: TM-T72899

  • (R)-IL-17 modulator 4
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    (R)-IL-17 modulator 4

    CAS:
    <p>(R)-IL-17 modulator 4, an R-isomer prodrug of IL-17 modulator 1, is potent and taken orally.</p>
    Formula:C27H34N6O2
    Color and Shape:Solid
    Molecular weight:474.6

    Ref: TM-T63089

  • Glu-urea-Glu-NHS ester
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    Glu-urea-Glu-NHS ester

    CAS:
    <p>Compound 21, Glu-urea-Glu-NHS ester, an activated N-hydroxysuccinamide (NHS) ester derivative of Glu-urea-Glu, serves as a pharmacophore for conjugation to prostate specific membrane antigen (PSMA) inhibitors [1].</p>
    Formula:C27H43N3O11
    Color and Shape:Solid
    Molecular weight:585.64

    Ref: TM-T84761

  • TLR7 agonist 14
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    TLR7 agonist 14

    CAS:
    <p>Compound 17b, a TLR7 agonist also known as TLR7 agonist 14, exhibits high potency with an EC50 of 18 nM.</p>
    Formula:C29H36N6O3
    Color and Shape:Solid
    Molecular weight:516.63

    Ref: TM-T79749

  • FCE-27164
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    FCE-27164

    CAS:
    <p>FCE-27164 inhibits PDGF-β and IL-7 receptor binding, potentially modulating inflammatory and immune responses for therapeutic applications.</p>
    Formula:C45H34N10Na6O23S6
    Purity:96.04%
    Color and Shape:Solid
    Molecular weight:1413.11

    Ref: TM-T70463

  • DNA polymerase-IN-1
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    DNA polymerase-IN-1

    CAS:
    <p>DNA polymerase-IN-1 exhibits antiproliferative activity against tumor cells and inhibits Taq DNA polymerase as a DNA polymerase inhibitor.</p>
    Formula:C10H7ClO4
    Purity:99.16%
    Color and Shape:Solid
    Molecular weight:226.61

    Ref: TM-T80644

  • CAY10464
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    CAY10464

    CAS:
    <p>CAY10464 (AHR antagonist 7) is an AHR antagonist for the study of cancer and metabolic diseases.</p>
    Formula:C15H12Cl2O
    Purity:99.96%
    Color and Shape:Solid
    Molecular weight:279.16

    Ref: TM-T84540

  • TLR7 agonist 15
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    TLR7 agonist 15

    CAS:
    <p>TLR7 agonist 15 (compound 16b) is a potent activator of mouse macrophages and hPBMCs, demonstrating an EC50 of 18 nM.</p>
    Formula:C26H31N5O
    Color and Shape:Solid
    Molecular weight:429.56

    Ref: TM-T79750

  • Tyrosinase-IN-22
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    Tyrosinase-IN-22

    CAS:
    <p>Tyrosinase-IN-22 (compound 4) serves as a potent inhibitor for tyrosinase substrates, namely L-tyrosine and L-dopa, exhibiting inhibitory concentrations (IC50s) of 60 nM and 30 nM, respectively. Additionally, it demonstrates significant antioxidant and anti-melanogenic properties, making it suitable for related research endeavors [1].</p>
    Formula:C7H5ClN2S
    Color and Shape:Solid
    Molecular weight:184.64

    Ref: TM-T84705

  • GSK840
    Targetmol
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    GSK840

    CAS:
    <p>GSK840 (GSK'840) is a receptor-interacting protein kinase 3 (RIP3 or RIPK3) inhibitor, which binds the RIP3 kinase domain (IC50: 0.9 nM), and inhibits kinase</p>
    Formula:C21H23N3O3
    Purity:99.7%
    Color and Shape:Solid
    Molecular weight:365.43

    Ref: TM-T11501