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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 3035 products of "Immunology and Inflammation"

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  • ASP-8731
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    ASP-8731

    CAS:
    <p>ASP8731 is a selective inhibitor of BACH1 that prevents inflammation and vascular occlusion, and induces fetal hemoglobin in sickle cell disease.</p>
    Formula:C20H21N5O4
    Color and Shape:Solid
    Molecular weight:395.41

    Ref: TM-T201687

  • ARG1-IN-1
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    ARG1-IN-1

    CAS:
    <p>ARG1-IN-1 is a human arginase 1 inhibitor with an IC 50 of 29 nM.</p>
    Formula:C11H21BN2O4
    Color and Shape:Solid
    Molecular weight:256.11

    Ref: TM-T39932

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    CD73-IN-2

    <p>CD73-IN-2 is a potent inhibitor of CD73 (IC50: 0.09 nM).</p>
    Formula:C17H25ClN5O7P
    Color and Shape:Solid
    Molecular weight:477.84

    Ref: TM-T63128

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    NLRP3/AIM2-IN-1

    <p>NLRP3/AIM2-IN-1 is an inhibitor of thermal sepsis (IC50 = 3.136 ± 0.7667 μM).</p>
    Formula:C15H16BNO4
    Color and Shape:Solid
    Molecular weight:285.1

    Ref: TM-T60563

  • Galectin-3-IN-6
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    Galectin-3-IN-6

    CAS:
    <p>Galectin-3-IN-6 (Compound 12) is an orally active galectin-3 (Gal-3) inhibitor, with an IC50 of 12 nM and a Kd of 13 nM for Gal-3. In a CCl4-induced mouse model of acute liver injury and fibrosis, Galectin-3-IN-6 significantly reduces fibrosis markers collagen-1 and α-smooth muscle actin (αSMA) by 64% and 71%, respectively, demonstrating notable anti-fibrotic activity. Galectin-3-IN-6 is applicable for research in fibrosis-related diseases, cancer, and cardiovascular disorders.</p>
    Formula:C28H29Cl2F3N4O6
    Color and Shape:Solid
    Molecular weight:645.454

    Ref: TM-T206457

  • SDH-IN-25
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    SDH-IN-25

    CAS:
    <p>SDH-IN-25 is an SDH inhibitor with an IC50 of 4.82 mg/L, demonstrating broad-spectrum and potent antifungal activity. By binding to SDH amino acid residues (TRP173, TYR58, and ARG43), it mimics the action mode of the commercial fungicide flutolanil. SDH-IN-25 induces changes in hyphal morphology, disrupts respiratory metabolism by binding to complex II, generates reactive oxygen species (ROS), and affects mitochondrial membrane potential (MMP) in hyphae. This compound is utilized in agricultural disease control research.</p>
    Formula:C19H15BrCl2N2O4
    Color and Shape:Solid
    Molecular weight:486.143

    Ref: TM-T206959

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    NOS-IN-2

    <p>NOS-IN-2: potent, selective imidamide NOS inhibitor, IC50=20μM for iNOS, spares eNOS, low toxicity, useful in inflammation research.</p>
    Formula:C18H20F3N3O2
    Color and Shape:Solid
    Molecular weight:367.37

    Ref: TM-T61426

  • IRAK4-IN-9
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    IRAK4-IN-9

    CAS:
    <p>IRAK4-IN-9 is a potent IRAK4 inhibitor with an IC50 of 1.5 nM, promising for inflammatory, autoimmune diseases, and cancer research.</p>
    Formula:C22H25N7
    Color and Shape:Solid
    Molecular weight:387.48

    Ref: TM-T61734

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    STING agonist-7

    <p>STING agonist-7 is an agonist of non-nucleotide STING that binds selectively to mouse STING but not human STING [1].</p>
    Formula:C17H12N4O4
    Color and Shape:Solid
    Molecular weight:336.3

    Ref: TM-T61043

  • BMY-25551
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    BMY-25551

    CAS:
    <p>BMY-25551, a Mitomycin A analog, exhibits cytotoxicity 8 to 20 times greater than Mitomycin C against both murine and human tumor cell lines. It is applicable in research pertaining to cancer and hematological disorders.</p>
    Formula:C17H21N3O7
    Color and Shape:Solid
    Molecular weight:379.36

    Ref: TM-T201024

  • TLR4/NF-κB/MAPK-IN-1
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    TLR4/NF-κB/MAPK-IN-1

    CAS:
    <p>TLR4/NF-κB/MAPK-IN-1 is a novel antineuroinflammatory agent that functions by inhibiting the TLR4/NF-κB/MAPK pathways.</p>
    Formula:C19H25BrO6
    Color and Shape:Solid
    Molecular weight:429.3

    Ref: TM-T62359

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    IRAK4-IN-18

    <p>IRAK4-IN-18: Potent IRAK4 inhibitor (IC50: 15 nM), reduces IL23 in cells, prevents rat arthritis.</p>
    Formula:C24H25FN6O3
    Color and Shape:Solid
    Molecular weight:464.49

    Ref: TM-T62950

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    ZM514

    <p>ZM514 inhibits CD73 (hCD73 IC50: 1.39 μM, mCD73 IC50: 14.65 μM) with low cytotoxicity, suitable for cancer research.</p>
    Formula:C36H57NO4
    Color and Shape:Solid
    Molecular weight:567.84

    Ref: TM-T64019

  • (S)-MALT1-IN-5
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    (S)-MALT1-IN-5

    CAS:
    <p>(S)-MALT1-IN-5: Potent MALT1 protease inhibitor, may help in abnormal T/B-cell signalling and MALT1-linked diseases.</p>
    Formula:C17H17ClF2N6O3
    Color and Shape:Solid
    Molecular weight:426.80

    Ref: TM-T62322

  • Carazostatin
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    Carazostatin

    CAS:
    <p>Carazostatin is an antioxidant, free radical scavenger, and potent lipid peroxidation inhibitor.</p>
    Formula:C20H25NO
    Purity:98%
    Color and Shape:Pale Yellow Solid
    Molecular weight:295.42

    Ref: TM-T23853

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    Galectin-3-IN-2

    <p>Galectin-3-IN-2 inhibits galactose lectin-3 (Gal-3) with an 8.3 μM IC50, impacting cancer-related metabolism.</p>
    Formula:C24H30FN3O10S
    Color and Shape:Solid
    Molecular weight:571.57

    Ref: TM-T64040

  • HEI3090
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    HEI3090

    CAS:
    <p>HEI3090 is an activator of the P2X7R receptor. This compound enhances the production of IL-18 by stimulating dendritic cells that express P2X7R, which in turn promotes the production of IFN-γ by natural killer cells and CD4T cells within tumors, triggering a sustained anti-tumor response. Additionally, HEI3090 can be used to improve the efficacy of αPD-1 therapy in non-small cell lung cancer (NSCLC).</p>
    Formula:C18H15Cl3N4O3
    Color and Shape:Solid
    Molecular weight:441.70

    Ref: TM-T89862

  • Glutathione monoethyl ester
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    Glutathione monoethyl ester

    CAS:
    <p>Glutathione monoethyl ester, a derivative of glutathione, can protect motor neuron cells (NSC-34) from TDP-43 pathology caused by mutations, which includes reducing aggregate formation, nuclear clearance, reactive oxygen species (ROS) production, and cell death.</p>
    Formula:C12H21N3O6S
    Color and Shape:Solid
    Molecular weight:335.377

    Ref: TM-T204308

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    NDT-30805

    <p>NDT-30805, a triazolopyridine, blocks IL-1β in PBMC (IC50: 0.013μM) &amp; NLRP3 inflammasome, for inflammation research.</p>
    Formula:C23H22N6S
    Color and Shape:Solid
    Molecular weight:414.53

    Ref: TM-T62139

  • Pelecopan
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    Pelecopan

    CAS:
    <p>Pelecopan (BCX9930), an oral complement factor D inhibitor, prevents hemolysis in PNH (IC50=14.3 nM).</p>
    Formula:C23H19FN2O4
    Color and Shape:Solid
    Molecular weight:406.41

    Ref: TM-T62020

  • Keap1-Nrf2-IN-5
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    Keap1-Nrf2-IN-5

    CAS:
    <p>Keap1-Nrf2-IN-5 is a potent inhibitor of Keap1-Nrf2 PPI (Keap1-Nrf2 protein-protein interaction) (IC50: 4.1 μM, Kd: 3.7 μM).</p>
    Formula:C23H30N4O6S
    Color and Shape:Solid
    Molecular weight:490.57

    Ref: TM-T63294

  • NLRP3-IN-69
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    NLRP3-IN-69

    CAS:
    <p>NLRP3-IN-69 (Compound 23) inhibits the activation of NF-κBp65 and the formation of the NLRP3 inflammasome. It suppresses the overexpression of IL-1β, iNOS, and COX-2 induced by LPS, and inhibits the production of NO (IC50=5.66 μM), thereby demonstrating anti-inflammatory activity.</p>
    Formula:C25H24O7
    Color and Shape:Solid
    Molecular weight:436.454

    Ref: TM-T205524

  • COX-2-IN-51
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    COX-2-IN-51

    CAS:
    <p>COX-2-IN-51 (E25) is a potent COX-2 inhibitor with an IC50 of 70.7 nM. It significantly suppresses LPS-induced release of NO and PGE2, the expression of COX-2 and iNOS, and the activation of the NF-κB pathway. Displaying anti-inflammatory and analgesic effects in various mouse models through NF-κB pathway inhibition, COX-2-IN-51 has lower gastrointestinal side effects compared to Indomethacin.</p>
    Formula:C23H18F4O3S
    Color and Shape:Solid
    Molecular weight:450.446

    Ref: TM-T204857

  • BMS-986458
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    BMS-986458

    CAS:
    <p>BMS-986458 is a highly selective, orally active BCL6 PROTAC degrader. It specifically targets cereblon (CRBN) and the BCL6 N-terminal BTB domain to catalyze proximity-induced BCL6 degradation. BMS-986458 is applicable for research in B-cell non-Hodgkin lymphoma.</p>
    Formula:C32H34ClN9O3
    Color and Shape:Solid
    Molecular weight:628.124

    Ref: TM-T206353

  • STING-IN-11
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    STING-IN-11

    CAS:
    <p>STING-IN-11 (Compound 42) is an orally active STING inhibitor with an IC50 of 37.8 nM. It impedes palmitoylation of the STING protein and the downstream signaling of STING, thereby inhibiting STING-mediated inflammation. STING-IN-11 demonstrates good in vivo safety and can be utilized for research on STING-related inflammatory and autoimmune diseases.</p>
    Formula:C21H20ClF2N3O
    Color and Shape:Solid
    Molecular weight:403.853

    Ref: TM-T205702

  • OP-5244
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    OP-5244

    CAS:
    <p>OP-5244 has comparable potency to bisphosphonic acid series and targets CD73.</p>
    Formula:C19H29ClN5O9P
    Purity:98%
    Color and Shape:Solid
    Molecular weight:537.89

    Ref: TM-T22392

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    COX-2-IN-7

    <p>COX-2-IN-7: potent, orally active COX-2 inhibitor with higher selectivity than Celecoxib, IC50 6.585 uM, anti-inflammatory, low ulcer risk.</p>
    Formula:C15H13N3O2S2
    Color and Shape:Solid
    Molecular weight:331.41

    Ref: TM-T60978

  • NLRP3-IN-78
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    NLRP3-IN-78

    CAS:
    <p>NLRP3-IN-78 (compound 21) is an NLRP3 inhibitor with a 46.72% inhibition rate of GSDMD-induced pyroptosis at 5 μM. It binds to the NLRP3 protein and prevents GSDMD-NT oligomerization. Additionally, NLRP3-IN-78 inhibits GSDMD cleavage and upstream NF-κB signaling, demonstrating anti-inflammatory activity.</p>
    Formula:C12H5Cl2N3O4S2
    Color and Shape:Solid
    Molecular weight:390.222

    Ref: TM-T206735

  • HG-12-6
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    HG-12-6

    CAS:
    <p>HG-12-6 is a type II IRAK4 inhibitor, targeting its inactive form with an IC50 of 165 nM, and is used in autoimmunity and inflammation.</p>
    Formula:C29H27F3N6O2S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:580.62

    Ref: TM-T11559

  • STAT1/3-IN-1
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    STAT1/3-IN-1

    CAS:
    <p>STAT1/3-IN-1 (Compound 6k) is an inhibitor of STAT1/3 phosphorylation. It prevents the phosphorylation and nuclear translocation of STAT1/3. Additionally, STAT1/3-IN-1 inhibits the inflammatory enzymes iNOS and COX-2. This compound exhibits anti-inflammatory properties by reducing pro-inflammatory cytokines, such as IL-1β, IL-6, and TNF-α, without significant cytotoxicity.</p>
    Formula:C28H25ClN6O5
    Color and Shape:Solid
    Molecular weight:560.988

    Ref: TM-T204879

  • 20-Hydroxyvitamin D3
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    20-Hydroxyvitamin D3

    CAS:
    <p>20-Hydroxyvitamin D3 (20(OH)D3) is a hydroxy metabolite of vitamin D3. It functions as a ligand for the vitamin D receptor (VDR), aryl hydrocarbon receptor (AhR), liver X receptor (LXR), and retinoic acid receptor-related orphan receptor (ROR). 20-Hydroxyvitamin D3 inhibits cell proliferation and induces differentiation. It is applicable in research on inflammatory and autoimmune diseases.</p>
    Formula:C27H44O2
    Color and Shape:Solid
    Molecular weight:400.637

    Ref: TM-T206693

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    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

    Ref: TM-T63389

  • CD73-IN-7
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    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

    Ref: TM-T60599

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    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

    Ref: TM-T60847

  • Hetrombopag olamine
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    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

    Ref: TM-T27536

  • RuDiOBn
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    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

    Ref: TM-T206205

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    MAO-B-IN-7

    <p>MAO-B-IN-7 inhibits MAO-B/AChE, crossing the blood-brain barrier; IC50: 41/87 nM (h/eel AChE), 0.3 μM (MAO-B). Reduces oxidative stress and neuroinflammation.</p>
    Formula:C25H31NO4
    Color and Shape:Solid
    Molecular weight:409.52

    Ref: TM-T62062

  • ODN 21158
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    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

    Ref: TM-T64279

  • IRAK4-IN-14
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    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

    Ref: TM-T63278

  • NP3-146 sodium
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    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

    Ref: TM-T200987

  • NLRP3-IN-58
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    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

    Ref: TM-T200969

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    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

    Ref: TM-T63315

  • C5aR-IN-3
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    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

    Ref: TM-T73262

  • Ocadusertib
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    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

    Ref: TM-T201183

  • NLRP3-IN-56
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    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

    Ref: TM-T200911

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    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

    Ref: TM-T60779

  • RGT-068A
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    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

    Ref: TM-T73389

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    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

    Ref: TM-T63956

  • oxLig-1
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    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

    Ref: TM-T201276

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    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

    Ref: TM-T62178