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Results for "

ifnγ

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    17
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    1
    TargetMol | Peptide_Products
  • Inhibitory Antibodies
    4
    TargetMol | Inhibitory_Antibodies
  • Recombinant Protein
    13
    TargetMol | Recombinant_Protein
TNF/IFNγ-IN-1
T83628876013-29-5
TNF IFNγ-IN-1 (TGA) is a dual inhibitor of TNF and IFN-γ. TNF IFNγ-IN-1 has potential antioxidant and anti-inflammatory activities for neurodegenerative diseases such as Alzheimer.
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Anti-IFNγ Antibody (B133.5)
T9901A-122
The Anti-IFNγ Antibody (B133.5) is a chimeric mouse IgG1 kappa targeting human IFNγ. Its isotype control is designated as Mouse IgG1 kappa, Isotype Control.
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PF-07038124 HCl
PF-07038124 HCl(2415085-44-6 Free base)
T60921L2415317-57-4In house
PF-07038124 HCl is a selective and potent PDE4 inhibitor with an IC50 of 0.5 nM for PDE4B2.PF-07038124 HCl inhibits IL-13, IL-4, and IFNγ, and can be used in the study of skin disorders such as atopic dermatitis and plaque psoriasis.
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RGS10 modulator-1
T2042671113116-62-3
RGS10 modulator-1 (compound 15) is an effective regulator of RGS10. It significantly reverses IFNγ-induced expression of both RGS10 protein and mRNA, as well as COX-2 mRNA and iNOS expression triggered by IFNγ.
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10-14 weeks
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N-Octanoyl dopamine
T204541105026-81-1
N-Octanoyl dopamine surpasses dopamine in preserving the contractile function of donor hearts from brain-dead individuals. Additionally, N-Octanoyl dopamine inhibits cytokine production in activated T cells and reduces the expression of MHC-II and adhesion molecules in endothelial cells stimulated by IFNγ.
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10-14 weeks
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Itaconic acid prodrug-1
T2045912641132-66-1
Itaconic acid prodrug-1 (Compound P2) is an orally active prodrug of Itaconic acid that efficiently delivers Itaconic acid to skin tissues upon oral administration. It exhibits immunomodulatory effects, significantly inhibiting Poly(I:C) IFNγ-induced inflammatory cytokines in human epidermal keratinocytes. Itaconic acid prodrug-1 is useful for research into alopecia areata and other inflammatory skin conditions.
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10-14 weeks
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pf-07038124
T609212415085-44-6
PF-07038124 is an inhibitor of PDE4. The IC50 value of PF-07038124 for PDE4B2 is 0.5 nM. PF-07038124 shows inhibitory activities against IFNγ, IL4, and IL-13 with IC50 values of 1.06, 4.1, and 125 nM, respectively [1].
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1-2 weeks
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tyk2-in-12
T624512244061-66-1
TYK2-IN-12 (compound 30) is a selective, orally active inhibitor of TYK2 (tyrosine kinase 2) (Ki: 0.51 nM). It inhibits IL-12-induced IFNγ in human and mouse whole blood with IC50 values of 2.7 and 7.0 μM, respectively, and can be used to study psoriasis.
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6-8 weeks
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JAK-IN-19
T63026
JAK-IN-19 is a potent JAK inhibitor with pIC50 values of 7.2 for PBMC (IFNγ) and 7.7 for HLF (Eotaxin). The compound also exhibits pIC50 values of 7.0 for VEGFR2 and 5.8 for Aurora B.
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10-14 weeks
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Feladilimab
GSK3359609
T774332252518-85-5
Feladilimab (GSK3359609) is an IgG4 monoclonal antibody that is an ICOS agonist. Feladilimab binds to ICOS-expressing T cells, induces IFNγ, and increases PD-1 L1 expression. Feladilimab has anti-tumor activity and can be used to study cancer.
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XY-52
T80759
XY-52 (Compound 32), an ST2 (Stimulation-2) inhibitor, exhibits IC50 values of 5.68 μM and 4.59 μM in the AlphaLISA and HEK-Blue assays, respectively. It promotes proinflammatory T-cell proliferation and diminishes plasma sST2 and IFNγ biomarkers in a graft versus host disease (GVHD) mouse model [1].
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QL-1200186
T813312848664-42-4
QL-1200186 is an orally active, selective TYK2 inhibitor that, upon dose-dependent oral administration, suppresses interferon-γ (IFNγ) production following interleukin-12 (IL-12) stimulation and markedly improves skin lesions in a psoriatic mouse model [1].
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8-10 weeks
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Soquelitinib
CPI-818, CPI818
T874292226636-04-8
Soquelitinib (CPI-818) is a covalent, irreversible, oral and selective ITK inhibitor that preferentially inhibits Th2 cytokine production over Th1, inhibits in vivo tumor growth in mice, and decreases markers of T-cell exhaustion, resulting in an increase in tumor infiltration and up-regulation of CXCR3, IFNγ, TNFα, and CD107a expression in normal CD8 cells.
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10-14 weeks
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Icotrokinra
PN-235,JNJ-77242113,JNJ-2113
T890732763602-16-8
Icotrokinra (JNJ-77242113) is an orally effective selective antagonist of the IL-23 receptor (IL-23 receptor), demonstrating high affinity with a dissociation constant (Kd) of 7.1 pM for the human IL-23 receptor (hIL-23R). It inhibits IL-23-induced STAT3 phosphorylation in PBMC with an IC50 of 5.6 pM and suppresses the production of IFNγ and IL-17A at the epidermal level induced by IL-23. Additionally, Icotrokinra exhibits anti-inflammatory activity in a rat model of TNBS-induced colitis.
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Anti-Mouse IFN gamma Antibody (XMG1.2)
T9901A-111
Anti-Mouse IFN gamma Antibody (XMG1.2) is a rat IgG1 kappa monoclonal antibody specifically targeting IFNγ in mice. The recommended isotype control for this antibody is Rat IgG1 kappa, Isotype Control.
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2-4 weeks
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Anti-Mouse IFN gamma Antibody (R4-6A2)
T9901A-175
Anti-Mouse IFN gamma Antibody (R4-6A2) is a rat-derived IgG1 kappa isotype antibody designed for in vivo targeting of mouse IFNγ. The recommended isotype control for this antibody is Rat IgG1 kappa, Isotype Control.
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FSL-1
FSL 1
TP2035322455-70-9
TLR2/6 agonist (also a putative TLR10 ligand). Activates NF-κB. Induces pro-inflammatory cytokines including IL-8, IL-1β, CCL20 and TNF-α in vitro. Synergizes with IFNγ to induce CXCL10 release from melanoma cells.
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