1. Signaling Pathways
  2. Apoptosis
  3. TNF Receptor
  4. CD40 Isoform

CD40

 

CD40 Related Products (41):

Cat. No. Product Name Effect Purity
  • HY-110203
    R-7050
    Antagonist 99.26%
    R-7050 (TNF-α Antagonist III) is a tumor necrosis factor receptor (TNFR) antagonist with greater selectivity toward TNFα.
  • HY-118250
    GSK2245035
    Activator 99.84%
    GSK2245035 is a highly potent and selective intranasal Toll-Like receptor 7 (TLR7) agonist with preferential Type-1 interferon (IFN)-stimulating properties.
  • HY-107390
    AX-024
    Inhibitor 99.29%
    AX-024 is an orally available, first-in-class inhibitor of the TCR-Nck interaction that selectively inhibits TCR-triggered T cell activation with an IC50 ~1 nM.
  • HY-133807
    Benpyrine
    Inhibitor 99.56%
    Benpyrine is a highly specific and orally active TNF-α inhibitor with a KD value of 82.1 μM.
  • HY-134471
    TNF-α-IN-2
    Inhibitor 98.12%
    TNF-α-IN-2 is a potent and orally active inhibitor of tumor necrosis factor alpha (TNFα), with an IC50 of 25 nM in the HTRF assay.
  • HY-P99167
    Lucatumumab
    Inhibitor
    Lucatumumab (HCD122) is a fully human anti-CD40 antagonist monoclonal antibody, which blocks CD40/CD40L-mediated signaling.
  • HY-P99670
    Iscalimab
    Inhibitor
    Iscalimab (CFZ-533) is a non-depleting IGg1 monoclonal antibody targeting CD40 (KD: 0.3 nM).
  • HY-P99325
    Toralizumab
    Inhibitor
    Toralizumab (IDEC-131) is a humanized monoclonal antibody (mAb) against CD40L (CD154) comprised of human gamma 1 heavy chains and human kappa light chains.
  • HY-119307
    Apratastat
    Inhibitor 99.67%
    Apratastat (TMI-005) is an orally active, non-selective and reversible TACE/MMPs inhibitor, can inhibit inhibit the release of TNF-α.
  • HY-P9953
    Certolizumab pegol
    Inhibitor 99.30%
    Certolizumab pegol (Certolizumab) is a recombinant, polyethylene glycolylated, antigen-binding fragment of a humanized monoclonal antibody that selectively targets and neutralizes tumour necrosis factor-α (TNF-α).
  • HY-N1949
    Homoplantaginin
    Inhibitor 99.90%
    Homoplantaginin is a flavonoid from a traditional Chinese medicine Salvia plebeia with antiinflammatory and antioxidant properties.
  • HY-107390A
    AX-024 hydrochloride
    Inhibitor 99.12%
    AX-024 hydrochloride is an orally available, first-in-class inhibitor of the TCR-Nck interaction that selectively inhibits TCR-triggered T cell activation with an IC50 ~1 nM.
  • HY-147045
    UCB-5307
    Inhibitor
    UCB-5307 is a potent TNF signaling inhibitor with a KD of 9 nM for human TNFα.
  • HY-135674
    SR-318
    Inhibitor 98.87%
    SR-318 is a potent and highly selective p38 MAPK inhibitor with IC50s of 5 nM, 32 nM and 6.11 μM for p38α, p38β and p38α/β, respectively.
  • HY-133807A
    (Rac)-Benpyrine
    Inhibitor 99.30%
    (Rac)-Benpyrine, a racemate of Benpyrine, is a potent and orally active TNF-α inhibitor.
  • HY-P99111
    Golimumab
    Inhibitor 99.68%
    Golimumab (CNTO-148) is a potent human IgG1 TNFα antagonist monoclonal antibody.
  • HY-115620
    AQX-016A
    Inhibitor 98.00%
    AQX-016A is an orally active and potent SHIP1 agonist.
  • HY-N7012
    7,3',4'-Tri-O-methylluteolin
    Inhibitor 99.28%
    7,3',4'-Tri-O-methylluteolin (5-Hydroxy-3',4',7-trimethoxyflavone), a flavonoid compound, possesses potent anti-inflammatory effects in LPS-induced macrophage cell line mediated by inhibition of release of inflammatory mediators, NO, PGE2, and pro-inflammatory cytokines.
  • HY-W082785A
    L6H21
    Inhibitor
    L6H21, a Chalcone (HY-121054) derivative, is an orally active, potent and specific myeloid differentiation 2 (MD-2) inhibitor.
  • HY-107352
    Fosfenopril
    Inhibitor
    Fosfenopril (Fosinoprilat) is a potent angiotensin converting enzyme (ACE) inhibitor.