Immunology & Inflammation related Inhibitors/Modulators

Cat.No. Product Name Information Product Use Citations Product Validations
S8141 Cl-amidine Cl-amidine is an irreversible pan-peptidylarginine deiminase (PAD) inhibitor with IC50 values of 5.9 ± 0.3 μM, 0.8 ± 0.3 μM, 6.2 ± 1.0 μM for PAD4, PAD1 and PAD3, respectively. Cl-amidine induces apoptosis.
Immunity, 2025, S1074-7613(25)00069-X
Cell Rep, 2025, 44(2):115226
Nat Commun, 2024, 15(1):8663
S1591 Bestatin (Ubenimex) Bestatin (Ubenimex) is a potent aminopeptidase-B and leukotriene (LT) A4 hydrolase inhibitor, used in the treatment of acute myelocytic leukemia.
PLoS One, November 16, 2015, e0142124
Aging (Albany NY), April 11, 2022, 3259-3275
Cell Reports, 2024, 114041
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S2286 Cyclosporin A Cyclosporin A, a non-polar cyclic oligopeptide, is an immunosuppressive agent that binds to cyclophilin and then inhibits calcineurin with IC50 of 7 nM in a cell-free assay. Cyclosporin A is generally given following transplant surgery to prevent rejection and has been used to test its toxic effect on a perfused 3D proximal tubule model.Cyclosporin A (NSC 290193) can be used to induce animal models of Chronic Rejection of Liver Transplantation.
Frontiers in Immunology, May 25, 2022, 861292
Circulation Research, March 27, 2026, e327680
Anticancer Research, March 2023, 1103-1112
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S8760 Iberdomide (CC-220) Iberdomide (CC-220) is a novel oral immunomodulatory compound that targets cereblon, part of the CRL4CRBN E3 ubiquitin ligase complex, with an IC50 of 60 nM in a competitive TR-FRET assay. Iberdomide (CC-220) induces apoptosis with antitumor and immunostimulatory activities.
Cell Rep Med, 2025, S2666-3791(25)00102-8
J Med Virol, 2025, 97(8):e70537
Cancer Res, 2025, 10.1158/0008-5472.CAN-24-1136
S3032 Bindarit (AF 2838) Bindarit exhibits selective inhibition against monocyte chemotactic proteins MCP-1/CCL2, MCP-3/CCL7 and MCP-2/CCL8.
International Journal of Biological Sciences, 2025, 21(14):6113-6131
Exp Mol Med, 2024, 56(2):408-421.
PLoS Pathog, 2024, 20(11):e1012747
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S1576 Sulfasalazine Sulfasalazine is a sulfa derivative of mesalazine, used as an anti-inflammatory agent to treat bowel disease and rheumatoid arthritis. This compound is a potent and specific inhibitor of nuclear factor kappa B (NF-κB), TGF-β and COX-2. It induces ferroptosis, apoptosis and autophagy.
Science Advances, August 27, 2021, eabj0364
Oncology Letters, April 1, 2026, 31
Med Oncol, 2024, 41(8):188
S1439 Tranilast Tranilast is an antiallergic drug by inhibiting lipid mediator and cytokine release from inflammatory cells, used for the treatment of allergic disorders such as asthma, allergic rhinitis and atopic dermatitis.
EMBO Mol Med, 2025, 17(4):747-774
Virol J, 2025, 22(1):301
PLoS One, 2025, 20(2):e0319381
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S2910 Tempol Tempol (4-Hydroxy-TEMPO) is a superoxide scavenger that displays neuroprotective, anti-inflammatory and analgesic effects. Phase 2.
Autophagy, 2025, 1791-1801
Cell Death Dis, 2024, 15(10):760
Cell Signal, 2023, 108:110712
S3648 Amlexanox Amlexanox is an anti-inflammatory antiallergic immunomodulator and also an inhibitor of the protein kinases TBK1 and IKK-ε.
Biomed Pharmacother, 2025, 186:117991
Cell Death Discov, 2025, 11(1):286
Sci Adv, 2025, 11(4):eadq2395
S5004 Pimecrolimus Pimecrolimus (Elidel,ASM 981,SDZ-ASM 981) is an immunophilin ligand, which binds specifically to the cytosolic receptor, immunophilin macrophilin-12 (FKBP-12); a calcineurin inhibitor.
PLoS Pathogens, November 20, 2020, e1009022
International Journal of Pharmaceutics, April 5, 2022, 121610
iScience, 2024, 27(10):110862
Verified customer review of Pimecrolimus