Complement System

Cat.No. Product Name Information Product Use Citations Product Validations
S1322 Dexamethasone Dexamethasone is a potent synthetic member of the glucocorticoid class of steroid drugs, and an interleukin receptor modulator that has anti-inflammatory and immunosuppressant effects. Dexamethasone induces autophagy and mitophagy. Dexamethasone is tested in hospitalized patients with COVID-19 and is found to have benefits for critically ill patients.
Blood, August 15 2024, 757-770
Signal Transduct Target Ther, 2025, 10(1):230
Signal Transduct Target Ther, 2025, 10(1):394
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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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S8522 Compstatin Compstatin binds to primates’ complement component C3 and inhibits complement activation with IC50 of 12 μM.
bioRxiv, September 27, 2025, nan
Proceedings of the National Academy of Sciences, May 13, 2025, e2412447122
ImmunoHorizons, March 1, 2024, 269-280
S8931 SB290157 trifluoroacetate SB290157 trifluoroacetate (SB 290157 TFA) is a potent, competitive and selective antagonist of C3a receptor (C3aR) with IC50 of 200 nM for RBL-C3aR.
Advanced Science, October 18, 2024, e2407967
bioRxiv, November 30, 2024, nan
Investigative Ophthalmology & Visual Science, May 1, 2025, 2
S0474 Avacopan (CCX168) Avacopan is an orally administered and selective C5a receptor (C5aR) antagonist.
British Journal of Cancer, 2025, Online ahead of print
Br J Cancer, 2025, 10.1038/s41416-025-03185-0
Nature Communications, 2024, 6519
S0803 Danicopan Danicopan is a potent, selective and orally active inhibitor of factor D with Kd of 0.54 nM for human Factor D. This compound inhibits alternative pathway of complement (APC) activity, and has potential to block the alternative pathway of complement in paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS).
Scientific Reports, 2024, 18494
iScience, 2023, 108018
S3240 Phaseoloidin Phaseoloidin, a homogentisic acid glucoside from Nicotiana attenuata trichomes, contributes to the plant's resistance against lepidopteran herbivores. This compound has anti-complement effects.
E1048 JR14a JR14a, a selective and potent human Complement C3a receptor antagonist, which is assessed by inhibition of intracellular calcium release (IC50=10 nM) induced in human monocyte-derived macrophages by C3a, inhibition of β-hexosaminidase secretion (IC50=8 nM) from human LAD2 mast cells degranulated by C3a, and selectivity for human C3aR over C5aR.
P1269New Pegcetacoplan acetate Pegcetacoplan acetate, a PEGylated cyclic peptide, is the first approved inhibitor of complement component C3/C3b designed to treat adults with Paroxysmal Nocturnal Hemoglobinuria (PNH). It binds C3 and C3b to inhibit convertase-mediated C3 cleavage, blocking C3b opsonization (extravascular hemolysis) and downstream MAC formation (intravascular hemolysis).
S3124 Dexamethasone Acetate Dexamethasone (NSC 39471,Dexamethasone 21-acetate) is a potent synthetic member of the glucocorticoid class of steroid drugs, and an interleukin receptor modulator that has anti-inflammatory and immunosuppressant effects.
Acta Pharm Sin B, 2024, 14(8):3528-3542
STAR Protoc, 2023, 4(2):102342
Exp Mol Med, 2022, 54(9):1450-1460
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