BP15242
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Carrageenan
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BP22477
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MCC950
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MCC950 (CP-456773, CRID3) is a potent and selective inhibitor of NLRP3 with IC50 values of 7.5 and 8.1 nM in BMDMs and HMDMs, respectively. nM and 8.1 nM in BMDMs and HMDMs, respectively.
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BP22567
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Concanamycin A
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Concanamycin A (Folimycin; Antibiotic X 4357B) is a macrolide antibiotic, a vacuolar type H+-ATPase (V-ATPase) inhibitor. Concanamycin A is also an inhibitor of lysosomal acidification, can be used to T cell-mediated inflammation research-.
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BP22568
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Fidaxomicin
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Fidaxomicin (OPT-80), a macrocyclic antibiotic, is an orally active and potent RNA polymerase inhibitor. Fidaxomicin has a narrow spectrum of antibacterial activity and a good anti-Clostridium difficile activity (MIC90=0.12 μg/mL). Fidaxomicin can be used for Clostridium difficile infection (CDI) research.
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BP22482
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TLR4-IN-C34
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TLR4-IN-C34 (TLR4-C34, C34, TLR4-C34-IN) is a potent and selective antagonist of Toll-like receptor 4 (TLR4).TLR4-IN-C34 reduces endotoxemia and systemic inflammation in a mouse model of necrotizing small intestinal colitis.
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BP22495
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Cyclosporin A
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Cyclosporin A (Cyclosporine A) is an immunosuppressant which binds to the cyclophilin and inhibits phosphatase activity of calcineurin with an IC50 of 5 nM. Cyclosporin A also inhibits CD11a/CD18 adhesion[8].
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Calcipotriol
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Calcipotriene (Calcipotriol, MC903) is a synthetic derivative of calcitriol that induces differentiation of keratinocytes, inhibits their proliferation, reverses abnormal changes of keratinocytes in psoriasis, and promotes normal epidermal growth.
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BP22566
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Staurosporine
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Staurosporine is a potent, ATP-competitive and non-selective inhibitor of protein kinases with IC50s of 6 nM, 15 nM, 2 nM, and 3 nM for PKC, PKA, c-Fgr, and Phosphorylase kinase respectively. Staurosporine also inhibits TAOK2 with an IC50 of 3 μM. Staurosporine is an apoptosis inducer.
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BP22573
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Chlorobutanol
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Chlorobutanol is a pharmaceutical preservative. Chlorobutanol is active against a wide variety of Gram-positive and Gram-negative bacteria, and several mold spores and fungi. Chlorobutanol is widely used in food and cosmetic industry.
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BP22476
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MCC950 sodium
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MCC950 Sodium (CP-456773 Sodium, CRID3 sodium salt) is a potent and selective inhibitor of NLRP3 with corresponding IC50 values of 7.5 nM and 8.1 nM in BMDMs and HMDMs, respectively.
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BP22478
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CY-09
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CY-09 is a specific inhibitor of the NLRP3 inflammasome and directly targets NLRP3. its IC50 values for the five major cytochrome P450 enzymes were 18.9, 8.18, >50, >50 and 26.0 µM, respectively.
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BP22484
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IAXO-102
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IAXO-102 is an antagonist of TLR4 that targets MD-2 and CD14 co-receptors.IAXO-102 inhibits MAPK and p65 NF-κB phosphorylation and downregulates TLR4-dependent pro-inflammatory protein expression.IAXO-102 inhibits the development of experimental abdominal aortic aneurysms.
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BP22510
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W-54011
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W-54011 is a potent and orally active non-peptide C5a receptor antagonist. W-54011 inhibits the binding of 125I-labeled C5a to human neutrophils with a Ki value of 2.2 nM. W-54011 also inhibits C5a-induced intracellular Ca2+ mobilization, chemotaxis, and generation of ROS in human neutrophils with IC50s of 3.1 nM, 2.7 nM, and 1.6 nM, respectively.
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BP22557
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Coenzyme Q10
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Coenzyme Q10 is an essential cofactor of the electron transport chain and a potent antioxidant agent.
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BP22562
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Ferrostatin-1
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Ferrostatin-1 (Fer-1), a potent and selective ferroptosis inhibitor, suppresses Erastin-induced ferroptosis in HT-1080 cells (EC50=60 nM). Ferrostatin-1, a synthetic antioxidant, acts via a reductive mechanism to prevent damage to membrane lipids and thereby inhibits cell death. Antifungal Activity.
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BP22570
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BRD-K98645985
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BRD-K98645985 is a BAF (mammalian SWI/SNF) transcriptional repression inhibitor with an EC50 of ~2.37 µM. BRD-K98645985 binds ARID1A-specific BAF complexes, prevents nucleosomal positioning, and potently reverses HIV-1 latency, without T cell activation or toxicity.
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BP22483
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MD2-TLR4-IN-1
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MD2-TLR4-IN-1 (compound 22m) is a potent inhibitor of myeloid differentiation protein 2/toll-like receptor 4 (MD2-TLR4). MD2-TLR4-IN-1 (compound 22m) inhibits lipopolysaccharide ( LPS-induced tumor necrosis factor alpha (TNF-α) and interleukin-6 (IL-6) expression in macrophages with corresponding IC50 values of 0.89 μM and 0.53 μM, respectively.
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BP22485
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Resatorvid
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Resatorvid (TAK-242, CLI-095), a small molecule inhibitor of TLR4 signaling pathway, blocks LPS-induced NO, TNF-α, and IL-6 production in macrophages with corresponding IC50 values of 1.8 nM, 1.9 nM, and 1.3 nM. Resatorvid downregulates the expression of TLR4 downstream signaling molecules MyD88 and TRIF. Resatorvid inhibits autophagy.
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(-)-Epigallocatechin Gallate
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(-)-Epigallocatechin Gallate (EGCG) is a potent antioxidant Polyphenol flavonoid isolated from green tea. EGCG inhibits telomerase and DNA methyltransferase, blocks the activation of EGF receptors and HER-2 receptors, inhibits fatty acid synthase and glutamate dehydrogenase activity.
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BP22536
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Celecoxib
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Celecoxib,a selective non-steroidal anti-inflammatory drug (NSAID), is a selective COX-2 inhibitor with an IC50 of 40 nM.
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