Immunology and Inflammation
Immunology and inflammation inhibitors are compounds that modulate the immune response and inflammatory processes. These inhibitors are crucial in studying the mechanisms of immune regulation, autoimmunity, and chronic inflammation, as well as in developing treatments for inflammatory diseases, allergies, and immune-related disorders. By targeting key pathways in the immune system, these inhibitors can help reduce excessive or inappropriate immune responses. At CymitQuimica, we provide a comprehensive selection of high-quality immunology and inflammation inhibitors to support your research in immunology, inflammation, and therapeutic development.
Subcategories of "Immunology and Inflammation"
- CCR(136 products)
- CXCR(147 products)
- Cell wall(5 products)
- IL Receptor(113 products)
- IκB/IKK(61 products)
- LTR(3 products)
- MALT(23 products)
- MRP(6 products)
- NADPH-oxidase(1 products)
- NF-κB(445 products)
- NOD(17 products)
- NOS(63 products)
- Nrf2(78 products)
- PGE Synthase(31 products)
- ROS(69 products)
- TGF-beta/Smad(58 products)
- TLR(66 products)
- Thioredoxin(12 products)
- gp120/CD4(4 products)
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Found 3035 products of "Immunology and Inflammation"
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Emlenoflast
CAS:<p>Emlenoflast (MCC7840) is a selective inhibitor of NLRP3 inflammasome.</p>Formula:C19H24N4O3SPurity:97.004% - 98.19%Color and Shape:SolidMolecular weight:388.48MALT1-IN-3
CAS:<p>MALT1-IN-3 is a potent inhibitor of MALT1 protease (IC50: 0.06 μM) with IC50 values of 0.14 and 0.13 μM for human IL6 and IL10, respectively, in OCI-LY3 cells.</p>Formula:C21H19F3N8O2Color and Shape:SolidMolecular weight:472.42Edasalonexent
CAS:<p>Edasalonexent (CAT-1004) is an orally available NF-κB inhibitor for the improvement of Duchenne muscular dystrophy.</p>Formula:C31H42N2O3Purity:99.13% - >99.99%Color and Shape:SolidMolecular weight:490.68Emlenoflast sodium
CAS:<p>Emlenoflast sodium (MCC7840 sodium), a sulfonylurea, is a selective NLRP3 inflammasome inhibitor with an IC50 value of less than 100 nM for NLRP3 inflammasome,</p>Formula:C19H24N4NaO3SColor and Shape:SolidMolecular weight:411.47MK-0703
CAS:<p>MK-0703 is a selective cyclooxygenase-2 inhibitor.</p>Formula:C17H22O5SPurity:98%Color and Shape:SolidMolecular weight:338.42Bay 65-1942 hydrochloride
CAS:<p>Bay 65-1942 hydrochloride is an inhibitor of ATP-competitive and selective IKKβ.</p>Formula:C22H26ClN3O4Color and Shape:SolidMolecular weight:431.91Insulin levels modulator
CAS:<p>Insulin level regulators can be used to treat diabetes.</p>Formula:C21H23N7OSPurity:98%Color and Shape:SolidMolecular weight:421.52COX-2/5-LOX-IN-1
CAS:<p>COX-2/5-LOX-IN-1, a benzothiophen-2-yl pyrazole, inhibits COX-2 & 5-LOX with IC50: COX-1 (12.13μM), COX-2 (0.4μM), 5-LOX (4.96μM). Better than Celecoxib.</p>Formula:C14H10ClN3O4S2Color and Shape:SolidMolecular weight:383.83IKKβ-IN-1
CAS:<p>IKKβ-IN-1 is a potent, orally active inhibitor of IkappaB (IKK-β) (IC50: 0.20 μM).</p>Formula:C31H30N4O4SColor and Shape:SolidMolecular weight:554.66MIND4-17
CAS:<p>MIND4-17 activates NRF2 by binding Keap1 C151, blocking Keap1-Nrf2, stabilizes Nrf2, and promotes its nuclear entry, with strong antioxidant effects.</p>Formula:C20H15N5O3SColor and Shape:SolidMolecular weight:405.43IRAK4-IN-21
CAS:<p>IRAK4-IN-21: Oral IRAK4 inhibitor, IC50: IRAK4 5 nM, TAK1 56 nM; curbs IL-23, aids autoimmune research.</p>Formula:C28H28FN7O2Color and Shape:SolidMolecular weight:513.57MitoB
CAS:<p>MitoB is a novel exon of mitochondrial hydrogen peroxide.</p>Formula:C25H23BBrO2PColor and Shape:SolidMolecular weight:477.14Heterophdoid A
CAS:<p>Heterophdoid A is an anti-inflammatory agent that inhibits NO production in BV-2 cells (IC50: 5.93 μM).</p>Formula:C26H42O10Color and Shape:SolidMolecular weight:514.61Ruzotolimod
CAS:<p>Ruzotolimod, an agonist of TLR7, exhibits promising potential for investigating HBV, COVID-19, and SARS-CoV-2 infections （WO2021130195A1）[1].</p>Formula:C14H18N4O5SColor and Shape:SolidMolecular weight:354.38COX-2/15-LOX-IN-1
CAS:<p>COX-2/15-LOX-IN-1 is a dual inhibitor for COX-2/15-LOX with anti-inflammatory properties (IC50: COX-1 10.65μM, COX-2 0.075μM, 15-LOX 2.98μM).</p>Formula:C21H21N7S3Color and Shape:SolidMolecular weight:467.63Clopirac
CAS:<p>Clopirac is a potent and orally active prostaglandin synthetase inhibitor that is an anti-inflammatory agent [1].</p>Formula:C14H14ClNO2Color and Shape:SolidMolecular weight:263.72NF-κB-IN-2
CAS:<p>NF-κB-IN-2 inhibits canonical NF-κB signaling induced by TNF-α in PC-3 cells.</p>Formula:C15H18O3Color and Shape:SolidMolecular weight:246.3Gue1654
CAS:<p>Gue1654 is an OXE-R inhibitor and cardiomyocyte apoptosis.Gue1654 can be used for the study of cardiovascular diseases.</p>Formula:C23H17N3OS3Purity:98.02% - 98.04%Color and Shape:SolidMolecular weight:447.6AVE3085
CAS:<p>AVE3085 is an enhancer of endothelial nitric oxide synthase that restores endothelial function and lowers blood pressure in spontaneously hypertensive rats.</p>Formula:C17H13F2NO3Purity:99.87%Color and Shape:SolidMolecular weight:317.29Methyl aminolevulinate
CAS:<p>Methyl aminolevulinate, a prodrug for protoporphyrin IX, sensitizes in PDT.</p>Formula:C6H11NO3Purity:98%Color and Shape:SolidMolecular weight:145.16Dihydrolipoic acid
CAS:<p>Dihydrolipoic acid (USAF XR-12), a dithiol carboxylic acid, is a potent antioxidant active against various reactive oxygen species at 0.01-0.5 mM.</p>Formula:C8H16O2S2Purity:97.51%Color and Shape:Yellow To Orange LiquidMolecular weight:208.34TPO agonist 1
CAS:<p>TPO agonist 1 is a thrombopoietin agonist. It would be useful as promoters of thrombopoiesis and megakaryocytopoiesis to treat thrombocytopenia.</p>Formula:C25H22N8O2Purity:98%Color and Shape:SolidMolecular weight:466.49(R)-MLT-985
CAS:<p>(R)-MLT-985 (compound 11) is a MALT1 protease inhibitor with IC50 of 3 nM, also blocking IL-2 in Jurkat cells and ABC-DLBCL cell growth.</p>Formula:C17H15Cl2N9O2Color and Shape:SolidMolecular weight:448.27COX-2-IN-18
CAS:<p>COX-2-IN-18 is a potent COX-2 inhibitor similar to Celecoxib, showing promise in cancer research. IC50=0.775μM.</p>Formula:C18H19N3O3S2Color and Shape:SolidMolecular weight:389.49MD13
<p>MD13 is a macrophage migration inhibitor (MIF) oriented PROTAC (Ki value: 71 nM). MD13 can be used to study cancer.</p>Color and Shape:LiquidSMA-12b
CAS:<p>SMA-12b is an analog of the immunomodulatory parasite product ES-62 that has immunomodulatory activity and can be used in the study of rheumatoid arthritis.</p>Formula:C13H22INO2SPurity:98.52% - 99.16%Color and Shape:SolidMolecular weight:383.29Sulfo-ara-F-NMN
CAS:<p>Sulfo-ara-F-NMN: cell-permeable, NMN analogue, activates SARM1, inhibits CD38 (IC50 ~10μM), induces cADPR, NAD loss, non-apoptotic death.</p>Formula:C11H14FN2O6PSPurity:98%Color and Shape:SolidMolecular weight:352.28Mercaptoethylguanidine (MEG) (dihydrobromide)
CAS:<p>MEG dihydrobromide inhibits inducible nitric oxide synthase and scavenges peroxynitrite, potentially aiding in inflammatory bowel disease studies.</p>Formula:C3H11Br2N3SColor and Shape:SolidMolecular weight:281.01AL-8417
CAS:<p>AL-8417 is an enzyme inhibitor with antioxidant, anti-inflammatory, and cytostatic properties; prevents vitrectomy-induced lens alterations.</p>Formula:C29H34O5Purity:98%Color and Shape:SolidMolecular weight:462.58IRAK inhibitor 4
CAS:<p>IRAK inhibitor 4 is an interleukin-1 receptor associated kinase 4 inhibitor.</p>Formula:C33H35F3N6O3Purity:98%Color and Shape:SolidMolecular weight:620.66L-NIL hydrochloride
CAS:<p>selective inhibitor of inducible nitric oxide synthase</p>Formula:C8H18ClN3O2Purity:98%Color and Shape:White To Off-White SolidMolecular weight:223.7IRAK4-IN-16
CAS:<p>IRAK4-IN-16 inhibits IRAK4 at 2.5nM; cytotoxic to OCI-LY10, TMD8, Ramos, HT cells with IC50s of 0.2, 0.2, 0.6, 2.7μM.</p>Formula:C17H20F2N8OColor and Shape:SolidMolecular weight:390.39CD73-IN-8
CAS:<p>CD73-IN-8 blocks CD73, hindering adenosine production that supports tumor growth, flagged as compound 57 in WO2022052886A1.</p>Formula:C17H13ClN4O2Color and Shape:SolidMolecular weight:340.76STING Agonist 12b
CAS:<p>STING agonist 12b activates human/mouse STING, binds with Kd 26.4 μM, prompts interferon, and induces TNF-a, IL-6, IP-10, IL-1b in THP-1 cells.</p>Formula:C16H15NO2Color and Shape:SolidMolecular weight:253.3GSK319347A
CAS:<p>GSK319347A is a dual inhibitor of TBK1 and IKKε that inhibits IKK2 and can be used to study bladder and lung adenocarcinomas.</p>Formula:C22H19N3O5S2Purity:98.42%Color and Shape:SolidMolecular weight:469.53Cyclic-di-GMP
CAS:<p>Cyclic-di-GMP is a STING agonist and ubiquitous second messenger, which regulates the formation, motility and virulence of biofilms in various bacterial species</p>Formula:C20H24N10O14P2Purity:98%Color and Shape:SolidMolecular weight:690.41AMT hydrochloride
CAS:<p>AMT hydrochloride is an iNOS inhibitor.</p>Formula:C5H11ClN2SPurity:98%Color and Shape:SolidMolecular weight:166.67Mivotilate
CAS:<p>Mivotilate, a potent, non-toxic aryl hydrocarbon receptor (AhR) activator, functions as a hepatoprotective agent.</p>Formula:C12H14N2O3S3Purity:98%Color and Shape:SolidMolecular weight:330.45AR-C102222 hydrochloride
CAS:<p>AR-C102222 hydrochloride: oral iNOS inhibitor, selective, IC50=37 nM, with anti-inflammatory and pain relief effects.</p>Formula:C19H17ClF2N6OPurity:98%Color and Shape:SolidMolecular weight:418.83NED-3238
CAS:<p>NED-3238 is a highly potent inhibitor of arginase I and II (IC50 of 1.3 nM and 8.1 nM, respectively).</p>Formula:C17H28BN3O4Purity:98%Color and Shape:SolidMolecular weight:349.23Xanthine oxidase-IN-6
<p>Xanthine oxidase-IN-6: potent oral mixed-type XOD inhibitor, IC50 1.37 µM, anti-hyperuricemia, renal protection.</p>Formula:C29H34N2O15Color and Shape:SolidMolecular weight:650.58MLT-747
CAS:<p>MLT-747 is an effective and allosteric inhibitor of MALT1. It binds MALT1 in the allosteric Trp580 pocket (IC50: 14 nM).</p>Formula:C20H21Cl2N7O3Color and Shape:SolidMolecular weight:478.33COX-2-IN-11
CAS:<p>COX-2-IN-11 (compound 7b2) is a potent and selective COX-2 inhibitor. COX-2-IN-11 has the potential in inflammation disease research[1].</p>Formula:C12H12OS3Color and Shape:SolidMolecular weight:268.42Carpro-AM1
CAS:<p>Carpro-AM1, dual FAAH/COX inhibitor, IC50: 94 nM.</p>Formula:C21H18ClN3OColor and Shape:SolidMolecular weight:363.84ASP-6537
CAS:<p>ASP-6537 is a selective and reversible inhibitor of cyclooxygenase-1.</p>Formula:C17H17N3O3Purity:98%Color and Shape:SolidMolecular weight:311.34CU-32
CAS:<p>CU-32 is a cGAS inhibitor with IC50=0.45 μM, blocks DNA-stimulated IFN-β production, and is selective over RIG-I-MAVS and TLRs pathways.</p>Formula:C11H10IN5O2Color and Shape:SolidMolecular weight:371.13PD 127443
CAS:<p>PD 127443 is a Leukotriene B4 antagonist, it is also a dual inhibitor of cyclooxygenase and 5-lipoxygenase.</p>Formula:C20H28N2OColor and Shape:SolidMolecular weight:312.45TFC-007
CAS:<p>TFC-007 is an H-PGDS inhibitor, reducing inflammation, useful for studying guinea pig allergic rhinitis induced by cedar pollen.</p>Formula:C27H29N5O4Purity:98.07%Color and Shape:SolidMolecular weight:487.55Vidarabine phosphate
CAS:<p>Vidarabine phosphate is an adenosine monophosphate analog.</p>Formula:C10H14N5O7PPurity:99.75%Color and Shape:White Crystalline PowderMolecular weight:347.22Safrole oxide
CAS:<p>Safrole oxide inhibits neuronal growth, induces apoptosis, elevates COX-2, IL-8, ROS, promoting endothelial-to-neuron-like cell transdifferentiation.</p>Formula:C10H10O3Purity:100%Color and Shape:SolidMolecular weight:178.18MIF degrader MD13
CAS:<p>MD13, a MIF-degrading PROTAC, disrupts vital protein interactions in cancer and inflammation, showing promise as a therapeutic research tool.</p>Formula:C35H35N5O8Color and Shape:SolidMolecular weight:653.686,2',4'-Trimethoxyflavone
CAS:<p>The compound is an Aryl hydrocarbon receptor antagonist (EC50 = 0.9 μM). It also has no short term agonist activity and no species or promoter dependence.</p>Formula:C18H16O5Purity:98%Color and Shape:SolidMolecular weight:312.32Naphazoline
CAS:<p>Naphazoline (Naphcon-a) is a sympathomimetic compound with marked alpha adrenergic activity.</p>Formula:C14H14N2Purity:99.79%Color and Shape:White Crystalline Powder SolidMolecular weight:210.271-Dehydro-[10]-gingerdione
CAS:<p>1-Dehydro-[10]-gingerdione blocks IKKβ, curbs IκBα phosphorylation, halts NF-κB activity, and aids inflammation research.</p>Formula:C21H30O4Color and Shape:SolidMolecular weight:346.46L-NMMA acetate
CAS:<p>L-NMMA acetate inhibits all NOS types (nNOS, eNOS, iNOS); Ki: 0.18, 0.4, 6 µM respectively.</p>Formula:C9H20N4O4Purity:99.72% - 99.8%Color and Shape:White To Off-White SolidMolecular weight:248.28IKK2-IN-4
CAS:<p>IKK2-IN-4(IKK2 Inhibitor VI) is a highly potent IKK-2 inhibitor with an IC50 value of 25 nM. IKK2-IN-4 inhibited the production of TNF-α in PBMC induced by LPS.</p>Formula:C12H11N3O2SPurity:>99.99%Color and Shape:SolidMolecular weight:261.3IL-17A modulator-3
CAS:<p>IL-17A modulator-3 inhibits IL-17A/A, IC50 <10 μM, for inflammation, cancer, autoimmune research.</p>Formula:C34H50FN7O4Color and Shape:SolidMolecular weight:639.8APY0201
CAS:<p>APY0201: potent, specific ATP-competitive PIKfyve inhibitor; IC50=5.2 nM; blocks PtdIns3P to PtdIns(3,5)P2 conversion.</p>Formula:C23H23N7OPurity:98% - 99.74%Color and Shape:SolidMolecular weight:413.48TYT-1
CAS:<p>TYT-1 is a West Nile virus (WNV) inhibitor, antiviral (IC₅₀ = 0.7 mM) by blocking the pre-assembly replication step following viral entry into cells.</p>Formula:C21H17N3O2S3Purity:98.49%Color and Shape:SolidMolecular weight:439.57Naproxen etemesil
CAS:<p>Naproxen, a COX-1/2 inhibitor, has IC50s of 8.72/5.15 μM. Its prodrug, naproxen etemesil, is lipophilic and converts to active form upon absorption.</p>Formula:C17H20O5SPurity:98%Color and Shape:SolidMolecular weight:336.4NLRP3-IN-25
CAS:<p>NLRP3-IN-25 (compound 32), an orally available NLRP3 inhibitor, exhibits anti-inflammatory properties by attenuating renal injury in a mouse model of doxorubicin-induced glomerulonephritis and inhibiting IL-1β secretion in THP-1 cells, with an IC 50 value of 21 nM [1].</p>Formula:C17H19F3N4O5SColor and Shape:SolidMolecular weight:448.42L 669083
CAS:<p>L 669083 is two classes of potent leukotriene biosynthesis inhibitors photoaffinity analogue.</p>Formula:C29H29IN4O5SPurity:98%Color and Shape:SolidMolecular weight:672.54LY 150310
CAS:<p>LY 150310, a histamine H1-receptor antagonist, can alter prostanoid concentrations in vitro and in vivo.</p>Formula:C13H14N2Color and Shape:SolidMolecular weight:198.26Fagaramide
CAS:<p>Fagaramide possesses Antiplasmodial activity.</p>Formula:C14H17NO3Purity:98%Color and Shape:SolidMolecular weight:247.29NCX-6560
CAS:<p>NCX-6560 is a novel NO-releasing derivative of atorvastatin, with those of atorvastatin.</p>Formula:C37H42FN3O8Color and Shape:SolidMolecular weight:675.74ZXX2-77
CAS:<p>ZXX2-77 is a cyclooxygenase-1 inhibitor.</p>Formula:C13H13ClN2O2SPurity:98%Color and Shape:SolidMolecular weight:296.77Tiazotic acid
CAS:<p>Tiazotic acid is an agent with the activity of antioxidant.</p>Formula:C5H7N3O2SPurity:98%Color and Shape:SolidMolecular weight:173.19L 748780
CAS:<p>L 748780 is a selective inducible COX-2 inhibitor.</p>Formula:C19H14Cl3NO4Purity:98%Color and Shape:SolidMolecular weight:426.68Oxyfenamate
CAS:<p>Oxyfenamate has anti-anxiety actions. It is also used in anxiety neuroses.</p>Formula:C11H15NO3Purity:98%Color and Shape:SolidMolecular weight:209.24Anisodine hydrobromide
CAS:<p>Anisodine hydrobromide is an inhibitor of adenosine kinase.</p>Formula:C17H22BrNO5Color and Shape:White Crystals Or Crystalline PowderMolecular weight:400.27FR20
CAS:<p>FR20 is a human microsomal prostaglandin synthase 1 (mPGES 1) inhibitor.</p>Formula:C31H25Cl2N3O2Color and Shape:SolidMolecular weight:542.46LC-R 505
CAS:<p>LC-R 505 is an anti-inflammatory.</p>Formula:C20H26N2O5SColor and Shape:SolidMolecular weight:406.5NCX1022
CAS:<p>NCX1022 is a NO-releasing derivative of Hydrocortisone. It is the most widely used anti-inflammatory drug for the treatment of skin inflammation.</p>Formula:C29H35NO9Purity:98%Color and Shape:SolidMolecular weight:541.59GSK223
CAS:<p>GSK223 is an iE-DAP-stimulated IL-8 release inhibitor via the NOD1 signaling pathway.</p>Formula:C21H18FN3O3S2Purity:98%Color and Shape:SolidMolecular weight:443.51MIP-1072
CAS:<p>MIP-1072 is the prostate-specific membrane antigen inhibitor.</p>Formula:C19H26IN3O7Purity:98%Color and Shape:SolidMolecular weight:535.33hDDAH-1-IN-1
CAS:<p>hDDAH-1-IN-1 is a selective non-amino acid catalytic site inhibitor of human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) (Ki: 18 μM).</p>Formula:C8H20N4OPurity:98%Color and Shape:SolidMolecular weight:188.27TL8-506
CAS:<p>TL8-506 is a selective and potent TLR8 agonist that induces cytokine and chemokine production.TL8-506 alleviates inflammatory and autoimmune diseases.</p>Formula:C20H17N3O2Purity:95% - 99.97%Color and Shape:SolidMolecular weight:331.37BPK-29
CAS:<p>BPK-29 disrupts NR0B1 binding and modifies C274, inhibiting growth in KEAP1-mutant cancers.</p>Formula:C26H32ClN3O3Purity:98%Color and Shape:SolidMolecular weight:4703-OH-Kynurenamine dihydroiodide
CAS:<p>3-OH-Kynurenamine dihydroiodide, the dihydroiodide form of 3-OH-Kynurenamine, functions as an activator of the aryl hydrocarbon receptor (AhR), thereby modulating the immune response. It enhances the expression of Ido1 and Tgfb1, reducing skin inflammation in psoriasis mouse models and kidney damage in nephrotoxic lupus mouse models .</p>Formula:C9H14I2N2O2Color and Shape:SolidMolecular weight:436.03UPF-648 sodium salt
CAS:<p>UPF-648 sodium salt is an inhibitor of kynurenine 3-monooxygenase (KMO) and exhibits highly active at 1 uM (81 ± 10% KMO inhibition).</p>Formula:C11H8Cl2NaO3Purity:98%Color and Shape:SolidMolecular weight:282.07AHR-6293
CAS:<p>AHR-6293 is used to distinguishing the effect of anti-platelet aggregating drug properties and the effect of anti-inflammatory properties.</p>Formula:C15H12ClNO3Color and Shape:SolidMolecular weight:289.71QM385
CAS:<p>QM385 is a potent inhibitor of sepiapterin reductase (SPR)(IC50 of 1.49 nM).</p>Formula:C17H18F3N7O2Purity:98%Color and Shape:SolidMolecular weight:409.37Loxoprofenol-SRS tromethamine
CAS:<p>Loxoprofenol-SRS tromethamine (HR1405-01), a metabolite of Loxoprofen, is a safe IV NSAID with strong anti-inflammatory and pain relief properties.</p>Formula:C19H31NO6Color and Shape:SolidMolecular weight:369.45Avenanthramide-C methyl ester
CAS:<p>Avenanthramide-C methyl ester blocks IKK/IκB phosphorylation, inhibits NF-κB, and reduces IL-6, IL-8, MCP-1 in endothelial cells (IC50 ~40 μM).</p>Formula:C17H15NO6Color and Shape:SolidMolecular weight:329.3BSP16
CAS:<p>BSP16: potent, oral STING agonist; boosts interferon genes; promising for cancer research.</p>Formula:C16H18O5SeColor and Shape:SolidMolecular weight:369.27NPD926
CAS:<p>NPD926 is an inducer of cancel cell death.</p>Formula:C29H35ClN2O2Color and Shape:SolidMolecular weight:479.05ML388
CAS:<p>ML388 is an inhibitor of human NAD(+)- dependent 15- hydroxyprostaglandin dehydrogenase.</p>Formula:C20H24N4Purity:98%Color and Shape:SolidMolecular weight:320.43TML-6
CAS:<p>TML-6, an oral derivative of curcumin, may help in Alzheimer's research by targeting amyloid production and various molecular pathways.</p>Formula:C30H37NO7Purity:99.71%Color and Shape:SolidMolecular weight:523.62MIF-IN-4 hydrochloride
CAS:<p>MIF-IN-4 hydrochloride inhibits MIF, a cytokine; has pIC50 of 5.01-6, affecting macrophage movement.</p>Formula:C26H29ClN6O2Color and Shape:SolidMolecular weight:493.01546C88
CAS:<p>546C88 is an inhibitor of nitric oxide synthase.</p>Formula:C7H17ClN4O2Purity:98%Color and Shape:SolidMolecular weight:224.69AXC-715 trihydrochloride
CAS:<p>AXC-715 trihydrochloride is a TLR7/8 agonist used to make PD-L1 adjuvanted antibody immunocouplings.</p>Formula:C18H28Cl3N5Purity:99.74%Color and Shape:SolidMolecular weight:420.81COX-2-IN-17
CAS:<p>COX-2-IN-17 is a potent, blood-brain barrier permeable COX-2 (cyclooxygenase-2) inhibitor (IC50: 0.02 μM) with anti-inflammatory and analgesic activity.</p>Formula:C20H23ClN6O2Color and Shape:SolidMolecular weight:414.89Etoricoxib HCl
CAS:<p>Etoricoxib HCl is a synthetic NSAID that inhibits COX-2, blocking prostaglandin production.</p>Formula:C18H16Cl2N2O2SColor and Shape:SolidMolecular weight:395.30ABD-350
CAS:<p>ABD-350 is ligand-induced inhibitor of nuclear factor kappaB phosphorylation.</p>Formula:C19H22F2O2Color and Shape:SolidMolecular weight:320.37L-Nabe
CAS:<p>L-Nabe (H-Arg(NO2)-Obzl) is a effective irreversible endothelium dependent relaxation inhibitor.</p>Formula:C13H19N5O4Purity:98.03%Color and Shape:SolidMolecular weight:309.32(R)-MALT1-IN-3
CAS:<p>(R)-MALT1-IN-3 (121) inhibits MALT1 protease (IC50: 20 nM) and IL6/IL10 in OCI-LY3 (IC50: 60/40 nM).</p>Formula:C21H19F3N8O2Color and Shape:SolidMolecular weight:472.42AI-3
CAS:<p>Nrf2/Keap1 and Keap1/Cul3 interaction inhibitor</p>Formula:C11H13ClO3S2Purity:98%Color and Shape:SolidMolecular weight:292.8Phox-I1
CAS:<p>Phox-I1 is a NOX2 inhibitor targeting the interactive site of p67phox with Rac GTPase.</p>Formula:C23H19N3O4Purity:98%Color and Shape:SolidMolecular weight:401.41Avanafil dibesylate
CAS:<p>Avanafil dibesylate is a PDE5 inhibitor.</p>Formula:C35H38ClN7O9S2Color and Shape:SolidMolecular weight:800.3K-80001
CAS:<p>K-80001 is a selective RXRα ligand and a COX-1/2 inhibitor, exhibiting IC50 values of 82.9μM for RXRα, 3.4μM for COX-1, and 1.2μM for COX-2, respectively [1].</p>Formula:C20H17FO2Color and Shape:SolidMolecular weight:308.35IMD-ferulic
<p>IMD-ferulic, a compound that forms covalent bonds, acts as an NF-κB modulator, enhancing the adjuvanticity of small molecule immune potentiators.</p>Formula:C36H41N7O4Color and Shape:SolidMolecular weight:635.76NCX 466
CAS:<p>cyclooxygenase (COX)-inhibiting nitric oxide (NO) donor</p>Formula:C20H24N2O9Purity:98%Color and Shape:SolidMolecular weight:436.41hDDAH-1-IN-1 TFA
CAS:<p>hDDAH-1-IN-1 TFA is a selective non-amino acid catalytic site inhibitor of human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) (Ki: 18 μM).</p>Formula:C12H22F6N4O5Purity:98%Color and Shape:SolidMolecular weight:416.32MIF-IN-5
CAS:<p>MIF-IN-5: reversible MIF inhibitor, IC50 4.8 μM, Ki 3.3 μM.</p>Formula:C18H14FN5O2Color and Shape:SolidMolecular weight:351.33COX-2-IN-26
CAS:<p>COX-2-IN-26: Oral, selective COX-2 inhibitor, low IC50s; anti-inflammatory with GI safety.</p>Formula:C23H21N7OS3Color and Shape:SolidMolecular weight:507.65AZD5718
CAS:<p>AZD5718: potent FLAP inhibitor (IC50=2.0 nM), treats Coronary Artery Disease, >90% leukotriene suppression, safe in animal studies, in phase 2a trial.</p>Formula:C29H34N6O4Color and Shape:SolidMolecular weight:530.62CYPMPO
CAS:<p>CYPMPO traps hydroxyl/superoxide radicals; decays in UV/H2O2 (15min) & hypoxanthine/xanthine (51min); outperforms DEPMPO in stability & shelf-life.</p>Formula:C10H18NO4PColor and Shape:SolidMolecular weight:247.23MHY884
CAS:<p>MHY884 inhibits tyrosinase and UVB-triggered NF-κB activation by reducing oxidative stress.</p>Formula:C15H14ClNO3SPurity:98%Color and Shape:SolidMolecular weight:323.79Interleukin 1β
CAS:<p>Interleukin 1beta is a bioactive chemical.</p>Formula:C15H28N4O5Purity:98%Color and Shape:SolidMolecular weight:344.41IACS-8803
CAS:<p>IACS-8803 is a potent cyclic dinucleotide STING agonist that exhibits strong systemic antitumor efficacy.</p>Formula:C20H23FN10O9P2S2Purity:98%Color and Shape:SolidMolecular weight:692.53Heme Oxygenase-1-IN-1 hydrochloride
CAS:<p>HO-1-IN-1 hydrochloride is a heme oxygenase 1 (HO-1) inhibitor (IC50: 250 nM).</p>Formula:C13H16BrClN2Color and Shape:SolidMolecular weight:315.64MIF-IN-6
CAS:<p>MIF-IN-6 is a potent MIF inhibitor with IC50 1.4 μM, Ki 0.96 μM, and hinders A549 cell growth.</p>Formula:C18H13ClFN5O2Color and Shape:SolidMolecular weight:385.78PC407-ws
CAS:<p>PC407-ws is a water-soluble novel COX-2 inhibitor.</p>Formula:C24H18F3N3Na2O5SPurity:98%Color and Shape:SolidMolecular weight:563.46Isocyclosporin A
CAS:<p>Isocyclosporin A is a rearranged degradation product. It is formed by acid treatment of cyclosporin A under aqueous and non-aqueous conditions.</p>Formula:C62H111N11O12Color and Shape:SolidMolecular weight:1202.61ND-2110
CAS:<p>ND-2110, a selective interleukin-1 receptor-associated kinase 4 inhibitors, is used for the treatment of autoimmune disorders and lymphoid malignancy.</p>Formula:C21H28N4O3SColor and Shape:SolidMolecular weight:416.54COX/5-LOX-IN-1
CAS:<p>Compound 6b is a potent dual inhibitor of COX/5-LOX with IC50s: 1.07μM (COX-1), 0.55μM (COX-2), 0.28μM (5-LOX) for inflammation research.</p>Formula:C18H30O3Color and Shape:SolidMolecular weight:294.43WIN 54954
CAS:<p>WIN 54954 is an orally available antiviral agent that inhibits Coxsackievirus and may be used in the study of small ribonucleic acid virus infections.</p>Formula:C18H20Cl2N2O3Purity:98.98%Color and Shape:SolidMolecular weight:383.27NOD2 antagonist 1
CAS:<p>NOD2 antagonist 1 (compound 32): Selective, effective (IC50: 5.23μM), blocks MDP-induced IL-8 in THP-1, IL-6/IL-10/TNF-α in PBMCs.</p>Formula:C26H26N4O3SColor and Shape:SolidMolecular weight:474.57Propoxur
CAS:<p>Propoxur: an insecticide causing temporary cholinergic effects in humans; chronic exposure leads to health issues; carcinogenicity unclassified by EPA.</p>Formula:C11H15NO3Purity:99.84% - 99.87%Color and Shape:Minute Crystals (Niosh 2016)Molecular weight:209.24Pifoxime
CAS:<p>Pifoxime: a NSAID with COX-1/2 inhibition, used in anti-inflammatory treatment and neuropsychiatric studies.</p>Formula:C15H20N2O3Color and Shape:SolidMolecular weight:276.33COX-2/5-LOX-IN-3
CAS:<p>COX-2/5-LOX-IN-3 inhibits COX-2/5-LOX with IC50s: COX-1 45.73μM, COX-2 5.45μM, 5-LOX 4.33μM; promising for inflammation research.</p>Formula:C17H16ClN3O2SColor and Shape:SolidMolecular weight:361.85Indolokine A5
CAS:<p>Indolokine A5, a catabolite of L-cysteine, is a potent AhR agonist .</p>Formula:C13H8N2O3SColor and Shape:SolidMolecular weight:272.28Isonixin
CAS:<p>Isonixin is used for the treatment of inflammation and pain associated with musculoskeletal and joint disorders.</p>Formula:C14H14N2O2Purity:98%Color and Shape:SolidMolecular weight:242.27AR-C 102222
CAS:<p>AR-C 102222 is an iNOS inhibitor.</p>Formula:C19H16F2N6OPurity:98%Color and Shape:SolidMolecular weight:382.37Bifenazate
CAS:<p>Bifenazate is a positive allosteric modulator of GABA receptor. Bifenazate is an acaricide that controls 100% of mites at a concentration of 25 ppm.</p>Formula:C17H20N2O3Purity:99.62%Color and Shape:Solid CrystallineMolecular weight:300.35Simvastatin acid calcium hydrate
CAS:<p>Simvastatin (Tenivastatin) calcium hydrate is an oral HMG-CoA reductase inhibitor that reduces ROS by blocking indoxyl sulfate.</p>Formula:C25H40O6Color and Shape:SolidMolecular weight:436.28249Tenosal
CAS:<p>Tenosal obtained by esterifying salicylic acid with 2-thiophene-carboxylic acid, and with analgesic and antipyretic properties, anti-inflammatory.</p>Formula:C12H8O4SPurity:98%Color and Shape:SolidMolecular weight:248.25Anti-inflammatory agent 1
CAS:<p>Anti-inflammatory agent 1 is an anti-inflammatory compound.</p>Formula:C17H16O3SPurity:98%Color and Shape:SolidMolecular weight:300.37MK-28
CAS:<p>MK-28 is a PERK agonist that reduces toxicity in a Huntington's disease model.MK-28 has a significant killing effect on MK28 gastric cancer cells.</p>Formula:C24H20N4O2Color and Shape:SolidMolecular weight:396.44B022
CAS:<p>B022 is an NF-κB-induced kinase (NIK) inhibitor that protects the liver from inflammation and injury caused by oxidative stress and toxins.</p>Formula:C19H16ClN5OSPurity:99.74%Color and Shape:SolidMolecular weight:397.88Imeglimin
CAS:<p>Imeglimin: first oral antidiabetic in its class, targets liver, muscle, & pancreatic β-cells for type 2 diabetes.</p>Formula:C6H13N5Purity:98.97%Color and Shape:SolidMolecular weight:155.2ER-34122
CAS:<p>ER-34122, a novel orally available dual 5-lipoxygenase/cyclooxygenase inhibitor with potent anti-inflammatory activity.</p>Formula:C27H26ClN3O5Purity:>99.99%Color and Shape:SolidMolecular weight:507.96YM-53403
CAS:<p>YM-53403: Antiviral that combats both RSV subgroup A/B, treats respiratory infections.</p>Formula:C36H29N3O3SPurity:98.49% - 98.85%Color and Shape:SolidMolecular weight:583.7CDDO-EA
CAS:<p>CDDO-EA (CDDO ethyl amide) is an activator of the Nrf2/antioxidant response element.</p>Formula:C33H46N2O3Purity:99.66%Color and Shape:SolidMolecular weight:518.73RIG012
CAS:<p>RIG012 is a potent RIG-I inhibitor with an IC50 value of 0.71 μM measured by NADH-coupled ATPase.RIG012 inhibited the expression of IFN-β and ISG hRsad2.</p>Formula:C23H21NO3Purity:99.53%Color and Shape:SolidMolecular weight:359.42ABI-1968
CAS:<p>ABI-1968 has antiviral and antitumor activity and can be used to study immune system diseases.</p>Formula:C35H58N5O6PPurity:98.54%Color and Shape:SolidMolecular weight:675.839Totrombopag
CAS:<p>Totrombopag (SB559448) is a candidate compound for action on RSV polymerase.</p>Formula:C25H22N8O2Purity:99.50%Color and Shape:SolidMolecular weight:466.49DDG-39
CAS:<p>DDG-39 (1-(2,3-dideoxy-2-fluoropentofuranosyl)cytosine) possesses antiviral activity with potent and selective anti-HIV-1 and HBV activity in cell culture.</p>Formula:C9H12FN3O3Purity:99.81% - >99.99%Color and Shape:SolidMolecular weight:229.21SC-75416
CAS:<p>SC-75416, a cyclooxygenase-2 (COX-2) inhibitor, is used potentially for the treatment of postoperative inflammation.</p>Formula:C15H14ClF3O3Purity:98.67% - 98.67%Color and Shape:SolidMolecular weight:334.72NFATc1-IN-1
CAS:<p>NFATc1-IN-1 (A04) inhibits RANKL-induced osteoclast formation with 1.57 μM IC50, blocking NFATc1 translocation.</p>Formula:C13H8F2INO2Purity:99.64%Color and Shape:SolidMolecular weight:375.11Selnoflast
CAS:<p>Selnoflast (RO-7486967) is an orally active, potent and selective NLRP3 inhibitor for the study of coronary arteries and ulcerative colitis.</p>Formula:C20H29N3O3SPurity:98.54% - 99.66%Color and Shape:SolidMolecular weight:391.53NLRP3/AIM2-IN-2
CAS:<p>NLRP3/AIM2-IN-2, potent species-specific NLRP3 and AIM2 inflammasome pyroptosis inhibitor; IC50 = 0.2392 ± 0.0233 μM.</p>Formula:C15H15NO3Purity:99.67%Color and Shape:SolidMolecular weight:257.28LMT-28
CAS:<p>LMT-28 is an inhibitor of IL-6 and selectively inhibits IL-6-induced phosphorylation of gp130, STAT3, and JAK2.</p>Formula:C17H29NO4Purity:99.88%Color and Shape:SolidMolecular weight:311.42Rabeximod
CAS:<p>Rabeximod, an immunomodulator, eases autoimmune diseases, inhibits arthritis, and aids brain recovery post-injury by blocking inflammation.</p>Formula:C22H24ClN5OPurity:99.99%Color and Shape:SolidMolecular weight:409.91NLRP3-IN-10
CAS:<p>NLRP3-IN-10 (ZVN26391) is a strong NLRP3 inhibitor, IC50 251.1 nM, that reduces IL-1β and ASC speck, hindering inflammasome activation.</p>Formula:C17H14BrFO3Purity:99.06%Color and Shape:SolidMolecular weight:365.19Desmosterol
CAS:<p>Desmosterol (24-Dehydrocholesterol) is a cholesterol biosynthesis intermediate that inhibits macrophage inflammatory vesicle activation .</p>Formula:C27H44OPurity:>99.99%Color and Shape:SolidMolecular weight:384.64IQP-0528
CAS:<p>IQP-0528: Potent NNRTI, blocks HIV entry, microbicidal gel, EC50: 0.2 nM for HIV-1, 100 nM for HIV-2.</p>Formula:C20H24N2O3Purity:98.36% - >99.99%Color and Shape:SolidMolecular weight:340.42BIT225
CAS:<p>BIT225 is an HIV-1 Vpu inhibitor with antiviral activity that inhibits HIV-1 replication in myeloid dendritic cells.</p>Formula:C16H15N5OPurity:98.8%Color and Shape:SolidMolecular weight:293.32FK-330
CAS:<p>FK-330 (FR-260330) is a novel nitric oxide synthase inhibitor that prevents ischemia and reperfusion injury in rat liver transplantation.</p>Formula:C29H28ClF3N6O4Purity:99.95%Color and Shape:SolidMolecular weight:617.02R 61837
CAS:<p>R 61837 is a novel rhinovirus inhibitor, a substituted phenylpyridazinamine, with antiviral activity.</p>Formula:C16H20N4OPurity:99.53%Color and Shape:SolidMolecular weight:284.36IL-4-inhibitor-1
CAS:<p>IL-4 inhibitor: Binds IL-4 (Kd=1.8 μM), blocks activity (EC50=1.81 μM), selective vs. IL-13, stops IL-4-JAK1-STAT6 in THP-1 monocytes (EC50=3.1 μM).</p>Formula:C18H12FN3O2Purity:98.78% - 99.53%Color and Shape:SolidMolecular weight:321.31BN-82451 2HCl
CAS:<p>BN-82451, a cyclooxygenase inhibitor, is used potentially for the treatment of Huntington’s disease.</p>Formula:C18H28Cl2N2OSPurity:99.84% - >99.99%Color and Shape:SolidMolecular weight:391.4F092
CAS:<p>F092 is a potent inhibitor of hematopoietic prostaglandin D synthetase (H-PGDS), which can be used to study allergic inflammation and vascular-related diseases.</p>Formula:C20H17N5O2Purity:99.63%Color and Shape:SolidMolecular weight:359.38TLR7/8-IN-1
CAS:<p>TLR7/8-IN-1, a crystalline TLR7/TLR8 inhibitor, is a valuable compound for autoimmune disease research.Cost-effective and quality-assured.</p>Formula:C29H40N8O2Purity:99.83%Color and Shape:SolidMolecular weight:532.68NDT 9513727
CAS:<p>NDT 9513727 is a potent, selective and competitive C5aR1 inverse agonist for the study of inflammatory and immune disorders.</p>Formula:C36H35N3O4Purity:99.21%Color and Shape:SolidMolecular weight:573.68LDC7559
CAS:<p>LDC7559 inhibits gasdermin D (GSDMD) by blocking neutrophil extracellular trap (NET) at late stage.</p>Formula:C20H19N3O3Purity:99.8%Color and Shape:SoildMolecular weight:349.38SM360320
CAS:<p>SM360320 (CL-087) is a selective TLR7 agonist that blocks HCV replication in hepatocytes and aids immunology research.</p>Formula:C15H17N5O3Purity:99.13%Color and Shape:SolidMolecular weight:315.33IL-2-IN-1
CAS:<p>IL-2-IN-1 is a potent inhibitor of IL-2 (IC50: 1978 nM) and exhibits anti-proliferative effects.</p>Formula:C17H12F6N4O2Purity:99.6%Color and Shape:SolidMolecular weight:418.29CMX-521
CAS:<p>CMX521: an antiviral for norovirus, effective against rotavirus; inhibits viral RNA polymerase.</p>Formula:C13H17N5O5Purity:99.57%Color and Shape:SolidMolecular weight:323.3Complement C5-IN-1
CAS:<p>Complement C5-IN-1 is a small-molecule inhibitor of complement component 5 protein (C5).</p>Formula:C24H32N2O6Purity:98.27%Color and Shape:SolidMolecular weight:444.52Zabedosertib
CAS:<p>Zabedosertib (BAY 1834845) is an inhibitor of IRAK4 with immunomodulatory potential.</p>Formula:C20H21F3N4O4SPurity:98.54%Color and Shape:SolidMolecular weight:470.47NFAT Transcription Factor Regulator-1
CAS:<p>NFAT Transcription Factor Regulator-1 is an synthesis inhibitor of IL-2 (IC50 of 182 nM).</p>Formula:C17H10F6N4O2Purity:99.90%Color and Shape:SolidMolecular weight:416.28IRAK4-IN-20
CAS:<p>IRAK4-IN-20 is a potent and orally active IRAK4 inhibitor (IC50:3.55 nM).</p>Formula:C22H25F3N4O3Purity:98.09%Color and Shape:SolidMolecular weight:450.45BBIQ
CAS:<p>BBIQ is a powerful vaccine adjuvant that enhances innate immune responses and a potent and selectively toll-like receptor 7 (TLR7) agonist with an EC50 of 59.1</p>Formula:C21H22N4Purity:99.71%Color and Shape:SolidMolecular weight:330.43BRD56491
CAS:<p>BRD56491 is a small molecule ROS enhancer and a bioprobe for the detection of cancer.</p>Formula:C20H14O2Purity:99.89%Color and Shape:SolidMolecular weight:286.32FEN1-IN-3
CAS:<p>FEN1-IN-3 is a human flap endonuclease-1 ( hFEN1 ) inhibitor that stabilizes hFEN1 with an EC 50 of 6.8 μM .</p>Formula:C15H12N2O4Purity:98.16%Color and Shape:SolidMolecular weight:284.27EIDD-2749
CAS:<p>EIDD-2749 (4'-Fluorouridine), an oral drug, inhibits RdRp, halts RSV/SARS-CoV-2 replication, and fights HCV/LCMV.</p>Formula:C9H11FN2O6Purity:97.39%Color and Shape:SolidMolecular weight:262.19HS271
CAS:<p>HS271 is a selective, highly potent and orally active IRAK4 inhibitor (IC50= 7.2 μM).</p>Formula:C21H24F3N5O2Purity:98.79%Color and Shape:SolidMolecular weight:435.44JC124
CAS:<p>JC124 is an inhibitor of NLRP3 Inflammasome and exhibits neuroprotective and anti-inflammatory activities.</p>Formula:C17H19ClN2O4SPurity:99.64%Color and Shape:SolidMolecular weight:382.86Antiviral agent 17
CAS:<p>Antiviral agent 17, EC50 0.015 μM in human assay, effective against murine norovirus, may aid infectious/malignant disease research.</p>Formula:C11H14N4O4Purity:99.89%Color and Shape:SolidMolecular weight:266.25Zharp2-1
CAS:<p>Zharp2-1 is a RIPK2 inhibitor that alleviates MDP-induced peritonitis symptoms in mice and can be used to study inflammatory bowel disease (IBD).</p>Formula:C19H18N3O2PSPurity:99.41%Color and Shape:SolidMolecular weight:383.4Rufigallol
CAS:<p>Rufigallol, an anthraquinone with six OH groups, induces DLC and fluoresces when aggregated, showing antimalarial effects with vitamin C and ketones.</p>Formula:C14H8O8Purity:98.92% - 99.27%Color and Shape:SolidMolecular weight:304.21T6167923
CAS:<p>T6167923 inhibits MyD88 signaling, binds TIR domain, blocks dimer formation, lowers SEAP activity, and has anti-inflammatory IC50s ~2.7 μM.</p>Formula:C17H20BrN3O3S2Purity:99.28%Color and Shape:SolidMolecular weight:458.39Azalanstat
CAS:<p>Azalanstat (RS 21607) is a mammalian lanosterol 14-alpha-demethylase inhibitor with hypocholesterolemic activity.</p>Formula:C22H24ClN3O2SPurity:99.41% - 99.85%Color and Shape:SolidMolecular weight:429.96M62812
CAS:<p>TLR4 inhibitor blocks LPS-induced NF-κB (IC50=2.4μg/mL), cytokines in PBMCs/HUVECs, and extends life in septic shock mice.</p>Formula:C13H13Cl2N3OSPurity:99.07%Color and Shape:SolidMolecular weight:330.23Dersalazine
CAS:<p>Dersalazine, a PAF inhibitor, reduces IL-17 to treat colitis in rodents, potentially aiding ulcerative colitis patients.</p>Formula:C35H32N6O4Purity:99.62%Color and Shape:SolidMolecular weight:600.67NO-prednisolone
CAS:<p>NO-prednisolone (NCX-1015) is a compound that effectively stimulates the production of IL-10 in vivo.</p>Formula:C29H33NO9Purity:98.65%Color and Shape:SolidMolecular weight:539.57ABT-963
CAS:<p>ABT-963: COX-2 inhibitor for osteoarthritis/pain with high selectivity, potency, and gastric safety.</p>Formula:C22H22F2N2O5SPurity:98% - 99.85%Color and Shape:SolidMolecular weight:464.48RIPK1-IN-9
CAS:<p>RIPK1-IN-9, a potent dihydronaphthone, selectively inhibits RIPK1 with IC50 of 2 nM (U937) and 1.3 nM (L929).</p>Formula:C26H25FN6O2Purity:99.85%Color and Shape:SolidMolecular weight:472.51AHR antagonist 2
CAS:<p>AHR antagonist 2 is an antagonist of the aryl hydrocarbon receptor. The IC50s for human AHR and mouse AHR are 0.885 and 2.03 nM, respectively.</p>Formula:C20H17F3N4O3Purity:99.38%Color and Shape:SolidMolecular weight:418.37C3a Receptor Agonist
CAS:<p>C3a Receptor Agonist activates C3aRs, inhibits neutrophil mobilization in ischemia, and promotes neural progenitor differentiation.</p>Formula:C27H35N3O2Purity:99.76%Color and Shape:SolidMolecular weight:433.59SP-100030
CAS:<p>SP-100030: Strong NF-κB/AP-1 inhibitor, IC50=50 nM. Reduces IL-2, IL-8, TNF-alpha, and murine CIA.</p>Formula:C14H5ClF9N3OPurity:99.79%Color and Shape:SolidMolecular weight:437.65Ezurpimtrostat hydrochloride
CAS:<p>Ethacrysta hydrochloride (GNS561 hydrochloride) is a PPT1 inhibitor with antifibrotic properties and may be used in studies of hepatocellular carcinoma.</p>Formula:C25H32Cl2N4Purity:99.84%Color and Shape:SolidMolecular weight:459.45Letosteine
CAS:<p>Letosteine, an oral expectorant, treats acute/chronic respiratory diseases by dissolving mucus and reducing inflammation.</p>Formula:C10H17NO4S2Purity:96.03%Color and Shape:SolidMolecular weight:279.38Thiodigalactoside
CAS:<p>Thiodigalactoside (TDG), a non-metabolizable disaccharide, serves as an orally active, potent galectin (GAL) inhibitor, exhibiting Kd values of 24 μM and 49 μM</p>Formula:C12H22O10SPurity:99.90%Color and Shape:SolidMolecular weight:358.36Biofor 389
CAS:<p>Biofor 389 (BF389) has anti-inflammatory activity and can be used to study arthritis.</p>Formula:C20H29NO3Purity:98.84% - 99.97%Color and Shape:SolidMolecular weight:331.45h-NTPDase8-IN-1
CAS:<p>h-NTPDase8-IN-1 is a specific aminosulfonylbenzamide inhibitor of h-NTPDases8, which can be used to study diseases caused by aberrant h-NTPDase expression.</p>Formula:C10H10ClNO4SPurity:98.78% - 99.59%Color and Shape:SolidMolecular weight:275.71Rociclovir
CAS:<p>Rociclovir has antiviral activity and is used to treat viral infections.</p>Formula:C15H25N5O3Purity:99.19%Color and Shape:SolidMolecular weight:323.39EG00229
CAS:<p>EG00229 blocks VEGF-A/NRP1 binding, IC50 of 3 μM; doesn't affect VEGFR-1/2. It's an NRP1 antagonist.</p>Formula:C19H20F3N7O7S3Purity:98.23%Color and Shape:SolidMolecular weight:611.6GSK2983559 free acid
CAS:<p>GSK2983559 free acid selectively inhibits RIP2, reducing inflammatory cytokines in human bowel disease.</p>Formula:C21H23N4O7PS2Purity:97.8700% - 98.61%Color and Shape:SolidMolecular weight:538.53Phox-I2
CAS:<p>Phox-I2 is an NOX2-specific inhibitor. Phox-I2 reverts ROS-accumulation and leads to refusion of mitochondrial networks.</p>Formula:C18H15N3O4Purity:99.73%Color and Shape:SolidMolecular weight:337.33Resiniferatoxin
CAS:<p>Resiniferatoxin ((+)-Resiniferatoxin) is a highly potent synthetic TRPV1 agonist.Cost-effective and quality-assured.</p>Formula:C37H40O9Purity:93.08% - 99.34%Color and Shape:SolidMolecular weight:628.71CPS-11
CAS:<p>CPS-11, a Thalidomide analogue, shows potent, broad antitumor activity, especially in multiple myeloma cells.</p>Formula:C14H12N2O5Purity:99.8% - 99.98%Color and Shape:SolidMolecular weight:288.26Cindunistat
CAS:<p>Cindunistat (free base) is an orally available selective iNOS inhibitor for the study of arthritis.</p>Formula:C8H17N3O2SPurity:99% - >99.99%Color and Shape:SolidMolecular weight:219.3Sonlicromanol hydrochloride
CAS:<p>Sonlicromanol hydrochloride (KH176 hydrochloride) is a ROS-redox modulator used in the treatment of mitochondrial diseases.</p>Formula:C19H29ClN2O3Purity:99.53%Color and Shape:SolidMolecular weight:368.9CT-2584
CAS:<p>CT-2584: angiogenesis & lysophosphatidic acid transferase inhibitor; alters phospholipid synthesis, increasing PI in tumor cells.</p>Formula:C30H55N5O3Purity:97.68% - 99.77%Color and Shape:SolidMolecular weight:533.79CPG-52364
CAS:<p>CPG-52364 is a small molecule compound that interacts between an endosomal TLR and its ligand and is a candidate for the treatment of psoriasis.</p>Formula:C27H36N6O3Purity:99.99%Color and Shape:SolidMolecular weight:492.61APX-115
CAS:<p>APX-115 (Ewha-18278) (Ewha-18278) is a potent, orally active pan NADPH oxidase (Nox) inhibitor (Kis: 1.08 μM, 0.57 μM, and 0.63 μM for Nox1, Nox2, and Nox4).</p>Formula:C17H18ClN3OPurity:98.62%Color and Shape:SolidMolecular weight:315.8AT791
CAS:<p>AT791 is an orally available TLR7 and TLR9 inhibitor, suppressing TLR7 and TLR9 signaling, used in autoimmune lupus research.</p>Formula:C23H31N3O3Purity:99.88%Color and Shape:SolidMolecular weight:397.51Epetirimod
CAS:<p>Epetirimod (S-30563) is a small molecule immunomodulator with antitumor and anti-infective activity for the study of papillomavirus infections.</p>Formula:C13H15N5Purity:99.08% - 99.53%Color and Shape:SolidMolecular weight:241.29
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