Immunologie et Inflammation
Les inhibiteurs en immunologie et inflammation sont des composés qui modulent la réponse immunitaire et les processus inflammatoires. Ces inhibiteurs sont cruciaux pour étudier les mécanismes de la régulation immunitaire, l'auto-immunité et l'inflammation chronique, ainsi que pour développer des traitements pour les maladies inflammatoires, les allergies et les troubles immunitaires. En ciblant des voies clés du système immunitaire, ces inhibiteurs peuvent aider à réduire les réponses immunitaires excessives ou inappropriées. Chez CymitQuimica, nous offrons une large sélection d'inhibiteurs de haute qualité en immunologie et inflammation pour soutenir vos recherches en immunologie, inflammation et développement thérapeutique.
Sous-catégories appartenant à la catégorie "Immunologie et Inflammation"
- RCC(136 produits)
- CXCR(147 produits)
- Paroi cellulaire(5 produits)
- Récepteur IL(113 produits)
- IκB/IKK(61 produits)
- LTR(3 produits)
- MALT(23 produits)
- MRP(6 produits)
- NADPH-oxydase(1 produits)
- NF-κB(445 produits)
- NOD(17 produits)
- NOS(63 produits)
- Nrf2(78 produits)
- PGE Synthase(31 produits)
- ROS(69 produits)
- TGF-beta/Smad(58 produits)
- TLR(66 produits)
- Thioredoxine(12 produits)
- gp120/CD4(4 produits)
Affichez 11 plus de sous-catégories
3035 produits trouvés pour "Immunologie et Inflammation"
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Emlenoflast
CAS :<p>Emlenoflast (MCC7840) is a selective inhibitor of NLRP3 inflammasome.</p>Formule :C19H24N4O3SDegré de pureté :97.004% - 98.19%Couleur et forme :SolidMasse moléculaire :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>Formule :C21H19F3N8O2Couleur et forme :SolidMasse moléculaire :472.42Edasalonexent
CAS :<p>Edasalonexent (CAT-1004) is an orally available NF-κB inhibitor for the improvement of Duchenne muscular dystrophy.</p>Formule :C31H42N2O3Degré de pureté :99.13% - >99.99%Couleur et forme :SolidMasse moléculaire :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>Formule :C19H24N4NaO3SCouleur et forme :SolidMasse moléculaire :411.47MK-0703
CAS :<p>MK-0703 is a selective cyclooxygenase-2 inhibitor.</p>Formule :C17H22O5SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :338.42Bay 65-1942 hydrochloride
CAS :<p>Bay 65-1942 hydrochloride is an inhibitor of ATP-competitive and selective IKKβ.</p>Formule :C22H26ClN3O4Couleur et forme :SolidMasse moléculaire :431.91Insulin levels modulator
CAS :<p>Insulin level regulators can be used to treat diabetes.</p>Formule :C21H23N7OSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C14H10ClN3O4S2Couleur et forme :SolidMasse moléculaire :383.83IKKβ-IN-1
CAS :<p>IKKβ-IN-1 is a potent, orally active inhibitor of IkappaB (IKK-β) (IC50: 0.20 μM).</p>Formule :C31H30N4O4SCouleur et forme :SolidMasse moléculaire :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>Formule :C20H15N5O3SCouleur et forme :SolidMasse moléculaire :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>Formule :C28H28FN7O2Couleur et forme :SolidMasse moléculaire :513.57MitoB
CAS :<p>MitoB is a novel exon of mitochondrial hydrogen peroxide.</p>Formule :C25H23BBrO2PCouleur et forme :SolidMasse moléculaire :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>Formule :C26H42O10Couleur et forme :SolidMasse moléculaire :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>Formule :C14H18N4O5SCouleur et forme :SolidMasse moléculaire :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>Formule :C21H21N7S3Couleur et forme :SolidMasse moléculaire :467.63Clopirac
CAS :<p>Clopirac is a potent and orally active prostaglandin synthetase inhibitor that is an anti-inflammatory agent [1].</p>Formule :C14H14ClNO2Couleur et forme :SolidMasse moléculaire :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>Formule :C15H18O3Couleur et forme :SolidMasse moléculaire :246.3Gue1654
CAS :<p>Gue1654 is an OXE-R inhibitor and cardiomyocyte apoptosis.Gue1654 can be used for the study of cardiovascular diseases.</p>Formule :C23H17N3OS3Degré de pureté :98.02% - 98.04%Couleur et forme :SolidMasse moléculaire :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>Formule :C17H13F2NO3Degré de pureté :99.87%Couleur et forme :SolidMasse moléculaire :317.29Methyl aminolevulinate
CAS :<p>Methyl aminolevulinate, a prodrug for protoporphyrin IX, sensitizes in PDT.</p>Formule :C6H11NO3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C8H16O2S2Degré de pureté :97.51%Couleur et forme :Yellow To Orange LiquidMasse moléculaire :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>Formule :C25H22N8O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C17H15Cl2N9O2Couleur et forme :SolidMasse moléculaire :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>Formule :C18H19N3O3S2Couleur et forme :SolidMasse moléculaire :389.49MD13
<p>MD13 is a macrophage migration inhibitor (MIF) oriented PROTAC (Ki value: 71 nM). MD13 can be used to study cancer.</p>Couleur et forme :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>Formule :C13H22INO2SDegré de pureté :98.52% - 99.16%Couleur et forme :SolidMasse moléculaire :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>Formule :C11H14FN2O6PSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :352.28Mercaptoethylguanidine (MEG) (dihydrobromide)
CAS :<p>MEG dihydrobromide inhibits inducible nitric oxide synthase and scavenges peroxynitrite, potentially aiding in inflammatory bowel disease studies.</p>Formule :C3H11Br2N3SCouleur et forme :SolidMasse moléculaire :281.01AL-8417
CAS :<p>AL-8417 is an enzyme inhibitor with antioxidant, anti-inflammatory, and cytostatic properties; prevents vitrectomy-induced lens alterations.</p>Formule :C29H34O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :462.58IRAK inhibitor 4
CAS :<p>IRAK inhibitor 4 is an interleukin-1 receptor associated kinase 4 inhibitor.</p>Formule :C33H35F3N6O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :620.66L-NIL hydrochloride
CAS :<p>selective inhibitor of inducible nitric oxide synthase</p>Formule :C8H18ClN3O2Degré de pureté :98%Couleur et forme :White To Off-White SolidMasse moléculaire :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>Formule :C17H20F2N8OCouleur et forme :SolidMasse moléculaire :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>Formule :C17H13ClN4O2Couleur et forme :SolidMasse moléculaire :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>Formule :C16H15NO2Couleur et forme :SolidMasse moléculaire :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>Formule :C22H19N3O5S2Degré de pureté :98.42%Couleur et forme :SolidMasse moléculaire :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>Formule :C20H24N10O14P2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :690.41AMT hydrochloride
CAS :<p>AMT hydrochloride is an iNOS inhibitor.</p>Formule :C5H11ClN2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :166.67Mivotilate
CAS :<p>Mivotilate, a potent, non-toxic aryl hydrocarbon receptor (AhR) activator, functions as a hepatoprotective agent.</p>Formule :C12H14N2O3S3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :330.45AR-C102222 hydrochloride
CAS :<p>AR-C102222 hydrochloride: oral iNOS inhibitor, selective, IC50=37 nM, with anti-inflammatory and pain relief effects.</p>Formule :C19H17ClF2N6ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C17H28BN3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C29H34N2O15Couleur et forme :SolidMasse moléculaire :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>Formule :C20H21Cl2N7O3Couleur et forme :SolidMasse moléculaire :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>Formule :C12H12OS3Couleur et forme :SolidMasse moléculaire :268.42Carpro-AM1
CAS :<p>Carpro-AM1, dual FAAH/COX inhibitor, IC50: 94 nM.</p>Formule :C21H18ClN3OCouleur et forme :SolidMasse moléculaire :363.84ASP-6537
CAS :<p>ASP-6537 is a selective and reversible inhibitor of cyclooxygenase-1.</p>Formule :C17H17N3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C11H10IN5O2Couleur et forme :SolidMasse moléculaire :371.13PD 127443
CAS :<p>PD 127443 is a Leukotriene B4 antagonist, it is also a dual inhibitor of cyclooxygenase and 5-lipoxygenase.</p>Formule :C20H28N2OCouleur et forme :SolidMasse moléculaire :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>Formule :C27H29N5O4Degré de pureté :98.07%Couleur et forme :SolidMasse moléculaire :487.55Vidarabine phosphate
CAS :<p>Vidarabine phosphate is an adenosine monophosphate analog.</p>Formule :C10H14N5O7PDegré de pureté :99.75%Couleur et forme :White Crystalline PowderMasse moléculaire :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>Formule :C10H10O3Degré de pureté :100%Couleur et forme :SolidMasse moléculaire :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>Formule :C35H35N5O8Couleur et forme :SolidMasse moléculaire :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>Formule :C18H16O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :312.32Naphazoline
CAS :<p>Naphazoline (Naphcon-a) is a sympathomimetic compound with marked alpha adrenergic activity.</p>Formule :C14H14N2Degré de pureté :99.79%Couleur et forme :White Crystalline Powder SolidMasse moléculaire :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>Formule :C21H30O4Couleur et forme :SolidMasse moléculaire :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>Formule :C9H20N4O4Degré de pureté :99.72% - 99.8%Couleur et forme :White To Off-White SolidMasse moléculaire :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>Formule :C12H11N3O2SDegré de pureté :>99.99%Couleur et forme :SolidMasse moléculaire :261.3IL-17A modulator-3
CAS :<p>IL-17A modulator-3 inhibits IL-17A/A, IC50 <10 μM, for inflammation, cancer, autoimmune research.</p>Formule :C34H50FN7O4Couleur et forme :SolidMasse moléculaire :639.8APY0201
CAS :<p>APY0201: potent, specific ATP-competitive PIKfyve inhibitor; IC50=5.2 nM; blocks PtdIns3P to PtdIns(3,5)P2 conversion.</p>Formule :C23H23N7ODegré de pureté :98% - 99.74%Couleur et forme :SolidMasse moléculaire :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>Formule :C21H17N3O2S3Degré de pureté :98.49%Couleur et forme :SolidMasse moléculaire :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>Formule :C17H20O5SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C17H19F3N4O5SCouleur et forme :SolidMasse moléculaire :448.42L 669083
CAS :<p>L 669083 is two classes of potent leukotriene biosynthesis inhibitors photoaffinity analogue.</p>Formule :C29H29IN4O5SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :672.54LY 150310
CAS :<p>LY 150310, a histamine H1-receptor antagonist, can alter prostanoid concentrations in vitro and in vivo.</p>Formule :C13H14N2Couleur et forme :SolidMasse moléculaire :198.26Fagaramide
CAS :<p>Fagaramide possesses Antiplasmodial activity.</p>Formule :C14H17NO3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :247.29NCX-6560
CAS :<p>NCX-6560 is a novel NO-releasing derivative of atorvastatin, with those of atorvastatin.</p>Formule :C37H42FN3O8Couleur et forme :SolidMasse moléculaire :675.74ZXX2-77
CAS :<p>ZXX2-77 is a cyclooxygenase-1 inhibitor.</p>Formule :C13H13ClN2O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :296.77Tiazotic acid
CAS :<p>Tiazotic acid is an agent with the activity of antioxidant.</p>Formule :C5H7N3O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :173.19L 748780
CAS :<p>L 748780 is a selective inducible COX-2 inhibitor.</p>Formule :C19H14Cl3NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :426.68Oxyfenamate
CAS :<p>Oxyfenamate has anti-anxiety actions. It is also used in anxiety neuroses.</p>Formule :C11H15NO3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :209.24Anisodine hydrobromide
CAS :<p>Anisodine hydrobromide is an inhibitor of adenosine kinase.</p>Formule :C17H22BrNO5Couleur et forme :White Crystals Or Crystalline PowderMasse moléculaire :400.27FR20
CAS :<p>FR20 is a human microsomal prostaglandin synthase 1 (mPGES 1) inhibitor.</p>Formule :C31H25Cl2N3O2Couleur et forme :SolidMasse moléculaire :542.46LC-R 505
CAS :<p>LC-R 505 is an anti-inflammatory.</p>Formule :C20H26N2O5SCouleur et forme :SolidMasse moléculaire :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>Formule :C29H35NO9Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :541.59GSK223
CAS :<p>GSK223 is an iE-DAP-stimulated IL-8 release inhibitor via the NOD1 signaling pathway.</p>Formule :C21H18FN3O3S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :443.51MIP-1072
CAS :<p>MIP-1072 is the prostate-specific membrane antigen inhibitor.</p>Formule :C19H26IN3O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C8H20N4ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C20H17N3O2Degré de pureté :95% - 99.97%Couleur et forme :SolidMasse moléculaire :331.37BPK-29
CAS :<p>BPK-29 disrupts NR0B1 binding and modifies C274, inhibiting growth in KEAP1-mutant cancers.</p>Formule :C26H32ClN3O3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C9H14I2N2O2Couleur et forme :SolidMasse moléculaire :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>Formule :C11H8Cl2NaO3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C15H12ClNO3Couleur et forme :SolidMasse moléculaire :289.71QM385
CAS :<p>QM385 is a potent inhibitor of sepiapterin reductase (SPR)(IC50 of 1.49 nM).</p>Formule :C17H18F3N7O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C19H31NO6Couleur et forme :SolidMasse moléculaire :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>Formule :C17H15NO6Couleur et forme :SolidMasse moléculaire :329.3BSP16
CAS :<p>BSP16: potent, oral STING agonist; boosts interferon genes; promising for cancer research.</p>Formule :C16H18O5SeCouleur et forme :SolidMasse moléculaire :369.27NPD926
CAS :<p>NPD926 is an inducer of cancel cell death.</p>Formule :C29H35ClN2O2Couleur et forme :SolidMasse moléculaire :479.05ML388
CAS :<p>ML388 is an inhibitor of human NAD(+)- dependent 15- hydroxyprostaglandin dehydrogenase.</p>Formule :C20H24N4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :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>Formule :C30H37NO7Degré de pureté :99.71%Couleur et forme :SolidMasse moléculaire :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>Formule :C26H29ClN6O2Couleur et forme :SolidMasse moléculaire :493.01546C88
CAS :<p>546C88 is an inhibitor of nitric oxide synthase.</p>Formule :C7H17ClN4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :224.69AXC-715 trihydrochloride
CAS :<p>AXC-715 trihydrochloride is a TLR7/8 agonist used to make PD-L1 adjuvanted antibody immunocouplings.</p>Formule :C18H28Cl3N5Degré de pureté :99.74%Couleur et forme :SolidMasse moléculaire :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>Formule :C20H23ClN6O2Couleur et forme :SolidMasse moléculaire :414.89Etoricoxib HCl
CAS :<p>Etoricoxib HCl is a synthetic NSAID that inhibits COX-2, blocking prostaglandin production.</p>Formule :C18H16Cl2N2O2SCouleur et forme :SolidMasse moléculaire :395.30ABD-350
CAS :<p>ABD-350 is ligand-induced inhibitor of nuclear factor kappaB phosphorylation.</p>Formule :C19H22F2O2Couleur et forme :SolidMasse moléculaire :320.37L-Nabe
CAS :<p>L-Nabe (H-Arg(NO2)-Obzl) is a effective irreversible endothelium dependent relaxation inhibitor.</p>Formule :C13H19N5O4Degré de pureté :98.03%Couleur et forme :SolidMasse moléculaire :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>Formule :C21H19F3N8O2Couleur et forme :SolidMasse moléculaire :472.42AI-3
CAS :<p>Nrf2/Keap1 and Keap1/Cul3 interaction inhibitor</p>Formule :C11H13ClO3S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :292.8Phox-I1
CAS :<p>Phox-I1 is a NOX2 inhibitor targeting the interactive site of p67phox with Rac GTPase.</p>Formule :C23H19N3O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :401.41Avanafil dibesylate
CAS :<p>Avanafil dibesylate is a PDE5 inhibitor.</p>Formule :C35H38ClN7O9S2Couleur et forme :SolidMasse moléculaire :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>Formule :C20H17FO2Couleur et forme :SolidMasse moléculaire :308.35
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