Inmunología e inflamación
Los inhibidores de inmunología e inflamación son compuestos que modulan la respuesta inmunitaria y los procesos inflamatorios. Estos inhibidores son cruciales para estudiar los mecanismos de regulación inmunitaria, la autoinmunidad y la inflamación crónica, así como para desarrollar tratamientos para enfermedades inflamatorias, alergias y trastornos relacionados con el sistema inmunológico. Al dirigirse a vías clave en el sistema inmunológico, estos inhibidores pueden ayudar a reducir las respuestas inmunitarias excesivas o inadecuadas. En CymitQuimica, ofrecemos una amplia selección de inhibidores de alta calidad para apoyar su investigación en inmunología, inflamación y desarrollo terapéutico.
Subcategorías de "Inmunología e inflamación"
- CCR(136 productos)
- CXCR(148 productos)
- Pared celular(5 productos)
- Receptor de IL(112 productos)
- IκB / IKK(60 productos)
- LTR(3 productos)
- MALT(23 productos)
- MRP(6 productos)
- NADPH-oxidasa(1 productos)
- NF-κB(444 productos)
- NOD(17 productos)
- NOS(63 productos)
- Nrf2(79 productos)
- PGE sintasa(31 productos)
- ROS(69 productos)
- TGF-beta / Smad(58 productos)
- TLR(66 productos)
- Tiorredoxina(12 productos)
- gp120 / CD4(4 productos)
Mostrar 11 subcategorías más
Se han encontrado 3045 productos de "Inmunología e inflamación"
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Naproxen glucuronide
CAS:<p>Naproxen glucuronide: NSAID, propionic class, eases pain, fever, inflammation. Nonselective COX blocker.</p>Fórmula:C20H22O9Forma y color:SolidPeso molecular:406.3812(R)-HETE
CAS:<p>12(R)-HETE made in invertebrates by lipoxygenation, in mammals by 12(R)-LOs/CYP450. Mainly proinflammatory, attracts leukocytes, reduces rabbit eye pressure.</p>Fórmula:C20H32O3Forma y color:SolidPeso molecular:320.47Feprazone
CAS:<p>Feprazone (DA-2370) possesses anti-inflammatory and antiadipogenic properties. Feprazone can be used in studies about the treatment of joint and muscular pain.</p>Fórmula:C20H20N2O2Pureza:99.6% - 99.89%Forma y color:SolidPeso molecular:320.39Nexinhib20
CAS:<p>Nexinhib20 is an inhibitor of exosome synthesis and transport with anti-inflammatory activity, inhibits RAB27A and neutral sphingomyelinase 2 (nSMase2) nsMase2.</p>Fórmula:C15H16N4O3Pureza:99.89%Forma y color:SolidPeso molecular:300.31Leptospermone
CAS:<p>Leptospermone is an essential oil from Leptospermum scoparium (manuka oil).</p>Fórmula:C15H22O4Forma y color:SolidPeso molecular:266.33Dibenzo(a,i)pyrene
CAS:<p>Dibenzo(a, i)pyrene is a polycyclic aromatic hydrocarbon with potent carcinogenic activity.</p>Fórmula:C24H14Forma y color:Greenish-Yellow Needles Prisms Or Lamellae Dibenz[A I]Pyrene Is A Colorless Solid Water InsolublePeso molecular:302.37Stigmane B
<p>Stigmane B activates Nrf2, decreases apoptosis and ROS, boosts antioxidants, and is neuroprotective.</p>Fórmula:C21H30O4Forma y color:SolidPeso molecular:346.46NBC 19
CAS:<p>Potent NLRP3 inflammasome inhibitor (IC50 = 60-80 nM). Inhibits nigericin- and ATP-induced IL-1β release.</p>Fórmula:C24H26BCl3N2O2Forma y color:SolidPeso molecular:491.65BBS-4
CAS:<p>BBS-4 inhibits NOS2 dimerization (IC50: 0.49 nM), guarding mice against sepsis-related heart issues.</p>Fórmula:C22H24N6O3Forma y color:SolidPeso molecular:420.46MIF-IN-3
CAS:<p>MIF-IN-3 inhibits MIF; useful in immunoinflammation research. (WO2021258272A1, compound 31)</p>Fórmula:C20H20N4O5SForma y color:SolidPeso molecular:428.46CK-119
CAS:<p>CK-119 inhibits IL-1, blocking corneal/conjunctival cell growth by halting DNA/RNA synthesis.</p>Fórmula:C21H23ClN4O5Forma y color:SolidPeso molecular:446.88HSR1304
CAS:<p>HSR1304 (5d) inhibits NFκB, key in diseases like cancer, offering research potential.</p>Fórmula:C24H21ClN2O3Forma y color:SolidPeso molecular:420.89Anti-inflammatory agent 21
CAS:<p>Compound 9o: orally active, low-toxicity anti-inflammatory; inhibits NO (IC50: 0.76 μM), blocks NF-κB/MAPK, reduces arthritis symptoms.</p>Fórmula:C24H21FO6Forma y color:SolidPeso molecular:424.42Fc 11a-2
CAS:<p>Fc 11a-2, an oral benzimidazole, potently inhibits NLRP3 inflammasome and caspase-1 to prevent colitis.</p>Fórmula:C16H16N2Forma y color:SolidPeso molecular:236.31COX-2-IN-22
CAS:<p>COX-2-IN-22 inhibits COX-2 (IC50: 8.6μM) and crosses the blood-brain barrier, also affects AChE, BChE, β-Secretase, LOX-5, DPPH.</p>Fórmula:C29H24O7Forma y color:SolidPeso molecular:484.5TNF-α-IN-18
CAS:<p>TNF-α-IN-18 is a small molecule TNF-α inhibitor that blocks NF-κB translocation, alleviates sepsis in models, and protects against rheumatoid arthritis in mice.</p>Fórmula:C16H7ClF2O4Pureza:99.77%Forma y color:SolidPeso molecular:336.67Simvastatin acid calcium hydrate
CAS:<p>Simvastatin (Tenivastatin) calcium hydrate is an oral HMG-CoA reductase inhibitor that reduces ROS by blocking indoxyl sulfate.</p>Fórmula:C25H40O6Forma y color:SolidPeso molecular:436.28249AR-C 102222
CAS:<p>AR-C 102222 is an iNOS inhibitor.</p>Fórmula:C19H16F2N6OPureza:98%Forma y color:SolidPeso molecular:382.37Indolokine A5
CAS:<p>Indolokine A5, a catabolite of L-cysteine, is a potent AhR agonist .</p>Fórmula:C13H8N2O3SForma y color:SolidPeso molecular:272.28COX-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>Fórmula:C17H16ClN3O2SForma y color:SolidPeso molecular:361.85Pifoxime
CAS:<p>Pifoxime: a NSAID with COX-1/2 inhibition, used in anti-inflammatory treatment and neuropsychiatric studies.</p>Fórmula:C15H20N2O3Forma y color:SolidPeso molecular:276.33NOD2 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>Fórmula:C26H26N4O3SForma y color:SolidPeso molecular:474.57COX/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>Fórmula:C18H30O3Forma y color:SolidPeso molecular:294.43MIF-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>Fórmula:C18H13ClFN5O2Forma y color:SolidPeso molecular:385.78Interleukin 1β
CAS:<p>Interleukin 1beta is a bioactive chemical.</p>Fórmula:C15H28N4O5Pureza:98%Forma y color:SolidPeso molecular:344.41CYPMPO
CAS:<p>CYPMPO traps hydroxyl/superoxide radicals; decays in UV/H2O2 (15min) & hypoxanthine/xanthine (51min); outperforms DEPMPO in stability & shelf-life.</p>Fórmula:C10H18NO4PForma y color:SolidPeso molecular:247.23AZD5718
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>Fórmula:C29H34N6O4Forma y color:SolidPeso molecular:530.62COX-2-IN-26
CAS:<p>COX-2-IN-26: Oral, selective COX-2 inhibitor, low IC50s; anti-inflammatory with GI safety.</p>Fórmula:C23H21N7OS3Forma y color:SolidPeso molecular:507.65MIF-IN-5
CAS:<p>MIF-IN-5: reversible MIF inhibitor, IC50 4.8 μM, Ki 3.3 μM.</p>Fórmula:C18H14FN5O2Forma y color:SolidPeso molecular:351.33IMD-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>Fórmula:C36H41N7O4Forma y color:SolidPeso molecular:635.76K-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>Fórmula:C20H17FO2Forma y color:SolidPeso molecular:308.35Avanafil dibesylate
CAS:<p>Avanafil dibesylate is a PDE5 inhibitor.</p>Fórmula:C35H38ClN7O9S2Forma y color:SolidPeso molecular:800.3(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>Fórmula:C21H19F3N8O2Forma y color:SolidPeso molecular:472.42COX-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>Fórmula:C20H23ClN6O2Forma y color:SolidPeso molecular:414.89AXC-715 trihydrochloride
CAS:<p>AXC-715 trihydrochloride is a TLR7/8 agonist used to make PD-L1 adjuvanted antibody immunocouplings.</p>Fórmula:C18H28Cl3N5Pureza:99.74%Forma y color:SolidPeso molecular:420.81MIF-IN-4 hydrochloride
CAS:<p>MIF-IN-4 hydrochloride inhibits MIF, a cytokine; has pIC50 of 5.01-6, affecting macrophage movement.</p>Fórmula:C26H29ClN6O2Forma y color:SolidPeso molecular:493.01TML-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>Fórmula:C30H37NO7Pureza:99.71%Forma y color:SolidPeso molecular:523.62NPD926
CAS:<p>NPD926 is an inducer of cancel cell death.</p>Fórmula:C29H35ClN2O2Forma y color:SolidPeso molecular:479.05Avenanthramide-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>Fórmula:C17H15NO6Forma y color:SolidPeso molecular:329.3Loxoprofenol-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>Fórmula:C19H31NO6Forma y color:SolidPeso molecular:369.453-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>Fórmula:C9H14I2N2O2Forma y color:SolidPeso molecular:436.03NLRP3-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>Fórmula:C17H19F3N4O5SForma y color:SolidPeso molecular:448.42IKK2-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>Fórmula:C12H11N3O2SPureza:>99.99%Forma y color:SolidPeso molecular:261.3L-NMMA acetate
CAS:<p>L-NMMA acetate inhibits all NOS types (nNOS, eNOS, iNOS); Ki: 0.18, 0.4, 6 µM respectively.</p>Fórmula:C9H20N4O4Pureza:99.72% - 99.8%Forma y color:White To Off-White SolidPeso molecular:248.281-Dehydro-[10]-gingerdione
CAS:<p>1-Dehydro-[10]-gingerdione blocks IKKβ, curbs IκBα phosphorylation, halts NF-κB activity, and aids inflammation research.</p>Fórmula:C21H30O4Forma y color:SolidPeso molecular:346.46Naphazoline
CAS:<p>Naphazoline (Naphcon-a) is a sympathomimetic compound with marked alpha adrenergic activity.</p>Fórmula:C14H14N2Pureza:99.79%Forma y color:White Crystalline Powder SolidPeso molecular:210.27Safrole oxide
CAS:<p>Safrole oxide inhibits neuronal growth, induces apoptosis, elevates COX-2, IL-8, ROS, promoting endothelial-to-neuron-like cell transdifferentiation.</p>Fórmula:C10H10O3Pureza:100%Forma y color:SolidPeso molecular:178.18Vidarabine phosphate
CAS:<p>Vidarabine phosphate is an adenosine monophosphate analog.</p>Fórmula:C10H14N5O7PPureza:99.75%Forma y color:White Crystalline PowderPeso molecular:347.22APY0201
CAS:<p>APY0201: potent, specific ATP-competitive PIKfyve inhibitor; IC50=5.2 nM; blocks PtdIns3P to PtdIns(3,5)P2 conversion.</p>Fórmula:C23H23N7OPureza:98% - 99.74%Forma y color:SolidPeso molecular: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>Fórmula:C21H17N3O2S3Pureza:98.49%Forma y color:SolidPeso molecular:439.57L 669083
CAS:<p>L 669083 is two classes of potent leukotriene biosynthesis inhibitors photoaffinity analogue.</p>Fórmula:C29H29IN4O5SPureza:98%Forma y color:SolidPeso molecular:672.54LY 150310
CAS:<p>LY 150310, a histamine H1-receptor antagonist, can alter prostanoid concentrations in vitro and in vivo.</p>Fórmula:C13H14N2Forma y color:SolidPeso molecular:198.26Fagaramide
CAS:<p>Fagaramide possesses Antiplasmodial activity.</p>Fórmula:C14H17NO3Pureza:98%Forma y color:SolidPeso molecular:247.29NCX-6560
CAS:NCX-6560 is a novel NO-releasing derivative of atorvastatin, with those of atorvastatin.Fórmula:C37H42FN3O8Forma y color:SolidPeso molecular:675.74ZXX2-77
CAS:<p>ZXX2-77 is a cyclooxygenase-1 inhibitor.</p>Fórmula:C13H13ClN2O2SPureza:98%Forma y color:SolidPeso molecular:296.77Tiazotic acid
CAS:<p>Tiazotic acid is an agent with the activity of antioxidant.</p>Fórmula:C5H7N3O2SPureza:98%Forma y color:SolidPeso molecular:173.19L 748780
CAS:<p>L 748780 is a selective inducible COX-2 inhibitor.</p>Fórmula:C19H14Cl3NO4Pureza:98%Forma y color:SolidPeso molecular:426.68Oxyfenamate
CAS:<p>Oxyfenamate has anti-anxiety actions. It is also used in anxiety neuroses.</p>Fórmula:C11H15NO3Pureza:98%Forma y color:SolidPeso molecular:209.24Anisodine hydrobromide
CAS:<p>Anisodine hydrobromide is an inhibitor of adenosine kinase.</p>Fórmula:C17H22BrNO5Forma y color:White Crystals Or Crystalline PowderPeso molecular:400.27FR20
CAS:<p>FR20 is a human microsomal prostaglandin synthase 1 (mPGES 1) inhibitor.</p>Fórmula:C31H25Cl2N3O2Forma y color:SolidPeso molecular:542.46LC-R 505
CAS:<p>LC-R 505 is an anti-inflammatory.</p>Fórmula:C20H26N2O5SForma y color:SolidPeso molecular: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>Fórmula:C29H35NO9Pureza:98%Forma y color:SolidPeso molecular:541.59GSK223
CAS:GSK223 is an iE-DAP-stimulated IL-8 release inhibitor via the NOD1 signaling pathway.Fórmula:C21H18FN3O3S2Pureza:98%Forma y color:SolidPeso molecular:443.51MIP-1072
CAS:<p>MIP-1072 is the prostate-specific membrane antigen inhibitor.</p>Fórmula:C19H26IN3O7Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C8H20N4OPureza:98%Forma y color:SolidPeso molecular:188.27BPK-29
CAS:<p>BPK-29 disrupts NR0B1 binding and modifies C274, inhibiting growth in KEAP1-mutant cancers.</p>Fórmula:C26H32ClN3O3Pureza:98%Forma y color:SolidPeso molecular:470UPF-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>Fórmula:C11H8Cl2NaO3Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C15H12ClNO3Forma y color:SolidPeso molecular:289.71QM385
CAS:<p>QM385 is a potent inhibitor of sepiapterin reductase (SPR)(IC50 of 1.49 nM).</p>Fórmula:C17H18F3N7O2Pureza:98%Forma y color:SolidPeso molecular:409.37546C88
CAS:<p>546C88 is an inhibitor of nitric oxide synthase.</p>Fórmula:C7H17ClN4O2Pureza:98%Forma y color:SolidPeso molecular:224.69Etoricoxib HCl
CAS:<p>Etoricoxib HCl is a synthetic NSAID that inhibits COX-2, blocking prostaglandin production.</p>Fórmula:C18H16Cl2N2O2SForma y color:SolidPeso molecular:395.30ABD-350
CAS:<p>ABD-350 is ligand-induced inhibitor of nuclear factor kappaB phosphorylation.</p>Fórmula:C19H22F2O2Forma y color:SolidPeso molecular:320.37AI-3
CAS:<p>Nrf2/Keap1 and Keap1/Cul3 interaction inhibitor</p>Fórmula:C11H13ClO3S2Pureza:98%Forma y color:SolidPeso molecular:292.8Phox-I1
CAS:<p>Phox-I1 is a NOX2 inhibitor targeting the interactive site of p67phox with Rac GTPase.</p>Fórmula:C23H19N3O4Pureza:98%Forma y color:SolidPeso molecular:401.41NCX 466
CAS:<p>cyclooxygenase (COX)-inhibiting nitric oxide (NO) donor</p>Fórmula:C20H24N2O9Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C12H22F6N4O5Pureza:98%Forma y color:SolidPeso molecular:416.32MHY884
CAS:<p>MHY884 inhibits tyrosinase and UVB-triggered NF-κB activation by reducing oxidative stress.</p>Fórmula:C15H14ClNO3SPureza:98%Forma y color:SolidPeso molecular:323.79PC407-ws
CAS:<p>PC407-ws is a water-soluble novel COX-2 inhibitor.</p>Fórmula:C24H18F3N3Na2O5SPureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C62H111N11O12Forma y color:SolidPeso molecular: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>Fórmula:C21H28N4O3SForma y color:SolidPeso molecular:416.54Propoxur
CAS:<p>Propoxur: an insecticide causing temporary cholinergic effects in humans; chronic exposure leads to health issues; carcinogenicity unclassified by EPA.</p>Fórmula:C11H15NO3Pureza:99.84% - 99.87%Forma y color:Minute Crystals (Niosh 2016)Peso molecular:209.24Isonixin
CAS:<p>Isonixin is used for the treatment of inflammation and pain associated with musculoskeletal and joint disorders.</p>Fórmula:C14H14N2O2Pureza:98%Forma y color:SolidPeso molecular:242.27Bifenazate
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>Fórmula:C17H20N2O3Pureza:99.62%Forma y color:Solid CrystallinePeso molecular:300.35Tenosal
CAS:<p>Tenosal obtained by esterifying salicylic acid with 2-thiophene-carboxylic acid, and with analgesic and antipyretic properties, anti-inflammatory.</p>Fórmula:C12H8O4SPureza:98%Forma y color:SolidPeso molecular:248.25Anti-inflammatory agent 1
CAS:<p>Anti-inflammatory agent 1 is an anti-inflammatory compound.</p>Fórmula:C17H16O3SPureza:98%Forma y color:SolidPeso molecular:300.37Carboxyamidotriazole
CAS:<p>Carboxyamidotriazole is a cytostatic inhibitor of non-voltage-operated calcium channels and calcium channel-mediated signaling pathways.</p>Fórmula:C17H12Cl3N5O2Pureza:98%Forma y color:SolidPeso molecular:424.67U-83836E
CAS:<p>U-83836E (lazaroid ) Possesses neuroprotective activity and anti-tumor activity, inhibits tumor necrosis factor and reverses endotoxin-induced shock.</p>Fórmula:C30H46Cl2N6O2Pureza:99.33%Forma y color:SolidPeso molecular:593.63NOC-5
CAS:<p>NOC-5 is an NO donor that induces airway relaxation and concentration-dependently triggers 10 μM DAF-2 fluorescence.</p>Fórmula:C6H16N4O2Pureza:98%Forma y color:SolidPeso molecular:176.22NOS1-IN-1
CAS:<p>NOS1-IN-1: selective, potent nNOS inhibitor (Ki: 120 nM), less effective on eNOS/iNOS, for neurological disorder research.</p>Fórmula:C14H24F9N7O8Pureza:99.7%Forma y color:SolidPeso molecular:589.37FK-330 dihydrate
CAS:<p>FK-330 dihydrate (FR-260330 dihydrate), as a NOS inhibitor, prevents tissue damage caused by ischemia and reperfusion. Cost-effective and quality-assured.</p>Fórmula:C29H32ClF3N6O6Pureza:99.52% - 99.98%Forma y color:SolidPeso molecular:653.05CID-2858522
CAS:<p>CID-2858522 is an effective and specific antigen receptor-mediated NF-κB activation inhibitor (IC50: 70 nM).</p>Fórmula:C28H39N3O3Pureza:96.12%Forma y color:SolidPeso molecular:465.63ROS inducer 3
CAS:<p>ROS inducer 3 is a ROS inducer used as a bactericide in the study of resistant plant bacterial diseases, inhibiting Streptomyces.</p>Fórmula:C22H22F3N3OPureza:99.88%Forma y color:SolidPeso molecular:401.43ROS inducer 2
CAS:<p>ROS inducer 2 is a reactive oxygen species (ROS) inducer with antibacterial activity, inhibiting Axonobacter species.</p>Fórmula:C23H24F3N3OPureza:99.53% - 99.97%Forma y color:SolidPeso molecular:415.45IND24
CAS:<p>IND24 has anti-prion activity and can be used to study neurodegenerative diseases.</p>Fórmula:C21H17N3SPureza:99.64%Forma y color:SolidPeso molecular:343.44HPN-01
CAS:<p>HPN-01 (IKK inhibitor XII) is an IKK inhibitor that inhibits IKK-α and IKK-ε, prolongs the lifespan of mice, and can be used to study immune disorders.</p>Fórmula:C19H16ClN3O3SPureza:98.07% - 98.17%Forma y color:SolidPeso molecular:401.87RIP2 Kinase Inhibitor 3
CAS:<p>RIP2 Kinase Inhibitor 3 is a potent and selective inhibitor of RIP2 with an IC50 of 1 nM.</p>Fórmula:C19H24N4O3SPureza:99.32% - 99.52%Forma y color:SolidPeso molecular:388.483-Bromo-7-nitroindazole
CAS:<p>3-Bromo-7-nitroindazole specifically inhibits nNOS, impacting NO synthesis in brain/body.</p>Fórmula:C7H4BrN3O2Pureza:98.2%Forma y color:Yellowish SolidPeso molecular:242.03AN3485 Hydrochloride
CAS:<p>AN3485 Hydrochloride is an anti-inflammatory agent and a TLRs inhibitor, reducing ear swelling induced by PMA.</p>Fórmula:C14H14BCl2NO3Pureza:98.34%Forma y color:SolidPeso molecular:325.98Bay 65-1942 free base
CAS:<p>Bay 65-1942 free base is an inhibitor of ATP-competitive and selective IKKβ.</p>Fórmula:C22H25N3O4Pureza:98%Forma y color:SolidPeso molecular:395.45Tin(IV) mesoporphyrin IX dichloride
CAS:<p>Tin(IV) mesoporphyrin IX dichloride (Stannsoporfin) is an effective heme oxygenase (HO) inhibitor used for the treatment of hyperbilirubinemia.</p>Fórmula:C34H36Cl2N4O4SnPureza:99.82%Forma y color:SolidPeso molecular:754.29CAY10575
CAS:<p>CAY10575 (IKK2-IN-3) is a potent IKK2 inhibitor with potential anti-inflammatory activity for the study of inflammatory and endocrine diseases.</p>Fórmula:C22H21N3O6S2Forma y color:SolidPeso molecular:487.55NLRP3-IN-16
CAS:<p>NLRP3-IN-16: potent NLRP3 inflammasome inhibitor; IC50=0.065μM; curbs IL-1β; used in inflammation studies.</p>Fórmula:C25H25NO5Pureza:98%Forma y color:SolidPeso molecular:419.478A8
CAS:<p>8A8 is a potent NO inhibitor with proinflammatory factor properties, exhibiting an IC50 of 4.7 μM.</p>Fórmula:C36H37BrClN5O9Pureza:98%Forma y color:SolidPeso molecular:799.06IMD-biphenylB
CAS:<p>IMD-biphenylB: Potent NF-κB inhibitor, curbs tumor growth with low inflammation and toxicity.</p>Fórmula:C35H33N5O3Pureza:98%Forma y color:SolidPeso molecular:571.67STING agonist-30
CAS:<p>STING agonist-30 is a STING agonist that stimulates STING-dependent immune activation and inhibits HSV, rotavirus and SARS-CoV-2.</p>Fórmula:C15H16N4O8Pureza:98.80%Forma y color:SolidPeso molecular:380.31CD38 inhibitor 3
CAS:<p>CD38 Inhibitor 3 (compound 1), with an IC50 of 11 nM, is a potent agent that enhances mitochondrial biogenesis, diminishes lactate levels, and augments both NAD</p>Fórmula:C16H14F3N7O3Pureza:98%Forma y color:SolidPeso molecular:409.32NLRP3-IN-20
CAS:<p>NLRP3-IN-20 (compound 11) is an orally administered inhibitor targeting the NLRP3 inflammasome, exhibiting potent inhibition with an IC50 of 25 nM against IL-1β</p>Fórmula:C22H27N3O3SPureza:98%Forma y color:SolidPeso molecular:413.53iNOS inhibitor-10
CAS:<p>iNOS Inhibitor-10, with an IC50 of 65 nM, exhibits antiproliferative effects on triple-negative breast cancer cells [1].</p>Fórmula:C22H23N3O2SPureza:98%Forma y color:SolidPeso molecular:393.5COX-2-IN-32
CAS:<p>COX-2-IN-32 (Compound 2f) is a dual inhibitor of iNOS and COX-2, known to downregulate NF-κB expression.</p>Fórmula:C25H24O6Pureza:98%Forma y color:SolidPeso molecular:420.45SZM679
<p>SZM679: Oral RIPK1 inhibitor, Kd 8.6 nM, weak RIPK3 affinity (>5000 nM). Reduces inflammation, Tau phosphorylation in AD research.</p>Fórmula:C27H18F5N3O5SPureza:98%Forma y color:SolidPeso molecular:591.51IMD-catechol
CAS:<p>IMD-catechol: an imidazoquinolinone-based dimer with NF-κB activity; improves CT26 cancer treatment, low toxicity.</p>Fórmula:C31H34N6O3Pureza:98%Forma y color:SolidPeso molecular:538.64NLRP3-IN-19
CAS:<p>JT001 (NLRP3-IN-19) is a potent, specific, and orally active NLRP3 inhibitor that impedes the assembly of the NLRP3 inflammasome.</p>Fórmula:C19H22N4O4SPureza:98%Forma y color:SolidPeso molecular:402.47NF-κB-IN-8
CAS:<p>NF-κB-IN-8 is a competitive antagonist of LPS for MD-2 binding, and it impedes the expression of inflammatory factors by engaging MD-2.</p>Fórmula:C24H21N3O3Pureza:98%Forma y color:SolidPeso molecular:399.44IMD-biphenylA
CAS:<p>IMD-biphenylA, a novel imidazoquinolinone-based dimer, functions as an NF-κB immunomodulator and enhances the adjuvant properties of small molecule immune</p>Fórmula:C35H33N5O2Pureza:98%Forma y color:SolidPeso molecular:555.67NF-κB-IN-11
CAS:<p>NF-κB-IN-11 (Compound 3i) is an inhibitor of NF-κB, effectively blocking TNF-α-induced NF-κB pathway activation and the nuclear translocation of NF-κB.</p>Fórmula:C19H18O5Pureza:98%Forma y color:SolidPeso molecular:326.34Nrf2 activator-4
CAS:<p>Nrf2 activator-4 is an Nrf2 activator for the treatment of fatty liver disease associated with metabolic dysfunction in humans.</p>Fórmula:C23H24ClF3N2O3Pureza:98.53%Forma y color:SolidPeso molecular:468.9CL264
CAS:<p>CL264, a selective agonist of TLR7, can be used in studies about innate immune signals.</p>Fórmula:C19H23N7O4Pureza:98.01%Forma y color:SolidPeso molecular:413.43BI605906
CAS:<p>BI605906 is an IKKβ inhibitor that can be used to study inflammatory skin diseases such as psoriasis.</p>Fórmula:C17H22F2N4O3S2Pureza:97.14%Forma y color:SolidPeso molecular:432.51DHMEQ racemate
CAS:<p>DHMEQ racemate is an NF-κB inhibitor. The activity of DHMEQ racemate is lower than (-)-DHMEQ.</p>Fórmula:C13H11NO5Pureza:98%Forma y color:SolidPeso molecular:261.23DSR-6434
CAS:<p>DSR-6434 is a selective agonist of TLR7 with antitumor effect. DSR-6434 exhibits EC50s of 7.2 nM and 4.6 nM for human and mouse.</p>Fórmula:C19H28N8O2Pureza:99.78%Forma y color:SolidPeso molecular:400.48CB2 modulator 1
CAS:<p>CB2 modulator 1 is a potent CB2 modulator. It can be used for the research for immune disorders, osteoporosis, inflammation, renal ischemia.</p>Fórmula:C18H19F3N4O2Pureza:99.6%Forma y color:SolidPeso molecular:380.36S-MTC
CAS:<p>S-MTC is a selective inhibitor of type I nitric oxide synthase.</p>Fórmula:C7H15N3O2SPureza:98%Forma y color:Off-White Powder / White SolidPeso molecular:205.28(R,1R)-Tenofovir amibufenamide
CAS:<p>(R,1R)-Tenofovir amibufenamide ((R,1R)-HS-10234) can be used as a Tenofovir prodrug, which can be taken orally and has antiviral activity.</p>Fórmula:C22H31N6O5PPureza:98.79% - 99.02%Forma y color:SolidPeso molecular:490.49AZD8848
CAS:<p>AZD8848 is a selective antedrug agonist of toll-like receptor 7 (TLR7). It is developed for the research of asthma and allergic rhinitis.</p>Fórmula:C29H43N7O5Forma y color:SolidPeso molecular:569.7Emlenoflast
CAS:<p>Emlenoflast (MCC7840) is a selective inhibitor of NLRP3 inflammasome.</p>Fórmula:C19H24N4O3SPureza:97.004% - 98.19%Forma y color:SolidPeso molecular:388.48Edasalonexent
CAS:<p>Edasalonexent (CAT-1004) is an orally available NF-κB inhibitor for the improvement of Duchenne muscular dystrophy.</p>Fórmula:C31H42N2O3Pureza:99.13% - >99.99%Forma y color:SolidPeso molecular: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>Fórmula:C19H24N4NaO3SForma y color:SolidPeso molecular:411.47Bay 65-1942 hydrochloride
CAS:<p>Bay 65-1942 hydrochloride is an inhibitor of ATP-competitive and selective IKKβ.</p>Fórmula:C22H26ClN3O4Forma y color:SolidPeso molecular:431.91Gue1654
CAS:<p>Gue1654 is an OXE-R inhibitor and cardiomyocyte apoptosis.Gue1654 can be used for the study of cardiovascular diseases.</p>Fórmula:C23H17N3OS3Pureza:98.02% - 98.04%Forma y color:SolidPeso molecular: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>Fórmula:C17H13F2NO3Pureza:99.87%Forma y color:SolidPeso molecular:317.29SMA-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>Fórmula:C13H22INO2SPureza:98.52% - 99.16%Forma y color:SolidPeso molecular:383.29GSK319347A
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>Fórmula:C22H19N3O5S2Pureza:98.42%Forma y color:SolidPeso molecular:469.53WIN 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>Fórmula:C18H20Cl2N2O3Pureza:98.98%Forma y color:SolidPeso molecular:383.27CD73-IN-1
CAS:<p>CD73-IN-1 is a CD73 inhibitor with anticancer activity.</p>Fórmula:C18H17N3O4SPureza:99.46% - 99.46%Forma y color:SolidPeso molecular:371.41AVE-9488
CAS:<p>AVE-9488 is a novel endothelial NO synthase (eNOS) enhancer that upregulates eNOS expression, induces NO production, and may ameliorate portal hypertension.</p>Fórmula:C16H14FNOPureza:99.87%Forma y color:SolidPeso molecular:255.29JAK2/STAT3-IN-1
CAS:<p>JAK2/STAT3-IN-1 is a GP130 inhibitor with anti-tumor effects and can be used to study inflammation, autoimmunity and cancer.</p>Fórmula:C34H35BrF3N5O2Pureza:97.35%Forma y color:SolidPeso molecular:682.57SARS-CoV-2 nsp13-IN-1
CAS:<p>SARS-CoV-2 nsp13-IN-1 (C1) inhibits nsp13 ssDNA+ATPase (IC50: 6 μM), not ssDNA-ATPase; useful for COVID-19 research.</p>Fórmula:C27H20N4O2Pureza:99.44%Forma y color:SolidPeso molecular:432.47M62812
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>Fórmula:C13H13Cl2N3OSPureza:99.07%Forma y color:SolidPeso molecular:330.23DDO-7263
CAS:<p>DDO-7263, a 1,2,4-Oxadiazole, boosts Nrf2 by binding Rpn6, blocking 26S proteasome assembly, and has anti-inflammatory effects.</p>Fórmula:C14H9F2N3OPureza:99.85%Forma y color:SolidPeso molecular:273.24NFAT Transcription Factor Regulator-1
CAS:<p>NFAT Transcription Factor Regulator-1 is an synthesis inhibitor of IL-2 (IC50 of 182 nM).</p>Fórmula:C17H10F6N4O2Pureza:99.90%Forma y color:SolidPeso molecular:416.28Zharp2-1
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>Fórmula:C19H18N3O2PSPureza:99.41%Forma y color:SolidPeso molecular:383.4LMT-28
CAS:<p>LMT-28 is an inhibitor of IL-6 and selectively inhibits IL-6-induced phosphorylation of gp130, STAT3, and JAK2.</p>Fórmula:C17H29NO4Pureza:99.88%Forma y color:SolidPeso molecular:311.42T6167923
CAS:<p>T6167923 inhibits MyD88 signaling, binds TIR domain, blocks dimer formation, lowers SEAP activity, and has anti-inflammatory IC50s ~2.7 μM.</p>Fórmula:C17H20BrN3O3S2Pureza:99.28%Forma y color:SolidPeso molecular:458.39Zabedosertib
CAS:<p>Zabedosertib (BAY 1834845) is an inhibitor of IRAK4 with immunomodulatory potential.</p>Fórmula:C20H21F3N4O4SPureza:98.54%Forma y color:SolidPeso molecular:470.47C3a Receptor Agonist
CAS:<p>C3a Receptor Agonist activates C3aRs, inhibits neutrophil mobilization in ischemia, and promotes neural progenitor differentiation.</p>Fórmula:C27H35N3O2Pureza:99.76%Forma y color:SolidPeso molecular:433.59NDT 9513727
CAS:<p>NDT 9513727 is a potent, selective and competitive C5aR1 inverse agonist for the study of inflammatory and immune disorders.</p>Fórmula:C36H35N3O4Pureza:99.21%Forma y color:SolidPeso molecular:573.68Ezurpimtrostat hydrochloride
CAS:<p>Ethacrysta hydrochloride (GNS561 hydrochloride) is a PPT1 inhibitor with antifibrotic properties and may be used in studies of hepatocellular carcinoma.</p>Fórmula:C25H32Cl2N4Pureza:99.84%Forma y color:SolidPeso molecular:459.45NLRP3/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>Fórmula:C15H15NO3Pureza:99.67%Forma y color:SolidPeso molecular:257.28AHR 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>Fórmula:C20H17F3N4O3Pureza:99.38%Forma y color:SolidPeso molecular:418.37F092
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>Fórmula:C20H17N5O2Pureza:99.63%Forma y color:SolidPeso molecular:359.38DDG-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>Fórmula:C9H12FN3O3Pureza:99.81% - >99.99%Forma y color:SolidPeso molecular:229.21Totrombopag
CAS:<p>Totrombopag (SB559448) is a candidate compound for action on RSV polymerase.</p>Fórmula:C25H22N8O2Pureza:99.50%Forma y color:SolidPeso molecular:466.49Thiodigalactoside
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>Fórmula:C12H22O10SPureza:99.90%Forma y color:SolidPeso molecular:358.36Sonlicromanol hydrochloride
CAS:<p>Sonlicromanol hydrochloride (KH176 hydrochloride) is a ROS-redox modulator used in the treatment of mitochondrial diseases.</p>Fórmula:C19H29ClN2O3Pureza:99.53%Forma y color:SolidPeso molecular:368.9h-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>Fórmula:C10H10ClNO4SPureza:98.78% - 99.59%Forma y color:SolidPeso molecular:275.71Imeglimin
CAS:<p>Imeglimin: first oral antidiabetic in its class, targets liver, muscle, & pancreatic β-cells for type 2 diabetes.</p>Fórmula:C6H13N5Pureza:98.97%Forma y color:SolidPeso molecular:155.2Resiniferatoxin
CAS:<p>Resiniferatoxin ((+)-Resiniferatoxin) is a highly potent synthetic TRPV1 agonist.Cost-effective and quality-assured.</p>Fórmula:C37H40O9Pureza:93.08% - 99.34%Forma y color:SolidPeso molecular:628.71BIT225
CAS:<p>BIT225 is an HIV-1 Vpu inhibitor with antiviral activity that inhibits HIV-1 replication in myeloid dendritic cells.</p>Fórmula:C16H15N5OPureza:98.8%Forma y color:SolidPeso molecular:293.32CMX-521
CAS:<p>CMX521: an antiviral for norovirus, effective against rotavirus; inhibits viral RNA polymerase.</p>Fórmula:C13H17N5O5Pureza:99.57%Forma y color:SolidPeso molecular:323.3EIDD-2749
CAS:<p>EIDD-2749 (4'-Fluorouridine), an oral drug, inhibits RdRp, halts RSV/SARS-CoV-2 replication, and fights HCV/LCMV.</p>Fórmula:C9H11FN2O6Pureza:97.39%Forma y color:SolidPeso molecular:262.19Rociclovir
CAS:<p>Rociclovir has antiviral activity and is used to treat viral infections.</p>Fórmula:C15H25N5O3Pureza:99.19%Forma y color:SolidPeso molecular:323.39NFATc1-IN-1
CAS:<p>NFATc1-IN-1 (A04) inhibits RANKL-induced osteoclast formation with 1.57 μM IC50, blocking NFATc1 translocation.</p>Fórmula:C13H8F2INO2Pureza:99.64%Forma y color:SolidPeso molecular:375.11Phox-I2
CAS:<p>Phox-I2 is an NOX2-specific inhibitor. Phox-I2 reverts ROS-accumulation and leads to refusion of mitochondrial networks.</p>Fórmula:C18H15N3O4Pureza:99.73%Forma y color:SolidPeso molecular:337.33Rufigallol
CAS:<p>Rufigallol, an anthraquinone with six OH groups, induces DLC and fluoresces when aggregated, showing antimalarial effects with vitamin C and ketones.</p>Fórmula:C14H8O8Pureza:98.92% - 99.27%Forma y color:SolidPeso molecular:304.21MK-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>Fórmula:C24H20N4O2Forma y color:SolidPeso molecular:396.44Cindunistat
CAS:<p>Cindunistat (free base) is an orally available selective iNOS inhibitor for the study of arthritis.</p>Fórmula:C8H17N3O2SPureza:99% - >99.99%Forma y color:SolidPeso molecular:219.3IRAK4-IN-20
CAS:<p>IRAK4-IN-20 is a potent and orally active IRAK4 inhibitor (IC50:3.55 nM).</p>Fórmula:C22H25F3N4O3Pureza:98.09%Forma y color:SolidPeso molecular:450.45RIPK1-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>Fórmula:C26H25FN6O2Pureza:99.85%Forma y color:SolidPeso molecular:472.51EG00229
CAS:<p>EG00229 blocks VEGF-A/NRP1 binding, IC50 of 3 μM; doesn't affect VEGFR-1/2. It's an NRP1 antagonist.</p>Fórmula:C19H20F3N7O7S3Pureza:98.23%Forma y color:SolidPeso molecular:611.6AT791
CAS:<p>AT791 is an orally available TLR7 and TLR9 inhibitor, suppressing TLR7 and TLR9 signaling, used in autoimmune lupus research.</p>Fórmula:C23H31N3O3Pureza:99.88%Forma y color:SolidPeso molecular: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>Fórmula:C13H15N5Pureza:99.08% - 99.53%Forma y color:SolidPeso molecular:241.29ER-34122
CAS:<p>ER-34122, a novel orally available dual 5-lipoxygenase/cyclooxygenase inhibitor with potent anti-inflammatory activity.</p>Fórmula:C27H26ClN3O5Pureza:>99.99%Forma y color:SolidPeso molecular:507.96Antiviral 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>Fórmula:C11H14N4O4Pureza:99.89%Forma y color:SolidPeso molecular:266.25IL-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>Fórmula:C18H12FN3O2Pureza:98.78% - 99.53%Forma y color:SolidPeso molecular:321.31ABT-963
CAS:<p>ABT-963: COX-2 inhibitor for osteoarthritis/pain with high selectivity, potency, and gastric safety.</p>Fórmula:C22H22F2N2O5SPureza:98% - 99.85%Forma y color:SolidPeso molecular:464.48CT-2584
CAS:<p>CT-2584: angiogenesis & lysophosphatidic acid transferase inhibitor; alters phospholipid synthesis, increasing PI in tumor cells.</p>Fórmula:C30H55N5O3Pureza:97.68% - 99.77%Forma y color:SolidPeso molecular:533.79Azalanstat
CAS:<p>Azalanstat (RS 21607) is a mammalian lanosterol 14-alpha-demethylase inhibitor with hypocholesterolemic activity.</p>Fórmula:C22H24ClN3O2SPureza:99.41% - 99.85%Forma y color:SolidPeso molecular:429.96ABI-1968
CAS:<p>ABI-1968 has antiviral and antitumor activity and can be used to study immune system diseases.</p>Fórmula:C35H58N5O6PPureza:98.54%Forma y color:SolidPeso molecular:675.839JC124
CAS:<p>JC124 is an inhibitor of NLRP3 Inflammasome and exhibits neuroprotective and anti-inflammatory activities.</p>Fórmula:C17H19ClN2O4SPureza:99.64%Forma y color:SolidPeso molecular:382.86IL-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>Fórmula:C17H12F6N4O2Pureza:99.6%Forma y color:SolidPeso molecular:418.29Desmosterol
CAS:<p>Desmosterol (24-Dehydrocholesterol) is a cholesterol biosynthesis intermediate that inhibits macrophage inflammatory vesicle activation .</p>Fórmula:C27H44OPureza:>99.99%Forma y color:SolidPeso molecular:384.64Biofor 389
CAS:<p>Biofor 389 (BF389) has anti-inflammatory activity and can be used to study arthritis.</p>Fórmula:C20H29NO3Pureza:98.84% - 99.97%Forma y color:SolidPeso molecular:331.45RIG012
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>Fórmula:C23H21NO3Pureza:99.53%Forma y color:SolidPeso molecular:359.42BN-82451 2HCl
CAS:<p>BN-82451, a cyclooxygenase inhibitor, is used potentially for the treatment of Huntington’s disease.</p>Fórmula:C18H28Cl2N2OSPureza:99.84% - >99.99%Forma y color:SolidPeso molecular:391.4Complement C5-IN-1
CAS:<p>Complement C5-IN-1 is a small-molecule inhibitor of complement component 5 protein (C5).</p>Fórmula:C24H32N2O6Pureza:98.27%Forma y color:SolidPeso molecular:444.52R 61837
CAS:<p>R 61837 is a novel rhinovirus inhibitor, a substituted phenylpyridazinamine, with antiviral activity.</p>Fórmula:C16H20N4OPureza:99.53%Forma y color:SolidPeso molecular:284.36Selnoflast
CAS:<p>Selnoflast (RO-7486967) is an orally active, potent and selective NLRP3 inhibitor for the study of coronary arteries and ulcerative colitis.</p>Fórmula:C20H29N3O3SPureza:98.54% - 99.66%Forma y color:SolidPeso molecular:391.53APX-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>Fórmula:C17H18ClN3OPureza:98.62%Forma y color:SolidPeso molecular:315.8Dersalazine
CAS:<p>Dersalazine, a PAF inhibitor, reduces IL-17 to treat colitis in rodents, potentially aiding ulcerative colitis patients.</p>Fórmula:C35H32N6O4Pureza:99.62%Forma y color:SolidPeso molecular:600.67CDDO-EA
CAS:<p>CDDO-EA (CDDO ethyl amide) is an activator of the Nrf2/antioxidant response element.</p>Fórmula:C33H46N2O3Pureza:99.66%Forma y color:SolidPeso molecular:518.73IQP-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>Fórmula:C20H24N2O3Pureza:98.36% - >99.99%Forma y color:SolidPeso molecular:340.42HS271
CAS:<p>HS271 is a selective, highly potent and orally active IRAK4 inhibitor (IC50= 7.2 μM).</p>Fórmula:C21H24F3N5O2Pureza:98.79%Forma y color:SolidPeso molecular:435.44NLRP3-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>Fórmula:C17H14BrFO3Pureza:99.06%Forma y color:SolidPeso molecular:365.19NO-prednisolone
CAS:<p>NO-prednisolone (NCX-1015) is a compound that effectively stimulates the production of IL-10 in vivo.</p>Fórmula:C29H33NO9Pureza:98.65%Forma y color:SolidPeso molecular:539.57Rabeximod
CAS:<p>Rabeximod, an immunomodulator, eases autoimmune diseases, inhibits arthritis, and aids brain recovery post-injury by blocking inflammation.</p>Fórmula:C22H24ClN5OPureza:99.99%Forma y color:SolidPeso molecular:409.91SM360320
CAS:<p>SM360320 (CL-087) is a selective TLR7 agonist that blocks HCV replication in hepatocytes and aids immunology research.</p>Fórmula:C15H17N5O3Pureza:99.13%Forma y color:SolidPeso molecular:315.33TLR7/8-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>Fórmula:C29H40N8O2Pureza:99.83%Forma y color:SolidPeso molecular:532.68SP-100030
CAS:SP-100030: Strong NF-κB/AP-1 inhibitor, IC50=50 nM. Reduces IL-2, IL-8, TNF-alpha, and murine CIA.Fórmula:C14H5ClF9N3OPureza:99.79%Forma y color:SolidPeso molecular:437.65FK-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>Fórmula:C29H28ClF3N6O4Pureza:99.95%Forma y color:SolidPeso molecular:617.02B022
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>Fórmula:C19H16ClN5OSPureza:99.74%Forma y color:SolidPeso molecular:397.88
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