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(148 products)
- Cell wall(5 products)
- IL Receptor(112 products)
- IκB/IKK(60 products)
- LTR(3 products)
- MALT(23 products)
- MRP(6 products)
- NADPH-oxidase(1 products)
- NF-κB(444 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 3034 products of "Immunology and Inflammation"
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CD73-IN-1
CAS:<p>CD73-IN-1 is a CD73 inhibitor with anticancer activity.</p>Formula:C18H17N3O4SPurity:99.46% - 99.46%Color and Shape:SolidMolecular weight:371.41TMV-IN-1
CAS:<p>TMV-IN-1: a chalcone inhibits TMV with EC50s of 70.7 and 60.8 μg/mL, applicable in infection and tumor studies.</p>Formula:C28H26O4Color and Shape:SolidMolecular weight:426.5TLR7/8 agonist 6
CAS:<p>Compound 4: Imidazoquinoline, potent TLR7/8 agonist, IC50: 0.18μM (TLR7), 5.34μM (TLR8).</p>Formula:C24H27N5O2Color and Shape:SolidMolecular weight:417.5Tin(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>Formula:C34H36Cl2N4O4SnPurity:99.82%Color and Shape:SolidMolecular weight:754.29LY 178002
CAS:<p>LY 178002 inhibits 5-LPO (IC50: 0.6 μM), PLA2, and LTB4 production; weak on cyclooxygenase.</p>Formula:C18H25NO2SPurity:98%Color and Shape:SolidMolecular weight:319.46APC-0576
CAS:<p>APC-0576, an (S,S)-isomer, blocks NF-kappaB gene activation and may reduce inflammation in human cells.</p>Formula:C23H27N3O3Color and Shape:SolidMolecular weight:393.48ADU-S100 ammonium salt
CAS:<p>ADU-S100 ammonium salt is an activator of stimulator of interferon genes (STING).Cost-effective and quality-assured.</p>Formula:C20H30N12O10P2S2Purity:98%Color and Shape:SolidMolecular weight:724.6COX-2-IN-20
CAS:<p>COX-2-IN-20 (Compound 5d) is a selective and orally active inhibitor of COX-2 (IC 50 = 17.9 nM) with anti-inflammatory activity [1].</p>Formula:C11H9ClFN3O2Color and Shape:SolidMolecular weight:269.66MitoTEMPOL
CAS:<p>MitoTEMPOL is a mitochondria-targeted antioxidant that prevents septal dysfunction by reversing sepsis-induced decreases in mitochondrial function.</p>Formula:C32H42BrNO2PColor and Shape:SolidMolecular weight:583.56NLRP3-IN-13
CAS:<p>NLRP3-IN-13 is an NLRP3 inhibitor that inhibits NLRP3-associated inflammation.NLRP3-IN-13 can be used in the study of neurological disorders and inflammation.</p>Formula:C19H15N3O3SPurity:99.16%Color and Shape:SolidMolecular weight:365.41C5aR-IN-2
CAS:<p>C5aR-IN-2, a potent C5aR inhibitor, shows promise for researching inflammatory diseases.</p>Formula:C36H40FN5O2Color and Shape:SolidMolecular weight:593.73Keap1-Nrf2-IN-13
CAS:<p>Keap1-Nrf2-IN-13 is a PPI inhibitor (IC50: 0.15 μM) that binds Keap1 strongly, useful for oxidative stress and inflammation research.</p>Formula:C28H32N2O10S2Color and Shape:SolidMolecular weight:620.69c-di-AMP
CAS:<p>c-di-AMP (Cyclic diadenylate) is a STING agonist. It binds to the transmembrane protein STING thereby activating the TBK3-IRF3 signaling pathway.</p>Formula:C20H24N10O12P2Purity:98%Color and Shape:SolidMolecular weight:658.41BC12-4
CAS:<p>BC12-4 is a novel potent inhibitor of IL-2 secretion, it has potent immunomodulatory activity.</p>Formula:C19H14N2O3Color and Shape:SolidMolecular weight:318.33STING modulator-4
CAS:<p>STING modulator-4: competitive, Ki=0.0933 μM (R232H STING), EC50 >10 μM (p-IRF3, THP-1 cells).</p>Formula:C17H18N8OColor and Shape:SolidMolecular weight:350.38L-Kynurenine sulfate
CAS:<p>L-Kynurenine sulfate activates AHR, leading naive T cells to anti-inflammatory Treg phenotype.</p>Formula:C10H14N2O7SColor and Shape:SolidMolecular weight:306.29GCPII-IN-1 TFA
CAS:<p>GCPII-IN-1 TFA (compound 2) is an inhibitor scaffold for glutamate carboxypeptidase II (GCPII, PSMA) with a Ki of 44.3±2.4 nM for use in prostate cancer.</p>Formula:C14H22F3N3O9Color and Shape:SoildMolecular weight:433.34OPC-163493
CAS:<p>OPC-163493 is an orally active, liver-targeted mitochondrial uncoupling agent that diminishes Δψ (delta psi) and mitochondrial ROS (reactive oxygen species)</p>Formula:C14H8F3N5SPurity:98%Color and Shape:SolidMolecular weight:335.31HPGDS inhibitor 3
CAS:<p>HPGDS inhibitor 3: oral, potent (IC50=9.4 nM; EC50=42 nM), selective, no CNS toxicity, good pharmacokinetics, anti-inflammatory.</p>Formula:C21H27N3O2Color and Shape:SolidMolecular weight:353.46IRAK4-IN-17
CAS:<p>IRAK4-IN-17 is a potent IRAK4 inhibitor with a 1.3 nM IC50, key for DLBCL research.</p>Formula:C17H20F2N8OColor and Shape:SolidMolecular weight:390.39T-5342126
CAS:<p>T-5342126: TLR4 antagonist, lowers LPS-induced NO in cells (IC50=27.8 μM) & cytokines in blood, cuts ethanol intake & Iba1 in mice.</p>Formula:C25H32ClN3O3Color and Shape:SolidMolecular weight:457.99CAY10575
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>Formula:C22H21N3O6S2Color and Shape:SolidMolecular weight:487.55Nω-Propyl-L-arginine hydrochloride
CAS:<p>Highly selective and potent inhibitor of nNOS (Ki = 57 nM). Displays 3158-fold and 149-fold selectivity over iNOS and eNOS respectively. Hypotensive in vivo.</p>Formula:C9H21ClN4O2Color and Shape:SolidMolecular weight:252.74NLRP3-IN-16
CAS:<p>NLRP3-IN-16: potent NLRP3 inflammasome inhibitor; IC50=0.065μM; curbs IL-1β; used in inflammation studies.</p>Formula:C25H25NO5Purity:98%Color and Shape:SolidMolecular weight:419.478A8
CAS:<p>8A8 is a potent NO inhibitor with proinflammatory factor properties, exhibiting an IC50 of 4.7 μM.</p>Formula:C36H37BrClN5O9Purity:98%Color and Shape:SolidMolecular weight:799.06IMD-biphenylB
CAS:<p>IMD-biphenylB: Potent NF-κB inhibitor, curbs tumor growth with low inflammation and toxicity.</p>Formula:C35H33N5O3Purity:98%Color and Shape:SolidMolecular weight: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>Formula:C15H16N4O8Purity:98.80%Color and Shape:SolidMolecular weight: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>Formula:C16H14F3N7O3Purity:98%Color and Shape:SolidMolecular weight: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>Formula:C22H27N3O3SPurity:98%Color and Shape:SolidMolecular weight: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>Formula:C22H23N3O2SPurity:98%Color and Shape:SolidMolecular weight: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>Formula:C25H24O6Purity:98%Color and Shape:SolidMolecular weight:420.45SZM679
<p>SZM679: Oral RIPK1 inhibitor, Kd 8.6 nM, weak RIPK3 affinity (>5000 nM). Reduces inflammation, Tau phosphorylation in AD research.</p>Formula:C27H18F5N3O5SPurity:98%Color and Shape:SolidMolecular weight:591.51Eltrombopag methyl ester
CAS:<p>Eltrombopag methyl ester, a Tpo receptor agonist derivative, boosts platelet production for thrombocytopenia research.</p>Formula:C26H24N4O4Color and Shape:SolidMolecular weight:456.49IMD-catechol
CAS:<p>IMD-catechol: an imidazoquinolinone-based dimer with NF-κB activity; improves CT26 cancer treatment, low toxicity.</p>Formula:C31H34N6O3Purity:98%Color and Shape:SolidMolecular weight: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>Formula:C19H22N4O4SPurity:98%Color and Shape:SolidMolecular weight: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>Formula:C24H21N3O3Purity:98%Color and Shape:SolidMolecular weight: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>Formula:C35H33N5O2Purity:98%Color and Shape:SolidMolecular weight: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>Formula:C19H18O5Purity:98%Color and Shape:SolidMolecular weight: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>Formula:C23H24ClF3N2O3Purity:98.53%Color and Shape:SolidMolecular weight:468.9Cyclic-di-GMP diammonium
CAS:<p>C-di-GMP diammonium activates STING, regulates biofilms, motility, and virulence in bacteria.</p>Formula:C20H30N12O14P2Color and Shape:SolidMolecular weight:724.47CL264
CAS:<p>CL264, a selective agonist of TLR7, can be used in studies about innate immune signals.</p>Formula:C19H23N7O4Purity:98.01%Color and Shape:SolidMolecular weight:413.43Tyrosinase-IN-12
CAS:<p>Tyrosinase-IN-12(Non-competitive tyrosinase inhibitor) is a potent non-competitive tyrosinase inhibitor with an IC50 of 49.33 ± 2.64 µM and a Ki of 31.25 ± 0.25</p>Formula:C16H12ClN3SPurity:99.2%Color and Shape:SoildMolecular weight:313.8NOS-IN-3
CAS:<p>NOS-IN-3: potent, selective iNOS inhibitor; IC50 of 4.6 µM; spares eNOS; low toxicity; potential for septic shock treatment.</p>Formula:C10H15N3OColor and Shape:SolidMolecular weight:193.25Isoandrographolide
CAS:<p>Isoandrographolide induces cell differentiation, protects the liver, blocks NLRP3, and reduces silicosis in mice.</p>Formula:C20H30O5Color and Shape:SolidMolecular weight:350.45AN-3485
CAS:<p>AN-3485 is a Toll-Like Receptor(TLR) inhibitor (IC50s: 18 to 580 nM).</p>Formula:C14H13BClNO3Color and Shape:SolidMolecular weight:289.52PHA-408
CAS:<p>PHA-408 is a novel potent, highly selective and ATP-competitive inhibitor of IKB kinase-2.</p>Formula:C29H27ClFN7O2Purity:98%Color and Shape:SolidMolecular weight:560.02STING Agonist 1a
CAS:<p>STING agonist 1a activates STING, induces IRF-SEAP, IFN-β, IL-6, CXCL10 (EC50=16.77 µM); effects reversed by STING KO/inhibitor H-151.</p>Formula:C19H11Cl2N5OColor and Shape:SolidMolecular weight:396.23BI605906
CAS:<p>BI605906 is an IKKβ inhibitor that can be used to study inflammatory skin diseases such as psoriasis.</p>Formula:C17H22F2N4O3S2Purity:97.14%Color and Shape:SolidMolecular weight:432.51DHMEQ racemate
CAS:<p>DHMEQ racemate is an NF-κB inhibitor. The activity of DHMEQ racemate is lower than (-)-DHMEQ.</p>Formula:C13H11NO5Purity:98%Color and Shape:SolidMolecular weight:261.23SNAP 398299
CAS:<p>SNAP 398299 is a Glycopeptide Receptor Type 3 (Gal3) antagonist with anxiolytic and antidepressant-like effects and is used in the study of mood disorders.</p>Formula:C27H24F3N3O2Purity:97.16%Color and Shape:SolidMolecular weight:479.49(+)-DHMEQ
CAS:<p>(+)-DHMEQ is an antioxidant transcription factor Nrf2 activator. (+)-DHMEQ is the enantiomer of (-)-DHMEQ.</p>Formula:C13H11NO5Color and Shape:SolidMolecular weight:261.23COX-2-IN-16
CAS:<p>COX-2-IN-16: potent, selective oral COX-2 blocker, IC50=102 μM, reduces NO, anti-inflammatory.</p>Formula:C19H12BrN3O2Color and Shape:SolidMolecular weight:394.22QD-394
CAS:<p>QD-394 promotes ROS, impairs GSH/GSSG ratio, and is cytotoxic to pancreatic cancer cells, with synergy with napabucasin.</p>Formula:C19H19N5O2Color and Shape:SolidMolecular weight:349.39Phortress
CAS:<p>Phortress (NSC-710305) is a potent AhR ligand with strong binding affinity, which subsequently triggers the transcription of CYP1A1 and induces antitumor</p>Formula:C20H25Cl2FN4OSPurity:99.89%Color and Shape:SolidMolecular weight:459.41NLRP3 antagonist 1
CAS:<p>Potential cancer research drug, NLRP3 antagonist 1, targets immune response in macrophages, neutrophils.</p>Formula:C16H18N6OColor and Shape:SolidMolecular weight:310.35AHR antagonist 5
CAS:<p>Potent, oral AHR blocker from WO2018195397; IC50 < 0.5μM; hinders tumor growth with anti-PD-1.</p>Formula:C25H27Cl3FN7Purity:98%Color and Shape:SolidMolecular weight:550.89KIN1400
CAS:<p>KIN1400 activates IRF3, boosts antiviral immunity, stimulates IFNbeta, and inhibits WNV, DV, and HCV.</p>Formula:C24H17F2N3O2SPurity:98%Color and Shape:SolidMolecular weight:449.47Tilarginine
CAS:<p>Tilarginine is a nitric oxide synthetase competitive inhibitor.</p>Formula:C7H16N4O2Purity:98%Color and Shape:SolidMolecular weight:188.23ARV-393
CAS:<p>ARV-393 is a PROTAC degrader targeting BCL6 orally available. ubiquitin proteasome for diffuse large b-cell lymphoma (DLBCL) and non-Hodgkin's lymphoma (NHL)</p>Formula:C46H53ClFN9O7Purity:99.96%Color and Shape:SoildMolecular weight:898.42DDX3-IN-2
CAS:<p>DDX3-IN-2 is a potent DDX3 inhibitor with an IC50 of 0.3 μM and shows broad antiviral effects, including against HIV resistance.</p>Formula:C20H23N5OColor and Shape:SolidMolecular weight:349.43TRAF-STOP inhibitor 6877002
CAS:<p>TRAF-STOP 6877002 inhibits CD40-TRAF6, curbing leukocyte recruitment and macrophage activation/proliferation in plaques.</p>Formula:C17H17NOPurity:99.76%Color and Shape:SolidMolecular weight:251.32MIF-IN-2
CAS:<p>MIF-IN-2 is a MIF inhibitor with anticancer activity for the study of cancer and autoimmune diseases.</p>Formula:C14H10ClN3O4Purity:98.55%Color and Shape:SolidMolecular weight:319.7TBK1/IKKε-IN-4
CAS:<p>TBK1/IKKε-IN-4, a 6-aminopyrazolopyrimidine derivative, serves as a potent, selective inhibitor for TBK1 and IKKε, demonstrating IC50 values of 13 nM and 59 nM</p>Formula:C28H35N7O4Color and Shape:SolidMolecular weight:533.62UC-781
CAS:<p>UC-781, a potent NNRTI, inhibits HIV-1 with a C50 of 5 nM and is stable across pH and temperatures.</p>Formula:C17H18ClNO2SPurity:92.17%Color and Shape:SolidMolecular weight:335.85DSR-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>Formula:C19H28N8O2Purity:99.78%Color and Shape:SolidMolecular weight:400.48NRP1 antagonist 2
CAS:<p>NRP1 antagonist 2 (Compound 1) is an NRP1 antagonist.</p>Formula:C20H17ClN6OS2Color and Shape:SolidMolecular weight:456.97OXSI-2
CAS:<p>OXSI-2 (Syk Inhibitor) is an inhibitor of Syk with an EC50 of 313 nM and an IC50 of 14 nM.</p>Formula:C18H15N3O3SPurity:98%Color and Shape:Dark Orange SolidMolecular weight:353.39Thiazolinobutazone
CAS:<p>Thiazolinobutazone is the 2-amino-2-thiazoline salt of phenylbutazone.</p>Formula:C22H26N4O2SColor and Shape:SolidMolecular weight:410.53CB2 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>Formula:C18H19F3N4O2Purity:99.6%Color and Shape:SolidMolecular weight:380.36COX/5-LO-IN-1
CAS:<p>COX/5-LO-IN-1 is a cyclooxygenase and 5-lipoxygenase (5-LO) inhibitor, and used for inflammatory and allergic disease states.</p>Formula:C16H15FN2O2SPurity:98%Color and Shape:SolidMolecular weight:318.37N-α-Tosyl-L-lysine chloromethyl ketone hydrochloride
CAS:<p>N-alpha-Tosyl-L-lysine chloromethyl ketone hydrochloride inhibits trypsin-like proteases and IFN-γ activities.</p>Formula:C14H22Cl2N2O3SPurity:97.44%Color and Shape:PowderMolecular weight:369.31COX-2-IN-14
CAS:<p>COX-2-IN-14 (2a) is a potent, selective COX-2 inhibitor with high affinity and notable anti-inflammatory effects in mice.</p>Formula:C18H18N4O6Color and Shape:SolidMolecular weight:386.364Hetrombopag
CAS:<p>Hetrombopag: potent thrombopoietin receptor agonist, well tolerated, safe, promising for immune thrombocytopenia research.</p>Formula:C25H22N4O5Color and Shape:SolidMolecular weight:458.47Ppc-1
CAS:<p>Ppc-1 inhibits Porphyromonas gingivalis, uncouples mitochondria, and blocks IL-2, with anti-obesity, antibacterial, anti-inflammatory effects.</p>Formula:C21H25NO4Purity:98%Color and Shape:SolidMolecular weight:355.43S-MTC
CAS:<p>S-MTC is a selective inhibitor of type I nitric oxide synthase.</p>Formula:C7H15N3O2SPurity:98%Color and Shape:Off-White Powder / White SolidMolecular weight:205.28Nrf2-Activator-12G
CAS:<p>Nrf2-Activator-12G is a potent Nrf-2 activator.</p>Formula:C15H13ClO3SPurity:98%Color and Shape:SolidMolecular weight:308.78(-)-Ibuprofenamide
CAS:<p>(-)-Ibuprofenamide is an amide prodrug of Ibuprofen with anti-inflammatory activity.</p>Formula:C13H19NOPurity:98%Color and Shape:SolidMolecular weight:205.3MALT1-IN-8
CAS:<p>MALT1-IN-8: potent MALT1 inhibitor, IC50=2 nM; hinders OCI-LY3 cells, IC50=1.16 μM; anticancer, from patent WO2018165385A1.</p>Formula:C20H15Cl2N7OColor and Shape:SolidMolecular weight:440.29IL-1β-IN-2
CAS:<p>IL-1β-IN-2, a cannabigerol derivative, serves as a potent inhibitor of IL-1β, exhibiting anti-inflammatory and pain-resolving properties [1].</p>Formula:C22H34O2Color and Shape:SolidMolecular weight:330.5CHS-111
CAS:<p>CHS-111 is a benzyl indazole that inhibits O2- generation, fMLP-induced PLD activity (IC50 3.9μM), and disrupts PLD1/Arf6 and RhoA interactions.</p>Formula:C21H18N2OPurity:98%Color and Shape:SolidMolecular weight:314.38AVE-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>Formula:C16H14FNOPurity:99.87%Color and Shape:SolidMolecular weight:255.29BAY32-5915
CAS:<p>BAY32-5915 is a selective inhibitor of IKKalpha.</p>Formula:C10H7NO3Purity:96.48% - 97%Color and Shape:Yellow Crystalline PowderMolecular weight:189.17UC-1V150
CAS:<p>UC-1V150: TLR7 agonist, triggers immune response, anti-tumor, precursor for ISAC synthesis.</p>Formula:C16H17N5O4Color and Shape:SolidMolecular weight:343.34YS-121
CAS:<p>YS121 inhibits mPGES-1 (IC50=3.4μM) & 5-LOX (IC50=6.5μM), and lowers PGE2 in A549 cells (EC50=12μM).</p>Formula:C20H26ClN3O2SColor and Shape:SolidMolecular weight:407.96NBC 6
CAS:<p>NLRP3-IN-NBC6: potent NLRP3 inflammasome inhibitor, IC50 574 nM, Ca2+ independent, inhibits inflammasome in THP-1 cells/BMDMs.</p>Formula:C18H16BCl3N2O2Color and Shape:SolidMolecular weight:409.5STING ligand-1
CAS:<p>STING ligand-1 is a lead STING ligand(IC50 of 68 nM for HAQ STING).</p>Formula:C29H27ClFNO5Purity:98%Color and Shape:SolidMolecular weight:523.98FD-IN-1
CAS:FD-IN-1: Factor D inhibitor, IC50=12 nM; blocks FXIa, Tryptase β2 (IC50s: 7.7 μM, 6.5 μM); key in innate immunity.Formula:C23H23NO4Color and Shape:SolidMolecular weight:377.43Anti-inflammatory agent 8
CAS:<p>Anti-inflammatory agent 8 targets COX-2 over COX-1, IC50 of 0.09 nM, orally bioavailable.</p>Formula:C18H15N5OS2Color and Shape:SolidMolecular weight:381.47M62812 free base
CAS:<p>M62812 (free base), a Toll-like receptor 4 (TLR4) signal transduction inhibitor, suppresses activation of endothelial cells and leukocytes and prevents lethal</p>Formula:C13H11N3OSColor and Shape:SolidMolecular weight:257.31iNOS-IN-2
CAS:<p>iNOS-IN-2 (Compound 53) is a potent inducible nitric oxide synthase (iNOS) protein down-regulator.</p>Formula:C25H31NO7Color and Shape:SolidMolecular weight:457.52JAK2/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>Formula:C34H35BrF3N5O2Purity:97.35%Color and Shape:SolidMolecular weight:682.57(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>Formula:C22H31N6O5PPurity:98.79% - 99.02%Color and Shape:SolidMolecular weight:490.49SARS-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>Formula:C27H20N4O2Purity:99.44%Color and Shape:SolidMolecular weight:432.47Prostaglandin G/H synthase 1 inhibitor
CAS:<p>Prostaglandin G/H synthase 1 inhibitor (CP 74006) is a selective D5D inhibitor with an IC(50) value of 20 nM.</p>Formula:C13H11ClN2OPurity:99.76%Color and Shape:SolidMolecular weight:246.697-NINA
CAS:<p>non-selective NOS inhibitor</p>Formula:C7H5N3NaO2Purity:98%Color and Shape:SolidMolecular weight:186.12R110
CAS:<p>R110 shows the potential for cancer research that is a potent, competitive MIF2 tautomerase inhibitor (IC 50 = 15 μM) [1].</p>Formula:C15H17ClN2OSColor and Shape:SolidMolecular weight:308.83TLR7 agonist 1
CAS:<p>TLR7 agonist 1 is a selective and oral TLR7 agonist (IC50: 90 nM).</p>Formula:C21H25N5OPurity:98%Color and Shape:SolidMolecular weight:363.46AZD8848
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>Formula:C29H43N7O5Color and Shape:SolidMolecular weight:569.7Emlenoflast
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:472.42
