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(149 productos)
- Pared celular(5 productos)
- Receptor de IL(112 productos)
- IκB / IKK(59 productos)
- LTR(3 productos)
- MALT(23 productos)
- MRP(6 productos)
- NADPH-oxidasa(1 productos)
- NF-κB(443 productos)
- NOD(18 productos)
- NOS(63 productos)
- Nrf2(78 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 3054 productos de "Inmunología e inflamación"
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Rademikibart
CAS:<p>Rademikibart (CBP-201) is a human monoclonal antibody selective for IL-4Rα, exhibiting strong affinity with a KD of 20.7 pM for human IL-4Rα epitopes, without</p>Pureza:95%Forma y color:LiquidAvizakimab
CAS:<p>Avizakimab (BOS161721) is a humanized lgG1 monoclonal antibody IL-21, with potential for the treatment of systemic lupus erythematosus (SLE).</p>Pureza:95% - 95%Forma y color:LiquidCC-90002
CAS:<p>CC-90002: humanized anti-CD47 mAb, high affinity, subnanomolar Kd. For hematologic and solid tumor research.</p>Forma y color:LiquidQNZ
CAS:Fórmula:C22H20N4OPureza:>98.0%(HPLC)Forma y color:White to Light yellow to Green powder to crystalPeso molecular:356.43Indometacin Farnesil
CAS:Fórmula:C34H40ClNO4Pureza:>98.0%(HPLC)Forma y color:Light yellow to Yellow to Orange clear liquidPeso molecular:562.15Azathioprine
CAS:Fórmula:C9H7N7O2SPureza:>98.0%(T)(HPLC)Forma y color:Light yellow to Yellow to Green powder to crystalPeso molecular:277.26Serotonin Creatinine Sulfate Monohydrate
CAS:Fórmula:C14H19N5O2·H2SO4·H2OPureza:>98.0%(T)Forma y color:White to Light yellow powder to crystalPeso molecular:405.43Nepafenac-d5
CAS:<p>Nepafenac D5 is the deuterium labeled Nepafenac, which is a selective inhibitor of COX-2 .</p>Fórmula:C15H14N2O2Pureza:98%Forma y color:SolidPeso molecular:259.31Maresin 1
CAS:Maresin 1 is biosynthesized by macrophages (MΦ) and possesses significant anti-inflammatory activity that attenuates LPS-induced lung injury in mice.Fórmula:C22H32O4Forma y color:SolidPeso molecular:360.49Ketorolac-d5
CAS:<p>Ketorolac-d5 is a deuterated compound of ketorolac for isotope tracing. Ketorolac is a non-steroidal anti-inflammatory agent and inhibitor of COX-1 and COX-2.</p>Fórmula:C15H8D5NO3Pureza:98.99%Forma y color:SolidPeso molecular:260.3Lusvertikimab
CAS:<p>Lusvertikimab (OSE-127) is a humanized anti-IL7R antibody with anti-leukemic efficacy and can be used to study leukemia.</p>Pureza:95% - 98.4% (SDS-PAGE); 99% (SEC-HPLC)Forma y color:LiquidBMS-378806
CAS:BMS-378806 (BMS-806) selectively inhibits the binding of HIV-1 gp120 to the CD4 receptor with EC50 of 0.85-26.5 nM in virus.Fórmula:C22H22N4O4Pureza:99.93%Forma y color:SolidPeso molecular:406.43Vopikitug
CAS:<p>Vopikitug is a humanized monoclonal antibody targeting IL-2RA with antitumor activity. It can be used to study cancer.</p>Pureza:99.1% (SDS-PAGE); 96.5% (SEC-HPLC) - 99.1% (SDS-PAGE); 96.5% (SEC-HPLC)Forma y color:Liquid(9α,13α,14α)-4-Hydroxy-3,7-dimethoxy-7,8-didehydromorphinan-6-one
CAS:(9α,13α,14α)-4-Hydroxy-3,7-dimethoxy-7,8-didehydromorphinan-6-one is a major mechanism of Sinomenine.Fórmula:C18H21NO4Pureza:97.85%Forma y color:SoildPeso molecular:315.36D228
CAS:<p>D228 is an oral anti-inflammatory,inhibi B and T lymphocytes, down-regulation of MyD88/TRAF6/p38 and up-regulation of IL-10,inflammatory bowel disease (IBD).</p>Fórmula:C22H28O12Pureza:99.91%Forma y color:SolidPeso molecular:484.45Amfenac
CAS:<p>Amfenac promotes apoptosis in ARPE-19 cell culture.</p>Fórmula:C15H13NO3Forma y color:SolidPeso molecular:255.27Avasopasem manganese
CAS:<p>Avasopasem manganese is a drug candidate of superoxide dismutase mimetic.</p>Fórmula:C21H35Cl2MnN5Pureza:98%Forma y color:SolidPeso molecular:483.38TMV-IN-9
CAS:<p>TMV-IN-9 (compound A6) is an antiviral agent that exhibits exceptional inactivation effects against Tobacco Mosaic Virus (TMV), with an EC50 of 62.8 μg/mL. It demonstrates strong binding capabilities to the TMV capsid protein, with a binding affinity of 1.862 μM. Moreover, TMV-IN-9 significantly disrupts the integrity of TMV particles, thereby preventing the virus from infecting the host.</p>Fórmula:C20H20O8Forma y color:SolidPeso molecular:388.37FAPI-2
CAS:<p>FAPI-2 is a specific inhibitor of fibroblast-activated protein based on the radiotracer FAP labeling, and has anticancer activity.</p>Fórmula:C40H56N10O10Pureza:98.76%Forma y color:SolidPeso molecular:836.933,4-DAA
CAS:<p>3,4-DAA has anti-inflammatory activity and inhibits EOC20 cell-induced nitric oxide synthase (iNOS) induced by IFN-γ and lipopolysaccharide.</p>Fórmula:C18H17NO6Pureza:98%Forma y color:SolidPeso molecular:343.33Azacyclonol hydrochloride
CAS:<p>Azacyclonol hydrochloride can be used in the treatment of chronic schizophrenia.</p>Fórmula:C18H22ClNOForma y color:Off White Crystalline PowderPeso molecular:303.83AZD4144
CAS:<p>AZD4144 is a potent and selective NLRP3 inhibitor (IC50 = 54 nM) that reducs IL-1β and IL-18 production for immune disorders.</p>Fórmula:C18H16F3N3O3Pureza:99.02%Forma y color:SoildPeso molecular:379.33Etokimab
CAS:<p>Etokimab (ANB-020) is a humanised monoclonal antibody targeting IL-33, neutrophil migration, atopic dermatitis, asthma, and sinusitis.</p>Pureza:95%Forma y color:LiquidAHR-10037
CAS:<p>AHR-10037, a NSAID, offers pain relief, fever reduction, safety, and low stomach risk, acting as a prodrug for COX inhibitors.</p>Fórmula:C15H13ClN2O2Pureza:98%Forma y color:SolidPeso molecular:288.73Kamebakaurin
CAS:<p>Kamebakaurin combats liver toxicity, cancer, inflammation, and neuroinflammation by blocking NF-κB, HIF-1α, and key signaling pathways.</p>Fórmula:C20H30O5Pureza:98.05%Forma y color:SolidPeso molecular:350.45Allopurinol Sodium
CAS:<p>Allopurinol Sodium is a xanthine oxidase inhibitor with an IC50 of 7.82±0.12 μM.</p>Fórmula:C5H4N4NaOPureza:99.93%Forma y color:SolidPeso molecular:159.1Catalase
CAS:<p>Catalase, an enzyme, metabolizes H2O2 and ROS; its expression and localization change significantly in tumors.</p>Pureza:≥98%Forma y color:Small Colorless Crystals Or Powder At Room Temperature Almost Odourless Small Colourless Crystals Or A White Crystalline PowderE3330
CAS:<p>E3330 is a potent and selective APE1(Ref-1) inhibitor, which suppressed NF-kappa B DNA-binding activity.</p>Fórmula:C21H30O6Pureza:99.52%Forma y color:SolidPeso molecular:378.46Pelubiprofen
CAS:<p>Pelubiprofen is a non-steroidal anti-inflammatory agent and a COX-2 inhibitor, which effectively reduces PGE(2) production by inhibiting COX activity.</p>Fórmula:C16H18O3Pureza:99.69%Forma y color:SolidPeso molecular:258.31K-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:420.81Naproxen glucuronide
CAS:<p>Naproxen glucuronide: NSAID, propionic class, eases pain, fever, inflammation. Nonselective COX blocker.</p>Fórmula:C20H22O9Forma y color:SolidPeso molecular:406.38CHD-5
CAS:<p>CHD-5 is a selective antagonist of the aryl hydrocarbon receptor (AhR).</p>Fórmula:C19H17N3O2Forma y color:SolidPeso molecular:319.36IRAK4-IN-22
CAS:<p>IRAK4-IN-22: oral IRAK4 inhibitor, IC50: IRAK4-3nM, TAK1-17nM, disrupts IL-23, targets autoimmune diseases.</p>Fórmula:C28H28FN7O2Forma y color:SolidPeso molecular:513.57Enflicoxib
CAS:<p>Enflicoxib is an effective treatment for canine osteoarthritis pain and inflammation, with faster onset than mavacoxib, improving veterinary outcomes.</p>Fórmula:C16H12F5N3O2SPureza:99.88%Forma y color:SolidPeso molecular:405.34MIF-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:523.62Tilarginine citrate
CAS:<p>Tilarginine citrate is a competitive nitric oxide synthetase inhibitor.</p>Fórmula:C13H24N4O9Pureza:98%Forma y color:SolidPeso molecular:380.354NPD926
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:369.45HE 3286
CAS:<p>Triolex, an NF-kB inhibitor, is used potentially for the treatment of rheumatoid arthritis, ulcerative colitis.</p>Fórmula:C21H30O3Forma y color:SolidPeso molecular:330.46COX-2-IN-21
CAS:<p>COX-2-IN-21 (Compound 5c) is an orally active, selective COX-2 inhibitor (IC50: 0.039 μM). COX-2-IN-21 has good anti-inflammatory potential.</p>Fórmula:C21H22N6O4Forma y color:SolidPeso molecular:422.44NF-κB-IN-3
CAS:<p>NF-κB-IN-3 (Compound 2) is an NF-κB inhibitor (IC50: 0.70 μM) and can be used as an anti-tumour agent.</p>Fórmula:C24H18ClF3N2O2Forma y color:SolidPeso molecular:458.863-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:436.03AChE/Nrf2 modulator 1
CAS:<p>AChE/Nrf2 modulator 1: oral, targets AChE/Nrf2, IC50s: 0.07 μM (eeAChE), 0.38 μM (hAChE); for Alzheimer's research.</p>Fórmula:C27H27FN4O2Forma y color:SolidPeso molecular:458.53Nrf2 activator-5
CAS:<p>Nrf2 activator-5 combats oxidative stress and inflammation in microglia, with potent antioxidant effects.</p>Fórmula:C25H30Cl2O6Forma y color:SolidPeso molecular:497.41Antimicrobial agent-2
CAS:<p>Compound V-a: broad-spectrum, low-toxicity antimicrobial with no resistance, high bioavailability, damages membranes, targets MRSA (MIC 1μg/mL).</p>Fórmula:C16H14N2O4SForma y color:SolidPeso molecular:330.36NLRP3-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:448.42iNOs-IN-3
CAS:<p>iNOs-IN-3: oral iNOS inhibitor, IC50 = 3.342 μM, anti-inflammatory, for LPS-induced ALI study.</p>Fórmula:C27H24N2O5SForma y color:SolidPeso molecular:488.55Keap1-Nrf2-IN-11
CAS:<p>Keap1-Nrf2-IN-11 (6k) inhibits Keap1-Nrf2, KD 0.21 nM; reduces ROS, NO, TNF-α; aids anti-inflammatory research.</p>Fórmula:C36H43N7O8S2Forma y color:SolidPeso molecular:765.910-Cl-BBQ
CAS:<p>10-Cl-BBQ is a ligand of aryl hydrocarbon receptor (AhR).</p>Fórmula:C18H9ClN2OForma y color:SolidPeso molecular:304.73IKK2-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:261.3NXPZ-2
CAS:<p>NXPZ-2, an oral Keap1-Nrf2 PPI inhibitor (Ki: 95 nM, EC50: 120-170 nM), may improve cognition and neuron health in AD.</p>Fórmula:C27H27N5O7S2Forma y color:SolidPeso molecular:597.66APHS
CAS:<p>APHS is a cyclooxygenase-2 (COX-2) inhibitor with anti-inflammatory action. It also more potent than aspirin in the inhibition of COX-1.</p>Fórmula:C15H18O2SForma y color:SolidPeso molecular:262.37Keap1-Nrf2-IN-12
CAS:<p>eap1-Nrf2-IN-12 is a potent inhibitor of Keap1-Nrf2 (IC50: 2.30 μM). eap1-Nrf2-IN-12 is metabolically stable in human liver microsomes.</p>Fórmula:C26H28N2O10S2Forma y color:SolidPeso molecular:592.64Piroxicam cinnamate
CAS:<p>Cinnoxicam is a COX inhibitor used for bone/joint inflammation, rheumatic issues, and varicocele-related oligospermia.</p>Fórmula:C24H19N3O5SForma y color:SolidPeso molecular:461.49IT-901
CAS:<p>IT-901: Oral NF-κB c-Rel inhibitor, IC50 0.1 µM. Blocks c-Rel/DNA binding, IC50 3 µM. Antitumor naphthalene derivative for lymphoma/myeloma therapy.</p>Fórmula:C17H14N2O4SPureza:98.06%Forma y color:SolidPeso molecular:342.37P2X7-IN-2
CAS:<p>P2X7-IN-2 is a P2X7 receptor blocker, halts IL-Iβ release (IC50: 0.01 nM), researched for autoimmunity and heart issues.</p>Fórmula:C22H21F4N3O2Forma y color:SolidPeso molecular:435.41PT4
CAS:<p>PT4: treats CL, disrupts parasite mitochondria, kills Leishmania spp., IC50- L. amazonensis 125.18 μM, L. braziliensis 233.18 μM, anti-inflammatory.</p>Fórmula:C18H14N4O2Forma y color:SolidPeso molecular:318.33COX-2/5-LOX-IN-2
CAS:<p>COX-2/5-LOX-IN-2, a benzothiophen derivative, inhibits COX-1, COX-2, 5-LOX with IC50s of 5.40, 0.01, 1.78 μM. More effective than Celecoxib, Indomethacin.</p>Fórmula:C18H13N3O4S2Forma y color:SolidPeso molecular:399.44DMX-129
CAS:<p>DMX-129 is a chemical compound acting as an inhibitor for both ΙΚΚε and TBK-1, demonstrating efficacy with IC50 values of below 30 nM for each [1].</p>Fórmula:C19H17FN8Forma y color:SolidPeso molecular:376.39CAY10589
CAS:<p>CAY10589 is an mPGES-1 inhibitor.</p>Fórmula:C25H28ClN3O2SForma y color:SolidPeso molecular:470.03COX-2-IN-19
CAS:<p>COX-2-IN-19, a potent COX-2 inhibitor, IC50 of 1.76 μM, has strong anti-inflammatory effects in vivo.</p>Fórmula:C18H18N4O2SForma y color:SolidPeso molecular:354.43COX-2-IN-24
CAS:<p>COX-2-IN-24 is an orally active COX-2 inhibitor (IC50: 0.17 μM) with anti-inflammatory and hypo-ulcerogenic effects.</p>Fórmula:C24H24BrN5O3S2Forma y color:SolidPeso molecular:574.51L-NMMA acetate
CAS:L-NMMA acetate inhibits all NOS types (nNOS, eNOS, iNOS); Ki: 0.18, 0.4, 6 µM respectively.Fórmula:C9H20N4O4Pureza:99.72% - 99.8%Forma y color:White To Off-White SolidPeso molecular:248.28PPM-18
CAS:<p>PPM-18 (NSC 73233), a potent anti-inflammatory, inhibits iNOS and NF-κB binding; also suppresses bladder cancer cell growth.</p>Fórmula:C17H11NO3Forma y color:SolidPeso molecular:277.271-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:346.46IRAK4-IN-13
CAS:<p>IRAK4-IN-13 (compound 21) is a potent IRAK4 inhibitor, IC50 0.6 nM, with high HLM clearance at 96 μL/min/mg.</p>Fórmula:C24H27N9OForma y color:SolidPeso molecular:457.53COX-2-IN-23
CAS:<p>COX-2-IN-23 selectively inhibits COX-2 (IC50=0.28μM), weakly affects COX-1 (IC50=20.14μM), and has anti-inflammatory and low ulcerogenic properties.</p>Fórmula:C24H25N5O3S2Forma y color:SolidPeso molecular:495.62IFN α-IFNAR-IN-1
CAS:<p>Nonpeptidic IFN-α/IFNAR blocker, halts MVA-triggered BM-pDC IFN-α response; IC50: 2-8 μM.</p>Fórmula:C18H17NSPureza:98%Forma y color:SolidPeso molecular:279.4COX-1/2-IN-3
CAS:<p>COX-1/2-IN-3 (Compound 7a) is a dual inhibitor of COX-1 and COX-2. COX-1/2-IN-3 has anti-inflammatory activity with low toxicity [1].</p>Fórmula:C14H8N2O8Forma y color:SolidPeso molecular:332.22Z-VRPR-FMK
CAS:<p>Z-VRPR-FMK: irreversible MALT1 inhibitor, halts growth/invasion of diffused B-cell lymphoma by blocking NF-κB activation and MMP expression.</p>Fórmula:C31H49FN10O6Forma y color:SolidPeso molecular:676.78COX-1/2-IN-1
CAS:<p>"COX-1/2-IN-2: Strong dual inhibitor of COX-1 (IC50 = 13.9 μM) and COX-2 (IC50 = 6.4 μM)."</p>Fórmula:C15H10BrClN2OForma y color:SolidPeso molecular:349.61β-Nor-lapachone
CAS:β-Nor-lapachone is an antibiofilm agent of Candida glabrata.Fórmula:C14H12O3Forma y color:SolidPeso molecular:228.24Keap1-Nrf2-IN-14
CAS:<p>Keap1-Nrf2-IN-14, a KEAP1-NRF2 inhibitor (IC50: 75 nM, Kd: 24 nM), boosts NRF2 gene expression, antioxidative and anti-inflammatory response.</p>Fórmula:C30H29NO8SForma y color:SolidPeso molecular:563.62COX-2/sEH-IN-1
CAS:<p>COX-2/sEH-IN-1, oral dual inhibitor: COX-2 (IC50=1.24 μM), sEH (IC50=0.40 μM); boosts anti-inflammatory action, cuts heart risk.</p>Fórmula:C23H18F3N5O3SForma y color:SolidPeso molecular:501.48Veledimex (S enantiomer)
CAS:Veledimex S is the oral S enantiomer of a gene therapy promoter activator and CYP3A4/5 inhibitor.Fórmula:C27H38N2O3Pureza:98%Forma y color:SolidPeso molecular:438.6PNRI-299
CAS:<p>PNRI-299 is a selective inhibitor of AP-1 transcription(IC50 of 20 uM ).</p>Fórmula:C21H15N5O4Pureza:98%Forma y color:SolidPeso molecular:401.37Naphazoline
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:Vidarabine phosphate is an adenosine monophosphate analog.Fórmula:C10H14N5O7PPureza:99.75%Forma y color:White Crystalline PowderPeso molecular:347.22TMV-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>Fórmula:C28H26O4Forma y color:SolidPeso molecular:426.5TLR7/8 agonist 6
CAS:<p>Compound 4: Imidazoquinoline, potent TLR7/8 agonist, IC50: 0.18μM (TLR7), 5.34μM (TLR8).</p>Fórmula:C24H27N5O2Forma y color:SolidPeso molecular:417.5APC-0576
CAS:<p>APC-0576, an (S,S)-isomer, blocks NF-kappaB gene activation and may reduce inflammation in human cells.</p>Fórmula:C23H27N3O3Forma y color:SolidPeso molecular:393.48COX-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>Fórmula:C11H9ClFN3O2Forma y color:SolidPeso molecular:269.66C5aR-IN-2
CAS:<p>C5aR-IN-2, a potent C5aR inhibitor, shows promise for researching inflammatory diseases.</p>Fórmula:C36H40FN5O2Forma y color:SolidPeso molecular: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>Fórmula:C28H32N2O10S2Forma y color:SolidPeso molecular: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>Fórmula:C20H24N10O12P2Pureza:98%Forma y color:SolidPeso molecular:658.41BC12-4
CAS:<p>BC12-4 is a novel potent inhibitor of IL-2 secretion, it has potent immunomodulatory activity.</p>Fórmula:C19H14N2O3Forma y color:SolidPeso molecular:318.33STING modulator-4
CAS:STING modulator-4: competitive, Ki=0.0933 μM (R232H STING), EC50 >10 μM (p-IRF3, THP-1 cells).Fórmula:C17H18N8OForma y color:SolidPeso molecular:350.38L-Kynurenine sulfate
CAS:<p>L-Kynurenine sulfate activates AHR, leading naive T cells to anti-inflammatory Treg phenotype.</p>Fórmula:C10H14N2O7SForma y color:SolidPeso molecular:306.29OPC-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>Fórmula:C14H8F3N5SPureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C21H27N3O2Forma y color:SolidPeso molecular: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>Fórmula:C17H20F2N8OForma y color:SolidPeso molecular: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>Fórmula:C25H32ClN3O3Forma y color:SolidPeso molecular:457.99Nω-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>Fórmula:C9H21ClN4O2Forma y color:SolidPeso molecular:252.74APY0201
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:Oxyfenamate has anti-anxiety actions. It is also used in anxiety neuroses.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:400.27Eltrombopag methyl ester
CAS:<p>Eltrombopag methyl ester, a Tpo receptor agonist derivative, boosts platelet production for thrombocytopenia research.</p>Fórmula:C26H24N4O4Forma y color:SolidPeso molecular:456.49FR20
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:535.33Cyclic-di-GMP diammonium
CAS:<p>C-di-GMP diammonium activates STING, regulates biofilms, motility, and virulence in bacteria.</p>Fórmula:C20H30N12O14P2Forma y color:SolidPeso molecular:724.47hDDAH-1-IN-1
CAS:hDDAH-1-IN-1 is a selective non-amino acid catalytic site inhibitor of human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) (Ki: 18 μM).Fórmula:C8H20N4OPureza:98%Forma y color:SolidPeso molecular:188.27BPK-29
CAS:BPK-29 disrupts NR0B1 binding and modifies C274, inhibiting growth in KEAP1-mutant cancers.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:289.71Tyrosinase-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>Fórmula:C16H12ClN3SPureza:99.2%Forma y color:SoildPeso molecular:313.8QM385
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:409.37NOS-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>Fórmula:C10H15N3OForma y color:SolidPeso molecular:193.25Isoandrographolide
CAS:<p>Isoandrographolide induces cell differentiation, protects the liver, blocks NLRP3, and reduces silicosis in mice.</p>Fórmula:C20H30O5Forma y color:SolidPeso molecular:350.45AN-3485
CAS:<p>AN-3485 is a Toll-Like Receptor(TLR) inhibitor (IC50s: 18 to 580 nM).</p>Fórmula:C14H13BClNO3Forma y color:SolidPeso molecular:289.52PHA-408
CAS:<p>PHA-408 is a novel potent, highly selective and ATP-competitive inhibitor of IKB kinase-2.</p>Fórmula:C29H27ClFN7O2Pureza:98%Forma y color:SolidPeso molecular:560.02546C88
CAS:<p>546C88 is an inhibitor of nitric oxide synthase.</p>Fórmula:C7H17ClN4O2Pureza:98%Forma y color:SolidPeso molecular:224.69STING 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>Fórmula:C19H11Cl2N5OForma y color:SolidPeso molecular:396.23Etoricoxib 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:401.41(+)-DHMEQ
CAS:(+)-DHMEQ is an antioxidant transcription factor Nrf2 activator. (+)-DHMEQ is the enantiomer of (-)-DHMEQ.Fórmula:C13H11NO5Forma y color:SolidPeso molecular:261.23NCX 466
CAS:<p>cyclooxygenase (COX)-inhibiting nitric oxide (NO) donor</p>Fórmula:C20H24N2O9Pureza:98%Forma y color:SolidPeso molecular:436.41COX-2-IN-16
CAS:<p>COX-2-IN-16: potent, selective oral COX-2 blocker, IC50=102 μM, reduces NO, anti-inflammatory.</p>Fórmula:C19H12BrN3O2Forma y color:SolidPeso molecular:394.22hDDAH-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:416.32QD-394
CAS:<p>QD-394 promotes ROS, impairs GSH/GSSG ratio, and is cytotoxic to pancreatic cancer cells, with synergy with napabucasin.</p>Fórmula:C19H19N5O2Forma y color:SolidPeso molecular: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>Fórmula:C20H25Cl2FN4OSPureza:99.89%Forma y color:SolidPeso molecular:459.41MHY884
CAS:<p>MHY884 inhibits tyrosinase and UVB-triggered NF-κB activation by reducing oxidative stress.</p>Fórmula:C15H14ClNO3SPureza:98%Forma y color:SolidPeso molecular:323.79NLRP3 antagonist 1
CAS:<p>Potential cancer research drug, NLRP3 antagonist 1, targets immune response in macrophages, neutrophils.</p>Fórmula:C16H18N6OForma y color:SolidPeso molecular:310.35AHR antagonist 5
CAS:<p>Potent, oral AHR blocker from WO2018195397; IC50 < 0.5μM; hinders tumor growth with anti-PD-1.</p>Fórmula:C25H27Cl3FN7Pureza:98%Forma y color:SolidPeso molecular:550.89PC407-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:416.54Tilarginine
CAS:<p>Tilarginine is a nitric oxide synthetase competitive inhibitor.</p>Fórmula:C7H16N4O2Pureza:98%Forma y color:SolidPeso molecular:188.23TBK1/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>Fórmula:C28H35N7O4Forma y color:SolidPeso molecular:533.62NRP1 antagonist 2
CAS:<p>NRP1 antagonist 2 (Compound 1) is an NRP1 antagonist.</p>Fórmula:C20H17ClN6OS2Forma y color:SolidPeso molecular:456.97Propoxur
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:209.24Thiazolinobutazone
CAS:<p>Thiazolinobutazone is the 2-amino-2-thiazoline salt of phenylbutazone.</p>Fórmula:C22H26N4O2SForma y color:SolidPeso molecular:410.53COX/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>Fórmula:C16H15FN2O2SPureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C14H22Cl2N2O3SPureza:97.44%Forma y color:PowderPeso molecular: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>Fórmula:C18H18N4O6Forma y color:SolidPeso molecular:386.364Isonixin
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:300.35Hetrombopag
CAS:<p>Hetrombopag: potent thrombopoietin receptor agonist, well tolerated, safe, promising for immune thrombocytopenia research.</p>Fórmula:C25H22N4O5Forma y color:SolidPeso molecular:458.47Tenosal
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:300.37Ppc-1
CAS:<p>Ppc-1 inhibits Porphyromonas gingivalis, uncouples mitochondria, and blocks IL-2, with anti-obesity, antibacterial, anti-inflammatory effects.</p>Fórmula:C21H25NO4Pureza:98%Forma y color:SolidPeso molecular:355.43Nrf2-Activator-12G
CAS:<p>Nrf2-Activator-12G is a potent Nrf-2 activator.</p>Fórmula:C15H13ClO3SPureza:98%Forma y color:SolidPeso molecular:308.78(-)-Ibuprofenamide
CAS:(-)-Ibuprofenamide is an amide prodrug of Ibuprofen with anti-inflammatory activity.Fórmula:C13H19NOPureza:98%Forma y color:SolidPeso molecular:205.3Carboxyamidotriazole
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:424.67MALT1-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>Fórmula:C20H15Cl2N7OForma y color:SolidPeso molecular:440.29U-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:593.63IL-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>Fórmula:C22H34O2Forma y color:SolidPeso molecular: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>Fórmula:C21H18N2OPureza:98%Forma y color:SolidPeso molecular:314.38NOC-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:176.22SARS-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:432.47UC-1V150
CAS:<p>UC-1V150: TLR7 agonist, triggers immune response, anti-tumor, precursor for ISAC synthesis.</p>Fórmula:C16H17N5O4Forma y color:SolidPeso molecular: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>Fórmula:C20H26ClN3O2SForma y color:SolidPeso molecular: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>Fórmula:C18H16BCl3N2O2Forma y color:SolidPeso molecular:409.5STING ligand-1
CAS:<p>STING ligand-1 is a lead STING ligand(IC50 of 68 nM for HAQ STING).</p>Fórmula:C29H27ClFNO5Pureza:98%Forma y color:SolidPeso molecular:523.98Anti-inflammatory agent 8
CAS:<p>Anti-inflammatory agent 8 targets COX-2 over COX-1, IC50 of 0.09 nM, orally bioavailable.</p>Fórmula:C18H15N5OS2Forma y color:SolidPeso molecular:381.47iNOS-IN-2
CAS:<p>iNOS-IN-2 (Compound 53) is a potent inducible nitric oxide synthase (iNOS) protein down-regulator.</p>Fórmula:C25H31NO7Forma y color:SolidPeso molecular:457.52NOS1-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:653.05Prostaglandin 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>Fórmula:C13H11ClN2OPureza:99.76%Forma y color:SolidPeso molecular:246.697-NINA
CAS:non-selective NOS inhibitorFórmula:C7H5N3NaO2Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C15H17ClN2OSForma y color:SolidPeso molecular:308.83CID-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:465.63MALT1-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>Fórmula:C21H19F3N8O2Forma y color:SolidPeso molecular:472.42MK-0703
CAS:<p>MK-0703 is a selective cyclooxygenase-2 inhibitor.</p>Fórmula:C17H22O5SPureza:98%Forma y color:SolidPeso molecular:338.42Insulin levels modulator
CAS:<p>Insulin level regulators can be used to treat diabetes.</p>Fórmula:C21H23N7OSPureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C14H10ClN3O4S2Forma y color:SolidPeso molecular:383.83IKKβ-IN-1
CAS:<p>IKKβ-IN-1 is a potent, orally active inhibitor of IkappaB (IKK-β) (IC50: 0.20 μM).</p>Fórmula:C31H30N4O4SForma y color:SolidPeso molecular: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>Fórmula:C20H15N5O3SForma y color:SolidPeso molecular: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>Fórmula:C28H28FN7O2Forma y color:SolidPeso molecular:513.57MitoB
CAS:<p>MitoB is a novel exon of mitochondrial hydrogen peroxide.</p>Fórmula:C25H23BBrO2PForma y color:SolidPeso molecular: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>Fórmula:C26H42O10Forma y color:SolidPeso molecular:514.61RWJ 63556
CAS:RWJ 63556 is an orally active inhibitor of COX-2 selective/5-lipoxygenase, shows anti-inflammatory activities.Fórmula:C11H10FNO3S2Pureza:99.92%Forma y color:SolidPeso molecular:287.33Nrf2 activator-3
CAS:Nrf2 activator-3 is an Nrf2 activator with potential anti-inflammatory, antioxidant and anti-tumor activity for the study of neurological diseases.Fórmula:C23H18F3N3O2Pureza:98.52% - 99.84%Forma y color:SolidPeso molecular:425.4Ruzotolimod
CAS:<p>Ruzotolimod, an agonist of TLR7, exhibits promising potential for investigating HBV, COVID-19, and SARS-CoV-2 infections （WO2021130195A1）[1].</p>Fórmula:C14H18N4O5SForma y color:SolidPeso molecular: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>Fórmula:C21H21N7S3Forma y color:SolidPeso molecular:467.63Clopirac
CAS:<p>Clopirac is a potent and orally active prostaglandin synthetase inhibitor that is an anti-inflammatory agent [1].</p>Fórmula:C14H14ClNO2Forma y color:SolidPeso molecular:263.72ROS 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:415.45NF-κB-IN-2
CAS:<p>NF-κB-IN-2 inhibits canonical NF-κB signaling induced by TNF-α in PC-3 cells.</p>Fórmula:C15H18O3Forma y color:SolidPeso molecular:246.3IND24
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:343.44Methyl aminolevulinate
CAS:<p>Methyl aminolevulinate, a prodrug for protoporphyrin IX, sensitizes in PDT.</p>Fórmula:C6H11NO3Pureza:98%Forma y color:SolidPeso molecular:145.16
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