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Inmunología e inflamación

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"

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Se han encontrado 3269 productos de "Inmunología e inflamación"

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  • Tenosal

    CAS:
    Tenosal obtained by esterifying salicylic acid with 2-thiophene-carboxylic acid, and with analgesic and antipyretic properties, anti-inflammatory.
    Fórmula:C12H8O4S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:248.25
  • Bay 65-1942 free base

    CAS:
    Bay 65-1942 free base is an inhibitor of ATP-competitive and selective IKKβ.
    Fórmula:C22H25N3O4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:395.45
  • KIN1400

    CAS:
    <p>KIN1400 activates IRF3, boosts antiviral immunity, stimulates IFNbeta, and inhibits WNV, DV, and HCV.</p>
    Fórmula:C24H17F2N3O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:449.47
  • PPM-18

    CAS:
    PPM-18 (NSC 73233), a potent anti-inflammatory, inhibits iNOS and NF-κB binding; also suppresses bladder cancer cell growth.
    Fórmula:C17H11NO3
    Forma y color:Solid
    Peso molecular:277.27
  • Eltrombopag methyl ester

    CAS:
    Eltrombopag methyl ester, a Tpo receptor agonist derivative, boosts platelet production for thrombocytopenia research.
    Fórmula:C26H24N4O4
    Forma y color:Solid
    Peso molecular:456.49
  • Bifenazate

    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:C17H20N2O3
    Pureza:99.62%
    Forma y color:Solid Crystalline
    Peso molecular:300.35
  • Naphazoline

    CAS:
    Naphazoline (Naphcon-a) is a sympathomimetic compound with marked alpha adrenergic activity.
    Fórmula:C14H14N2
    Pureza:99.79%
    Forma y color:White Crystalline Powder Solid
    Peso molecular:210.27
  • ARV-393

    CAS:
    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)
    Fórmula:C46H53ClFN9O7
    Pureza:99.96%
    Forma y color:Soild
    Peso molecular:898.42
  • Isonixin

    CAS:
    Isonixin is used for the treatment of inflammation and pain associated with musculoskeletal and joint disorders.
    Fórmula:C14H14N2O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:242.27
  • BSP16

    CAS:
    BSP16: potent, oral STING agonist; boosts interferon genes; promising for cancer research.
    Fórmula:C16H18O5Se
    Forma y color:Solid
    Peso molecular:369.27
  • Cyclic-di-GMP diammonium

    CAS:
    C-di-GMP diammonium activates STING, regulates biofilms, motility, and virulence in bacteria.
    Fórmula:C20H30N12O14P2
    Forma y color:Solid
    Peso molecular:724.47
  • Propoxur

    CAS:
    Propoxur: an insecticide causing temporary cholinergic effects in humans; chronic exposure leads to health issues; carcinogenicity unclassified by EPA.
    Fórmula:C11H15NO3
    Pureza:99.84% - 99.87%
    Forma y color:Minute Crystals (Niosh 2016)
    Peso molecular:209.24
  • COX-2-IN-24

    CAS:
    COX-2-IN-24 is an orally active COX-2 inhibitor (IC50: 0.17 μM) with anti-inflammatory and hypo-ulcerogenic effects.
    Fórmula:C24H24BrN5O3S2
    Forma y color:Solid
    Peso molecular:574.51
  • DDX3-IN-2

    CAS:
    DDX3-IN-2 is a potent DDX3 inhibitor with an IC50 of 0.3 μM and shows broad antiviral effects, including against HIV resistance.
    Fórmula:C20H23N5O
    Forma y color:Solid
    Peso molecular:349.43
  • COX/5-LOX-IN-1

    CAS:
    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.
    Fórmula:C18H30O3
    Forma y color:Solid
    Peso molecular:294.43
  • TRAF-STOP inhibitor 6877002

    CAS:
    TRAF-STOP 6877002 inhibits CD40-TRAF6, curbing leukocyte recruitment and macrophage activation/proliferation in plaques.
    Fórmula:C17H17NO
    Pureza:99.76%
    Forma y color:Solid
    Peso molecular:251.32
  • Ophthalmic acid

    CAS:
    Ophthalmic acid is a glutathione analog in which cysteine is substituted by L-aminobutyrate.
    Fórmula:C11H19N3O6
    Forma y color:Solid
    Peso molecular:289.29
  • IND24

    CAS:
    <p>IND24 has anti-prion activity and can be used to study neurodegenerative diseases.</p>
    Fórmula:C21H17N3S
    Pureza:99.64%
    Forma y color:Solid
    Peso molecular:343.44
  • MIF-IN-2

    CAS:
    MIF-IN-2 is a MIF inhibitor with anticancer activity for the study of cancer and autoimmune diseases.
    Fórmula:C14H10ClN3O4
    Pureza:98.55%
    Forma y color:Solid
    Peso molecular:319.7
  • CB2 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:C18H19F3N4O2
    Pureza:99.6%
    Forma y color:Solid
    Peso molecular:380.36
  • LY 178002

    CAS:
    LY 178002 inhibits 5-LPO (IC50: 0.6 μM), PLA2, and LTB4 production; weak on cyclooxygenase.
    Fórmula:C18H25NO2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:319.46
  • Dibenzo(a,i)pyrene

    CAS:
    Dibenzo(a, i)pyrene is a polycyclic aromatic hydrocarbon with potent carcinogenic activity.
    Fórmula:C24H14
    Forma y color:Greenish-Yellow Needles Prisms Or Lamellae Dibenz[A I]Pyrene Is A Colorless Solid Water Insoluble
    Peso molecular:302.37
  • 6,2',4'-Trimethoxyflavone

    CAS:
    The compound is an Aryl hydrocarbon receptor antagonist (EC50 = 0.9 μM). It also has no short term agonist activity and no species or promoter dependence.
    Fórmula:C18H16O5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:312.32
  • AR-C 102222

    CAS:
    AR-C 102222 is an iNOS inhibitor.
    Fórmula:C19H16F2N6O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:382.37
  • Safrole 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:C10H10O3
    Pureza:100%
    Forma y color:Solid
    Peso molecular:178.18
  • IRAK4-IN-16

    CAS:
    IRAK4-IN-16 inhibits IRAK4 at 2.5nM; cytotoxic to OCI-LY10, TMD8, Ramos, HT cells with IC50s of 0.2, 0.2, 0.6, 2.7μM.
    Fórmula:C17H20F2N8O
    Forma y color:Solid
    Peso molecular:390.39
  • OXSI-2

    CAS:
    OXSI-2 (Syk Inhibitor) is an inhibitor of Syk with an EC50 of 313 nM and an IC50 of 14 nM.
    Fórmula:C18H15N3O3S
    Pureza:98%
    Forma y color:Dark Orange Solid
    Peso molecular:353.39
  • AHR-6293

    CAS:
    AHR-6293 is used to distinguishing the effect of anti-platelet aggregating drug properties and the effect of anti-inflammatory properties.
    Fórmula:C15H12ClNO3
    Forma y color:Solid
    Peso molecular:289.71
  • IMD-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:C36H41N7O4
    Forma y color:Solid
    Peso molecular:635.76
  • COX-2-IN-21

    CAS:
    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.
    Fórmula:C21H22N6O4
    Forma y color:Solid
    Peso molecular:422.44
  • UPF-648 sodium salt

    CAS:
    UPF-648 sodium salt is an inhibitor of kynurenine 3-monooxygenase (KMO) and exhibits highly active at 1 uM (81 ± 10% KMO inhibition).
    Fórmula:C11H8Cl2NaO3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:282.07
  • MALT1-IN-8

    CAS:
    MALT1-IN-8: potent MALT1 inhibitor, IC50=2 nM; hinders OCI-LY3 cells, IC50=1.16 μM; anticancer, from patent WO2018165385A1.
    Fórmula:C20H15Cl2N7O
    Forma y color:Solid
    Peso molecular:440.29
  • (-)-Ibuprofenamide

    CAS:
    (-)-Ibuprofenamide is an amide prodrug of Ibuprofen with anti-inflammatory activity.
    Fórmula:C13H19NO
    Pureza:98%
    Forma y color:Solid
    Peso molecular:205.3
  • Nrf2-Activator-12G

    CAS:
    <p>Nrf2-Activator-12G is a potent Nrf-2 activator.</p>
    Fórmula:C15H13ClO3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:308.78
  • BPK-29

    CAS:
    BPK-29 disrupts NR0B1 binding and modifies C274, inhibiting growth in KEAP1-mutant cancers.
    Fórmula:C26H32ClN3O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:470
  • HE 3286

    CAS:
    Triolex, an NF-kB inhibitor, is used potentially for the treatment of rheumatoid arthritis, ulcerative colitis.
    Fórmula:C21H30O3
    Forma y color:Solid
    Peso molecular:330.46
  • Simvastatin acid calcium hydrate

    CAS:
    Simvastatin (Tenivastatin) calcium hydrate is an oral HMG-CoA reductase inhibitor that reduces ROS by blocking indoxyl sulfate.
    Fórmula:C25H40O6
    Forma y color:Solid
    Peso molecular:436.28249
  • Ppc-1

    CAS:
    Ppc-1 inhibits Porphyromonas gingivalis, uncouples mitochondria, and blocks IL-2, with anti-obesity, antibacterial, anti-inflammatory effects.
    Fórmula:C21H25NO4
    Pureza:98%
    Forma y color:Solid
    Peso molecular:355.43
  • Bay 65-1942 hydrochloride

    CAS:
    Bay 65-1942 hydrochloride is an inhibitor of ATP-competitive and selective IKKβ.
    Fórmula:C22H26ClN3O4
    Forma y color:Solid
    Peso molecular:431.91
  • Pifoxime

    CAS:
    Pifoxime: a NSAID with COX-1/2 inhibition, used in anti-inflammatory treatment and neuropsychiatric studies.
    Fórmula:C15H20N2O3
    Forma y color:Solid
    Peso molecular:276.33
  • Naproxcinod

    CAS:
    Naproxcinod is a derivative of naproxen, analgesic and anti-inflammatory, a COX-inhibitory nitric oxide donor (CINOD), osteoarthritis and inflammatory.
    Fórmula:C18H21NO6
    Pureza:99.85%
    Forma y color:Solid
    Peso molecular:347.36
  • CU-32

    CAS:
    <p>CU-32 is a cGAS inhibitor with IC50=0.45 μM, blocks DNA-stimulated IFN-β production, and is selective over RIG-I-MAVS and TLRs pathways.</p>
    Fórmula:C11H10IN5O2
    Forma y color:Solid
    Peso molecular:371.13
  • COX-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:C18H18N4O6
    Forma y color:Solid
    Peso molecular:386.364
  • N-α-Tosyl-L-lysine chloromethyl ketone hydrochloride

    CAS:
    N-alpha-Tosyl-L-lysine chloromethyl ketone hydrochloride inhibits trypsin-like proteases and IFN-γ activities.
    Fórmula:C14H22Cl2N2O3S
    Pureza:97.44%
    Forma y color:Powder
    Peso molecular:369.31
  • TMV-IN-1

    CAS:
    TMV-IN-1: a chalcone inhibits TMV with EC50s of 70.7 and 60.8 μg/mL, applicable in infection and tumor studies.
    Fórmula:C28H26O4
    Forma y color:Solid
    Peso molecular:426.5
  • hDDAH-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:C8H20N4O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:188.27
  • COX/5-LO-IN-1

    CAS:
    COX/5-LO-IN-1 is a cyclooxygenase and 5-lipoxygenase (5-LO) inhibitor, and used for inflammatory and allergic disease states.
    Fórmula:C16H15FN2O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:318.37
  • Thiazolinobutazone

    CAS:
    <p>Thiazolinobutazone is the 2-amino-2-thiazoline salt of phenylbutazone.</p>
    Fórmula:C22H26N4O2S
    Forma y color:Solid
    Peso molecular:410.53
  • NRP1 antagonist 2

    CAS:
    NRP1 antagonist 2 (Compound 1) is an NRP1 antagonist.
    Fórmula:C20H17ClN6OS2
    Forma y color:Solid
    Peso molecular:456.97
  • TBK1/IKKε-IN-4

    CAS:
    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
    Fórmula:C28H35N7O4
    Forma y color:Solid
    Peso molecular:533.62