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Transportador de membrana / canal de iones

Transportador de membrana / canal de iones

Los inhibidores de transportadores de membrana y canales iónicos son compuestos que bloquean la función de proteínas responsables del transporte de iones, nutrientes y otras moléculas a través de las membranas celulares. Estos inhibidores son cruciales para estudiar la regulación de la homeostasis celular, la transducción de señales y la neurotransmisión. Los inhibidores de transportadores de membrana y canales iónicos también son importantes para desarrollar tratamientos para trastornos como la epilepsia, las enfermedades cardiovasculares y los síndromes metabólicos. En CymitQuimica, ofrecemos una amplia selección de inhibidores de alta calidad de transportadores de membrana y canales iónicos para apoyar su investigación en fisiología, neurociencia y farmacología.

Subcategorías de "Transportador de membrana / canal de iones"

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Se han encontrado 2290 productos de "Transportador de membrana / canal de iones"

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  • mGAT3/4-IN-2

    CAS:
    <p>mGAT3/4-IN-2 are potent inhibitors of mGAT3/mGAT4 with their pIC50 values of 5.44 and 5.25, respectively.</p>
    Fórmula:C26H32ClN3OS2
    Forma y color:Solid
    Peso molecular:502.13
  • GDC-6599

    CAS:
    <p>GDC-6599 (Example 8) is an orally active inhibitor of the TRPA1 channel, potentially useful for researching TRPA1-mediated conditions, including pain [1].</p>
    Fórmula:C20H19ClN6O3
    Forma y color:Solid
    Peso molecular:426.86
  • M084 hydrochloride

    CAS:
    <p>M084 hydrochloride, a TRPC4/5 channel blocker, exhibits IC50 values of 10.3 μM and 8.2 μM, respectively. This compound is noted for its antidepressant and anxiolytic effects [1] [2].</p>
    Fórmula:C11H16ClN3
    Forma y color:Solid
    Peso molecular:225.72
  • MONIRO-1

    CAS:
    <p>MONIRO-1 blocks T/N-type Ca²⁺ channels: hCav2.2 (IC50: 34μM), hCav3.1 (3.3μM), hCav3.2 (1.7μM), hCav3.3 (7.2μM).</p>
    Fórmula:C23H24ClFN4O3
    Forma y color:Solid
    Peso molecular:458.92
  • NMDA receptor modulator 6

    CAS:
    <p>NMDA receptor regulator 6 (Compound 183) is an effective NMDA receptor regulator and has research value in neurological disorders.</p>
    Fórmula:C20H17FN2O4S
    Forma y color:Solid
    Peso molecular:400.42
  • Clobutinol hydrochloride

    CAS:
    <p>Clobutinol hydrochloride, an antitussive agent, influences heart rate and blood pressure, and is utilized in cough-related research [1] [2] [3].</p>
    Fórmula:C14H23Cl2NO
    Pureza:98%
    Forma y color:Solid
    Peso molecular:292.25
  • CFTR corrector 12

    CAS:
    <p>CFTR corrector 12 is a CFTR corrector that rescues all mutant proteins except M760R ABCA3 and can be used to study cystic fibrosis.</p>
    Fórmula:C19H21ClN4O2S2
    Pureza:99.47%
    Forma y color:Solid
    Peso molecular:436.98
  • CFTR corrector 6

    CAS:
    <p>CFTR corrector 6, a potent CFTR potentiator, aids cystic fibrosis research and related disorders.</p>
    Fórmula:C22H13F4N9
    Forma y color:Solid
    Peso molecular:479.39
  • LG 83-6-05

    CAS:
    <p>LG 83-6-05 is a novel kind of sodium channel blocking agent.</p>
    Fórmula:C21H30ClNO3S
    Forma y color:Solid
    Peso molecular:411.99
  • TRPC5 modulator-1

    CAS:
    <p>TRPC5 modulator-1 (Compound 9) is a TRPC5 modulator (IC50&lt;1 nM) that can be used to study neuropsychiatric disorders.</p>
    Fórmula:C23H27FN2O4
    Forma y color:Solid
    Peso molecular:414.47
  • ROMK-IN-32

    CAS:
    <p>ROMK-IN-32 is an inhibitor of the extra-renal medullary potassium channel (ROMK) (IC50: 35 nM) and also inhibits hERG (IC50: 22 μM).</p>
    Fórmula:C24H28N4O5
    Forma y color:Solid
    Peso molecular:452.5
  • Dibutyryl-cGMP sodium

    CAS:
    Bt2cGMP sodium is a cGMP analog, activates PKG, inhibits platelet [3H]-arachidonate, and induces analgesia via K+ channels.
    Fórmula:C18H24N5NaO9P
    Pureza:98%
    Forma y color:Solid
    Peso molecular:508.38
  • CGP-54626 free base

    CAS:
    CGP-54626 is a selective antagonist of the GABAB receptor (IC50 = 4 nM ).
    Fórmula:C18H28Cl2NO3P
    Pureza:98%
    Forma y color:Solid
    Peso molecular:408.3
  • GSK3395879

    CAS:
    <p>GSK3395879 is a selective and orally bioavailable antagonist of transient receptor potential vanilloid-4 (TRPV4) (IC50: 1 nM for hTRPV4).</p>
    Fórmula:C20H15F4N3O5S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:485.41
  • SN40 hydrochloride

    CAS:
    <p>SN40 hydrochloride is a potent inhibitor of amino acid transport (AAT), exhibiting inhibitory constants (Kis) of 7.29 μM, 2.42 μM, 2.94 μM, 5.55 μM, 24.43 μM, and 5.55 μM for rat ASCT2, human ASCT2, EAAT1, EAAT2, EAAC1, and EAAT5, respectively. It is utilized in cancer research. [1]</p>
    Fórmula:C18H21ClN2O2
    Forma y color:Solid
    Peso molecular:332.82
  • AMPA-IN-1

    CAS:
    <p>AMPA-IN-1: Potent AMPA receptor inhibitor; key in regulating brain excitatory transmission and plasticity.</p>
    Fórmula:C23H12F2N4O2
    Forma y color:Solid
    Peso molecular:414.36
  • L-822179

    CAS:
    <p>L-822179 (α5IA) is a selective inverse agonist for the Α5 subtype of GABAA receptor with higher intrinsic activity at the A5 subtype than other drugs.</p>
    Fórmula:C17H14N8O2
    Pureza:98.5% - 99.61%
    Forma y color:Solid
    Peso molecular:362.35
  • KCa1.1 channel activator-1


    <p>A selective vascular KCa1.1 channel stimulator with CaV1.2 blocking ability and mild myorelaxant effects.</p>
    Fórmula:C25H16O10
    Forma y color:Solid
    Peso molecular:476.39
  • Afizagabar

    CAS:
    <p>Afizagabar, a first-in-class α5-GABAAR antagonist, IC50: 585 nM, Ki: 66 nM, may boost memory.</p>
    Fórmula:C19H12FN3O2S
    Forma y color:Solid
    Peso molecular:365.38
  • JM-1232

    CAS:
    <p>JM-1232 is a sedative and hypnotic drug being researched as a potential anesthetic.</p>
    Fórmula:C24H27N3O2
    Forma y color:Solid
    Peso molecular:389.49