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Transportador de Membranas/Canal Iónico

Transportador de Membranas/Canal Iónico

Os inibidores de transportadores de membrana e canais iônicos são compostos que bloqueiam a função de proteínas responsáveis pelo transporte de íons, nutrientes e outras moléculas através das membranas celulares. Esses inibidores são cruciais para o estudo da regulação da homeostase celular, transdução de sinais e neurotransmissão. Os inibidores de transportadores de membrana e canais iônicos também são importantes no desenvolvimento de tratamentos para distúrbios como epilepsia, doenças cardiovasculares e síndromes metabólicas. Na CymitQuimica, oferecemos uma ampla seleção de inibidores de alta qualidade de transportadores de membrana e canais iônicos para apoiar sua pesquisa em fisiologia, neurociência e farmacologia.

Subcategorias de "Transportador de Membranas/Canal Iónico"

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Foram encontrados 2290 produtos de "Transportador de Membranas/Canal Iónico"

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  • Ibutilide Fumarate

    CAS:
    <p>Ibutilide Fumarate is a class III antiarrhythmic, prolonging action potentials by enhancing sodium influx, and can extend QT interval.</p>
    Fórmula:(C20H36N2O3S)2·C4H4O4
    Pureza:99.68% - 99.74%
    Cor e Forma:Solid
    Peso molecular:885.23
  • Ko 143

    CAS:
    <p>Ko 143 is a selective inhibitor of ATP-binding cassette sub-family G member 2 (ABCG2; BCRP).</p>
    Fórmula:C26H35N3O5
    Pureza:99.01% - 99.89%
    Cor e Forma:Solid
    Peso molecular:469.57
  • BAY-8002

    CAS:
    <p>BAY-8002 is a potent dual MCT1/2 inhibitor (IC50 values are 3, 8, and 12 nM at rat (C6), human (DLD-1) and mouse (4T1) MCT1 respectively).</p>
    Fórmula:C20H14ClNO5S
    Pureza:98.7% - 99.13%
    Cor e Forma:Solid
    Peso molecular:415.85
  • Phe-Met-Arg-Phe, amide acetate


    <p>Phe-Met-Arg-Phe amide acetate (ED50=23 nM) triggers K+ current in caudodorsal neurons, co-localizes with neuropeptide Y in brain areas.</p>
    Fórmula:C31H46N8O6S
    Pureza:99.4%
    Cor e Forma:Solid
    Peso molecular:658.82
  • Benzamil

    CAS:
    <p>Benzamil blocks ENaC, inhibiting sodium transport (IC50=4 nM) and binds with Kd=5 nM to bovine kidney membranes.</p>
    Fórmula:C13H14ClN7O
    Pureza:99.79%
    Cor e Forma:Solid
    Peso molecular:319.75
  • Tetraethylammonium chloride

    CAS:
    <p>Tetraethylammonium chloride is a quaternary ammonium compound.</p>
    Fórmula:C8H20ClN
    Pureza:≥95%
    Cor e Forma:White Solid Solid Particulate/Powder
    Peso molecular:165.7
  • SAR7334 hydrochloride

    CAS:
    <p>SAR7334 hydrochloride is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).</p>
    Fórmula:C21H24Cl3N3O
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:440.79
  • Pikamilone

    CAS:
    <p>Pikamilone (Picamilon) is an intelligent medicine.</p>
    Fórmula:C10H12N2O3
    Pureza:99.38%
    Cor e Forma:White Crystalline Powder
    Peso molecular:208.21
  • BRITE-338733

    CAS:
    <p>BRITE-338733 is a novel inhibitor of ATPase. BRITE 338733 inhibits the expression of RecA in bacteria (IC50=4.7 μM) for the bacterial infections treatment.</p>
    Fórmula:C27H35N3O2
    Pureza:99.85%
    Cor e Forma:Solid
    Peso molecular:433.59
  • Raxatrigine

    CAS:
    Raxatrigine (CNV 1014802) has been investigated for the treatment of Bipolar Disorder and Bipolar Depression.
    Fórmula:C18H19FN2O2
    Pureza:98% - 99.43%
    Cor e Forma:Solid
    Peso molecular:314.35
  • VU590

    CAS:
    <p>VU590 is an inhibitor of extrarenal medullary potassium ROMK.VU590 inhibits Kir7.1 and modulates uterine myometrial contractility and melanocortin signalling.</p>
    Fórmula:C24H32N4O7
    Pureza:98.06%
    Cor e Forma:Solid
    Peso molecular:488.53
  • Darigabat

    CAS:
    <p>Darigabat (PF-06372865) is a GABAA receptor modulator with anxiolytic activity that inhibits α2, α1 PAM, and α2 PAM.</p>
    Fórmula:C22H21FN4O3S
    Pureza:98.42% - 99.29%
    Cor e Forma:Solid
    Peso molecular:440.49
  • Methionine

    CAS:
    <p>Methionine (D-Methionine) (MRX-1024; D-Methionine) is an effective chemoprotective agent which can also inhibit the neuronal activity through GABAA receptor</p>
    Fórmula:C5H11NO2S
    Pureza:99.13% - 99.62%
    Cor e Forma:Solid
    Peso molecular:149.21
  • Riluzole

    CAS:
    <p>Riluzole (RP-54274) is an anticonvulsant, glutamate antagonist, and prolongs ALS patient survival.</p>
    Fórmula:C8H5F3N2OS
    Pureza:99.71% - 99.88%
    Cor e Forma:Powder
    Peso molecular:234.2
  • VB124

    CAS:
    <p>VB124 is an orally active, potent and selective MCT4 inhibitor. VB124 blocked lactate importand expor in MDA-MB-231 cells.Cost-effective and quality-assured.</p>
    Fórmula:C23H23ClN2O4
    Pureza:99.21% - 99.57%
    Cor e Forma:Soild
    Peso molecular:426.89
  • Dimiracetam

    CAS:
    <p>Dimiracetam, a NMDA-receptor antagonist, is used potentially for the treatment of neuropathic pain.</p>
    Fórmula:C6H8N2O2
    Pureza:>99.99% - >99.99%
    Cor e Forma:Solid
    Peso molecular:140.14
  • ZT-1a

    CAS:
    <p>ZT-1a is a SPAK inhibitor.ZT-1a inhibits SPAK.ZT-1a can be used for the prevention and treatment of neurodegenerative and neurocognitive disorders.</p>
    Fórmula:C22H15Cl3N2O2
    Pureza:99.77%
    Cor e Forma:Solid
    Peso molecular:445.73
  • Mtb ATP synthase-IN-1

    CAS:
    Mtb ATP synthase-IN-1 is a potent, low-toxicity M. tuberculosis inhibitor with good oral bioavailability and metabolic stability.
    Fórmula:C17H13N3O4
    Pureza:98.28%
    Cor e Forma:Solid
    Peso molecular:323.30
  • CX717

    CAS:
    <p>CX 717 is a positive allosteric modulator of AMPA receptor which has an antidepressant-like effect.</p>
    Fórmula:C11H11N3O3
    Pureza:99.81%
    Cor e Forma:Soild
    Peso molecular:233.23
  • Lanicemine dihydrochloride

    CAS:
    <p>Lanicemine dihydrochloride (AZD-6765 dihydrochloride) is an NMDA channel blocker with antidepressant activity and can be used to study neurological diseases.</p>
    Fórmula:C13H16Cl2N2
    Pureza:98.37%
    Cor e Forma:Solid
    Peso molecular:271.19
  • SRI-41315

    CAS:
    <p>SRI-41315 is an eRF1 degrader that acts as a molecular glue at the ribosomal decoding center.SRI-41315 induces extended pauses at the termination codon.</p>
    Fórmula:C22H19N3O2
    Pureza:99.87%
    Cor e Forma:Solid
    Peso molecular:357.41
  • Ro 25-6981 Maleate

    CAS:
    <p>Ro 25-6981 Maleate is an NMDA receptor antagonist used in the study of neurological disorders such as Parkinson's and epilepsy.</p>
    Fórmula:C26H33NO6
    Pureza:99.42%
    Cor e Forma:Solid
    Peso molecular:455.54
  • Propoxycaine hydrochloride

    CAS:
    Propoxycaine hydrochloride is an ester local anesthetic that inhibits voltage-gated sodium channels, modulates nerve impulses, and induces loss of sensation.
    Fórmula:C16H27ClN2O3
    Pureza:97.25%
    Cor e Forma:Solid
    Peso molecular:330.85
  • JNJ-28583113

    CAS:
    <p>JNJ-28583113 is a TRPM2 antagonist, inducing phosphorylation of GSK3α and β subunits, protecting cells from oxidative stress-induced cell death.</p>
    Fórmula:C19H21F3N2O2
    Pureza:98.57%
    Cor e Forma:Solid
    Peso molecular:366.38
  • PF 03716556

    CAS:
    <p>PF 03716556 (PF-3716556) , an effective and specific P-CAB (potassium-competitive acid blocker), is utilized for the treatment of gastroesophageal reflux</p>
    Fórmula:C22H26N4O3
    Pureza:99.79% - 99.85%
    Cor e Forma:Solid
    Peso molecular:394.47
  • HUP30

    CAS:
    <p>HUP30 is a potent vasodilating agent. HUP30 can stimulate soluble guanylyl cyclase, activate K+ channels, and block extracellular Ca2+ influx.</p>
    Fórmula:C14H15N3O3S
    Pureza:99.96%
    Cor e Forma:Solid
    Peso molecular:305.35
  • Bupivacaine

    CAS:
    <p>Bupivacaine (AH-250) is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels</p>
    Fórmula:C18H28N2O
    Pureza:99.83%
    Cor e Forma:Solid
    Peso molecular:288.43
  • N-Methyl-L-leucin

    CAS:
    <p>N-Methyl-L-leucine ((S)-4-Methyl-2-(methylamino)pentanoic acid) is a novel calcium channel antagonist used in pain research.</p>
    Fórmula:C7H15NO2
    Pureza:99.87%
    Cor e Forma:Solid
    Peso molecular:145.2
  • Safinamide

    CAS:
    <p>Safinamide: reversible MAO-B inhibitor, enhances dopamine, blocks glutamate release, sodium, calcium channels; may treat Parkinson's, RLS, epilepsy.</p>
    Fórmula:C17H19FN2O2
    Pureza:99.92%
    Cor e Forma:Solid
    Peso molecular:302.34
  • BL-1249

    CAS:
    <p>BL-1249 is a selective and potent non-steroidal potassium channel activator with anti-inflammatory activity that activates K2P2.1 (TREK-1) and K2P10.1 (TREK-2).</p>
    Fórmula:C17H17N5
    Pureza:98% - 98.25%
    Cor e Forma:Solid
    Peso molecular:291.35
  • Doxapram

    CAS:
    Doxapram (Dopram) is a respiratory stimulant that inhibits TASK-1, TASK-3, and TASK-1/TASK-3 heterodimer channels.
    Fórmula:C24H30N2O2
    Pureza:99.42%
    Cor e Forma:Solid
    Peso molecular:378.51
  • Apinocaltamide

    CAS:
    Apinocaltamide (ACT-709478) is an orally available and selective T-type calcium channel blocker that cross BBB for Cav3.1, Cav3.2, and Cav3.3,epilepsy.
    Fórmula:C22H18F3N5O
    Pureza:99.80%
    Cor e Forma:Solid
    Peso molecular:425.41
  • Bupivacaine-d9

    CAS:
    Bupivacaine-d9 is a deuterated compound of Bupivacaine. Bupivacaine has a CAS number of 38396-39-3. Bupivacaine is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain.
    Fórmula:C18H19D9N2O
    Cor e Forma:Solid
    Peso molecular:297.48
  • Eleclazine

    CAS:
    <p>Eleclazine (GS-6615) is a novel and selective voltage-gated sodium channel inhibitor with antiarrhythmic properties that reduces peak sodium current (INaP).</p>
    Fórmula:C21H16F3N3O3
    Pureza:98.67%
    Cor e Forma:Solid
    Peso molecular:415.37
  • SAR7334

    CAS:
    <p>SAR7334 (TRCP6-IN-1) is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).</p>
    Fórmula:C21H22ClN3O
    Pureza:99.62% - 99.71%
    Cor e Forma:Solid
    Peso molecular:367.87
  • FSC231

    CAS:
    <p>FSC231 is a PICK1 inhibitor with analgesic activity, activating GSK-3β and ERK1/2.</p>
    Fórmula:C13H10Cl2N2O3
    Pureza:99.66%
    Cor e Forma:Solid
    Peso molecular:313.14
  • Amlodipine hydrochloride

    CAS:
    <p>Amlodipine hydrochloride is a salt of Amlodipine --- a medication used to lower blood pressure and prevent chest pain.</p>
    Fórmula:C20H26Cl2N2O5
    Cor e Forma:Solid
    Peso molecular:445.34
  • Amlodipine besilate impurity G

    CAS:
    <p>Amlodipine besilate impurity G is a Calcium Channel antagonist with potential application in the study of neurological diseases and is an impurity in the</p>
    Fórmula:C17H18ClNO4
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:335.78
  • Flavoxate

    CAS:
    <p>Flavoxate is an anticholinergic with antimuscarinic effects.</p>
    Fórmula:C24H25NO4
    Cor e Forma:Solid
    Peso molecular:391.46
  • Cinepazide

    CAS:
    <p>Cinepazide: a vasodilator targeting adenosine A2 receptors, treats various vascular diseases.</p>
    Fórmula:C22H31N3O5
    Cor e Forma:White Powder
    Peso molecular:417.5
  • VGSC blocker-1

    CAS:
    <p>VGSC blocker-1 inhibits 34.9% INa in nNav1.5 at 1 μM, reduces MDA-MB-231 invasion by 0.3%, non-toxic.</p>
    Fórmula:C24H32F2N2
    Cor e Forma:Solid
    Peso molecular:386.52
  • MCT-IN-1

    CAS:
    <p>MCT-IN-1 (compound 2) acts as a potent inhibitor of the monocarboxylate transporter (MCT), demonstrating IC50 values of 9 nM for MCT1 and 14 nM for MCT4.</p>
    Fórmula:C19H26N2O3
    Cor e Forma:Solid
    Peso molecular:330.42
  • Eperisone

    CAS:
    <p>Eperisone: a muscle relaxant for stiffness and pain, relaxes muscles, improves circulation, and mitigates pain by inhibiting reflexes and vasodilation.</p>
    Fórmula:C17H25NO
    Cor e Forma:Solid
    Peso molecular:259.39
  • Dofetilide D4

    CAS:
    Dofetilide D4 (UK 68789 D4), a deuterium-labeled version of Dofetilide, is categorized as a Class III antiarrhythmic medication.
    Fórmula:C19H27N3O5S2
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:445.59
  • Nifedipine-d6

    CAS:
    <p>Nifedipine D6 is deuterium labeled nifedipine which is a potent blocker of calcium channel.</p>
    Fórmula:C17H18N2O6
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:352.37
  • Propafenone D7 hydrochloride

    CAS:
    <p>Propafenone D7 hydrochloride is the deuterium labeled Propafenone, and is a classic anti-arrhythmic medication.</p>
    Fórmula:C21H28ClNO3
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:384.95
  • Topiramate D12

    CAS:
    <p>Topiramate D12 is a deuterium labeled Topiramate. Topiramate is an agent of broad-spectrum antiepileptic. Topiramate is an antagonist of GluR5 receptor.</p>
    Fórmula:C12H21NO8S
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:351.44
  • PBFI-AM

    CAS:
    <p>PBFI-AM is a useful tool to determine intracellular K + content [1] .</p>
    Fórmula:C58H62N2O24
    Cor e Forma:Solid
    Peso molecular:1171.11
  • BAY-390

    CAS:
    <p>BAY-390, a selective TRPA1 inhibitor, crosses species, penetrates brains, with IC50s: 16-82 nM. Used in inflammation research.</p>
    Fórmula:C13H15F4NO
    Cor e Forma:Solid
    Peso molecular:277.26
  • Bumetanide-d5

    CAS:
    Bumetanide D5 is a deuterium-labeled Bumetanide. Bumetanide is a Na+-K+-Cl- (NKCC1) inhibitor (IC50s: 0.68 and 4.0 μM for hNKCC1A and hNKCC2A).
    Fórmula:C17H20N2O5S
    Pureza:98%
    Cor e Forma:Solid
    Peso molecular:369.45