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Neurociencia

Neurociencia

Los inhibidores en neurociencia son compuestos diseñados para modular la actividad de proteínas, enzimas o receptores específicos dentro del sistema nervioso. Estos inhibidores son cruciales para estudiar los mecanismos moleculares subyacentes a la función neuronal, la transmisión sináptica y las enfermedades neurodegenerativas. Al dirigirse a los receptores de neurotransmisores, canales iónicos y vías de señalización, los inhibidores en neurociencia ayudan en la exploración de la función cerebral y en el desarrollo de estrategias terapéuticas para trastornos neurológicos como el Alzheimer, Parkinson y la epilepsia. En CymitQuimica, ofrecemos una amplia gama de inhibidores de neurociencia de alta calidad para apoyar su investigación en neurobiología, neurofarmacología y ciencias cognitivas.

Subcategorías de "Neurociencia"

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Se han encontrado 5398 productos de "Neurociencia"

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  • F 14679
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    F 14679

    CAS:
    <p>F 14679 is a potent 5-HT1A agonist (pKi=10.23) with a maximum Ca2t response similar to 5-HT.</p>
    Fórmula:C21H25ClF2N4O
    Pureza:99.09%
    Forma y color:Solid
    Peso molecular:422.9

    Ref: TM-T62269

  • VU6016235
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    VU6016235

    CAS:
    <p>VU6016235 is a structurally unique, orally available, and highly selective tricyclic M4 muscarinic acetylcholine receptor positive allosteric modulator.</p>
    Fórmula:C21H22N4OS
    Forma y color:Solid
    Peso molecular:378.49

    Ref: TM-T201326

  • Mesulergine hydrochloride
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    Mesulergine hydrochloride

    CAS:
    <p>5-HT2A and 2C receptor antagonist</p>
    Fórmula:C18H27ClN4O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:398.95

    Ref: TM-T22970

  • Zanapezil fumarate
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    Zanapezil fumarate

    CAS:
    <p>Zanapezil is an acetylcholinesterase (AChE) inhibitor. Zanapezil increases choline acetyltransferase activity in cultured rat septal cholinergic neurons.</p>
    Fórmula:C29H36N2O5
    Forma y color:Solid
    Peso molecular:492.61

    Ref: TM-T29203

  • LB-102
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    LB-102

    CAS:
    <p>LB-102 is an orally active inhibitor of dopamine D2, D3, and serotonin 5-HT7 receptors, utilized in the study of schizophrenia and other psychiatric disorders.</p>
    Fórmula:C18H29N3O4S
    Forma y color:Solid
    Peso molecular:383.51

    Ref: TM-T200914

  • Glutaminyl Cyclase Inhibitor 3
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    Glutaminyl Cyclase Inhibitor 3

    CAS:
    <p>Designed anti-Alzheimer’s compound; potent Glutaminyl Cyclase inhibitor; IC50 at 4.5 nM; reduces brain Aβ; improves cognition.</p>
    Fórmula:C24H32N6O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:468.61

    Ref: TM-T11422

  • SB 243213 hydrochloride
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    SB 243213 hydrochloride

    CAS:
    <p>SB 243213 hydrochloride is an orally active, selective and high-affinity antagonist of 5-hydroxytryptamine (5-HT)2C receptor(pKi of 9.37 and a pKb of 9.8).It</p>
    Fórmula:C22H20ClF3N4O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:464.87

    Ref: TM-T12859

  • HDAC6-IN-9
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    HDAC6-IN-9

    CAS:
    <p>HDAC6-IN-9 is a γ-secretase modulator that can significantly reduce the level of Aβ42 in mouse brain and can be used to study neurological diseases.</p>
    Fórmula:C19H16N2O3
    Pureza:98.84%
    Forma y color:Solid
    Peso molecular:320.34

    Ref: TM-T60856

  • CPPG
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    CPPG

    CAS:
    <p>CPPG: potent group II/III mGlu receptor antagonist, 20x more selective for group III (IC50: 2.2 nM) than II (46.2 nM) in rat cortex.</p>
    Fórmula:C11H14NO5P
    Forma y color:Solid
    Peso molecular:271.21

    Ref: TM-T10880

  • (RS)-AMPA hydrochloride
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    (RS)-AMPA hydrochloride

    CAS:
    <p>(RS)-AMPA ((±)-AMPA) hydrochloride is a glutamate analog and serves as an efficient selective agonist for the excitatory neurotransmitter L-glutamic acid (L-glutamic acid). It does not interfere with the binding sites of alginate or NMDA receptors.</p>
    Fórmula:C7H11ClN2O4
    Forma y color:Solid
    Peso molecular:222.63

    Ref: TM-T200780

  • Lu 26-046
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    Lu 26-046

    CAS:
    <p>Lu 26-046 is a muscarinic receptor agonist.</p>
    Fórmula:C10H12N2OS
    Forma y color:Solid
    Peso molecular:208.28

    Ref: TM-T70651

  • Remlifanserin
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    Remlifanserin

    CAS:
    <p>Remlifanserin is a potent inverse agonist of the serotonin receptor (5-HT2A).</p>
    Fórmula:C24H29F2N3O2
    Forma y color:Solid
    Peso molecular:429.50

    Ref: TM-T201055

  • SB 243213 dihydrochloride
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    SB 243213 dihydrochloride

    CAS:
    <p>SB 243213 dihydrochloride is an orally active, selective and high-affinity antagonist of 5-hydroxytryptamine (5-HT)2C receptor(pKi of 9.37 and a pKb of 9.8 for</p>
    Fórmula:C22H21Cl2F3N4O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:501.33

    Ref: TM-T12859L

  • Cyproflanilide
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    Cyproflanilide

    CAS:
    <p>Cyproflanilide is a GABAR antagonist that exhibits high activity against a variety of pests, including those from the Lepidoptera, Coleoptera, and Thysanoptera orders.</p>
    Fórmula:C28H17BrF12N2O2
    Forma y color:Solid
    Peso molecular:721.33

    Ref: TM-T201028

  • P2X7 receptor antagonist-5
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    P2X7 receptor antagonist-5

    CAS:
    <p>P2X7 receptor antagonist-5 (compound 13a) is a potent, orally active, and long-lasting antagonist of the P2X7 receptor.</p>
    Fórmula:C21H17F3N6O3S2
    Forma y color:Solid
    Peso molecular:522.52

    Ref: TM-T201089

  • Logo de CymitQuimica
    Targetmol
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    AChE/BChE-IN-3 hydrochloride

    <p>AChE/BChE-IN-3 (BMC-1) HCl is a dual inhibitor with IC50s: eqBChE 0.383 μM, elAChE 6.08 μM.</p>
    Fórmula:C15H25ClN2O3
    Forma y color:Solid
    Peso molecular:316.82

    Ref: TM-T60831

  • Logo de CymitQuimica
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    AZD 2066 hydrate

    <p>AZD 2066 hydrate is a selective, orally active, and brain-penetrant antagonist of mGluR5. It exhibits antinociceptive effects [1].</p>
    Fórmula:C19H18ClN5O3
    Forma y color:Solid
    Peso molecular:386.33

    Ref: TM-T61708

  • AChE/BChE/MAO-B-IN-5
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    AChE/BChE/MAO-B-IN-5

    CAS:
    <p>AChE/BChE/MAO-B-IN-5 is a multi-target inhibitor capable of crossing the blood-brain barrier, targeting cholinesterases (AChE and BChE) and monoamine oxidase MAO-B. It exhibits IC50 values of 0.24 µM for AChE, 6.29 µM for BChE, and 0.11 µM for MAO-B. AChE/BChE/MAO-B-IN-5 holds potential for research in neurodegenerative diseases such as Alzheimer's disease.</p>
    Fórmula:C22H14F3NO2
    Forma y color:Solid
    Peso molecular:381.347

    Ref: TM-T206229

  • LY367385 hydrochloride
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    LY367385 hydrochloride

    CAS:
    <p>LY367385 hydrochloride: selective mGluR1a antagonist, IC50 = 8.8 μM, neuroprotective, anticonvulsant, antiepileptic.</p>
    Fórmula:C10H12ClNO4
    Forma y color:Solid
    Peso molecular:245.66

    Ref: TM-T60355

  • MAO-B-IN-42
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    MAO-B-IN-42

    CAS:
    <p>MAO-B-IN-42 (Compound 4f) is a selective and reversible monoamine oxidase-B (MAO-B) inhibitor, with an IC50 value of 0.184 μM. By blocking the oxidative deamination of monoamines catalyzed by MAO-B, it helps maintain neurotransmitter levels. MAO-B-IN-42 shows potential for research into Parkinson's disease.</p>
    Fórmula:C19H12FNO2
    Forma y color:Solid
    Peso molecular:305.302

    Ref: TM-T206712