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Neuroscience

Neuroscience

Neuroscience inhibitors are compounds designed to modulate the activity of specific proteins, enzymes, or receptors within the nervous system. These inhibitors are crucial for studying the molecular mechanisms underlying neural function, synaptic transmission, and neurodegenerative diseases. By targeting neurotransmitter receptors, ion channels, and signaling pathways, neuroscience inhibitors aid in the exploration of brain function and the development of therapeutic strategies for neurological disorders such as Alzheimer's, Parkinson's, and epilepsy. At CymitQuimica, we offer a comprehensive range of high-quality neuroscience inhibitors to support your research in neurobiology, neuropharmacology, and cognitive sciences.

Subcategories of "Neuroscience"

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Found 5389 products of "Neuroscience"

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  • Serotonin maleate

    CAS:
    <p>Serotonin hydrogen maleate serves as a monoaminergic neurotransmitter and an endogenous 5-HT receptor agonist within the central nervous system (CNS). It also functions as an inhibitor of catechol O-methyltransferase (COMT), exhibiting a Ki value of 44 μM.</p>
    Formula:C14H16N2O5
    Color and Shape:Solid
    Molecular weight:292.287
  • BRD0418

    CAS:
    <p>BRD0418 acts as an upregulator of TRIB1 expression by leading to reprogramming of hepatic lipoprotein metabolism from adipogenesis to clearance it.</p>
    Formula:C29H32N2O5
    Purity:99.57%
    Color and Shape:Solid
    Molecular weight:488.57
  • Relicpixant

    CAS:
    <p>Relicpixant is a potent purine receptor (P2X) antagonist.</p>
    Formula:C20H19ClF2N4O5S
    Color and Shape:Solid
    Molecular weight:500.9
  • Carlina oxide

    CAS:
    <p>Carlina oxide is both an AChE inhibitor and an antioxidant, effective in eliminating mosquito larvae (LC50=1.39 μg/mL). Furthermore, Carlina oxide exhibits cytotoxicity in vertebrate cells, human dermis, and HCT116 and MDA-MB231 cell lines.</p>
    Formula:C13H10O
    Color and Shape:Solid
    Molecular weight:182.22
  • Amyloid-β-IN-2

    CAS:
    <p>Amyloid-β-IN-2 (Compound EX.112) is a selective inhibitor of γ-secretase. In H4 cells, it demonstrates inhibitory activity on Aβ42 secretion, with an EC50 value of 226 nM. Amyloid-β-IN-2 holds potential for research in Alzheimer's disease (AD) and diseases associated with Aβ deposition.</p>
    Formula:C22H21F2N3O2
    Color and Shape:Solid
    Molecular weight:397.42
  • Amyloid-β-IN-3

    CAS:
    <p>Amyloid-β-IN-3 (EX.113) is a selective inhibitor of γ-secretase. It demonstrates inhibitory activity on Aβ42 secretion in H4 cells, with an EC50 value of 148 nM. By modulating the catalytic activity of γ-secretase, Amyloid-β-IN-3 decreases Aβ42 production, thereby alleviating neurotoxicity caused by Aβ deposition. It holds potential for Alzheimer's disease (AD) research.</p>
    Formula:C22H21F2N3O2
    Color and Shape:Solid
    Molecular weight:397.42
  • LRRK2-IN-3

    CAS:
    <p>LRRK2-IN-3: potent, selective oral LRRK2 blocker, BBB-penetrant, IC50 of 0.6 nM in hPBMCs, for Parkinson's research.</p>
    Formula:C25H29ClF2N6O2
    Color and Shape:Solid
    Molecular weight:518.99
  • K203


    <p>K203 is a potent tabun-inhibited AChE reactivator and is an important antidote to organophosphorus poisoning.</p>
    Formula:C16H18Br2N4O2
    Color and Shape:Solid
    Molecular weight:458.15
  • Fletazepam

    CAS:
    Fletazepam, a benzodiazepine derivative, exhibits sedative, anti-anxiety, and muscle-relaxant properties. It is utilized in neurological research.
    Formula:C17H13ClF4N2
    Color and Shape:Solid
    Molecular weight:356.74
  • DSP-1053 benzenesulfonate

    CAS:
    <p>DSP-1053: Benzylpiperidine-based, potent SERT inhibitor (Ki=1.02nM), partial 5-HT1A receptor agonist (Ki=5.05nM), antidepressant.</p>
    Formula:C32H38BrNO7S
    Color and Shape:Solid
    Molecular weight:660.62
  • UB 165

    CAS:
    <p>Subtype-selective nicotinic agonist</p>
    Formula:C13H15ClN2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:234.72
  • CPPG

    CAS:
    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.
    Formula:C11H14NO5P
    Color and Shape:Solid
    Molecular weight:271.21
  • 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>
    Formula:C15H25ClN2O3
    Color and Shape:Solid
    Molecular weight:316.82
  • AAZ-A 154 hydrobromide

    CAS:
    <p>AAZ-A 154 hydrobromide is a selective, competitive, non-hallucinogenic 5-HT2AR antagonist. It promotes neuronal growth in rodents and yields enduring beneficial behavioral effects.</p>
    Formula:C14H21BrN2O
    Color and Shape:Solid
    Molecular weight:313.23
  • LY2794193

    CAS:
    LY2794193, a potent and selective mGlu3 receptor agonist, reduces akathisia seizures and increases GAT1, GLAST and GLT-1 protein levels in rats.
    Formula:C16H18N2O6
    Purity:98.15%
    Color and Shape:Solid
    Molecular weight:334.32
  • AAZ-A 154 benzoate

    CAS:
    <p>AAZ-A 154 benzoate is a selective, competitive, and non-hallucinogenic 5-HT2AR antagonist. This compound facilitates neuronal growth in rodents and produces lasting beneficial behavioral effects.</p>
    Formula:C21H26N2O3
    Color and Shape:Solid
    Molecular weight:354.44
  • AAZ-A 154 hydrochloride

    CAS:
    <p>AAZ-A 154 hydrochloride is a selective, competitive, non-hallucinogenic antagonist of 5-HT2AR. It promotes neuronal growth in rodents and results in enduring beneficial behavioral effects.</p>
    Formula:C14H21ClN2O
    Color and Shape:Solid
    Molecular weight:268.78
  • AAZ-A 154 mesylate

    CAS:
    <p>AAZ-A 154 mesylate mesylate is a selective, competitive, and non-hallucinogenic antagonist of 5-HT2AR. It enhances neuronal growth in rodents and produces enduring beneficial behavioral effects.</p>
    Formula:C15H24N2O4S
    Color and Shape:Solid
    Molecular weight:328.43
  • LRRK2-IN-6


    <p>LRRK2-IN-6 is an oral, selective LRRK2 inhibitor crossing the blood-brain barrier, targeting GS (IC50: 4.6μM) and WT LRRK2 (IC50: 49μM).</p>
    Formula:C23H24F2N4O2S
    Color and Shape:Solid
    Molecular weight:458.52
  • P2X4 antagonist-1

    CAS:
    <p>P2X4 antagonist-1 is a potent P2X4 receptor antagonist used in the study of neurological, cardiovascular, and immune system diseases.</p>
    Formula:C20H15Cl3N2O4S
    Purity:99.9%
    Color and Shape:Solid
    Molecular weight:485.77