1. Neurological Disease

Neurological Disease

A range of neurological disorders, including epilepsy and dystonia, may involve dysfunctional intracortical inhibition, and may respond to treatments that modify it. Parkinson’s is a neurodegenerative disease characterized by increased activity of GABA in basal ganglia and the loss of dopamine in nigrostriatum, associated with rigidity, resting tremor, gait with accelerating steps, and fixed inexpressive face. Neurological deficits, along with neuromuscular involvement, are characteristic of mitochondrial disease, and these symptoms can have a dramatic impact on patient quality of life. Neurological features may be manifold, ranging from neural deafness, ataxia, peripheral neuropathy, migraine, seizures, stroke‐like episodes and dementia and depend on the part of the nervous system affected.

Neurological Disease Related Products (1126):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-15608
    MPTP hydrochloride 23007-85-4 99.16%
    MPTP (hydrochloride) is a prodrug to the neurotoxin MPP which causes permanent symptoms of Parkinson's disease.
    MPTP hydrochloride
  • HY-17366
    Clozapine N-oxide 34233-69-7 99.98%
    Clozapine N-oxide is a pharmacologically inert metabolite of Clozapine, which is a potent 5-HT1C receptor antagonist. Clozapine N-oxide (CNO) is a DREADD (designer receptors exclusively activated by designer drug) agonist.
    Clozapine N-oxide
  • HY-13027
    DAPT 208255-80-5 99.25%
    DAPT is a γ-secretase inhibitor, reduces the total beta-amyloid peptide () production with IC50 of 20 nM in HEK 293 cells.
  • HY-B0726
    Pilocarpine Hydrochloride 54-71-7 99.63%
    Pilocarpine HCl is a nonselective muscarinic acetylcholine receptor agonist used to produce an experimental model of epilepsy.
    Pilocarpine Hydrochloride
  • HY-15084
    (+)-MK 801 Maleate 77086-22-7 99.98%
    (+)-MK 801 (Maleate) is a potent, selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes.
    (+)-MK 801 Maleate
  • HY-12526
    Tetrodotoxin 4368-28-9 99.99%
    Tetrodotoxin is a highly selective sodium channel blocker, with IC50 of 33 nM for Nav1.6.
  • HY-12012
    SB 216763 280744-09-4
    SB 216763 is potent and selective glycogen synthase kinase-3 (GSK-3) inhibitor, with IC50 value of 34 nM.
    SB 216763
  • HY-B0215
    Acetylcysteine 616-91-1 99.27%
    Acetylcysteine is used mainly as a mucolytic, which protects against acetaminophen overdose-induced hepatotoxicity by maintaining or restoring hepatic concentrations of glutathione.
  • HY-13291
    WIN 55,212-2 Mesylate 131543-23-2 98.98%
    WIN 55,212-2 (Mesylate) is a potent aminoalkylindole cannabinoid (CB) receptor agonist with Kis of 62.3 and 3.3 nM for human recombinant CB1 and CB2 receptors, respectively.
    WIN 55,212-2 Mesylate
  • HY-10095
    Olcegepant 204697-65-4 99.32%
    Olcegepant is the first potent and selective non-peptide antagonist of the calcitonin gene-related peptide 1 (CGRP1) receptor with IC50 of 0.03 nM and with a Ki of 14.4 pM for human CGRP.
  • HY-B0407A
    Chlorpromazine hydrochloride 69-09-0 99.85%
    Chlorpromazine Hydrochloride is an antagonist of the dopamine D2 receptors, 5-HT2A receptors, potassium channel, sodium channel, with Ki of 363 nM and 8.3 nM for dopamine D2 receptor and serotonin 5-HT2A receptor, respectively.
    Chlorpromazine hydrochloride
  • HY-B1756
    Rotenone 83-79-4 >98.0%
    Rotenone is an inhibitor of mitochondrial electron transport at NADH:ubiquinone oxidoreductase, and is used to induce a Parkinson-like syndrome as an experimental model in rats.
  • HY-B0075
    Melatonin 73-31-4 >98.0%
    Melatonin, a hormone produced in the brain, is a potent melatonin receptor activator, and possesses important antioxidative and anti-inflammatory properties.
  • HY-10889
    Preladenant 377727-87-2 99.08%
    Preladenant is a potent competitive antagonist of the human A2A receptor (Ki=1.1 nM) and has >1000-fold selectivity over all other adenosine receptors.
  • HY-14992
    Bay 60-7550 439083-90-6 98.12%
    Bay 60-7550 is a selective inhibitor of PDE2 with Ki of 3.8±0.2 nM, also is a modulator of NO.
    Bay 60-7550
  • HY-14557
    Pimavanserin 706779-91-1 99.73%
    Pimavanserin is a potent 5-hydroxytryptamine (5-HT)2A receptor inverse agonist, displays potent inverse agonist activity in the cell-based functional assay receptor selection and amplification technology (R-SAT), with a mean pIC50 of 8.7.
  • HY-B0150
    Nicotinamide 98-92-0 99.94%
    Nicotinamide is a water-soluble vitamin, an active component of coenzymes NAD and NADP, and acts as poly (ADP-ribose) polymerase (PARP) inhibitor.
  • HY-B0617
    Ademetionine 29908-03-0 >98.0%
    Ademetionine(S-adenosyl-l-methionine; SAMe) is a naturally-occurring substance which is a major source of methyl groups in the brain.
  • HY-19370
    FPS-ZM1 945714-67-0 99.31%
    FPS-ZM1 is a high-affinity RAGE specific inhibitor with a Ki of 25 nM.
  • HY-16759
    Verubecestat 1286770-55-5 99.79%
    MK-8931 is a BACE1 inhibitor. MK-8931 binds significantly to β-secretase.