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"
- 5-HT Receptor(942 products)
- ACK(1 products)
- AChR(576 products)
- ATP Citrate Lyase(16 products)
- Adrenergic Receptor(2,949 products)
- BACE(36 products)
- Beta Amyloid(205 products)
- CaMK(69 products)
- Cyclooxygenase (COX) Inhibitors(565 products)
- Dopamine Receptor(410 products)
- GABA Receptor(337 products)
- Gamma-secretase(59 products)
- GluR(255 products)
- GlyT(24 products)
- Histamine Receptor(359 products)
- LRRK2(33 products)
- Melatonin Receptor(24 products)
- NMDAR(26 products)
- OX Receptor(40 products)
- Opioid Receptor(298 products)
Show 12 more subcategories
Found 5389 products of "Neuroscience"
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FPTQ
CAS:<p>FPTQ is a highly effective antagonist of mGluR 1, displaying IC50 values of 6 nM and 1.4 nM for human and mouse mGluR1 respectively [1].</p>Formula:C17H12FN5Purity:99.68% - 99.88%Color and Shape:SolidMolecular weight:305.31JM-1232
CAS:<p>JM-1232 is a sedative and hypnotic drug being researched as a potential anesthetic.</p>Formula:C24H27N3O2Color and Shape:SolidMolecular weight:389.49RAGE/SERT-IN-1
CAS:<p>RAGE/SERT-IN-1 is a potent, orally active inhibitor of advanced glycation end products (RAGE) and serotonin transporter (SERT), with IC50 values of 8.26 μM and</p>Formula:C38H41ClN4OSColor and Shape:SolidMolecular weight:637.28(+)-Bicuculline methiodide
CAS:<p>(+)-Bicuculline methiodide is a GABAA receptor blocker that blocks epileptogens and may be used in the study of neurological disorders.</p>Formula:C21H20INO6Purity:99.24%Color and Shape:SolidMolecular weight:509.29Bisnorcymserine
CAS:<p>Bisnorcymserine reversibly inhibits butyrylcholinesterase, binding Ser(200) and His(440) non-covalently and stacking with Trp(84).</p>Formula:C21H25N3O2Purity:98%Color and Shape:SolidMolecular weight:351.443β-Hydroxy-lup-20(29)-en-16-one
CAS:<p>3β-Hydroxy-lup-20(29)-en-16-one (compound 9) serves as a dual inhibitor of both AChE and BChE, displaying a preference for BChE with an IC50 of 28.9 μM [1].</p>Formula:C30H48O2Color and Shape:SolidMolecular weight:440.7rel-HDMP 28 hydrochloride
CAS:<p>Rel-HDMP-28 hydrochloride (Compound 2g) is an analogue of methylphenidate, exhibiting selective affinity for the serotonin transporter (SERT) with a binding constant (Ki) of 105 nM [1].</p>Formula:C18H22ClNO2Color and Shape:SolidMolecular weight:319.83L-772,405
CAS:<p>L-772,405 is a highly selective agonists of h5-HT(1D) receptor.</p>Formula:C26H31FN6OPurity:98%Color and Shape:SolidMolecular weight:462.56BMS 433796
CAS:<p>BMS 433796 is a γ-secretase inhibitor that demonstrates Aβ-lowering activity within a transgenic mouse model of Alzheimer's disease.</p>Formula:C21H20F2N4O4Purity:99.17%Color and Shape:SolidMolecular weight:430.4Zamifenacin fumarate
CAS:<p>Zamifenacin fumarate (UK-76654 fumarate) is a potent and gut-selective antagonist of muscarinic M3 receptor.</p>Formula:C31H33NO7Purity:99.88%Color and Shape:SolidMolecular weight:531.6CGP-54626 free base
CAS:CGP-54626 is a selective antagonist of the GABAB receptor (IC50 = 4 nM ).Formula:C18H28Cl2NO3PPurity:98%Color and Shape:SolidMolecular weight:408.3Pomaglumetad methionil hydrochloride
CAS:<p>LY2140023 hydrochloride: oral methionine prodrug of LY404039, a selective mGlu2/3 agonist, studied for schizophrenia.</p>Formula:C12H19ClN2O7S2Purity:98.57%Color and Shape:SolidMolecular weight:402.87AAK1-IN-4
CAS:<p>AAK1-IN-4 selectively inhibits AAK1 with IC50 of 4.6 nM; penetrates CNS, oral bioactive, potential for studying neuropathic pain.</p>Formula:C20H28N4O3Color and Shape:SolidMolecular weight:372.46MAO-B-IN-1
CAS:<p>MAO-B-IN-1 is a monoamine oxidase B inhibitor and can be used for the research of neurological diseases.</p>Formula:C16H14F3N3O2SPurity:98%Color and Shape:SolidMolecular weight:369.36AChE-IN-19
CAS:<p>AChE-IN-19: strong AChE blocker (IC50: 0.56 μM), hinders Aβ clumps, neuro-protective, non-toxic to SH-SY5Y, for Alzheimer's research.</p>Formula:C30H33NO7Color and Shape:SolidMolecular weight:519.59Anti-amyloid agent-1
CAS:<p>Anti-amyloid agent-1 is a potent compound that inhibits amyloid aggregation, offering a promising approach for research into the treatment of amyloidosis [1].</p>Formula:C21H17F3N2O3Color and Shape:SolidMolecular weight:402.37FPPQ
CAS:<p>FPPQ blocks 5-HT3 and 5-HT6 receptors (Ki: 0.9 & 3 nM) and may improve psychosis and cognition.</p>Formula:C21H19FN4O2SColor and Shape:SolidMolecular weight:410.46GR-127935
CAS:<p>GR-127935 is a potent and selective 5-HT1B/1D receptor antagonist.</p>Formula:C29H31N5O3Color and Shape:SolidMolecular weight:497.59LY108742
CAS:<p>LY108742 is an antagonist of 5-HT2.</p>Formula:C21H28N2O3Purity:98%Color and Shape:SolidMolecular weight:356.465-HT3-In-1
CAS:5-HT3-In-1 (compound example 8) exhabits with 5-HT3 inhibition activity.Formula:C16H21ClN4O3Purity:98%Color and Shape:SolidMolecular weight:352.82
