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"
- Receptor 5-HT(942 productos)
- ACK(1 productos)
- AChR(576 productos)
- ATP Citrato Liasa(16 productos)
- Receptor adrenérgico(2.949 productos)
- BACE(36 productos)
- Beta amiloide(205 productos)
- CAMK(69 productos)
- Inhibidores de ciclooxigenasa (COX)(565 productos)
- Receptor de dopamina(410 productos)
- Receptor GABA(337 productos)
- Gamma-secretasa(59 productos)
- GluR(255 productos)
- GlyT(24 productos)
- Receptor de histamina(359 productos)
- LRRK2(33 productos)
- Receptor de melatonina(24 productos)
- NMDAR(26 productos)
- Receptor de OX(40 productos)
- Receptor de opioides(298 productos)
Mostrar 12 subcategorías más
Se han encontrado 5389 productos de "Neurociencia"
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5-Methyltryptamine hydrochloride
CAS:<p>5-Methyltryptamine hydrochloride is a high-affinity 5-HT1C receptor ligand and a partial agonist of 5-HT. 5-Methyltryptamine hydrochloride protects mice subjected to burn, tourniquet and endotoxin shock.</p>Fórmula:C11H15ClN2Pureza:99.45%Forma y color:SolidPeso molecular:210.7037-Acetoxy-1-methylquinolinium iodide
CAS:<p>7-Acetoxy-1-methylquinolinium iodide (AMQI) is a cholinesterase substrate for inhibitor detection with 320 nm Ex and 410 nm Em.</p>Fórmula:C12H12INO2Forma y color:SolidPeso molecular:329.13Dianicline dihydrochloride
CAS:<p>Dianicline dihydrochloride is a partial agonist of α4β2 nicotinic acetylcholine receptor. It increases cessation rates in a dose-dependent manner.</p>Fórmula:C13H16N2OPureza:98%Forma y color:SolidPeso molecular:216.28Aβ1-42 aggregation inhibitor 1
CAS:<p>Aβ1-42 aggregation inhibitor 1 effectively inhibits acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE), demonstrating IC50 values of 2.64 μM and 1.29</p>Fórmula:C29H32N4SForma y color:SolidPeso molecular:468.66Catestatin
CAS:Non-competitive inhibitor of nicotinic receptors; blocks cationic signalling and catecholamine release; stimulates histamine release. IC50 ~200-250nM.Fórmula:C107H173N37O26SPureza:98%Forma y color:SolidPeso molecular:2425.84Penbutolol sulfate
CAS:<p>Penbutolol sulfate ((-)-Terbuclomine) is able to bind to both β2-adrenergic receptor and β1-adrenergic receptor, thus making it a non-selective β blocker.</p>Fórmula:C18H29NO2H2O4SPureza:98.55%Forma y color:SolidPeso molecular:340.47VU0477886
CAS:<p>VU0477886: Potent mGlu4 PAM, effective in preclinical Parkinson's model HIC.</p>Fórmula:C20H13ClN4O3Pureza:98%Forma y color:SolidPeso molecular:392.80Aprofene
CAS:<p>Aprofene blocks acetylcholine receptors, used for peptic ulcers, endarteritis, cholecystitis, and colitis.</p>Fórmula:C21H27NO2Forma y color:SolidPeso molecular:325.447-Desmethyl-3-hydroxyagomelatine
CAS:<p>7-Desmethyl-3-hydroxyagomelatine, less active than parent drug Agomelatine, is a melatonergic agonist and 5-HT2C antagonist.</p>Fórmula:C14H15NO3Pureza:98%Forma y color:SolidPeso molecular:245.27VU0029767
CAS:<p>VU0029767 is an allosteric enhancer of the M1 muscarinic receptor, capable of modulating the receptor's activity. This compound enhances M1 receptor activity by increasing agonist affinity. However, VU0029767 demonstrates distinct characteristics from other compounds, particularly under varying experimental conditions such as its interaction with mutated M1 receptors and its effects on downstream signaling pathways.</p>Fórmula:C21H21N3O3Forma y color:SolidPeso molecular:363.41Diclofensine
CAS:<p>Diclofensine (Ro 8-4650) inhibits the uptake of serotonin, noradrenaline and dopamine.</p>Fórmula:C17H17Cl2NOPureza:97.01% - 98.13%Forma y color:SolidPeso molecular:322.23Nalfurafine N-Oxide
CAS:Producto controlado<p>Stability Hygroscopic<br>Applications Nalfurafine N-Oxide, is an impurity of Nalfurafine (N255600), which is a κ-opioid receptor agonist marketed as a treatment for uremic pruritus in hemodialysis patients.<br>References Fujii, H., et al.: Bioorg. Med. Chem., 12, 4133 (2004), Mori, T., et al.: Life Sci., 75, 2433 (2004), Fujii, H., et al.: Curr. Med. Chem., 13, 1109 (2006), Nagase, H., et al.: Bioorg. Med. Chem. Lett., 20, 6302 (2010),<br></p>Fórmula:C28H32N2O6Forma y color:NeatPeso molecular:492.562-(4-Chlorophenyl)-2-(methylamino)cyclohexanone Hydrochloride
CAS:Producto controladoFórmula:C13H17Cl2NOForma y color:NeatPeso molecular:274.192Z-Nalfurafine
CAS:Producto controlado<p>Applications 2Z-Nalfurafine is a geometric isomer of Nalfurafine (N255600), a on-narcotic opioid drug for intractable itch caused by hemodialysis. It showed significant opioid κ-agonist activity and induced neither aversion nor preference in rats on the CPP (Conditioned Place Preference) test. Nalfurafine is a new therapeutic agent for the treatment of uremic pruritus in hemodialysis patients.<br>References Fujii, H., et al.: Bioorg. Med. Chem., 12, 4133 (2004); Mori, T., et al.: Life Sci., 75, 2433 (2004); Fujii, H., et al.: Curr. Med. Chem., 13, 1109 (2006); Nagase, H., et al.: Bioorg. Med. Chem. Lett., 20, 6302 (2010)<br></p>Fórmula:C28H32N2O5Forma y color:NeatPeso molecular:476.562-(3-Chlorophenyl)-2-(methylamino)cyclohexanone Hydrochloride
CAS:Producto controladoFórmula:C13H17Cl2NOForma y color:NeatPeso molecular:274.196S-Nalfurafine
CAS:Producto controlado<p>Applications 6S-Nalfurafine is a stereoisomer of Nalfurafine (N255600), a on-narcotic opioid drug for intractable itch caused by hemodialysis. It showed significant opioid κ-agonist activity and induced neither aversion nor preference in rats on the CPP (Conditioned Place Preference) test. Nalfurafine is a new therapeutic agent for the treatment of uremic pruritus in hemodialysis patients.<br>References Fujii, H., et al.: Bioorg. Med. Chem., 12, 4133 (2004); Mori, T., et al.: Life Sci., 75, 2433 (2004); Fujii, H., et al.: Curr. Med. Chem., 13, 1109 (2006); Nagase, H., et al.: Bioorg. Med. Chem. Lett., 20, 6302 (2010)<br></p>Fórmula:C28H32N2O5Forma y color:NeatPeso molecular:476.56LY 344864
CAS:<p>LY 344864, a specifc receptor agonist, is an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor.</p>Fórmula:C21H22FN3OPureza:98%Forma y color:SolidPeso molecular:351.42Paroxetine hydrochloride hemihydrate
CAS:<p>Paroxetine hydrochloride hemihydrate (Paxil) is an effective and selective serotonin reuptake inhibitor (SSRI).</p>Fórmula:C38H44Cl2F2N2O7Pureza:99.949%Forma y color:SolidPeso molecular:749.67Dolasetron Mesylate
CAS:<p>Dolasetron Mesylate (MDL-73147EF) is an antagonist of the 5-HT3 receptor and can be used in research on the treatment of vomiting and nausea following</p>Fórmula:C20H24N2O6SPureza:99.05%Forma y color:White PowderPeso molecular:420.48hMAO-B-IN-7
CAS:<p>Compound 11n (hMAO-B-IN-7) is a potent inhibitor of human monoamine oxidase-B (hMAO-B) that can cross the blood-brain barrier (BBB). It demonstrates an IC 50 value of 0.79±0.05 μM and is useful in research related to Alzheimer's disease (AD) and Parkinson's disease (PD) [1].</p>Fórmula:C23H19FN2O5Forma y color:SolidPeso molecular:422.41SIB-1553A hydrochloride
CAS:SIB-1553A hydrochloride is a nicotinic acetylcholine receptor agonist and a selective neuronal nAChR ligandFórmula:C13H20ClNOSPureza:99.56% - 99.73%Forma y color:SolidPeso molecular:273.82SSAO inhibitor-3
CAS:<p>SSAO inhibitor-3 targets human AOC1/SSAO in atherosclerosis, diabetes, obesity, CKD, and more, with IC50s of 0.1-10 μM/<10 nM.</p>Fórmula:C15H23FN4O3Forma y color:SolidPeso molecular:326.37PF-03463275
CAS:<p>PF-03463275 is an orally active and selective reversible inhibitor of competitive glycine transporter protein-1 (GlyT1) with a Ki of 11.6 nM.PF-03463275 has CNS</p>Fórmula:C19H22ClFN4OPureza:99.86%Forma y color:SolidPeso molecular:376.86Mirisetron
CAS:<p>Mirisetron (WAY-100579, SEC-579) is a 5-HT3 receptor antagonist, cognitive-enhancing effects. counteracts learning deficits.</p>Fórmula:C24H31N3O2Pureza:99.88%Forma y color:SolidPeso molecular:393.52Phaclofen
CAS:<p>GABAB antagonist</p>Fórmula:C9H13ClNO3PPureza:99.32%Forma y color:White SolidPeso molecular:249.63S 14506 hydrochloride
CAS:<p>S 14506 hydrochloride is a 5-HT1A receptor full agonist.</p>Fórmula:C24H27ClFN3O2Pureza:99.92%Forma y color:SolidPeso molecular:443.94AP-521 (Free base)
CAS:<p>AP-521, a 5-HT1A receptor antagonist, is used potentially for the treatment of anxiety.</p>Fórmula:C20H18N2O3SForma y color:SolidPeso molecular:366.43Tilapertin
CAS:Tilapertin is an oral glycine transporter type-1 inhibitor.Fórmula:C20H21F3N2O2Pureza:98%Forma y color:SolidPeso molecular:378.39CP94253 hydrochloride
CAS:<p>CP94253 hydrochloride: selective 5-HT1B agonist, Ki=2 nM; less active on 5-HT1A/D/C/2 (Ki=89/49/860/1600 nM).</p>Fórmula:C15H20ClN3OPureza:99.78%Forma y color:SolidPeso molecular:293.79Iferanserin
CAS:Iferanserin (S-MPEC) is a selective antagonist of the 5-HT receptor (serotonin receptor) with an affinity for 5-HT2A receptors.Fórmula:C23H28N2OForma y color:SolidPeso molecular:348.48F13714 fumarate
CAS:<p>F13714 fumarate is a 5-HT1A receptor-biased agonist.</p>Fórmula:C25H29ClF2N4O5Pureza:98.86%Forma y color:SolidPeso molecular:538.97Enciprazine
CAS:Enciprazine (D-3112) shows anxiolytic activity, is used to treat anxiety disorders, and can be used to study depression.Fórmula:C23H32N2O6Pureza:98.63%Forma y color:SolidPeso molecular:432.51TC-N 22A
CAS:TC-N 22A is a strong, selective, oral active mGlu4 forward allosteric regulator (PAM) that can cross the blood-brain barrier.Fórmula:C14H13N5SPureza:99.95%Forma y color:SolidPeso molecular:283.35UoS 12258
CAS:<p>UoS 12258 is a positive allosteric modulator of AMPA receptors, used for studying cognitive impairments.</p>Fórmula:C17H19FN2O2SPureza:99.84%Forma y color:SolidPeso molecular:334.41SB-269970
CAS:SB-269970 is a antagonist of 5-HT7 receptor(pKi of 8.3).Fórmula:C18H28N2O3SPureza:98%Forma y color:SolidPeso molecular:352.49MAO-B-IN-22
CAS:<p>MAO-B-IN-22 (compound 6h) represents a powerful MAO-B inhibitor, boasting an IC50 value of 0.014 μM, and exhibits high antioxidant activity alongside effective</p>Fórmula:C20H18FNO2Pureza:98%Forma y color:SolidPeso molecular:323.36E2730
CAS:<p>E2730 is a non-competitive GABA transporter 1 (GAT1) inhibitor with anti-epileptic activity, useful in studying neurological disorders.</p>Fórmula:C9H8F4N2O2SPureza:98.22% - 98.54%Forma y color:SolidPeso molecular:284.23MHP 133
CAS:<p>MHP 133 is a drug with multiple CNS targets(AChE with Ki of 69 μM).</p>Fórmula:C17H20ClN5O3Pureza:98%Forma y color:SolidPeso molecular:377.83PD-102807
CAS:<p>PD-102807 is a selective and competitive M4 muscarinic receptor antagonist for Parkinson's disease research, inhibit airway smooth muscle (ASM) contraction.</p>Fórmula:C23H24N2O4Pureza:98.90%Forma y color:SolidPeso molecular:392.45Nexopamil racemate
CAS:<p>Nexopamil racemate（(Rac)-Nexopamil） is a racemate of Nexopamil. The Nexopamil racemate has potential anti-asthmatic and anti-ulcer activity.</p>Fórmula:C24H40N2O3Pureza:98.61%Forma y color:SolidPeso molecular:404.59Nelonicline citrate
CAS:<p>Nelonicline citrate (ABT-126) is a selective α7 nAChR agonist with a Ki of 12.3 nM, studied for schizophrenia and Alzheimer's.</p>Fórmula:C23H27N3O8SForma y color:SolidPeso molecular:505.54Tarafenacin D-tartrate
CAS:Tarafenacin D-tartrate is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over the M2 receptor.Fórmula:C25H26F4N2O8Pureza:99.86%Forma y color:SolidPeso molecular:558.48DMeOB
CAS:DMeOB (3,3'-Dimethoxybenzaldazine) is a negative regulator with mGluR5 agonist activity and is used in the study of neurological disorders.Fórmula:C16H16N2O2Pureza:98.34%Forma y color:SolidPeso molecular:268.31VU6001376
CAS:<p>VU6001376 is an effective and selective positive allosteric modulator of the metabotropic glutamate receptor 4 (EC50: 50.1 nM).</p>Fórmula:C18H14F2N6OSPureza:98%Forma y color:SolidPeso molecular:400.41HexylHIBO
CAS:<p>HexylHIBO is a type I mGluR antagonist that inhibits mGlu1a and mGlu5a, with Kb values of 140 and 110 μM, respectively.HexylHIBO decreases sEPSC in rats.</p>Fórmula:C12H20N2O4Pureza:99.55%Forma y color:SolidPeso molecular:256.3P-gp inhibitor 1
CAS:<p>P-gp inhibitor 1 inhibits reversing P-glycoprotein-mediated multidrug resistance with an EC50 of 57.9 nM (K562/A02 cells).</p>Fórmula:C32H31N5O2Pureza:98.65%Forma y color:SolidPeso molecular:517.622-Iodomelatonin
CAS:<p>2-Iodomelatonin, Ki 28 pM, is an MT1 agonist, >5x selective over MT2, used to map melatonin sites in brain/tissues.</p>Fórmula:C13H15IN2O2Pureza:99.7%Forma y color:SolidPeso molecular:358.17Flosulide
CAS:<p>Flosulide is an effective selective COX-2 inhibitor for the treatment of inflammatory diseases.</p>Fórmula:C16H13F2NO4SPureza:98%Forma y color:SolidPeso molecular:353.34Tilmacoxib
CAS:Tilmacoxib is a highly selective, time-dependent, and irreversible inhibitor of human COX-2 ( IC50: 85 nM in an enzyme assay).Fórmula:C16H19FN2O3SPureza:98%Forma y color:SolidPeso molecular:338.4(1R,2S)-VU0155041
CAS:<p>(1R,2S)-VU0155041 is the cis regioisomer of VU0155041 and a partial agonist of mGluR4.</p>Fórmula:C14H15Cl2NO3Pureza:98.85%Forma y color:SolidPeso molecular:316.18
