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(939 products)
- ACK(1 products)
- AChR(575 products)
- ATP Citrate Lyase(16 products)
- Adrenergic Receptor(2,945 products)
- BACE(36 products)
- Beta Amyloid(205 products)
- CaMK(69 products)
- Cyclooxygenase (COX) Inhibitors(561 products)
- Dopamine Receptor(407 products)
- GABA Receptor(336 products)
- Gamma-secretase(59 products)
- GluR(255 products)
- GlyT(24 products)
- Histamine Receptor(358 products)
- LRRK2(33 products)
- Melatonin Receptor(24 products)
- NMDAR(28 products)
- OX Receptor(40 products)
- Opioid Receptor(297 products)
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Found 5398 products of "Neuroscience"
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(-)-Deguelin
CAS:Formula:C23H22O6Purity:>95.0%(HPLC)Color and Shape:White to Yellow to Green powder to crystalMolecular weight:394.42CHIR 99021 [Optimized for Cell Culture]
CAS:Formula:C22H18Cl2N8Purity:>97.0%(HPLC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:465.341,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic Acid
CAS:Formula:C22H24N2O10Purity:>97.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:476.44KB-R 7943
CAS:Formula:C16H17N3O3S·CH4O3SPurity:>98.0%(HPLC)Color and Shape:White to Yellow to Green powder to crystalMolecular weight:427.49Pipamperone
CAS:Formula:C21H30FN3O2Purity:>98.0%(HPLC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:375.49Dantrolene Sodium Salt Hydrate
CAS:Formula:C14H9N4NaO5·xH2OPurity:>98.0%(T)(HPLC)Color and Shape:Orange to Brown powder to crystalMolecular weight:336.24 (as Anhydrous)Brexpiprazole-d8
CAS:<p>Brexpiprazole D8 is a deuterium-modified partial agonist of 5-HT1A and dopamine receptors, with Ki values of 0.12 nM and 0.3 nM respectively.</p>Formula:C25H27N3O2SPurity:98%Color and Shape:SolidMolecular weight:441.62Amitriptyline-d6 Hydrochloride
CAS:<p>Amitriptyline-d6 Hydrochloride is a deuterated compound of Amitriptyline Hydrochloride. Amitriptyline Hydrochloride has a CAS number of 549-18-8. Amitriptyline Hydrochloride is the hydrochloride salt of the tricyclic dibenzocycloheptadiene amitriptyline with antidepressant and antinociceptive activities.</p>Formula:C20H18D6ClNColor and Shape:SolidMolecular weight:319.90Mirtazapine D3
CAS:<p>Mirtazapine D3 is a deuterium labeled Mirtazapine. Mirtazapine is an inhibitor of 5-HT receptor .</p>Formula:C17H19N3Purity:98%Color and Shape:SolidMolecular weight:268.37Homotaurine-d6
CAS:<p>Homotaurine-d6 is a deuterated compound of Homotaurine. Homotaurine has a CAS number of 3687-18-1. Because of its similarity in structure to the neurotransmitter gamma-aminobutyric acid (GABA), it has GABAergic effects and may be useful as an anticonvulsant. Homotaurine has also been investigated as a potential treatment for Alzheimer's disease. It binds to soluble amyloid beta and inhibits the formation of neurotoxic aggregates that lead to amyloid plaque deposition in the brain. However, clinical trials failed to show improvement compared to placebo.</p>Formula:C3D6H3NO3SColor and Shape:SolidMolecular weight:145.21Hydroxy ziprasidone
CAS:<p>Hydroxy ziprasidone is an impurity of Ziprasidone. Ziprasidone, an antipsychotic agent, is a 5-HT and dopamine receptor antagonist.</p>Formula:C21H21ClN4O2SPurity:98%Color and Shape:SolidMolecular weight:428.947-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>Formula:C12H12INO2Color and Shape:SolidMolecular weight:329.13Diclofensine
CAS:<p>Diclofensine (Ro 8-4650) inhibits the uptake of serotonin, noradrenaline and dopamine.</p>Formula:C17H17Cl2NOPurity:97.01% - 98.13%Color and Shape:SolidMolecular weight:322.23Ketanserinol
CAS:<p>Ketanserinol is a metabolite of the antihypertensive drug ketanserin, which blocks 5-HT2 receptors to treat protamine-induced pulmonary hypertension.</p>Formula:C22H24FN3O3Color and Shape:SolidMolecular weight:397.44Aβ1-42 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>Formula:C29H32N4SColor and Shape:SolidMolecular weight:468.66Catestatin
CAS:Non-competitive inhibitor of nicotinic receptors; blocks cationic signalling and catecholamine release; stimulates histamine release. IC50 ~200-250nM.Formula:C107H173N37O26SPurity:98%Color and Shape:SolidMolecular weight: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>Formula:C18H29NO2H2O4SPurity:98.55%Color and Shape:SolidMolecular weight:340.47SB 271046 hydrochloride
CAS:<p>SB 271046 hydrochloride (SB 271046A) is selective, orally active 5-HT6 antagonist and is > 200-fold selective over 55 other receptors, enzymes and ion channels.</p>Formula:C20H22ClN3O3S2·HClPurity:99.77%Color and Shape:SolidMolecular weight:488.45Aprofene
CAS:<p>Aprofene blocks acetylcholine receptors, used for peptic ulcers, endarteritis, cholecystitis, and colitis.</p>Formula:C21H27NO2Color and Shape:SolidMolecular weight:325.44Aftin-5
CAS:<p>Aftin-5 is an inducer of amyloid beta protein 42 (Aβ42). It functions by modifying the ultrastructure of mitochondria, leading to an upregulation of Aβ42 and a downregulation of Aβ38 through a β-secretase and γ-secretase-dependent mechanism. Aftin-5 exhibits mild cytotoxicity in SH-SY5Y, HT22, N2a, and N2a-AβPP695 cells, with IC50 values of 180, 194, 178, and 150 μM, respectively.</p>Formula:C19H26N6OColor and Shape:SolidMolecular weight:354.45Pardoprunox
CAS:<p>Pardoprunox (SLV-308) is a partial dopamine D2 agonist and noradrenergic agonist with serotonin 5-HT1A agonist properties.</p>Formula:C12H15N3O2Purity:98%Color and Shape:SolidMolecular weight:233.27Dianicline dihydrochloride
CAS:<p>Dianicline dihydrochloride is a partial agonist of α4β2 nicotinic acetylcholine receptor. It increases cessation rates in a dose-dependent manner.</p>Formula:C13H16N2OPurity:98%Color and Shape:SolidMolecular weight:216.28Biperiden lactate
CAS:<p>Biperiden lactate is a biochemical.</p>Formula:C24H35NO4Color and Shape:SolidMolecular weight:401.54VU0477886
CAS:<p>VU0477886: Potent mGlu4 PAM, effective in preclinical Parkinson's model HIC.</p>Formula:C20H13ClN4O3Purity:98%Color and Shape:SolidMolecular weight:392.807-Desmethyl-3-hydroxyagomelatine
CAS:<p>7-Desmethyl-3-hydroxyagomelatine, less active than parent drug Agomelatine, is a melatonergic agonist and 5-HT2C antagonist.</p>Formula:C14H15NO3Purity:98%Color and Shape:SolidMolecular weight:245.275-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>Formula:C11H15ClN2Purity:99.45%Color and Shape:SolidMolecular weight:210.703Nicardipine pyridine metabolite II
CAS:<p>Nicardipine pyridine metabolite II is a biaoctive chemical.</p>Formula:C26H27N3O6Color and Shape:SolidMolecular weight:477.514-(6-Bromo-2-benzothiazolyl)-N-methylbenzenamine
CAS:<p>4-(6-Bromo-2-benzothiazolyl)-N-methylbenzenamine is a potent amyloid imaging agent that binds to Amyloid-β (1-40) (KD: 1.7 nM).</p>Formula:C14H11BrN2SPurity:98%Color and Shape:SolidMolecular weight:319.22VU0029767
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>Formula:C21H21N3O3Color and Shape:SolidMolecular weight:363.412-(3-Chlorophenyl)-2-(methylamino)cyclohexanone Hydrochloride
CAS:Controlled ProductFormula:C13H17Cl2NOColor and Shape:NeatMolecular weight:274.192-(4-Chlorophenyl)-2-(methylamino)cyclohexanone Hydrochloride
CAS:Controlled ProductFormula:C13H17Cl2NOColor and Shape:NeatMolecular weight:274.192Z-Nalfurafine
CAS:Controlled Product<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>Formula:C28H32N2O5Color and Shape:NeatMolecular weight:476.56Nalfurafine N-Oxide
CAS:Controlled Product<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>Formula:C28H32N2O6Color and Shape:NeatMolecular weight:492.566S-Nalfurafine
CAS:Controlled Product<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>Formula:C28H32N2O5Color and Shape:NeatMolecular weight:476.56Dolasetron 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>Formula:C20H24N2O6SPurity:99.05%Color and Shape:White PowderMolecular weight:420.48LY 344864
CAS:<p>LY 344864, a specifc receptor agonist, is an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor.</p>Formula:C21H22FN3OPurity:98%Color and Shape:SolidMolecular weight:351.42Paroxetine hydrochloride hemihydrate
CAS:<p>Paroxetine hydrochloride hemihydrate (Paxil) is an effective and selective serotonin reuptake inhibitor (SSRI).</p>Formula:C38H44Cl2F2N2O7Purity:99.949%Color and Shape:SolidMolecular weight:749.67SB-737050A
CAS:<p>SB-737050A, a 5-HT antagonist, is used potentially for the treatment of schizophrenia.</p>Formula:C22H23ClN2O3S2Color and Shape:SolidMolecular weight:463.01γ-Secretase modulator 4
CAS:<p>γ-Secretase modulator 4 is a potent γ-secretase modulator, reduces the Aβ42 level with IC50s of 0.017 μM and 0.014 μM in mouse and human, respectively.</p>Formula:C23H19FN4O2Purity:98%Color and Shape:SolidMolecular weight:402.42BChE-IN-8
CAS:<p>BChE-IN-8, compound 20, is a potent oral BChE inhibitor effective on eqBChE and hBChE, crosses blood-brain barrier, and may help in Alzheimer's research.</p>Formula:C18H12BrN7O2Color and Shape:SolidMolecular weight:438.24GABAA receptor agent 6
CAS:<p>GABAA receptor agent 6 (compound 2027) is a potent γ-GABAAR antagonist with low cellular membrane permeability (Ki = 0.56 μM) [1].</p>Formula:C18H25N3O2Color and Shape:SolidMolecular weight:315.41EMD 386088 hydrochloride
CAS:<p>EMD 386088 hydrochloride is a 5-HT6 receptor agonist.</p>Formula:C14H16Cl2N2Purity:98%Color and Shape:SolidMolecular weight:283.2TB 21007
CAS:<p>GABAA receptor inverse agonist</p>Formula:C15H17NO2S3Purity:98%Color and Shape:SolidMolecular weight:339.5(R)-Praziquantel
CAS:<p>(R)-Praziquantel is an active enantiomer of praziquantel.</p>Formula:C19H24N2O2Purity:98%Color and Shape:SolidMolecular weight:312.41Methacholine bromide
CAS:<p>Methacholine bromide is a potent M3 agonist for diagnosing asthma by identifying bronchial hyperresponsiveness.</p>Formula:C8H18BrNO2Color and Shape:SolidMolecular weight:240.141SL-651498
CAS:<p>SL-651498, a GABAA receptor agonist, is used potentially for the treatment of anxiety.</p>Formula:C23H20FN3O2Purity:98%Color and Shape:SolidMolecular weight:389.42D-NMAPPD
CAS:<p>Litifilimab (BIIB059) is a humanized antibody targeting BDCA2 and CLEC4C for the study of cutaneous lupus erythematosus.</p>Formula:C23H38N2O5Color and Shape:SolidMolecular weight:422.56BACE-IN-1
CAS:<p>BACE-IN-1 is an imidazo[1,2-a]pyridine derivative that inhibits the β-site amyloid precursor protein cleavage enzyme (BACE) sentence.BACE-IN-1 has the potential</p>Formula:C22H16ClN5O2Purity:98%Color and Shape:SolidMolecular weight:417.85PNU-96415E
CAS:<p>dopamine D4 and serotonergic 5-HT2A receptor antagonist</p>Formula:C21H27Cl2FN2OPurity:98%Color and Shape:SolidMolecular weight:413.36CGS-12066 maleate salt
CAS:<p>CGS-12066 maleate salt is an agonist of 5-HT1B serotonin receptor.</p>Formula:C21H21F3N4O4Color and Shape:SolidMolecular weight:450.41TAK-070
CAS:<p>TAK-070 is a non-competitive inhibitor of BACE1.</p>Formula:C27H31NOPurity:98%Color and Shape:SolidMolecular weight:385.54TMPPAA
CAS:<p>TMPPAA is an allosteric agonist of 5-HT3 receptor.</p>Formula:C15H21NO2Purity:98%Color and Shape:SolidMolecular weight:247.33Org37684
CAS:<p>5-HT2 receptors agonist</p>Formula:C14H20ClNO2Purity:98%Color and Shape:SolidMolecular weight:269.77HTL14242
CAS:<p>HTL14242 is a mGlu5 Negative Allosteric Modulator.</p>Formula:C16H8ClFN4Color and Shape:SolidMolecular weight:310.71THK-523
CAS:<p>THK-523 selectively binds to tau in Alzheimer's, potent in vitro/vivo. 18F-THK523 excels in tau imaging.</p>Formula:C17H15FN2OColor and Shape:SolidMolecular weight:282.31GR 196429
CAS:<p>GR 196429: MT1-selective melatonin receptor agonist; induces sleep, alters circadian rhythm, stimulates melatonin in mice.</p>Formula:C14H18N2O2Purity:98%Color and Shape:SolidMolecular weight:246.3Chlorisondamine diiodide
CAS:<p>long lasting nicotinic antagonist</p>Formula:C14H20Cl4I2N2Color and Shape:SolidMolecular weight:611.94Bifeprunox
CAS:<p>Bifeprunox: potent antipsychotic, partial agonist at D2-like/5-HT1A receptors; treats schizophrenia.</p>Formula:C24H23N3O2Purity:98%Color and Shape:SolidMolecular weight:385.46Clovoxamine
CAS:<p>Clovoxamine fumarate (DU 23811 fumarate) is a 5-HT reuptake, serotonin and norepinephrine inhibitor with antidepressant and anticonvulsant activity.</p>Formula:C14H21ClN2O2Purity:99.44% - 99.75%Color and Shape:SolidMolecular weight:284.785-HT4 antagonist 1
CAS:<p>5-HT4 antagonist 1 is an antagonist of 5-HT4 (pKi = 9.6).</p>Formula:C23H36N4O5SPurity:99.75%Color and Shape:SolidMolecular weight:480.62(RS)-PPG
CAS:<p>(RS)-PPG: Potent, selective III mGluRs agonist; EC50s: hmGluR4a 5.2μM, hmGluR6 4.7μM, hmGluR7b 185μM, hmGluR8a 0.2μM; neuroprotective, anticonvulsive.</p>Formula:C8H10NO5PPurity:98%Color and Shape:SolidMolecular weight:231.14ML381
CAS:<p>ML381 is a M5-orthosteric antagonist with a high selectivity of muscarinic subtype.</p>Formula:C21H21N3O4Color and Shape:SolidMolecular weight:379.41tCFA15
CAS:<p>tCFA15: A trimethylated long-chain fatty alcohol with a 15-carbon side chain; may regulate Notch signaling and neuron differentiation.</p>Formula:C24H44O2Purity:98%Color and Shape:SolidMolecular weight:364.61L-775,606
CAS:<p>L-775,606 is a selective agonist of 5-hydroxytryptamine 1D.</p>Formula:C25H29FN6Purity:98%Color and Shape:SolidMolecular weight:432.54VU0431316
CAS:<p>VU0431316 is a negative mGlu5 allosteric modulator. It has activity in a mouse model of anxiety.</p>Formula:C14H9ClN6O2Purity:98%Color and Shape:SolidMolecular weight:328.71JNJ-40418677
CAS:<p>JNJ-40418677 is a γ-secretase modulator that selectively blocks γ-site cleavage of the APP without affecting the processing of Notch.</p>Formula:C26H22F6O2Purity:98%Color and Shape:SolidMolecular weight:480.44Zamifenacin
CAS:<p>Zamifenacin obviously decreases colonic motility in irritable bowel syndrome. Zamifenacin is an effective gut-selective muscarinic M3 receptor antagonist.</p>Formula:C27H29NO3Purity:98%Color and Shape:SolidMolecular weight:415.52Ro 41-3290
CAS:<p>Ro 41-3290 is the desethylated derivative of Ro 41-3696, which is an agonist of nonbenzodiazepine partial at the benzodiazepine receptor.</p>Formula:C24H21ClN2O3Purity:98%Color and Shape:SolidMolecular weight:420.89PF-0713
CAS:<p>PF 0713, a GABAA receptor agonist, is used as an intravenous sedative-hypnotic for general anaesthesia, ICU sedation, procedural sedation, chemotherapy.</p>Formula:C14H22OPurity:98%Color and Shape:SolidMolecular weight:206.32AChE-IN-21
CAS:<p>AChE-IN-21 (I-8), potent, selective AChE inhibitor, IC50: 2.66 nM, good BBB permeability.</p>Formula:C24H29NO4Color and Shape:SolidMolecular weight:395.49VU0366248
CAS:<p>VU0366248 is a mGlu5 negative allosteric modulator.</p>Formula:C14H7ClF2N2OPurity:98%Color and Shape:SolidMolecular weight:292.67DH97
CAS:<p>MT2 melatonin receptor antagonist</p>Formula:C22H26N2OPurity:98%Color and Shape:SolidMolecular weight:334.45BGT1-IN-9
CAS:<p>BGT1-IN-9 is an M1 muscarinic agonist.</p>Formula:C5H10ClN3O2Color and Shape:SolidMolecular weight:179.605DCG-IV
CAS:<p>DCG-IV: Class II mGluR agonist; anticonvulsant; neuroprotective; EC50: mGlu2R-0.35μM, mGlu3R-0.09μM; antagonizes Group I/III mGluRs.</p>Formula:C7H9NO6Purity:98%Color and Shape:SolidMolecular weight:203.15(+/-)-Marmesin
CAS:<p>Marmesin is a novel angiogenesis inhibitor.</p>Formula:C14H14O4Purity:98.00% - 98.00%Color and Shape:SolidMolecular weight:246.26MS 245 oxalate
CAS:<p>MS 245 oxalate is a 5-HT6 antagonist.</p>Formula:C21H24N2O7SPurity:98%Color and Shape:SolidMolecular weight:448.49SKF-83566 hydrobromide
CAS:<p>D1-like dopamine receptor antagonist</p>Formula:C17H19BrClNOPurity:98%Color and Shape:SolidMolecular weight:368.7GABAA receptor agent 5
CAS:<p>Compound 018 is a potent γ-GABAAR antagonist, Ki of 0.020 μM, with low membrane permeability.</p>Formula:C21H25N3O2SColor and Shape:SolidMolecular weight:383.51γ-secretase modulator 2
CAS:<p>Gamma-secretase modulator 2 selectively targets Alzheimer's by reducing Aβ(1-42), aiding in prevention and treatment.</p>Formula:C25H22F4N6O2Purity:98%Color and Shape:SolidMolecular weight:514.47T 82
CAS:<p>T 82 is an antagonist of 5-HT3 and inhibitor of acetylcholinesterase (AChE) and used for the treatment of Alzheimer's Disease.</p>Formula:C56H62N6O8Purity:98%Color and Shape:SolidMolecular weight:947.146VU0410425
CAS:<p>VU0410425 is a metabotropic glutamate receptor subtype 1 negative allosteric modulator.</p>Formula:C19H16ClN3O3Purity:98%Color and Shape:SolidMolecular weight:369.8HZ166
CAS:<p>HZ-166 is a positive GABAA receptor modulator and a GABAA receptor subtype-selective benzodiazepine site ligand.</p>Formula:C21H16N4O2Purity:98%Color and Shape:SolidMolecular weight:356.38Pregabalin arenacarbil
CAS:<p>Pregabalin arenacarbil is a gabamimetic.</p>Formula:C15H27NO6Color and Shape:SolidMolecular weight:317.38NCS-382
CAS:<p>γ-Hydroxybutyric acid antagonist</p>Formula:C13H14O3Purity:98%Color and Shape:SolidMolecular weight:218.25BNC375
CAS:<p>BNC375 is a α7 nAChRs type I positive allosteric modulator (EC50: 1.9 μM).</p>Formula:C19H23ClN2O3SPurity:98%Color and Shape:SolidMolecular weight:394.925-HT3 antagonist 2
CAS:<p>5-HT3 antagonist 2 is an antagonist of 5-HT3 receptor.</p>Formula:C18H21N3OPurity:98%Color and Shape:SolidMolecular weight:295.38BChE-IN-14
CAS:<p>BChE-IN-14 reverses cognitive decline, is safe for primary cells, crosses the blood-brain barrier, and selectively inhibits BChE (IC50: 0.011 μM for hBChE).</p>Formula:C24H29NColor and Shape:SolidMolecular weight:331.49PF-3246799
CAS:<p>PF-3246799 is an effective and selective agonist of the 5-HT2C receptor.</p>Formula:C15H17N3Purity:98%Color and Shape:SolidMolecular weight:239.32Telenzepine
CAS:<p>Telenzepine is a potent and selective M1 antimuscarinic.</p>Formula:C19H22N4O2SPurity:98%Color and Shape:SolidMolecular weight:370.47AR-A 2
CAS:<p>AR-A 2, a selective 5-HT1B antagonist; high guinea pig 5-HT1B/1D affinity (Ki: 0.24, 0.47 nM); 10x less for 5-HT1D (Ki: 5 nM).</p>Formula:C27H36N4O2Purity:98%Color and Shape:SolidMolecular weight:448.6Amitriptylinoxide
CAS:<p>Amitriptylinoxide is an antidepressant.</p>Formula:C20H23NOPurity:98%Color and Shape:SolidMolecular weight:293.4Ro 19-4603
CAS:<p>Benzodiazepine inverse agonist</p>Formula:C15H17N3O3SPurity:98%Color and Shape:SolidMolecular weight:319.38SB 206553 hydrochloride
CAS:<p>SB 206553 hydrochloride is a 5-HT2C inverse agonist and a 5-HT2C/5-HT2B receptor antagonist with anxiolytic activity, useful for studying neurological disorders</p>Formula:C17H17ClN4OPurity:99.56%Color and Shape:SolidMolecular weight:328.8Levemopamil HCl
CAS:<p>Levemopamil HCl is used as a calcium channel blocker.</p>Formula:C23H31ClN2Purity:98%Color and Shape:SolidMolecular weight:370.96MPDC
CAS:<p>MPDC acts as a competitive inhibitor against the Na+-dependent high-affinity glutamate transporter within forebrain synaptosomes.</p>Formula:C7H9NO4Purity:98%Color and Shape:SolidMolecular weight:171.15Alaproclate (hydrochloride)
CAS:<p>Alaproclate, an SSRI, enhances serotonin and SIRT1, hinders NMDA and K+ currents in neurons, and shows antidepressant-like effects in rats.</p>Formula:C13H19Cl2NO2Color and Shape:SolidMolecular weight:292.2BGC 20-761
CAS:<p>BGC20-761: selective 5-HT6/Dopamine antagonist; enhances memory, potential antipsychotic. K i - 5-HT6: 20 nM, 5-HT2A: 69 nM, D2: 140 nM.</p>Formula:C19H22N2OColor and Shape:SolidMolecular weight:294.39LY 2365109 hydrochloride
CAS:<p>glycine transporter 1 (GlyT1) inhibitor</p>Formula:C22H27NO5Purity:98%Color and Shape:SolidMolecular weight:385.45hMAO-B-IN-2
CAS:<p>hMAO-B-IN-2: selective oral hMAO-B inhibitor, crosses BBB, IC50=4 nM, potential for Alzheimer's research, neuroprotective, low toxicity.</p>Formula:C18H23NO3Color and Shape:SolidMolecular weight:301.38PF-4479745
CAS:<p>PF-4479745 ia a potent and selective agonist of 5-HT2C receptor.</p>Formula:C17H22N4Purity:98%Color and Shape:SolidMolecular weight:282.38
![CHIR 99021 [Optimized for Cell Culture]](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3B%2Fthumb-webp%2FC4010.webp&w=3840&q=75)
