Neurociência
Os inibidores de neurociência são compostos projetados para modular a atividade de proteínas, enzimas ou receptores específicos no sistema nervoso. Esses inibidores são cruciais para estudar os mecanismos moleculares subjacentes à função neural, transmissão sináptica e doenças neurodegenerativas. Ao direcionar receptores de neurotransmissores, canais iônicos e vias de sinalização, os inibidores de neurociência ajudam na exploração da função cerebral e no desenvolvimento de estratégias terapêuticas para distúrbios neurológicos como Alzheimer, Parkinson e epilepsia. Na CymitQuimica, oferecemos uma ampla gama de inibidores de neurociência de alta qualidade para apoiar sua pesquisa em neurobiologia, neurofarmacologia e ciências cognitivas.
Subcategorias de "Neurociência"
- Receptor 5-HT(1.025 produtos)
- ACK(1 produtos)
- AChR(648 produtos)
- ATP Citrato Liase(17 produtos)
- Receptor adrenérgico(3.029 produtos)
- BACE(37 produtos)
- Beta Amilóide(231 produtos)
- CaMK(73 produtos)
- COX(602 produtos)
- Receptor de Dopamina(445 produtos)
- Receptor GABA(372 produtos)
- Gama-secretase(63 produtos)
- GluR(265 produtos)
- GlyT(26 produtos)
- Receptor de Histamina(385 produtos)
- LRRK2(42 produtos)
- Receptor de Melatonina(26 produtos)
- NMDAR(10 produtos)
- Receptor OX(42 produtos)
- Receptor opioide(327 produtos)
Exibir 12 mais subcategorias
Foram encontrados 5636 produtos de "Neurociência"
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Adinazolam Mesylate
CAS:Adinazolam Mesylate is an anxiolytic and antidepressant agent. Adinazolam Mesylate binds to peripheral-type benzodiazepine receptors that interact allosterically with GABA receptors as an agonist to produce inhibitory effects.Fórmula:C20H22ClN5O3SPureza:98%Cor e Forma:SolidPeso molecular:447.94Ro 14-7437
CAS:Ro 14-7437 is an antagonist of GABA-benzodiazepine receptor.Fórmula:C15H15N3O3Cor e Forma:SolidPeso molecular:285.3Profadol hydrochloride
CAS:Profadol hydrochloride acts as a mixed agonist-antagonist of the μ-opioid receptor with analgesic activity.Fórmula:C14H22ClNOPureza:98%Cor e Forma:SolidPeso molecular:255.78(S)-MCPG
CAS:(S)-MCPG is the active isomer of (RS)-MCPG, non-selective group I/group II metabotropic glutamate receptor antagonist.Fórmula:C10H11NO4Pureza:98.72%Cor e Forma:SolidPeso molecular:209.20SCH-50910 free base
CAS:SCH-50910 is an antagonist of GABAB receptor.Fórmula:C8H15NO3Cor e Forma:SolidPeso molecular:173.21WAY 629
CAS:WAY 629 is a selective SR-2C agonist that also act as potent 5-HT2C receptor agonists.Fórmula:C15H18N2Cor e Forma:SolidPeso molecular:226.32(R)-Duloxetine Hydrochloride
CAS:(R)-Duloxetine Hydrochloride, naphthalenyloxy amine, binds human serum albumin, less effective than (S)-enantiomer as SNRI.Fórmula:C18H20ClNOSCor e Forma:SolidPeso molecular:333.87Glutaminyl Cyclase Inhibitor 5
Glutaminyl Cyclase Inhibitor 5 is a potent, selective inhibitor of human glutaminyl cyclase (hQC), demonstrating an inhibition concentration half-max (IC 50) ofFórmula:C22H30N6OCor e Forma:SolidPeso molecular:394.51Elzasonan
CAS:Elzasonan is a selective 5-hydroxytryptamine 1B receptor antagonist used to treat patients with major depressive disorder and obsessive compulsive disorder.Fórmula:C22H23Cl2N3OSCor e Forma:SolidPeso molecular:448.41ZK-91296
CAS:ZK-91296: GABA agonist, lowers anxiety without sedation, may target specific BZ receptor subtype.Fórmula:C23H22N2O4Pureza:98%Cor e Forma:SolidPeso molecular:390.43AS19
CAS:AS19 is a potent, selective 5-HT7 receptor agonist (IC50: 0.83 nM; Ki: 0.6 nM).Fórmula:C18H25N3Pureza:98%Cor e Forma:SolidPeso molecular:283.41AVN-101 free base
CAS:AVN-101: potent 5-HT7 antagonist, also targets 5-HT6, 5-HT2A, 5-HT2C. Aims to treat CNS disorders.Fórmula:C21H24N2Cor e Forma:SolidPeso molecular:304.43mCPBG
CAS:mCPBG is a potent high affinity agonist of 5-HT3 receptor.Fórmula:C8H10ClN5Cor e Forma:SolidPeso molecular:211.65Ro 22-8515
CAS:Ro 22-8515 is the ligand of benzodiazepine receptor.Fórmula:C18H12Cl2N2OCor e Forma:SolidPeso molecular:343.21(1R,2S)-VU0155041
CAS:(1R,2S)-VU0155041 is the cis regioisomer of VU0155041 and a partial agonist of mGluR4.Fórmula:C14H15Cl2NO3Pureza:98.85%Cor e Forma:SolidPeso molecular:316.18Octamylamine hydrochloride
CAS:Octamylamine hydrochloride is a P450 inhibitor.Fórmula:C13H30ClNCor e Forma:SolidPeso molecular:235.84YM-58790
CAS:YM-58790 is a potent mAChR blocker with Ki values of 28 nM (M1), 260 nM (M2), 15 nM (M3), and reduces bladder contractions in rats.Fórmula:C27H31N3O2Pureza:99.87%Cor e Forma:SoildPeso molecular:429.55DAU 5884 HCl
CAS:DAU 5884 HCl is an M3 receptor antagonistFórmula:C17H21N3O3Cor e Forma:SolidPeso molecular:315.37TC-1698 dihydrochloride
CAS:TC-1698 dihydrochloride: selective α7 nicotinic agonist, with some β-receptor activity; neuroprotectant.Fórmula:C13H20Cl2N2Cor e Forma:SolidPeso molecular:275.22Alfadolone
CAS:Alfadolone is an anesthetic derivative of pregnanedione.Fórmula:C21H32O4Cor e Forma:SolidPeso molecular:348.48Cgp 52608
CAS:CGP 52608 is a selective ligand for RAR-associated orphan receptor alpha.Fórmula:C8H12N4OS2Cor e Forma:SolidPeso molecular:244.34AZD-9164 bromide
CAS:AMG-221, a selective 11β-HSD1 inhibitor, suppresses enzyme activity, lowers glucose/insulin, and reduces weight in obese mice.Fórmula:C29H38BrFN2O2Cor e Forma:SolidPeso molecular:545.53Caramiphen hydrochloride
CAS:Caramiphen hydrochloride: antimuscarinic, anticholinergic, NMDA receptor antagonist salt.Fórmula:C18H28ClNO2Cor e Forma:SolidPeso molecular:325.88Metanicotine
CAS:Metanicotine is a selective nicotinic agonist with antinociceptive properties.Fórmula:C10H14N2Cor e Forma:SolidPeso molecular:162.23LC kinetic stabilizer-2
CAS:LC Kinetic Stabilizer-2 is a powerful stabilizer for amyloidogenic immunoglobulin light chains (LC), demonstrating significant efficacy with an EC50 of 24 nM.Fórmula:C28H31N3O3Cor e Forma:SolidPeso molecular:457.56N-Nitroso Fluoxetine
CAS:N-Nitroso fluoxetine is a derivative of fluoxetine.1It is genotoxic toS. typhimuriumwhen used at concentrations ranging from 0.06 to 0.12 mg/ml.Fórmula:C17H17F3N2O2Cor e Forma:SolidPeso molecular:338.32Octamylamine sulfamate
CAS:Octamylamine sulfamate is a P450 inhibitor.Fórmula:C13H32N2O3SCor e Forma:SolidPeso molecular:296.47Zimelidine
CAS:Zimelidine, a withdrawn antidepressant, posed Guillain-Barre risk.Fórmula:C16H17BrN2Pureza:98%Cor e Forma:SolidPeso molecular:317.22Fonazine mesylate
CAS:Fonazine mesylate is a phenothiazine drug used for the treatment of migraine. It is a serotonin antagonist and histamine antagonist.Fórmula:C20H29N3O5S3Cor e Forma:SolidPeso molecular:487.65Hadacidin sodium
CAS:Hadacidin sodium is an inhibitor of AMP synthesis. Hadacidin and hadacidin analogues have anticancer activity and activity against adenylosuccinate synthetase.Fórmula:C3H4NNaO4Cor e Forma:SolidPeso molecular:141.06RJR-2429
CAS:RJR-2429 is a potent AChR agonist.Fórmula:C12H16N2Cor e Forma:SolidPeso molecular:188.27VER-3323
CAS:VER-3323 is a selective agonist for the 5-HT2B and 5-HT2C serotonin receptor with potent anorectic effects in animal studies.Fórmula:C11H15BrN2Pureza:98%Cor e Forma:SolidPeso molecular:255.15Iferanserin HCl
CAS:Iferanserin HCl is a selective serotonin receptor antagonist.Fórmula:C23H29ClN2OCor e Forma:SolidPeso molecular:384.95Echothiophate chloride
CAS:Echothiophate: long-lasting cholinesterase inhibitor for chronic glaucoma treatment; binds irreversibly, inactivating the enzyme.Fórmula:C9H23ClNO3PSCor e Forma:SolidPeso molecular:291.7708PF-06663195
CAS:PF-06663195 is a potent inhibitor of β-site amyloid precursor protein (APP) Cleaving Enzyme 1 (BACE1, β-Secretase 1).Fórmula:C18H18F3N3O2SCor e Forma:SolidPeso molecular:397.41A-850002
CAS:A-850002 is a bioactive chemical.Fórmula:C18H16N4OSCor e Forma:SolidPeso molecular:336.41SH-053-S-CH3-2'F
CAS:SH-053-S-CH3-2'F is a potent and selective agonist of GABAA receptors.Fórmula:C23H18FN3O2Cor e Forma:SolidPeso molecular:387.41SCH 50911 hydrochloride
CAS:SCH 50911 hydrochloride is a selective, orally-active and competitive antagonist of γ-Aminobutyric acid B GABA(B) receptor(IC50 : 1.1 μM).Fórmula:C8H16ClNO3Pureza:98%Cor e Forma:SolidPeso molecular:209.67Lintopride
CAS:Lintopride is an antagonist of 5HT4. It has moderate 5HT3 antagonist properties.Fórmula:C14H19ClN4O2Pureza:98%Cor e Forma:SolidPeso molecular:310.78VU 0469650
CAS:VU 0469650 is a potent and selective negative allosteric modulator of mGluR1 (IC50 = 99 nM).Fórmula:C22H28N4OPureza:98.03%Cor e Forma:SolidPeso molecular:364.48Ref: TM-T29118
1mg42,00€5mg79,00€1mL*10mM (DMSO)90,00€10mg108,00€25mg210,00€50mg313,00€100mg464,00€200mg640,00€Milacemide HCl
CAS:Milacemide HCl is an MAO-B inhibitor and glycine prodrug.Fórmula:C7H17ClN2OPureza:98%Cor e Forma:SolidPeso molecular:180.68DH-97
CAS:DH-97 is a potent MT2 melatonin receptor antagonist (pKi value = 8.03).Fórmula:C22H26N2OCor e Forma:SolidPeso molecular:334.45PD-102807
CAS:PD-102807 is a selective and competitive M4 muscarinic receptor antagonist for Parkinson's disease research, inhibit airway smooth muscle (ASM) contraction.Fórmula:C23H24N2O4Pureza:98.90%Cor e Forma:SolidPeso molecular:392.45Methacholine iodide
CAS:Methacholine iodide is a muscarinic acetylcholine receptor agonist.Fórmula:C8H18INO2Cor e Forma:SolidPeso molecular:287.14Pancopride
CAS:Pancopride（LAS 30451） is a novel, orally available, long-acting, selective 5-HT3 receptor antagonist that blocks nitrogen mustard and dacarbazine-inducedFórmula:C18H24ClN3O2Pureza:93.64%Cor e Forma:SolidPeso molecular:349.86MHP 133
CAS:MHP 133 is a drug with multiple CNS targets(AChE with Ki of 69 μM).Fórmula:C17H20ClN5O3Pureza:98%Cor e Forma:SolidPeso molecular:377.83γ-secretase modulator 1
CAS:gamma-secretase modulator 1 is a modulator of γ secretase and can be used in studies about the treatment of Alzheimer's disease.Fórmula:C24H24N4OSPureza:99.75% - 99.96%Cor e Forma:SolidPeso molecular:416.54VU0486321
CAS:VU0486321: potent mGlu1 PAM, rat PK CLp 13.3 mL/min/kg, t1/2 54 min, human fu 0.05, rat fu 0.03, great CNS penetration Kp 1.02.Fórmula:C20H12ClFN2O4Cor e Forma:SolidPeso molecular:398.77Neopterin, L-erythro-
CAS:Neopterin, L-erythro- can be used as a cholinergic receptor.Fórmula:C9H11N5O4Cor e Forma:SolidPeso molecular:253.21Asoxime dichloride
CAS:Asoxime dichloride (HI-6) blocks AChRs, including α7 nAChR, and boosts vaccination in the nervous system.Fórmula:C14H16Cl2N4O3Pureza:99.75% - 99.86%Cor e Forma:SolidPeso molecular:359.21ETAP
CAS:ETAP, a dual inhibitor of both monoamine oxidase A (MAO-A) and monoamine oxidase B (MAO-B), exhibits antidepressant-like effects and is utilized in the researchFórmula:C18H17N3OPureza:98%Cor e Forma:SolidPeso molecular:291.35E2730
CAS:E2730 is a non-competitive GABA transporter 1 (GAT1) inhibitor with anti-epileptic activity, useful in studying neurological disorders.Fórmula:C9H8F4N2O2SPureza:98.22% - 98.54%Cor e Forma:SolidPeso molecular:284.23LRRK2-IN-10
CAS:LRRK2-IN-10 (compound 34) is a potent, mutation-selective, brain-penetrant inhibitor targeting G2019S-LRRK2 kinase with IC50 values of 11 nM for G2019S-LRRK2Fórmula:C20H15N5OPureza:98%Cor e Forma:SolidPeso molecular:341.37MAO-B-IN-22
CAS: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 effectiveFórmula:C20H18FNO2Pureza:98%Cor e Forma:SolidPeso molecular:323.36MAO-B-IN-21
CAS:MAO-B-IN-21: MAO-B inhibitor with antioxidant, anti-amyloid aggregation, neuroprotective properties, BBB permeable, improves memory in Alzheimer's mice.Fórmula:C24H25ClN2O4Pureza:98%Cor e Forma:SolidPeso molecular:440.92MAO-B-IN-23
CAS:MAO-B-IN-23, also known as Compound 11f, is a reversible and competitive monoamine oxidase B (MAO-B) inhibitor with an IC50 value of 1.44 μM and a Ki of 0.51 μMFórmula:C19H18BrNOPureza:98%Cor e Forma:SolidPeso molecular:356.26Thiothixene hydrochloride
CAS:Thiothixene hydrochloride is an antipsychotic agent that can be used in the study of schizophrenia and bipolar mania.Fórmula:C23H30ClN3O2S2Cor e Forma:SolidPeso molecular:480.08GTS-21
CAS:GTS-21 (DMXB-A) is an α7 nAChR agonist. GTS-21 suppresses inflammation associated with rheumatoid arthritis by inhibiting RA Th1 cell differentiation.Fórmula:C19H20N2O2Pureza:98%Cor e Forma:SolidPeso molecular:308.375-HT3 antagonist 2
CAS:5-HT3 antagonist 2 is an antagonist of 5-HT3 receptor.Fórmula:C18H21N3OPureza:98%Cor e Forma:SolidPeso molecular:295.38PF-06767832
CAS:PF-06767832: selective M1 PAM (EC50=60 nM), no M2-M5 activity, good CNS penetration, but has GI and cardiovascular risks.Fórmula:C22H23N3O3SCor e Forma:SolidPeso molecular:409.5q-FTAA
CAS:q-FTAA targets Aβ1-42 fibrils (330-630 nM) and ADPBC (300-500 nM), useful in Alzheimer's disease research.Fórmula:C21H14O6S4Cor e Forma:SolidPeso molecular:490.59Bitopertin (R enantiomer)
CAS:Bitopertin R enantiomer (RG1678 R enantiomer) is the R-enantiomer of Bitopertin.Fórmula:C21H20F7N3O4SPureza:98%Cor e Forma:SolidPeso molecular:543.46ELN318463 racemate
CAS:ELN318463 racemate (ELN 318463 racemate) is the racemate of ELN318463 which is an amyloid precursor protein (APP) selective γ-secretase inhibitor.Fórmula:C19H20BrClN2O3SPureza:99.69%Cor e Forma:SolidPeso molecular:471.8Ref: TM-T11178L
1mg154,00€5mg370,00€1mL*10mM (DMSO)424,00€10mg583,00€25mg858,00€50mg1.170,00€100mg1.575,00€Anxiolytic/nonsedative agent-1
CAS:TCS 1205: Selective GABAA agonist, BzR affinity in bovine brain (Kis: 14-239 nM), α2 efficacy in vitro, anxioselective in vivo.Fórmula:C18H15N3O4Pureza:98.61%Cor e Forma:SolidPeso molecular:337.33Ref: TM-T23445
1mg60,00€2mg92,00€5mg109,00€10mg142,00€25mg314,00€50mg447,00€100mg622,00€500mg1.224,00€Almoxatone
CAS:Almoxatone, also known as MD 780236, is a monoamine oxidase (MAO) inhibitor.Fórmula:C18H19ClN2O3Cor e Forma:SolidPeso molecular:346.81SB-269970
CAS:SB-269970 is a antagonist of 5-HT7 receptor(pKi of 8.3).Fórmula:C18H28N2O3SPureza:98%Cor e Forma:SolidPeso molecular:352.49Levomepromazine Maleate
CAS:Levomepromazine Maleate: TCA and SNRI with antihistamine, antiadrenergic, and anticholinergic properties.Fórmula:C23H28N2O5SCor e Forma:SolidPeso molecular:444.546F-15599 tosylate
CAS:F-15599 tosylate is a selective 5-HT(1A) agonist.Fórmula:C26H29ClF2N4O4SCor e Forma:SolidPeso molecular:567.05Neostigmine hydroxide
CAS:Neostigmine hydroxide, a cholinesterase inhibitor, treats myasthenia gravis and reverses muscle relaxants; doesn't cross the blood-brain barrier.Fórmula:C12H20N2O3Cor e Forma:SolidPeso molecular:240.3Atropine Oxide Hydrochloride
CAS:Atropine Oxide, a derivative of anticholinergic Atropine, treats poisonings, slow heart rate, and reduces saliva during surgery.Fórmula:C17H24ClNO4Cor e Forma:SolidPeso molecular:341.83Tropatepine
CAS:Tropatepine: oral anticholinergic, treats extrapyramidal symptoms, anti-Parkinson's.Fórmula:C22H23NSCor e Forma:SolidPeso molecular:333.49(E/Z)-VU0029767
CAS:VU0029767 enhances M1 muscarinic receptor function, increasing acetylcholine potency and efficacy.Fórmula:C21H21N3O3Cor e Forma:SolidPeso molecular:363.41Dexetimide HCl
CAS:Dexetimide HCl is a muscarinic antagonist that has been used to treat neuroleptic-induced parkinsonism. Benzetimide is the (-)-enantimorph of dexetimide.Fórmula:C23H27ClN2O2Cor e Forma:SolidPeso molecular:398.93NW-1772 free base
CAS:NW-1772 free base is a monoamine oxidase B inhibitor.Fórmula:C18H16ClNO3Cor e Forma:SolidPeso molecular:329.78UH-AH 37
CAS:UH-AH 37 is a antagonist of human muscarinic acetylcholine receptor.Fórmula:C21H23Cl2N3O2Pureza:98%Cor e Forma:SolidPeso molecular:420.33Fonazine hydrochloride
CAS:Fonazine hydrochloride is a phenothiazine drug used for the treatment of migraine. It is a serotonin antagonist and histamine antagonist.Fórmula:C19H26ClN3O2S2Cor e Forma:SolidPeso molecular:428.01SC 53116 Hydrochloride
CAS:SC 53116 Hydrochloride is selective agonist of the newly identified serotonin 5-HT4 receptor subtype.Fórmula:C16H23Cl2N3O2Cor e Forma:SolidPeso molecular:360.28Way 100135
CAS:WAY-100135: research drug, phenylpiperazine, potent 5-HT1A antagonist, partial 5-HT1D agonist, minor 5-HT1B activity.Fórmula:C24H33N3O2Cor e Forma:SolidPeso molecular:395.54AQ-RA 721
CAS:AQ-RA 721 is a selective muscarinic antagonist with high affinity for M1- and M3-receptors. AQ-RA 721 may be used as a bronchodilator.Fórmula:C22H23N3O2Cor e Forma:SolidPeso molecular:361.44Glutaminyl Cyclase Inhibitor 2
CAS:Glutaminyl Cyclase Inhibitor 2 is a glutaminyl cyclase inhibitor (IC50: 1.23 μM).Fórmula:C19H20FN3Pureza:98%Cor e Forma:SolidPeso molecular:309.384-Chloro Trazodone hydrochloride
CAS:4-Chloro Trazodone HCl is a Trazodone isomer, an antidepressant for anxiety disorders.Fórmula:C19H23Cl2N5OCor e Forma:SolidPeso molecular:408.32BMT-046091
CAS:BMT-046091 is a potent and selective radioligand which inhibits adaptor-associated kinase 1 (AAK1).Fórmula:C18H21N3O2Cor e Forma:SolidPeso molecular:311.385-HT3 antagonist 3
CAS:5-HT3 antagonist 3 (Compound 15b) is a high-affinity 5-HT3 receptor antagonist. It binds to 5-HT3 receptors in rat brain cortical membranes (Ki: 0.25 nM).Fórmula:C20H21N3OPureza:99.9%Cor e Forma:SolidPeso molecular:319.4Ref: TM-T10162
500mgA consultar1mg109,00€2mg163,00€5mg243,00€10mg355,00€25mg532,00€50mg750,00€100mg1.009,00€Metitepine
CAS:Metitepine is a serotonin receptor antagonist in the CNS used as an antipsychotic.Fórmula:C20H24N2S2Cor e Forma:SolidPeso molecular:356.55Eptapirone fumarate
CAS:Eptapirone (F11440) is a strong 5HT1A agonist with high anxiolytic and antidepressant effects, more potent than buspirone and flesinoxan.Fórmula:C20H27N7O6Cor e Forma:SolidPeso molecular:461.479KL8604166
CAS:KL8604166 (UCB-11056) is a potential puzzle compound.UCB-11056 amplifies the formation of inducible cyclic AMP in rat brain tissue.Fórmula:C12H21N5O2Pureza:99.21%Cor e Forma:SolidPeso molecular:267.33Ref: TM-T29038
1mg264,00€1mL*10mM (DMSO)590,00€5mg650,00€10mg888,00€25mg1.369,00€50mg1.783,00€100mg2.250,00€SZV558
CAS:SZV558: Strong MAO-B inhibitor, non-mutagenic, hERG-safe, high-dose tolerant, neuroprotective in PD model.Fórmula:C13H16ClNPureza:98%Cor e Forma:SolidPeso molecular:221.73Pridinol
CAS:Pridinol is an antispasmodic and muscle relaxant.Fórmula:C20H25NOPureza:98%Cor e Forma:Crystals SolidPeso molecular:295.42HOCPCA
CAS:HOCPCA: potent, selective GHB site ligand; 27x higher affinity than GHB; crosses blood-brain barrier.Fórmula:C6H8O3Pureza:98%Cor e Forma:SolidPeso molecular:128.13LY 81067
CAS:LY 81067, a new anticonvulsant, prevents PTZ- and picrotoxin-induced seizures in mice via picrotoxin site interaction.Fórmula:C22H24N4OCor e Forma:SolidPeso molecular:360.45trans-4-Hydroxycrotonic acid
CAS:trans-4-Hydroxycrotonic acid (T-HCA) is a selective and competitive ligand for the γ-hydroxybutyric acid (GHB) binding site.Fórmula:C4H6O3Pureza:99.19%Cor e Forma:SolidPeso molecular:102.09CB-6673567
CAS:CB-6673567 is a selective inhibitor of adenylyl cyclase.Fórmula:C19H14N4O3Cor e Forma:SolidPeso molecular:346.34DAT 582
CAS:DAT 582 is a novel serotonin3 receptor antagonist. It is also an effective and long-lasting antiemetic agentFórmula:C22H28ClN5OPureza:98%Cor e Forma:SolidPeso molecular:413.95Ro 04-6790 dihydrochloride
CAS:Ro 04-6790 dihydrochloride is an effective and selective antagonist of the serotonin 5-HT6 receptor.Fórmula:C12H18Cl2N6O2SPureza:98%Cor e Forma:SolidPeso molecular:381.28Siltenzepine
CAS:Siltenzepine is an agent of anti-acid agent,and used in the treatment of peptic ulcers.Fórmula:C19H20ClN3O4Pureza:98%Cor e Forma:SolidPeso molecular:389.83LP 20 hydrochloride
CAS:ligand of the 5-HT7 receptorFórmula:C17H21ClN2OPureza:98%Cor e Forma:SolidPeso molecular:304.81Aβ42-IN-2
CAS:Aβ42-IN-2 is a γ-secretase modulator. Aβ42-IN-2 has an IC 50 of 6.5 nM for Αβ 42. Aβ42-IN-2 can be used for the Alzheimer's disease research[1].Fórmula:C24H26N6O2Pureza:98.09% - 99.87%Cor e Forma:SolidPeso molecular:430.5Ref: TM-T9641
1mg42,00€1mL*10mM (DMSO)93,00€5mg94,00€10mg134,00€25mg215,00€50mg304,00€100mg420,00€200mg582,00€GSK931145
CAS:GSK931145 is a positron emission tomography (PET) radioligand, it is suitable for quantifying glycine transporter (GlyT1) availability in the living brain.Fórmula:C23H30N2OPureza:98%Cor e Forma:SolidPeso molecular:350.5Vesamicol
CAS:Vesamicol is an experimental drug. It acting presynaptically by inhibiting acetylcholine uptake into synaptic vesicles and reducing its release.Fórmula:C17H25NOPureza:98%Cor e Forma:SolidPeso molecular:259.39Flutropium Bromide
CAS:Flutropium Bromide is a competitive antagonist of acetylcholine. It is used to treat asthma and chronic obstructive pulmonary.Fórmula:C24H29BrFNO3Pureza:98%Cor e Forma:SolidPeso molecular:478.39
