Neuroscience
Les inhibiteurs en neurosciences sont des composés conçus pour moduler l'activité de protéines, d'enzymes ou de récepteurs spécifiques au sein du système nerveux. Ces inhibiteurs sont cruciaux pour étudier les mécanismes moléculaires sous-jacents au fonctionnement neuronal, à la transmission synaptique et aux maladies neurodégénératives. En ciblant les récepteurs des neurotransmetteurs, les canaux ioniques et les voies de signalisation, les inhibiteurs en neurosciences facilitent l'exploration du fonctionnement cérébral et le développement de stratégies thérapeutiques pour des troubles neurologiques tels que la maladie d'Alzheimer, de Parkinson et l'épilepsie. Chez CymitQuimica, nous offrons une gamme complète d'inhibiteurs en neurosciences de haute qualité pour soutenir vos recherches en neurobiologie, neuropharmacologie et sciences cognitives.
Sous-catégories appartenant à la catégorie "Neuroscience"
- récepteur 5-HT(1.025 produits)
- ACK(1 produits)
- AChR(645 produits)
- ATP Citrate Lyase(17 produits)
- Récepteur adrénergique(3.018 produits)
- BACE(37 produits)
- Bêta-amyloïde(228 produits)
- CaMK(73 produits)
- COX(600 produits)
- Récepteur de la dopamine(445 produits)
- Récepteur GABA(372 produits)
- Gamma-sécrétase(61 produits)
- GluR(265 produits)
- GlyT(26 produits)
- Récepteur de l'histamine(385 produits)
- LRRK2(43 produits)
- Récepteur de la mélatonine(26 produits)
- NMDAR(10 produits)
- Récepteur OX(41 produits)
- Récepteur opioïde(327 produits)
Affichez 12 plus de sous-catégories
5548 produits trouvés pour "Neuroscience"
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YM-202074
CAS :YM-202074: Selective mGlu1 antagonist, binds allosteric site (Ki=4.8 nM), inhibits mGlu1 (IC50=8.6 nM).Formule :C22H30N4O2SCouleur et forme :SolidMasse moléculaire :414.56HDAC6-IN-9
CAS :HDAC6-IN-9 is a γ-secretase modulator that can significantly reduce the level of Aβ42 in mouse brain and can be used to study neurological diseases.Formule :C19H16N2O3Degré de pureté :98.84%Couleur et forme :SolidMasse moléculaire :320.34(R)-(-)-Pirlindole mesylate
CAS :(R)-(–)-Pirlindole acts as a monoamine oxidase A (MAO-A) inhibitor with an IC50 value of 0.43 µM, exhibiting selectivity for MAO-A compared to MAO-B. When administered at 50 mg/kg, it reduces immobility time in the forced swim test in mice and, at 25 mg/kg, inhibits reserpine-induced palpebral ptosis in mice.Formule :C16H22N2O3SCouleur et forme :SolidMasse moléculaire :322.42Aβ42-IN-1
CAS :Aβ42-IN-1, compound 1v, is a novel, potent and orally active γ-secretase modulator (GSM).Formule :C29H27ClN4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :499(9R)-RO7185876
CAS :(9R)-RO7185876 (Compound example 16) is a γ-secretase inhibitor. It reduces the secretion of Αβ42. This compound can be employed in the research of Alzheimer's disease, cerebral amyloid angiopathy, hereditary cerebral hemorrhage with amyloidosis, multi-infarct dementia, senile dementia, or Down syndrome.Formule :C25H28F3N7Couleur et forme :SolidMasse moléculaire :483.53225C-NBF hydrochloride
CAS :25C-NBF hydrochloride is an agonist of 5-HT receptors, specifically activating 5-HT2A and 5-HT2C receptors, with an EC50 of approximately 0.3 μM.Formule :C17H20Cl2FNO2Masse moléculaire :360.251BPN-15606 besylate
BPN-15606 besylate is a potent oral γ-secretase regulator reducing Aβ42 and Aβ40 with good pharmacokinetics. IC50: 7 nM (Aβ42), 17 nM (Aβ40).Formule :C29H29FN6O4SCouleur et forme :SolidMasse moléculaire :576.64DSP-1053 benzenesulfonate
CAS :DSP-1053: Benzylpiperidine-based, potent SERT inhibitor (Ki=1.02nM), partial 5-HT1A receptor agonist (Ki=5.05nM), antidepressant.Formule :C32H38BrNO7SCouleur et forme :SolidMasse moléculaire :660.62Rocavorexant
CAS :Rocavorexant is an antagonist of the orexin-1 receptor (orexin-1 receptor), exhibiting a pIC50 value of 9.1 for human OX1 and a pIC50 of 6.0 for human OX2.Formule :C18H19F3N8OCouleur et forme :SolidMasse moléculaire :420.392SGE-516
CAS :SGE516: neuroactive steroid, enhances GABAA, lowers neuronal activity, protects from seizures.Formule :C23H35N3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :385.54(R)-Norfluoxetine
CAS :(R)-Norfluoxetine is the (R)-enantiomer of Norfluoxetine. It functions as a potent serotonin reuptake inhibitor, with a Ki value of 13 nM. This compound is utilized in the research of depression.Formule :C16H16F3NOCouleur et forme :SolidMasse moléculaire :295.299VU6005806
CAS :VU6005806 is a potent M4 PAM with EC50s: 94 nM (human), 28 nM (rat), 87 nM (dog), 68 nM (cyno); studied for neuropsychiatric disorders.Formule :C17H16F3N7O2SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :439.41Illudinine
CAS :Illudinine is a sesquiterpene alkaloid that acts as an inhibitor of monoamine oxidase B (MAO-B), with an IC50 value of 18.3 μM. It is applicable in research focused on neurological disorders.Formule :C16H17NO3Couleur et forme :SolidMasse moléculaire :271.31BACE1-IN-2
CAS :BACE1-IN-2 is a BACE1 inhibitor (IC50: 22 nM).Formule :C19H15F4N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :421.35Nedemelteon
CAS :Nedemelteon is an agonist of the melatonin receptor (melatonin receptor).Formule :C15H18N2O2Couleur et forme :SolidMasse moléculaire :258.32SB 243213 hydrochloride
CAS :SB 243213 hydrochloride is an orally active, selective and high-affinity antagonist of 5-hydroxytryptamine (5-HT)2C receptor(pKi of 9.37 and a pKb of 9.8).ItFormule :C22H20ClF3N4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :464.87BGT1-IN-1
CAS :BGT1-IN-1 (compound 9) is an effective inhibitor of BGT1, demonstrating IC50 values of 13.9 µM for hBGT1 and 58.3 µM for GAT3. It exhibits no cytotoxic effects and possesses neuroprotective activity.Formule :C6H9NO2Couleur et forme :SolidMasse moléculaire :127.14(E)-CHBO4
CAS :(E)-CHBO4 is an MAO-B inhibitor with an IC50 value of 0.023 μM, making it a potential candidate for research into Parkinson's disease treatment.Formule :C15H10BrFOCouleur et forme :SolidMasse moléculaire :305.142Aβ42 agonist-1
CAS :Aβ42 agonist-1 is a small molecule compound with anti-cancer activity and NF-κB inhibitory properties, inducing Aβ42 aggregation.Formule :C15H11NO2Degré de pureté :99.77%Couleur et forme :SolidMasse moléculaire :237.25MAO-B-IN-28
CAS :MAO-B-IN-28 (compound 10e) is a potent hMAO-B inhibitor with an IC50 value of 1.9±0.5 nM, potentially serving as a candidate molecule for neurodegenerative disease research.Formule :C19H10F3NO4SMasse moléculaire :405.35CGS-9895
CAS :CGS-9895 is a GABA antagonist that operates by interacting with the benzodiazepine binding site on GABA receptors containing the γ subunit (ag).Formule :C17H13N3O2Couleur et forme :SolidMasse moléculaire :291.304OX2R agonist 1
CAS :OX2R agonist 1 is an OX2R activator with an EC50 of less than 100 nM. It is utilized in research related to narcolepsy and cataplexy.Formule :C21H28F2N2O5SCouleur et forme :SolidMasse moléculaire :458.52AM-6494
CAS :AM-6494 is a potent and orally active BACE1 inhibitor (IC50: 0.4 nM) with in vivo selectivity over BACE2 (IC50: 18.6 nM).Formule :C22H21F2N5O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :473.5CTW0404
CAS :CTW0404 is an effective positive allosteric modulator (PAM) of the 5-HT receptor, with promising implications for research into neuropsychiatric disorders.Formule :C21H33N3O2Masse moléculaire :359.51TP003
CAS :TP003 is a novel non-selective GABAA receptor benzodiazepine site agonist with affinity for α1β2gam2, α2β3gam2, α3β3gam2, α5β2gam2, EC50 of 20.3, 10.6, 3.24, 5.
Formule :C23H16F3N3ODegré de pureté :99.17%Couleur et forme :SolidMasse moléculaire :407.39Flucopride
CAS :Flucopride (Compound 4a) acts as an acetylcholinesterase inhibitor (AChE) with an IC50 value of 24 nM and serves as a partial agonist for the human 5-HT4 receptor (5-HT4R) with a Ki of 9.6 nM for (h)5-HT4R. It promotes non-amyloidogenic processing of APP in COS-7 cells transiently expressing (h)5-HT4R with an EC50 of 23.0 nM. Flucopride is also likely to exhibit significant gastrointestinal tract (GIT) penetration and blood-brain barrier (BBB) permeability, as determined in PAMPA experiments.Formule :C22H33FN2O2Couleur et forme :SolidMasse moléculaire :376.51R-137696
CAS :R-137696 is an orally active 5-HT1A receptor agonist that facilitates the relaxation of the proximal stomach. It is utilized in research related to functional dyspepsia.Formule :C17H23N3O2Couleur et forme :SolidMasse moléculaire :301.385-HT2A receptor agonist-8
CAS :5-HT2A receptor agonist-8 (compound 8) is a potent 5-HT2A receptor agonist with an EC50 of 0.6784 nM. It is suitable for research related to depression and bipolar disorder.Formule :C22H27N3OCouleur et forme :SolidMasse moléculaire :349.47BMS-986163
CAS :BMS-986163, GluN2B negative allosteric modulator prodrug, converts to BMS-986169 (Ki=4 nM), antidepressant-like activity.Formule :C23H28FN2O5PDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :462.45LY 541850
CAS :LY541850 is a selective orthosteric mGlu2 agonist and mGlu3 antagonist with IC50 values of 0.161 μM and 0.038 μM, respectively.LY 541850 is claimed from humanFormule :C9H13NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :199.2p-F-HHSiD hydrochloride
CAS :p-F-HHSiD (p-Fluorohexahydrosiladifenidol) hydrochloride is a selective M3mAChR antagonist. It is capable of inhibiting acetylcholine-mediated vasodilation in human umbilical vein endothelial cells (HUVEC).Formule :C20H33ClFNOSiMasse moléculaire :386.019LRRK2-IN-12
CAS :LRRK2-IN-12 (compound 1) is a potent inhibitor of LRRK2 (G20195) with an IC 50 of 0.45 nM, LRRK2 WT with an IC 50 of 1.1 nM, and LRRK2 WT ADP-Glo with an IC 50 of 0.46 nM. This compound is utilized in research related to Alzheimer's Disease [1].Formule :C18H17ClN8O2Couleur et forme :SolidMasse moléculaire :412.83QP5020
CAS :QP5020 is a QPCTL inhibitor with an IC50 value of 15 nM, demonstrating antitumor efficacy.Formule :C20H19FN6Masse moléculaire :362.40Fletazepam
CAS :Fletazepam, a benzodiazepine derivative, exhibits sedative, anti-anxiety, and muscle-relaxant properties. It is utilized in neurological research.Formule :C17H13ClF4N2Couleur et forme :SolidMasse moléculaire :356.74LY3020371 hydrochloride
CAS :LY3020371 HCl: potent mGlu2/3 antagonist, antidepressant-like; Ki: 5.3/2.5 nM, IC50: 16.2 nM for cAMP inhibition.Formule :C15H16ClF2NO5SCouleur et forme :SolidMasse moléculaire :395.81BRD0418
CAS :BRD0418 acts as an upregulator of TRIB1 expression by leading to reprogramming of hepatic lipoprotein metabolism from adipogenesis to clearance it.Formule :C29H32N2O5Degré de pureté :99.57%Couleur et forme :SolidMasse moléculaire :488.57BACE1-IN-4
CAS :BACE1-IN-4 is a potent and highly selective BACE1 inhibitor (IC50: 3.8 nM; Ki: 1.9 nM), more selective at BACE1 over BACE2.Formule :C21H23F2N5O4S2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :511.57Beloxepin
CAS :Beloxepin is an oral dual selective inhibitor of serotonin and norepinephrine uptake.Formule :C19H21NO2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :295.38LY593093
CAS :LY593093 is a selective partial orthosteric agonist of M1 muscarinic acetylcholine receptor.Formule :C32H30FN3O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :507.6β-CCM
CAS :β-CCM is a benzodiazepine receptor inverse agonist with anxiogenic and convulsant effects. It enhances emotional reactivity and reduces interference sensitivity in spatial working memory tasks. β-CCM is applicable in research related to anxiety disorders.Formule :C13H10N2O2Couleur et forme :SolidMasse moléculaire :226.231AChE/BChE-IN-10
CAS :AChE/BChE-IN-10 inhibits AChE/BChE (IC50: 0.176/0.47 μM), crosses the blood-brain barrier, and prevents Aβ-aggregation.
Formule :C26H30N2O2Degré de pureté :99.55% - 99.88%Couleur et forme :SoildMasse moléculaire :402.53BMS 299897
CAS :BMS 299897, a sulfonamide γ-secretase inhibitor, inhibits Aβ production with an IC50 of 7 nM in HEK293 cells overexpressing APP.Formule :C24H21ClF3NO4SDegré de pureté :99.82%Couleur et forme :SolidMasse moléculaire :511.94Umibecestat
CAS :Umibecestat inhibits human and mouse BACE-1 (IC50: 11 nM & 10 nM), potentially for Alzheimer's research.Formule :C19H15ClF7N5O2Degré de pureté :99.88%Couleur et forme :SolidMasse moléculaire :513.8Ref: TM-T13253
1mg163,00€5mg334,00€10mg485,00€25mg807,00€50mg1.099,00€100mg1.485,00€1mL*10mM (DMSO)376,00€AChE-IN-26
CAS :AChE-IN-26 (compound 4a) is an AChE (acetylcholinesterase) inhibitor (IC50: 0.42 μM).
Formule :C21H21BrN2O3Degré de pureté :99.24% - 99.85%Couleur et forme :SoildMasse moléculaire :429.31NB-360
CAS :NB-360: potent, brain-penetrant BACE1/2 inhibitor; IC50s: 5-6 nM; high selectivity vs pepsin, cathepsin E/D.Formule :C21H19F4N5O2Degré de pureté :99.72%Couleur et forme :SolidMasse moléculaire :449.4Ref: TM-T12188
1mg104,00€5mg215,00€10mg318,00€25mg510,00€50mg692,00€100mg888,00€500mg1.783,00€1mL*10mM (DMSO)235,00€LY2979165
CAS :LY2979165 (mGlu2 agonist) is an orthosteric agonist of mGluR2 and can be used in studies about serving as an anti-depressant.Formule :C13H22N6O6SDegré de pureté :98.41%Couleur et forme :SolidMasse moléculaire :390.42Iclepertin
CAS :Iclepertin (BI-425809) is a GlyT1 inhibitor.Iclepertin is used for the treatment of Alzheimer;s disease and other CNS disorders.Formule :C20H18F6N2O5SDegré de pureté :98.89% - 98.93%Couleur et forme :SolidMasse moléculaire :512.42Ref: TM-T37089
1mg90,00€2mg114,00€5mg160,00€10mg212,00€25mg349,00€50mg522,00€100mg783,00€200mg1.054,00€1mL*10mM (DMSO)173,00€SB-224289 hydrochloride
CAS :SB-224289 hydrochloride (SB-224289A) is a selective antagonist of 5-HT1B receptor, with anxiolytic effect.Formule :C32H33ClN4O3Degré de pureté :98.99% - 99.96%Couleur et forme :SolidMasse moléculaire :557.084-Amino-6-hydroxypyrazolo[3,4-d]pyrimidine
CAS :Formule :C5H5N5ODegré de pureté :>93.0%(HPLC)Couleur et forme :White to Light yellow to Light orange powder to crystallineMasse moléculaire :151.13Xanthocillin X permethyl ether
CAS :Xanthocillin X permethyl ether, a natural product extracted from fungal sources, exhibits Aβ-42 lowering activity.Formule :C20H16N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :316.35
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