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Receptor 5-HT

Receptor 5-HT

Los receptores 5-HT, también conocidos como receptores de serotonina, son un grupo de receptores acoplados a proteínas G (GPCR) que median los efectos de la serotonina, un neurotransmisor involucrado en la regulación del estado de ánimo, la ansiedad, el sueño, el apetito y otros procesos fisiológicos. Estos receptores se dividen en varios subtipos, cada uno con funciones y propiedades farmacológicas distintas. Los moduladores de los receptores 5-HT se estudian ampliamente por su papel en el tratamiento de la depresión, los trastornos de ansiedad y otras afecciones neuropsiquiátricas. En CymitQuimica, ofrecemos una gama de moduladores de receptores 5-HT de alta calidad para apoyar su investigación en neurofarmacología, trastornos del estado de ánimo y señalización GPCR.

Se han encontrado 993 productos de "Receptor 5-HT"

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  • ASP-2205

    CAS:
    <p>ASP-2205, a 5-HT2C receptor agonist (human 5-HT2C receptor, EC50=0.85 nM; rat 5-HT2C receptor, EC50=2.5 nM), enhances the urethral closure reflex mediated by the genital nerve, thereby preventing urinary incontinence.</p>
    Fórmula:C19H28N2O
    Forma y color:Solid
    Peso molecular:300.44
  • Remlifanserin

    CAS:
    Remlifanserin is a potent inverse agonist of the serotonin receptor (5-HT2A).
    Fórmula:C24H29F2N3O2
    Forma y color:Solid
    Peso molecular:429.50
  • YM-31636 free base

    CAS:
    <p>YM-31636 (free base) is an orally active, potent, and selective agonist of the 5-HT3 receptor with a pKi value of 9.67. This compound induces contraction in isolated guinea pig distal colon and provokes tachycardia in isolated guinea pig right atrium, demonstrating a relative intrinsic activity of about 0.23. YM-31636 (free base) holds potential for research in constipation management.</p>
    Fórmula:C14H11N3S
    Forma y color:Solid
    Peso molecular:253.32
  • Tiprenolol hydrochloride

    CAS:
    Tiprenolol hydrochloride is a β-adrenoceptor (β-adrenoceptor) antagonist. This compound is effective in eliminating ventricular arrhythmias in dogs caused by intravenous administration of adrenaline, following inhalation of halothane.
    Fórmula:C13H22ClNO2S
    Forma y color:Solid
    Peso molecular:291.84
  • 5-HT6R/MAO-B modulator 1


    5-HT6R/MAO-B modulator 1 blocks 5-HT6R and permanently inhibits MAO-B, protects glial cells, and reverses memory loss.
    Fórmula:C33H38N4O3S
    Forma y color:Solid
    Peso molecular:570.74
  • PDE4B/7A-IN-1

    CAS:
    5-HT1A antagonist; Ki=8nM, Kb=0.04nM. PDE4B IC50=80.4μM; PDE7A IC50=151.3μM. Good biofilm penetration, stable, anticognitive, antidepressant.
    Fórmula:C25H35N3O3
    Forma y color:Solid
    Peso molecular:425.56
  • AAZ-A 154 hydrochloride

    CAS:
    <p>AAZ-A 154 hydrochloride is a selective, competitive, non-hallucinogenic antagonist of 5-HT2AR. It promotes neuronal growth in rodents and results in enduring beneficial behavioral effects.</p>
    Fórmula:C14H21ClN2O
    Forma y color:Solid
    Peso molecular:268.78
  • SB 243213 dihydrochloride

    CAS:
    SB 243213 dihydrochloride 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 for
    Fórmula:C22H21Cl2F3N4O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:501.33
  • LK-732

    CAS:
    LK-732 is a thrombin inhibitor with antithrombotic activity. It exhibits dose-dependent inhibition in models of hypercoagulability, with an IC50 value of 1.3 mg/kg. LK-732 is used in cardiovascular and cerebrovascular research.
    Fórmula:C25H29N5O3S
    Forma y color:Solid
    Peso molecular:479.59
  • Befiradol hydrochloride

    CAS:
    <p>Befiradol HCl (NLX-112) is a selective 5-HT1A receptor agonist with anxiolytic effects and prevents ATXN3 aggregation.</p>
    Fórmula:C20H23Cl2F2N3O
    Pureza:99.1%
    Forma y color:Solid
    Peso molecular:430.32
  • (-)-5-HT2C agonist-3

    CAS:
    <p>Compound (−)-19, also known as (-)-5-HT2C agonist-3, is a selective 5-HT2C agonist exhibiting a preference for Gq signaling. It demonstrates efficiency with EC50 values for 5-HT2 receptor subtypes as follows: 5-HT2C at 103 nM, 5-HT2B at 570 nM, and 5-HT2A at 72 nM. This compound is utilized in research on antipsychotics.</p>
    Fórmula:C19H23ClFNO2
    Forma y color:Solid
    Peso molecular:351.84
  • (S)-Praziquantel

    CAS:
    (S)-Praziquantel is the inactive isomer of R-praziquantel.
    Fórmula:C19H24N2O2
    Forma y color:Solid
    Peso molecular:312.406
  • CB2R/5-HT1AR agonist 1

    CAS:
    <p>Compound 2o, also known as CB2R/5-HT1AR agonist 1, serves as a partial orally active agonist for the CB2 receptor (EC50 = 479.6 nM) and a full agonist for the 5-HT1A receptor (EC50 = 2.7 μM). This compound demonstrates both anti-anxiety and anti-depressive effects and has favorable pharmacokinetic properties [1].</p>
    Fórmula:C24H33NO3
    Forma y color:Solid
    Peso molecular:383.52
  • SEP-363856 mesylate

    CAS:
    <p>SEP-363856 (SEP-856) mesylate is an orally active compound that acts as an agonist for both TAAR1 and 5-HT1A receptors. This compound exhibits antipsychotic activity in the central nervous system and has potential for the study of schizophrenia.</p>
    Fórmula:C10H17NO4S2
    Forma y color:Solid
    Peso molecular:279.38
  • 5-HT1A antagonist 1


    <p>Compound 6f is a potent, selective 5-HT1A receptor blocker (Ki: 35 nM), useful in CNS disorder research.</p>
    Fórmula:C23H29ClN6O2
    Forma y color:Solid
    Peso molecular:456.97
  • AChE-IN-5


    AChE-IN-5: oral, crosses blood-brain barrier, targets AChE/5-HT1A/SERT, potent with 2.29 nM IC50.
    Fórmula:C38H45N5O
    Forma y color:Solid
    Peso molecular:587.8
  • Mesulergine hydrochloride

    CAS:
    5-HT2A and 2C receptor antagonist
    Fórmula:C18H27ClN4O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:398.95
  • Sulamserod hydrochloride

    CAS:
    <p>Sulamserod hydrochloride is a 5-HT4 receptor antagonist. It is utilized in research related to gastrointestinal disorders.</p>
    Fórmula:C19H29Cl2N3O5S
    Forma y color:Solid
    Peso molecular:482.42
  • Flucopride

    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.
    Fórmula:C22H33FN2O2
    Forma y color:Solid
    Peso molecular:376.51
  • R-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.
    Fórmula:C17H23N3O2
    Forma y color:Solid
    Peso molecular:301.38