133 Results for "

postsynaptic

" in MedChemExpress (MCE) Product Catalog:
Products (133)

133 Results for "postsynaptic" in MCE Product Catalog:

Cat. No.: HY-129517
CAS No.: 773109-55-0
Target:  

iGluR

Research Areas:  

Neurological Disease

UBP714 exhibts agonistic activity for recombinant GluN1/GluN2 receptor by binding to the positive allosteric site (PAM) of NMDARs. UBP714 enhances NMDAR-mediated field excitatory postsynaptic potentials (f-EPSPs) in Xenopus oocytes .
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Cat. No.: HY-B0718
CAS No.: 76-38-0
Synonyms: DA-759
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Methoxyflurane disrupts neuronal transmission by interfering with the release and re-uptake of neurotransmitters at post-synaptic terminals, or altering ionic conductance following receptor activation . Methoxyflurane is an analgesic agent that provides rapid short-term analgesia. Methoxyflurane may shows a effective non-opioid treatment option for trauma pain .
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Cat. No.: HY-105328
CAS No.: 153607-44-4
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

S-14489 is an orally active selective postsynaptic 5-HT1A receptor antagonist with a pKi of 9.2. S-14489 can act as a 5-HT1A autoreceptor agonist and inhibit striatal 5-hydroxytryptophan accumulation. S-14489 can be used for the research of neurological disease .
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Cat. No.: HY-164703
CAS No.: 1469777-40-9
Lumateperone metabolite 1 (Formula T) is a metabolite of Lumateperone (HY-17637) . Lumateperone (ITI-007) is an orally active 5-HT2A receptor antagonist (Ki = 0.54 nM), a partial agonist of presynaptic D2 receptors and an antagonist of postsynaptic D2 receptors (Ki = 32 nM), and a dopamine D1 receptor modulator
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Cat. No.: HY-106781
CAS No.: 111073-34-8
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

OPC-4392 is a orally active presynaptic dopamine autoreceptor agonist and postsynaptic D2 receptor antagonist. OPC 4392 reverses the Reserpine (HY-N0480)-induced dopamine accumulation, inhibits Apomorphine (HY-12723)-induced stereotypic and climbing behaviors in mouse models. OPC-4392 can be used as antipsychotic agent .
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Cat. No.: HY-14785A
CAS No.: 2436760-81-3
Purity:  99.93%
Synonyms: NLX-112 hydrochloride; F 13640 hydrochloride
Target:  

5-HT Receptor

Befiradol (NLX-112) hydrochloride is a highly selective 5-HT1A receptor agonist that acts on both presynaptic and postsynaptic sites. Befiradol hydrochloride attenuates sedative agent-induced respiratory depression in neonatal and adult rats. Befiradol reduces the duration of sedative agent-induced analgesia and sedation in adult rats. Befiradol hydrochloride can be used in studies related to opioid-induced respiratory depression .
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Cat. No.: HY-17637S2
CAS No.: 2102683-55-4
Synonyms: ITI-007-d4
Lumateperone-d4 (ITI-007-d4) is deuterium labeled Lumateperone. Lumateperone (ITI-007) is an orally active 5-HT2A receptor antagonist (Ki = 0.54 nM), a partial agonist of presynaptic D2 receptors and an antagonist of postsynaptic D2 receptors (Ki = 32 nM), and a dopamine D1 receptor modulator. Lumateperone has anticancer activity and can also be used for the study of schizophrenia and bipolar depression .
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Cat. No.: HY-101599
CAS No.: 58013-09-5
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

IP-66 is a potent postsynaptic alpha-receptor antagonist. IP-66 can be used for the research of cardiovascular disease, such as hypertension .
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Cat. No.: HY-B0098S
CAS No.: 1126848-44-9
Synonyms: UK 33274-d8
Doxazosin-d8 is a deuterium labeled Doxazosin (UK 33274). Doxazosin is a quinazoline-derivative that selectively antagonizes postsynaptic α1 adrenergic receptors .
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Cat. No.: HY-145454A
CAS No.: 85966-89-8
Synonyms: (-)-3-PPP
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Preclamol is a dopamine (DA) agonist with autoreceptor as well as postsynaptic receptor stimulatory properties. Preclamol inhibits the locomotor activity of mice and rats in low doses .
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Cat. No.: HY-B1789
CAS No.: 80880-90-6
Target:  

mAChR

Research Areas:  

Neurological Disease

Telenzepine is an antimuscarinic agent with Kis of 0.94 nM (M1 mAChR) and 17.8 nM (M2 mAChR) binding to muscarinic receptors. Telenzepine effectively blocks synaptic transmission promoted by muscarinic or M1 receptor agonists. Thus, Telenzepine can reduce the amplitude of extracellular slow excitatory postsynaptic potentials (EC50=38 nM) and slow inhibitory postsynaptic potentials (EC50=253 nM) .
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Cat. No.: HY-P2590
CAS No.: 113611-68-0
Target:  

Inhibitory Antibodies

Research Areas:  

Others

Tnrnflrfamide is a neuropeptide that modulates the receptor muscles of the lobster abdominal stretch receptors and their exoskeletal muscle homologues. Tnrnflrfamide enhances motor performance, including the amplitude of excitatory postsynaptic potentials and the development of nerve-evoked tension .
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Cat. No.: HY-174146
CAS No.: 2410053-15-3
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

5-HT1A agonist 1 (Compound Ex.37) is a highly selective 5-HT1a receptor agonist (EC50=0.18 nM). 5-HT1A agonist 1 mimicks serotonin binding to the receptor, promotes postsynaptic membrane hyperpolarization, inhibits neuronal hyperexcitability, and reduces the release of anxiety-related neurotransmitters. 5-HT1A agonist 1 is promising for research of neuropsychiatric diseases .
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Cat. No.: HY-131885
CAS No.: 2417096-44-5
Purity:  82.94%
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

RuBi-Glutamate hexafluorophosphate sodium is a neuronal activator. RuBi-Glutamate hexafluorophosphate sodium photocleaves to release glutamate upon one- or two-photon excitation, activating glutamate receptors in cortical pyramidal neurons. RuBi-Glutamate hexafluorophosphate sodium reduces peak amplitude of evoked GABAergic inhibitory postsynaptic currents in its caged form. RuBi-Glutamate hexafluorophosphate sodium can be used for the research of Huntington's disease .
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Cat. No.: HY-145475
CAS No.: 887405-21-2
Synonyms: NEA
Nervonoyl ethanolamide (NEA) is an endogenous cannabinoid that can act as a presynaptic and postsynaptic neuromodulator. Nervonoyl ethanolamide can also be used in the research of inflammation .
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Cat. No.: HY-108698A
CAS No.: 89874-80-6
Purity:  ≥98.0%
Synonyms: (+)-3-PPP hydrochloride
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

(R)-Preclamol hydrochloride ((+)-3-PPP hydrochloride) is the R-enantiomer of Preclamol hydrochloride. (R)-Preclamol hydrochloride is a DA agonist with autoreceptor as well as postsynaptic receptor stimulatory properties .
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Cat. No.: HY-B1396R
CAS No.: 82752-99-6
Synonyms: BMY-13754 (Standard); MJ-13754-1 (Standard)
Nefazodone (hydrochloride) (Standard) is the analytical standard of Nefazodone (hydrochloride). This product is intended for research and analytical applications. Nefazodone hydrochloride (BMY-13754) is a potent and selective 5HT2A (Ki=5.8 nM) antagonist with moderate inhibition of 5-HT and noradrenaline uptake (IC50 of 290 and 300 nM, respectively). Nefazodone hydrochloride is a phenylpiperazine antidepressant with less alpha-adrenergic blocking activity .
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Cat. No.: HY-124910
CAS No.: 114667-74-2
BU-E-75 is a guanidine-type H2 receptor agonist that exhibits antagonism at postsynaptic α-adrenoceptors, which can relax the noradrenaline-precontracted vessels .
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Cat. No.: HY-A0171A
CAS No.: 10085-81-1
Synonyms: Ba-30803
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Benzoctamine hydrochloride (Ba-30803) is a psychoactive agent with anti-anxiety effect. Benzoctamine hydrochloride blocks the central postsynaptic serotonin receptors and decreases 5-HT turnover in the brain .
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Cat. No.: HY-100785A
CAS No.: 2935387-13-4
Synonyms: γDGG acetate; γ-D-Glutamylglycine acetate
Target:  

iGluR

Research Areas:  

Neurological Disease

gamma-DGG acetate (γDGG acetate) is a competitive AMPA receptor blocker. gamma-DGG acetate is also a reversible Excitatory post-synaptic potentials (e.p.s.p.s) antagonist .
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