109 Results for "

presynaptic

" in MedChemExpress (MCE) Product Catalog:
Products (109)

109 Results for "presynaptic" in MCE Product Catalog:

Cat. No.: HY-W010178
CAS No.: 54947-74-9
4-Methyloctanoic acid is an endogenous branched-chain medium-chain fatty acid and a negative regulator of the cAMP/PKA signaling pathway. 4-Methyloctanoic acid exerts antiepileptic effects by inhibiting epileptiform discharges and terminating behavioral and electroencephalographic seizures. 4-Methyloctanoic acid has neuroprotective effects; its polar metabolites can cross the blood-brain barrier, repair presynaptic release defects, improve motor function and alleviate neuromuscular degeneration in ALS models. 4-Methyloctanoic acid regulates phosphatidylinositol metabolism, reduces PIP/PIP2 levels and increases inositol levels. 4-Methyloctanoic acid can be used in studies related to epilepsy and amyotrophic lateral sclerosis .
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Cat. No.: HY-107516
CAS No.: 201730-11-2
Purity:  95.03%
Synonyms: (S)-3,4-Dicarboxyphenylglycine
Target:  

mGluR

Research Areas:  

Neurological Disease

(S)-3,4-DCPG ((S)-3,4-Dicarboxyphenylglycine) is a potent and selective mGlu8a receptor agonist with an EC50 of 31 nM for human mGlu8a. (S)-3,4-DCPG inhibits Forskolin (HY-15371)-stimulated cAMP formation by activating mGlu8, and modulates presynaptic glutamatergic transmission and synaptic plasticity. (S)-3,4-DCPG can be used in research on inflammatory pain, neuropathic pain, autism spectrum disorder, and glutamatergic synaptic plasticity .
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Cat. No.: HY-10965
CAS No.: 136199-02-5
Purity:  99.68%
Synonyms: KW-3902
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease

Rolofylline (KW-3902) is a potent, selective adenosine A1 receptor antagonist that is under development for the treatment of patients with acute congestive heart failure and renal impairment. Rolofylline is metabolized primarily to the pharmacologically active M1-trans and M1-cis metabolites by cytochrome P450 (CYP450) . Rolofylline is alleviating the presynaptic dysfunction and restores neuronal activity as well as dendritic spine levels in vitro, is an interesting candidate to combat the hypometabolism and neuronal dysfunction associated with Tau-induced neurodegenerative diseases .
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Cat. No.: HY-16934
CAS No.: 1649450-12-3
Target:  

Cholinesterase (ChE)

Research Areas:  

Neurological Disease

ML352 is a noncompetitive inhibitor of the presynaptic choline transporter (CHT) with Ki values of 92 and 166 nM for HEK293 cells expressing human CHT and mouse forebrain synaptosomes, respectively .
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Cat. No.: HY-124501
CAS No.: 1814-64-8
Purity:  99.24%
Synonyms: p-NH2-PE-TFMPP
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

LY 165163 is a potent 5-HT presynaptic receptor agonist. LY 165163 significantly decreases 5-HTP accumulation and increases DOPA accumulation in the cortex and striatum .
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Cat. No.: HY-110146
CAS No.: 196928-50-4
Purity:  99.99%
Target:  

mGluR

Research Areas:  

Neurological Disease

XAP044 is a potent and selective antagonist of mGlu7. The metabotropic glutamate receptor subtype 7 (mGlu7) is an important presynaptic regulator of neurotransmission in the mammalian CNS. XAP044 demonstrates good brain exposure and wide spectrum anti-stress and antidepressant- and anxiolytic-like efficacy in rodent behavioral paradigms .
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Cat. No.: HY-B0495R
CAS No.: 84057-84-1
Synonyms: LTG (Standard); BW430C (Standard)
Research Areas:  

Neurological Disease

Lamotrigine (Standard) is the analytical standard of Lamotrigine. This product is intended for research and analytical applications. Lamotrigine (BW430C) is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine selectively blocks voltage-gated Na + channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine can be used for the research of epilepsy, focal seizure, et al .
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Cat. No.: HY-B0590B
CAS No.: 1026016-83-0
Synonyms: (+)-TBZ; (3R,11bR)-TBZ; (3R,11bR)-Tetrabenazine
Target:  

Monoamine Transporter

Research Areas:  

Cancer

(+)-Tetrabenazine ((+)-TBZ) is the enantiomer of Tetrabenazine (HY-B0590) and is also a Vesicular Monoamine Transporter 2 (VMAT2) inhibitor with a rat Ki of 4.61 nM. (+)-Tetrabenazine inhibits monoamine uptake into granular vesicles of presynaptic neurons. (+)-Tetrabenazine is 3 times more active than (-)-Tetrabenazine. (+)-Tetrabenazine can be used for the research of Huntington's disease and hyperkinetic movement disorders (including chorea) .
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Cat. No.: HY-W795507
CAS No.: 69906-85-0
Research Areas:  

Neurological Disease

Cyanopindolol is an β3-adrenoceptor antagonist. Cyanopindolol is a potent and selective antagonist at the presynaptic serotonin autoreceptor in the rat brain cortex. Cyanopindolol has binding affinity for 5-HT1A and 5-HT1B receptor (Ki: 2.1 and 3 nM respectively) .
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Cat. No.: HY-P3095
CAS No.: 65988-34-3
Target:  

Endogenous Metabolite

Research Areas:  

Neurological Disease

α-Latrotoxin, a potent neurotoxin from black widow spider venom, triggers synaptic vesicle exocytosis from presynaptic nerve terminals .
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Cat. No.: HY-100454
CAS No.: 104391-26-6
Purity:  99.65%
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

CGP 25454A is a selective presynaptic dopamine autoreceptor antagonist which induces the increase of dopamine and acetyl choline. CGP 25454A can be used for major depression research .
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Cat. No.: HY-P3089A
Target:  

Potassium Channel

Research Areas:  

Others

Dendrotoxin K TFA is a Kv1.1 channel blocker. Dendrotoxin K TFA determines glutamate release in CA3 neurons in a time-dependent manner through the control of the presynaptic spike waveform .
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Cat. No.: HY-B1423
CAS No.: 90-69-7
Synonyms: α-Lobeline; L-Lobeline
Lobeline (α-Lobeline) is a brain-penetrant nicotinic receptor agonist. Lobeline increases dopamine (DA) release by inhibiting DA uptake into synaptic vesicles, and altering presynaptic DA storage. Lobeline is effective in smoking cessation .
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Cat. No.: HY-P3140A
Target:  

α-synuclein

Research Areas:  

Neurological Disease

α-Synuclein (61-75) TFA is the 61-75 fragment of α-Synuclein. α-Synuclein is an abundant neuronal protein that is highly enriched in presynaptic nerve terminals. α-Synuclein is a potential biomarker for Parkinson's disease (PD) .
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Cat. No.: HY-117575A
CAS No.: 149055-79-8
Purity:  98.32%
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

WAY-100135 dihydrochloride is a selective antagonist at presynaptic and postsynaptic 5-HT1A receptor, with an IC50 of 34 nM at the rat hippocampal 5-HT1A receptor. WAY-100135 dihydrochloride has potential antipsychotic properties .
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Cat. No.: HY-B0495S4
CAS No.: 1188265-38-4
Synonyms: LTG-13C3; BW430C-13C3
Lamotrigine- 13C3 is the 13C-labeled Lamotrigine. Lamotrigine (BW430C) is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine selectively blocks voltage-gated Na+ channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine can be used for the research of epilepsy, focal seizure, et al .
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Cat. No.: HY-119468
CAS No.: 32359-34-5
Purity:  99.34%
Target:  

Dopamine Transporter

Research Areas:  

Neurological Disease

Medifoxamine is an orally active monoamine reuptake inhibitor and antidepressant. Medifoxamine preferentially inhibits presynaptic dopamine reuptake. Medifoxamine acts as an intraocular pressure-lowering agent to reduce intraocular pressure, and also functions as a miotic agent to decrease pupil diameter. Medifoxamine exhibits characteristic properties of antidepressant compounds, including preventing hypothermia induced by Reserpine (HY-N0480) or Apomorphine (HY-12723), potentiating the toxic effects of Yohimbine (HY-N0127) in mice, and reducing immobility behavior in mice and rats in the "behavioral despair" model. Medifoxamine has no anticholinergic activity. Medifoxamine can be used in research related to depression .
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Cat. No.: HY-141554
CAS No.: 3466-75-9
Purity:  99.23%
Synonyms: DHTBZ
Target:  

Monoamine Transporter

Research Areas:  

Neurological Disease

Dihydrotetrabenazine (DHTBZ) is the active metabolite of Tetrabenazine (HY-B0590). Dihydrotetrabenazine is the inhibitor for human vesicular monoamine transporter 2 (VMAT2), that reduces monoamine content in presynaptic neurons, and can be used in movement disorder research .
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Cat. No.: HY-P3140
CAS No.: 440645-08-9
Target:  

α-synuclein

Research Areas:  

Neurological Disease

α-Synuclein (61-75) is the 61-75 fragment of α-Synuclein. α-Synuclein is an abundant neuronal protein that is highly enriched in presynaptic nerve terminals. α-Synuclein is a potential biomarker for Parkinson's disease (PD) .
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Cat. No.: HY-119615
CAS No.: 50335-55-2
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease Endocrinology

Mezilamine is a potent antidopaminergic agent. Mezilamine induces a concentration dependent increase in the electrically stimulated overflow of 3H-noradrenaline from rat cortical slices, without affecting the basal overflow. Mezilamine acts as a presynaptic α-adrenoceptor antagonist and a postsynaptic α-adrenoceptor agonist .
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