39 Results for "

Ganglionic blocker

" in MedChemExpress (MCE) Product Catalog:
Products (39)

39 Results for "Ganglionic blocker" in MCE Product Catalog:

7
7 Publications Verification
Art. -Nr.: HY-B1395
CAS. Nr.: 826-39-1
Mecamylamine hydrochloride is an orally active, nonselective, noncompetitive nAChR antagonist. Mecamylamine hydrochloride is also a ganglionic blocker. Mecamylamine hydrochloride can across the blood-brain barrier. Mecamylamine hydrochloride can be used in the research of neuropsychiatric disorders, hypertension, antidepressant area .
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5
5 Cited Publications
Art. -Nr.: HY-121119
CAS. Nr.: 212329-37-8
Reinheit:  99.97%
MRS 1523 is a potent and selective adenosine A3 receptor antagonist with Ki values of 18.9 nM and 113 nM for human and rat A3 receptors, respectively. In rat this corresponds to selectivities of 140- and 18-fold vs A1 and A2A receptors, respectively. MRS 1523 can exert antihyperalgesic effect through N-type Ca channel block and action potential inhibition in isolated rat dorsal root ganglion (DRG) neurons .
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5
5 Cited Publications
Art. -Nr.: HY-B1661
CAS. Nr.: 60-25-3
Synonyms: Hexone chloride
Hexamethonium Chloride Dihydrate is a synthetic organic compound commonly used as a ganglion blocking agent, which means it blocks the transmission of nerve impulses between ganglion cells in the autonomic nervous system. Hexamethonium Chloride Dihydrate is used in various medical applications such as lowering blood pressure or inhibiting certain types of neuropathic pain. It works by inhibiting the release of acetylcholine, a neurotransmitter that plays a key role in regulating many bodily functions.
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1
1 Cited Publications
Art. -Nr.: HY-W008350
CAS. Nr.: 492-08-0
Synonyms: Pachycarpine
(+)-Sparteine is a natural alkaloid acting as a ganglionic blocking agent. (+)-Sparteine competitively blocks nicotinic ACh receptor in the neurons.
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1
1 Cited Publications
Art. -Nr.: HY-N0340
CAS. Nr.: 149-64-4
Synonyms: Hyoscine butylbromide; (-)-Scopolamine butylbromide; Butylscopolamine bromide
Scopolamine butylbromide (Hyoscine butylbromide) is an orally active anticholinergic agent and spasmolytic. Scopolamine butylbromide binds with high affinity to rat cardiac M2 (Ki 83 nmol/L), hM2 (Ki 233 nmol/L), rat intestinal M3 (Ki 290 nmol/L) and hM3 (Ki 643 nmol/L) muscarinic receptors. Scopolamine butylbromide exerts a dose-dependent antagonistic effect on Carbachol-induced gastrointestinal smooth muscle spasm. Scopolamine butylbromide can be used for the research of abdominal colic and pain associated with gastrointestinal spasm, functional abdominal pain, chronic gastropathy and gastric ulcer .
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1
1 Cited Publications
Art. -Nr.: HY-B0530
CAS. Nr.: 115-46-8
Synonyms: γ-pipradol
Target:  

Histamine Receptor

Forschungsgebiete:  

Neurological Disease

Azacyclonol (γ-pipradol), a metabolite of Terfenadine, is a central depressant agent. Azacyclonol is a ganglion-blocking agent. Azacyclonol can be used to diminish psychoses-induced hallucinations .
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1
1 Cited Publications
Art. -Nr.: HY-B1304A
Synonyms: (+)-Lupinidine sulfate pentahydrate
(+)-sparteine (sulfate pentahydrate) is a ganglionic blocking agent. (+)-Sparteine competitively blocks nicotinic ACh receptor in the neurons .
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Art. -Nr.: HY-B1382
CAS. Nr.: 79-55-0
Synonyms: 1,2,2,6,6-Pentamethylpiperidine
Target:  

nAChR

Pempidine (1,2,2,6,6-Pentamethylpiperidine) is an orally active ganglionic blocking agent used in hypertension-related conditions. Pempidine is a nicotinic receptor blocker. Pempidine can antagonize the nicotine-induced increase of the striatal dopamine (DA) in vitro .
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Art. -Nr.: HY-120751
CAS. Nr.: 1309601-26-0
Target:  

Calcium Channel

Forschungsgebiete:  

Neurological Disease

TROX-1 is a selective, orally active and brain-penetrant N-type calcium channel (Cav2.2) inhibitor with an IC50 value of 0.11 μM. TROX-1 exerts state-dependent and use-dependent inhibition, preferentially targets open/inactivated channels, blocks depolarization-associated calcium influx, and fully blocks calcium influx in rat dorsal root ganglion neurons. TROX-1 reverses inflammatory-induced hyperalgesia, nerve injury-induced allodynia. TROX-1 can be used for the research of pain .
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Art. -Nr.: HY-101347
CAS. Nr.: 96750-66-2
Reinheit:  ≥98.0%
Target:  

nAChR

Forschungsgebiete:  

Neurological Disease

Chlorisondamine (diiodide) is a potent nicotinic acetylcholine receptor (nAChR) antagonist and a ganglion blocker. Chlorisondamine antagonizes some of nicotine's central actions in a potent, long-lasting and pharmacologically selective way .
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Art. -Nr.: HY-119926
CAS. Nr.: 15358-48-2
Synonyms: Hydroxylupanine
Target:  

Integrin

13-Hydroxylupanine (Hydroxylupanine) is the typical alkaloid profile of sweet lupins.13-Hydroxylupanine blocks ganglionic transmission, decreases cardiac contractility and contracts uterine smooth muscle .
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Art. -Nr.: HY-P10227
CAS. Nr.: 2040964-58-5
Synonyms: ONL-1204
Xelafaslatide (ONL-1204) is a Fas receptor antagonist. Xelafaslatide blocks the Fas receptor signaling pathway and inhibits downstream apoptosis and inflammatory pathways. Xelafaslatide suppresses neuroinflammation and microglial activation in glaucoma models, protects retinal ganglion cells and prevents axonal degeneration. Xelafaslatide is applicable to relevant research on glaucoma .
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Art. -Nr.: HY-B1219
CAS. Nr.: 52-62-0
Target:  

nAChR

Forschungsgebiete:  

Neurological Disease

Pentolinium tartrate is a ganglionic blocking agent. Pentolinium tartrate lowers blood pressure and permits regression of the signs and symptoms associated with severe hypertension .
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Art. -Nr.: HY-B1191
CAS. Nr.: 504-03-0
Synonyms: 2,6-Lupetidine
Nanofin (2,6-Lupetidine) is a ganglionic blocker. Nanofin is used in research on eczema, neurodermatitis and hypertension .
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Art. -Nr.: HY-W127668
CAS. Nr.: 5957-17-5
Triethylcholine iodide is a choline acetyltransferase inhibitor and a regulator of the acetylcholine synthesis pathway. Triethylcholine iodide inhibits acetylcholine synthesis in brain tissues and blocks neuromuscular and autonomic ganglionic transmission. Triethylcholine iodide exerts weak curare-like effects at extremely high concentrations. Triethylcholine iodide elevates the pentylenetetrazol seizure threshold, alters electroencephalogram patterns in Felis catus, but does not affect the maximal electroshock seizure threshold in Oryctolagus cuniculus. Triethylcholine iodide can be used in seizure-related research .
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Art. -Nr.: HY-P3071
CAS. Nr.: 172450-46-3
Synonyms: Stichodactyla helianthus neurotoxin
ShK toxin blocks voltage-dependent potassium channel (Kv1.3 channel). ShK toxin can be isolated from the whole body extract of the Caribbean sea anemone (Stichodactylu helianthus). ShK toxin competes with dendrotoxin I and α-dendrotoxin for binding to synaptosomal membranes of rat brain, facilitates acetylcholine release. ShK toxin suppresses K+ currents in cultured rat dorsal root ganglion neurons. ShK toxin also inhibits T lymphocyte proliferation .
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Art. -Nr.: HY-B1395A
CAS. Nr.: 60-40-2
Mecamylamine is an orally active, nonselective, noncompetitive nAChR antagonist. Mecamylamine is also a ganglionic blocker. Mecamylamine can across the blood-brain barrier. Mecamylamine can be used in the research of neuropsychiatric disorders, hypertension, antidepressant area .
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Art. -Nr.: HY-N0789
CAS. Nr.: 509-18-2
Delsoline, a major alkaloid of Delphinium anthriscifolium Hance, has both a curare-like effect and a ganglion-blocking effect and is used to relieve muscle tension or hyperkinesia. D. anthriscifolium Hance has effects of dispelling wind and dampness, activating collaterals, and relieving pains and is used to treat rheumatism, hemiplegia, indigestion, and cough .
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Art. -Nr.: HY-164183
CAS. Nr.: 21035-85-8
Target:  

Adrenergic Receptor

Forschungsgebiete:  

Cardiovascular Disease

Trimethaphan bromide is a ganglionic blocking agent and can be used for study of hypertension .
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Art. -Nr.: HY-167741
CAS. Nr.: 69-27-2
Target:  

nAChR

Chlorisondamine is a nicotinic antagonist that acts as a ganglionic blocker and has been utilized to evaluate the neurogenic contributions to blood pressure and sympathetic vasomotor tone in animal models. Chlorisondamine has demonstrated antihypertensive properties, primarily being assessed through its effects on blood pressure, cardiac output, and heart rate in various experimental settings, particularly in mice.
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