Arecoline hydrobromide (Standard)
Arecoline hydrobromide (Standard) is the analytical standard of Arecoline hydrobromide. This product is intended for research and analytical applications. Arecoline hydrobromide, a naturally brain-penetrant and orally active occurring psychoactive alkaloid, is a partial agonist of nicotinic and muscarinic acetylcholine receptor. Arecoline hydrobromide exhibits stimulation, alertness, anxiolysis and anti-parasitic effects. Arecoline hydrobromide also can induce oxidative stress.
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- Pureza : 98%
- No. CAS: 300-08-3
- Fòrmula: C8H14BrNO2
- Peso molecular:236.11
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Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Product Information
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Chemical Information
- Pureza y Documentación
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Help & FAQs
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HY-B0489
Arecoline hydrobromidenAChR/mAChR Agonist -
HY-B0282
Acetylcholine chlorideCholinergic Agonist -
HY-10448
CapsaicinTRPV1 Agonist -
HY-W009724
2-Aminoethyl diphenylborinateIP3R Inhibitor -
HY-N0175
CytisiniclinenAChR Agonist -
HY-B0228
AdenosineEndogenous Autacoid -
HY-B0282R
Acetylcholine chloride (Standard)Reference Standard -
HY-B0726
Pilocarpine HydrochloridemAChR Agonist -
HY-B0451A
Dopamine hydrochlorideCatecholamine Neurotransmitter -
HY-B0820
NitenpyramnAChR Agonist -
HY-10448R
Capsaicin (Standard)Analytical Standard -
HY-16560
CamptothecinTopo I inhibitor
Product Information
Information
Aplicación
The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
Chemical Information
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No. CAS 300-08-3
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Peso molecular 236.11
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Fòrmula C8H14BrNO2
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SMILES
O=C(C1=CCCN(C)C1)OC.Br
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Synonyms
methyl 1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxylate hydrobromide (Standard)
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Structure Classification
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Initial Source
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureza y Documentación
Referencias
[1]. Thangjam GS, et, al. Regulation of oxidative-stress responsive genes by arecoline in human keratinocytes. J Periodontal Res. 2009 Oct;44(5):673-82. [Content Brief]
[2]. Liu YJ, et, al. The pharmacology, toxicology and potential applications of arecoline: a review. Pharm Biol. 2016 Nov;54(11):2753-2760. [Content Brief]
[3]. Volgin AD, et, al. DARK Classics in Chemical Neuroscience: Arecoline. ACS Chem Neurosci. 2019 May 15;10(5):2176-2185. [Content Brief]
[4]. Kuo TM, et, al. Arecoline induces TNF-alpha production and Zonula Occludens-1 redistribution in mouse Sertoli TM4 cells. J Biomed Sci. 2014 Sep 9;21(1):93. [Content Brief]
[5]. Chen QY, et al. Inhibition of cortical synaptic transmission, behavioral nociceptive, and anxiodepressive-like responses by arecoline in adult mice. Mol Brain. 2024 Jun 17;17(1):39. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Arecoline hydrobromide (Standard) Related Classifications
HY-B0489R Related Classifications
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