Interbiotech Arecoline Bromide

Interbiotech Arecoline Bromide

InterBioTech FT-AYM126 Arecoline bromide Product Description Catalog #: AYM126, 500mg AYM127, 1g Also available as 10 mM * 1 mL in DMSO Name: Arecoline bromide Syn.: Taeniolin CAS [300-08-3] ; MW : 236.11 Purity : >98 % Solubility : DMSO 47 mg/mL; Water 47 mg/m Storage: Store at -20°C in a tightly closed container. (M) Can be stored at RT for short term For Research Use Only Mechanism: Arecoline Hydrobromide is a muscarinic acetylcholine receptor agonist. Target: mAChR General information Biological Activity: Arecoline is an alkaloid found in the areca nut. Arecoline. a drug obtained from the Areca Catechu L., induced a dose- dependent antinociception (0.3-1 mg kg(-1) i.p.) which was prevented by the muscarinic antagonists pirenzepine (0.1 microg per mouse i.c.v.) and S-(-)-ET-126 (0.01 microg per mouse i.c.v.) [1]. Arecoline exerts its excitatory actions by binding to M2-muscarinic receptors on the cell membrane of neurons of the locus coeruleus [2]. Arecoline (1 nM - 1 microM) produced a concentration-dependent contraction in both the longitudinal and the circular smooth muscle of rabbit colon. Atropine (10 microM) abolished the arecoline (80 nM)--induced contraction. M3 receptor antagonist, 4 - DAMP (0.4 microM), abolished the arecoline (80 nM)--related response, whereas M2 receptor antagonist, gallamine (0.4 microM), did not affect the effect of arecoline. These results suggest that arecoline excites the colonic motility via M3 receptor in rabbits [3]. References: [1]. Ghelardini, C., et al., M1 receptor activation is a requirement for arecoline analgesia. Farmaco, 2001. 56(5-7): p. 383-5. [2]. Yang, Y.R., et al., Arecoline excites rat locus coeruleus neurons by activating the M2-muscarinic receptor. Chin J Physiol, 2000. 43(1): p. 23-8. [3]. Xie, D.P., et al., Arecoline excites the colonic smooth muscle motility via M3 receptor in rabbits. Chin J Physiol, 2004. 47(2): p. 89-94. Preparing Stock Solutions Volume of DMSO: concentration mass 1 mg 5 mg 10 mg mM 4.2353 mL 21.1766 mL 42.3531 mL 5 mM 0.8471 mL 4.2353 mL 8.4706 mL 10 mM 0.4235 mL 2.1177 mL 4.2353 mL P.1 InterBioTech FT-AYM126 Related mAChR Products (R)-5-Hydroxymethyl Tolterodine (PNU-200577; Desfesoterodine) a potent and selective muscarinic receptor antagonist with a Kb and a pA2 of 0.84 nM and 9.14, respectively. Acetylcholine chloride a neurotransmitter that can induce the opening of calcium channels. Aclidinium Bromide (LAS 34273; LAS-W 330) a long-acting, inhaled muscarinic antagonist as a maintenance treatment for chronic obstructive pulmonary disease (COPD). Anisodamine an anticholinergic and (alpha)1-adrenergic receptor antagonist used in the treatment of acute circulatory shock, is also a naturally occurring tropane alkaloid found in some plants of the Solanaceae family. Benzetimide hydrochloride a muscarinic acetylcholine receptor antagonist. Benztropine mesylate a centrally-acting, antimuscarinic agent used as an adjunct in the treatment of Parkinson(acute)s disease. Camylofine Camylofin is an antimuscarinic, is a smooth muscle relaxant. Carbamoylcholine chloride used to study responses mediated by nAChR and mAChR, including smooth muscle contraction, gut motility, and neuronal signaling. Clidinium bromide an anticholinergic (specifically a muscarinic antagonist) drug, may help symptoms of cramping and abdominal/stomach pain by decreasing stomach acid, and slowing the intestines. Diphenidol hydrochloride a muscarinic antagonist employed as an antiemetic and as an antivertigo agent. Ordering information Catalog size quantities and prices may be found at http://www.interchim.com. Please inquire for higher quantities (availability, shipment conditions). Please contact InterBioTech – Interchim for any other information Hotline : +33(0)4 70 03 73 06 – [email protected] Disclaimer : Materials are sold for research use only, and are not intended for food, drug, household, or cosmetic use. Interchim® is not liable for any damage resulting from handling or contact with this product. R04E P.2 .

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