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Diphenidol-d10
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Diphenidol-d10图片
规格:98%
分子量:319.5
包装与价格:
包装价格(元)
500ug电议
1mg电议
5mg电议

产品介绍
An internal standard for the quantification of diphenidol
货号:ajcx25236
CAS:N/A
分子式:C21H17D10NO
分子量:319.5
溶解度:DMSO: soluble,Methanol: soluble
纯度:98%
存储:Store at -20°C
库存:现货

Background:

Diphenidol-d10is intended for use as an internal standard for the quantification of diphenidol by GC- or LC-MS. Diphenidol is an antagonist of muscarinic acetylcholine receptors (mAChRs; Kis = 0.43, 2.8, 1.1, 0.91, and 1.28 µM in CHO cell membranes expressing M1-5receptors, respectively).1It also inhibits Kvchannels in Neuro2A cells (IC50= 28.2 µM), as well as L-type voltage-gated calcium channels in differentiated NG 108-15 cells in a concentration-dependent manner.2Microiontophoretic application of diphenidol inhibits rotation-induced firing of medial vestibular nucleus neurons in a cat model of vertigo.3Diphenidol (3.2 mg/kg, i.v.) prevents apomorphine-induced emesis in dogs.4Formulations containing diphenidol have been used in the treatment of vertigo and as antiemetics.


1.Varoli, L., Andreani, A., Burnelli, S., et al.Diphenidol-related diamines as novel muscarinic M4 receptor antagonistsBioorg. Med. Chem. Lett.18(9)2972-2976(2008) 2.Leung, Y.M., Wong, K.L., Cheng, K.S., et al.Inhibition of voltage-gated K+ channels and Ca2+ channels by diphenidolPharmacol. Rep.64(3)739-744(2012) 3.Kawabata, A., Sasa, M., Kishimoto, T., et al.Effects of anti-vertigo drugs on medial vestibular nucleus neurons activated by horizontal rotationJpn. J. Pharmacol.55(1)101-106(1991) 4.Nakayama, H., Yamakuni, H., Nakayama, A., et al.Diphenidol has no actual broad antiemetic activity in dogs and ferretsJ. Pharmacol. Sci.96(3)301-306(2004)