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Cilnidipine-d7

An internal standard for the quantification of cilnidipine

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Cilnidipine-d7的二维码
  • 库存: 现货
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  • 1mg
    ¥10787.00
    8630.00
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  • 货号: ajcx24116
  • CAS: N/A
  • 别名: FRC-8653-d7
  • 分子式: C27H21D7N2O7
  • 分子量: 499.6
  • 纯度: >98%
  • 溶解度: DMSO: soluble,Methanol: soluble
  • 储存: -20°C
  • 库存: 现货

Background

Cilnidipine-d7 is intended for use as an internal standard for the quantification of cilnidipine by GC- or LC-MS. Cilnidipine is a dihydropyridine calcium channel blocker that blocks L- and N-type high-voltage-activated calcium currents in rat hippocampal CA1 pyramidal neurons when used at a concentration of 10 μM.1 Cilnidipine (3 mg/kg) reduces the pressor response to acute cold stress, as well as mean blood pressure, in spontaneously hypertensive rats.2 It dose-dependently reduces mean blood pressure and cerebral vascular resistance without affecting cerebral blood flow in anesthetized rats at doses ranging from 3-100 μg/kg.3 Cilnidipine (100 μg/kg, i.p.) reduces cerebral infarction area in a rat model of focal brain ischemia.



1.Murai, Y., Uneyama, H., Ishibashi, H., et al.Preferential inhibition of L- and N-type calcium channels in the rat hippocampal neurons by cilnidipineBrain Res.854(1-2)6-10(1999) 2.Hosono, M., Hiruma, T., Watanabe, K., et al.Inhibitory effect of cilnidipine on pressor response to acute cold stress in spontaneously hypertensive ratsJpn. J. Pharmacol.69(2)119-125(1995) 3.Takahara, A., Konda, T., Enomoto, A., et al.Neuroprotective effects of a dual L/N-type Ca2+ channel blocker cilnidipine in the rat focal brain ischemia modelBiol. Pharm. Bull.27(9)1388-1391(2004)

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