>>Signaling Pathways>> GPCR/G protein>> Adrenergic Receptor>>Piperoxan hydrochloride (Benodaine hydrochloride)

Piperoxan hydrochloride (Benodaine hydrochloride) (Synonyms: DL-Piperoxan)

Catalog No.GC31782

Piperoxan(Benodaine) 염산염은 α2 아드레날린 수용체 길항제입니다.

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Piperoxan hydrochloride (Benodaine hydrochloride) Chemical Structure

Cas No.: 135-87-5

Size 가격 재고 수량
10mM (in 1mL DMSO)
US$103.00
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2mg
US$70.00
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5mg
US$139.00
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10mg
US$232.00
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25mg
US$324.00
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50mg
US$417.00
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100mg
US$510.00
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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

Piperoxan hydrochloride is an α2 adrenoceptor antagonist.

When the medulla is superfused with α2 adrenoceptor antagonist Piperoxane (50 μM; 5 min) while the pons is with artificial cerebrospinal fluid (ACSF), the three inactive preparations display rhythmic phrenic bursts at a low frequency (2-4 c/min), and the phrenic burst frequency of the 12 active ones significantly increases during the last 3 min of Piperoxane applications (163±12% of the previous mean frequency). In active medullary preparations, the effects of NA applications (25 μM; 5 min) are compared when the preparations sre superfused either by ACSF (n=8) or by the α2 adrenoceptor antagonist Piperoxane (50 μM; PIP-ACSF; n=5). NA applications either alone (NA-ACSF) or with Piperoxane (PIP-ACSF+NA) significantly increases the phrenic burst frequency. However, the blockage of the medullary α2 adrenoceptors by Piperoxane potentiates a phrenic burst frequency increase: during the fifth minute of NA applications, the phrenic burst frequency reached 171±11% of the mean control value when ACSF is applied alone and 234±21% of the mean control value when PIP-ACSF is applied in control condition[1].

[1]. Viemari JC, et al. Nasal trigeminal inputs release the A5 inhibition received by the respiratory rhythm generator of the mouse neonate. J Neurophysiol. 2004 Feb;91(2):746-58. [2]. Bentley GA, et al. The antinociceptive action of some beta-adrenoceptor agonists in mice. Br J Pharmacol. 1986 Jul;88(3):515-21.

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