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(-)-p-Bromotetramisole Oxalate (Synonyms: (-)-p-Bromotetramisole, L-para-Bromotetramisole)

Catalog No.GC14520 Copy One-Click Copy Product Info

(-)-p-Bromotetramisole Oxalate(L-p-bromotetramisole) es un inhibidor potente e inespecífico de la fosfatasa alcalina.

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(-)-p-Bromotetramisole Oxalate Chemical Structure

Cas No.: 62284-79-1

Tamaño Precio Disponibilidad Cantidad
10mM (in 1mL DMSO)
40,00 $
Disponible
10mg
48,00 $
Disponible
5mg
76,00 $
Disponible
50mg
121,00 $
Disponible
500mg
896,00 $
Disponible
1g
1.638,00 $
Disponible
20g
6.600,00 $
Disponible

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Sample solution is provided at 25 µL, 10mM.



Description of (-)-p-Bromotetramisole Oxalate

(-)-p-Bromotetramisole Oxalate(L-p-bromotetramisole) es un inhibidor potente e inespecífico de la fosfatasa alcalina [1-2].

(-)-p-Bromotetramisole Oxalate (1 mM) aumentó el eflujo de yoduro estimulado por cAMPy, por sí mismio, estimuló un flujo mayor que el evocado por los agonista de cAMP, lo que sugiere que puede promover la apertura del regulador de conductancia transmembrana de la fibrosis quística humana (CFTR) en células CHO[3]. En las células PC12, (-)-p-Bromotetramisole Oxalate (0.3 mM) mejora la liberación de norepinefrina (NA) estimulada por innomicina[4].

(-)-p-Bromotetramisole Oxalate(30 mg/kg; ivgtt) inhibió significativamente la elevación del MABP inducida por norepinefrina y la resistencia vascular renal. Reduce la respuesta vascular renal y de la presión arterial a la norepinefrina[5]. La infusión sistémica de (-)-p-Bromotetramisole Oxalate (0.8 ml/min de 10 mM I-p-Bromotetramisole oxalate; ivgtt) aumenta la excreción fraccional de fosfato (FEPi) en ratas de Sprague-Dawley[6].

References:[1]. Borgers M. The cytochemical application of new potent inhibitors of alkaline phosphatases. J Histochem Cytochem. 1973 Sep;21(9):812-24. doi: 10.1177/21.9.812. PMID: 4741290.[2]. Borgers M, Thoné F. The inhibition of alkaline phosphatase by L-p-bromotetramisole. Histochemistry, 1975, 44(3): 277-280.[3]. Lansdell KA, Kidd JF, et,al. Regulation of murine cystic fibrosis transmembrane conductance regulator Cl- channels expressed in Chinese hamster ovary cells. J Physiol. 1998 Nov 1;512 ( Pt 3)(Pt 3):751-64. doi: 10.1111/j.1469-7793.1998.751bd.x. PMID: 9769419; PMCID: PMC2231228.[4]. Kitamura T, Murayama T, et,al. Enhancement of Ca2+-induced noradrenaline release by vanadate in PC12 cells: possible involvement of tyrosine phosphorylation. Brain Res. 2000 Jan 31;854(1-2):165-71. doi: 10.1016/s0006-8993(99)02299-4. PMID: 10784118.[5]. Jackson EK, Zhang Y,et,al. Alkaline Phosphatase Inhibitors Attenuate Renovascular Responses to Norepinephrine. Hypertension. 2017 Mar;69(3):484-493. doi: 10.1161/HYPERTENSIONAHA.116.08623. Epub 2017 Jan 30. PMID: 28137984; PMCID: PMC5310812.[6]. Onsgard-Meyer M, McCoy AL, et,al. Effect of bromotetramisole on renal phosphate excretion. Proc Soc Exp Biol Med. 1996 Nov;213(2):193-5. doi: 10.3181/00379727-213-44050. PMID: 8931664.

Protocol of (-)-p-Bromotetramisole Oxalate

Experimentos celulares [1]:

Líneas celulares

Células PC12

Método de preparación

Las células PC12 premarcadas se incubaron con vehículo o 5 µM de ionomicina en presencia de 2 mM de CaCl2. (-)-p-Bromotetramisole Oxalate (BTO) se añadió aún más a la mezcla de ensayo.

Condiciones de reacción

0.3 mM

Áreas de aplicación

(-)-p-Bromotetramisole Oxalate (0.3 mM) mejora la liberación de norepinefrina (NA) estimulada por ionomicina.
Experimentos con animales [2]:

Modelos animales

Ratas Sprague-Dawley

Método de preparación

Se midió la excreción fraccionada de fosfato (FEPi) en ratas tiroparatiroidectomizadas antes y durante una infusión sistémica a 0.8 ml/min de 10 mM (-)-p-Bromotetramisole Oxalate.

Forma de dosificación

0.8 ml/min de 10 mM (-)-p-Bromotetramisole Oxalate; ivgtt

Áreas de aplicación

La infusión sistémica de (-)-p-Bromotetramisole Oxalate aumenta la excreción fraccional de fosfato (FEPi) en ratas.

References:

[1]. Kitamura T, Murayama T, et,al. Enhancement of Ca2+-induced noradrenaline release by vanadate in PC12 cells: possible involvement of tyrosine phosphorylation. Brain Res. 2000 Jan 31;854(1-2):165-71. doi: 10.1016/s0006-8993(99)02299-4. PMID: 10784118.
[2]. Onsgard-Meyer M, McCoy AL, et,al. Effect of bromotetramisole on renal phosphate excretion. Proc Soc Exp Biol Med. 1996 Nov;213(2):193-5. doi: 10.3181/00379727-213-44050. PMID: 8931664.

Chemical Properties of (-)-p-Bromotetramisole Oxalate

Cas No. 62284-79-1 SDF
Sinónimos (-)-p-Bromotetramisole, L-para-Bromotetramisole
Canonical SMILES BrC(C=C1)=CC=C1[C@H]2N=C3SCCN3C2.OC(C(O)=O)=O
Formula C13H13BrN2O4S M.Wt 373.22
Solubility ≥ 18.65mg/mL in DMSO Storage Desiccate at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of (-)-p-Bromotetramisole Oxalate

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.6794 mL 13.3969 mL 26.7938 mL
5 mM 535.9 μL 2.6794 mL 5.3588 mL
10 mM 267.9 μL 1.3397 mL 2.6794 mL
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