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Rimeporide

Catalog No. T5319   CAS 187870-78-6
Synonyms: EMD-87580

Rimeporide (EMD-87580) (EMD-87580) is a potent and selective Sodium hydrogen exchange 1 (NHE-1) inhibitor.

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Rimeporide Chemical Structure
Rimeporide, CAS 187870-78-6
Pack Size Availability Price/USD Quantity
1 mg In stock $ 40.00
2 mg In stock $ 59.00
5 mg In stock $ 97.00
10 mg In stock $ 178.00
25 mg In stock $ 397.00
50 mg In stock $ 582.00
100 mg In stock $ 829.00
1 mL * 10 mM (in DMSO) In stock $ 116.00
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Purity: 99.98%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Rimeporide (EMD-87580) (EMD-87580) is a potent and selective Sodium hydrogen exchange 1 (NHE-1) inhibitor.
In vitro Treatment for 24 h with 10 μM phenylephrine significantly increased cell surface area to 129.6 3.1% of control values. The hypertrophic effect of phenylephrine was completely abrogated by 5 μM of EMD87580 [1].
Cell Research To induce hypertrophy, myocytes were treated for 10 min or 24 h as appropriate and noted under Results with 10 μM phenylephrine in the absence or presence of the following agents: the NHE-1 inhibitor EMD87580 (5 μM) or cariporide (5 μM), the JNK1/2 inhibitor SP600125, the p38 inhibitor SB203580, the ERK1/2 inhibitor PD98059 (all at 10 μM), and the reverse mode Na+-Ca2+ exchange inhibitor KB-R7943 or SN-6 (both at 10 μM). All drugs were added 30 min before the addition of phenylephrine [1].
Animal Research Two groups were studied. The treatment group (n = 5) received EMD 87580 at a dose of 5 mg/kg IV bolus 5 min before aortic cross-clamping and 10 mol/L EMD 87580 in the cardioplegic solution. The control group (n = 9) received the same volume of saline vehicle. Systemic pretreatment was used to ensure drug availability during the ischemic period prior to CPA. Direct infusion via cardioplegia ensures drug delivery at the time of ischemia (CPA), and it decreases the variability of drug delivery that may occur during the hemodilution with CPB initiation. Incorporation into the cardioplegia also minimizes the potential variable of drug/extracorporeal circuit interactions. Using this dosing regimen, the plasma concentration of EMD 87580 was in the 2,500 to 3,000 ng/mL range at 10 min after CPB. This concentration has been shown to be effective at Na+/H+ exchanger inhibition in vitro [2].
Synonyms EMD-87580
Molecular Weight 333.38
Formula C11H15N3O5S2
CAS No. 187870-78-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 15 mg/mL (50 mM)

TargetMolReferences and Literature

1. Stanbouly S, et al. Sodium hydrogen exchange 1 (NHE-1) regulates connexin 43 expression in cardiomyocytes via reverse mode sodium calcium exchange and c-Jun NH2-terminal kinase-dependent pathways. J Pharmacol Exp Ther. 2008 Oct;327(1):105-13. 2. Cox CS Jr, et al. Improved myocardial function using a Na+/H+ exchanger inhibitor during cardioplegic arrest and cardiopulmonary bypass. Chest. 2003 Jan;123(1):187-94.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Drug Library Drug Repurposing Compound Library Inhibitor Library Anti-Cancer Clinical Compound Library Sodium Channel Blocker Library Human Metabolite Library Bioactive Compound Library Ion Channel Inhibitor Library Bioactive Compounds Library Max Clinical Compound Library

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Keywords

Rimeporide 187870-78-6 Membrane transporter/Ion channel Sodium Channel Inhibitor EMD87580 Sodium-hydrogen Exchanger EMD 87580 Sodium/hydrogen Exchanger inhibit Na+/H+ Exchanger (NHE) EMD-87580 inhibitor

 

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