A NHE-1 inhibitor
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Eniporide

Item No. 20984

Technical Information
Formal Name
N-(aminoiminomethyl)-2-methyl-5-(methylsulfonyl)-4-(1H-pyrrol-1-yl)-benzamide
CAS Number
176644-21-6
Molecular Formula
C14H16N4O3S
Formula Weight
Purity
≥95%
A crystalline solid
DMF: 20 mg/mLDMF:PBS(pH 7.2)(1:1): 0.5 mg/mLDMSO: 5 mg/mL
SMILES
CC1=C(C(NC(N)=N)=O)C=C(S(C)(=O)=O)C(N2C=CC=C2)=C1
InChi Code
InChI=1S/C14H16N4O3S/c1-9-7-11(18-5-3-4-6-18)12(22(2,20)21)8-10(9)13(19)17-14(15)16/h3-8H,1-2H3,(H4,15,16,17,19)
InChi Key
UADMBZFZZOBWBB-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Eniporide is a selective inhibitor of human Na+/H+ exchanger isoform 1 (NHE-1) (IC50 = 4.5 nM).1 Inhibition with eniporide prevents calcium overload-induced myocardial ischemia-reperfusion injury in vitro and in vivo.2,3,4,5

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kawamoto, T., Kimura, H., Kusumoto, K., et al. Potent and selective inhibition of the human Na+/H+ exchanger isoform NHE1 by a novel aminoguanidine derivative T-162559. Eur. J. Pharmacol. 420(1), 1-8 (2001).

    2. Counillon, L., Scholz, W., Lang, H.J., et al. Pharmacological characterization of stably transfected Na+/H+ antiporter isoforms using amiloride analogs and a new inhibitor exhibiting anti-ischemic properties. Mol. Pharmacol. 44(5), 1041-1045 (1993).

    3. Masereel, B., Pochet, L., and Laeckmann, D. An overview of inhibitors of Na+/H+ exchanger. Eur. J. Med. Chem. 38(6), 547-554 (2003).

    4. An, J., Varadarajan, S.G., Camara, A.C., Q., et al. Blocking Na+/H+ exchange reduces [Na+]i and [Ca2+]i load after ischemia and improves function in intact hearts. Am. J. Physiol. Heart Circ. Physiol. 281(6), H2398-H2409 (2001).

    5. Knight, D.R., Smith, A.H., Flynn, D.M., et al. A novel sodium-hydrogen exchanger isoform-1 inhibitor, zoniporide, reduces ischemic myocardial injury in vitro and in vivo. J. Pharmacol. Exp. Ther. 297(1), 254-259 (2001).