A Kir7.1 inhibitor
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ML-418

Item No. 43042

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
N-[1-[(5-chloro-8-hydroxy-7-quinolinyl)methyl]-4-piperidinyl]-carbamic acid, 1-methylethyl ester
CAS Number
1928763-08-9
Molecular Formula
C19H24ClN3O3
Formula Weight
377.9
Purity
≥98%
Formulation
A solid
Solubility(Learn about Variance in Solubility)
DMSO: Slightly soluble: 0.1-1 mg/mlEthanol: Slightly soluble: 0.1-1 mg/ml
SMILES
O=C(NC1CCN(CC1)CC2=CC(Cl)=C3C=CC=NC3=C2O)OC(C)C
InChi Code
InChI=1S/C19H24ClN3O3/c1-12(2)26-19(25)22-14-5-8-23(9-6-14)11-13-10-16(20)15-4-3-7-21-17(15)18(13)24/h3-4,7,10,12,14,24H,5-6,8-9,11H2,1-2H3,(H,22,25)
InChi Key
CWIXCQOSULUGBT-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    5 mg

    $65

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    10 mg

    $117

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    25 mg

    $228

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    50 mg

    $423

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    Product Description

    ML-418 is an inhibitor of inward-rectifier potassium channel 7.1 (Kir7.1; IC50 = 0.31 µM).1 It is selective for Kir7.1 over Kir1.1, Kir2.1, and Kir4.1 (IC50s = >30 µM for all) but does inhibit sulfonylurea receptor 1 (SUR1) linked to ATP-sensitive potassium channel Kir6.2 (SUR1/Kir6.2; IC50 = 1.9 µM).

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Swale, D.R., Kurata, H., Kharade, S.V., et al. ML418: The first selective, sub-micromolar pore blocker of Kir7.1 potassium channels. ACS Chem. Neurosci. 7(7), 1013-1023 (2016).