Startseite>>Signaling Pathways>> Membrane Transporter/Ion Channel>> Potassium Channel>>ML 418

ML 418

Katalog-Nr.GC50596

ML 418 ist der erste wirksame, selektive und ZNS-durchdringende Blocker des Kir7.1-Kaliumkanals (IC50, 310 nM), der auch Kir6.2/SUR1 wirksam hemmt und eine überlegene Selektivität gegenüber anderen Kir-Kanälen aufweist.

Products are for research use only. Not for human use. We do not sell to patients.

ML 418 Chemische Struktur

Cas No.: 1928763-08-9

Größe Preis Lagerbestand Menge
10 mg
143,00 $
Auf Lager
50 mg
607,00 $
Auf Lager

Tel:(909) 407-4943 Email: sales@glpbio.com

Kundenbewertungen

Basiert auf Kundenrezensionen.

  • GlpBio Citations

    GlpBio Citations
  • Bioactive Compounds Premium Provider

    Bioactive Compounds Premium Provider

Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Kir7.1 inhibitor (IC50 = 0.31 μM). Also inhibits Kir6.2 with similar potency. Displays >17-fold selectivity for Kir7.1 over Kir1.1, Kir2.1, Kir2.2, Kir2.3, Kir3.1/3.2 and Kir4.1. Active in vivo.

Swale et al (2016) ML418: the first selective, sub-micromolar pore blocker of Kir7.1 potassium channels. ACS Chem.Neurosci. 7 1013 PMID:27184474 |Kharade (2017) Pore polarity and charge determine differential block of Kir1.1 and Kir7.1 potassium channels by small-molecule inhibitor VU590. Mol.Pharmacol. 92 338 PMID:28619748

Bewertungen

Review for ML 418

Average Rating: 5 ★★★★★ (Based on Reviews and 21 reference(s) in Google Scholar.)

5 Star
100%
4 Star
0%
3 Star
0%
2 Star
0%
1 Star
0%
Review for ML 418

GLPBIO products are for RESEARCH USE ONLY. Please make sure your review or question is research based.

Required fields are marked with *

You may receive emails regarding this submission. Any emails will include the ability to opt-out of future communications.