Startseite>>Signaling Pathways>> Apoptosis>> Other Apoptosis>>9-ING-41

9-ING-41 (Synonyms: Elraglusib)

Katalog-Nr.GC39152

9-ING-41 ist ein Maleimid-basierter ATP-kompetitiver und selektiver Glykogen-Synthase-Kinase-3β (GSK-3β)-Inhibitor mit einem IC50 von 0,71 μM. 9-ING-41 fÜhrt signifikant zu Zellzyklusstillstand, Autophagie und Apoptose in Krebszellen. 9-ING-41 hat AntikrebsaktivitÄt und hat das Potenzial, die Antitumorwirkung von Chemotherapeutika zu verstÄrken.

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

9-ING-41 Chemische Struktur

Cas No.: 1034895-42-5

Größe Preis Lagerbestand Menge
10mM (in 1mL DMSO)
92,00 $
Auf Lager
5mg
84,00 $
Auf Lager
10mg
140,00 $
Auf Lager
25mg
294,00 $
Auf Lager
50mg
525,00 $
Auf Lager
100mg
910,00 $
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

9-ING-41 is a potent glycogen synthase kinase-3 (GSK-3) inhibitor[1]. 9-ING-41 induces apoptosis and cell cycle arrest at prophase by targeting centrosomes and microtubule-bound GSK-3β. 9-ING-41 has anticancer activity[2].

[1]. Ugolkov AV, et al. 9-ING-41, a small-molecule glycogen synthase kinase-3 inhibitor, is active in neuroblastoma. Anticancer Drugs. 2018 Sep;29(8):717-724. [2]. Wu X, et al. Targeting glycogen synthase kinase 3 for therapeutic benefit in lymphoma. Blood. 2019 Jul 25;134(4):363-373.

Bewertungen

Review for 9-ING-41

Average Rating: 5 ★★★★★ (Based on Reviews and 27 reference(s) in Google Scholar.)

5 Star
100%
4 Star
0%
3 Star
0%
2 Star
0%
1 Star
0%
Review for 9-ING-41

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.