Startseite>>Signaling Pathways>> Tyrosine Kinase>> ROS>>F-1

F-1

Katalog-Nr.GC36021

F-1 ist ein potenter dualer ALK- und ROS1-Inhibitor, der Phospho-ALK und seine relativ nachgeschalteten Signalwege unterdrÜckt, mit IC50-Werten von 2,1 nM, 2,3 nM, 1,3 nM und 3,9 nM fÜr ALKWT, ROS1WT, ALKL1196M bzw. ALKG1202R.

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

F-1 Chemische Struktur

Cas No.: 2244775-31-1

Größe Preis Lagerbestand Menge
100mg Please Inquire Please Inquire
250mg Please Inquire Please Inquire
500mg Please Inquire Please Inquire

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

F-1 is a potent ALK and ROS1 dual inhibitor, suppresses phospho-ALK and its relative downstream signaling pathways, with IC50s of 2.1 nM, 2.3 nM, 1.3 nM and 3.9 nM for ALKWT, ROS1WT, ALKL1196M and ALKG1202R, respectively[1].

[1]. Guo M, et al. Dual potent ALK and ROS1 inhibitors combating drug-resistant mutants: Synthesis and biological evaluation of aminopyridine-containing diarylaminopyrimidine derivatives. Eur J Med Chem. 2018 Sep 6;158:322-333.

Bewertungen

Review for F-1

Average Rating: 5 ★★★★★ (Based on Reviews and 38 reference(s) in Google Scholar.)

5 Star
100%
4 Star
0%
3 Star
0%
2 Star
0%
1 Star
0%
Review for F-1

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.