Inicio>>Signaling Pathways>> Angiogenesis>>PD 168368

PD 168368

Catalog No.GC44584

PD 168368 es un antagonista potente, competitivo y selectivo del receptor de neuromedina B (NMB-R) con Ki de 15-45 nM. PD 168368 es un antagonista del receptor de neuromedina B (NMBR; IC50 = 96 nM)/receptor del péptido liberador de gastrina (GRPR IC50 = 3500 nM). PD 168368 también es un agonista mixto de FPR1/FPR2/FPR3 con EC50 de 0,57, 0,24 y 2,7 nM, respectivamente.

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

PD 168368 Chemical Structure

Cas No.: 204066-82-0

Tamaño Precio Disponibilidad Cantidad
500μg
35,00 $
Disponible
1mg
67,00 $
Disponible
5mg
278,00 $
Disponible
10mg
488,00 $
Disponible

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

Reseñas de cliente

Based on customer reviews.

  • 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

PD 168368 is a competitive antagonist of neuromedin B (NMB) receptors (Kis = 15-45 nM for rat and human receptors expressed in various cell lines). It blocks the elevation of intracellular calcium and release of inositol phosphate induced by NMB in cells expressing NMB receptors. PD 168368 is selective for NMB receptors over those for related peptide agonists, including bombesin and gastrin-releasing peptide. It is also an agonist of formyl-peptide receptors (FPRs) at higher concentrations (EC50s = 0.57 and 0.24 µM for FPR1 and FPR2, respectively). PD 168368 induces cell cycle arrest and apoptosis in MDA-MB-231 breast cancer cells and blocks neovascularization and cancer cell growth in breast cancer xenograft tumors in mice.

Reseñas

Review for PD 168368

Average Rating: 5 ★★★★★ (Based on Reviews and 14 reference(s) in Google Scholar.)

5 Star
100%
4 Star
0%
3 Star
0%
2 Star
0%
1 Star
0%
Review for PD 168368

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.