halofuginone; 7-bromo-6-chloro-3-[3-[(3R)-3-hydroxypiperidin-2-yl]-2-oxopropyl]quinazolin-4-one; stenorol; tempostatin

From Aaushi
Jump to navigation Jump to search

Introduction

extracted from plants

Indications

Mechanism of action

More general terms

References

  1. Sundrud MS et al. Halofuginone inhibits TH17 cell differentiation by activating the amino acid starvation response. Science 2009 Jun 5; 324:1334. <PubMed> PMID: https://www.ncbi.nlm.nih.gov/pubmed/19498172 <Internet> http://dx.doi.org/10.1126/science.1172638
  2. 2.0 2.1 Pines M et al Halofuginone to treat fibrosis in chronic graft-versus-host disease and scleroderma. Biol Blood Marrow Transplant. 2003 Jul;9(7):417-25. PMID: https://www.ncbi.nlm.nih.gov/pubmed/12869955

Database