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Halofuginone (hydrochloride)

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    Halofuginone (hydro<wbr/>chloride)
  • Halofuginone (hydro<wbr/>chloride)
Cat No: 13370
Cayman

Halofuginone is a halogenated derivative of febrifugine, a natural quinazolinone-containing compound found in the Chinese herb D. febrifuga.{26479} It has antimalarial and anticoccidial actions.{26479} In mammals, halofuginone at 10 ng/ml down-regulat...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 7-bromo-6-chloro-3-[3-[(2R,3S)-3-hydroxy-2-piperidinyl]-2-oxopropyl]-4(3H)-quinazolinone, monohydrochloride
Correlated keywords:
  • 55837-20-2 inhibitors inhibitions inhibits cancers genes regulations autoimmunity infectious diseases immunology HCl TGF-? TGF-.beta. TGF-beta TGF-b TGF ? .beta. beta b signals signaling TH17 differentiation derivatives febrifugine D. D febrifuga antimalarial anti-malarial anti malarial malaria anticoccidial anti-coccidial coccidial Smad3 fibroblasts myofibroblasts epithelial cells mesenchymal fibrosis tumors competitive competitively prolyl-tRNA prolyl tRNA synthetase monohydrochloride autoimmune diseases
Product Overview:
Halofuginone is a halogenated derivative of febrifugine, a natural quinazolinone-containing compound found in the Chinese herb D. febrifuga.{26479} It has antimalarial and anticoccidial actions.{26479} In mammals, halofuginone at 10 ng/ml down-regulates Smad3, blocking TGF-β signaling and preventing both the differentiation of fibroblasts to myofibroblasts and the transitioning of epithelial cells to mesenchymal cells.{26479,26481} Through this action, halofuginone blocks fibrosis and tumor progression in a variety of different models.{26479,26482} This compound also competitively inhibits prolyl-tRNA synthetase (Ki = 18.3 nM), activating the amino acid starvation response.{26480,17217} This prevents the differentiation of TH17 cells, blunting an autoimmune response.{17217}
Size 500 µg
Shipping dry ice
CAS Number 1217623-74-9
Molecular Formula C16H17BrClN3O3 • HCl
SMILES BrC1=C(Cl)C=C2C(N=CN(CC(C[C@H]3NCCC[C@@H]3O)=O)C2=O)=C1.Cl
Molecular Weight 451,1
Formulation A crystalline solid
Purity ≥95%
Custom Code 2903.99
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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