About: Halofuginone     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/drugbank/Drug, within Data Space : linked.opendata.cz associated with source document(s)

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http://linked.open...gbank/description
  • Halofuginone is a low molecular weight quinazolinone alkaloid, and a potent inhibitor of collagen alpha1(I) and matrix metalloproteinase 2 (MMP-2) gene expression. Halofuginone also effectively suppresses tumor progression and metastasis in mice. (en)
http://linked.open...generalReferences
  • # Elkin M, Miao HQ, Nagler A, Aingorn E, Reich R, Hemo I, Dou HL, Pines M, Vlodavsky I: Halofuginone: a potent inhibitor of critical steps in angiogenesis progression. FASEB J. 2000 Dec;14(15):2477-85. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/11099465 (en)
http://linked.open...gy/drugbank/group
  • investigational (en)
http://linked.open...drugbank/halfLife
  • 23.8 to 72.1 hours (en)
http://linked.open...ugbank/indication
  • For the treatment of scleroderma, cancer, and restenosis. (en)
sameAs
Title
  • Halofuginone (en)
adms:identifier
http://linked.open...mechanismOfAction
  • Halofuginone is a potent inhibitor of collagen a1(I) and matrix metalloproteinase 2 (MMP-2) gene expression. Halofuginone also suppresses extracellular matrix deposition and cell proliferation. The profound antitumoral effect of halofuginone is attributed to its combined inhibition of the tumor stromal support, vascularization, invasiveness, and cell proliferation. (en)
http://linked.open.../drugbank/synonym
  • Tempostatin (Collgard Biopharmaceuticals) (en)
http://linked.open...ogy/drugbank/salt
  • (en)
http://linked.open...ugbank/IUPAC-Name
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  • Readily bioavailable and rapidly absorbed following oral administration. (en)
http://linked.open.../affectedOrganism
  • Humans and other mammals (en)
  • Protozoa (en)
http://linked.open...casRegistryNumber
  • 55837-20-2 (en)
http://linked.open...drugbank/category
  • (en)
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