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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
  • Tolrestat (INN) (AY-27773) is an aldose reductase inhibitor which was approved for the control of certain diabetic complications. While it was approved for marketed in several countries, it failed a Phase III trial in the U.S. due to toxicity and never received FDA approval. It was discontinued by Wyeth in 1997 because of the risk of severe liver toxicity and death. It was sold under the tradename Alredase. [Wikipedia] (en)
http://linked.open...generalReferences
  • # Sestanj K, Bellini F, Fung S, Abraham N, Treasurywala A, Humber L, Simard-Duquesne N, Dvornik D: N-[5-(trifluoromethyl)-6-methoxy-1-naphthalenyl]thioxomethyl]- N-methylglycine (Tolrestat), a potent, orally active aldose reductase inhibitor. J Med Chem. 1984 Mar;27(3):255-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/6422042 # Kador PF, Kinoshita JH, Sharpless NE: Aldose reductase inhibitors: a potential new class of agents for the pharmacological control of certain diabetic complications. J Med Chem. 1985 Jul;28(7):841-9. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/3925146 (en)
http://linked.open...gy/drugbank/group
  • withdrawn (en)
http://linked.open...ugbank/indication
  • For the pharmacological control of certain diabetic complications. (en)
sameAs
Title
  • Tolrestat (en)
adms:identifier
http://linked.open...drugbank/toxicity
  • Oral, mouse: LD50 = 300 mg/kg; Oral, rabbit: LD50 = 3200 mg/kg; Oral, rat: LD50 = 980 mg/kg. (en)
http://linked.open...ugbank/IUPAC-Name
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http://linked.open.../affectedOrganism
  • Humans and other mammals (en)
http://linked.open...casRegistryNumber
  • 82964-04-3 (en)
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http://linked.open...strongest-acidic-
http://linked.open...-strongest-basic-
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