About: Cycloserine     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)

AttributesValues
rdf:type
http://linked.open...gbank/description
  • Antibiotic substance produced by Streptomyces garyphalus. [PubChem] (en)
http://linked.open...y/drugbank/dosage
http://linked.open...gy/drugbank/group
  • approved (en)
http://linked.open...drugbank/halfLife
  • Half-life in patients with normal renal function is 10 hours, and is prolonged in patients with impaired renal function. (en)
http://linked.open...ugbank/indication
  • Used in combination with up to 5 other drugs as a treatment for Mycobacterium avium complex (MAC) and is also used to treat tuberculosis (TB). (en)
http://linked.open...bank/manufacturer
sameAs
Title
  • Cycloserine (en)
adms:identifier
http://linked.open...mechanismOfAction
  • Cycloserine is an analog of the amino acid D-alanine. It interferes with an early step in bacterial cell wall synthesis in the cytoplasm by competitive inhibition of two enzymes, L-alanine racemase, which forms D-alanine from L-alanine, and D-alanylalanine synthetase, which incorporates D-alanine into the pentapeptide necessary for peptidoglycan formation and bacterial cell wall synthesis. (en)
http://linked.open...drugbank/packager
http://linked.open.../drugbank/synonym
  • Cycloserine (en)
  • Orientomycin (en)
  • Seromycin (en)
  • Cicloserina (en)
  • D-Cycloserine (en)
  • alpha-Cycloserine (en)
  • (+)-4-Amino-3-isoxazolidinone (en)
  • (+)-Cycloserine (en)
  • (R)-4-AMINO-isoxazolidin-3-one (en)
  • Cycloserinum (en)
  • D-(+)-Cycloserine (en)
  • D-4-amino-3-Isoxazolidinone (en)
  • D-4-amino-3-Isoxazolidone (en)
  • DCS (en)
  • PA 94 (en)
  • PA-94 (en)
  • Ro-1-9213 (en)
  • cyclo-D-Serine (en)
  • α-Cycloserine (en)
http://linked.open...drugbank/toxicity
  • Oral LD<sub>50</sub> in mouse is 5290 mg/kg, and in rat is over 5000 mg/kg. Symptoms of a cycloserine overdose include drowsiness, confusion, headache, dizziness, irritability, numbness and tingling, difficulty speaking, paralysis, abnormal behavior, seizures, and unconsciousness. (en)
http://linked.open...ynthesisReference
  • Norman P. Jensen, "N-substituted cycloserine compounds, salts thereof, and processes for preparing them." U.S. Patent US3932439, issued December, 1956. (en)
foaf:page
http://linked.open...ugbank/IUPAC-Name
http://linked.open...gy/drugbank/InChI
http://linked.open...Molecular-Formula
http://linked.open.../Molecular-Weight
http://linked.open...noisotopic-Weight
http://linked.open...y/drugbank/SMILES
http://linked.open.../Water-Solubility
http://linked.open...ogy/drugbank/logP
http://linked.open...ogy/drugbank/logS
http://linked.open...l/drug/hasATCCode
http://linked.open...nd-Acceptor-Count
http://linked.open...-Bond-Donor-Count
http://linked.open...drugbank/InChIKey
http://linked.open...urface-Area--PSA-
http://linked.open...nk/Polarizability
http://linked.open...bank/Refractivity
http://linked.open...atable-Bond-Count
http://linked.open...ugbank/absorption
  • Rapidly and almost completely absorbed (70 to 90%) from the gastrointestinal tract following oral administration. (en)
http://linked.open.../affectedOrganism
  • Enteric bacteria and other eubacteria (en)
  • Mycobacterium tuberculosis (en)
http://linked.open...casRegistryNumber
  • 68-41-7 (en)
http://linked.open...drugbank/category
  • (en)
http://linked.open...gbank/containedIn
http://linked.open...k/Bioavailability
http://linked.open...bank/Ghose-Filter
http://linked.open...nk/MDDR-Like-Rule
http://linked.open...ank/Melting-Point
http://linked.open...k/Number-of-Rings
http://linked.open...siological-Charge
http://linked.open...bank/Rule-of-Five
http://linked.open...tional-IUPAC-Name
http://linked.open...strongest-acidic-
http://linked.open...-strongest-basic-
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