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rdf:type
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http://linked.open...gbank/description
| - Antibiotic substance produced by Streptomyces garyphalus. [PubChem] (en)
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http://linked.open...y/drugbank/dosage
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http://linked.open...gy/drugbank/group
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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)
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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)
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http://linked.open...bank/manufacturer
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sameAs
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Title
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adms:identifier
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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)
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http://linked.open...drugbank/packager
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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)
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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)
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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)
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foaf:page
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http://linked.open...ugbank/IUPAC-Name
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http://linked.open...gy/drugbank/InChI
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http://linked.open...Molecular-Formula
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http://linked.open.../Molecular-Weight
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http://linked.open...noisotopic-Weight
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http://linked.open...y/drugbank/SMILES
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http://linked.open.../Water-Solubility
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http://linked.open...ogy/drugbank/logP
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http://linked.open...ogy/drugbank/logS
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http://linked.open...l/drug/hasATCCode
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http://linked.open...nd-Acceptor-Count
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http://linked.open...-Bond-Donor-Count
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http://linked.open...drugbank/InChIKey
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http://linked.open...urface-Area--PSA-
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http://linked.open...nk/Polarizability
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http://linked.open...bank/Refractivity
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http://linked.open...atable-Bond-Count
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http://linked.open...ugbank/absorption
| - Rapidly and almost completely absorbed (70 to 90%) from the gastrointestinal tract following oral administration. (en)
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http://linked.open.../affectedOrganism
| - Enteric bacteria and other eubacteria (en)
- Mycobacterium tuberculosis (en)
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http://linked.open...casRegistryNumber
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http://linked.open...drugbank/category
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http://linked.open...gbank/containedIn
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http://linked.open...k/Bioavailability
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http://linked.open...bank/Ghose-Filter
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http://linked.open...nk/MDDR-Like-Rule
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http://linked.open...ank/Melting-Point
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http://linked.open...k/Number-of-Rings
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http://linked.open...siological-Charge
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http://linked.open...bank/Rule-of-Five
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http://linked.open...tional-IUPAC-Name
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http://linked.open...strongest-acidic-
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http://linked.open...-strongest-basic-
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