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rdf:type
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http://linked.open...gbank/description
| - One of the first narrow spectrum macrocyclic antibiotic, it is a natural compound and is structurally similar to compounds in lipiarmycin-a fermentation mixture. FDA approved on May 27, 2011. (en)
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http://linked.open...y/drugbank/dosage
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http://linked.open...generalReferences
| - # Artsimovitch I, Seddon J, Sears P: Fidaxomicin is an inhibitor of the initiation of bacterial RNA synthesis. Clin Infect Dis. 2012 Aug;55 Suppl 2:S127-31. doi: 10.1093/cid/cis358. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/22752861 # Crawford T, Huesgen E, Danziger L: Fidaxomicin: a novel macrocyclic antibiotic for the treatment of Clostridium difficile infection. Am J Health Syst Pharm. 2012 Jun 1;69(11):933-43. doi: 10.2146/ajhp110371. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/22610025 (en)
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http://linked.open...gy/drugbank/group
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http://linked.open...drugbank/halfLife
| - 200 mg, healthy subjects = 11.7 hours (en)
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http://linked.open...ugbank/indication
| - Treatment of Clostridium difficile-associated diarrhea (en)
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sameAs
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Title
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adms:identifier
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http://linked.open...mechanismOfAction
| - Fidaxomicin is a bactericidal-type antibiotic that inhibits RNA polymerase sigma subunit. RNA polymerase is responsible for transcription in the bacteria therefore fidaxomicin will inhibit protein synthesis. As a result, apoptosis is triggered in susceptible organisms such as C. difficile. (en)
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http://linked.open...y/drugbank/patent
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http://linked.open...outeOfElimination
| - Feces (>92% as unchanged drugs and metabolites) and urine (<1% of drug was excreted) (en)
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http://linked.open.../drugbank/synonym
| - Dificid (en)
- Difimicin (en)
- Lipiarmicin (en)
- Lipiarmycin (en)
- Lipiarrmycin (en)
- OPT 80 (en)
- OPT-80 (en)
- PAR 101 (en)
- PAR-101 (en)
- Tiacumicin B (en)
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http://linked.open...umeOfDistribution
| - Fidaxomicin is largely confined in the gastrointestinal tract and is not distributed extensively in the systemic. (en)
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http://linked.open.../drug/hasAHFSCode
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http://linked.open...k/foodInteraction
| - Food decreases Cmax of fidaxomicin and its metabolites however this is not considered clinically significant. (en)
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http://linked.open...ynthesisReference
| - Youe-Kong Shue, Chi-Jen Frank Du, Ming-Hsi Chiou, Mei-Chiao Wu, Yuan-Ting Chen, Franklin W. Okumu, Jonathan James Duffield, "Medium for the Production of Tiacumicin B." U.S. Patent US20100028970, issued February 04, 2010. (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
| - Fidaxomicin is not systemically absorbed as shown by a plasma concentrations below the lower limit of quantification after single-dose or multiple-dose. In contrast, fecal concentrations of fidaxomicin are much higher and are concentration-dependent. Cmax = 2 hours; Tmax = 5.2 ng/mL; AUC = 14 ng•hr/mL (en)
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http://linked.open.../affectedOrganism
| - Gram-positive Bacteria (en)
- Peptoclostridium difficile (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...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...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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