This is an old revision of this page, as edited by Beetstra (talk | contribs) at 14:25, 6 December 2011 (Saving copy of the {{drugbox}} taken from revid 461256786 of page Sitagliptin for the Chem/Drugbox validation project (updated: '').). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
Revision as of 14:25, 6 December 2011 by Beetstra (talk | contribs) (Saving copy of the {{drugbox}} taken from revid 461256786 of page Sitagliptin for the Chem/Drugbox validation project (updated: '').)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)This page contains a copy of the infobox ({{drugbox}}) taken from revid 461256786 of page Sitagliptin with values updated to verified values. |
Clinical data | |
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AHFS/Drugs.com | Monograph |
MedlinePlus | a606023 |
License data |
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Routes of administration | Oral |
ATC code | |
Legal status | |
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Pharmacokinetic data | |
Bioavailability | 87% |
Protein binding | 38% |
Metabolism | Hepatic (CYP3A4- and CYP2C8-mediated) |
Elimination half-life | 8 to 14 h |
Excretion | Renal (80%) |
Identifiers | |
IUPAC name
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CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
ChEBI | |
ChEMBL | |
Chemical and physical data | |
Formula | C16H15F6N5O |
Molar mass | 407.314 g/mol g·mol |
3D model (JSmol) | |
SMILES
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InChI
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(what is this?) (verify) |
- ^ Herman GA (2005). "Pharmacokinetics and pharmacodynamics of sitagliptin, an inhibitor of dipeptidyl peptidase IV, in healthy subjects: results from two randomized, double-blind, placebo-controlled studies with single oral doses". Clin Pharmacol Ther. 78 (6): 675–88. doi:10.1016/j.clpt.2005.09.002. PMID 16338283.
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