Gliquidone

Chemical compound
  • C
Routes of
administrationOral (tablets)ATC code
  • A10BB08 (WHO)
Legal statusLegal status
  • UK: POM (Prescription only)
  • In general: ℞ (Prescription only)
Pharmacokinetic dataBioavailabilityHigh (Tmax = 2–3 hours)MetabolismExtensive hepaticOnset of action1–1.5 hoursExcretionBiliary (95%), renal (5%)Identifiers
  • 1-cyclohexyl-3-[4-[2-(7-methoxy-4,4-dimethyl-1,3-dioxoisoquinolin-2-yl)ethyl]phenyl]sulfonylurea
CAS Number
  • 33342-05-1
PubChem CID
  • 91610
DrugBank
  • DB01251 checkY
ChemSpider
  • 82719 checkY
UNII
  • C7C2QDD75P
KEGG
  • D02430 checkY
ChEMBL
  • ChEMBL383634 checkY
CompTox Dashboard (EPA)
  • DTXSID4023096 Edit this at Wikidata
ECHA InfoCard100.046.770 Edit this at WikidataChemical and physical dataFormulaC27H33N3O6SMolar mass527.64 g·mol−13D model (JSmol)
  • Interactive image
  • O=C(NC1CCCCC1)NS(=O)(=O)c2ccc(cc2)CCN4C(=O)c3c(ccc(OC)c3)C(C4=O)(C)C
  • InChI=1S/C27H33N3O6S/c1-27(2)23-14-11-20(36-3)17-22(23)24(31)30(25(27)32)16-15-18-9-12-21(13-10-18)37(34,35)29-26(33)28-19-7-5-4-6-8-19/h9-14,17,19H,4-8,15-16H2,1-3H3,(H2,28,29,33) checkY
  • Key:LLJFMFZYVVLQKT-UHFFFAOYSA-N checkY
  (verify)

Gliquidone (INN, sold under the trade name Glurenorm) is an anti-diabetic medication in the sulfonylurea class.[1] It is classified as a second-generation sulfonylurea. It is used in the treatment of diabetes mellitus type 2. It is marketed by the pharmaceutical company Boehringer Ingelheim (Germany).

Contraindications

Pharmacokinetics

Gliquidone is fully metabolized by the liver. Its metabolites are excreted virtually completely with bile (even with long-term administration), thus allowing the use of medication in diabetic patients with kidney disease and diabetic nephropathy.[2]

References

  1. ^ Malaisse WJ (2006). "Gliquidone contributes to improvement of type 2 diabetes mellitus management: a review of pharmacokinetic and clinical trial data". Drugs in R&D. 7 (6): 331–7. doi:10.2165/00126839-200607060-00002. PMID 17073516. S2CID 10155445.
  2. ^ a b "Glurenorm (gliquidone) 30 mg Tablets, for Oral Use. Full Prescribing Information". Russian State Register of Medicinal Products (in Russian). Boehringer Ingelheim. Archived from the original on 14 August 2016. Retrieved 12 July 2016.
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Oral diabetes medication, insulins and insulin analogs, and other drugs used in diabetes (A10)
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inhalable
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Non-insulins
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Combinations
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Calcium
VDCCsTooltip Voltage-dependent calcium channels
Blockers
Activators
Potassium
VGKCsTooltip Voltage-gated potassium channels
Blockers
Activators
IRKsTooltip Inwardly rectifying potassium channel
Blockers
Activators
  • GIRKTooltip G protein-coupled inwardly rectifying potassium channel-specific: ML-297 (VU0456810)
KCaTooltip Calcium-activated potassium channel
Blockers
  • BKCa-specific: Ethanol (alcohol)
  • GAL-021
Activators
K2PsTooltip Tandem pore domain potassium channel
Blockers
Activators
Sodium
VGSCsTooltip Voltage-gated sodium channels
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Activators
ENaCTooltip Epithelial sodium channel
Blockers
Activators
  • Solnatide
ASICsTooltip Acid-sensing ion channel
Blockers
Chloride
CaCCsTooltip Calcium-activated chloride channel
Blockers
Activators
CFTRTooltip Cystic fibrosis transmembrane conductance regulator
Blockers
Activators
Unsorted
Blockers
Others
TRPsTooltip Transient receptor potential channels
  • See here instead.
LGICsTooltip Ligand gated ion channels
  • See here instead.
See also: Receptor/signaling modulators • Transient receptor potential channel modulators


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