Glibornuride
Names | |
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IUPAC name
1-(6-hydroxy-1,7,7-trimethyl-5-bicyclo[2.2.1]heptanyl)-3-(4-methylphenyl)sulfonylurea | |
Identifiers | |
26944-48-9 | |
DrugBank | DB08962 |
Jmol interactive 3D | Image |
KEGG | D02427 |
PubChem | 33649 |
UNII | VP83E7434R |
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Properties | |
C18H26N2O4S | |
Molar mass | 366.48 g/mol |
Pharmacology | |
ATC code | A10 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Glibornuride (INN) is an anti-diabetic drug from the group of sulfonylureas.[1]
Synthesis
Gliburnide is an endo-endo derivative made from camphor-3-carboxamode by borohydride reduction (exo approach), followed by Hofmann rearrangement to carbamate, followed by displacement with sodium tosylamide.
References
- ↑ Haupt E, Köberich W, Beyer J, Schöffling K (December 1971). "Pharmacodynamic aspects of tolbutamide, glibenclamide, glibornuride and glisoxepide. I. Dose response relations and repeated administration in diabetic subjects". Diabetologia 7 (6): 449–54. doi:10.1007/bf01212061. PMID 5004178.
- ↑ Bretschneider, H.; Hohenlohe-Oehringen, K.; Graßmayr, K. (1969). "Arylsulfonylureido- und Arylsulfonylamidoacyl-derivate von Oxy- und Oxo-cycloalkanen als potentielle Antidiabetica". Monatshefte für Chemie 100 (6): 2133. doi:10.1007/BF01151769.
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