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Adosopine

From Wikipedia, the free encyclopedia
Adosopine
Names
Preferred IUPAC name
N-(5-Methyl-6,11-dioxo-6,11-dihydro-5H-dibenzo[b,e]azepin-10-yl)acetamide
Other names
Adosupine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard100.081.230Edit this at Wikidata
UNII
  • InChI=1S/C17H14N2O3/c1-10(20)18-13-8-5-7-12-15(13)16(21)11-6-3-4-9-14(11)19(2)17(12)22/h3-9H,1-2H3,(H,18,20)
    Key: KLSKLNWJEDXFSD-UHFFFAOYSA-N
  • InChI=1/C17H14N2O3/c1-10(20)18-13-8-5-7-12-15(13)16(21)11-6-3-4-9-14(11)19(2)17(12)22/h3-9H,1-2H3,(H,18,20)
    Key: KLSKLNWJEDXFSD-UHFFFAOYAV
  • CC(=O)NC1=CC=CC2=C1C(=O)C3=CC=CC=C3N(C2=O)C
Properties
C17H14N2O3
Molar mass294.310 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Adosopine is adibenzoazepinedrug that has been studied for the treatment ofurinary incontinence.[1][2]

References

[edit]
  1. ^Perico, A; Triolo, A; Viti, G; Mannucci, C; Caviglioli, G; Cocchini, A; Pestellini, V; Paoli, P; Dapporto, P (1994). "Synthesis, characterization, and analytical studies of adosupine, a potential new drug for urinary incontinence".Journal of Pharmaceutical Sciences.83 (2):137–42.doi:10.1002/jps.2600830206.PMID 8169779.
  2. ^d'Aranno, V; Mancinelli, A; Manzini, S (1992). "Determination of the tricyclic compound adosupine and its three metabolites in plasma and brain of rat using high-performance liquid chromatography".Journal of Chromatography.574 (2):319–25.doi:10.1016/0378-4347(92)80046-s.PMID 1618966.


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