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Dyclonine
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Dyclonine

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Dyclonine
Dyclonine Structural Formula V.1.svg
Clinical data
Trade names Sucrets
AHFS/Drugs.com Monograph
Routes of
administration
Lozenge
ATC code
Legal status
Legal status
Identifiers
  • 1-(4-butoxyphenyl)-3-(1-piperidyl)propan-1-one
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
Formula C18H27NO2
Molar mass 289.419 g·mol−1
3D model (JSmol)
  • O=C(c1ccc(OCCCC)cc1)CCN2CCCCC2
  • InChI=1S/C18H27NO2/c1-2-3-15-21-17-9-7-16(8-10-17)18(20)11-14-19-12-5-4-6-13-19/h7-10H,2-6,11-15H2,1H3 checkY
  • Key:BZEWSEKUUPWQDQ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Dyclonine (Dyclocaine) is an oral anaesthetic that is the active ingredient of Sucrets, an over-the-counter throat lozenge. It is also found in some varieties of the Cepacol sore throat spray. It is a local anesthetic, used topically as the hydrochloride salt.

History

The product Sucrets was introduced in Baltimore, Maryland, by Sharp & Dohme in 1932.

In 1966 the Federal Trade Commission ordered Merck and Company to discontinue the false claims of germ-killing and pain-relieving properties for its Sucrets and Children's Sucrets throat lozenges. In 1977, it was acquired by Beecham, later merging with SmithKline Beckman in 1989 to form SmithKline Beecham. By 1994 the brand switched from a metal container to a plastic container. SmithKline Beecham, after announcing a merger with GlaxoWellcome to form GlaxoSmithKline, sold the brand in 2000 to Insight Pharmaceuticals. In 2011, Sucrets reintroduced their product back into the familiar tin due to popular demand and nostalgia.

See also

External links



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