Adrenalone

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Adrenalone
Adrenalone.svg
Systematic (IUPAC) name
1-(3,4-dihydroxyphenyl)-2-(methylamino)ethanone
Clinical data
Pregnancy cat.
  • No data
Legal status
?
Routes Topical
Pharmacokinetic data
Metabolism MAO, COMT
Excretion Renal
Identifiers
CAS number 99-45-6 N
62-13-5 (hydrochloride)
ATC code A01AD06 B02BC05
PubChem CID 7436
ChemSpider 7158 YesY
UNII EGU41QL329 YesY
KEGG D02774 YesY
ChEMBL CHEMBL2103996 N
Chemical data
Formula C9H11NO3 
Mol. mass 181.189 g/mol
Physical data
Melt. point 235–236 °C (455–457 °F) (decomposes)
 N (what is this?)  (verify)

Adrenalone is an adrenergic agonist used as a topical vasoconstrictor and hemostatic. Formerly, it was also used to prolong the action of local anesthetics. It is the ketone form of epinephrine (adrenaline). Contrary to epinephrine, adrenalone mainly acts on alpha-1 adrenergic receptors, but has little affinity for beta receptors. The drug is largely obsolete, being superseded by other hemostatics such as thrombin, fibrinogen, and vasopressin analogues.[1]

Contraindications and interactions[edit]

Adrenalone does not stop bleeding from large blood vessels. It is not approved for systemic use. Combination with antithrombotics is not useful because they contravene the action of adrenalone.[1]

Side effects[edit]

Vasoconstriction by adrenalone may lead to local necrosis.[1]

Pregnancy and lactation[edit]

Adrenalone passes into breast milk, but adverse effects are unlikely because of its very low systemic resorption.[1]

Chemical properties[edit]

Adrenalone is a derivative of epinephrine, having the alcohol function replaced with a ketone. As a consequence, it is not optically active any more.

Solubility in water, ethanol and diethyl ether is low. The substance is typically used in form of the hydrochloride, a white crystalline powder which tastes bitter and slightly acidic, and is soluble in water (1:8) and 94% ethanol (1:45). The melting point of the hydrochloride is 243 °C (469 °F).[1]

Pharmacology[edit]

After local application, only traces of adrenalone are found in the blood, which is partly a consequence of the vasoconstriction caused by the drug via alpha-1 adrenergic receptors. In an (unspecified) pharmacological model, hypertensive (blood pressure increasing) action has been found to be about 0.5% that of epinephrine at equivalent plasma concentrations. Therefore, systemic effects are unlikely.

Like epinephrine, adrenalone is metabolised by catechol-O-methyl transferase (COMT), yielding 3O-methyladrenalone, which in turn is N-demethylized by monoamine oxidase (MAO). Alternatively, it can first undergo metabolization by MAO and then by COMT; in both cases, the resulting 3O-methyl-N-demethyladrenalone is conjugated to sulfate or glucuronide and excreted by the kidney. No reduction to epinephrine has been observed in vivo.[1]

References[edit]

  1. ^ a b c d e f Dinnendahl, V.; Fricke, U., eds. (2010). Arzneistoff-Profile (in German) 4 (23 ed.). Eschborn, Germany: Govi Pharmazeutischer Verlag. ISBN 978-3-7741-9846-3.