Corbadrine

Chemical compound
title: "Corbadrine" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public tags: ["alpha1-adrenergic-agonists", "alpha2-adrenergic-agonists", "beta-adrenergic-agonists", "beta-hydroxyamphetamines", "catecholamines", "decongestants", "human-drug-metabolites", "norepinephrine-releasing-agents", "vasoconstrictors"] description: "Chemical compound" topic_path: "general/alpha1-adrenergic-agonists" source: "https://en.wikipedia.org/wiki/Corbadrine" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0
::summary Chemical compound ::
| Verifiedfields = verified | verifiedrevid = 462091113 | IUPAC_name = 4-[(1R,2S)-2-amino-1-hydroxypropyl]benzene-1,2-diol | image = Corbadrine.svg | image_class = skin-invert-image | width = 200px
| tradename = Neo-Cobefrine | pregnancy_category = | legal_status = Rx-only | routes_of_administration =
| bioavailability = | metabolism = | elimination_half-life = | excretion =
| CAS_number_Ref = | CAS_number = 829-74-3 | ATC_prefix = None | ATC_suffix = | PubChem = 164739 | IUPHAR_ligand = 508 | DrugBank_Ref = | DrugBank = DB06707 | ChemSpiderID_Ref = | ChemSpiderID = 144416 | UNII_Ref = | UNII = V008L6478D | KEGG_Ref = | KEGG = D02388 | ChEMBL_Ref = | ChEMBL = 677 | synonyms = Levonordefrin; α-Methylnorepinephrine; (–)-3,4-Dihydroxynorephedrine; 3,4,β-Trihydroxy-α-methylphenethylamine; 3,4,β-Trihydroxyamphetamine
| C=9 | H=13 | N=1 | O=3 | SMILES = Oc1ccc(cc1O)C@@HC@@HC | StdInChI_Ref = | StdInChI = 1S/C9H13NO3/c1-5(10)9(13)6-2-3-7(11)8(12)4-6/h2-5,9,11-13H,10H2,1H3/t5-,9-/m0/s1 | StdInChIKey_Ref = | StdInChIKey = GEFQWZLICWMTKF-CDUCUWFYSA-N
Corbadrine, sold under the brand name Neo-Cobefrine and also known as levonordefrin and α-methylnorepinephrine, is a catecholamine sympathomimetic used as a topical nasal decongestant and vasoconstrictor in dentistry in the United States. It is usually used in a pre-mixed solution with local anesthetics, such as mepivacaine.
The drug acts as a non-selective agonist of the α1-, α2-, and β-adrenergic receptors. It is said to have preferential activity at the α2-adrenergic receptor.
Corbadrine is also a metabolite of the antihypertensive drug methyldopa and plays a role in its pharmacology and effects.
Pharmacology
Pharmacokinetics
Corbadrine is metabolized primarily by catechol O-methyltransferase (COMT).
Chemistry
Corbadrine, also known as 3,4,β-trihydroxy-α-methylphenethylamine or as 3,4,β-trihydroxyamphetamine, as well as α-methylnorepinephrine or (–)-3,4-dihydroxynorephedrine, is a substituted phenethylamine and amphetamine derivative.
Analogues of corbadrine include α-methyldopamine, dioxifedrine (3,4-dihydroxyephedrine; α-methylepinephrine), dioxethedrin (3,4-dihydroxy-N-ethylnorephedrine; α-methyl-N-ethylnorepinephrine), and hydroxyamphetamine (4-hydroxyamphetamine; α-methyltyramine).
Society and culture
Names
Corbadrine is the generic name of the drug and its . It is also known as levonordefrin, which is its . Synonyms of corbadrine include α-methylnorepinephrine and (–)-3,4-dihydroxynorephedrine. The drug has been sold under the brand name Neo-Cobefrine.
References
References
- Elks, J.. (2014). "The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies". Springer US.
- (31 October 1999). "Concise Dictionary of Pharmacological Agents: Properties and Synonyms". Springer Science & Business Media.
- (January 2000). "Index Nominum 2000: International Drug Directory". Taylor & Francis.
- "DailyMed — Search results for levonordefrin".
- Logothetis, D.D.. (2016). "Local Anesthesia for the Dental Hygienist". Elsevier Health Sciences.
- Abraham, Donald J.. (15 January 2003). "Burger's Medicinal Chemistry and Drug Discovery". Wiley.
- (October 2002). "Vasoconstrictors: indications and precautions". Dent Clin North Am.
- (October 1963). "Studies on the Metabolism and Mechanism of Action of Methyldopa". Circulation.
- "Levonordefrin".
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