Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Corbadrine

From Wikipedia, the free encyclopedia
(Redirected fromLevonordefrin)
Chemical compound
Pharmaceutical compound
Corbadrine
Clinical data
Trade namesNeo-Cobefrine
Other namesLevonordefrin; α-Methylnorepinephrine; (–)-3,4-Dihydroxynorephedrine; 3,4,β-Trihydroxy-α-methylphenethylamine; 3,4,β-Trihydroxyamphetamine
ATC code
  • None
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • 4-[(1R,2S)-2-amino-1-hydroxypropyl]benzene-1,2-diol
CAS Number
PubChemCID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.113.606Edit this at Wikidata
Chemical and physical data
FormulaC9H13NO3
Molar mass183.207 g·mol−1
3D model (JSmol)
  • Oc1ccc(cc1O)[C@@H](O)[C@@H](N)C
  • InChI=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 checkY
  • Key:GEFQWZLICWMTKF-CDUCUWFYSA-N checkY
  (verify)

Corbadrine, sold under the brand nameNeo-Cobefrine and also known aslevonordefrin andα-methylnorepinephrine, is acatecholaminesympathomimetic used as atopicalnasaldecongestant andvasoconstrictor indentistry in theUnited States.[1][2][3] It is usually used in a pre-mixed solution withlocal anesthetics, such asmepivacaine.[4]

The drug acts as anon-selectiveagonist of theα1-,α2-, andβ-adrenergic receptors.[5][6][7] It is said to have preferential activity at the α2-adrenergic receptor.[5][7]

Corbadrine is also ametabolite of theantihypertensive drugmethyldopa and plays a role in itspharmacology and effects.[8]

Pharmacology

[edit]

Pharmacokinetics

[edit]

Corbadrine ismetabolized primarily bycatecholO-methyltransferase (COMT).[7]

Chemistry

[edit]

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 asubstituted phenethylamine andamphetaminederivative.[1][3]

Analogues of corbadrine includeα-methyldopamine,dioxifedrine (3,4-dihydroxyephedrine; α-methylepinephrine),dioxethedrin (3,4-dihydroxy-N-ethylnorephedrine; α-methyl-N-ethylnorepinephrine), andhydroxyamphetamine (4-hydroxyamphetamine; α-methyltyramine).

Society and culture

[edit]

Names

[edit]

Corbadrine is thegeneric name of the drug and itsINNTooltip International Nonproprietary Name.[1][3][2] It is also known aslevonordefrin, which is itsUSANTooltip United States Adopted Name.[1][3][2] Synonyms of corbadrine includeα-methylnorepinephrine and(–)-3,4-dihydroxynorephedrine.[9] The drug has been sold under the brand nameNeo-Cobefrine.[3]

References

[edit]
  1. ^abcdElks, J. (2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 55.ISBN 978-1-4757-2085-3. Retrieved30 August 2024.
  2. ^abcMorton I, Morton IK, Hall JM (31 October 1999).Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 164–.ISBN 978-0-7514-0499-9.
  3. ^abcdeIndex Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 275–.ISBN 978-3-88763-075-1.
  4. ^"DailyMed — Search results for levonordefrin".DailyMed. Retrieved20 February 2016.
  5. ^abLogothetis, D.D. (2016).Local Anesthesia for the Dental Hygienist. Elsevier Health Sciences. p. 46.ISBN 978-0-323-43050-0. Retrieved30 August 2024.
  6. ^Abraham, Donald J. (15 January 2003).Burger's Medicinal Chemistry and Drug Discovery. Wiley.doi:10.1002/0471266949.bmc093.ISBN 978-0-471-26694-5.
  7. ^abcNaftalin LW, Yagiela JA (October 2002). "Vasoconstrictors: indications and precautions".Dent Clin North Am.46 (4):733–746, ix.doi:10.1016/s0011-8532(02)00021-6.PMID 12436828.
  8. ^Sjoerdsma A, Vendsalu A, Engelman K (October 1963)."Studies on the Metabolism and Mechanism of Action of Methyldopa".Circulation.28 (4):492–502.doi:10.1161/01.CIR.28.4.492.PMID 14068757.
  9. ^"Levonordefrin".PubChem. Retrieved30 August 2024.

External links

[edit]
Decongestants and other nasal preparations (R01)
Topical
Sympathomimetics, plain
Antiallergic agents,
excluding corticosteroids
Corticosteroids
Other nasal preparations
Combination products
Systemic use:
Sympathomimetics
Adamantanes
Adenosine antagonists
Alkylamines
Ampakines
Arylcyclohexylamines
Benzazepines
Cathinones
Cholinergics
Convulsants
Eugeroics
Oxazolines
Phenethylamines
Phenylmorpholines
Piperazines
Piperidines
Phenethylpyrrolidines
Racetams
Psychedelics
Tropanes
Tryptamines
Others
α1
Agonists
Antagonists
α2
Agonists
Antagonists
β
Agonists
Antagonists
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Retrieved from "https://en.wikipedia.org/w/index.php?title=Corbadrine&oldid=1312020127"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp