Corbadrine

In this article we will address the topic of Corbadrine, which has sparked great interest and debate in recent years. Corbadrine has aroused the curiosity of researchers, academics and the general public, due to its relevance in different areas of society. From its impact on the economy, politics, culture, to its influence on people's daily lives, Corbadrine has become a central topic of discussion and reflection. Along these lines we will analyze different perspectives and opinions about Corbadrine, with the aim of offering a broad and enriching vision of this topic that is so relevant today.
Corbadrine
Clinical data
ATC code
  • none
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • 4-benzene-1,2-diol
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.113.606 Edit this at Wikidata
Chemical and physical data
FormulaC9H13NO3
Molar mass183.207 g·mol−1
3D model (JSmol)
  • Oc1ccc(cc1O)(O)(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
 ☒NcheckY (what is this?)  (verify)

Corbadrine (INN; marketed as Neo-Cobefrine), also known as levonordefrin (USAN) and α-methylnorepinephrine, is a catecholamine sympathomimetic used as a topical nasal decongestant and vasoconstrictor in dentistry in the United States, (usually in a pre-mixed solution with local anesthetics, such as mepivacaine).

Corbadrine is also a metabolite of the antihypertensive drug methyldopa, and plays a role in its pharmacology and effects.

See also

References

  1. ^ Morton 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.
  2. ^ Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 275–. ISBN 978-3-88763-075-1.
  3. ^ "DailyMed — Search results for levonordefrin". DailyMed. Retrieved 20 February 2016.
  4. ^ 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.

External links