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Anisodine

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This is an old revision of this page, as edited by Machinexa (talk | contribs) at 13:48, 21 December 2020 (https://bpspubs.onlinelibrary.wiley.com/doi/10.1111/j.1476-5381.1986.tb10201.x It is concluded that both anisodamine and to a lesser extent anisodine possess α‐adrenoceptor blocking properties; this antagonistic activity of anisodamine may contribute to its salutary effects on the microcirculation. However, it is unlikely that anisodine produces a significant adrenoceptor blockade in the clinically used dose‐range.). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Anisodine
Clinical data
ATC code
  • none
Identifiers
  • 9-methyl-3-oxa-9-azatricyclo[3.2.1.02,4]non-7-yl α-hydroxy-α-(hydroxymethyl)benzeneacetate
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC17H21NO5
Molar mass319.357 g·mol−1
3D model (JSmol)
  • O=C(OC1CC2N(C(C1)C3OC23)C)C(O)(c4ccccc4)CO
  • InChI=1S/C17H21NO5/c1-18-12-7-11(8-13(18)15-14(12)23-15)22-16(20)17(21,9-19)10-5-3-2-4-6-10/h2-6,11-15,19,21H,7-9H2,1H3/t11?,12-,13+,14-,15+,17-/m1/s1 checkY
  • Key:JEJREKXHLFEVHN-QDXGGTILSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Anisodine, also known as daturamine and α-hydroxyscopolamine, is an antispasmodic and anticholinergic drug used in the treatment of acute circulatory shock in China.[1][2] It is a tropane alkaloid and is found naturally in plants of the family Solanaceae.[2] Anisodine acts as a muscarinic acetylcholine receptor antagonist and α1-adrenergic receptor antagonist.[1]

See also

References

  1. ^ a b Varma DR, Yue TL (March 1986). "Adrenoceptor blocking properties of atropine-like agents anisodamine and anisodine on brain and cardiovascular tissues of rats". British Journal of Pharmacology. 87 (3): 587–94. doi:10.1111/j.1476-5381.1986.tb10201.x. PMC 1916562. PMID 2879586.
  2. ^ a b Ganellin, C. R.; Triggle, David J. (21 November 1996). Dictionary of pharmacological agents - Google Books. ISBN 9780412466304.


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