Mepyramine

First generation antihistamine

  • R06AC01 (WHO) D04AA02 (WHO)
Legal statusLegal status
  • In general: Over-the-counter (OTC)
Identifiers
  • N-(4-methoxybenzyl)-N',N'-dimethyl-N-pyridin-2-ylethane-1,2-diamine
CAS Number
  • 91-84-9 checkY
    59-33-6 (maleate)
PubChem CID
  • 4992
IUPHAR/BPS
  • 1227
DrugBank
  • DB06691 ☒N
ChemSpider
  • 4818 checkY
UNII
  • HPE317O9TL
KEGG
  • D08183 checkY
ChEBI
  • CHEBI:6762 ☒N
ChEMBL
  • ChEMBL511 checkY
CompTox Dashboard (EPA)
  • DTXSID9023542 Edit this at Wikidata
ECHA InfoCard100.001.912 Edit this at WikidataChemical and physical dataFormulaC17H23N3OMolar mass285.391 g·mol−13D model (JSmol)
  • Interactive image
  • O(c1ccc(cc1)CN(c2ncccc2)CCN(C)C)C
InChI
  • InChI=1S/C17H23N3O/c1-19(2)12-13-20(17-6-4-5-11-18-17)14-15-7-9-16(21-3)10-8-15/h4-11H,12-14H2,1-3H3 checkY
  • Key:YECBIJXISLIIDS-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Mepyramine, also known as pyrilamine, is a first generation antihistamine, targeting the H1 receptor as an inverse agonist.[1] Mepyramine rapidly permeates the brain, often causing drowsiness.[2] It is often sold as a maleate salt, pyrilamine maleate.

The medication has negligible anticholinergic activity, with 130,000-fold selectivity for the histamine H1 receptor over the muscarinic acetylcholine receptors (for comparison, diphenhydramine had 20-fold selectivity for the H1 receptor).[3]

It was patented in 1943 and came into medical use in 1949.[4] It was marketed under the names Histadyl, Histalon, Neo-Antergan, Neo-Pyramine, and Nisaval.[5] In the 1960s and 70s it was a very common component in over-the-counter sleep aids such as Alva-Tranquil, Dormin, Sedacaps, Sominex, Nytol, and many others.[5] The US FDA included it in the list of chemicals and compounds barred from use in over-the-counter nighttime sleep aid products in 1989.[6]

It is used in over-the-counter combination products to treat the common cold and menstrual symptoms such as Midol Complete.[7] It is also the active ingredient of the topical antihistamine creams Anthisan[8] and Neoantergan[1] sold for the treatment of insect bites, stings, and nettle rash.

See also

References

  1. ^ a b Parsons, Mike E.; Ganellin, C. Robin (January 2006). "Histamine and its receptors". British Journal of Pharmacology. 147 (Suppl 1) (published 2 February 2009): S127–S135. doi:10.1038/sj.bjp.0706440. PMC 1760721. PMID 16402096.
  2. ^ "Mepyramine". drugbank.com. Retrieved 8 May 2021.
  3. ^ Kubo, Nobuo; Shirakawa, Osamu; Kuno, Takayoshi; Tanaka, Chikako (March 1987). "Antimuscarinic effects of antihistamines: quantitative evaluation by receptor-binding assay". Japanese Journal of Pharmacology. 43 (3): 277–282. doi:10.1254/jjp.43.277. PMID 2884340.
  4. ^ Fischer, János; Gannelin, C. Robin, eds. (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 545. ISBN 9783527607495.
  5. ^ a b Thornton, William E. (September 1977). "Sleep aids and sedatives". Journal of the American College of Emergency Physicians. 6 (9): 408–412. doi:10.1016/S0361-1124(77)80006-3. PMID 330911.
  6. ^ 54 FR 6826
  7. ^ "Active Ingredients for Midol Complete". Bayer HealthCare LLC. Archived from the original on 2 December 2009. Retrieved 8 December 2009.
  8. ^ "Anthisan Cream - Patient Information Leaflet (PIL)". Medicines.org.
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See also: Receptor/signaling modulators • Monoamine releasing agents • Adrenergics • Dopaminergics • Serotonergics • Monoamine metabolism modulators • Monoamine neurotoxins
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See also: Receptor/signaling modulators
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