Triprolidine
Verifiedfieldschanged
Watchedfieldschanged
Verifiedrevid470617213
Iupac name2-[(E)-1-(4-methylphenyl)-3-pyrrolidin-1-yl-
prop-1-enyl]pyridine
TradenameFlonase Nighttime Allergy Relief, Actidil, others
Pregnancy categoryC (US)
Legal usotc
Routes of administrationBy mouth
BioavailabilityOral: 4%
Protein bound90%
MetabolismHepatic (CYP2D6)
Elimination half-life4–6 hours
ExcretionRenal
Cas number486-12-4
Atc prefixR06
Atc suffixAX07
Pubchem5282443
Iuphar ligand1228
DrugbankDB00427
Chemspiderid4445597
Unii2L8T9S52QM
KeggD01782
Chebi84116
Chembl855
C19
H22
N2
Smilesn3c(\C(=C\CN1CCCC1)c2ccc(cc2)C)cccc3
Stdinchi1S/C19H22N2/c1-16-7-9-17(10-8-16)18(19-6-2-3-12-20-19)11-15-21-13-4-5-14-21/h2-3,6-12H,4-5,13-15H2,1H3/b18-11+
StdinchikeyCBEQULMOCCWAQT-WOJGMQOQSA-N
Melting point60
Solubility500

Triprolidine is an over-the-counter first-generation antihistamine with strong anticholinergic properties.[1] It is used to combat the symptoms associated with allergies and is sometimes combined with other medications in preparations designed to provide general relief for flu-like symptoms.[2] As with many antihistamines, the most common side effect is drowsiness.[1]

Triprolidine was patented in 1948 and came into medical use in 1953,[3] and has mostly been replaced in popular cold and flu medications by other drugs such as diphenhydramine, promethazine, chlorpheniramine, loratadine and fexofenadine.

See also

References

  1. ^ Goldsmith P, Dowd PM (January 1993). "The new H1 antihistamines. Treatment of urticaria and other clinical problems". Dermatologic Clinics. 11 (1): 87–95. doi:10.1016/S0733-8635(18)30285-7. PMID 8094649
  2. ^ Williams BO, Liao SH, Lai AA, Arnold JD, Perkins JG, Blum MR, Findlay JW (1984). "Bioavailability of pseudoephedrine and triprolidine from combination and single-ingredient products". Clinical Pharmacy. 3 (6): 638–43. PMID 6509877
  3. ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 546. ISBN 9783527607495.