Almitrine

Chemical compound
  • R07AB07 (WHO)
Identifiers
  • 6-[4-[bis(4-fluorophenyl)methyl]piperazin-1-yl]-N,N'-
    diprop-2-enyl-1,3,5-triazine-2,4-diamine
CAS Number
  • 27469-53-0 checkY
PubChem CID
  • 33887
DrugBank
  • DB01430 checkY
ChemSpider
  • 31235 checkY
UNII
  • 9A1222NBG4
KEGG
  • D07126 checkY
ChEBI
  • CHEBI:53778 checkY
ChEMBL
  • ChEMBL1183717 ☒N
CompTox Dashboard (EPA)
  • DTXSID4057899 Edit this at Wikidata
ECHA InfoCard100.044.054 Edit this at WikidataChemical and physical dataFormulaC26H29F2N7Molar mass477.564 g·mol−13D model (JSmol)
  • Interactive image
Melting point181 °C (358 °F)
  • Fc1ccc(cc1)C(c2ccc(F)cc2)N4CCN(c3nc(nc(n3)NC\C=C)NC\C=C)CC4
InChI
  • InChI=1S/C26H29F2N7/c1-3-13-29-24-31-25(30-14-4-2)33-26(32-24)35-17-15-34(16-18-35)23(19-5-9-21(27)10-6-19)20-7-11-22(28)12-8-20/h3-12,23H,1-2,13-18H2,(H2,29,30,31,32,33) checkY
  • Key:OBDOVFRMEYHSQB-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Almitrine (marketed as Duxil by Servier) is a diphenylmethylpiperazine derivative classified as a respiratory stimulant by the ATC. It enhances respiration by acting as an agonist of peripheral chemoreceptors located on the carotid bodies. The drug increases arterial oxygen tension while decreasing arterial carbon dioxide tension in patients with chronic obstructive pulmonary disease. It may also prove useful in the treatment of nocturnal oxygen desaturation without impairing the quality of sleep. A significant literature exists for this compound, including over 60 papers that Medline labels as reviews.

The clinical efficacy of almitrine-raubasine combination therapy for age related cerebral disorders and functional rehabilitation after stroke has been reviewed by Allain and Bentué-Ferrer.[1] They summarize two studies in which almitrine-raubasine improved some symptoms significantly more than placebo, especially in vascular cases. Their paper also suggests that other studies have shown a beneficial effect of this compound on neurosensory vascular disorders, specifically chorioretinal dysfunctions (visual symptomatology) and vertigo associated with electronystagmographic modifications. This paper further claims that the dosage and tolerance of the compound have been confirmed in a French multi-center study of 5,361 outpatients.

Under the brand names Albasine, Aruxil, and Truxil, almitrine-raubasine has been marketed for rehabilitation after stroke, age related neurological disorders, visual disorders related to circulation, and tinnitus in Bangladesh.[2]

See also

References

  1. ^ Allain H, Bentué-Ferrer D (1998). "Clinical efficacy of almitrine-raubasine. An overview". European Neurology. 39 (Suppl. 1): 39–44. doi:10.1159/000052069. PMID 9516074. S2CID 46780859.
  2. ^ "Almitrine Bismesylate + Raubasine | অ্যালমিট্রিন বিসমিসাইলেট + রবাসিন | Indications, Pharmacology, Dosage, Side Effects & other Generic info with Available Brand names in Bangladesh | MedEx". MedEx. Retrieved 2022-04-07.
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Simple piperazines
(no additional rings)
Phenylpiperazines
Benzylpiperazines
Diphenylalkylpiperazines
(benzhydrylalkylpiperazines)
Pyrimidinylpiperazines
Pyridinylpiperazines
Benzo(iso)thiazolylpiperazines
Tricyclics
(piperazine attached via side chain)
Others/Uncategorized


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