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1 See also  





2 References  














Almitrine






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This article needs additional citations for verification. Please help improve this articlebyadding citations to reliable sources. Unsourced material may be challenged and removed.
Find sources: "Almitrine" – news · newspapers · books · scholar · JSTOR
(October 2011) (Learn how and when to remove this message)

Almitrine

Skeletal formula of almitrine

Ball-and-stick model of the almitrine molecule

Clinical data

AHFS/Drugs.com

International Drug Names

ATC code

Identifiers

  • 6-[4-[bis(4-fluorophenyl)methyl]piperazin-1-yl]-N,N'-
    diprop-2-enyl-1,3,5-triazine-2,4-diamine

CAS Number

PubChem CID

DrugBank

ChemSpider

UNII

KEGG

ChEBI

ChEMBL

CompTox Dashboard (EPA)

ECHA InfoCard

100.044.054 Edit this at Wikidata

Chemical and physical data

Formula

C26H29F2N7

Molar mass

477.564 g·mol−1

3D model (JSmol)

Melting point

181 °C (358 °F)

  • Fc1ccc(cc1)C(c2ccc(F)cc2)N4CCN(c3nc(nc(n3)NC\C=C)NC\C=C)CC4

  • 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 DuxilbyServier) 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 tinnitusinBangladesh.[2]

    See also[edit]

    References[edit]

    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.
  • ^ "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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  • Zacopride
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  • Nitric oxide
  • BW373U86
  • CX-546
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  • Simple piperazines
    (no additional rings)

  • Diethylcarbamazine
  • HEPPS
  • Midafotel
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  • DPI-221
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  • DPI-3290
  • GBR-12,783
  • GBR-12,935
  • GBR-13,069
  • GBR-13,098
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  • Hydroxyzine
  • Lidoflazine
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  • MT-45
  • Oxatomide
  • SNC-80
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  • t
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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Almitrine&oldid=1202463410"

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