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Bromantane information


Bromantane
Clinical data
Trade namesLadasten
Other namesBromantan; Bromontan; ADK-709; Adamantylbromphenylamine
Routes of
administration
Oral (tablets)
ATC code
  • None
Legal status
Legal status
  • US: Unscheduled not FDA approved
  • Rx-only (RU)
Pharmacokinetic data
Bioavailability27.5%
Elimination half-life11.21 hours (in humans),[1]
7 hours (in rats)[2]
Identifiers
IUPAC name
  • N-(4-Bromophenyl)adamantan-2-amine
CAS Number
  • 87913-26-6 checkY
PubChem CID
  • 4660557
ChemSpider
  • 3849628 ☒N
UNII
  • N1ILS53XWK
CompTox Dashboard (EPA)
  • DTXSID40405333 Edit this at Wikidata
ECHA InfoCard100.213.907 Edit this at Wikidata
Chemical and physical data
FormulaC16H20BrN
Molar mass306.247 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • C1C2CC3CC1CC(C2)C3NC4=CC=C(C=C4)Br
InChI
  • InChI=1S/C16H20BrN/c17-14-1-3-15(4-2-14)18-16-12-6-10-5-11(8-12)9-13(16)7-10/h1-4,10-13,16,18H,5-9H2 ☒N
  • Key:LWJALJDRFBXHKX-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Bromantane, sold under the brand name Ladasten, is an atypical psychostimulant and anxiolytic drug of the adamantane family related to amantadine and memantine which is used in Russia in the treatment of neurasthenia. Although the effects of the bromantane have been determined to be dependent on the dopaminergic and possibly serotonergic neurotransmitter systems, its exact mechanism of action is unknown,[3][4] and it is distinct in its properties relative to typical psychostimulants such as amphetamine. Because of its unique aspects, bromantane has sometimes been described instead as an actoprotector.[5][6]

  1. ^ "Ladasten (adamantylbromphenylamine) Tablets for Oral Use. Full Prescribing Information". Russian State Register of Medicines (in Russian). Lekko CJSC. p. 1. Archived from the original on 3 February 2016. Retrieved 27 January 2016.
  2. ^ Neild PJ, Gazzard BG (September 1997). "HIV-1 infection in China". Lancet. 350 (9082): 963. doi:10.1016/S0140-6736(05)63309-0. PMID 9314899. S2CID 40317188.
  3. ^ Grekhova TV, Gainetdinov RR, Sotnikova TD, Krasnykh LM, Kudrin VS, Sergeeva SA, Morozov IS (1995). "Effect of bromantane, a new immunostimulating agent with psychostimulating activity, on the release and metabolism of dopamine in the striatum of freely moving rats. A microdialysis study". Bulletin of Experimental Biology and Medicine. 119 (3): 294–296. doi:10.1007/BF02445840. ISSN 0007-4888. S2CID 33214442.
  4. ^ Iezhitsa IN, Spasov AA, Bugaeva LI (2001). "Effects of bromantan on offspring maturation and development of reflexes". Neurotoxicology and Teratology. 23 (2): 213–222. doi:10.1016/S0892-0362(01)00119-2. PMID 11348840.
  5. ^ Spasov AA, Khamidova TV, Bugaeva LI, Morozov IS (2000). "Adamantane derivatives: Pharmacological and toxicological properties (review)". Pharmaceutical Chemistry Journal. 34 (1): 1–7. doi:10.1007/BF02524549. ISSN 0091-150X. S2CID 41620120.
  6. ^ Morozov IS, Ivanova IA, Lukicheva TA (2001). "Actoprotector and Adaptogen Properties of Adamantane Derivatives (A Review)". Pharmaceutical Chemistry Journal. 35 (5): 235–238. doi:10.1023/A:1011905302667. ISSN 0091-150X. S2CID 29475883.

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