Delucemine

Last updated

Delucemine
Delucemine.svg
Clinical data
ATC code
  • none
Identifiers
  • 3,3-Bis(3-fluorophenyl)-N-methylpropan-1-amine
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
Formula C16H17F2N
Molar mass 261.316 g·mol−1
3D model (JSmol)
  • CNCCC(C1=CC(=CC=C1)F)C2=CC(=CC=C2)F
  • InChI=1S/C16H17F2N/c1-19-9-8-16(12-4-2-6-14(17)10-12)13-5-3-7-15(18)11-13/h2-7,10-11,16,19H,8-9H2,1H3 X mark.svgN
  • Key:MUGNLPWYHGOJEG-UHFFFAOYSA-N X mark.svgN
 X mark.svgNYes check.svgY  (what is this?)    (verify)

Delucemine (NPS-1506) is a drug which acts as an NMDA antagonist and a serotonin reuptake inhibitor, and has neuroprotective effects. [1] [2] It was originally investigated for the treatment of stroke and in 2004 was studied as a potential antidepressant. [3] [4] [5]

Contents

Origin

The structure of delucemine is based on argiotoxin 636, a NMDA antagonist isolated from the venom of Argiope aurantia . [6] [7] [8]

See also

References

  1. Mueller AL, Artman LD, Balandrin MF, Brady E, Chien Y, Delmar EG, George K, Kierstead A, Marriott TB, Moe ST, Newman MK, Raszkiewicz JL, Sanguinetti EL, van Wagenen BC, Wells D (December 1999). "NPS 1506, a novel NMDA receptor antagonist and neuroprotectant. Review of preclinical and clinical studies". Annals of the New York Academy of Sciences. 890 (1): 450–7. Bibcode:1999NYASA.890..450M. doi:10.1111/j.1749-6632.1999.tb08023.x. PMID   10668449. S2CID   5629889.
  2. Leoni MJ, Chen XH, Mueller AL, Cheney J, McIntosh TK, Smith DH (December 2000). "NPS 1506 attenuates cognitive dysfunction and hippocampal neuron death following brain trauma in the rat". Experimental Neurology. 166 (2): 442–9. doi:10.1006/exnr.2000.7513. PMID   11085909. S2CID   39222349.
  3. "NPS Pharmaceuticals Inc, Form 10-Q, Quarterly Report, Filing Date May 17, 2004". secdatabase.com. Retrieved May 14, 2018.
  4. CA 2599721,Pyke R, Ceci A,"Pharmaceutical compositions for the treatment and/or prevention of depression"
  5. WO 2014015047,Ichinose F, Marutani E, Kida K,"Compositions and methods to treat neurodegenerative diseases"
  6. Nentwig W (2013-02-15). Spider Ecophysiology. Springer Science & Business Media. ISBN   9783642339899.
  7. Oldrati V, Bianchi E, Stöcklin R (February 2013). "Spider Venom Components as Drug Candidates". Spider Ecophysiology. pp. 491–503. doi:10.1007/978-3-642-33989-9_37. ISBN   978-3-642-33988-2.
  8. Monge-Fuentes V, Gomes FM, Campos GA, Silva Jd, Biolchi AM, Dos Anjos LC, Gonçalves JC, Lopes KS, Mortari MR (August 2015). "Neuroactive compounds obtained from arthropod venoms as new therapeutic platforms for the treatment of neurological disorders". The Journal of Venomous Animals and Toxins Including Tropical Diseases. 21 (31): 31. doi: 10.1186/s40409-015-0031-x . PMC   4529710 . PMID   26257776.