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FGIN-127

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
FGIN-127
Identifiers
  • 2-[2-(4-fluorophenyl)-1H-indol-3-yl]-N,N-dihexylacetamide
CAS Number
PubChemCID
ChemSpider
ChEBI
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC28H37FN2O
Molar mass436.615 g·mol−1
3D model (JSmol)
  • CCCCCCN(CCCCCC)C(=O)Cc1c2ccccc2[nH]c1c3ccc(cc3)F
  • InChI=1S/C28H37FN2O/c1-3-5-7-11-19-31(20-12-8-6-4-2)27(32)21-25-24-13-9-10-14-26(24)30-28(25)22-15-17-23(29)18-16-22/h9-10,13-18,30H,3-8,11-12,19-21H2,1-2H3 ☒N
  • Key:VUWXAQFLTSBUDB-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

FGIN-1-27 is ananxiolytic drug which acts as a selectiveagonist at theperipheral benzodiazepine receptor, also known as the mitochondrial 18 kDa translocator protein or TSPO. It is thought to produce anxiolytic effects by stimulatingsteroidogenesis ofneuroactive steroids such asallopregnanolone.[1][2][3][4][5][6]

References

[edit]
  1. ^Romeo E, Auta J, Kozikowski AP, Ma D, Papadopoulos V, Puia G, Costa E, Guidotti A (September 1992). "2-Aryl-3-indoleacetamides (FGIN-1): a new class of potent and specific ligands for the mitochondrial DBI receptor (MDR)".The Journal of Pharmacology and Experimental Therapeutics.262 (3):971–8.PMID 1326631.
  2. ^Romeo E, Cavallaro S, Korneyev A, Kozikowski AP, Ma D, Polo A, Costa E, Guidotti A (October 1993). "Stimulation of brain steroidogenesis by 2-aryl-indole-3-acetamide derivatives acting at the mitochondrial diazepam-binding inhibitor receptor complex".The Journal of Pharmacology and Experimental Therapeutics.267 (1):462–71.PMID 8229777.
  3. ^Guillon J, Boulouard M, Lelong V, Dallemagne P, Rault S, Jarry C (November 2001)."Synthesis and preliminary behavioural evaluation in mice of new 3-aryl-3-pyrrol-1-ylpropanamides, analogues of FGIN-1-27 and FGIN-1-43".The Journal of Pharmacy and Pharmacology.53 (11):1561–8.doi:10.1211/0022357011777945.PMID 11732760.S2CID 11838769.
  4. ^Petralia SM, Frye CA (March 2005). "In the ventral tegmental area picrotoxin blocks FGIN 1-27-induced increases in sexual behavior of rats and hamsters".Psychopharmacology.178 (2–3):174–82.doi:10.1007/s00213-004-2001-9.PMID 15338106.S2CID 22649389.
  5. ^Opatz T, Ferenc D (September 2006). "Preparation of indoles from alpha-aminonitriles: A short synthesis of FGIN-1-27".Organic Letters.8 (20):4473–5.doi:10.1021/ol061617+.PMID 16986928.
  6. ^James ML, Selleri S, Kassiou M (2006)."Development of ligands for the peripheral benzodiazepine receptor"(PDF).Current Medicinal Chemistry.13 (17):1991–2001.doi:10.2174/092986706777584979.hdl:2158/222808.PMID 16842193.
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