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FGIN-143

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
FGIN-143
Identifiers
  • 2-[2-(4-chlorophenyl)-5-chloro-1H-indol-3-yl]-N,N-dihexylacetamide
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC28H36Cl2N2O
Molar mass487.51 g·mol−1
3D model (JSmol)
  • c3cc(Cl)ccc3-c2[nH]c1ccc(Cl)cc1c2CC(=O)N(CCCCCC)CCCCCC
  • InChI=1S/C28H36Cl2N2O/c1-3-5-7-9-17-32(18-10-8-6-4-2)27(33)20-25-24-19-23(30)15-16-26(24)31-28(25)21-11-13-22(29)14-12-21/h11-16,19,31H,3-10,17-18,20H2,1-2H3
  • Key:XTZUPNNVXIMWAR-UHFFFAOYSA-N
  (verify)

FGIN-1-43 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, and is several times more potent than the related drugFGIN-127.[1][2][3][4]

References

[edit]
  1. ^Romeo E, Auta J, Kozikowski AP, Ma D, Papadopoulos V, Puia G, et al. (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. ^Kozikowski AP, Ma D, Brewer J, Sun S, Costa E, Romeo E, Guidotti A (October 1993). "Chemistry, binding affinities, and behavioral properties of a new class of "antineophobic" mitochondrial DBI receptor complex (mDRC) ligands".Journal of Medicinal Chemistry.36 (20):2908–20.doi:10.1021/jm00072a010.PMID 8411007.
  3. ^Costa E, Auta J, Guidotti A, Korneyev A, Romeo E (June 1994)."The pharmacology of neurosteroidogenesis".The Journal of Steroid Biochemistry and Molecular Biology.49 (4–6):385–9.doi:10.1016/0960-0760(94)90284-4.PMID 8043504.S2CID 33492066.
  4. ^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.
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