^“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 Therapeutics262 (3): 971–8. (September 1992). PMID1326631.
^“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 Therapeutics267 (1): 462–71. (October 1993).
PMID8229777.
^“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 Pharmacology53 (11): 1561–8. (November 2001). doi:10.1211/0022357011777945.
PMID11732760.
^“In the ventral tegmental area picrotoxin blocks FGIN 1-27-induced increases in sexual behavior of rats and hamsters”. Psychopharmacology178 (2–3): 174–82. (March 2005). doi:10.1007/s00213-004-2001-9.
PMID15338106.
^“Preparation of indoles from alpha-aminonitriles: A short synthesis of FGIN-1-27”. Organic Letters8 (20): 4473–5. (September 2006). doi:10.1021/ol061617+.
PMID16986928.