Okazaki H, Ishizaka N, Sakurai T, Kurokawa K, Goto K, Kumada M, Takuwa Y (February 1993). "Molecular cloning of a novel putative G protein-coupled receptor expressed in the cardiovascular system". Biochem. Biophys. Res. Commun. 190 (3): 1104–9. doi:10.1006/bbrc.1993.1163. PMID8382486.
MacLennan AJ, Browe CS, Gaskin AA, Lado DC, Shaw G (June 1994). "Cloning and characterization of a putative G-protein coupled receptor potentially involved in development". Mol. Cell. Neurosci. 5 (3): 201–9. doi:10.1006/mcne.1994.1024. PMID8087418. S2CID34088289.
Gräler MH, Bernhardt G, Lipp M (October 1998). "EDG6, a novel G-protein-coupled receptor related to receptors for bioactive lysophospholipids, is specifically expressed in lymphoid tissue". Genomics. 53 (2): 164–9. doi:10.1006/geno.1998.5491. PMID9790765.
Sharma, N; et al. (2013). "Sphingosine-1-phosphate suppresses TLR-induced CXCL8 secretion from human T cells". J Leukoc Biol. 93 (4): 521–528. doi:10.1189/jlb.0712328. PMID23345392.
Clemens JJ, Davis MD, Lynch KR, Macdonald TL (August 2005). "Synthesis of 4(5)-phenylimidazole-based analogues of sphingosine-1-phosphate and FTY720: discovery of potent S1P1 receptor agonists". Bioorg. Med. Chem. Lett. 15 (15): 3568–72. doi:10.1016/j.bmcl.2005.05.097. PMID15982878.
Hale JJ, Lynch CL, Neway W, Mills SG, Hajdu R, Keohane CA, Rosenbach MJ, Milligan JA, Shei GJ, Parent SA, Chrebet G, Bergstrom J, Card D, Ferrer M, Hodder P, Strulovici B, Rosen H, Mandala S (December 2004). "A rational utilization of high-throughput screening affords selective, orally bioavailable 1-benzyl-3-carboxyazetidine sphingosine-1-phosphate-1 receptor agonists". J. Med. Chem. 47 (27): 6662–5. doi:10.1021/jm0492507. PMID15615513.
Nakamura T, Asano M, Sekiguchi Y, Mizuno Y, Tamaki K, Kimura T, Nara F, Kawase Y, Shimozato T, Doi H, Kagari T, Tomisato W, Inoue R, Nagasaki M, Yuita H, Oguchi-Oshima K, Kaneko R, Watanabe N, Abe Y, Nishi T (February 2012). "Discovery of CS-2100, a potent, orally active and S1P3-sparing S1P1 agonist". Bioorg. Med. Chem. Lett. 22 (4): 1788–92. doi:10.1016/j.bmcl.2011.12.019. PMID22264485.
Okazaki H, Ishizaka N, Sakurai T, Kurokawa K, Goto K, Kumada M, Takuwa Y (February 1993). "Molecular cloning of a novel putative G protein-coupled receptor expressed in the cardiovascular system". Biochem. Biophys. Res. Commun. 190 (3): 1104–9. doi:10.1006/bbrc.1993.1163. PMID8382486.
MacLennan AJ, Browe CS, Gaskin AA, Lado DC, Shaw G (June 1994). "Cloning and characterization of a putative G-protein coupled receptor potentially involved in development". Mol. Cell. Neurosci. 5 (3): 201–9. doi:10.1006/mcne.1994.1024. PMID8087418. S2CID34088289.
Gräler MH, Bernhardt G, Lipp M (October 1998). "EDG6, a novel G-protein-coupled receptor related to receptors for bioactive lysophospholipids, is specifically expressed in lymphoid tissue". Genomics. 53 (2): 164–9. doi:10.1006/geno.1998.5491. PMID9790765.
Sharma, N; et al. (2013). "Sphingosine-1-phosphate suppresses TLR-induced CXCL8 secretion from human T cells". J Leukoc Biol. 93 (4): 521–528. doi:10.1189/jlb.0712328. PMID23345392.
Clemens JJ, Davis MD, Lynch KR, Macdonald TL (August 2005). "Synthesis of 4(5)-phenylimidazole-based analogues of sphingosine-1-phosphate and FTY720: discovery of potent S1P1 receptor agonists". Bioorg. Med. Chem. Lett. 15 (15): 3568–72. doi:10.1016/j.bmcl.2005.05.097. PMID15982878.
Hale JJ, Lynch CL, Neway W, Mills SG, Hajdu R, Keohane CA, Rosenbach MJ, Milligan JA, Shei GJ, Parent SA, Chrebet G, Bergstrom J, Card D, Ferrer M, Hodder P, Strulovici B, Rosen H, Mandala S (December 2004). "A rational utilization of high-throughput screening affords selective, orally bioavailable 1-benzyl-3-carboxyazetidine sphingosine-1-phosphate-1 receptor agonists". J. Med. Chem. 47 (27): 6662–5. doi:10.1021/jm0492507. PMID15615513.
Nakamura T, Asano M, Sekiguchi Y, Mizuno Y, Tamaki K, Kimura T, Nara F, Kawase Y, Shimozato T, Doi H, Kagari T, Tomisato W, Inoue R, Nagasaki M, Yuita H, Oguchi-Oshima K, Kaneko R, Watanabe N, Abe Y, Nishi T (February 2012). "Discovery of CS-2100, a potent, orally active and S1P3-sparing S1P1 agonist". Bioorg. Med. Chem. Lett. 22 (4): 1788–92. doi:10.1016/j.bmcl.2011.12.019. PMID22264485.