〈Front Matter〉. 《Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book)》. Cambridge: The Royal Society of Chemistry. 2014. 697쪽. doi:10.1039/9781849733069-FP001. ISBN978-0-85404-182-4. The prefixes ‘mercapto’ (–SH), and ‘hydroseleno’ or selenyl (–SeH), etc. are no longer recommended.
Smalley, Keiran S.M; Tim G. Eisen (2002년 4월 1일). “Farnesyl thiosalicylic acid inhibits the growth of melanoma cells through a combination of cytostatic and pro-apoptotic effects”. 《International Journal of Cancer》 98 (4): 514–522. doi:10.1002/ijc.10213. PMID11920610.
George, Jacob; Arnon Afek; Pnina Keren; Itzhak Herz; Iris Goldberg; Roni Haklai; Yoel Kloog; Gad Keren (2002). “Functional Inhibition of Ras by S-trans,trans-Farnesyl Thiosalicylic Acid Attenuates Atherosclerosis in Apolipoprotein E Knockout Mice”. 《Circulation》 105 (20): 2416–2422. doi:10.1161/01.CIR.0000016065.90068.96. PMID12021230.
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ncbi.nlm.nih.gov
Smalley, Keiran S.M; Tim G. Eisen (2002년 4월 1일). “Farnesyl thiosalicylic acid inhibits the growth of melanoma cells through a combination of cytostatic and pro-apoptotic effects”. 《International Journal of Cancer》 98 (4): 514–522. doi:10.1002/ijc.10213. PMID11920610.
George, Jacob; Arnon Afek; Pnina Keren; Itzhak Herz; Iris Goldberg; Roni Haklai; Yoel Kloog; Gad Keren (2002). “Functional Inhibition of Ras by S-trans,trans-Farnesyl Thiosalicylic Acid Attenuates Atherosclerosis in Apolipoprotein E Knockout Mice”. 《Circulation》 105 (20): 2416–2422. doi:10.1161/01.CIR.0000016065.90068.96. PMID12021230.
