Tham khảo Romidepsin

  1. ↑ "Romidepsin". National Cancer Institute. Truy cập 2009-09-11.
  2. ↑ "Romidepsin". Gloucester Pharmaceuticals. Truy cập 2009-09-11.[permanent dead link]
  3. 1 2 3 Ueda H, Nakajima H, Hori Y, et al. (March 1994). "FR901228, a novel antitumor bicyclic depsipeptide produced by Chromobacterium violaceum No. 968. I. Taxonomy, fermentation, isolation, physico-chemical and biological properties, and antitumor activity". Journal of Antibiotics. 47 (3): 301–10. doi:10.7164/antibiotics.47.301. PMID 7513682.
  4. ↑ Li KW, Wu J, Xing W, Simon JA (July 1996). "Total synthesis of the antitumor depsipeptide FR-901,228". Journal of the American Chemical Society. 118 (30): 7237–8. doi:10.1021/ja9613724.
  5. ↑ Nakajima H, Kim YB, Terano H, Yoshida M, Horinouchi S (May 1998). "FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor". Experimental Cell Research. 241 (1): 126–33. doi:10.1006/excr.1998.4027. PMID 9633520.
  6. 1 2 3 Masuoka Y, Shindoh N, Inamura N (2008). "Histone deacetylase inhibitors from microorganisms: the Astellas experience". In Petersen F, Amstutz R (eds.). Natural compounds as drugs. 2. Basel: Birkhäuser. pp. 335–59. ISBN 978-3-7643-8594-1. Retrieved on ngày 8 tháng 11 năm 2009 through Google Book Search.
  7. ↑ http://chembl.blogspot.com/2009/11/new-drug-approvals-pt-xxiii-romidepsin.html
  8. ↑ http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Reports.MonthlyApprovalsAll
  9. ↑ Wei, D (2014). “Histone Deacetylase Inhibitor Romidepsin Induces HIV Expression in CD4 T Cells from Patients on Suppressive Antiretroviral Therapy at Concentrations Achieved by Clinical Dosing”. PLoS Pathog. 10 (4): e1004071. doi:10.1371/journal.ppat.1004071. PMC 3983056. PMID 24722454. Đã bỏ qua tham số không rõ |displayauthors= (gợi ý |display-authors=) (trợ giúp)
  10. ↑ Qin, Luye; Ma, Kaijie; Wang, Zi-Jun; Hu, Zihua; Matas, Emmanuel; Wei, Jing; Yan, Zhen (2018). “Social deficits in Shank3-deficient mouse models of autism are rescued by histone deacetylase (HDAC) inhibition”. Nature Neuroscience. 21 (4): 564. doi:10.1038/s41593-018-0110-8. PMC 5876144. PMID 29531362.
  11. ↑ Bates, Susan E.; Zhan, Zhirong; Steadman, Kenneth; Obrzut, Tomasz; Luchenko, Victoria; Frye, Robin; Robey, Robert W.; Turner, Maria; Gardner, Erin R. (tháng 1 năm 2010). “Laboratory correlates for a phase II trial of romidepsin in cutaneous and peripheral T-cell lymphoma”. British Journal of Haematology. 148 (2): 256–267. doi:10.1111/j.1365-2141.2009.07954.x. ISSN 0007-1048. PMC 2838427.
  12. ↑ Nakajima, Hidenori; Kim, Young Bae; Terano, Hiroshi; Yoshida, Minoru; Horinouchi, Sueharu (tháng 5 năm 1998). “FR901228, a Potent Antitumor Antibiotic, Is a Novel Histone Deacetylase Inhibitor”. Experimental Cell Research. 241 (1): 126–133. doi:10.1006/excr.1998.4027. ISSN 0014-4827.
  13. ↑ Bradner, James E; West, Nathan; Grachan, Melissa L; Greenberg, Edward F; Haggarty, Stephen J; Warnow, Tandy; Mazitschek, Ralph (ngày 7 tháng 2 năm 2010). “Chemical phylogenetics of histone deacetylases”. Nature Chemical Biology. 6 (3): 238–243. doi:10.1038/nchembio.313. ISSN 1552-4450. PMC 2822059.
  14. ↑ Nakajima, Hidenori; Kim, Young Bae; Terano, Hiroshi; Yoshida, Minoru; Horinouchi, Sueharu (tháng 5 năm 1998). “FR901228, a Potent Antitumor Antibiotic, Is a Novel Histone Deacetylase Inhibitor”. Experimental Cell Research. 241 (1): 126–133. doi:10.1006/excr.1998.4027. ISSN 0014-4827.
  15. ↑ Shigematsu, N.; Ueda, H.; Takase, S.; Tanaka, H.; Yamamoto, K.; Tada, T. (1994). “FR901228, a novel antitumor bicyclic depsipeptide produced by Chromobacterium violaceum No. 968. II. Structure determination”. J. Antibiot. 47 (3): 311–314. doi:10.7164/antibiotics.47.311. PMID 8175483.
  16. ↑ Ueda, H.; Manda, T.; Matsumoto, S.; Mukumoto, S.; Nishigaki, F.; Kawamura, I.; Shimomura, K. (1994). “FR901228, a novel antitumor bicyclic depsipeptide produced by Chromobacterium violaceum No. 968. III. Antitumor activities on experimental tumors in mice”. J. Antibiot. 47 (3): 315–323. doi:10.7164/antibiotics.47.315. PMID 8175484.
  17. ↑ Greshock, Thomas J.; Johns, Deidre M.; Noguchi, Yasuo; Williams, Robert M. (2008). “Improved Total Synthesis of the Potent HDAC Inhibitor FK228 (FR-901228)”. Organic Letters. 10 (4): 613–616. doi:10.1021/ol702957z. PMC 3097137. PMID 18205373.
  18. 1 2 [No authors listed] (October 2014). "ISTODEX Label Information (updated to October 2014)" (PDF). U.S. Food and Drug Administration.

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