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romidepsin(Istodax) 被引量:1

romidepsin(Istodax)
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作者 隋娜 郭长彬
机构地区 首都师范大学
出处 《中国药物化学杂志》 CAS CSCD 2010年第3期239-239,共1页 Chinese Journal of Medicinal Chemistry
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参考文献4

  • 1WEN S J, PACKHAM G H, GANESAN A. Macrolactamization versus macrolactonization: total synthesis of FK228, the depsipeptide histone deacetylase inhibitor [ J ]. J Org Chem, 2008,73(23) :9353 -9361. 被引量:1
  • 2BOWERS A A,GRESHOCK T J,WEST N, et al. Synthesis and conformation-activity relationships of the peptide isosteres of FK228 and largazole[J]. J Am Chem Soc,2009,131 (8) : 2900 - 2905. 被引量:1
  • 3WHITCHCAD R P, RANKIN C, HOFF P M G, et al. Phase II trial of romidepsin ( NSC-630176 ) in previouslytreated colorectal cancer patients with advanced disease a southwest oncology group study( S0336 ) [ J]. Invest New Drugs,2009, 27(5) :469 -475. 被引量:1
  • 4US FDA. HighLights of prescribing information [ EB/OL ]. [2009 - 11 - 09 ]. http://www, accessdata, fda. gov/drug- sat - fda_docs/label/2009/0223931 bl. pdf. 被引量:1

同被引文献12

  • 1BERTINO E M, O'FFERSON G: A. Romidepsin: a novel histone deacetylase inhibitor for cancer [ J ]. Expert Opin Investig Drugs, 2011,20 ( 8 ) : 1151 - 1158. 被引量:1
  • 2UEDA H,NAKAJIMA H,HORI Y,et al. FR901228,a novel antitumor bicyclic depsipeptide produced by chromobacterium violaceum No. 968. I. Taxonomy,fer- mentation, isolation, physico-chemical and biological properties,and antitumor activity [ J ]. Jantibiot, 1994,47(3) :301. 被引量:1
  • 3MARO S D, AHN J M. Development of an efficient solid-phase synthetic methodology to construct a combinatorial library of a potent HDAC inhibitor [ J]. Peptides for Youth,2009 (611 ) : 17 - 18. 被引量:1
  • 4CHENG Y Q,YANG M,MATTER A M. Characteri- zation of a gene cluster responsible for the biosynthe- sis of anticancer agent FK228 in chromobacterium violaceum No. 968 [ J ]. Appl Environ Microbiol, 2007,73( 11 ) :3460 -3469. 被引量:1
  • 5GRESHOCK T J, JOHNS D M,NOGUCHI Y, et al. Improved total synthesis of the potent HDAC inhibi- tor FK228 ( FR-901228 ) [ J ]. Org Lett, 2008, 10 (4) :613 -616. 被引量:1
  • 6LI K W, WU J, XING W, et al. Total synthesis of the antitumor depsipeptide FR-901,228 [ J]. J Am Chem Soc, 1996,118 (30) : 7237 - 7238. 被引量:1
  • 7CHEN Y,GAMBS C,ABE Y,et al. Total synthesis of the depsipeptide FR-901375 [ J ]. J Org Chem, 2003,68 (23) : 8902 - 8905. 被引量:1
  • 8WEN S, PACKHAM G, GANESAN A. Macrolac- tamization versus macrolactonization: total synthesis of FK228, the depsipeptide histone deacetylase inhi- bitor[ J ]. J Org Chem,2008,73 (23) :9353 - 9361. 被引量:1
  • 9NARITA K,KIKUCHI T,WATANABE K,et al. To- tal synthesis of the bicyclic depsipeptide HDAC in- hibitors spiruchostatins A and B, 5"-epi-spiruchosta- tin B, FK228 (FR901228) and preliminary evaluation of their biological activity[J]. Chem Eur J,2009,15 (42) :11174 - 11186. 被引量:1
  • 10BLAKEMORE P R. The modified Julia olefination : al- kene synthesis via the condensation of metallated hete- roarylalkylsulfones with carbonyl compounds [ J ]. J Chem Soc ,Perkin Trans 1,2002 (23) :2563 - 2585. 被引量:1

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