Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Identification of Vimentin Binding to the Derivative of Saurolactam with Antiresorptive Activity by Using Its Chemical Affinity Probe

  • Kim, Myung-Hee (Laboratory of Chemical Genomics, Pharmacology Research Center, Korea Research Institute of Chemical Technology) ;
  • Choi, Young-Lok (Medicinal Chemistry Research Center, Korea Research Institute of Chemical Technology) ;
  • Heo, Jung-Nyoung (Medicinal Chemistry Research Center, Korea Research Institute of Chemical Technology) ;
  • Min, Yong-Ki (Laboratory of Chemical Genomics, Pharmacology Research Center, Korea Research Institute of Chemical Technology) ;
  • Kim, Seong-Hwan (Laboratory of Chemical Genomics, Pharmacology Research Center, Korea Research Institute of Chemical Technology)
  • Received : 2010.02.18
  • Accepted : 2010.05.03
  • Published : 2010.07.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Han, S. Y.; Kim, S. H. Arch. Pharm. (Weinheim) 2007, 340, 169. https://doi.org/10.1002/ardp.200600153
  2. Chen, Y. J.; Chen, S. H.; Chien, Y. Y.; Chang, Y. W.; Liao, H.K.; Chang, C. Y.; Jan, M. D.; Wang, K. T.; Lin, C. C. Chembiochem2005, 6, 1169. https://doi.org/10.1002/cbic.200500023
  3. Tomohiro, T.; Hashimoto, M.; Hatanaka, Y.Chem. Rec. 2006, 5, 385. https://doi.org/10.1002/tcr.20058
  4. Kim, M. H.; Han, S. Y.; Kim, B. T.;Min, Y. K.; Kim, S. H. Bull. Korean Chem. Soc. 2006, 27, 1285. https://doi.org/10.5012/bkcs.2006.27.9.1285
  5. Harding, M. W.; Galat, A.; Uehling, D. E.; Schreiber, S. L. Nature1989, 341, 758. https://doi.org/10.1038/341758a0
  6. Oda, Y.; Owa, T.; Sato, T.; Boucher, B.;Daniels, S.; Yamanaka, H.; Shinohara, Y.; Yokoi, A.; Kuromitsu,J.; Nagasu, T. Anal. Chem. 2003, 75, 2159. https://doi.org/10.1021/ac026196y
  7. Boyle, W. J.; Simonet, W. S.; Lacey, D. L. Nature 2003, 423, 337. https://doi.org/10.1038/nature01658
  8. Kim, M. H.; Ryu, S. Y.; Choi, J. S.; Min, Y. K.; Kim, S. H. J. Cell. Physiol. (in press)
  9. Hsu, H.; Lacey, D. L.; Dunstan, C. R.; Solovyev, I.; Colombero,A.; Timms, E.; Tan, H. L.; Elliott, G.; Kelley, M. J.; Sarosi, I.;Wang, L.; Xia, X. Z.; Elliott, R.; Chiu, L.; Black, T.; Scully, S.;Capparelli, C.; Morony, S.; Shimamoto, G.; Bass, M. B.; Boyle,W. J. Proc. Natl. Acad. Sci. USA 1999, 96, 3540. https://doi.org/10.1073/pnas.96.7.3540
  10. Kim, M. H.; Ryu, S. Y.; Bae, M. A.; Choi, J. S.; Min, Y. K.; Kim, S.H. Food Chem. Toxicol. 2008, 46, 3375. https://doi.org/10.1016/j.fct.2008.08.016
  11. Kim, J. K.; Kim, Y. H.; Nam, H, T.; Kim, B. T.; Heo, J.-N. Org. Lett. 2008, 10, 3543.
  12. Choi, Y. L.; Kim, J. K.; Choi, S.-U.; Min, Y.-K.; Bae, M.-A.; Kim, B. T.; Heo, J.-N. Bioorg. Med. Chem. Lett. 2009, 19, 3036. https://doi.org/10.1016/j.bmcl.2009.04.020
  13. Kim, Y. H.; Lee, H.; Kim, Y. J.; Kim, B. T.; Heo,J.-N. J. Org. Chem. 2008, 73, 495. https://doi.org/10.1021/jo702001n
  14. Geen, G. R.; Mann, I. S.; Mullane, M. V.; McKillop, A. Tetrahedron1998, 54, 9875. https://doi.org/10.1016/S0040-4020(98)00540-7
  15. Matsuzawa, K.; Kosako, H.; Inagaki, N.; Shibata, H.; Mukai, H.; Ono, Y.; Amano, M.; Kaibuchi, K.; Matsuura, Y.; Azuma, I.; Inagaki, M. Biochem. Biophys. Res. Commun. 1997, 234, 621. https://doi.org/10.1006/bbrc.1997.6669
  16. Okayama, N.; Fowler, M. R.; Jennings, S. R.; Specian, R.; Alexander,B.; Jackson, T. H.; Oshima, T.; Shannon, T.; Alexander, J. S.In Vitro Cell Dev. Biol. Anim. 2000, 36, 228. https://doi.org/10.1290/1071-2690(2000)036<0228:COJAHG>2.0.CO;2

Cited by

  1. Direct Lactamization of Azido Amides via Staudinger-Type Reductive Cyclization vol.33, pp.1, 2012, https://doi.org/10.5012/bkcs.2012.33.1.333
  2. SnH-Mediated Reductive Cyclization of Azido Amides vol.33, pp.2, 2012, https://doi.org/10.5012/bkcs.2012.33.2.739
  3. An Efficient and Practical Total Synthesis of Sauristolactam vol.32, pp.12, 2010, https://doi.org/10.5012/bkcs.2011.32.12.4431