Kinamycin

Kinamycins are a group of bacterial polyketide secondary metabolites containing a diazo group. Kinamycins are known for their cytotoxicity and are considered of interest for potential use in anti-cancer therapies.[1][2]

Chemical structure of kinamycin A

Synthesis

In 2006 and 2007 the means to totally and enantioselectively synthesize kinamycins C, F, and J were discovered.[3][4] In 2010 a method was found to allow easier synthesis of these compounds in fewer steps, making research into their properties more feasible.[5]

gollark: Also, the processor in the graphing ones was manufactured after 1990, probably.
gollark: They are, at least, more reasonably priced and customizable.
gollark: Because convention or something Casio is more popular here.
gollark: Indeed.
gollark: My computer can calculate things! It literally has 6TFLOP/s of computing power!

References
  1. Ballard, T. E.; Melander, C. (2008). "Kinamycin-mediated DNA cleavage under biomimetic conditions". Tetrahedron Letters. 49 (19): 3157. doi:10.1016/j.tetlet.2008.03.019.
  2. O'Hara, K. A.; Wu, X.; Patel, D.; Liang, H.; Yalowich, J. C.; Chen, N.; Goodfellow, V.; Adedayo, O.; Dmitrienko, G. I.; Hasinoff, B. B. (2007). "Mechanism of the cytotoxicity of the diazoparaquinone antitumor antibiotic kinamycin F". Free Radical Biology and Medicine. 43 (8): 1132–1144. doi:10.1016/j.freeradbiomed.2007.07.005. PMC 2753228. PMID 17854709.
  3. Lei, X.; Porco Ja, J. (2006). "Total synthesis of the diazobenzofluorene antibiotic (-)-kinamycin C1". Journal of the American Chemical Society. 128 (46): 14790–14791. doi:10.1021/ja066621v. PMID 17105273.
  4. Nicolaou, K. C.; Li, H.; Nold, A. L.; Pappo, D.; Lenzen, A. (2007). "Total Synthesis of Kinamycins C, F, and J". Journal of the American Chemical Society. 129 (34): 10356–7. doi:10.1021/ja074297d. PMID 17676854.
  5. Woo, C. M.; Lu, L.; Gholap, S. L.; Smith, D. R.; Herzon, S. B. (2010). "Development of a Convergent Entry to the Diazofluorene Antitumor Antibiotics: Enantioselective Synthesis of Kinamycin F". Journal of the American Chemical Society. 132 (8): 2540–1. doi:10.1021/ja910769j. PMID 20141138.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.