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Needs context
editRifleman 82 (talk) 03:57, 17 December 2012 (UTC)
Reactions
edit- C9H23NO6P2 C4H4O3 C51C64N4O13 C4H6BrClO → C60H79N5O23P2[1]
This reaction exhibits the creation of the molecule ryfamicin VIII. Ryfamicin is the original molecule of which rifalazil is the derivative. The purpose of this reaction is to use rifalazil to make a different derivative of the molecule so the substance can be delivered to osseous tissue in the body. This allows the medication to be released at different points in time to the rest of the body in through the blood stream as opposed to all at once.
References
- ^ Reddy, Ranga; Dietrich, Evelyne; Lafontaine, Yanick; Houghton, Tom J.; Belanger, Odette; Dubois, Anik; Arhin, Francis F.; Sarmiento, Ingrid; Fadhil, Ibtihal (2008). "Bisphosphonated Benzoxazinorifamycin Prodrugs for the Prevention and Treatment of Osteomyelitis". ChemMedChem. 3 (12): 1863–8. doi:10.1002/cmdc.200800255. PMID 18973169.1863-8&rft.date=2008&rft_id=info:doi/10.1002/cmdc.200800255&rft_id=info:pmid/18973169&rft.aulast=Reddy&rft.aufirst=Ranga&rft.au=Dietrich, Evelyne&rft.au=Lafontaine, Yanick&rft.au=Houghton, Tom J.&rft.au=Belanger, Odette&rft.au=Dubois, Anik&rft.au=Arhin, Francis F.&rft.au=Sarmiento, Ingrid&rft.au=Fadhil, Ibtihal&rfr_id=info:sid/en.wikipedia.org:Talk:Rifalazil" class="Z3988">