Maria Del Rayo Camacho Corona

Summary

Publications

  1. Favela Hernández J, González Santiago O, Ramírez Cabrera M, Esquivel Ferriño P, Camacho Corona M. Chemistry and Pharmacology of Citrus sinensis. Molecules. 2016;21:247 pubmed publisher
    ..This review reveals the therapeutic potential of C. sinensis as a source of natural compounds with important activities that are beneficial for human health that could be used to develop new drugs. ..
  2. Favela Hernández J, González Santiago O, Ramírez Cabrera M, Esquivel Ferriño P, Camacho Corona M. Chemistry and Pharmacology of Citrus sinensis. Molecules. 2016;21:247 pubmed publisher
    ..This review reveals the therapeutic potential of C. sinensis as a source of natural compounds with important activities that are beneficial for human health that could be used to develop new drugs. ..
  3. Favela Hernández J, Clemente Soto A, Balderas Rentería I, Garza González E, Camacho Corona M. Potential mechanism of action of 3'-demethoxy-6-O-demethyl-isoguaiacin on methicillin resistant Staphylococcus aureus. Molecules. 2015;20:12450-8 pubmed publisher
    ..This molecular mechanism is not present in any antibacterial commercial drug and could be a new target for the development of novel antibacterial agents. ..
  4. Reyes Melo K, Garcia A, Romo Mancillas A, Garza Gonzalez E, Rivas Galindo V, Miranda L, et al. meso-Dihydroguaiaretic acid derivatives with antibacterial and antimycobacterial activity. Bioorg Med Chem. 2017;25:5247-5259 pubmed publisher
    ..The amino-ether 31 exhibited a selectivity index value of 23, which indicate it was more toxic to M. tuberculosis than to mammalian cells. Therefore, 31 can be considered as a promising antitubercular agent for further studies. ..
  5. Favela Hernández J, Clemente Soto A, Balderas Rentería I, Garza González E, Camacho Corona M. Potential Mechanism of Action of 3'-Demethoxy-6-O-demethyl-isoguaiacin on Methicillin Resistant Staphylococcus aureus. Molecules. 2015;20:12450-8 pubmed publisher
    ..This molecular mechanism is not present in any antibacterial commercial drug and could be a new target for the development of novel antibacterial agents. ..

Detail Information

Publications5