Browsing by Author "Soto Morales, Francisco"

Now showing items 1-5 of 5

    • A THEORETICAL STUDY OF THE INHIBITION OF WILD-TYPE AND DRUG-RESISTANT HIV-1 REVERSE TRANSCRIPTASE BY SOME ... 
      Soto Morales, Francisco; Gómez Jeria, Juan (Sociedad Chilena de Química, 2007-05-02)
      We present the results of a quantum chemical study of the relationship between the electronic-conformational structure of a group of thiazolidenebenzenesulfo namide derivatives (TBS) and their Immunodeficiency Type 1 Virus ...
    • A Zindo/1 Study of the Cannabinoid-Mediated Inhibition of Adenylyl Cyclase 
      Gómez Jeria, Juan; Soto Morales, Francisco; Larenas Gutiérrez, Gipsy (University of Tehran., 2003-09-06)
      We present here the results of a formal structure-property relationship study carried out for 1 CB - and 2 CB -mediated inhibition of adenylyl cyclase (ADC) by a group of classical cannabinoid derivatives. The wave ...
    • A Zindo/1 Study of the Cannabinoid-Mediated Inhibition of Adenylyl Cyclase 
      Gómez Jeria, Juan; Soto Morales, Francisco; Larenas Gutiérrez, Gipsy (University of Tehran, 2003-09-06)
      We present here the results of a formal structure-property relationship study carried out for 1 CB - and 2 CB -mediated inhibition of adenylyl cyclase (ADC) by a group of classical cannabinoid derivatives. The wave ...
    • Short nanotubes or big molecules? The concept of minimal length 
      Gómez Jeria, Juan; Soto Morales, Francisco (SOCIEDAD CHILENA DE QUIMICA, 2005-12)
      We have studied the problem of what must be the minimal length of a nanotube with a given diameter to reasonably assert that its electronic properties can be extrapolated to longer structures. For this purpose the variation ...
    • A theoretical structure-affinity relationship study of some cannabinoid derivatives 
      Gómez Jeria, Juan; Soto Morales, Francisco; Rivas, Jorge; Sotomayor, Alejandra (SOC CHILENA QUIMICA, 2008-03)
      A ZINDO/1 quantum-chemical structure-affinity relationship study with the KPG model is presented for the in vitro interaction of a group of classical, indole-derived and aminoalkylindole-derived cannabinoids with CB1 and ...