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Quantitative Structure Antitumoral-Activity Relationships of Thiadiazinthione Derivatives Using the Novel Hybrid Molecular Index pMRc / s. t
Carrasco, Ramón; Padrón, Juan A; Pérez, Rolando; Rodríguez, Hortensia; Suárez, Margarita; Ochoa, Carmen.
Affiliation
  • Carrasco, Ramón; Centro de Química Farmacéutica. La Habana. Cuba
  • Padrón, Juan A; Universidad de La Habana. Facultad de Química. Laboratorio de Química Computacional y Teórica. La Habana. Cuba
  • Pérez, Rolando; Universidad de La Habana. Facultad de Química. Laboratorio de Síntesis Orgánica. La Habana. Cuba
  • Rodríguez, Hortensia; Universidad de La Habana. Facultad de Química. Laboratorio de Síntesis Orgánica. La Habana. Cuba
  • Suárez, Margarita; Universidad de La Habana. Facultad de Química. Laboratorio de Síntesis Orgánica. La Habana. Cuba
  • Ochoa, Carmen; Instituto de Química Médica. Madrid. España
J Pharm Pharmaceut Sci ; 8(3)Dec. 2005. ilus, graf
Article in English | CUMED | ID: cum-40038
Responsible library: CU1.1
ABSTRACT
The recently defined molar-refractivity-partition index was applied to a family of 1,3,5- thiadiazin-2-thione derivatives in order to establish quantitative structure-antitumoral models. The goal of this effort is to establish the relationships between the structure and biological response of these compounds. Method. After the splitting of the sample in two sets, their indices were correlated against the measured biological activity. The combined use of our index with others had been able to describe not only the topologic but also the London dispersive forces of any fragment in relation to the biological response of the sets. Results. The obtained models showed correlation coefficients of 0,87 and 0,81 respectively linking structural and biological features of the molecules. The mean relative error values were less than 7 percent. According to the models, the activity of the first sample is related mostly to molecular topology and dispersive forces. Sample two activity was associated to the size and branching of the substituents, and also to the London forces. Conclusion. The index was able to discriminate between pure topological features and those related to dispersive forces(AU)
Subject(s)
Full text: Available Collection: National databases / Cuba Database: CUMED Main subject: Thiadiazines / Thiones / HeLa Cells / Quantitative Structure-Activity Relationship / Antineoplastic Agents Limits: Humans Language: English Journal: J Pharm Pharmaceut Sci Year: 2005 Document type: Article Institution/Affiliation country: Centro de Química Farmacéutica/Cuba / Instituto de Química Médica/España / Universidad de La Habana/Cuba
Full text: Available Collection: National databases / Cuba Database: CUMED Main subject: Thiadiazines / Thiones / HeLa Cells / Quantitative Structure-Activity Relationship / Antineoplastic Agents Limits: Humans Language: English Journal: J Pharm Pharmaceut Sci Year: 2005 Document type: Article Institution/Affiliation country: Centro de Química Farmacéutica/Cuba / Instituto de Química Médica/España / Universidad de La Habana/Cuba
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