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[5] C. T. Lowden and K. F. Bastow, “Cell Culture Replication of Herpes Simplex Virus and, or Human Cytomegalovirus Is Inhibited by 3, 7-Dialkoxylated, 1-Hydroxyacridone Derivatives,” Antiviral Research, Vol. 59, No. 3, 2003, pp. 143-154.

has been cited by the following article:

• TITLE: 3D-QSAR Topomer CoMFA Studies on 10 N-Substituted Acridone Derivatives

  AUTHORS: Adeayo O. Ajala, Cosmas O. Okoro

  KEYWORDS: Acridone; Topomer; Acyclic; CoMFA; Cross-Validated; SAR

  JOURNAL NAME: Open Journal of Medicinal Chemistry, Vol.2 No.3, September 27, 2012

  ABSTRACT: Topomer CoMFA models have been used to optimize the potency of 15 biologically active acridone derivatives se- lected from the literature. Their 3D chemical structures were sliced into three acyclic R groups, to produce a fragment that is present in each training set. The analysis was successful with 3 as the number of components that provided the highest q2 results: q2 is 0.56, which is the cross-validated coefficient for the specified number of components, giving rise to 0.37 standard error of estimate (q2 stderr), and a conventional coefficient (r2) of 0.82, whose standard error of estimate is 0.24. These results provide structure-activity relationship (sar) among the compounds. The result of the To-pomer CoMFA studies was used to design novel derivatives for future studies.