Literature DB >> 17416442

An atom counting strategy towards analyzing the biological activity of sex hormones.

D R Roy1, N Pal, A Mitra, P Bultinck, R Parthasarathi, V Subramanian, P K Chattaraj.   

Abstract

A simple and effective molecular descriptor, viz., the number of atoms in a molecule (N(A)) is made use of in the development of the quantitative structure-activity relationship (QSAR). A series of testosterone derivatives with various biological activities and estrogen derivatives with the activities in terms of relative binding affinity (RBA) are considered to find out the potential of N(A) in predicting the activities of those molecules. It is heartening to note that N(A) along with the electrophilicity index (omega) is capable of explaining the biological activities of the male and female hormones.

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Year:  2007        PMID: 17416442     DOI: 10.1016/j.ejmech.2007.01.028

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  2 in total

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Authors:  Bachir Zouchoune
Journal:  Struct Chem       Date:  2020-07-15       Impact factor: 1.887

Review 2.  Conceptual density functional theory based electronic structure principles.

Authors:  Debdutta Chakraborty; Pratim Kumar Chattaraj
Journal:  Chem Sci       Date:  2021-03-31       Impact factor: 9.825

  2 in total

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