Literature DB >> 1994153

The concept of molecular structure in structure-activity relationship studies and drug design.

B Testa1, L B Kier.   

Abstract

We can justify the use of any model, method, or algorithm if we clearly state our goals, understand the basis of our procedures, and fully appreciate the true nature and limitations of the results. As we have illustrated here, the creation of new wisdom may appear to be a consequence of our labors. There are cases, however, where this creation may be only an illusion. In any analysis of structure-activity, property-activity, or structure-property relationships, the degree of understanding of the nature of the starting data therefore determines the level of confidence ascribable to any result and prediction. This is, in essence, the message of our inquisitive meditations on the deep nature of structure-activity relationships.

Mesh:

Year:  1991        PMID: 1994153     DOI: 10.1002/med.2610110104

Source DB:  PubMed          Journal:  Med Res Rev        ISSN: 0198-6325            Impact factor:   12.944


  2 in total

1.  Octanol/water partition coefficients for environmentally important organic compounds : Test of three RP-HPLC-methods and new experimental results.

Authors:  S Ritter; W H Hauthal; G Maurer
Journal:  Environ Sci Pollut Res Int       Date:  1995-11       Impact factor: 4.223

2.  Comparative QSAR analysis of cyclo-oxygenase2 inhibiting drugs.

Authors:  Arumugam Mohanapriya; Dayalan Achuthan
Journal:  Bioinformation       Date:  2012-04-30
  2 in total

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