Back to Search
Start Over
Quantitative structure-activity relationships of phenolic compounds causing apoptosis.
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2003 Feb 20; Vol. 11 (4), pp. 617-20. - Publication Year :
- 2003
-
Abstract
- A study of a variety of phenolic compounds (simple phenols, estradiol, bisphenol A, diethylstilbesterol) on their action on L1210 leukemia cells led to the formulation of the following QSAR for apoptosis:log 1/C=-3.16 Clog P+2.77 CMR-3.76n=11, r(2)=0.939, s=0.630, q(2)=0.892C is the molar concentration causing 25% apoptosis, Clog P is the calculated octanol/water partition coefficient and CMR is the calculated molecular refractivity. Our results imply the significance of characterization of the phenolic compounds with apoptotic activity and the development of new agents for cancer therapy.
- Subjects :
- Algorithms
Animals
Cell Line
DNA biosynthesis
DNA drug effects
DNA Repair drug effects
Drug Design
Flow Cytometry
Leukemia L1210 drug therapy
Leukemia L1210 pathology
Mice
Quantitative Structure-Activity Relationship
Tumor Cells, Cultured
Apoptosis drug effects
Phenols chemical synthesis
Phenols pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0968-0896
- Volume :
- 11
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 12538027
- Full Text :
- https://doi.org/10.1016/s0968-0896(02)00326-7