Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Chemical Compound Review:

SureCN36454 4-[(4- hydroxyphenyl)methyl]phenol

Synonyms: CHEMBL138061, CCRIS 9461, B47006_ALDRICH, NSC-401136, KSC-19-052, ...

Hopp, L. et al., Watanabe, N. et al., Cabaton, N. et al.

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High impact information on NSC401136

Six compounds with chemical structures related to those of 5 and 1 were tested for ability to induce the release of 86Rb from COS-7 cells preloaded with this isotope: 4,4'-(9-fluorenylidene)diphenol (2), 4, 4'-(9-fluorenylidene)dianiline, 4, 4'-(9-fluorenylidene)bisphenoxyethanol, 1,1'-bi-2-naphthol, 4, 4'-biphenol, and bis(4-hydroxyphenyl)methane [1].
The distribution of bisphenol F (4,4'-dihydroxydiphenyl-methane, BPF) was studied in female Sprague-Dawley rats [2].
The decomposition of structurally similar substances of 4,4'-ethylidenebisphenol (EBP) and 4,4'-methylenebisphenol (MBP) was compared [3].

References

Bisphenols that stimulate cells to release alkali metal cations: a structure-activity study. Hopp, L., Megee, S.O., Lloyd, J.B. J. Med. Chem. (1998) [Pubmed]
Disposition and metabolic profiling of bisphenol F in pregnant and nonpregnant rats. Cabaton, N., Chagnon, M.C., Lhuguenot, J.C., Cravedi, J.P., Zalko, D. J. Agric. Food Chem. (2006) [Pubmed]
Photodegradation mechanism for bisphenol A at the TiO2/H2O interfaces. Watanabe, N., Horikoshi, S., Kawabe, H., Sugie, Y., Zhao, J., Hidaka, H. Chemosphere (2003) [Pubmed]

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