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Inhibition of MMPs by alcohols.
Tezvergil-Mutluay A, Agee KA, Hoshika T, Uchiyama T, Tjäderhane L, Breschi L, Mazzoni A, Thompson JM, McCracken CE, Looney SW, Tay FR, Pashley DH. Tezvergil-Mutluay A, et al. Dent Mater. 2011 Sep;27(9):926-33. doi: 10.1016/j.dental.2011.05.004. Epub 2011 Jun 14. Dent Mater. 2011. PMID: 21676453 Free PMC article.
Based on the molar concentration required to inhibit rhMMP-9 fifty percent, 2-hydroxyethylmethacrylate (HEMA), 3-hexanol, 3-heptanol and 1-octanol gave the strongest inhibition. SIGNIFICANCE: The results indicate that alcohols with 4 methylene groups inhibit MMPs mo …
Based on the molar concentration required to inhibit rhMMP-9 fifty percent, 2-hydroxyethylmethacrylate (HEMA), 3-hexanol, 3-heptan …
Identification of centrolobol as the platyphylloside metabolite responsible for the observed effect on in vitro digestibility of hay.
Sunnerheim K, Bratt K. Sunnerheim K, et al. J Agric Food Chem. 2004 Sep 22;52(19):5869-72. doi: 10.1021/jf040135e. J Agric Food Chem. 2004. PMID: 15366834
Syntheses of the metabolites from platyphylloside, a phenol causing digestibility inhibition in rumen fluid, have been performed to identify the active metabolite. 1,7-Bis(4'-hydroxyphenyl)-3-heptanone (3-platyphyllone), racemic, and the two enantiomers of 1,7-bis(4'-hydroxypheny …
Syntheses of the metabolites from platyphylloside, a phenol causing digestibility inhibition in rumen fluid, have been performed to identify …
Communication: Supramolecular structures in monohydroxy alcohols: insights from shear-mechanical studies of a systematic series of octanol structural isomers.
Hecksher T, Jakobsen B. Hecksher T, et al. J Chem Phys. 2014 Sep 14;141(10):101104. doi: 10.1063/1.4895095. J Chem Phys. 2014. PMID: 25217896
A recent study [C. Gainaru, R. Figuli, T. Hecksher, B. Jakobsen, J. C. Dyre, M. Wilhelm, and R. ...In this work, we apply broadband shear-mechanical spectroscopy to a systematic series of octanol structural isomers, x-methyl-3-heptanol (with x ranging …
A recent study [C. Gainaru, R. Figuli, T. Hecksher, B. Jakobsen, J. C. Dyre, M. Wilhelm, and R. ...In this work, we apply broa …
Can the pi-facial selectivity of solvation be predicted by atomistic simulation?
Berardi R, Cainelli G, Galletti P, Giacomini D, Gualandi A, Muccioli L, Zannoni C. Berardi R, et al. J Am Chem Soc. 2005 Aug 3;127(30):10699-706. doi: 10.1021/ja052199r. J Am Chem Soc. 2005. PMID: 16045358
We study, using molecular dynamics simulations, the facial solvation of (R)-2-phenyl-propionaldehyde in n-pentane and n-octane at a number of temperatures and compare it with experimental selectivity data for the nBuLi addition leading to syn- and anti-(2R)-2-phenyl-3 …
We study, using molecular dynamics simulations, the facial solvation of (R)-2-phenyl-propionaldehyde in n-pentane and n-octane at a n …