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The observed ATPase inhibitory activities (IC50) of these compounds range between 0.36 and 5.45 μM.
The ionization potentials of these compounds range from 5.45 to 5.97 as determined by the electron photoemission method.
Target compounds range in volatility from acetylene and freons to phthalates and PCBs and include apolar, polar and reactive species.
Organometallic compounds range in polar power from methylpotassium, in which the bond is almost like certain ionic bonds, to lead, which bonds with carbon with very little polarization.
The compounds range from C6 to >C33, including n-alkanols, n-alkanoic acids, n-alkyl formates, n-alkanones, and n-alkanes, all with no carbon number preferences.
Lipophilicity parameters relying on solid-supported lipid membranes correlate well with octanol water partition coefficients Kow for neutral organic compounds (range of log Kow = 1.5 5, n = 7, r = 0.93).
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Activity of compounds ranged widely with AC50 values ranging between 0.01μM for phenylarsine oxide up to 7.32 μM for aristolochic acid.
Next, proliferation of Tg and Nc was tested in the presence of a concentration series of these compounds ranging from 0 to 20 nM.
Lag-times for the start of degradation of these compounds ranged from < 15 to 30 days.
The binding affinity of the new compounds ranged from 6 to 133 nM.
The MIC value of these compounds ranged from 1.56 μg/mL to 100 μg/mL.
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