Skip to main content
. 2012 Apr;53(4):718–725. doi: 10.1194/jlr.M023689

TABLE 1.

Evaluation of the alkylating properties 5,6α-EC, 5,6β-EC, and SO

Compound Solvent Temperature Nucleophile Reaction
5,6α-EC Ethanol RT NR
Ethanol RT AE NR
Ethanol RT ME NR
Ethanol RT G NR
CM RT NR
Ethanol 37°C NR
Ethanol 37°C AE NR
Ethanol 37°C ME NR
Ethanol 37°C G NR
CM 37°C NR
5,6β-EC Ethanol RT NR
Ethanol RT AE NR
Ethanol RT ME NR
Ethanol RT G NR
CM RT NR
Ethanol 37°C NR
Ethanol 37°C AE NR
Ethanol 37°C ME NR
Ethanol 37°C G NR
CM 37°C NR
SO Ethanol RT NR
Ethanol RT AE +
Ethanol RT ME +
Ethanol RT G +
C.M. RT +
Ethanol 37°C NR
Ethanol 37°C AE +
Ethanol 37°C ME +
Ethanol 37°C G +
CM 37°C +

Compounds were incubated at a concentration of 8 mg/ml for 48 h in the absence or presence of AE, ME, or G at a concentration 0.32 mol/l or in complete growth CM for eukaryote cells at the indicated temperatures. The reaction was followed as described in Materials and Methods.

+, reaction; AE, 2-aminoethanol; CM, culture medium; G, guanine; ME, 2-mercaptoethanol; NR, no reaction, RT, room temperature; SO, styrene oxide.