An Optimal Energy Efficient Design of Artificial Noise for Preventing Power Leakage based Side-Channel Attacks

Side-channel attacks (SCAs), which infer secret information (for example secret keys) by exploiting information that leaks from the implementation (such as power consumption), have been shown to be a non-negligible threat to modern cryptographic implementations and devices in recent years. Hence, how to prevent side-channel attacks on cryptographic devices has become an important problem. One of the widely used countermeasures to against power SCAs is the injection of random noise sequences into the raw leakage traces. However, the indiscriminate injection of random noise can lead to significant increases in energy consumption in device, and ways must be found to reduce the amount of energy in noise generation while keeping the side-channel invisible. In this paper, we propose an optimal energy-efficient design for artificial noise generation to prevent side-channel attacks. This approach exploits the sparsity among the leakage traces. We model the side-channel as a communication channel, which allows us to use channel capacity to measure the mutual information between the secret and the leakage traces. For a given energy budget in the noise generation, we obtain the optimal design of the artificial noise injection by solving the side-channel's channel capacity minimization problem. The experimental results also validate the effectiveness of our proposed scheme

Poly[[tetra­aquadi-μ3-oxalato-μ2-oxalato-diprasedymium(III)] dihydrate]

In the title compound, {[Pr2(C2O4)3(H2O)4]·2H2O}n, the three-dimensional network structure has the PrIII ion coordinated by nine O atoms in a distorted tricapped trigonal-prismatic geometry. The coordinated and uncoordinated water mol­ecules inter­act with the carboxyl­ate O atoms to consolidate the network via O—H⋯O hydrogen bonds

Metabolism and Metabolic Inhibition of Xanthotoxol in Human Liver Microsomes

Cytochrome p450 (CYP450) enzymes are predominantly involved in Phase I metabolism of xenobiotics. In this study, the CYP450 isoforms involved in xanthotoxol metabolism were identified using recombinant CYP450s. In addition, the inhibitory effects of xanthotoxol on eight CYP450 isoforms and its pharmacokinetic parameters were determined using human liver microsomes. CYP1A2, one of CYP450s, played a key role in the metabolism of xanthotoxol compared to other CYP450s. Xanthotoxol showed stronger inhibition on CYP3A4 and CYP1A2 compared to other isoenzymes with the IC50 of 7.43 μM for CYP3A4 and 27.82 μM for CYP1A2. The values of inhibition kinetic parameters (Ki) were 21.15 μM and 2.22 μM for CYP1A2 and CYP3A4, respectively. The metabolism of xanthotoxol obeyed the typical monophasic Michaelis-Menten kinetics and Vmax, Km, and CLint values were calculated as 0.55 nmol·min−1·mg−1, 8.46 μM, and 0.06 mL·min−1·mg−1. In addition, the results of molecular docking showed that xanthotoxol was bound to CYP1A2 with hydrophobic and π-π bond and CYP3A4 with hydrogen and hydrophobic bond. We predicted the hepatic clearance (CLh) and the CLh value was 15.91 mL·min−1·kg−1 body weight. These data were significant for the application of xanthotoxol and xanthotoxol-containing herbs

The Analysis of Gravity on Tourism Resource of Shijiazhuang with Anion, Hebei

AbstractThis paper analyzes the decisive factor of The Shijiazhuang coastal economic zone's tourist resource from the perspective of the actual data by adopting Gravity model; meanwhile, presents an overall aspect of Shijiazhuang city, its current development of the tourism industry, and the advantages and characteristics as well. Further proposal is also produced to contribute to the tourist development based on the analysis of the model data

Poly[μ2-aqua-aqua-μ5-naphthalene-2,7-disulfonato-strontium]

In the crystal structure of the polymeric title compound, [Sr(C10H6O6S2)(H2O)2]n, the naphthalene-2,7-disulfonate dianion uses one –SO3 unit to bind to two SrII cations and the other –SO3 unit to bind to three SrII cations; of the two coordinated water mol­ecules, one is monodentate to one SrII cation, whereas the other bridges two SrII cations. The μ5-bridging mode of the dianon and the μ2-bridging mode of the water mol­ecule generate a polymeric three-dimensional network which is consolidated by O—H⋯O hydrogen bonds. The SrII cation exists in an undefined eight-coordinate environment