Fault-Based Attack on Montgomery��s Ladder Algorithm

In this paper we present invalid-curve attacks that apply to the Montgomery ladder elliptic curve scalar multiplication (ECSM) algorithm. An elliptic curve over the binary field is defined using two parameters, a and b. We show that with a different “value” for curve parameter a, there exists a cryptographically weaker group in nine of the ten NIST-recommended elliptic curves over \mathbbF_2^m\mathbb{F}_{2^{m}}. Thereafter, we present two attacks that are based on the observation that parameter a is not utilized for the Montgomery ladder algorithms proposed by López and Dahab (CHES 1999: Cryptographic Hardware and Embedded Systems, LNCS, vol. 1717, pp. 316–327, Springer, Berlin, 1999). We also present the probability of success of such attacks for general and NIST-recommended elliptic curves. In addition we give some countermeasures to resist these attacks.     

Hexadecyltrimethylammonium bromide micellization in glycine,diglycine, and triglycine aqueous solutions as a function of surfactant concentration and temperatures

Micellization behavior of hexadecyltrimethylammonium bromide (HTAB) was investigated conductometrically in aqueous solutions containing 0.02 mol kg^?1glycine (Gly), diglycine (Gly-Gly), and triglycine (Gly-Gly-Gly) as a function of surfactant concentration at different temperatures. The critical micelle concentration (CMC) of HTAB exhibits a decreasing trend as the number of carbon atoms increases from Gly to Gly-Gly-Gly, favoring the micelle formation. The values of CMC and the degree of counterion dissociation of the micelles were utilized to evaluate the standard free energy for transferring the surfactant hydrophobic chain out of the solvent to the interior of the micelle, ΔG _HP ^○ , free energy associated with the surface contributions, ΔG _S ^○ , standard free energy, ΔG _m ^○ , enthalpy, ΔH _m ^○ , and entropy, ΔS _m ^○ of micellization were also calculated. The results show that the micellization of HTAB in aqueous solutions as well as in aqueous Gly/Gly-Gly/Gly-Gly-Gly solutions is primarily governed by the entropy gain due to the transfer of the hydrophobic groups of the surfactant from the solvent to the interior part of the micelle. The CMC obtained by fluorometric method is in close agreement with those obtained conductometrically. Furthermore, decrease in the I ₁/I ₃ ratio of pyrene fluorescence intensity suggests the solubilization of the additives by the surfactant micelles and that this solubilization increases as the hydrophobicity increases from Gly to Gly-Gly-Gly.     

Synthesis,spectroscopy, and biological activity of heterobimetallic complexes containing Sn(IV) and Pd(II) with 4-(hydroxymethyl)piperidine-1-carbodithioic acid

4-(Hydroxymethyl)piperidine-1-carbodithioic acid has been synthesized by reacting 4-piperidinemethanol with carbon disulfide at room temperature. The synthesized ligand was treated with organotin(IV) chlorides to yield organotin complexes. These complexes by further treatment with palladium chloride afford heterobimetallic complexes containing Sn(IV) and Pd(II). The synthesized complexes along with ligand has been characterized by elemental analysis, FTIR, NMR (¹H, ¹³C) spectroscopy. The IR data confirmed the complexation through the sulfur and oxygen donor sites of the ligand. NMR data revealed the tetrahedral geometry in the solution. Biological activity was checked against selected bacterial and fungal strains. All complexes along with the ligand were found to be biologically active with few exceptions.     

A simple,direct and reliable extraction method applied to GaN devices

In this article, a simple, direct and reliable extraction method has been developed and applied to different sizes of Gallium Nitride (GaN) high electron mobility transistors (HEMTs). Instead of high-voltage gate-forward measurements with risk of device damage, the proposed approach uses only uncritical cold S-parameters at pinch-off (V_GS < V_p, V_DS = 0 V) and in the off-state (V_GS = 0 V, V_DS = 0 V). The extraction procedure is validated by small- and large-signal measurements. Very good agreement is obtained. Scaling of parasitic elements with the device size is confirmed.     

克尔透镜锁模超短脉冲的时空往返模型

本文解决了由克尔透镜锁模的飞秒脉冲固体激光的时空模型中脉冲和波束形状的相互关系.根据随时间变化的脉冲的形状和KLM飞秒脉冲激光对于谐振腔中的空间光束参数建立了时空往返模型.     

Multifaced Assessment of Antioxidant Power,Phytochemical Metabolomics,In-Vitro Biological Potential and In-Silico Studies of Neurada procumbens L.: An Important Medicinal Plant

This work was undertaken to explore the phytochemical composition, antioxidant, and enzyme-inhibiting properties of Neurada procumbens L. extracts/fractions of varying polarity (methanol extract and its fractions including n-hexane, chloroform, n-butanol, and aqueous fractions). A preliminary phytochemical study of all extracts/fractions, HPLC-PDA polyphenolic quantification, and GC-MS analysis of the n-hexane fraction were used to identify the phytochemical makeup. Antioxidant (DPPH), enzyme inhibition (against xanthine oxidase, carbonic anhydrase, and urease enzymes), and antibacterial activities against seven bacterial strains were performed for biological investigation. The GC-MS analysis revealed the tentative identification of 22 distinct phytochemicals in the n-hexane fraction, the majority of which belonged to the phenol, flavonoid, sesquiterpenoid, terpene, fatty acid, sterol, and triterpenoid classes of secondary metabolites. HPLC-PDA analysis quantified syringic acid, 3-OH benzoic acid, t-ferullic acid, naringin, and epicatechin in a significant amount. All of the studied extracts/fractions displayed significant antioxidant capability, with methanol extract exhibiting the highest radical-scavenging activity, as measured by an inhibitory percentage of 81.4 ± 0.7 and an IC₅₀ value of 1.3 ± 0.3. For enzyme inhibition experiments, the n-hexane fraction was shown to be highly potent against xanthine oxidase and urease enzymes, with respective IC₅₀ values of 2.3 ± 0.5 and 1.1 ± 0.4 mg/mL. Similarly, the methanol extract demonstrated the strongest activity against the carbonic anhydrase enzyme, with an IC₅₀ value of 2.2 ± 0.4 mg/mL. Moreover, all the studied extracts/fractions presented moderate antibacterial potential against seven bacterial strains. Molecular docking of the five molecules β-amyrin, campesterol, ergosta-4,6,22-trien-3β-ol, stigmasterol, and caryophyllene revealed the interaction of these ligands with the investigated enzyme (xanthine oxidase). The results of the present study suggested that the N. procumbens plant may be evaluated as a possible source of bioactive compounds with multifunctional therapeutic applications.     

The Potential Role of Apigenin in Cancer Prevention and Treatment

Cancer is the leading cause of death worldwide. In spite of advances in the treatment of cancer, currently used treatment modules including chemotherapy, hormone therapy, radiation therapy and targeted therapy causes adverse effects and kills the normal cells. Therefore, the goal of more effective and less side effects-based cancer treatment approaches is still at the primary position of present research. Medicinal plants or their bioactive ingredients act as dynamic sources of drugs due to their having less side effects and also shows the role in reduction of resistance against cancer therapy. Apigenin is an edible plant-derived flavonoid that has received significant scientific consideration for its health-promoting potential through modulation of inflammation, oxidative stress and various other biological activities. Moreover, the anti-cancer potential of apigenin is confirmed through its ability to modulate various cell signalling pathways, including tumor suppressor genes, angiogenesis, apoptosis, cell cycle, inflammation, apoptosis, PI3K/AKT, NF-κB, MAPK/ERK and STAT3 pathways. The current review mainly emphases the potential role of apigenin in different types of cancer through the modulation of various cell signaling pathways. Further studies based on clinical trials are needed to explore the role of apigenin in cancer management and explain the possible potential mechanisms of action in this vista.     

N‐{4‐Bromo‐2‐[(3‐bromo‐1‐phenylsulfonyl‐1H‐indol‐2‐yl)methyl]‐5‐methoxyphenyl}acetamide

In the title compound, C₂₄H₂₀Br₂N₂O₄S, the indole ring system is planar and the S atom has a distorted tetrahedral configuration. The sulfonyl‐bound phenyl ring is orthogonal to the indole ring system and the conformation of the phenyl­sulfonyl substituent with respect to the indole moiety is influenced by intramolecular C—H⃛O hydrogen bonds involving the two sulfonyl O atoms. The mean plane through the acetyl­amido group makes a dihedral angle of 57.0 (1)° with the phenyl ring of the benzyl moiety. In the crystal, glide‐related mol­ecules are linked together by N—H⃛O hydrogen bonds and C—H⃛π interactions to form molecular chains, which extend through the crystal. Inversion‐related chains are interlinked by C—H⃛π interactions to form molecular layers parallel to the bc plane. These layers are interconnected through π–π interactions involving the five‐ and six‐membered rings of the indole moiety.     

Nepetanal and nepetanoate: a new diterpene aldehyde and a benzene derivative ester from Nepeta juncea

One new tricyclic clerodane type diterpene aldehyde nepetanal (1) and one new benzene derivative nepetanoate (2) have been isolated from a plant Nepeta juncea together with two known compounds oleanolic acid (3) and ursolic acid (4). The structures of the isolated compounds were elucidated by means of modern spectroscopic techniques and comparison with literature data. Copyright © 2009 John Wiley & Sons, Ltd.