A Labeling DOM-Based Tree Walking Algorithm for Mapping XML Documents into Relational Databases

XML has emerged as the standard format for representing and exchanging data on the World Wide Web. For practical purposes, it is found to be critical to have efficient mechanisms to store and query XML data, as well as to exploit the full power of this new technology. Several researchers have proposed to use relational databases to store and query XML data. With the understanding the limitations of current approaches, this thesis aims to propose an algorithm for automatic mapping XML documents to RDBMS with XML-API as a database utility. The algorithm uses best fit auto mapping technique, and dynamic shredding, of a specified selected XML document type (datacentric, document-centric, and mixed documents).e. The propose algorithm use DOM(Data Object Model) as a warehouse and stack as a data structure to mapping the XML document into relational database and reconstructing the XML document from the relational database. The experiment study show that the algorithm mapping document and reconstructing it again well. Finally, the algorithm compare with other algorithms the result is good in time and efficiency, also the algorithm complexity is O(11n+2)

Nonrigid Medical Image Registration using Adaptive Gradient Optimizer

Medical image registration has a significant role in several applications. It has sequential processes, including transformation, similarity metric calculation, diffusion regularization, and optimization of the transformation parameters (i.e., rotation, translation, and shear). The optimization process for determining the optimal set of the transformation vectors is considered the main stage affecting the performance of the registration process. Hence, medical image registration can be deliberated as an optimization problem for computing the geometric transformations to realize maximum similarity between the moving image and the fixed one. In this work, a mono-modal nonrigid image registration using B-spline is designed for the alignment of Computed Tomography (CT) images of thorax using Adaptive Gradient algorithm (AdaGrad) optimizer. In addition, a comparative study with other first order optimizers, such as Stochastic Gradient Descent (SGD), Adaptive Moment Estimation (Adam) algorithm (AdaMaX), AdamP, and RangerQH were conducted. Also, a comparison with the limited memory Broyden-Fletcher-Goldfarb-Shannon (LBFGS) as a second order optimizer was also carried out. The results showed the superiority of the AdaGrad optimizer by 56.99% and 48.37% improvement in the compared to the target registration error (TRE) compared to the SGD, and the LBFGS optimizer, respectively

Effect of Irradiated Crumb Rubber on Cold Recycled Bitumen Emulsion Mixes Properties

Recycling is one of the most innovative and interesting techniques for the rehabilitation of distressed road pavements. In recent years the increased interest in this process has led to the development of various alternative methods for the recovery and the reuse of road bituminous materials. Cold recycling is among the recycling techniques. Many researches involve the use of Crumb Rubber within a mixture containing 100% Reclaimed Asphalt Pavement. The goal of this research is to analyze and evaluate the different physical and mechanical characteristics from addition of irradiated crumb rubber to asphalt emulsion cold mixes. The results indicated that the existence of the irradiated crumb in asphalt emulsion could improve the indirect tensile strength, high temperature stability, moisture resistance and fatigue performance of asphalt emulsion cold recycled mixes

Simple approach to thieno[3,2-d]pyrimidines as new scaffolds of antimicrobial activities

6-(4-Chlorophenyl)-spiro[cyclohexane-1,2-thieno[3,2-d][1,3]oxazin]-4(1H)-one (1) was synthesized and used as a starting material for the synthesis of a novel series of spiro compounds having biologically active sulfonamide (2a-e) and 3-(4-acetylphenyl)-6-(4-chlorophenyl)-1H-spiro[cyclohexane-1,2-thieno[3,2-d]pyrimidine-4(3H)-one (3). Compound 2a was used as a key intermediate for the synthesis of sulfonyl carbothioamide derivatives (4a-c). Also, compound 3 was used as an intermediate for the synthesis of 3H-spiro[cyclohexane-1,2-thieno[3,2-d]pyrimidin]-3-yl]phenyl}-2-imino-4-(substituted phenyl and/or thienyl)-1,2-dihydropyridine-3-carbonitrile derivatives (5a-e), 3H-spiro[cyclohexane-1,2-thieno[3,2-d]pyrimidin]-3-yl]phenyl}-2-oxo-4-(substituted phenyl and/or thienyl)-1,2-dihydropyridine-3-carbonitrile derivatives (6a-e), and 4-[(2Z)-3-substituted-arylprop-2-enoyl]phenyl-1H-spiro[cyclohexane-1,2-thieno[3,2-d]pyrimidine derivatives (7a-e). Cyclocondensation of 7a-e with hydrazine hydrate produced 6-(4-chlorophenyl)-3-[4-(5-substituted aryl-4,5-dihydro-1H-pyrazol-3-yl)phenyl]-1H-spiro[cyclohexane-1,2-thieno-[3,2-d]pyrimidin]-4(3H)-ones (8a-e), but with hydroxylamine hydrochloride afforded the corresponding isoxazoline derivatives (9a-e). Also, cyclocondensation by thiourea afforded 2-thioxo-1,2-dihydropyrimidin-4-yl)-phenyl-spiro-{cyclohexanethieno[3,2-d]pyrimidin}-4-one derivatives (10a-e). The new compounds were investigated for antimicrobial activity. Compounds 2c, 8b, c, 9b and 10b were the most potent ones against both Gram-negative and Gram-positive bacteria. Compound 8c exhibited higher antifungal activity towards the examined fungi with MIC of 1–2 µmol mL–1 compared to ketoconazole (MIC 2–3 µmol mL–1)

Toward sustainable cities: Monitoring thermal environment for buildings and pedestrian space using drone-captured 3D thermal imaging

UAE's average temperature has risen in recent years and is expected to rise more in the next 40 years, creating a massive heat island agglomeration. Therefore, the demand for energy saving and diversified personal thermal management requires innovative solutions combining advanced building materials and structural designs to provide personal thermal comfort during indoor and outdoor activities. However, due to the complexities of structural designs and their associated materials, analytical and numerical strategies are for revealing real-world scenarios are limited. Therefore, full-scale experiments are required for exploring and demonstrating dynamic scenarios under thermal stress. This study aimed to explore the feasibility of using drone along with various thermal image analysis software that enables thermal photogrammetric mapping for monitoring and classification of heat rates based on building components surveyed across the UAEU campus. Thermal aerial images were collected in March 2022 and analyzed using SPSS, Agisoft Metashape Professional, DJI Thermal Tool, and FLIR for two buildings, A and B, and pedestrian spaces across UAEU's main campus in shaded, unshaded, and green zones. Noramilty and Kruskal-Wallis H tests were applied to examine if there was a statistically significant variation in surface temperatures. The pedestrian space thermal analysis showed that the natural shaded grass surface has the most tolerable heat environment (mean rank = 7.6), while the unshaded sand surface has the most unfriendly thermal environment (mean rank = 52.0), with an 18°C difference in mean surface temperature. The study also revealed the temperature evolution process and its dependence on building materials and structural designs, providing first-hand research data based on building components for the UAE climate, setting the path for future research in the era of sustainability and urban development

Synthesis and evaluation of antitumor activity of new 4-substituted thieno[3,2-d]-pyrimidine and thienotriazolopyrimidine derivatives

3-Methyl-6-phenyl-2-thioxo-2,3-dihydro-thieno[3,2-d]pyrimidin-4(1H)-one (2), on treatment with phosphorous oxychoride, affored 4-chloro-3-methyl-6-phenyl -thieno[3,2-d]pyrimidine-2(3H)-thione (3). A series of novel 6-phenyl-thieno[3,2-d]pyrimidine derivatives 4-9 bearing different functional groups were synthesized via treatment of compound 3 with different reagents. On the other hand, compound 2 was used to synthesize ethyl-[(3-methyl-6-phenyl-2-thioxo-2,3-dihydro-thieno[3,2-d]pyrimidin-4-yl)-oxy]acetate (10), 2-hydrazinyl-3-methyl-6-phenyl-thieno[3,2-d]pyrimidin-4(3H)-one (11), 3-methyl-2-(methyl-sulfanyl)-6-phenyl-thieno[3,2-d]pyrimidin-4(3H)-one (12) and N-(phenyl)/4-chlorophenyl or methoxy-phenyl)-2-[(3-methyl-4-oxo-6-phenyl-3,4-dihydro-thieno[3,2-d]pyrimidin-2-yl)-sulfanyl]-acetamide (13a-c). In addition, compound 12 was used to synthesize thieno[1,2,4]triazolopyrimidine derivatives 14 and 15 and 3-methyl-2-(methyl-sulfonyl)-6-phenyl-thieno[3,2-d]pyrimidin-4(3H)-one (16) through the reaction with the respective reagents. Moreover, the reaction of 16 with 4-phenylenediamine gave 2-[(4-aminophenyl)-amino]-3-methyl-6-phenyl-thieno[3,2-d]pyrimidin-4(3H)-one (17), which reacted with methanesulfonyl chloride to afford N-{4-[(3-methyl-4-oxo-6-phenyl-3H,4H-thieno[3,2-d]pyrimidin-2-yl)-amino]phenyl}-methanesulfonamide (18). The majority of the newly synthesized compounds displayed potent anticancer activity, comparable to that of doxorubicin, on three human cancer cell lines, including the human breast adenocarcinoma cell line (MCF-7), cervical carcinoma cell line (HeLa) and colonic carcinoma cell line (HCT-116). Compounds 18, 13b and 10 were nearly as active as doxorubicin whereas compounds 6, 7b and 15 exhibited marked growth inhibition, but still lower than doxorubicin

Synthesis of thiophene and N-substituted thieno[3,2-d]pyrimidine derivatives as potent antitumor and antibacterial agents

This paper describes the synthesis of 1,4-dihydropyridine compounds (DHPs) endowed with good muscle relaxant activity and stability to light. Six new condensed DHPs were synthesized by the microwave irradiation method. A long-chain ester moiety [2-(methacryloyloxy)ethyl] and various substituents on the phenyl ring were demonstrated to affect the muscle relaxant activity occurring in isolated rabbit gastric fundus smooth muscle strips. Forced photodegradation conditions were applied to the molecules according to the ICH rules. The degradation profile of the drugs was monitored by spectrophotometry coupled with the multivariate curve resolution technique. Formation of the oxidized pyridine derivative was observed for all the studied DHPs, except for one compound, which showed very fast degradation and formation of a second photoproduct. Pharmacological tests on the molecules showed a good muscle relaxing effect, with a mechanism similar to that of nifedipine, however, proving to be more stable to light

One-Pot Microwave Synthesis of Pyrimido[4,5-b]quinoline and its C- and S-Glycosides with Anti-Inflammatory and Anticancer Activities

An efficient one-pot synthesis of 2-thioxopyrimido[4,5-b]quinoline 3a,b has been accomplished from a three-component reaction of 6-aminothiouracil, cyclohexanone and aromatic aldehyde under microwave irradiation. Compound 3a,b was used as a key intermediate for the synthesis of S- and C-nucleoside analogs of types, 5-(4-fluorophenyl / 4-anisyl)-2-S-(β-D-ribofuranosyl / arabinofuranosyl)-6,7,8,9-tetrahydro-3H-pyrimido[4,5-b]quinolin-4-one (6a–d) and 5-(4-fluorophenyl / 4-anisyl)-2-S-(β-D-gluco / galactopyranosyl)-6,7,8,9-tetrahydro-3H-pyrimido[4,5-b]quinolin-4-one (8a–d). Also. the 2-hydrazino compounds 9a,b were used for the synthesis of 3-(glycosyl)-6-(4-substituted phenyl)-7,8,9,10-tetrahydro[1,2,4]triazolo[4\u27,3\u27:1,2]pyrimido[4,5-b]quinoline-5-(1H)-one (11a–d and 13a–d). The title compounds were investigated for anti-inflammatory and anticancer activities. Compounds 11a exhibited the comparable anti-inflammatory activity (83.4 %) to the standard drug Indomethacin (85.2 %). 5-(4-Fluorophenyl)-2-S-(β-D-ribofuranosyl)-6,7,8,9-tetrahydro-3H-pyrimido[4,5-b]quinolin-4-one 6a and 3-(ribosyl)-5-(4-fluorophenyl)-7,8,9,10-tetrahydro[1,2,4]triazolo[4\u27,3\u27:1,2]pyrimido[4,5-b]quinolin-5-one (13a) exhibited the maximum cytotoxic effect against the three human cancer cell lines with inhibitory effects higher than the reference doxorubicin. This work is licensed under a Creative Commons Attribution 4.0 International License

Facile heterocyclic synthesis and antimicrobial activity of polysubstituted and condensed pyrazolopyranopyrimidine and pyrazolopyranotriazine derivatives

Reaction of 6-amino-3-methyl-4-(substituted phenyl)-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile (1) with triethylorthoformate followed by treatment with hydrazine hydrate, formic acid, acetic acid, phenylisocyanate, ammonium thiocyanate and formamide afforded the corresponding pyranopyrimidine derivatives 2–6. Cyclocondensation of 1 with cyclohexanone afforded pyrazolopyranoquinoline 7. One-pot process of diazotation and de-diazochlorination of 1 afforded pyrazolopyranotriazine derivative 8, which upon treatment with secondary amines afforded 9 and 10a-c. Condensation of 2 with aromatic aldehyde gave the corresponding Schiff bases 11a,b, the oxidative cyclization of the hydrazone with appropriate oxidant afforded 11-(4-fluorophenyl))-2-(4-substitutedphenyl)-10-methyl-8,11-dihydropyrazolo-[4\u27,3\u27:5,6]pyrano[3,2-e][1,2,4]triazolo[1,5-c]pyrimidines (12a,b). Structures of the synthesized compounds were confirmed by spectral data and elemental analysis. All synthesized compounds were evaluated for antibacterial and antifungal activities compared to norfloxacin and fluconazole as standard drugs. Compounds 9, 10c, 12a and 15 were found to be the most potent antibacterial agents, with activity equal to that of norfloxacin. On the other hand, compound 5 exhibited higher antifungal activity compared to fluconazole