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Abdel‐Baki Abdel‐Azeem S.,Aboelhadid Shawky M.,Sokmen Atalay,Al‐Quraishy Saleh,Hassan Ahmed O.,Kamel Asmaa A. 한국곤충학회 2021 Entomological Research Vol.51 No.11
The present study was designed to evaluate the insecticidal activity of different concentrations of Foeniculum vulgare and two of its components, trans-anethole and fenchone, against the different stages of Musca domestica. The tested concentrations were applied through a residual film method and topical application on larvae and pupae respectively. Trans-anethole achieved the best results against larvae when compared with those of the fennel or fenchone with LC50 values of 0.58%, 1.57%, and 17.22%, respectively. Moreover, tans-anethole killed 100% of larvae at concentration of 2.5% and fennel achieved the same effect at concentration of 10%, meanwhile fenchone did not reach such an effect at any of the tested concentrations. At the concentration of 10%, fennel oil and trans-anethole induced morphological deformation in the dead larvae such as shrunk bodies with dark colored integument. Regarding the pupicidal activity, fennel oil showed percentage inhibition rate (PIR) of 100% at the concentration of 10% while the same effect was achieved by trans-anethole at concentration of 5%. On the contrary, fenchone did not show any pupicidal activity. Treatment of the third instar house fly larvae with LC5o of fennel oil, trans-anethole, and fenchone significantly inhibited the acetylcholinestrase (AchE) when compared with the control untreated larvae. Additionally, the glutathione-s-transferase (GST) and malondialdehyde (MDA) production significantly increased in the larvae treated with trans-anethole. The results of the present study indicate that the insecticidal activity of fennel oil was mainly attributed to the presence of trans-anethole as a major constituent.
Abdel‐Raheem Mohamed,ALghamdi Huda A.,Reyad Naglaa F. 한국곤충학회 2020 Entomological Research Vol.50 No.5
The red palm weevil, Rhynchophorus ferrugineus, is the biggest pest of various palm species. The aim of this study was to evaluate the impact of the essential oils of purslane, mustard and castor (bulk and nano) on R. ferrugineus and to evaluate the oviposition deterrent effect to prevent new infestations. Prepared concentrations of essential oils (bulk and nano) were tested for their impact on R. ferrugineus larvae, pupae and adults. The most effective oil was purslane oil (bulk and nano), followed by mustard and the least effective was castor. The percent mortality of larvae was 75.2, 45.3 and 17.9% (bulk phase) and 92.5, 84.4 and 65.5% (nano phase) in purslane, mustard and castor, respectively, when treated with the high concentration. The percent mortality of adults was 67.2, 40.0 and 15.6% (bulk phase) and 83.5, 72.9 and 60.0% (nano phase) in purslane, mustard and castor, respectively, when treated with the high concentration. The number of eggs laid decreased with increasing concentration of the tested oils. Purslane essential oil showed good impact on R. ferrugineus larvae and adults followed by mustard and castor oils as bulk and as nano.
Abdel-Alim Mohamed Abdel-Alim,Abdel-Nasser Ahmed El-Shorbagi,Samia Galal Abdel-Moty,Hajjaj Hassan Mohamed Abdel-Allah 대한약학회 2005 Archives of Pharmacal Research Vol.28 No.6
This work includes the synthesis of 15 final compounds (6a-h and 7b-h) as prodrugs of 5-ASA in the form of the acid itself, esters and amides linked by an amide linkage through a spacer to the endocyclic ring N of nicotinamide. Also, 15 new intermediate compounds were prepared. The target compounds (6b, 6f, 7b, and 7e-h) revealed potent analgesic and anti-inflammatory activities in comparison to sulfasalazine and 5-ASA. In addition, ulcerogenicity, LD50, in vivo and in vitro metabolism of compound 7f were determined.
Abdel-Alim Abdel-Alim Mohamed,EI-Shorbagi Abdel-Nasser Ahmed,Abdel-Moty Samia Galal,Abdel-Allah Hajjaj Hassan Mohamed The Pharmaceutical Society of Korea 2005 Archives of Pharmacal Research Vol.28 No.6
This work includes the synthesis of 15 final compounds (6a-h and 7b-h) as prod rugs of 5-ASA in the form of the acid itself, esters and amides linked by an amide linkage through a spacer to the endocyclic ring N of nicotinamide. Also, 15 new intermediate compounds were prepared. The target compounds (6b, 6f, 7b, and 7e-h) revealed potent analgesic and anti-inflammatory activities in comparison to sulfasalazine and 5-ASA. In addition, ulcerogenicity, $LD_{50}$, in vivo and in vitro metabolism of compound 7f were determined.
Enas Nashaat Amin,Abdel-Alim M. Abdel-Alim,Samia G. Abdel-Moty,Abdel-Naser A. El-Shorbagi,Mahran Sh. Abdel-Rahman 대한약학회 2010 Archives of Pharmacal Research Vol.33 No.1
4,5-dihydro-3(2H)pyridazinones such as CI-914, CI-930 and pimobendan along with tetrahydropyridopyridazine (endralazine) and perhydropyridazinodiazepine (cilazopril) have been used as potent positive inotropes, antihypertensives as well as platelet aggregation inhibitors. Accordingly, the present work involves the synthesis of 24 target compounds; 4,5-dihydro-3(2H)pyridazinones in addition to seven reported intermediates. The chemical structures of the new compounds were assigned by microanalysis, IR, 1H-NMR spectral analysis and some representatives by mass spectrometry. The positive inotropic effect of the final compounds and the intermediates 12a-12d as well as the reported intermediate compound 10 was determined in-vitro on isolated rabbit heart in comparison to digoxin. Data obtained revealed that twelve of the test compounds exhibited higher effective response than digoxin, nine compounds elicited comparable effects to digoxin and eight compounds were less active than digoxin. In addition, four compounds approved marked significant hypotensive effect better than that of the previously reported compound 10. Moreover, two compounds induced complete platelet aggregation inhibition. The last two compounds were also subjected to determination of their LD50 and they showed no signs of toxicity up to the dose level 300 mg/kg (i.p.), while the reported oral LD50 of digoxin is 17.78 mg/kg. Correlation of cardiotonic and hypotensive activities with structures of compounds was tried and pharmacophore models were computed to get useful insight onto the essential structural features required for inhibiting phosphodiesterase-III in the heart muscles and blood vessels.
Abdel-aziz Khairy Abdel-aal,Yuji Yagi 한국지질과학협의회 2017 Geosciences Journal Vol.21 No.2
We estimated moment tensor and centroid depth of eight small/moderate local earthquakes occurred between 2011 and 2013 in the northern Red Sea Triple Junction using a moment tensor inversion of near-source waveform data recorded by very broadband stations of the Egyptian National Seismic Network (ENSN). We also estimated the focal mechanism using the P-wave polarity data set and then compared it with the moment tensor inversion results. The moment tensor solutions are consistent with the focal mechanism obtained from the P-wave polarity data. We also estimated the stress field in the study area using the Multiple Inverse Method (MIM). Our results indicate that the axis of the minimum principal stress is a nearly horizontal NE-SW direction, while the axis of the maximum principal stress is nearly vertical. The direction of the minimum principal stress is consistent with the opening direction of the northern Red Sea zone, where the southern part of Gulf of Suez is currently under an extensional stress field with a NE-SW trending horizontal extension. These results are compatible with the kinematics of the Red Sea-Gulf of Suez rift.
Synthesis and Anticonvulsant Evaluation of N-Substituted-Isoindolinedione Derivatives
Abdel-Hafez, Atef Abdel-Monem The Pharmaceutical Society of Korea 2004 Archives of Pharmacal Research Vol.27 No.5
A series of N-substituted-1,3-isoindolinedione derivatives (2-16) were synthesized for the purpose of defining the effect of N-substitution on the anticonvulsant activity of these derivatives. The target compounds (2-16) were obtained by condensation of phthalic anhydride with the corresponding amine derivative. The structures of the synthesized derivatives (2-16) were confirmed by means of IR, $^1$H-NMR, $^{13}$ C-NMR, MS and elemental analyses. The anticonvulsant activity of all compounds (2-16) were evaluated by subcutaneous pentylenetetrazole seizure threshold test at doses of 0.2, 0.4 and 0.8 mmol/kg compared with sodium valproate as a positive control. Their neurotoxicity were determined by the rotorod test. Many of the present series of compounds showed good anticonvulsant activity at the tested doses, as compared to sodium valproate. Three of them (4, 6 and 11) exhibited 100 % protection against convulsions, neurotoxicity and death at all tested doses. Out of the series, two compounds (12 and 13) were completely inactive with 100% mortality. 3-(p-chlorophenyl)-4-(1 ,3-dioxo-2,3-dihydro-1 H-2-isoindolyl) butanoic acid derivative (11) has emerged as the most active compound which is 20 times more active than valproate with ED$_{50}$ 8.7, 169 mg/kg; TD$_{50}$ 413, 406 mg/kg and PI 47.5, 2.4. The results revealed the importance of the combination of baclofenic and phthalimide moieties (compound 11) as a promising anticonvulsant candidate.