Thesis
Biochemical and Cytochemical Studies of Blood Esteratic Profile in Cancer Patients
A study of the Effect of Some Antimicrobials against Various Species of Leishmania (In Vitro Study)
Clindamycin LD50 value against L.donovani promastigotes (1.07mg/ml) was more potent than control in opposite axenic and intramacrophage amastigotes (0.07 and 0.15 mg/ml) was less potent than control respectively, against L.major promastigotes, axenic and intramacrophage amastigotes (1.0, 0.015 and 0.64 mg/ml) was less potent than control respectively and against L.tropica promastigotes, axenic and intramacrophage amastigotes (0.63, 0.21 and 0.53 mg/ml) was less potent than control respectively.
Indoor RFID network planning based on particle swarm optimization
Design and implementation of PSO-based PID controller for MA2000 robotic manipulator
Construction and study of new polymeric membrane electrodes for clarithromycin determination
SYNTHESIS, CHARACTERIZATION AND EVALUATION OF BIOLOGICAL ACTIVITY FOR SOME FIVE MEMBEREDAND FUSED HETEROCYCLIC DERIVATIVES
Preparation of some Organic Compounds containHetero- atoms as Corrosion Inhibiters forMild Steel in Acidic Media.
1- This work involves preparation of some organic compounds contain hetero-atoms, that starting from (E)-2-benzylidenehydrazinecarbothioamide[1]to (E)-5-(2-chloroethylthio)-N-(1-phenylethylidene)-1,3,4-thiadiazol-2-amine [21],are summarized below: - First set of organic compounds was prepared in one step by a condensation reaction between the carbonyl group of aldehydes or ketones and the amino group ofThiosemicarbazide derivatives to produce the compounds: [1]- (E)-2-benzylidenehydrazinecarbothioamide.
SPECTROSCOPIC INVESTIGATION FOR SOME TRANSITION METAL SALTS IN IONIC LIQUID
Separation of isomeric hydrocarbons by Gas Chromatography using Liquid Crystalline Materials as Stationary Phases
The synthesized compounds were characterized using FTIR, 1HNMR 13CNMR, EI-Mass spectroscopy and CHN analysis. The liquid crystalline properties of the prepared compounds which were verified using differential scanning calorimete (DSC) and hot-stage polarizing optical microscope (POM) were discussed. The
Synthesis and Cytotoxic Activity of Some Pyrimidine Derivatives
This research is divided into two parts: Part one: This part involved in the synthesis of some pyrimidine derivativeswhich play an important role in the medicinal chemistry because they possess promising cytotoxic activity. The synthesized compounds: 1. 5,6-diaminouracil-2,4-diol hydrochloride. 2.5,6-diamino- 2-mercaptopyrimidine-4-ol hydrochloride. 3.2-mercapto-6-methylpyrimidin-4(3H)-one. 4.2-hydrazinyl-6-methylpyrimidin-4(3H)-one 5.2-(2-(4-(dimethylamino)benzylidene)hydrazinyl)-6-methylpyrimidin-4(3H)-one.