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Acetophenone thiosemicarbazone (APTSC) was synthesized. Solubility of APTSC was determined in ethanol and methanol at different temperatures. Thiosemicarbazone p-Substituted Acetophenone Derivatives Promote the Loss of Mitochondrial, GSH Depletion, and Death in K Cells. Sample records for acetophenone thiosemicarbazones synthesis The complex compounds of rhenium with methyl ident thiosemicarbazone were synthesized.

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Full Text Available Eastern spruce budworm Choristoneura fumiferiana Clemens ESBW is a major forest pest which feeds on young shoots of white spruce Picea glauca and can cause landscape level economic and ecological losses.

This structure endows high thhiosemicarbazone to the molecules and favors transport through membranes. All drugs presented a dose dependent cytotoxicity against cancer cells at submicromolar concentrations. Inversion from octahedral to square-planar configuration occurred upon heating the parent Ni-HIAT complex to form the corresponding pyrolytic product.

A principal reason is that the sample contained higher percentage of DMPA has higher light-absorbed efficiency.

Oxidative Medicine and Cellular Longevity

Another probable mechanism thiosemicarbazonr operates in aerobic conditions is the alkylation of GSH, as described for nitrocompounds [ 45 ]. The method was used for the determination of mercury in surface water fishes. Extractive spectrophotometric determination of molybdenum using p-chloroisonitroso acetophenone hydrazone. Additionally, one died of an ileus in cycle 1 considered related to treatment and two stopped treatment due to toxicity.

Cu II bis thiosemicarbazone radiopharmaceutical binding to serum albumin: Determination of mercury by liquid chromatography in fresh water fishes using 2-thiophenealdehydephenyl thiosemicarbazone.

acetophenone thiosemicarbazones synthesis: Topics by

The paper presents the synthesis of the ligand 1- 2-hydroxyphenyl ethanone N 4 -allyl thiosemicarbazone H2L and six coordination compounds of copper, nickel and cobalt with this ligand. Our results suggest that I-Ph possess indispensable characteristics acetophenonr an efficient radiopharmaceutical for tumour diagnosis.

Antiproliferative activity was measured using a human colon cancer cell line HCT Highly efficient ultrasonic-assisted removal of Hg II ions on graphene oxide modified with 2-pyridinecarboxaldehyde thiosemicarbazone: The study showed how variation in structures of Schiff bases alters their antioxidant and anti-enzymatic activities.

All metal complexes possess higher antimicrobial activity comparing with the free thiosemicarbazone ligand. The lipophilicity of the synthesized compounds was measured using HPLC and then calculated.


Acetophenone thiosemicarbazone |

In the present paper, solvent extraction technique has been used to develop methods for the separation and spectrophotometric determination of Mo VI with p-chloroisonitroso acetophenone hydrazone was extracted into chloroform from aqueous solution in the pH range 8 to 8.

Present findings show that, in U cells, 1-indanone thiosemicarbazones coordinated to palladium II were more cytotoxic than those complexed with platinum IIalthough the latter were found to be more selective for leukemic cells suggesting that they are promising compounds with potential therapeutic application against hematological malignancies.

However, they do not depend simply on the angle of torsion phi of the functional group as anticipated hitherto. The activity against MRSA is an interesting observation as the commercially available gentamycin is found to be inactive against this bacterial strain.

Characterization of the anti tumoral activity of the thiosemicarbazones derived from N 4 -methyl-tolyl-2acetylpyridine And 2-pyridinoformamide and its metal complex: Therefore, synergistic effects of metal chelation, changes in membrane fluidity, and GSH depletion might contribute to cell death. Only a few compounds showed moderate activity against fungi, and E quinolinylvinyl-N,N-dimethylhydrazine-carbothioamide appeared to be more effective than fluconazole against most of the fungal strains tested.

In the present work, cross-resistance assays were performed with the most active compounds. The antifungal activity against the tested organisms showed that some metal complexes enhanced the activity with respect to the parent ligands. Urease is an important enzyme acftophenone breaks urea into ammonia and carbon dioxide during metabolic processes. An enantioselective synthesis of S-[gamma]-[ 4-trifluoromethyl phenoxy]benzenepropanamine-[3-[sup 14]C] hydrochloride, an important metabolite of fluoxetine hydrochloride.

Studies of zinc II in pharmaceutical and biological samples by extractive spectrophotometry: List, Nanna Holmgaard, E-mail: The formation of the complexes fully inhibited the photoinduced generation of reactive oxygen tiosemicarbazone, and only subtle changes were found in the electronic absorption spectra of the complexes in aqueous and DMSO solutions upon UVA steady-state irradiation.

The transition metal complex of TSCs can redox cycle, leading to the generation of free radical species; this process is an important contributing factor for the antitumor activity of these compounds [ 18 ]. During their replication in a TSC-free medium, some virus populations presented a kind of interaction with the host cell that resembled a persistent infection: The kinetic and thermodynamic parameters for the different thermal decomposition steps in the complexes have been evaluated.


TSCs that possess a coordinating ring- N were previously reported to be efficient metal chelators due to their capacity to form a tridentate complex [ 51 ]. The effect of diverse ions on the extraction of silver I was investigated. The reagent 6-methylpyridinecarboxaldehydephenyl thiosemicarbazone MPAPT has been examined for the pre-concentration of metal ions and determination using air acetylene flame atomic absorption spectrometer.

Acetopuenone, the hydrophobic characteristic of BZTS limits its administration and results in low oral bioavailability.

Full Text Available Pd-loaded hierarchical FAU Pd-FAU membranes, containing an intrinsic secondary non-zeolitic mesoporosity, were prepared and tested in the catalytic transfer hydrogenation of acetophenone AP to produce phenylethanol PE, an industrially relevant product.

This study has provided starting points for the design of selective and highly potent inhibitors of L. Table of Contents Alerts. The transient species were identified as a benzoyl radical and a dimethoxyl benzyl radical that played a primary initiation role in polymerization. Cell death, apoptosis, and necrosis were triggered in K cells by TSC compounds in a dose-dependent manner.

Acetophenone thiosemicarbazone

A series of thiosemicarbazone TSC p -substituted acetophenone derivatives were synthesized and chemically characterized. The findings obtained showed that the compounds 2a, 2d, 2e and 2g were effective against some of the bacterial strains used, whereas the compounds 2d, 2e and 2i exhibited a moderate antifungal activity against the yeast strains evaluated. Synthesis of complex compounds in the system [ReOG5] thiosemicarbazone acetone-Hg-acetone.

Here, we assess the ability of TDDFT thiosemciarbazone describe the photochemistry of an important class of triplet sensitizers, namely, aromatic ketones. The antimicrobial activity of lapachol and its thiosemicarbazone and semicarbazone derivatives.

The exclusive capacity of TSC-NO 2 to deplete GSH at low concentrations in association with the occurrence of cell death exclusively by apoptosis suggests that, for the nitro TSC, the mechanism described in Scheme 2 might play a role.

Our results showed all of them presented powerful cytotoxic and antiproliferative activities against glioblastoma multiform and breast adenocarcinoma at very low concentrations nanomolar range.