Search results for "ANTIPROLIFERATIVE ACTIVITY"

showing 6 items of 106 documents

Chamazulene-Rich Artemisia arborescens Essential Oils Affect the Cell Growth of Human Melanoma Cells

2020

Artemisia arborescens is an aromatic shrub whose essential oils are considered a potential source of molecules with industrial and pharmaceutical interest. The chemical profile of A. arborescens essential oils (EOs) was shown to be quite variable and various chemotypes have been identified. In this study, we compared the EOs composition of A. arborescens leaves and flowers collected from four different locations in Sicily. The EOs were assayed for their antiproliferative activity against A375 human malignant melanoma cells, also testing cell viability and cell membrane integrity. The evaluation of DNA fragmentation and caspase-3 activity assay was employed for the detection of apoptosis. Th…

antiproliferative activitymelanoma cancer cellArtemisia arborescensPlant ScienceArticleessential oillaw.inventionSuperoxide dismutase03 medical and health scienceschemistry.chemical_compound0302 clinical medicinemelanoma cancer cellslawcamphor<i>Artemisia arborescens</i>Viability assayEcology Evolution Behavior and SystematicsEssential oil030304 developmental biology0303 health sciencesEcologybiologyChemistryCell growthChamazuleneBotanychamazuleneArtemisia arborescensbiology.organism_classificationBiochemistryApoptosis030220 oncology & carcinogenesisQK1-989Artemisia arborescenbiology.proteinDNA fragmentationPlants
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3-(6-Phenylimidazo [2,1-

2019

A new series of imidazo[2,1-b][1,3,4]thiadiazole derivatives was efficiently synthesized and screened for their in vitro antiproliferative activity on a panel of pancreatic ductal adenocarcinoma (PDAC) cells, including SUIT-2, Capan-1 and Panc-1. Compounds 9c and 9l, showed relevant in vitro antiproliferative activity on all three pre-clinical models with half maximal inhibitory concentration (IC50) ranging from 5.11 to 10.8 µM, while the compounds 9e and 9n were active in at least one cell line. In addition, compound 9c significantly inhibited the migration rate of SUIT-2 and Capan-1 cells in the scratch wound-healing assay. In conclusion, our results will support further studies to increa…

antiproliferative activitymigration assayIndolesimidazo[21-b][134]thiadiazole derivativespancreatic cancerAntineoplastic AgentsAdenocarcinomaindole compoundsArticlePancreatic NeoplasmsresistanceStructure-Activity RelationshipTumor Cells CulturedHumansDrug Screening Assays AntitumorCarcinoma Pancreatic DuctalCell ProliferationMolecules (Basel, Switzerland)
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Photochemotherapeutic haterocyclic agents having antiproliferative and antineoplastic activity

2011

antiproliferative activityphotochemotherapeutic agentangelicinpyrrolo[32-h]quinolinonesSettore CHIM/08 - Chimica Farmaceutica
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Phytochemical investigation and antitumor activity of coumarins from Sicilian accession of Ferulago nodosa (L.) Boiss. roots

2023

Ferulago nodosa (L.) Boiss. (Apiaceae) is a species occurring in the Balkan-Tyrrhenian area being present in Crete, Greece, Albania, and probably in Macedonia. From the roots of this accession of species, not previously investigated, four coumarins, grandivittin, aegelinol benzoate, felamidin and aegelinol, and two terpenoids, (2E)-3-methyl-4-[(3-methyl-1-oxo-2-buten-1yl)oxy]-2-butenoic acid and pressafonin-A, were isolated and spectroscopically characterized. The last one was never detected in Ferulago species. The evaluation of the anti-tumor effects of F. nodosa coumarins on colon cancer HCT116 cells showed only a modest effect on reduction of tumor cell viability. For aegelinol, the red…

antiproliferative activityrootscoumarinsOrganic ChemistryapiaceaePlant ScienceFerulago nodosa (L.) BoissBiochemistryNMRAnalytical ChemistryNatural Product Research
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Synthesis of alkyl-5,8-dimethyl-6-phenyl-5,6-dihydropyrazolo[3,4-f] [1,2,3,5]tetrazepin-4(3H)-ones of pharmaceutical interest

2006

The multistep synthesis of two pyrazolo[3,4-f][1,2,3,5]tetrazepin-4(3H)-one derivatives, a new class of fused 1,2,3,5-tetrazepinones with potential antiproliferative activity, has been carried out. Owing to the instability of the above compounds, the last step of the synthesis was performed at -5/0 degrees C. The obtained tetrazepinones, when allowed to stand at r.t. for 24 h, afforded quantitatively 1-phenyl-3,6-dimethylpyrazolo [3,4-d][1,2,3] triazole.

lcsh:QD241-441chemistry.chemical_classificationchemistry.chemical_compoundlcsh:Organic chemistryChemistryOrganic ChemistryTriazole1235-tetrazepinones pyrazoles pyrazolo[34-f][1235]-tetrazepinones drug resistance antiproliferative activityCombinatorial chemistryAlkyl
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Synthesis and biological evaluation of some new 2-phenylpropiolamidobenzamides as potential antagonists of the HMDM2-p53 protein-protein interactions

2009

phenylpropiolamidobenzamides/antiproliferative activitySettore CHIM/08 - Chimica Farmaceutica
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