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Ministry points: Help
Year | Points | List |
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Year 2024 | 100 | Ministry scored journals list 2024 |
Year | Points | List |
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2024 | 100 | Ministry scored journals list 2024 |
2023 | 140 | Ministry Scored Journals List |
2022 | 100 | Ministry Scored Journals List 2019-2022 |
2021 | 100 | Ministry Scored Journals List 2019-2022 |
2020 | 100 | Ministry Scored Journals List 2019-2022 |
2019 | 100 | Ministry Scored Journals List 2019-2022 |
2018 | 25 | A |
2017 | 25 | A |
2016 | 25 | A |
2015 | 25 | A |
2014 | 25 | A |
2013 | 25 | A |
2012 | 25 | A |
2011 | 25 | A |
2009 | 20 | List of scored magazines |
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Points CiteScore:
Year | Points |
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Year 2022 | 7.4 |
Year | Points |
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2022 | 7.4 |
2021 | 5.6 |
2020 | 5.1 |
2019 | 4.9 |
2018 | 5.3 |
2017 | 4.4 |
2016 | 4.3 |
2015 | 3.8 |
2014 | 3.5 |
2013 | 3.7 |
2012 | 4.1 |
2011 | 4.1 |
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Papers published in journal
Filters
total: 28
Catalog Journals
Year 2023
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Gαi-derived peptide binds the µ-opioid receptor
Publication
Year 2020
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Proof-of-concept study on improved efficacy of rHuEPO administered as a long-term infusion in rats
Publication -
Population pharmacokinetics of standard-dose meropenem in critically ill patients on continuous renal replacement therapy: a prospective observational trial
Publication
Year 2018
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Modulation of UDP-glucuronidation by acridinone antitumor agents C-1305 and C-1311 in HepG2 and HT29 cell lines, despite slight impact in noncellular systems.
PublicationBackground Among the studied antitumor acridinone derivatives developed in our laboratory, 5-dimethylaminopropylamino-8-hydroxytriazoloacridinone (C-1305) and 5-diethylaminoethylamino-8-hydroxyimidazoacridinone (C-1311) exhibited cytotoxic and antitumor properties against several cancer types and were selected to be evaluated in preclinical and early-phase clinical trials. In the present work, we investigated the impact of C-1305...
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Drug-drug interaction potential of antitumor acridine agent C-1748: The substrate of UDP-glucuronosyltransferases 2B7, 2B17 and the inhibitor of 1A9 and 2B7
PublicationBackground The compound 9-(2′-hydroxyethylamino)-4-methyl-1-nitroacridine (C-1748), the promising antitumor agent developed in our laboratory was determined to undergo phase I metabolic pathways. The present studies aimed to know its biotransformation with phase II enzymes – UDP-glucuronosyltransferases (UGTs) and its potential to be engaged in drug-drug interactions arising from the modulation of UGT activity. Methods UGT-mediated...
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Comparison of the effects of rosuvastatin monotherapy and atorvastatin-ezetimibe combined therapy on the structure of erythrocyte membranes in patients with coronary artery disease
Publication
Year 2017
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Temozolomide and sorafenib as programmed cell death inducers of human glioma cells
Publication -
High-dose testosterone enanthate supplementation boosts oxidative stress, but exerts little effect on the antioxidant barrier in sedentary adolescent male rat liver
Publication -
Effect of intensive lipid-lowering therapies on cholinesterase activity in patients with coronary artery disease
Publication
Year 2016
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Imidazoacridinone antitumor agent C-1311 as a selective mechanism- based inactivator of human cytochrome P450 1A2 and 3A4 isoenzymes.
Publication5-Diethylaminoethylamino-8-hydroxyimidazoacridinone (C-1311), a promising antitumor agent that is also active against autoimmune diseases, was determined to be a selective inhibitor of the cytochrome P450 (CYP) 1A2 and 3A4 isoenzymes. Therefore, C-1311 might modulate the effectiveness of other drugs used in multidrug therapy. The present work aimed to identify the mechanism of the observed C-1311-mediated inactivation of CYP1A2...
Year 2015
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The effect of interleukin-35 on the integrity, ICAM-1 expression and apoptosis of human aortic smooth muscle cells
Publication -
Mesoporous silica nanoflakes – Biocompatibility, cellular uptake and drug transport
Publication -
Detrimental effects of chemotherapeutics and other drugs on the endothelium: A call for endothelial toxicity profiling
Publication
Year 2014
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The influence of the time of day on midazolam pharmacokinetics and pharmacodynamics in rabbits
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Pharmacokinetics and pharmacodynamics of propofol in children undergoing different types of surgeries
Publication -
Chronic treatment with zinc hydroaspartate induces anti-inflammatory and anti-ulcerogenic activity in rats
Publication -
Catalase activity in blood fractions of patients with sporadic ALS
Publication
Year 2013
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Possible contribution of IGF-1 to depressive disorder
Publication -
Assessing circadian rhythms during prolonged midazolam infusion in the pediatric intensive care unit (PICU) children
Publication
Year 2012
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Potential pitfalls of propofol target controlled infusion delivery related to its pharmacokinetics and pharmacodynamics
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Pharmacokinetics and pharmacodynamics of propofol in patients undergoing abdominal aortic surgery
Publication -
New conjugates of muramyl dipeptide and nor-muramyl dipeptide linked to tuftsin and retro-tuftsin derivatives significantly influence their biological activity
PublicationOpisano syntezę nowych koniugatów MDP i nor-MDP z pochodnymi tuftsyny i retro-tuftsyny zawierającymi wiązanie izopeptydowe pomiędzy epsilon-aminową grupą lizyny, a karboksylową grupą Ala, Gly czy Val. Zbadano ich aktywność biologiczną, m.in. profil cytokinowy.
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Maternal immune activation leads to age-related behavioral and immunological changes in male rat offspring - the effect of antipsychotic drugs
Publication -
Diversity of frequency-modulated 50-kHz vocalization response to intermittent amphetamine treatment in Sprague-Dawley rats
Publication
Year 2011
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Therapeutic potential of adenosine analogues and conjugates
PublicationZaprezentowano przegląd literatury chemicznej na temat analogów i koniugatów adenozyny oraz ich potencjalne zastosowanie terapeutyczne. Zwrócono także uwagę na ich oddziaływanie z receptorami adenozyny.
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Natural and synthetic acridines/acridones as antitumor agents: their biological activities and methods of synthesis.
PublicationPraca stanowi przegląd opisanych w literaturze chemicznej modyfikacji struktur naturalnych i syntetycznych pochodnych akrydyny i akrydonu. Artykuł obejmuje swym zakresem metody syntezy, a także wpływ budowy cząsteczek tych związków na ich aktywność przeciwnowotworową oraz mechanizm działania.
Year 2009
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