• Phenacetin in Pharmacokinetic Research: Solubility, Organ...

  2025-09-23

  Explore the scientific utility of Phenacetin (N-(4-ethoxyphenyl)acetamide) as a non-opioid analgesic in advanced pharmacokinetic studies, with emphasis on drug solubility in ethanol and DMSO and the application of hiPSC-derived intestinal organoids for in vitro research.

• Phenacetin in Contemporary Non-Opioid Analgesic Research:...

  2025-09-22

  This article explores the application of Phenacetin (N-(4-ethoxyphenyl)acetamide) as a reference non-opioid analgesic in advanced pharmacokinetic studies, emphasizing its solubility properties and nephrotoxicity profile. We discuss its integration into next-generation in vitro models, including hiPSC-derived intestinal organoids, and provide technical insights for scientific research use.

• Phenacetin in Modern Pharmacokinetic Research: Solubility...

  2025-09-19

  This article explores Phenacetin (N-(4-ethoxyphenyl)acetamide) as a model non-opioid analgesic in advanced pharmacokinetic studies, emphasizing its solubility in ethanol and DMSO and its relevance in hiPSC-derived intestinal organoid systems for scientific research use.

• Phenacetin in Advanced Pharmacokinetic Models: A Research...

  2025-09-18

  Explore the scientific potential of Phenacetin, a non-opioid analgesic, in state-of-the-art pharmacokinetic studies using human stem cell-derived intestinal organoids. This article examines its solubility, research applications, and relevance for mechanistic investigations in drug metabolism.

• The excellent potencies selectivities and improved PK

  2025-03-03

  

  The excellent potencies, selectivities and improved PK associated with the piperazine class triggered more extensive off-target screenings of the highlighted compounds. A screen of more than 100 enzymes, receptors, and ion channels resulted in activity at the norepinephrine transporter (NET). This m

• It is important to note that stable

  2025-03-03

  

  It is important to note that stable amnesia is, apparently, a general biological phenomenon and can be found in different animal species. In studies on rats, it was found that if reconsolidation of conditioned olfactory aversion memory was impaired by the antagonist of NMDA glutamate receptors, amne

• br Conflict of interest br Acknowledgements The authors

  2025-03-03

  

  Conflict of interest Acknowledgements The authors would like to thank Mrs. Amparo Pacheco from CMPL, PUC, for her technical and secretarial assistance. This work was supported by the Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT 1150344, 1050377, 11150083), and the Direccioń

• The fact that the BPloopAsn regains

  2025-03-03

  

  The fact that the α1-BPloopAsn141 regains its α-Btx binding with a Kd similar to that of the wild type α1 ECD [18], suggests that the AChBP Cys-loop does not interfere with the correct conformation of the mutant ECD. Data from analogous mutants of the human neuronal α7 subunit ECD showed improved li

• br Materials and methods br Results

  2025-03-03

  

  Materials and methods Results Discussion Prostate cancer represents an ideal candidate for chemoprevention because of its high incidence and long latency to clinically significant disease [17]. The precancerous lesion PIN may also be a suitable target for ablation in chemoprevention strateg

• br Regulation and pharmacology of mPGES mPGES

  2025-03-03

  

  Regulation and pharmacology of mPGES-1 mPGES-1 (16 kDa, 152 amino acids) is a trimeric integral membrane protein of the endoplasmic reticulum with each monomer containing four transmembrane domains (Samuelsson et al., 2007; Sjogren et al., 2013). The three active site cavities are located at the

• Considering the physicochemical stability results

  2025-03-03

  

  Considering the physicochemical stability results on Fig. 5, it was observed that the particles are stable when they are stored at 4 °C for 30 days. After day 30, a significant increase was observed in particle size, but at the end of the 90 days the SLN particle size is still below 100 nm. Stabilit

• Finally not only can ERs pair with

  2025-03-01

  

  Finally, not only can ERs pair with different mGluRs in different ttp stock regions, but it is becoming increasingly clear that the same mGluRs can pair with distinct downstream signaling partners to have differential effects both within and across brain regions (Gross et al., 2016; Mannaioni et al

• Thus a majority of known chemical

  2025-03-01

  

  Thus, a majority of known chemical and physico-chemical methods of metallic ions assay has a number of disadvantages, such as a low sensitivity and selectivity, high costs and complexity of the equipment. Therefore, the development of simple cost-effective sensitive methods of quantitative analysis

• According to the present observations the Ampk isoform

  2025-03-01

  

  According to the present observations, the Ampkα1 isoform promotes AP-1 transcriptional activity and thereby fosters NNC 55-0396 of AP-1 target genes in cardiomyocytes via activation of Pkcζ. The transcription factor AP-1 plays a decisive role during cardiac remodeling [24], [25], [26], [37]. AP-1 m

• br Materials and methods br Results br Discussion Recently w

  2025-03-01

  

  Materials and methods Results Discussion Recently, we showed that stimulation of TRPM3 and TRPC6 channels triggers a signaling cascade leading to the activation of AP-1 [11], [12], [13], [15]. The objective of this study was to investigate whether stimulation of TRPV1 channels leads to an a

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