Acridine and its derivatives: a patent review (2009–2013)

B Zhang, X Li, B Li, C Gao, Y Jiang - Expert opinion on therapeutic …, 2014 - Taylor & Francis
Introduction: Acridine derivatives have been extensively explored as potential therapeutic
agents for the treatment of a number of diseases, such as cancer, Alzheimer's, and bacterial …

The role of glucuronidation in drug resistance

Z Mazerska, A Mróz, M Pawłowska… - Pharmacology & …, 2016 - Elsevier
The final therapeutic effect of a drug candidate, which is directed to a specific molecular
target strongly depends on its absorption, distribution, metabolism and excretion (ADME) …

[HTML][HTML] Hypoxia increases chemoresistance in human medulloblastoma DAOY cells via hypoxia‑inducible factor 1α‑mediated downregulation of the CYP2B6 …

J Valencia‑Cervantes, S Huerta‑Yepez… - Oncology …, 2019 - spandidos-publications.com
Medulloblastomas are among the most frequently diagnosed pediatric solid tumors, and
drug resistance remains as the principal cause of treatment failure. Hypoxia and the …

Novel multi-substituted benzyl acridone derivatives as survivin inhibitors for hepatocellular carcinoma treatment

B Zhang, N Wang, C Zhang, C Gao, W Zhang… - European journal of …, 2017 - Elsevier
Sorafenib was the only small-molecule drug approved by FDA for treatment of the advanced
hepatocellular carcinoma (HCC). Recent study indicated that YM155 was a promising agent …

Screening of a chemical library reveals novel PXR-activating pharmacologic compounds

M Ratajewski, I Grzelak, K Wiśniewska, K Ryba… - Toxicology Letters, 2015 - Elsevier
The pregnane X receptor (PXR) is one of the master regulators of xenobiotic transformation.
Interactions between pharmacologic compounds and PXR frequently result in drug-to-drug …

Genistein affects expression of cytochrome P450 (CYP450) genes in hepatocellular carcinoma (HEPG2/C3A) cell line

SR Lepri, D Sartori, SC Semprebon… - Drug Metabolism …, 2018 - ingentaconnect.com
Background: Genistein (5, 7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one) is the
most abundant isoflavone in soybean, which has been associated with a lower risk of …

Combined anticancer therapy with imidazoacridinone analogue C‐1305 and paclitaxel in human lung and colon cancer xenografts—Modulation of tumour …

M Świtalska, B Filip‐Psurska… - Journal of Cellular …, 2022 - Wiley Online Library
Abstract The acridanone derivative 5‐dimethylaminopropylamino‐8‐
hydroxytriazoloacridinone (C‐1305) has been described as a potent inhibitor of cancer cell …

Enhanced activity of P4503A4 and UGT1A10 induced by acridinone derivatives c-1305 and c-1311 in MCF-7 and HCT116 cancer cells: Consequences for the drugs' …

M Pawłowska, A Kwaśniewska, Z Mazerska… - International Journal of …, 2020 - mdpi.com
Activity modulation of drug metabolism enzymes can change the biotransformation of
chemotherapeutics and cellular responses induced by them. As a result, drug-drug …

A strong preference for the TA/TA dinucleotide step discovered for an acridine-based, potent antitumor dsDNA intercalator, C-1305: NMR-driven structural and …

T Laskowski, W Andrałojć, J Grynda, P Gwarda… - Scientific Reports, 2020 - nature.com
Triazoloacridinone C-1305, a potent antitumor agent recommended for Phase I clinical trials,
exhibits high activity towards a wide range of experimental colon carcinomas, in many cases …

Suppression of carboxylesterases by imatinib mediated by the down‐regulation of pregnane X receptor

W Luo, Y Xin, X Zhao, F Zhang, C Liu… - British Journal of …, 2017 - Wiley Online Library
Background and Purpose Imatinib mesylate (IM) is a first‐line treatment for chronic myeloid
leukaemia (CML) as a specific inhibitor of BCR‐ABL tyrosine kinase. As IM is widely used in …