Recent advances in metabolism and toxicity of tyrosine kinase inhibitors

Q Zhao, ZE Wu, B Li, F Li - Pharmacology & Therapeutics, 2022 - Elsevier
Small molecule tyrosine kinase inhibitors (TKIs) are widely used as anticancer drugs
approved by US FDA. However, the toxicities of TKIs to multiple organs have greatly limited …

[HTML][HTML] Benzbromarone in the treatment of gout

VF Azevedo, IA Kos, AB Vargas-Santos… - Advances in …, 2019 - SciELO Brasil
Background Benzbromarone is a uricosuric drug that has been used in the treatment of gout
over the last 30 years. Due to its potent inhibition of the dominant apical (luminal) urate …

Less is more: a new perspective for toxicity of emerging contaminants by structures, protein adducts and proteomics

X Hu, S Gong, Q He, JL Wu, N Li - TrAC Trends in Analytical Chemistry, 2023 - Elsevier
Emerging contaminants, as a group of trace contaminants arising from pharmaceuticals,
personal care products, etc., are of growing concern due to their potential hazard to the …

Determination and regulation of hepatotoxic pyrrolizidine alkaloids in food: A critical review of recent research

C Ma, Y Liu, L Zhu, H Ji, X Song, H Guo, T Yi - Food and Chemical …, 2018 - Elsevier
Pyrrolizidine alkaloids (PAs) are secondary metabolites of plants. PAs have been reported to
be hepatotoxic, mutagenic, and carcinogenic; they are a significant group of natural toxins …

Drug-induced idiosyncratic agranulocytosis-infrequent but dangerous

B Rattay, RA Benndorf - Frontiers in pharmacology, 2021 - frontiersin.org
Drug-induced agranulocytosis is a life-threatening side effect that usually manifests as a
severe form of neutropenia associated with fever or signs of sepsis. It can occur as a …

Elucidation of the relationship between evodiamine-induced liver injury and CYP3A4-mediated metabolic activation by UPLC-MS/MS analysis

T Peng, J Rao, T Zhang, Y Wang, N Li, Q Gao… - Analytical and …, 2023 - Springer
Evodiamine (EVD), which has been reported to cause liver damage, is the main constituent
of Evodia rutaecarpa (Juss.) Benth and may be bioactivated into reactive metabolites …

Design, synthesis and biological evaluation of tetrahydroquinoline-based reversible LSD1 inhibitors

X Wang, C Zhang, X Zhang, J Yan, J Wang… - European Journal of …, 2020 - Elsevier
The targeted regulation of LSD1, which is highly expressed in a variety of tumor cells, is a
promising cancer therapy strategy. Several LSD1 inhibitors are currently under clinical …

[HTML][HTML] In vivo anti-hyperuricemia and anti-gouty arthritis effects of the ethanol extract from Amomumvillosum Lour.

L Dong, S Zhang, L Chen, J Lu, F Zhao, T Long… - Biomedicine & …, 2023 - Elsevier
The incidence of hyperuricemia and gout has been increasing year by year, and it is
showing a younger trend. However, the first-line drugs currently used for hyperuricemia and …

Lycium barbarum polysaccharides protect mice from hyperuricaemia through promoting kidney excretion of uric acid and inhibiting liver xanthine oxidase

X Yu, L Zhang, P Zhang, J Zhi, R Xing… - Pharmaceutical …, 2020 - Taylor & Francis
Abstract Context Lycium barbarum L.(Solanaceae) polysaccharides (LBPs) are important
active constituents that have demonstrated kidney protection. Objective This study …

Benzbromarone mitigates cisplatin nephrotoxicity involving enhanced peroxisome proliferator-activated receptor-alpha (PPAR-α) expression

EAN Abdel-Razek, AM Abo-Youssef, AA Azouz - Life sciences, 2020 - Elsevier
Aim Despite the great efficacy reported for cisplatin as a widely used chemotherapeutic
agent, its clinical use is limited by the challenge of facing its serious side effect; …