1. Academic Validation
  2. Preclinical Pharmacokinetics and in vitro Metabolism of FHND5071, a Novel Selective RET Kinase Inhibitor

Preclinical Pharmacokinetics and in vitro Metabolism of FHND5071, a Novel Selective RET Kinase Inhibitor

  • Eur J Drug Metab Pharmacokinet. 2023 Sep;48(5):595-614. doi: 10.1007/s13318-023-00844-6.
Yiran Han 1 Tiantian Wen 2 Jia Wang 3 Jinmiao Shi 3 Yongqiang Zhu 4
Affiliations

Affiliations

  • 1 School of Life Sciences, Fudan University, No. 2005 Songhu Road, Shanghai, 200438, China.
  • 2 School of Life Science, Nanjing Normal University, No. 1 Wenyuan Road, Nanjing, 210046, China.
  • 3 Jiangsu Chia Tai Fenghai Pharmaceutical Co. Ltd, No. 9 Weidi Road, Nanjing, 210046, China.
  • 4 School of Life Science, Nanjing Normal University, No. 1 Wenyuan Road, Nanjing, 210046, China. zhyqscu@hotmail.com.
Abstract

Background and objectives: Rearranged during transfection (RET) is a transmembrane receptor tyrosine kinase that plays a crucial role in tumorigenesis. FHND5071, a potent and selective RET kinase inhibitor, could exert antitumor effects by inhibiting RET autophosphorylation. The present work aims to profile the pharmacokinetics of FHND5071 in in vivo and in vitro experiments as a ground work for further clinical research.

Methods: The absorption, distribution, metabolism, and excretion properties of FHND5071 were examined, along with metabolite production and Cytochrome P450 (CYP) phenotyping assay. Additionally, plasma protein binding and pharmacokinetics in mice were investigated.

Results: Microsomal stability assay corroborated moderate to high clearance of FHND5071, and the use of UPLC-Q-TOF-MS identified a total of six metabolites and suggested a possible metabolic pathway involving oxidation, demethylation, and N-dealkylation. Primary contributors to the CYP-mediated metabolism of FHND5071 were found to be CYP2C8 and CYP3A4, and FHND5071 displayed low permeability and acted as a substrate for the P-glycoprotein (P-gp). FHND5071 had a moderate to high binding in plasma and exhibited a moderate absorption degree (absolute bioavailability > 60%) The distribution of FHND5071 in mouse tissues was rapid (mostly peaking at 1-4 h) and wide (detectable in almost all tissues and organs), with the highest exposure in the spleen. A small fraction of FHND5071 was excreted via the urine and feces, and a presumed metabolic pathway involving 20 metabolites in mice is proposed.

Conclusion: Pharmacokinetic characteristics of FHND5071 were systemically profiled, which may lay the foundation for further clinical development as a drug candidate.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-149413
    RET激酶抑制剂
    RET