Molecular docking analysis of docetaxel analogues as duel lipocalin 2 inhibitors.

Bioinformation

Department of Biochemistry, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai - 600 077, India.

Published: June 2020

AI Article Synopsis

  • Lipocalin 2 is a key protein associated with breast cancer and a target for treatment.
  • Researchers evaluated 10 drug analogues derived from Docetaxel to enhance their binding efficiency with Lipocalin 2.
  • The findings highlight potential new drug candidates that could improve treatment options for breast cancer.

Article Abstract

Lipocalin 2 (Lcn2, also called as neutrophil gelatinase-associated lipocalin) is a member of the lipocalin family and a known target for breast cancer. Therefore, it is of interest to use Docetaxel as a scaffold to design molecules with improved efficiency from naturally derived phytochemicals. We document 10 analogues (4Deacetyltaxol, 7Acetyltaxol, Cabazitaxel, Cephalomannine, Docetaxal, Deacetyltaxol, Docetaxeltrihydrate, Ortataxel, Paclitaxel, Taxoline) having optimal binding with Lipocalin 2 in comparison with Docetaxel. This data is highly useful for consideration in the design and development of drugs for breast cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452746PMC
http://dx.doi.org/10.6026/97320630016438DOI Listing

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