| Literature DB >> 32551021 |
Yuzo Iwaki1, Akira Ohhata1, Shingo Nakatani1, Katsuya Hisaichi1, Yasuyuki Okabe1, Atsushi Hiramatsu1, Toshihide Watanabe1, Shingo Yamamoto1, Taihei Nishiyama1, Juta Kobayashi1, Yasuo Hirooka1, Hideki Moriguchi1, Tatsuo Maeda1, Makoto Katoh1, Yuka Komichi1, Hiroto Ota1, Naoya Matsumura1, Masahiro Okada1, Tetsuya Sugiyama1, Hiroshi Saga1, Akira Imagawa1.
Abstract
Lysophosphatidic acid (LPA) is a bioactive lipid mediator that elicits a number of biological functions, including smooth muscle contraction, cell motility, proliferation, and morphological change. LPA is endogenously produced by autotaxin (ATX) from extracellular lysophosphatidylcholine (LPC) in plasma. Herein, we report our medicinal chemistry effort to identify a novel and highly potent ATX inhibitor, ONO-8430506 (20), with good oral availability. To enhance the enzymatic ATX inhibitory activity, we designed several compounds by structurally comparing our hit compound with the endogenous ligand LPC. Further optimization to improve the pharmacokinetic profile and enhance the ATX inhibitory activity in human plasma resulted in the identification of ONO-8430506 (20), which enhanced the antitumor effect of paclitaxel in a breast cancer model.Entities:
Year: 2020 PMID: 32551021 PMCID: PMC7294725 DOI: 10.1021/acsmedchemlett.0c00200
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345