Eicosanoid regulation of debris-stimulated metastasis was written by Deng, Jianjun;Yang, Haixia;Haak, Victoria M.;Yang, Jun;Kipper, Franciele C.;Barksdale, Chantal;Hwang, Sung Hee;Gartung, Allison;Bielenberg, Diane R.;Subbian, Selvakumar;Ho, Koc-Kan;Ye, Xiang;Fan, Daidi;Sun, Yongkui;Hammock, Bruce D.;Panigrahy, Dipak. And the article was included in Proceedings of the National Academy of Sciences of the United States of America in 2021.Synthetic Route of C16H20F3N3O3 The following contents are mentioned in the article:
Cancer therapy reduces tumor burden via tumor cell death (debris), which can accelerate tumor progression via the failure of inflammation resolution Thus, there is an urgent need to develop treatment modalities that stimulate the clearance or resolution of inflammation-associated debris. Here, we demonstrate that chemotherapy-generated debris stimulates metastasis by up-regulating soluble epoxide hydrolase (sEH) and the prostaglandin E2 receptor 4 (EP4). Therapy-induced tumor cell debris triggers a storm of proinflammatory and proangiogenic eicosanoid-driven cytokines. Thus, targeting a single eicosanoid or cytokine is unlikely to prevent chemotherapy-induced metastasis. Pharmacol. abrogation of both sEH and EP4 eicosanoid pathways prevents hepato-pancreatic tumor growth and liver metastasis by promoting macrophage phagocytosis of debris and counterregulating a protumorigenic eicosanoid and cytokine storm. Therefore, stimulating the clearance of tumor cell debris via combined sEH and EP4 inhibition is an approach to prevent debris-stimulated metastasis and tumor growth. This study involved multiple reactions and reactants, such as 1-(1-Propionylpiperidin-4-yl)-3-(4-(trifluoromethoxy)phenyl)urea (cas: 1222780-33-7Synthetic Route of C16H20F3N3O3).
1-(1-Propionylpiperidin-4-yl)-3-(4-(trifluoromethoxy)phenyl)urea (cas: 1222780-33-7) belongs to piperidine derivatives. The piperidine structural motif is present in numerous natural alkaloids. These include piperine, which gives black pepper its spicy taste. Piperidine derivatives bearing a masked aldehyde function in the 蔚-position are easily transformed into quinolizidine compounds through intramolecular reductive amination.Synthetic Route of C16H20F3N3O3
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem