Web17. aug 2024 · One such strategy is inhibition of SphK2. Our group and others have shown that Sphk2 −/− or wild-type mice treated with an SphK2 inhibitor were protected against … Web11. apr 2024 · RedHill's key clinical late-stage development programs include: (i) RHB-204 , with an ongoing Phase 3 study for pulmonary nontuberculous mycobacteria (NTM) disease; (ii) opaganib (ABC294640), a...
Emerging role of sphingosine-1-phosphate signaling in head and …
Web13. okt 2024 · Inhibition of Sphk2 sustains long-term self-renewal, increases regenerative potential, and functionally attenuates the aging of HSCs. Loss of Sphk2 improves … WebOur studies demonstrate that SLP120701, a SphK2-selective inhibitor (Ki = 1 μM), decreases S1P levels in histiocytic lymphoma (U937) cells. Surprisingly, homologation with a single methylene unit between the oxadiazole and heterocyclic ring afforded a SphK1-selective inhibitor in SLP7111228 (Ki = 48 nM), which also decreased S1P levels in ... flat pedal biking shoes for women
Sphingosine-1-Phosphate (S1P) and S1P Signaling Pathway
Web10. apr 2024 · Sphingosine-1-phosphate (S1P) is a lipid mediator and its binding to the S1P receptor 2 (S1PR2) is reported to regulate cytoskeletal organization. Epidermal growth factor (EGF) has been shown to induce migration and invasion in tumour cells. Since binding of S1P to S1PR2 and EGF to the EGF receptors exhibit some overlapping functionality, this … Web13. okt 2024 · Here, we show that the enzyme Sphk2 (sphingosine kinase 2), which generates the lipid metabolite sphingosine-1-phosphate, is highly expressed in HSCs. The … Web15. aug 2008 · 有效的生物活性鞘脂介质 1-磷酸鞘氨醇 (S1P) 由 2 种鞘氨醇激酶同工酶 SphK1 和 SphK2 产生。SphK1 的表达在癌症(包括白血病)中上调,并与癌症进展相关。筛选出的鞘氨醇类似物鉴定为 (2R,3S,4E)-N-methyl-5-(4'-pentylphenyl)-2-aminopent-4-ene-1,3-diol,命名为 SK1-I (BML-258) ,作为 SphK1 的有效、水溶性、同工酶特异性 ... checkr inc. zoominfo