PF-06649298 |
| Catalog No.GC66038 |
PF-06649298은 나트륨 결합 구연산염 수송체(NaCT 또는 SLC13A5) 억제제입니다. 821d96072c2d58d8970e76f526b0f6b8PF-06649298은 IC50 값이 16.2 μM인 NaCT와 특이적으로 상호작용하여 인간 간세포에서 구연산염의 수송을 억제합니다. 821d96072c2d58d8970e76f526b0f6b8PF-06649298은 포도당 대사 및 지질 대사 조절 연구에 사용할 수 있습니다.821d96072c2d58d8970e76f526b0f6b8
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1854061-16-7
Sample solution is provided at 25 µL, 10mM.
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IC50: 408 nM (citrate uptake in HEKNaCT), 16.2 μM (citrate uptake in Human Heps), 4.5 μM (citrate uptake in Mouse Heps), ??100 μM (citrate uptake in HEKNaCD1), ??100 μM (citrate uptake in HEKNaCD3)[1][2]
PF-06649298 is a sodium-coupled citrate transporter (NaCT or SLC13A5) inhibitor. PF-06649298 specifically interacts with NaCT with an IC50 value of 16.2 μM to inhibits the transport of citrate in human hepatocytes. PF-06649298 can be used for the research of regulating glucose metabolism and lipid metabolism[1][2].
PF-06649298 (0-100 μM; 30 min) inhibits citrate uptaken in cells[1].
Cell Viability Assay[1]
| Cell Line: | HEK-293 cells expressing NaCT, NaDC1 or NaDC3, human hepatocytes and mouse epatocytes |
| Concentration: | 0-100 μM |
| Incubation Time: | 30 min |
| Result: | Showed a selectivity for NaCT over the dicarboxylate transporters NaDC1 and NaDC3. Inhibited citrate uptake in HEK-293 cells expressing NaCT, NaDC1 or NaDC3, human hepatocytes and mouse epatocytes with IC50s of 408 nM, ??100 μM, ??100 μM, 16.2 μM and 4.5 μM, respectively. |
PF-06649298 (250 mg/kg; p.o. twice a day; for 21 days) reverses glucose intolerance of high fat diet (HFD) mice[2].
| Animal Model: | Mice with high fat diet (HFD) administration[2] |
| Dosage: | 250 mg/kg |
| Administration: | Oral gavage; 250mg/kg twice a day; for 21 days |
| Result: | Decreased plasma glucose, hepatic triglycerides, diacylglycerides, and acyl-carnitines concentration of livers in HFD mice. Totally reversed glucose intolerance of HFD mice. |
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