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|---|---|---|---|---|---|---|---|
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| 描述 | IDO-IN-7 is a potent human IDO inhibitor with IC50 of < 1 μM. |
| Concentration | Treated Time | Description | References | |
| UM-SCC1 cells | 10 µM | Assessed the effect of Navoximod nanoformulation on the metabolic activity of UM-SCC1 cells, showing no changes up to 10 μM. | Bioeng Transl Med. 2023 Oct 28;9(1):e10599. | |
| UM-SCC1 cells | 10 µM | Evaluated the efficiency of Navoximod nanoformulation in inhibiting the IDO enzyme, showing an IC50 of 3.33 μM for the nanoformulation compared to 6.66 μM for free Navoximod. | Bioeng Transl Med. 2023 Oct 28;9(1):e10599. |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6 mice | Orthotopic head and neck cancer model | 10 mg/kg | Six doses of Navoximod nanoformulation and four doses of aPD-1 | Evaluated the anti-tumor effects of Navoximod nanoformulation in combination with aPD-1, showing significant inhibition of tumor growth with an average tumor volume of 52.7 ± 25.8 mm3 in the combination group compared to single therapy and control groups. | Bioeng Transl Med. 2023 Oct 28;9(1):e10599. | |
| C57BL/6J male mice | Intra-abdominal sepsis model induced by caecal ligation and puncture (CLP) or lipopolysaccharide (LPS) injection | Oral | 100 mg/kg and 200 mg/kg | Started 48 hours before CLP or LPS injection, once every 24 hours, continued until the end of the experiment | Navoximod significantly mitigated IAS-induced skeletal muscle loss and increased the phosphorylated AKT and myosin heavy chain protein expression. | J Cachexia Sarcopenia Muscle. 2023 Apr;14(2):1046-1059 |
| C57BL/6 mice | Subcutaneous HCC model | Intratumoral injection | 120 μg | Single dose | To evaluate the anti-tumor effect of Navoximod combined with HSV-1, results showed that the combination therapy significantly inhibited tumor growth and improved survival rate. | Commun Biol. 2023 Jun 9;6(1):621 |
| C57BL/6 mice | Intracranial and subcutaneous TRP tumor models | Oral | 200 mg/kg | Twice daily for 2-3 weeks | To evaluate the anti-tumor efficacy of GDC-0919 alone or in combination with radiation therapy (RT). Results showed that GDC-0919 alone had no anti-tumor activity but significantly enhanced therapeutic response when combined with RT, particularly with a hypofractionated regimen. | Clin Cancer Res. 2018 Aug 1;24(15):3632-3643 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
3.16mL 0.63mL 0.32mL |
15.80mL 3.16mL 1.58mL |
31.61mL 6.32mL 3.16mL |
|
| CAS号 | 1402837-78-8 |
| 分子式 | C18H21FN2O2 |
| 分子量 | 316.37 |
| SMILES Code | O[C@H](CC1)CC[C@]1([H])[C@H](O)C[C@@H]2N3C(C4=C2C(F)=CC=C4)=CN=C3 |
| MDL No. | MFCD29472253 |
| 别名 | GDC-0919; NLG-919 |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, store in freezer, under -20°C |
| 溶解方案 |
DMSO: 105 mg/mL(331.89 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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