Ambeed.cn

首页 / / / IDO / Navoximod

Navoximod {[allProObj[0].p_purity_real_show]}

货号:A451279 同义名: GDC-0919; NLG-919

Navoximod是一种强效的人类 IDO 抑制剂,IC50 小于 1 μM。

Navoximod 化学结构 CAS号:1402837-78-8
Navoximod 化学结构
CAS号:1402837-78-8
Navoximod 3D分子结构
CAS号:1402837-78-8
Navoximod 化学结构 CAS号:1402837-78-8
Navoximod 3D分子结构 CAS号:1402837-78-8
规格 价格 会员价 库存 数量
{[ item.pr_size ]}

{[ getRatePriceInt(item.pr_rmb, 1,1) ]}

{[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]}

{[ getRatePriceInt(item.pr_rmb, 1,1) ]}

{[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]}
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} 现货 1周 咨询 - +
购物车0 收藏 询单

Navoximod 纯度/质量文件 产品仅供科研

货号:A451279 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

全球学术期刊中引用的产品

Nature, 2025, 645, 793-800. Ambeed. [ A201204 , A444152 , A344107 , A952055 ]
Cell, 2025. Ambeed. [ A122167 ]
Science, 2025, 387(6729): eadp5637. Ambeed. [ A875019 ]
Sig. Transduct. Target. Ther., 2025, 10, 257. Ambeed. [ A104916 ]
Nat. Nanotechnol., 2025. Ambeed. [ A243018 , A1216705 , A522597 , A125401 , A1355641 ]
更多 >

Navoximod 生物活性

描述 IDO-IN-7 is a potent human IDO inhibitor with IC50 of < 1 μM.

Navoximod 细胞实验

Cell Line
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.

Navoximod 动物实验

Species
Animal Model
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

Navoximod 参考文献

[1]WO2012142237A1

Navoximod 实验方案

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

Navoximod 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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
方案 一
方案 二
方案 三
方案 四
方案 五
方案 六
AmBeed 相关网站 AmBeed.cn AmBeed.com
AmBeed
关于我们
联系我们
资讯中心
网站地图
产品手册
  • 批次文件查询
  • 客户支持
    技术支持
    专业术语
    缩略词释义
    质量手册
    产品咨询
    计算器
    活动政策
    订购方法
    积分商城
    活动声明
    联系我们
    400-920-2911 sales@ambeed.cn tech@ambeed.cn
    AmBeed 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务,不为任何个人或者非科研性质用途提供服务。