AG-636
目录号: PL03689 纯度: ≥98%
CAS No. :1623416-31-8
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中文名称
AG-636
英文名称
AG-636
英文别名
AG-636;1-methyl-5-(2'-methyl-[1,1'-biphenyl]-4-yl)-1H-benzo[d][1,2,3]triazole-7-carboxylic acid;1-methyl-5-(2'-methyl[1,1'-biphenyl]-4-yl)-1H-benzotriazole-7-carboxylic acid;s9776;R4P;US11147801, Compound 1;BDBM520617;1-methyl-5-(2''-methyl-[1,1''-biphenyl]-4-yl)-1H-benzo[d][1,2,3]triazole-7- carboxylic acid;
Cas No.
1623416-31-8
分子式
C21H17N3O2
分子量
343.38
包装储存
Powder -20°C 3 years;In solvent -80°C 6 months
产品详情
AG-636 是一种有效,可逆,选择性和具有口服活性的二氢乳清酸脱氢酶 (DHODH) 抑制剂,IC50 为 17 nM。AG-636 具有很强的抗癌作用。
生物活性
AG-636 is a potent, reversible, selective and orally active dihydroorotate dehydrogenase (DHODH) inhibitor with an IC 50 of 17 nM. AG-636 has strong anticancer effects.
性状
Solid
IC50 & Target[1][2]
IC50: 17 nM (Dihydroorotate dehydrogenase (DHODH))
体外研究(In Vitro)
AG-636 has strong growth-inhibitory activity in cancer cell lines of hematologic versus solid tumor origin. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
AG-636 (10-100 mg/kg ; oral gavage; twice daily; for 14 days) treatment results in robust tumor growth inhibition in the OCILY19 DLBCL tumor xenograft model. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;In solvent -80°C 6 months
ClinicalTrial
参考文献
[1]. Gabrielle McDonald, et al. Selective Vulnerability to Pyrimidine Starvation in Hematologic Malignancies Revealed by AG-636, a Novel Clinical-Stage Inhibitor of Dihydroorotate Dehydrogenase. Mol Cancer Ther. 2020 Dec;19(12):2502-2515.
溶解度数据
In Vitro: DMSO : 31.25 mg/mL (91.01 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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