产品详情
SAR131675是一种有效的选择性VEGFR-3-TK抑制剂,具有抗淋巴显形、抗肿瘤和抗转移活性。
靶点信息
VEGFR3 (Cell-free assay) | ||||
23 nM |
In vitro (25°C) | DMSO | 29 mg/mL (80.91 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
In vivo | 5% DMSO+30% PEG 300+5% Tween 80+ddH2O | 2 mg/mL | |
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 27.91 mL | 139.55 mL | 279.1 mL |
0.5 mM | 5.58 mL | 27.91 mL | 55.82 mL |
1 mM | 2.79 mL | 13.96 mL | 27.91 mL |
5 mM | 0.56 mL | 2.79 mL | 5.58 mL |
*The above data is based on the productmolecular weight 358.29. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
目录号 | A13377 |
---|---|
作用机制 | Inhibitor (抑制剂) |
M. Wt | 358.29 |
Formula | C18H22N4O4 |
Purity | >99% |
Storage | Store lyophilized at -20ºC, keep desiccated. |
CAS No. | 1433953-83-3 |
Synonyms | 0 |
SMILES | CCN1C(=C(C(=O)C2=C1N=C(C=C2)C#C[C@](C)(COC)O)C(=O)NC)N |
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