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Vorasidenib (AG-881)是一种有效且选择性的口服抑制剂,可抑制细胞质中异柠檬酸脱氢酶1型(IDH1,IDH1 [NADP+]可溶)和2型(IDH2异柠檬酸脱氢酶[NADP+])的突变形式。线粒体中的线粒体,具有潜在的抗肿瘤活性。
In vitro | DMSO | 75 mg/mL (180.83 mM) | |
Water | Insoluble | ||
Ethanol | 75 mg/mL (180.83 mM) | ||
* <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 | 24.11 mL | 120.56 mL | 241.11 mL |
0.5 mM | 4.82 mL | 24.11 mL | 48.22 mL |
1 mM | 2.41 mL | 12.06 mL | 24.11 mL |
5 mM | 0.48 mL | 2.41 mL | 4.82 mL |
*The above data is based on the productmolecular weight 414.74. 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 | A16908 |
---|---|
作用机制 | Inhibitor (抑制剂) |
M. Wt | 414.74 |
Formula | C14H13ClF6N6 |
Purity | >99% |
Storage | Store lyophilized at -20ºC, keep desiccated. |
CAS No. | 1644545-52-7 |
Synonyms | AG-881, AG 881, AG881 |
SMILES | C[C@@H](NC1=NC(C2=NC(Cl)=CC=C2)=NC(N[C@H](C)C(F)(F)F)=N1)C(F)(F)F |
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