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Ticagrelor (AZD6140)是第一个可逆结合的口服P2Y(12)受体拮抗剂,可阻断ADP诱导的血小板聚集。
In vitro (25°C) | DMSO | 99 mg/mL (189.45 mM) | |
Water | Insoluble | ||
Ethanol | 52 mg/mL (99.51 mM) | ||
In vivo | 2% DMSO+30% PEG 300+5% Tween 80+ddH2O | 9 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 | 19.14 mL | 95.68 mL | 191.35 mL |
0.5 mM | 3.83 mL | 19.14 mL | 38.27 mL |
1 mM | 1.91 mL | 9.57 mL | 19.14 mL |
5 mM | 0.38 mL | 1.91 mL | 3.83 mL |
*The above data is based on the productmolecular weight 522.6 . 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 | A11238 |
---|---|
作用机制 | Antagonist (拮抗剂) |
M. Wt | 522.6 |
Formula | C23H28F2N6O4S |
Purity | >99% |
Storage | Store lyophilized at -20ºC, keep desiccated. |
CAS No. | 274693-27-5 |
Synonyms | AZD 6140 |
SMILES | CCCSC1=NC2=C(C(=N1)N[C@@H]3C[C@H]3C4=CC(=C(C=C4)F)F)N=NN2[C@@H]5C[C@@H]([C@H]([C@H]5O)O)OCCO |
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