Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Iloprost is a second generation structural analog of prostacyclin (PGI2) with about ten-fold greater potency than the first generation stable analogs, typified by carbaprostacyclin. Iloprost binds with equal affinity to the recombinant human IP and EP1 receptors with a Ki value of 11 nM. Most preparations of iloprost contain 16(S) and 16(R) stereoisomers. 16(S)-Iloprost potently inhibits platelet aggregation with an IC50 value of 3.5 nM.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
500 μg | 35 days | $ 560.00 | |
1 mg | 35 days | $ 1,060.00 | |
5 mg | 35 days | $ 4,440.00 |
Description | Iloprost is a second generation structural analog of prostacyclin (PGI2) with about ten-fold greater potency than the first generation stable analogs, typified by carbaprostacyclin. Iloprost binds with equal affinity to the recombinant human IP and EP1 receptors with a Ki value of 11 nM. Most preparations of iloprost contain 16(S) and 16(R) stereoisomers. 16(S)-Iloprost potently inhibits platelet aggregation with an IC50 value of 3.5 nM. |
Molecular Weight | 360.49 |
Formula | C22H32O4 |
CAS No. | 74843-14-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMF: 30 mg/mL
Ethanol: 30 mg/mL
PBS (pH 7.2): 1 mg/mL
DMSO: 25 mg/mL
You can also refer to dose conversion for different animals. More
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16(S)-Iloprost 74843-14-4 16(S) Iloprost 16Iloprost 16(S)Iloprost inhibitor inhibit