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Catalog: | HY-111341 |
Brand: | MCE |
CAS: | 618913-30-7 |
MDL | MFCD31619279 |
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Molecular Weight | 252.29 |
Molecular Formula | C10H12N4O2S |
SMILES | O=C1NC(N(C[C@@H]2OCCC2)C3=C1N=CN3)=S |
AZD5904 is a selective and irreversible inhibitor of human Myeloperoxidase ( MPO ) with an IC 50 of 140 nM and has similar potency in mouse and rat.
IC50: 140 nM (human MPO) [1]
AZD5904 is a pselective and irreversible inhibitor of human Myeloperoxidase (MPO) with an IC 50 of 140 nM and has similar potency in mouse and rat. It is 10 to 19-fold selective compare to the closely related lactoperoxidase and thyroid peroxidase; >70-fold to a broad panel of other enzymes, ion channels, and receptors. In isolated human neutrophils, 1 µM AZD5904 inhibits PMA stimulated HOCl by >90% [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : 100 mg/mL ( 396.37 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 3.9637 mL | 19.8185 mL | 39.6369 mL |
5 mM | 0.7927 mL | 3.9637 mL | 7.9274 mL |
10 mM | 0.3964 mL | 1.9818 mL | 3.9637 mL |
Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)
Solubility: ≥ 2.08 mg/mL (8.24 mM); Clear solution
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