CRDWMOVRQCMROH-HIKRQZGHSA-N - Names and Identifiers
CRDWMOVRQCMROH-HIKRQZGHSA-N - Physico-chemical Properties
Molecular Formula | C23H34N3Na2O10P
|
Molar Mass | 589.483 |
Solubility | H2O: ≥ 140 mg/mL |
Storage Condition | -20℃ |
In vitro study | Phosphoramidon is a potent inhibitor of thermolysin without inhibiting other endopeptidases such as trypsin, papain, and chymotrypsin. Phosphoramidon reduces tumor cell invasion in CC531 cells. |
In vivo study | In rats bearing colon cancer CC531 xenografts, Phosphoramidon (250 mg/rat, I. P.) significantly reduced tumor cell growth. Intranasal phosphodipeptide increases β-amyloid levels in wild-type and NEP/nep2-deficient mice, allowing it to be used to mimic Alzheimer's disease (AD). |
CRDWMOVRQCMROH-HIKRQZGHSA-N - Preparation solution concentration reference
| 1mg | 5mg | 10mg |
---|
1 mM | 1.702 ml | 8.511 ml | 17.022 ml |
5 mM | 0.34 ml | 1.702 ml | 3.404 ml |
10 mM | 0.17 ml | 0.851 ml | 1.702 ml |
5 mM | 0.034 ml | 0.17 ml | 0.34 ml |
Last Update:2024-01-02 23:10:35
CRDWMOVRQCMROH-HIKRQZGHSA-N - Reference Information
biological activity | phospho-aminidon diisodium Salt is a metabolite inhibitor that is widely used as a biochemical tool. Phosphoramidon inhibited ECE, NEP and ACE activities with IC50 values of 3.5 μm, 0.034 μm and 78 μm, respectively. |
Target | Value |
Last Update:2024-04-10 22:29:15