Phosphoramidon Disodium Salt
Phosphoramidon Disodium Salt is a potent inhibitor of metalloproteinase [1].
Metalloproteinase is an enzyme whose catalytic mechanism involves a metal. Most metalloproteases require zinc and some require cobalt.
Phosphoramidon Disodium Salt is a potent metalloproteinase inhibitor. In porcine aortic endothelial cells, phosphoramidon (10-4 M) inhibited immunoreactive-endothelin (IR-ET) release by 10-20% and increased IR-CTF levels. These results suggested that phosphoramidon reduced the IR-ET release through affecting the conversion of big ET-1 to ET-l [1]. In cultured endothelial cells, phosphoramidon inhibited the increase of ET-1 and C-terminal fragment (CTF) of big ET-1. However, phosphoramidon increased big ET-1 secretion [2].
In anesthetized rats, phosphoramidon inhibited the hypertensive effect of big ET-1 [2]. In mice, phosphoramidon inhibited big ET-1 induced lethality and increased plasma IR-ET-1 through inhibition of the enzyme that converted big ET-1 to ET-1 [3].
References:
[1]. Ikegawa R, Matsumura Y, Tsukahara Y, et al. Phosphoramidon, a metalloproteinase inhibitor, suppresses the secretion of endothelin-1 from cultured endothelial cells by inhibiting a big endothelin-1 converting enzyme. Biochem Biophys Res Commun, 1990, 171(2): 669-675.
[2]. Matsumura Y, Ikegawa R, Hisaki K, et al. Conversion of big endothelin-1 to endothelin-1 by phosphoramidon-sensitive metalloproteinase derived from aortic endothelial cells. J Cardiovasc Pharmacol, 1991, 17 Suppl 7: S65-7.
[3]. Matsuura A, Okumura H, Ashizawa N, et al. Big endothelin-1-induced sudden death is inhibited by phosphoramidon in mice. Life Sci, 1992, 50(21): 1631-1638.
| Physical Appearance | A solid |
| Storage | Desiccate at -20°C |
| M.Wt | 587.47 |
| Cas No. | 164204-38-0 |
| Formula | C23H32N3Na2O10P |
| Solubility | ≥58.7 mg/mL in DMSO; insoluble in EtOH; ≥52.5 mg/mL in H2O |
| Chemical Name | sodium (S)-3-(1H-indol-3-yl)-2-((S)-4-methyl-2-((oxido(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)phosphoryl)amino)pentanamido)propanoate |
| SDF | Download SDF |
| Canonical SMILES | O=C([O-])[C@@H](NC([C@@H](NP(O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O)([O-])=O)CC(C)C)=O)CC2=CNC3=C2C=CC=C3.[Na+].[Na+] |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |
| Cell experiment [1]: | |
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Cell lines |
ECs isolated from fresh porcine thoracic aortas |
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Preparation method |
The solubility of this compound in DMSO is >10mM. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months. |
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Reacting condition |
10- 7-10-4 M |
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Applications |
In ECs, phosphoramidon (10- 7-10-4 M) suppressed dose-dependently the apparent converting activity of the membrane fraction and suppressed the membrane fraction induced apparent conversion of big ET-l to ET-l ( Endothelin-1 ). ET-l is a 21 amino acid peptide isolated from the culture medium of vascular endothelial cells (ECs), the secretion of ET-l from cultured ECs was abolished by the addition of phosphoramidon. |
| Animal experiment [2]: | |
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Animal models |
Wild-type mice, NEP/NEP2-deficient mice |
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Dosage form |
24 μl (30 mM) once per day for 5 days. |
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Application |
Intranasal administration of phosphoramidon produced significantly elevated cerebral Aβ (Beta-amyloid peptide) levels in wild-type mice. In NEP/NEP2-deficient mice, Aβ levels were significantly elevated by phosphoramidon, in the absence of NEP (Aβ degrading enzymes) and NEP2, phosphoramidon clearly elevates Aβ1–40 levels relative to Aβ1–42 levels. NEP and NEP2 may be the major “NEP-like” Aβ1–42-degrading (phosphoramidon-sensitive) enzymes in the rodent brain. |
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Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
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References: [1]. Matsumura Y, Ikegawa R, Hisaki K., et al. Conversion of big endothelin-1 to endothelin-1 by phosphoramidon-sensitive metalloproteinase derived from aortic endothelial cells. J Cardiovasc Pharmacol, 1991, 17 Suppl 7: S65-7. [2] . Hanson LR., et al. Intranasal phosphoramidon increases beta-amyloid levels in wild-type and NEP/NEP2-deficient mice.J MolNeurosci. 2011 Mar;43(3):424-7. |
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Quality Control & MSDS
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