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R7385

Sigma-Aldrich

Phosphoramidon disodium salt

powder, ≥97% (HPLC)

Synonyme(s) :

N-(α-Rhamno­pyranosyl­oxy­hydroxy­phosphinyl)-Leu-Trp disodium salt, N-(α-Rhamno­pyranosyl­phos­phono)-L-leucyl-L-tryptophan disodium salt

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About This Item

Formule empirique (notation de Hill):
C23H32N3Na2O10P
Numéro CAS:
Poids moléculaire :
587.47
Numéro Beilstein :
8105669
Numéro MDL:
Code UNSPSC :
12352202
ID de substance PubChem :
Nomenclature NACRES :
NA.77

product name

Phosphoramidon disodium salt, ≥97% (HPLC)

Source biologique

Streptomyces sp.

Pureté

≥97% (HPLC)

Forme

powder

Solubilité

H2O: 50 mg/mL

Température de stockage

−20°C

Chaîne SMILES 

[Na+].[Na+].CC(C)C[C@H](NP([O-])(=O)O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O)C(=O)N[C@@H](Cc2c[nH]c3ccccc23)C([O-])=O

InChI

1S/C23H34N3O10P.2Na/c1-11(2)8-16(26-37(33,34)36-23-20(29)19(28)18(27)12(3)35-23)21(30)25-17(22(31)32)9-13-10-24-15-7-5-4-6-14(13)15;;/h4-7,10-12,16-20,23-24,27-29H,8-9H2,1-3H3,(H,25,30)(H,31,32)(H2,26,33,34);;/q;2*+1/p-2/t12-,16-,17-,18-,19+,20+,23-;;/m0../s1

Clé InChI

OQKHVXFOYFBMDJ-ODIUWQMJSA-L

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Description générale

Phosphoramidon [N-(α-rhamnopyranosyl-oxyhydroxyphosphinyl)-Leu-Trp] is a competitive inhibitor of several soluble zinc metalloproteases. Phosphoramidate is produced naturally by Streptomyces tanashiensis.

Application

Phosphoramidon disodium salt has been used:
  • as the neprilysin (NEP) inhibitor: in amyloid beta (Aβ) uptake and degradation
  • to study its effect on keratinase activity
  • to treat primary microglia from wild-type mice

Identification of phosphoramidon as a metallo-endopeptidase inhibitor was used to characterize endothelin converting enzyme as a metallo-endopeptidase. Phosphoramidon increases the production of β-amyloid protein, but not amyloid precursor protein, indicating that abnormal amyloid processing in Alzheimer′s disease may be carried out by a metallo-endopeptidase.

Actions biochimiques/physiologiques

Phosphoramidon can inhibit ZMPSTE24, an integral membrane protein zinc metalloprotease. It is capable of blocking thermolysin.
Phosphoramidon is a potent inhibitor of thermolysin and other metallo-endopeptidases. It trongly inhibits mammalian enkephalinase and it does not inhibit trypsin, papain, chymotrypsin or pepsin. It weakly inhibits collagenase.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

SIRT1 facilitates amyloid beta peptide degradation by upregulating lysosome number in primary astrocytes
Li MZ, et al.
Neural Regeneration Research, 13(11), 2005-2005 (2018)
J R Wu-Wong et al.
Molecular pharmacology, 44(2), 422-429 (1993-08-01)
Endothelin (ET) is generated from prepro-ET by dibasic pair proteolysis, followed by specific proteolytic cleavage between Trp21 and Val22. Currently, intense research efforts are focused on the investigation of a metalloprotease-like ET-converting enzyme that is inhibited by phosphoramidon but not
Deacetylation of TFEB promotes fibrillar A beta degradation by upregulating lysosomal biogenesis in microglia
Bao J, et al.
Protein & cell, 7(6), 417-433 (2016)
Phosphoramidon inhibits the integral membrane protein zinc metalloprotease ZMPSTE24
Goblirsch BR, et al.
Acta crystallographica. Section D, Structural biology, 74(Pt 8), 739-739 (2018)
Christoph Nicolaus et al.
Journal of ethnopharmacology, 196, 94-103 (2016-12-14)
Calendula officinalis (pot marigold) flower extracts have a long-lasting tradition in ethnopharmacology. Currently, the European Medicines Agency (EMA) has approved its lipophilic and aqueous alcoholic extracts as traditional medicinal products for the treatment of minor inflammation of the skin and

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