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36357-77-4

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Biosynthetic reconstitution of deoxysugar phosphoramidate metalloprotease inhibitors using an N-P-bond-forming kinase
Phosphoramidon is a potent metalloprotease inhibitor and a widespread tool in cell biology research. It contains a dipeptide backbone that is uniquely linked to a 6-deoxysugar via a phosphoramidate bridge. Herein, we report the identification of a gene cluster for the formation of phosphoramidon and its detailed characterization. In vitro reconstitution of the biosynthesis established TalE as a phosphoramidate-forming kinase and TalC as the glycosyltransferase which installs the l-rhamnose moiety by phosphoester linkage.
Baulig, Alexandra,Helmle, Irina,Bader, Marius,Wolf, Felix,Kulik, Andreas,Al-Dilaimi, Arwa,Wibberg, Daniel,Kalinowski, J?rn,Gross, Harald,Kaysser, Leonard
p. 4486 - 4490
(2019)
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Synthesis of the endothelin converting enzyme inhibitor phosphoramidon
Phosphoramidon, an endothelin converting enzyme inhibitor, is synthesized by coupling of a rhamnose derivative with a dichlorophosphate and a suitably protected dipeptide.
De Nanteuil, Guillaume,Benoist, Alain,Remond, Georges,Descombes, Jean-Jacques,Barou, Veronique,Verbeuren, Tony J.
p. 1435 - 1438
(2007/10/02)

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Chemical Properties

Density: 1.48 g/cm³
Solubility:H2O: 1 mM Stock solution stable for 1 month at –20&#
Storage Temp.:−20°C
PKA: -0.66±0.50(Predicted)
PSA: 220.48000
LogP: 1.01040

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