Phosphoramidon
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Phosphoramidon

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Phosphoramide is an inhibitor of pyrolytic enzyme derived from the culture of Streptomyces tanashiensis.

Category
Peptide Inhibitors
Catalog number
BAT-010282
CAS number
119942-99-3
Molecular Formula
C23H34N3O10P.xNa
Molecular Weight
543.50 (free acid)
Phosphoramidon
IUPAC Name
sodium; (2S)-3-(1H-indol-3-yl)-2-[[(2S)-4-methyl-2-[[oxido-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphosphoryl]amino]pentanoyl]amino]propanoate
Synonyms
N-(alpha-Rhamnopyranosyloxyhydroxyphosphinyl)-L-leucyl-L-tryptophan
Appearance
Solid Powder
Purity
>98%
Storage
Store at -20°C
Solubility
Soluble in DMSO
InChI
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
InChI Key
OQKHVXFOYFBMDJ-ODIUWQMJSA-L
Canonical SMILES
CC1C(C(C(C(O1)OP(=O)(NC(CC(C)C)C(=O)NC(CC2=CNC3=CC=CC=C32)C(=O)[O-])[O-])O)O)O.[Na+].[Na+]
1.S 17162 is a novel selective inhibitor of big ET-1 responses in the rat.
Descombes JJ1, Mennecier P, Versluys D, Barou V, de Nanteuil G, Laubie M, Verbeuren TJ. J Cardiovasc Pharmacol. 1995;26 Suppl 3:S61-4.
Endothelin-1 (ET-1) is a powerful renal vasoconstrictor peptide that may be implicated in acute renal failure. The aim of the present study was to test the effects of the novel endothelin-converting enzyme inhibitor S 17162 (N-(2,3 dihydroxy propyl phosphonyl)-(S)-Leu-(S)-Trp-OH, disodium salt) on pressor responses to ET-1 and its precursor, big ET-1, in isolated perfused rat kidneys and in pithed rats. In both models, phosphoramidon selectively inhibited the pressor responses to big ET-1 without influencing those to ET-1, angiotensins (AT-I and AT-II) or norepinephrine. S 17162 was active against big ET-1 in both test systems. It selectively inhibited the pressor responses to big ET-1 with ID50 values of 160 micrograms/kg/min (phosphoramidon: 120 micrograms/kg/min) in the spinal rat and 6 microM (phosphoramidon: 5 microM) in the perfused rat kidney. In the nonanesthetized rat, S 17162 at 20 mg/kg p.o. inhibited the pressor responses to big ET-1, demonstrating its oral bioavailability.
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