Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	69920
Common Name:	Phosphoramidon
Systematic Name:	(2S)-2-[[(2S)-2-[[hydroxy-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-phosphoryl]amino]-4-methyl-pentanoyl]amino]-3-(1H-indol-3-yl)propanoic acid
RefMet Name:	Phosphoramidon
Synonyms:	Phosphoramidon disodium salt; Phosphramidon; Phosporamidon [PubChem Synonyms]
Exact Mass:	543.1982 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C23H34N3O10P
InChIKey:	ZPHBZEQOLSRPAK-XLCYBJAPSA-N
ClassyFire superclass:	Organic acids and derivatives [C0000264]
ClassyFire class:	Carboxylic acids and derivatives [C0000265]
ClassyFire subclass:	Amino acids, peptides, and analogues [C0000013]
ClassyFire direct parent:	Dipeptides [C0004830]
MoNA MS spectra:	View MS spectra
NP-MRD NMR spectra:	View NMR spectra
SMILES:	CC(C)C[C@@H](C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)O)NP(=O)(O)O[C@H]1[C@@H]([C@@H]([C@H]([C@H](C)O1)O)O)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

Calculated physicochemical properties (?):

Heavy Atoms:	37
Rings:	3
Aromatic Rings:	2
Rotatable Bonds:	11
van der Waals Molecular volume:	472.47 Å3 molecule-1
Toplogical Polar Sufrace Area:	212.74 Å2 molecule-1
Hydrogen Bond Donors:	8
Hydrogen Bond Acceptors:	10
logP:	2.25
Molar Refractivity:	134.59
Fraction sp3 Carbons:	0.57
sp3 Carbons:	13

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y