Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	50458
Common Name:	Myo-inositol 1,3,4,5,6-pentakisphosphate
Systematic Name:	myo-inositol 1,3,4,5,6-pentakis(dihydrogen phosphate)
Synonyms:	[PubChem Synonyms]
Exact Mass:	579.8950 (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:	C6H17O21P5
InChIKey:	CTPQAXVNYGZUAJ-KXXVROSKSA-N
ClassyFire superclass:	Organic oxygen compounds [C0004603]
ClassyFire class:	Organooxygen compounds [C0000323]
ClassyFire subclass:	Alcohols and polyols [C0000129]
ClassyFire direct parent:	Inositol phosphates [C0002511]
SMILES:	[C@@H]1([C@H]([C@@H]([C@H]([C@@H]([C@H]1OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)O
Studies:	-

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	439468
CHEBI ID:	16322
HMDB ID:	HMDB0003529
KEGG ID:	C01284
MetaCyc ID:	CPD-1107
Plant Metabolite Hub(Pmhub):	MS000017193

Calculated physicochemical properties (?):

Heavy Atoms:	32
Rings:	1
Aromatic Rings:	0
Rotatable Bonds:	10
van der Waals Molecular volume:	383.74 Å3 molecule-1
Toplogical Polar Sufrace Area:	354.03 Å2 molecule-1
Hydrogen Bond Donors:	11
Hydrogen Bond Acceptors:	21
logP:	0.17
Molar Refractivity:	92.29
Fraction sp3 Carbons:	1.00
sp3 Carbons:	6

Human Pathway links:

HMDB and KEGG pathways containing this metabolite

REACTOME pathways containing this metabolite

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