Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	56370
Common Name:	N(6)-methyl-AMP
Systematic Name:	N-methyladenosine 5'-(dihydrogen phosphate)
Synonyms:	N(6)-methyl-5'-adenylic acid; N(6)-methyl-5'-phosphoadenosine; N(6)-methyl-[5']adenylic acid; N(6)-methyladenosine 5'-monophosphate; N6-METHYLADENOSINE-5'-MONOPHOSPHATE [PubChem Synonyms]
Exact Mass:	361.0787 (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:	C11H16N5O7P
InChIKey:	WETVNPRPZIYMAC-IOSLPCCCSA-N
ClassyFire superclass:	Nucleosides, nucleotides, and analogues [C0000289]
ClassyFire class:	Purine nucleotides [C0001506]
ClassyFire subclass:	Purine ribonucleotides [C0001544]
ClassyFire direct parent:	Purine ribonucleoside monophosphates [C0001617]
SMILES:	CNc1c2c(ncn1)n(cn2)[C@H]1[C@@H]([C@@H]([C@@H](COP(=O)(O)O)O1)O)O
Studies:	-

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	16760025
CHEBI ID:	40196

Calculated physicochemical properties (?):

Heavy Atoms:	24
Rings:	3
Aromatic Rings:	2
Rotatable Bonds:	5
van der Waals Molecular volume:	265.78 Å3 molecule-1
Toplogical Polar Sufrace Area:	174.15 Å2 molecule-1
Hydrogen Bond Donors:	5
Hydrogen Bond Acceptors:	11
logP:	0.08
Molar Refractivity:	80.54
Fraction sp3 Carbons:	0.55
sp3 Carbons:	6

Human Pathway links:

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