Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	43068
Common Name:	Etoposide
Systematic Name:	(10R,11R,15R,16S)-16-{[(2R,4aR,6R,7R,8R,8aS)-7,8-dihydroxy-2-methyl-hexahydro-2H-pyrano[3,2-d][1,3]dioxin-6-yl]oxy}-10-(4-hydroxy-3,5-dimethoxyphenyl)-4,6,13-trioxatetracyclo[7.7.0.0^{3,7}.0^{11,15}]hexadeca-1(9),2,7-trien-12-one
RefMet Name:	Etoposide
Synonyms:	[PubChem Synonyms]
Exact Mass:	588.1843 (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:	C29H32O13
InChIKey:	VJJPUSNTGOMMGY-MRVIYFEKSA-N
ClassyFire superclass:	Lignans, neolignans and related compounds [C0001392]
ClassyFire class:	Lignan lactones [C0001510]
ClassyFire subclass:	Podophyllotoxins [C0000047]
ClassyFire direct parent:	Podophyllotoxins [C0000047]
MoNA MS spectra:	View MS spectra
SMILES:	C[C@@H]1OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)O[C@@H]2c3cc4c(cc3[C@@H](c3cc(c(c(c3)OC)O)OC)[C@@H]3[C@@H]2COC3=O)OCO4)O)O)O1
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

Calculated physicochemical properties (?):

Heavy Atoms:	42
Rings:	7
Aromatic Rings:	2
Rotatable Bonds:	5
van der Waals Molecular volume:	497.73 Å3 molecule-1
Toplogical Polar Sufrace Area:	173.25 Å2 molecule-1
Hydrogen Bond Donors:	3
Hydrogen Bond Acceptors:	13
logP:	3.63
Molar Refractivity:	142.40
Fraction sp3 Carbons:	0.55
sp3 Carbons:	16

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