Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	68884
Common Name:	Taccalonolide A
Systematic Name:	(2R,3R,5S)-2-(1-hydroxy-1-methyl-ethyl)-5-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]tetrahydropyran-3-ol
RefMet Name:	Taccalonolide A
Synonyms:	AC1L9BGV; CHEMBL1821838; C08635 [PubChem Synonyms]
Exact Mass:	702.2888 (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:	C36H46O14
InChIKey:	PTTJLTMUKRRHAT-VJAKQJMOSA-N
LIPID MAPS Category:	Sterol Lipids [ST]
LIPID MAPS mainclass:	Sterols [ST01]
SMILES:	C[C@@H]1C=C2[C@@](C)([C@H]3[C@H]1[C@]1(C)[C@H]([C@H]4[C@H]([C@@H]([C@@H]1OC(=O)C)OC(=O)C)[C@]1(C)[C@H](C[C@H]5[C@@H]([C@@H]1OC(=O)C)O5)C(=O)[C@@H]4O)[C@H]3OC(=O)C)[C@@](C)(C(=O)O2)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	441685
LIPID MAPS ID:	LMST01160016
CHEBI ID:	9388
KEGG ID:	C08635
Plant Metabolite Hub(Pmhub):	MS000020071

Calculated physicochemical properties (?):

Heavy Atoms:	50
Rings:	7
Aromatic Rings:	0
Rotatable Bonds:	8
van der Waals Molecular volume:	649.42 Å3 molecule-1
Toplogical Polar Sufrace Area:	203.63 Å2 molecule-1
Hydrogen Bond Donors:	2
Hydrogen Bond Acceptors:	14
logP:	3.70
Molar Refractivity:	169.83
Fraction sp3 Carbons:	0.78
sp3 Carbons:	28

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