Metabolomics Structure Database

 
MW REGNO: 35101
Common Name:Sarsasapogenenin
Systematic Name:(25S)-5beta-spirostan-3beta-ol
Synonyms:Parigenin; Sarsasapogenin [PubChem Synonyms]
Exact Mass:
416.3290 (neutral)    Calculate m/z:
Formula:C27H44O3
InChIKey:GMBQZIIUCVWOCD-WWASVFFGSA-N
LIPID MAPS Category:Sterol Lipids [ST]
LIPID MAPS mainclass:Sterols [ST01]
LIPID MAPS subclass:Spirostanols and derivatives [ST0108]
Massbank MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:C[C@H]1CC[C@@]2([C@@H](C)[C@H]3[C@H](C[C@H]4[C@@H]5CC[C@@H]6C[C@H](CC[C@]6(C)[C@H]5CC[C@]34C)O)O2)OC1
Studies:Available studies(via PubChem CID)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:92095
LIPID MAPS ID:LMST01080007
CHEBI ID:15578
HMDB ID:HMDB0030024
KEGG ID:C03963
Chemspider ID:83145
NP-MRD ID(NMR):NP0030539
Plant Metabolite Hub(Pmhub):MS000015961
PhytoHub ID:PHUB000017

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
NPClassifier classification: "NPClassifier: A Deep Neural Network-Based Structural Classification Tool for Natural Products", Kim HW, Wang M, Leber CA, Nothias LF, Reher R, Kang KB, van der Hooft JJJ, Dorrestein PC, Gerwick WH and Cottrell GW. J Nat Prod. 2021 Nov 26;84(11):2795-2807.DOI: 10.1021/acs.jnatprod.1c00399.

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