Metabolomics Structure Database

 
MW REGNO: 36309
Common Name:beta-Muricholic acid
Systematic Name:3alpha,6beta,7beta-trihydroxy-5beta-cholan-24-oic acid
RefMet Name:beta-Muricholic acid
Synonyms:beta-MCA; MCA(b) [PubChem Synonyms]
Exact Mass:
408.2876 (neutral)    Calculate m/z:
Formula:C24H40O5
InChIKey:DKPMWHFRUGMUKF-CRKPLTDNSA-N
LIPID MAPS Category:Sterol Lipids [ST]
LIPID MAPS mainclass:Bile acids and derivatives [ST04]
LIPID MAPS subclass:C24 bile acids, alcohols, and derivatives [ST0401]
Massbank MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@H]3[C@H](CC[C@]12C)[C@@]1(C)CC[C@H](C[C@H]1[C@@H]([C@@H]3O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:5283853
LIPID MAPS ID:LMST04010067
CHEBI ID:81298
HMDB ID:HMDB0000415
KEGG ID:C17726
Chemspider ID:4446941
METLIN ID:5404
NP-MRD ID(NMR):NP0000912

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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