Metabolomics Structure Database

 
MW REGNO: 70479
Common Name:Oligomycin C
Systematic Name:(1R,4S,5E,5'R,6'R,7E,10S,11R,12R,14R,15R,16S,18R,19S,20R,21E,25S,26R,27S,29S)-4-ethyl-11,15,19-trihydroxy-6'-[(2S)-2-hydroxypropyl]-5',10,12,14,16,18,20,26,29-nonamethyl-spiro[24,28-dioxabicyclo[23.3.1]nonacosa-5,7,21-triene-27,2'-tetrahydropyran]-13,17,23-trione
RefMet Name:Oligomycin C
Synonyms:AC1NQZ9I; Ambotz11052-72-5; O5251_SIGMA; C11313 [PubChem Synonyms]
Exact Mass:
774.5282 (neutral)    Calculate m/z:
Formula:C45H74O10
InChIKey:CMMLZMMKTYEOKV-JEKNLLRFSA-N
ClassyFire superclass:Phenylpropanoids and polyketides [C0000261]
ClassyFire class:Macrolides and analogues [C0000147]
ClassyFire subclass:Macrolides and analogues [C0000147]
ClassyFire direct parent:Aliphatic heteropolycyclic compounds
SMILES:CC[C@@H]1/C=C/C=C/C[C@H](C)[C@H]([C@@H](C)C(=O)[C@H](C)[C@H]([C@H](C)C(=O)[C@H](C)[C@H]([C@H](C)/C=C/C(=O)O[C@H]2[C@@H](C)[C@@H](CC1)O[C@@]1(CC[C@@H](C)[C@@H](C[C@H](C)O)O1)[C@@H]2C)O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:5281901
KEGG ID:C11313
Plant Metabolite Hub(Pmhub):MS000022230

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

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