Metabolomics Structure Database

 
MW REGNO: 52696
Common Name:Latrunculin A
Systematic Name:(4R)-4-[(1R,4Z,8E,10Z,12S,15R,17R)-17-hydroxy-5,12-dimethyl-3-oxo-2,16-dioxabicyclo[13.3.1]nonadeca-4,8,10-trien-17-yl]-1,3-thiazolidin-2-one
Synonyms:(+)-latrunculin A; 2-Thiazolidinone, 4-((1R,4Z,8E,10Z,12S,15R,17R)-17-hydroxy-5,12-dimethyl-3-oxo-2,16-dioxabicyclo(13.3.1)nonadeca-4,8,10-trien-17-yl)-, (4R)-; LAT-A; LatA; NSC 613011 [PubChem Synonyms]
Exact Mass:
421.1923 (neutral)    Calculate m/z:
Formula:C22H31NO5S
InChIKey:DDVBPZROPPMBLW-IZGXTMSKSA-N
ClassyFire superclass:Phenylpropanoids and polyketides
ClassyFire class:Macrolides and analogues
ClassyFire subclass:Macrolides and analogues
ClassyFire direct parent:Aliphatic heteropolycyclic compounds
SMILES:C[C@@H]1/C=CC=CCC/C(=CC(=O)O[C@@H]2C[C@@H](CC1)O[C@](C2)([C@@H]1CSC(=O)N1)O)/C
Studies:Available studies(via PubChem CID)

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External database links:

PubChem CID:445420
CHEBI ID:69136
EPA CompTox DB:DTXCID401332729
Marine Natural Products DB:CMNPD3753

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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