Metabolomics Structure Database

 
MW REGNO: 51962
Common Name:Neocarzinostatin chromophore
Systematic Name:[(4S,6R,9E,11R,12R)-11-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-6-methyl-3-(methylamino)oxan-2-yl]oxy-4-[(4R)-2-oxo-1,3-dioxolan-4-yl]-5-oxatricyclo[8.3.0.04,6]trideca-1(13),9-dien-2,7-diyn-12-yl] 2-hydroxy-7-methoxy-5-methylnaphthalene-1-carboxylate
RefMet Name:Neocarzinostatin chromophore
Synonyms:Ncs-chrom; Neocarzinostatin chromophore [PubChem Synonyms]
Exact Mass:
659.2003 (neutral)    Calculate m/z:
Formula:C35H33NO12
InChIKey:QZGIWPZCWHMVQL-UIYAJPBUSA-N
ClassyFire superclass:Organic oxygen compounds
ClassyFire class:Organooxygen compounds
ClassyFire subclass:Carbohydrates and carbohydrate conjugates
ClassyFire direct parent:Aminoglycosides
SMILES:Cc1cc(cc2c1ccc(c2C(=O)O[C@@H]1C=C2C#C[C@]3([C@@H](C#C/C=C/[C@H]1O[C@@H]1[C@@H]([C@H]([C@H]([C@@H](C)O1)O)O)NC)O3)[C@H]1COC(=O)O1)O)OC
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:447545
CHEBI ID:29655
HMDB ID:HMDB0255490
Natural Products Atlas ID:NP020312
Plant Metabolite Hub(Pmhub):MS000022799

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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