MassBank Record: AC000743



 Oxaline; LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: AC000743
RECORD_TITLE: Oxaline; LC-ESI-ITFT; MS2; CE: 20; R=17500; [M+H]+
DATE: 2017.07.07
AUTHORS: , Megan J. Kelman, Justin B. Renaud, Mark W. Sumarah, Agriculture and Agri-Food Canada
LICENSE: CC BY-SA
COPYRIGHT: Copyright (C) 2017
PUBLICATION: Visagie, C. M.; Renaud, J. B.; Burgess, K. M. N.; Malloch, D. W.; Clark, D.; Ketch, L.; Urb, M.; Louis-Seize, G.; Assabgui, R.; Sumarah, M. W.; et al. Fifteen New Species of Penicillium. Persoonia - Molecular Phylogeny and Evolution of Fungi 2016, 36 (1), 247–80. DOI:10.3767/003158516x691627
COMMENT: CONFIDENCE Penicillium amphipolaria

CH$NAME: Oxaline CH$COMPOUND_CLASS: Natural Product; Fungal metabolite CH$FORMULA: C24H25N5O4 CH$EXACT_MASS: 447.19064 CH$SMILES: CC(C)(C=C)[C@@]12C=C(C(=O)N\3[C@]1(NC(=O)/C3=C\C4=CN=CN4)N(C5=CC=CC=C25)OC)OC CH$IUPAC: InChI=1S/C24H25N5O4/c1-6-22(2,3)23-12-19(32-4)21(31)28-18(11-15-13-25-14-26-15)20(30)27-24(23,28)29(33-5)17-10-8-7-9-16(17)23/h6-14H,1H2,2-5H3,(H,25,26)(H,27,30)/b18-11+/t23-,24-/m0/s1 CH$LINK: INCHIKEY SOHAVULMGIITDH-ZXPSTKSJSA-N CH$LINK: CAS 55623-37-5 CH$LINK: PUBCHEM CID:70698220 CH$LINK: CHEMSPIDER 10225680 CH$LINK: KNAPSACK C00011266
AC$INSTRUMENT: Q-Exactive Orbitrap Thermo Scientific AC$INSTRUMENT_TYPE: LC-ESI-ITFT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: ION_MODE POSITIVE AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: IONIZATION_VOLTAGE 3.9 kV AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD AC$MASS_SPECTROMETRY: COLLISION_ENERGY 20(NCE) AC$MASS_SPECTROMETRY: RESOLUTION 17500 AC$CHROMATOGRAPHY: COLUMN_NAME Agilent RRHD Eclipse 50 x 2 mm, 1.8 uM AC$CHROMATOGRAPHY: FLOW_GRADIENT 100:0 at 0 min, 100:0 at 0.5 min, 0:100 at 3.5 min, 0:100 at 5.5 min, 100:0 at 7 min AC$CHROMATOGRAPHY: FLOW_RATE 0.3 mL min-1 AC$CHROMATOGRAPHY: RETENTION_TIME 2.73 AC$CHROMATOGRAPHY: NAPS_RTI 705 AC$CHROMATOGRAPHY: SOLVENT A H2O 0.1% FA AC$CHROMATOGRAPHY: SOLVENT B ACN 0.1% FA
MS$FOCUSED_ION: BASE_PEAK 417.1785 MS$FOCUSED_ION: PRECURSOR_M/Z 448.1974 MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+ MS$DATA_PROCESSING: DEPROFILE Proteowizard MS$DATA_PROCESSING: RECALIBRATE based on Fragment ion formula determination MS$DATA_PROCESSING: INTENSITY CUTOFF 0.05 Base Peak
PK$SPLASH: splash10-014j-0004900000-516c6f79f542554bfc74 PK$ANNOTATION: m/z tentative_formula mass_error(ppm) 332.0876 C18H12N4O3+ -8.36 348.1082 C18H14N5O3+ -2.58 349.1161 C18H15N5O3+ -2.36 374.1603 C21H20N5O2+ -2.26 386.1603 C22H20N5O2+ -2.19 416.1709 C23H22N5O3+ -1.94 417.1785 C23H23N5O3+ -2.47 448.1966 C24H26N5O4+ -2.95 PK$NUM_PEAK: 8 PK$PEAK: m/z int. rel.int. 332.0904 831623.0625 31 348.1091 7506994.0 294 349.1169 3936626.25 153 374.1611 939862.1875 35 386.1611 1790251.125 69 416.1717 1310166.25 50 417.1795 25444462.0 999 448.1979 2685199.75 104 //

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