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RefMet: Metabolite Nomenclature
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Clustering data with hclust algorithm for (Study ST003857)
None (Direct infusion) POSITIVE ION MODE (Analysis AN006338)
Metabolite
Structure
F1
F2
SM(d18:0/24:1)
ME1019824
0.07
1.31
TG(18:1/14:0/18:1)
ME1019826
NA
1.00
TG(16:0/18:0/18:2)
ME1019828
NA
1.00
phosphatidylethanolamine (15:0/16:0)
ME1019800
NA
1.00
PC(20:2/14:0)
ME1019813
NA
1.00
PC(18:3/18:0)
ME1019816
NA
1.00
PC(18:1/20:3)
ME1019823
NA
1.00
PC(18:0/14:0)
ME1019812
NA
1.00
PC(14:0/18:1)
ME1019810
NA
1.00
PA(16:0/18:2)
ME1019801
NA
1.00
NCGC00384912-01_C38H61NO9_(3beta,9xi,16alpha)-3-[(2-Acetamido-2-deoxy-beta-D-glucopyranosyl)oxy]-16-hydroxyolean-12-en-28-oic acid
ME1019799
NA
1.00
PA(16:0/18:1)
ME1019802
NA
1.00
PAz-PC
ME1019798
0.98
1.02
TG(18:0/14:0/18:1)
ME1019827
1.00
NA
POV-PC
ME1019795
1.00
NA
PE (15:0-18:1-d7)_791638
ME1019811
1.00
NA
PC(22:2/16:1)
ME1019821
1.00
NA
PC(20:3/16:1)
ME1019819
1.00
NA
PC(16:1/16:1)
ME1019808
1.00
NA
PC(16:0/14:0)
ME1019804
1.00
NA
PA(18:1/18:1)
ME1019806
1.00
NA
NCGC00380734-01_C39H65NO10_2-{6-[5-Hydroxy-3-(2-hydroxy-2-propanyl)-6a,9b-dimethyldodecahydrocyclopenta[f]chromen-7-yl]-4a-methyl-3,4,4a,7,8,8a-hexahydro-2H-chromen-2-yl}-2-propanyl 2-acetamido-2-deoxy-6-O-methylhexopyranoside
ME1019805
1.00
NA
Malyngamide J
ME1019796
1.00
NA
Arg Tyr Gln Lys
ME1019794
1.00
NA
4^-Methyl-(-)-epigallocatechin 7-glucuronide
ME1019793
1.00
NA
4S,5S-antillatoxin A
ME1019790
1.00
NA
Ser Lys Phe Leu Lys
ME1019797
1.13
0.62
Ubiquinol 8
ME1019809
1.14
0.57
PC(18:1/16:0)
ME1019814
1.25
0.25
PC(20:2/16:0)
ME1019817
1.24
0.28
PC(18:2/16:0)
ME1019815
1.56
0.16
SM(d18:1/16:0)
ME1019807
1.52
0.48
Factors:
F1
Treatment:control
F2
Treatment:DOX treatment
Data matrix
UCSD Metabolomics Workbench, a resource sponsored by the Common Fund of the National Institutes of Health
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