Metabolomics Workbench : NIH Data Repository

Clustering data with hclust algorithm for (Study ST003998)

Reversed phase POSITIVE ION MODE (Analysis AN006590)

Metabolite	Structure	F1	F2	F3	F4	F5
Sorbic acid	ME1058477	0.46	0.13	4.25	0.13	0.03
2^-O-Methyladenosine	ME1058440	2.43	0.69	1.28	0.51	0.09
Adenosine 3^5^-cyclic monophosphate	ME1058452	1.50	0.89	1.69	0.82	0.10
9S,13R-12-Oxophytodienoic acid	ME1058449	4.57	0.16	0.12	0.12	0.04
L-Phenylalanine	ME1058469	4.83	0.04	0.01	0.04	0.08
Apigetrin	ME1058453	4.98	0.01	0.01	0.00	0.00
trans-3-Indoleacrylic acid	ME1058480	4.97	0.00	0.02	0.00	0.00
1-Tetradecylamine	ME1058436	3.47	0.53	0.31	0.33	0.36
Inosine	ME1058460	3.41	0.58	0.01	0.45	0.54
Nicotinic acid	ME1058473	3.92	0.21	0.01	0.27	0.59
D-(+)-Pyroglutamic Acid	ME1058455	3.92	0.54	0.01	0.51	0.02
Scutellarein 7-methyl ether 6-glucoside	ME1058476	3.91	0.38	0.24	0.33	0.14
5-methyl-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H-chromen-2-one	ME1058445	2.72	0.65	0.28	0.68	0.68
Adenosine	ME1058451	2.98	0.46	0.04	0.69	0.82
Luteolin-3^,7-Diglucoside	ME1058471	2.55	0.96	0.34	0.90	0.25
trans-Zeatin	ME1058481	3.05	0.88	0.05	1.01	0.01
Tangeritin	ME1058478	0.08	0.74	0.01	3.52	0.65
Leucine	ME1058466	0.02	1.23	0.01	1.12	2.62
Galangin	ME1058459	0.44	0.94	0.02	0.77	2.84
Leucylproline	ME1058467	0.31	1.18	0.01	0.79	2.71
4-Pyridoxic acid	ME1058444	0.03	2.04	0.14	1.80	1.00
4-(4-hydroxy-2,2,6-trimethyl-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}cyclohexylidene)but-3-en-2-one	ME1058441	0.35	1.85	0.08	1.71	1.01
Trifolin	ME1058482	0.36	1.97	0.02	1.71	0.93
9-Oxo-10(E),12(E)-octadecadienoic acid	ME1058448	0.42	1.29	0.51	1.29	1.49
4-Indolecarbaldehyde	ME1058443	0.31	1.33	0.14	1.24	1.99
1-Methyladenine	ME1058435	0.01	1.35	0.03	1.58	2.03
(6-{[3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl (2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	ME1058434	0.04	1.22	0.18	1.32	2.24
Acetylarginine	ME1058450	0.01	2.00	0.14	1.30	1.57
N1-(2-oxopropyl)-2-phenylacetamide	ME1058472	0.03	1.89	0.03	1.54	1.51
Kuromanin	ME1058463	0.09	1.57	0.04	1.79	1.50
L(+)-Ornithine	ME1058465	0.00	1.64	0.03	1.47	1.85
Tetramethylpyrazine	ME1058479	0.01	1.67	0.01	1.46	1.85
8-{3-Oxo-2-[(2E)-2-penten-1-yl]-1-cyclopenten-1-yl}octanoic acid	ME1058447	0.26	1.58	0.12	1.45	1.59
4H-1-Benzopyran-4-one	ME1058442	0.20	1.62	0.01	1.53	1.64
L-Tyrosine	ME1058470	0.19	1.67	0.03	1.53	1.58
2,3,4,9-Tetrahydro-1H-β-carboline-3-carboxylic acid	ME1058437	0.15	2.87	1.12	0.78	0.09
7-methoxy-6-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2H-chromen-2-one	ME1058446	0.08	1.51	1.59	1.50	0.32
Nobiletin	ME1058474	0.46	1.44	1.43	0.89	0.78
2-Hydroxycinnamic acid	ME1058439	0.01	2.55	0.16	2.26	0.02
Diosmetin	ME1058458	0.58	2.03	0.23	2.13	0.02
Quinoline	ME1058475	0.46	2.33	0.16	2.05	0.01
Desthiobiotin	ME1058457	0.34	2.18	0.08	2.38	0.02
L-Glutamic acid	ME1058468	0.34	2.35	0.02	2.22	0.06
2-Amino-1,3,4-octadecanetriol	ME1058438	1.40	2.76	0.03	0.77	0.04
Isonaringin	ME1058461	1.28	1.57	0.61	1.15	0.38
D-(+)-Proline	ME1058454	0.26	0.01	0.01	0.20	4.52
Kaempferol	ME1058462	0.08	0.19	0.01	0.18	4.55
D-Carnitine	ME1058456	2.14	0.56	0.04	0.77	1.50
Kynurenic acid	ME1058464	1.58	0.35	0.02	0.23	2.83
Valylproline	ME1058483	1.50	0.47	0.01	0.38	2.63

Factors:

F1	Sample source:Leaves \| Treatment:Acetone Crude Extract
F2	Sample source:Leaves \| Treatment:Chloroform Crude Extract
F3	Sample source:Leaves \| Treatment:Ethanol Crude Extract
F4	Sample source:Leaves \| Treatment:Methanol Crude Extract
F5	Sample source:Leaves \| Treatment:Water Crude Extract

Data matrix