#METABOLOMICS WORKBENCH prats1988_20210404_005908 DATATRACK_ID:2563 STUDY_ID:ST001779 ANALYSIS_ID:AN002889 PROJECT_ID:PR001132
VERSION             	2
CREATED_ON             	May 8, 2021, 11:06 am
#PROJECT
PR:PROJECT_TYPE                  	Untargeted quantitative metabolomics analysis
PR:PROJECT_SUMMARY               	A549 lung cancer cells were treated in vitro with control, 0.5 mM ATP and 10
PR:PROJECT_SUMMARY               	ng/ml TGF-beta for 2, 6 and 12 hours The untargeted metabolomics data was
PR:PROJECT_SUMMARY               	generated from these studies.
PR:INSTITUTE                     	Ohio University
PR:DEPARTMENT                    	Biological Sciences
PR:LABORATORY                    	Dr. Xiaozhuo Chen, Edison biotechnology Institute
PR:FIRST_NAME                    	Pratik
PR:ADDRESS                       	Room 425, Parks Hall, College of Pharmacy, Ohio State University, Columbus Ohio.
PR:ADDRESS                       	43210
PR:EMAIL                         	ps774614@ohio.edu
PR:PHONE                         	7406033801
PR:FUNDING_SOURCE                	This study was funded by NIH R15 grant CA242177-01 to Dr. Xiaozhuo Chen.
PR:PROJECT_TITLE                 	Untargeted metabolomics analysis of A549 cancer cells treated in control, 0.5 mM
PR:PROJECT_TITLE                 	ATP and 10 ng/ml TGF-beta for 2, 6 and 12 hours
PR:LAST_NAME                     	Shriwas
#STUDY
ST:STUDY_TITLE                   	Untargeted Metabolomics analysis of A549 treated with 0.5 mM extracellular ATP
ST:STUDY_TITLE                   	and 10 ng/ml TGF-beta
ST:STUDY_SUMMARY                 	Control, 0.5 mM extracellular ATP and 10 ng/ml TGF-beta were used to treated 5
ST:STUDY_SUMMARY                 	million A549 lung cancer cells in vitro for 2, 6 and 12 hours. The untargeted
ST:STUDY_SUMMARY                 	metabolomics analysis was performed on the cell lysates. The main objective of
ST:STUDY_SUMMARY                 	the study was to determine changes in metabolite abundances in lung cancer after
ST:STUDY_SUMMARY                 	treatment with extracellular ATP and TGF-beta (a known EMT inducer).
ST:INSTITUTE                     	Ohio University
ST:DEPARTMENT                    	Biological Sciences
ST:LABORATORY                    	Dr. Xiaozhuo Chen, Edison biotechnology Institute
ST:LAST_NAME                     	Shriwas
ST:FIRST_NAME                    	Pratik
ST:ADDRESS                       	Room 425, Parks Hall, College of Pharmacy, Ohio State University, Columbus Ohio.
ST:ADDRESS                       	43210
ST:EMAIL                         	ps774614@ohio.edu
ST:NUM_GROUPS                    	7
ST:STUDY_TYPE                    	Untargeted metabolomics analysis in lung cancer cells
ST:PHONE                         	7406033801
#SUBJECT
SU:SUBJECT_TYPE                  	Cultured cells
SU:SUBJECT_SPECIES               	Homo sapiens
SU:TAXONOMY_ID                   	9606
SU:CELL_BIOSOURCE_OR_SUPPLIER    	ATCC
SU:CELL_STRAIN_DETAILS           	Human Lung epithelial A549 cancer cells
SU:CELL_PASSAGE_NUMBER           	10
SU:CELL_COUNTS                   	5 million cells
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data
SUBJECT_SAMPLE_FACTORS           	-	Control_1	Treatment:Control	RAW_FILE_NAME=ControlA_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	Control_2	Treatment:Control	RAW_FILE_NAME=ControlA_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	Control_3	Treatment:Control	RAW_FILE_NAME=ControlB_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	Control_4	Treatment:Control	RAW_FILE_NAME=ControlB_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h ATP_1	Treatment:2h ATP	RAW_FILE_NAME=2hATP1_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h ATP_2	Treatment:2h ATP	RAW_FILE_NAME=2hATP1_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h ATP_3	Treatment:2h ATP	RAW_FILE_NAME=2hATP2_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h ATP_4	Treatment:2h ATP	RAW_FILE_NAME=2hATP2_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h ATP_5	Treatment:2h ATP	RAW_FILE_NAME=2hATP3_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h ATP_6	Treatment:2h ATP	RAW_FILE_NAME=2hATP3_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	6h ATP_1	Treatment:6h ATP	RAW_FILE_NAME=6hATP1_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	6h ATP_2	Treatment:6h ATP	RAW_FILE_NAME=6hATP1_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	6h ATP_3	Treatment:6h ATP	RAW_FILE_NAME=6hATP2_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	6h ATP_4	Treatment:6h ATP	RAW_FILE_NAME=6hATP2_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h ATP_1	Treatment:12h ATP	RAW_FILE_NAME=12hATP1_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h ATP_2	Treatment:12h ATP	RAW_FILE_NAME=12hATP1_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h ATP_3	Treatment:12h ATP	RAW_FILE_NAME=12hATP2_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h ATP_4	Treatment:12h ATP	RAW_FILE_NAME=12hATP2_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h ATP_5	Treatment:12h ATP	RAW_FILE_NAME=12hATP3_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h ATP_6	Treatment:12h ATP	RAW_FILE_NAME=12hATP3_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h TGF-?_1	Treatment:2h TGF-?	RAW_FILE_NAME=2hTGF1_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h TGF-?_2	Treatment:2h TGF-?	RAW_FILE_NAME=2hTGF1_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h TGF-?_3	Treatment:2h TGF-?	RAW_FILE_NAME=2hTGF2_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h TGF-?_4	Treatment:2h TGF-?	RAW_FILE_NAME=2hTGF2_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h TGF-?_5	Treatment:2h TGF-?	RAW_FILE_NAME=2hTGF3_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	2h TGF-?_6	Treatment:2h TGF-?	RAW_FILE_NAME=2hTGF3_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	6h TGF-?_1	Treatment:6h TGF-?	RAW_FILE_NAME=6hTGF1_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	6h TGF-?_2	Treatment:6h TGF-?	RAW_FILE_NAME=6hTGF1_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	6h TGF-?_3	Treatment:6h TGF-?	RAW_FILE_NAME=6hTGF2_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	6h TGF-?_4	Treatment:6h TGF-?	RAW_FILE_NAME=6hTGF2_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h TGF-?_1	Treatment:12h TGF-?	RAW_FILE_NAME=12hTGF1_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h TGF-?_2	Treatment:12h TGF-?	RAW_FILE_NAME=12hTGF1_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h TGF-?_3	Treatment:12h TGF-?	RAW_FILE_NAME=12hTGF2_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h TGF-?_4	Treatment:12h TGF-?	RAW_FILE_NAME=12hTGF2_2.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h TGF-?_5	Treatment:12h TGF-?	RAW_FILE_NAME=12hTGF3_1.mzxml
SUBJECT_SAMPLE_FACTORS           	-	12h TGF-?_6	Treatment:12h TGF-?	RAW_FILE_NAME=12hTGF3_2.mzxml
#COLLECTION
CO:COLLECTION_SUMMARY            	A549 lung cancer cells were treated with control, ATP, TGF-beta and then
CO:COLLECTION_SUMMARY            	collected according to sample preparation protocol.
CO:COLLECTION_PROTOCOL_FILENAME  	Collection protocol
CO:SAMPLE_TYPE                   	Lung
CO:COLLECTION_METHOD             	Ice cold methanol (80%) using cell scrappers
CO:COLLECTION_LOCATION           	150mm dish
CO:COLLECTION_FREQUENCY          	Once
CO:COLLECTION_DURATION           	1-2 sec
CO:VOLUMEORAMOUNT_COLLECTED      	1 ml
CO:STORAGE_CONDITIONS            	-80?
CO:COLLECTION_VIALS              	Polypropylene 1.5 ml tubes
CO:STORAGE_VIALS                 	Polypropylene 1.5 ml
CO:COLLECTION_TUBE_TEMP          	4C
CO:TISSUE_CELL_QUANTITY_TAKEN    	5 million
#TREATMENT
TR:TREATMENT_SUMMARY             	5 million A549 cells were treated with control (no treatment), 0.5 mM ATP or 10
TR:TREATMENT_SUMMARY             	ng/ml TGF-beta for 2, 6 and 12 hours.
TR:TREATMENT                     	In vitro treatment with small molecules
TR:TREATMENT_DOSEVOLUME          	10 ml DMEM media containing appropriate compounds
TR:CELL_STORAGE                  	37C; 5% CO2 incubator
TR:CELL_GROWTH_CONTAINER         	150 mm Dish tissue culture treated
TR:CELL_MEDIA                    	DMEM (10% FBS; 1% Pen/Strep)
TR:CELL_HARVESTING               	after 2, 6 and 12 hours
TR:CELL_PCT_CONFLUENCE           	80%
TR:CELL_MEDIA_LASTCHANGED        	NA
TR:TREATMENT_COMPOUND            	0.5 mM ATP and 10 ng/ml TGF-beta
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	5 × 106 A549 cells were treated with control (no treatment), 0.5 mM ATP or 10
SP:SAMPLEPREP_SUMMARY            	ng/ml TGF-beta for 2, 6 and 12 hours. After treatment, cells were washed twice
SP:SAMPLEPREP_SUMMARY            	with deionized water and polar metabolites were then extracted with
SP:SAMPLEPREP_SUMMARY            	cryogenically cold 80% methanol/water mixture. LC-MS grade water, methanol, and
SP:SAMPLEPREP_SUMMARY            	acetonitrile (Fischer Scientific, PA, USA) were used. Methanol-extracted samples
SP:SAMPLEPREP_SUMMARY            	were then sonicated in cycles of sonication phase and rest phase for 10 minutes
SP:SAMPLEPREP_SUMMARY            	(5 second sonication phase and 10 seconds halt). The samples were then
SP:SAMPLEPREP_SUMMARY            	centrifuged at 13,000 rpm for 10 minutes and supernatant was then collected.
SP:SAMPLEPREP_SUMMARY            	Supernatants collected from in vitro and in vivo extraction were then
SP:SAMPLEPREP_SUMMARY            	lyophilized. Briefly, the supernatant was then lyophilized by using a speed
SP:SAMPLEPREP_SUMMARY            	vacuum evaporator. The samples were then dissolved into a mixture of
SP:SAMPLEPREP_SUMMARY            	acetonitrile/water (1:1; v/v).
SP:SAMPLEPREP_PROTOCOL_FILENAME  	Sample preparation protocol
SP:PROCESSING_METHOD             	CEll scrapping Quenching
SP:PROCESSING_STORAGE_CONDITIONS 	-80?
SP:EXTRACTION_METHOD             	Quenching with Ice cold methanol
SP:EXTRACT_ENRICHMENT            	Speed vaccum evaporator
SP:EXTRACT_STORAGE               	-80?
SP:SAMPLE_RESUSPENSION           	Acetonitrile/water (1:1)
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_SUMMARY        	The entire LC/MS-MS experiment was performed in the Campus Chemical
CH:CHROMATOGRAPHY_SUMMARY        	Instrumentation Center’s Mass Spectrometry and Proteomics facility at The Ohio
CH:CHROMATOGRAPHY_SUMMARY        	State University. Lyophilized samples were dissolved in equal amounts of LC-MS
CH:CHROMATOGRAPHY_SUMMARY        	grade water and acetonitrile and run with LC/MS-MS analysis, using an untargeted
CH:CHROMATOGRAPHY_SUMMARY        	metabolomics approach by utilizing Agilent Q-TOF 6545 mass spectrometer
CH:CHROMATOGRAPHY_SUMMARY        	connected to an Agilent 1290 UHPLC system with a Poroshell 120 SB-C18 (2 x 100
CH:CHROMATOGRAPHY_SUMMARY        	mm, 2.7 µm particle size) column. The LC gradient consisted of solvent A, H2O
CH:CHROMATOGRAPHY_SUMMARY        	with 0.1 % Formic acid, and solvent B, 100 % acetonitrile at a 200 µL/min flow
CH:CHROMATOGRAPHY_SUMMARY        	rate with an initial 2 % solvent B with a linear ramp to 95 % B at 15 min,
CH:CHROMATOGRAPHY_SUMMARY        	holding at 95% B for 1 minutes, and back to 2 % B from 16 min and equilibration
CH:CHROMATOGRAPHY_SUMMARY        	of 2 % B until min 32. A 5 µL volume sample was injected for each run and the
CH:CHROMATOGRAPHY_SUMMARY        	top 5 ions were selected for data-dependent analysis with a 15 second exclusion
CH:CHROMATOGRAPHY_SUMMARY        	window.
CH:CHROMATOGRAPHY_TYPE           	Reversed phase
CH:INSTRUMENT_NAME               	Agilent 1290
CH:COLUMN_NAME                   	Poroshell 120 SB-C18 (2.1 x 100 mm x 2.7 µm)
CH:FLOW_GRADIENT                 	an initial 2 % solvent B with a linear ramp to 95 % B at 15 min, holding at 95%
CH:FLOW_GRADIENT                 	B for 1 minutes, and back to 2 % B from 16 min and equilibration of 2 % B until
CH:FLOW_GRADIENT                 	min 32.
CH:FLOW_RATE                     	200 µL/min
CH:COLUMN_TEMPERATURE            	40
CH:SOLVENT_A                     	H2O with 0.1 % Formic acid
CH:SOLVENT_B                     	100 % acetonitrile
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
AN:LABORATORY_NAME               	Campus Center for Chemical Instrumentation (CCIC)
#MS
MS:INSTRUMENT_NAME               	Agilent 6545 QTOF
MS:INSTRUMENT_TYPE               	QTOF
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	NEGATIVE
MS:MS_COMMENTS                   	Masshunter software was used to collect the raw data. Progenesis was used for
MS:MS_COMMENTS                   	peak intergration.
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS	normalized
MS_METABOLITE_DATA_START
Samples	Control_1	Control_2	Control_3	Control_4	2h ATP_1	2h ATP_2	2h ATP_3	2h ATP_4	2h TGF-?_1	2h TGF-?_2	2h TGF-?_3	2h TGF-?_4
Factors	Treatment:Control	Treatment:Control	Treatment:Control	Treatment:Control	Treatment:2h ATP	Treatment:2h ATP	Treatment:2h ATP	Treatment:2h ATP	Treatment:2h TGF-?	Treatment:2h TGF-?	Treatment:2h TGF-?	Treatment:2h TGF-?
D-glucose	180871.632	155945.6778	108028.4886	104402.9947	78839.74905	85242.05611	60614.97795	59749.29751	62000.47622	69113.92096	61821.18276	63305.78447
fructose-6-phosphate	108652.7831	113442.9838	101617.833	107619.6798	157699.2985	138380.9583	127504.1583	139665.6394	86733.57814	80194.96147	83990.47581	84488.61864
Fructose 1,6-bisphosphate	168828.2037	149177.5662	665758.3249	630921.2057	698882.5107	691736.3535	631672.2715	652749.9638	200882.3149	186185.3748	308911.3652	190311.5511
Dihydroxyacetone phosphate	403254.5628	444441.2613	545070.6032		649191.3628	634123.3158	634123.3158		286943.5153	294878.0796	280738.9848	279249.4544
2-Phosphoglycerate		47073.16003	51566.05788	57316.24788	58308.27312	47550.38252	47969.96964	50910.56659	41519.16996	43143.44111	33455.92417	33608.83334
Pyruvic acid	76072.8415	84177.61543		60142.82689	65608.99229	61622.93244	64340.00074	69347.5298	50249.44972	58455.82322	53227.70587	58297.79217
L-Lactic acid	90771.13666	98022.23754	122993.4062	134833.0798	41344.11362	58963.75902	58963.75902	28261.79525	55811.73775	56920.39771	31009.62537	69319.53517
L-Glutamic acid	710496.604	676775.9899	1116337.183	1075631.557	659082.8565	774086.3579	694834.8322	640777.2211	439033.9826	513353.3698	405548.8024	547766.1365
Oxoglutaric acid		23653.57037	22139.81353	28315.34195	11732.14612	13215.39986	11806.56515	9978.930114	13090.35466	9834.016906	9087.907292	6916.593616
L-Aspartic acid	43981.80493	41190.39788		68638.19089	71916.92879	76292.68749	76818.31479	69401.10106	52174.61891	51486.70749	61880.86784	64954.8084
Oxalacetic acid	101658.5072	92233.32717	84399.79539	98249.65837	66683.74156	69797.4527	73238.44135	73405.35754	95316.12473	92734.22456	112109.3542	127271.5843
Glutathione	7272884.285	7744367.879	10062766.55		10803037.98	11356232.01	12674648.53	10861963.7	12120642.76		12933273.8	12025747.79
Oxidized Glutathione	2673139.343	3034161.983	6773703.111		7030776.01	7607149.483	5659046.245	6548066.536		10217288.06	9067432.331	10132139.43
Glycine		27101.20389	45294.35487	34886.29831	31376.84759	30309.63276	36557.42001		19168.23792	21590.36787	20516.32801	26790.12944
Acetyl-CoA	4850.471688	6219.514105	11252.96551		15272.18273	13267.02367	15524.25492	12122.90255	20454.71726	19825.77331	19254.21466	22086.7727
Citric acid	4374210.795	4879821.671	3230198.559	3139679.891	4030733.622	4270204.053	4100164.069	4204844.563	4810954.617	4392899.705	4112454.902	4106534.708
cis-Aconitic acid	292954.0616	264251.4851	285104.851	227440.616	331380.5934	341854.6757	334824.6748	330093.3035	512163.9311	505435.555	521079.7336	472515.5865
Succinyl-CoA	3223.100333	3552.717209	2037.363439		1191.078626	2806.222126	3704.565211	1732.297693	3823.77642	5184.842766	5258.99672	3906.539424
Succinic acid	800496.8317	875186.4758	1160137.074	1112538.082	953844.2706	968193.6116	869383.2121	949124.6734	525286.7966	582278.7404	624104.5299	641490.8725
fumaric acid	265758.3716	323465.8319	260131.2553	221480.2787	134217.9263	112933.9642	126089.5124	183695.081	195164.108	181610.488	114675.3273	205552.4569
Malic acid	1303503.138	1577512.156	1679568.861		1908545.329	2049257.638	1717979.85	1880342.162	1412869.815	1371362.035	1188249.46	1406914.553
Coenzyme A	6380.182928	7527.09858	9593.579425		11454.71803	16146.2739	11525.29601		18622.78236	16800.47879	13613.77461	11634.7926
Guanosine diphosphate	167361.5949	235830.6054	342440.9087	350654.8394	116708.6638	115731.8189	171885.3336	186910.7322	167951.078	184681.6131	184430.5036	276832.077
NAD	277420.5361	315257.3727	253265.2725	288909.4183	395627.274	342643.8471	348114.0684	451238.5385	180779.8092	254751.3093	236546.8188	223521.776
FAD	440240.8346	426299.8268	916454.6465	1080478.074	634732.413	674630.689	672205.6323	638229.664	849485.6005	888096.6359	753230.1234	815346.4388
Phosphorylcholine		42639.38468	30362.53348	36300.32893		10925.85392	16726.28758	19164.74603		7138.525219	9828.463308	8837.477535
LysoPC(16:0)		12971.20699	21149.74965	15265.30071		4956.081214	5321.371999	6827.593009		2846.79835	3477.906443	2835.742259
Phosphatidylinositol-3,4,5-trisphosphate		16213.49502	19233.0199	16570.40632		20457.97856	22589.74084	20885.26642		19284.32375	20474.10801	23773.70479
Arachidonic acid		162714.8731	139235.8577	159440.3653		271258.2418	279712.4534	122324.4237		160067.8528	116332.6167	178420.0286
Thromboxane a2		52850.78953	31920.78269	99193.19941		35414.27619	49127.56733	74768.51556		119487.0977	100616.1232	103719.9255
Prostaglandin D2		3152.854781	3145.715439	3340.243838		1564.785459	3406.361938	3809.758901		2372.503629	630.2070965	862.7063276
Prostaglandin E2		360889.8949	337384.3162	484712.8096		379676.8793	334910.0197	487043.3875		303542.7643	221641.0789	275253.326
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
Metabolite_name	KEGG ID	HMDB ID	PUBCHEM ID	Mode	retention time_m/z	m/z
D-glucose	C00221	HMDB0000122	5793	Negative	1.40_215.0338m/z	215.0337908
fructose-6-phosphate	C00085	HMDB0000124	69507	Negative	1.43_260.0313n	260.0312509
Fructose 1,6-bisphosphate	C05378	HMDB0001058	10267	Negative	2.02_338.9909m/z	338.9908581
Dihydroxyacetone phosphate	C00111	HMDB0001473	668	Negative	1.60_169.9992n	338.9908202
2-Phosphoglycerate	C00631	HMDB0000362	59	Negative	14.75_370.9787m/z	370.9786937
Pyruvic acid	C00022	HMDB0000243	1060	Negative	1.93_87.0093m/z	87.00933104
L-Lactic acid	C00186	HMDB0000190	107689	Negative	1.31_179.0572m/z	179.0572277
L-Glutamic acid	C00025	HMDB0000148	33032	Negative	1.34_146.0470m/z	146.0469686
Oxoglutaric acid	C00026	HMDB0000208	51	Negative	1.83_145.0148m/z	145.0148367
L-Aspartic acid	C00049	HMDB0000191	5960	Negative	1.34_132.0311m/z	132.0310582
Oxalacetic acid	C00036	HMDB0000223	970	Negative	13.87_262.9934m/z	262.9934231
Glutathione	C00051	HMDB0062697	745	Negative	2.33_307.0861n	306.0788438
Oxidized Glutathione	C00127	HMDB0003337	65359	Negative	4.92_612.1551n	611.1478583
Glycine	C00037	HMDB0000123	750	Negative	1.29_74.0254m/z	74.02537056
Acetyl-CoA	C00024	HMDB0001206	444493	Negative	8.38_808.0797m/z	808.0796604
Citric acid	C00158	HMDB0000094	311	Negative	14.28_226.9929m/z	226.9928819
cis-Aconitic acid	C00417	HMDB0000072	643757	Negative	3.37_173.0100m/z	173.0100124
Succinyl-CoA	C00091	HMDB0001022	439161	Negative	12.08_906.0920m/z	906.0920187
Succinic acid	C00042	HMDB0000254	1110	Negative	3.16_117.0201m/z	117.0201424
fumaric acid	C00122	HMDB0000134	444972	Negative	2.93_115.0043m/z	115.0043117
Malic acid	C03668	HMDB0000744	525	Negative	1.72_133.0152m/z	133.0152414
Coenzyme A	C00010	HMDB0001423	87642	Negative	9.71_766.1110m/z	766.1110235
Guanosine diphosphate	C00035	HMDB0001201	8977	Negative	3.35_444.0296m/z	444.0296018
NAD	C00003	HMDB0000902	5893	Negative	3.87_663.1158m/z	663.1157954
FAD	C00016	HMDB0001248	643975	Negative	9.09_784.1532m/z	784.1532207
Phosphorylcholine	C00588	HMDB0001565	1014	Negative	7.92_219.0456m/z	219.0455678
Choline	C00114	HMDB0000097	305	Positive	10.21_143.0694m/z	143.0693893
LysoPC(16:0)	C04230	HMDB0010382	460602	Negative	15.74_530.2924m/z	530.2924336
Phosphatidylinositol-3,4,5-trisphosphate	C05981	HMDB0004249	53477782	Negative	15.12_642.9822m/z	642.9821693
Arachidonic acid	C00219	HMDB0001043	444899	Negative	16.50_303.2350m/z	303.2350214
Thromboxane a2	C02198	HMDB0001452	5280497	Negative	13.83_352.2272n	351.2199179
Prostaglandin D2	C00696	HMDB0001403	448457	Negative	13.86_387.1986m/z	387.1986467
Prostaglandin E2	C00584	HMDB0001220	5283116	Negative	14.10_351.2200m/z	351.2199929
METABOLITES_END
#END