Table 9 Differential metabolites of each group.

From: Integrated network pharmacology and metabolomics reveal the mechanisms of Jasminum elongatum in anti-ulcerative colitis

No.	Identification	MW	RT (min)	Iron Mode	Model/control	JE/Model
1	P-xylene	107.0852	14.4087	[M+H]⁺	↑	↓
2	Cinnamic acid	131.0487	6.9346	[M+H]⁺	↓	↑
3	5-Hydroxyindole	134.0594	5.7819	[M+H]⁺	↓	↑
4	(+)-Pulegone	135.1165	15.6783	[M+H]⁺	↑	↓
5	Butylbenzene	135.1164	16.0706	[M+H]⁺	↑	↓
6	4-Propylphenol	137.0957	7.2539	[M+H]⁺	↑	↓
7	MLS000575022-01	225.1098	7.4197	[M+H]⁺	↓	↑
8	Pirlindole mesylate	227.1640	9.0905	[M+H]⁺	↓	↑
9	O-1918	287.1955	1.0157	[M+H]⁺	↓	↑
10	Aspartame	295.1290	5.5636	[M+H]⁺	↑	↓
11	Ajmaline	327.2171	15.8019	[M+H]⁺	↑	↓
12	Rimexolone	371.2583	8.6013	[M+H]⁺	↑	↓
13	5-hydroxy-2,2-dimethyl-7,10-bis(2-methylbut-3-en-2-yl)pyrano[3,2-g]chromen-8-one	381.2053	16.3180	[M+H]+	↑	↓
14	HTMT	383.2012	16.3198	[M+H]⁺	↑	↓
15	N-stearoyl tyrosine	448.3429	11.7405	[M+H]⁺	↑	↓
16	Cer-AS d27:4	450.3497	11.7665	[M+H]⁺	↑	↓
17	Strophanthidin Semicarbazide	462.2681	7.8092	[M+H]⁺	↓	↑
18	Cytochalasin B	480.2789	7.7958	[M+H]⁺	↓	↑
19	Taurocholic acid	516.3005	7.8138	[M+H]⁺	↓	↑
19	Taurocholic acid	514.2841	7.8508	[M-H]⁻	↓	↑
20	Scutellarein 6,4'-dimethyl ether 7-(6''-acetylglucoside)	519.1399	21.7285	[M+H]⁺	↑	↓
21	Calcimycin	524.2779	9.5045	[M+H]⁺	↓	↑
22	Fumitremorgin A	580.2942	12.0851	[M+H]⁺	↓	↑
23	Lanceotoxin A	621.2857	11.3963	[M+H]⁺	↑	↓
24	3-Hydroxybutyrate	103.0399	2.9730	[M-H]⁻	↑	↓
25	Ethyl everninate	209.0795	6.9414	[M-H]⁻	↓	↑
26	Ellipticine	245.1143	4.8547	[M-H]⁻	↑	↓
27	Arachidonic acid	303.2329	15.8049	[M-H]⁻	↑	↓
28	Icosatrienoic acid	305.2400	15.8063	[M-H]⁻	↑	↓
29	Glutamyltyrosine	309.1094	4.9120	[M-H]⁻	↑	↓
30	3α,7α,12β-Trihydroxy-5β-cholanate	407.2802	8.3662	[M-H]⁻	↑	↓
31	LPA (18:2(9Z,12Z)/0:0)	433.2375	21.7105	[M-H]⁻	↑	↓
32	FAHFA 29:6	455.3181	10.9142	[M-H]⁻	↑	↓
33	2-(Methoxycarbonyl)-5-methyl-2,4-bis(3-methyl-2-butenyl)-6-(2-methyl-1-oxopropyl)-5-(4-methyl-3-pentenyl) cyclohexanone	457.3343	12.3855	[M-H]⁻	↑	↓
34	(17α,23S)-Epoxy-28,29-dihydroxy-27-norlanost-8-ene-3,24-dione	471.3120	8.6663	[M-H]⁻	↑	↓
35	1-Hydroxy-2-(9Z,12Z,15Z-octadecatrienoyl)-sn-glycero-3-phosphoethanolamine	474.2638	10.7485	[M-H]⁻	↑	↓
36	Lucidenic acid G	475.2684	8.3518	[M-H]⁻	↑	↓
37	LPA (22:6)	481.2372	13.5786	[M-H]⁻	↑	↓
38	LPG 18:1	509.2905	15.1871	[M-H]⁻	↑	↓
39	LPC (20:4(8Z,11Z,14Z,17Z))	588.3314	11.6640	[M-H]⁻	↑	↓
40	LPC (20:3(5Z,8Z,11Z))	590.3467	12.2839	[M-H]⁻	↑	↓
41	LPI 20:4	619.2895	11.6448	[M-H]⁻	↑	↓
42	LPI 20:3	621.3058	13.0770	[M-H]⁻	↑	↓
43	LPI 22:6	643.2906	11.9968	[M-H]⁻	↑	↓
44	LPI 22:5	645.3083	13.4158	[M-H]⁻	↑	↓
45	LPI 22:4	647.3227	14.4554	[M-H]⁻	↑	↓

Back to article page

Table 9 Differential metabolites of each group.

Search

Quick links