Return to study ST000142 main page   Show: (1)HMDB and KEGG pathways   (2)REACTOME pathways containing these metabolites

SelectMetabolite Name Metabolite Id Refmet Name Ret. Index Quant. m/z Analysis Display
2,3',4,6-Tetrahydroxybenzophenone-13C0[+Na]+ ME683707 2,3',4,6-Tetrahydroxybenzophenone -269.04148MS positive ion mode
2,3',4,6-Tetrahydroxybenzophenone-13C0[+QDA adduct... ME684103 2,3',4,6-Tetrahydroxybenzophenone -523.3148MS positive ion mode
2,3',4,6-Tetrahydroxybenzophenone-13C1[+Na]+ ME683618 2,3',4,6-Tetrahydroxybenzophenone -270.046MS positive ion mode
2,3',4,6-Tetrahydroxybenzophenone-13C8[+Na]+ ME683869 2,3',4,6-Tetrahydroxybenzophenone -277.06944MS positive ion mode
3,5-Dichloro-4-hydroxyphenylpyruvate-13C0[+Na]+ ME682896 3,5-Dichloro-4-hydroxyphenylpyruvate -270.95363MS positive ion mode
4-Chlorobenzaldehyde-13C0[+Na]+ ME682404 4-Chlorobenzaldehyde -162.99199MS positive ion mode
4-Chlorobenzaldehyde-13C0[+QDA adduct]+ ME682492 4-Chlorobenzaldehyde -395.28163MS positive ion mode
Acetohexamide-13C0[+QDA adduct]+ ME683862 Acetohexamide -579.39345MS positive ion mode
Acrovestone-13C0[+13CD3 QDA]+ ME683527 Acrovestone -813.59026MS positive ion mode
Amphenone B-13C0[+H]+ ME683591 Amphenone B -255.14908MS positive ion mode
Aurin-13C0[+13CD3 QDA]+ ME684305 Aurin -549.39518MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C0[+13CD3 QDA]+ ME682617 Benzyl 2-methyl-3-oxobutanoate -465.39599MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C0[+H]+ ME684836 Benzyl 2-methyl-3-oxobutanoate -207.10149MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C0[+QDA adduct]+ ME682771 Benzyl 2-methyl-3-oxobutanoate -461.37339MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C10[+QDA adduct]+ ME683017 Benzyl 2-methyl-3-oxobutanoate -471.40684MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C1[+13CD3 QDA]+ ME683605 Benzyl 2-methyl-3-oxobutanoate -466.39941MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C12[+QDA adduct]+ ME682191 Benzyl 2-methyl-3-oxobutanoate -473.41329MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C1[+QDA adduct]+ ME684519 Benzyl 2-methyl-3-oxobutanoate -462.37715MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C2[+13CD3 QDA]+ ME682601 Benzyl 2-methyl-3-oxobutanoate -467.40309MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C3[+QDA adduct]+ ME682855 Benzyl 2-methyl-3-oxobutanoate -464.38376MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C4[+QDA adduct]+ ME684716 Benzyl 2-methyl-3-oxobutanoate -465.38658MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C6[+13CD3 QDA]+ ME683347 Benzyl 2-methyl-3-oxobutanoate -471.41587MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C7[+13CD3 QDA]+ ME683671 Benzyl 2-methyl-3-oxobutanoate -472.41929MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C8[+13CD3 QDA]+ ME683600 Benzyl 2-methyl-3-oxobutanoate -473.42231MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C8[+QDA adduct]+ ME683058 Benzyl 2-methyl-3-oxobutanoate -469.4002MS positive ion mode
Benzyl 2-methyl-3-oxobutanoate-13C9[+13CD3 QDA]+ ME682359 Benzyl 2-methyl-3-oxobutanoate -474.42641MS positive ion mode
Calcimycin-13C0[+13CD3 QDA]+ ME682557 Calcimycin -782.56867MS positive ion mode
Calcimycin-13C0[+H]+ ME683277 Calcimycin -524.27649MS positive ion mode
Citrinin-13C0[+H]+ ME683494 Citrinin -251.09047MS positive ion mode
Citrinin-13C0[+QDA adduct+Na]+ ME684158 Citrinin -527.34501MS positive ion mode
Fenofibrate-13C0[+QDA adduct]+ ME683414 Fenofibrate -615.39284MS positive ion mode
Hydroxybenzophenone-13C0[+H]+ ME682550 Hydroxybenzophenone -199.07601MS positive ion mode
Hydroxybenzophenone-13C0[+Na]+ ME683339 Hydroxybenzophenone -221.05826MS positive ion mode
Hydroxybenzophenone-13C0[+QDA adduct+Na]+ ME683793 Hydroxybenzophenone -475.32971MS positive ion mode
Hydroxybenzophenone-13C1[+QDA adduct+Na]+ ME684207 Hydroxybenzophenone -476.3328MS positive ion mode
Ingenol 3,20-dibenzoate-13C0[+H]+ ME684319 Ingenol 3,20-dibenzoate -557.25365MS positive ion mode
Ingenol 3,20-dibenzoate-13C0[+Na]+ ME683549 Ingenol 3,20-dibenzoate -579.23614MS positive ion mode
Ingenol 3,20-dibenzoate-13C0[+QDA adduct+Na]+ ME684358 Ingenol 3,20-dibenzoate -833.50756MS positive ion mode
Ketoprofen glucuronide-13C0[+Na]+ ME682677 Ketoprofen glucuronide -453.11553MS positive ion mode
Phenylacetone-13C0[+13CD3 QDA]+ ME683118 Phenylacetone -393.37476MS positive ion mode
Phenylacetone-13C0[+Na]+ ME684193 Phenylacetone -157.06298MS positive ion mode
Phenylacetone-13C0[+QDA adduct]+ ME682958 Phenylacetone -389.35271MS positive ion mode
Phenylacetone-13C1[+13CD3 QDA]+ ME684865 Phenylacetone -394.37807MS positive ion mode
Phenylacetone-13C1[+Na]+ ME683184 Phenylacetone -158.06619MS positive ion mode
Phenylacetone-13C1[+QDA adduct]+ ME682405 Phenylacetone -390.35592MS positive ion mode
Phenylacetone-13C6[+13CD3 QDA]+ ME683755 Phenylacetone -399.39453MS positive ion mode
Phenylacetone-13C6[+Na]+ ME685016 Phenylacetone -163.08182MS positive ion mode
Phenylacetone-13C7[+13CD3 QDA]+ ME683664 Phenylacetone -400.39866MS positive ion mode
Phenylacetone-13C7[+Na]+ ME682569 Phenylacetone -164.08656MS positive ion mode
Phenylacetone-13C8[+13CD3 QDA]+ ME683468 Phenylacetone -401.40106MS positive ion mode
Phenylacetone-13C8[+QDA adduct]+ ME683987 Phenylacetone -397.37896MS positive ion mode
Resistomycin-13C0[+H]+ ME683049 Resistomycin -377.10159MS positive ion mode
Resistomycin-13C0[+QDA adduct+Na]+ ME683890 Resistomycin -653.35588MS positive ion mode
Sarothralin-13C0[+QDA adduct+Na]+ ME683713 Sarothralin -811.48759MS positive ion mode
Tolcapone-13C0[+QDA adduct]+ ME684910 Tolcapone -528.34233MS positive ion mode


  logo