Metabolite List
metabolites which its exact mass nearly 169.0504 with tolerance error 0.01 da.
Phosphodimethylethanolamine (BioCAD00000016243)
Formula: C4H12NO4P (Exact Mass: 169.0504)
Phosphomonomethylethanolamine, phosphodimethylethanolamine and phosphocholine were weak competitive inhibitors of the cytidylyltransferase catalyzed reaction when phosphoethanolamine was used as a substrate, with Ki values of 7.0, 6.8 and 52.9 mM, respectively. (PMID: 8130268) Unlike the plant and Plasmodium PEAMT, which catalyze all three methylations in the pathway, PMT-2 catalyzes only the last two steps in the pathway, i.e., the methylation of phosphomonomethylethanolamine (P-MME) to phosphodimethylethanolamine (P-DME) and of P-DME to phosphocholine. (PMID: 16681378)
(1R,6S)-1,6-dihydroxy-4-methylcyclohexa-2,4-diene-1-carboxylate (BioCAD00000472312)
Formula: C8H9O4 (Exact Mass: 169.0501)
Conjugate base of (1R,6S)-1,6-dihydroxy-4-methylcyclohexa-2,4-diene-1-carboxylic acid." []
1,6-dihydroxy-2-methylcyclohexa-2,4-diene-1-carboxylate (BioCAD00000472806)
Formula: C8H9O4 (Exact Mass: 169.0501)
The conjugate base of 1,6-dihydroxy-2-methylcyclohexa-2,4-dienecarboxylic acid; major species at pH 7.3." []
[2-(dimethylamino)ethoxy]sulfonic acid (BioCAD00000511539)
Formula: C4H11NO4S (Exact Mass: 169.0409)
2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (BioCAD00000580240)
Formula: C6H7N3O3 (Exact Mass: 169.0487)
A member of the class of imidazo[2,1-b][1,3]oxazines in which the hydrogen at position 2 is substituted by a nitro group and in which the oxazine ring is fully saturated." []