Modomics - A Database of RNA Modifications

The molecule is shown in a ball-and-stick representation with the following colors for atoms :
Hydrogen (H): white Carbon (C): gray Oxygen (O): red Phosphorus (P): orange Nitrogen (N): blue Selenium (Se): gold Sulfur (S): yellow


Full name5-carboxyhydroxymethyluridine-5'-monophosphate
Short namepchm5U
MODOMICS code new2000520551U
MODOMICS code520551U
Nature of the modified residueNatural
RNAMods code
Residue unique ID357
Related nucleosides73

Chemical information

Sum formulaC11H13N2O12P
Type of moietynucleotide
Number of atoms26
Number of Hydrogen Bond Acceptors 1 (HBA1)10
Number of Hydrogen Bond Acceptors 2 (HBA2)13
Number of Hydrogen Bond Donors (HBD)5
Search the molecule in external databases ChEMBL  ChemAgora  ChEBI  PubChem Compound Database  Ligand Expo  ChemSpider  WIPO 

* Chemical properties calculated with Open Babel - O'Boyle et al. Open Babel: An open chemical toolbox. J Cheminform 3, 33 (2011) (link)

Download Structures

2D   .png .mol .mol2 .sdf .pdb .smi
3D   .mol .mol2 .sdf .pdb


Tautomers SMILES
OC(=O)C(=O)C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C(=O)NC1=O tautomer #0
OC(O)C(=O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(=O)[nH]c1=O tautomer #1
OC(=O)C(O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(=O)[nH]c1=O tautomer #2
OC(=O)C(O)=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C(=O)NC1=O tautomer #3
OC(=O)C(=O)C=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C(=O)NC1O tautomer #4
OC(O)C(=O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(O)nc1=O tautomer #5
OC(=O)C(O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(O)nc1=O tautomer #6
OC(=O)C(=O)C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C(O)=NC1=O tautomer #7
OC(O)C(=O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(=O)nc1O tautomer #8
OC(=O)C(O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(=O)nc1O tautomer #9
OC(=O)C(=O)C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C(=O)N=C1O tautomer #10
OC(O)=C(O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(=O)[nH]c1=O tautomer #11
OC(=O)C(O)=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C(O)=NC1=O tautomer #12
OC(=O)C(=O)C=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C(O)=NC1O tautomer #13
OC(=O)C(O)=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C(=O)N=C1O tautomer #14
OC(O)=C(O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(O)nc1=O tautomer #15
OC(O)=C(O)c1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c(=O)nc1O tautomer #16
Tautomer image Show Image

Predicted CYP Metabolic Sites

pchm5U pchm5U pchm5U

* CYP Metabolic sites predicted with SMARTCyp. SMARTCyp is a method for prediction of which sites in a molecule that are most liable to metabolism by Cytochrome P450. It has been shown to be applicable to metabolism by the isoforms 1A2, 2A6, 2B6, 2C8, 2C19, 2E1, and 3A4 (CYP3A4), and specific models for the isoform 2C9 (CYP2C9) and isoform 2D6 (CYP2D6). CYP3A4, CYP2D6, and CYP2C9 are the three of the most important enzymes in drug metabolism since they are involved in the metabolism of more than half of the drugs used today. The three top-ranked atoms are highlighted. See: SmartCYP and SmartCYP - background; Patrik Rydberg, David E. Gloriam, Lars Olsen, The SMARTCyp cytochrome P450 metabolism prediction server, Bioinformatics, Volume 26, Issue 23, 1 December 2010, Pages 2988–2989 (link)

LC-MS Information

Monoisotopic massNone
Average mass396.201
[M+H]+ not available
Product ions not available
Normalized LC elution time * not available
LC elution order/characteristics not available

* normalized to guanosine (G), measured with a RP C-18 column with acetonitrile/ammonium acetate as mobile phase.

Last modification of this entry: Sept. 22, 2023