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

Summary

Full name7-aminomethyl-7-deazaguanosine-5'-monophosphate
Short nameppreQ1
MODOMICS code new2000101551G
MODOMICS code101551G
Nature of the modified residueNatural
Residue unique ID408
Related nucleosides123

Chemical information

Sum formulaC12H16N5O8P
Type of moietynucleotide
SMILESNCc1c[n]([C@@H]2O[C@H](COP(=O)([O-])[O-])[C@@H](O)[C@H]2O)c2nc(N)[nH]c(=O)c12
logP-0.3481
TPSA234.64
Number of atoms26
Number of Hydrogen Bond Acceptors 1 (HBA1)9
Number of Hydrogen Bond Acceptors 2 (HBA2)12
Number of Hydrogen Bond Donors (HBD)5
PDB exact match , link to the most similar ligand PQ1
InChIInChI=1S/C12H18N5O8P/c13-1-4-2-17(9-6(4)10(20)16-12(14)15-9)11-8(19)7(18)5(25-11)3-24-26(21,22)23/h2,5,7-8,11,18-19H,1,3,13H2,(H2,21,22,23)(H3,14,15,16,20)/p-2/t5-,7-,8-,11-/m1/s1
InChIKeyGIQSPNMTDJCDKB-IOSLPCCCSA-L
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

Tautomers SMILES
N=Cc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3NC(=N)NC(O)c13 tautomer #0
NCc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(=N)[nH]c(=O)c13 tautomer #1
NCc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3nc(N)nc(O)c13 tautomer #2
N=Cc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3NC(N)=NC(O)c13 tautomer #3
NCc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(N)nc(=O)c13 tautomer #4
NCc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3nc(N)[nH]c(=O)c13 tautomer #5
NCc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3nc(=N)[nH]c(O)c13 tautomer #6
N=CC1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3nc(N)nc(O)c13 tautomer #7
NC=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3nc(N)nc(O)c13 tautomer #8
N=CC1=CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3NC(=N)NC(=O)C13 tautomer #9
N=CC=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3NC(=N)NC(=O)C13 tautomer #10
NCC1=CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)NC(=O)C13 tautomer #11
N=CC1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)NC(=O)C13 tautomer #12
N=CC=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)NC(O)C13 tautomer #13
NCC=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)NC(=O)C13 tautomer #14
N=CC1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(=N)[nH]c(=O)c13 tautomer #15
NC=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)NC(=O)C13 tautomer #16
NC=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(=N)[nH]c(=O)c13 tautomer #17
NCc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3nc(N)nc(O)c13 tautomer #18
N=CC1=CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3NC(N)=NC(=O)C13 tautomer #19
N=CC=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3NC(N)=NC(=O)C13 tautomer #20
NCC1=CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(N)=NC(=O)C13 tautomer #21
N=CC1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(N)=NC(=O)C13 tautomer #22
N=CC=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(N)=NC(O)C13 tautomer #23
NCC=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(N)=NC(=O)C13 tautomer #24
N=CC1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(N)nc(=O)c13 tautomer #25
NC=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(N)=NC(=O)C13 tautomer #26
NCc1cn(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(=N)nc(O)c13 tautomer #27
NC=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(N)nc(=O)c13 tautomer #28
N=CC1=CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3NC(=N)NC(O)=C13 tautomer #29
N=CC1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3nc(=N)[nH]c(O)c13 tautomer #30
NC=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3nc(=N)[nH]c(O)c13 tautomer #31
N=CC1=CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3NC(N)=NC(O)=C13 tautomer #32
N=CC1=CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3NC(=N)N=C(O)C13 tautomer #33
N=CC=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3NC(=N)N=C(O)C13 tautomer #34
NCC1=CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)N=C(O)C13 tautomer #35
N=CC1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)N=C(O)C13 tautomer #36
NCC=1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)N=C(O)C13 tautomer #37
N=CC1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(=N)nc(O)c13 tautomer #38
NC=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)C3=NC(=N)N=C(O)C13 tautomer #39
NC=C1CN(C2OC(COP(=O)([O-])[O-])C(O)C2O)c3[nH]c(=N)nc(O)c13 tautomer #40
Tautomer image Show Image

Predicted CYP Metabolic Sites

CYP3A4 CYP2D6 CYP2C9
ppreQ1 ppreQ1 ppreQ1

* 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 mass389.258
[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