Detail Information

Number qtl-m0189
Declustering Potential(DP) 20
Collision Energy(CE) 20
Observed mass(Da) 284.0989
Exact mass(Da) 284.0917
Accurate mass error(ppm) 0.16
Molecular formula C10H13N5O5
Ionization model
Ret. Time(min)
Precursor ions(Q1) 284.1
Product ions(Q3) 152.1
Main fragments 152.1, 238.2, 181.1, 135.1, 110.1, 95.2
Compound Crotonoside
Identification putative
class Nucleotide
Organism
Reference Harborne et. al (1999)
CV(%)
H2
ChEBI_ID CHEBI:3927
Agricola Citation Links
ArrayExpress Database Links
BRAND Names
Beilstein Registry Numbers
BioModels Database Links
CAS Registry Numbers 1818-71-9;;
COMe Database Links
ChEBI ID
ChEBI Name Crotonoside;;
Charge
Chinese Abstracts Citation Links
CiteXplore Citation Links
Definition
DrugBank Database Links
Formulae C10H13N5O5;;
Gmelin Registry Numbers
INN
IUPAC Names
InChI InChI=1S/C10H13N5O5/c11-7-4-8(14-10(19)13-7)15(2-12-4)9-6(18)5(17)3(1-16)20-9/h2-3,5-6,9,16-18H,1H2,(H3,11,13,14,19)/t3-,5-,6-,9-/m1/s1;;
InChIKey MIKUYHXYGGJMLM-UUOKFMHZSA-N;;
IntAct Database Links
IntEnz Database Links
KEGG COMPOUND Database Links C08432
KEGG DRUG Database Links
KEGG GLYCAN Database Links
LIPID MAPS class Database Links
LIPID MAPS instance Database Links
Last Modified 28 Jul 2014;;
Mass
MolBase Database Links
PDBeChem Database Links
Patent Database Links
PubChem Database Links 223439392;;
PubMed Central Citation Links
PubMed Citation Links
RESID Database Links
Reactome Database Links
Rhea Database Links
SABIO-RK Database Links
SMILES Nc1nc(=O)[nH]c2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O;;
Secondary ChEBI ID
Star 2;;
Synonyms Isoguanosine;;Crotonoside;;
UM-BBD compID Database Links
UniProt Database Links
ChEBI Image