Spectrum ML003101 for cytidine

Rating: (*)(*)(*)(*)(*)

Compound Information

Chemical Names

Compound Classification (provided by ClassyFire)

ClassyFire is a freely accessible computational tool that uses the ChemOnt taxonomy to classify chemical entities based on their structure. ClassyFire combines structure search, IUPAC name parsing, and evaluation of logical expressions to retrieve structural features, which are then mapped to the corresponding ChemOnt classes.

Compound Metadata

NameValue
InChI=1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)/t4-,6-,7-,8-/m1/s1
UHDGCWIWMRVCDJ-XVFCMESISA-N
C9H13N3O5
243.08552051599997
N=C1N=C(O)N(C=C1)C2OC(CO)C(O)C2O

Mass Spectral Metadata

NameValue
98/2/0.2 Acetonitrile/Water/Formic Acid
loess on assigned fragments and MS1
ML003101
2014.11.12
Mark Earll, Stephan Beisken, EMBL-EBI
CC BY-SA
Copyright (C) 2014, European Molecular Biology Laboratory - European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
Beisken S et al (2014) Scientific Data, 1:140029, DOI:10.1038/sdata.2014.29. http://www.ebi.ac.uk/metabolights/MTBLS38
243.0855
LTQ Orbitrap Velos Thermo Scientific
LC-ESI-ITFT
MS2
ESI
HCD
50 % (nominal)
7500
HSS T3 1.7 um, 2x150 mm, Waters
100/0 at 0 min, 90/10 at 7.5 min, 0/100 at 10 min, 0/100 at 12 min, 100/0 at 18 min, 100/0 at 25 min
250 uL/min at 0 min, 400 uL/min at 7.5 min
3.2 min
0.2% Formic Acid
Peaks with additional N2/O included
RMassBank 1.7.0
positive
0.09666349222824955
0.1394559408727045
244.0928
[M+H]+
2.8289076939724622 ppm
-6.905159999632815E-4 Da