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About This Item
Empirical Formula (Hill Notation):
C11H15N3O6
CAS Number:
Molecular Weight:
285.25
UNSPSC Code:
41106305
PubChem Substance ID:
EC Number:
223-195-6
MDL number:
assay
≥98%
mp
199 °C (dec.) (lit.)
storage temp.
−20°C
SMILES string
CC(=O)NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O
InChI
1S/C11H15N3O6/c1-5(16)12-7-2-3-14(11(19)13-7)10-9(18)8(17)6(4-15)20-10/h2-3,6,8-10,15,17-18H,4H2,1H3,(H,12,13,16,19)/t6-,8-,9-,10-/m1/s1
InChI key
NIDVTARKFBZMOT-PEBGCTIMSA-N
Regulatory Information
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Clement T Y Chan et al.
PLoS genetics, 6(12), e1001247-e1001247 (2010-12-29)
Decades of study have revealed more than 100 ribonucleoside structures incorporated as post-transcriptional modifications mainly in tRNA and rRNA, yet the larger functional dynamics of this conserved system are unclear. To this end, we developed a highly precise mass spectrometric
G Kawai et al.
Nucleic acids symposium series, (21)(21), 61-62 (1989-01-01)
The conformational characteristics of a modified nucleoside 4-acetylcytidine (ac4C) was analyzed by proton nuclear magnetic resonance spectroscopy. This nucleoside was found to take the C3'-endo form predominantly. The enthalpy difference between the C2'-endo form and the C3'-endo form of the
Marcus J O Johansson et al.
RNA (New York, N.Y.), 10(4), 712-719 (2004-03-24)
The biogenesis of transfer RNA is a process that requires many different factors. In this study, we describe a genetic screen aimed to identify gene products participating in this process. By screening for mutations lethal in combination with a sup61-T47:2C