Absolute configurations of spiroiminodihydantoin and allantoin stereoisomers: comparison of computed and measured electronic circular dichroism spectra.
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Crystal Structure of DNA Polymerase β with DNA Containing the Base Lesion Spiroiminodihydantoin in a Templating PositionAbsolute configurations of DNA lesions determined by comparisons of experimental ECD and ORD spectra with DFT calculationsThermodynamic profiles and nuclear magnetic resonance studies of oligonucleotide duplexes containing single diastereomeric spiroiminodihydantoin lesions.Reconciliation of chemical, enzymatic, spectroscopic and computational data to assign the absolute configuration of the DNA base lesion spiroiminodihydantoin.Characterization of 2'-deoxyguanosine oxidation products observed in the Fenton-like system Cu(II)/H2O2/reductant in nucleoside and oligodeoxynucleotide contextsInfluence of substrate complexity on the diastereoselective formation of spiroiminodihydantoin and guanidinohydantoin from chromate oxidation.Spirodi(iminohydantoin) products from oxidation of 2'-deoxyguanosine in the presence of NH4Cl in nucleoside and oligodeoxynucleotide contexts.Effect of Base-Pairing Partner on the Thermodynamic Stability of the Diastereomeric Spiroiminodihydantoin Lesion.Endonuclease and Exonuclease Activities on Oligodeoxynucleotides Containing Spiroiminodihydantoin Depend on the Sequence Context and the Lesion Stereochemistry.Determination of Absolute Configuration of Natural Products: Theoretical Calculation of Electronic Circular Dichroism as a ToolA new flavone C-glycoside and a new bibenzyl from Bulbophyllum retusiusculum.Formation and processing of DNA damage substrates for the hNEIL enzymes.The R- and S-diastereoisomeric effects on the guanidinohydantoin-induced mutations in DNA.Computational studies of electronic circular dichroism spectra predict absolute configuration assignments for the guanine oxidation product 5-carboxamido-5-formamido-2-iminohydantoin.Enantioselective determination of the chiral pesticide isofenphos-methyl in vegetables, fruits, and soil and its enantioselective degradation in pak choi using HPLC with UV detection.Simultaneous determination of chiral pesticide flufiprole enantiomers in vegetables, fruits, and soil by high-performance liquid chromatography.A new phenylpropanoid glucoside and a chain compound from the roots of Allium tuberosum.Conformational stabilities of iminoallantoin and its base pairs in DNA: implications for mutagenicity.
P2860
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P2860
Absolute configurations of spiroiminodihydantoin and allantoin stereoisomers: comparison of computed and measured electronic circular dichroism spectra.
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Absolute configurations of spi ...... ic circular dichroism spectra.
@ast
Absolute configurations of spi ...... ic circular dichroism spectra.
@en
type
label
Absolute configurations of spi ...... ic circular dichroism spectra.
@ast
Absolute configurations of spi ...... ic circular dichroism spectra.
@en
prefLabel
Absolute configurations of spi ...... ic circular dichroism spectra.
@ast
Absolute configurations of spi ...... ic circular dichroism spectra.
@en
P2093
P2860
P356
P1476
Absolute configurations of spi ...... ic circular dichroism spectra.
@en
P2093
Alexander Durandin
Alexander Kolbanovskiy
Conor Crean
Nicholas E Geacintov
Shuang Ding
Suse Broyde
P2860
P304
P356
10.1021/TX900107Q
P577
2009-06-01T00:00:00Z