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1 ication after exposure in vivo to styrene or styrene oxide.
2 yrene in the enantioselective synthesis of S-styrene oxide.
3 from phenylacetaldehyde and phenylketene to styrene oxide.
4 ept for particularly activated cases such as styrene oxide.
5 such as 1-butene oxide, 1-hexene oxide, and styrene oxide.
6 cal damage to ds-DNA from known damage agent styrene oxide.
7 n peaks for DNA bases during incubation with styrene oxide.
8 gle adenine by either R- or S-enantiomers of styrene oxide.
9 peaks increased with time of incubation with styrene oxide.
10 at the alpha-carbon than the beta-carbon of styrene oxide.
12 enyl)styrene oxide and (S)-beta-(N(6)-adenyl)styrene oxide adducts at position X(6) in d(CGGACXAGAAG)
14 uctures of the (R)- and (S)-alpha-(N2-guanyl)styrene oxide adducts at X6 in d(GGCAGXTGGTG).d(CACCACCT
15 ational studies of R- and S-alpha-(N6-adenyl)styrene oxide adducts mismatched with deoxycytosine at p
16 resis and HPLC-MS suggested the formation of styrene oxide adducts of DNA bases under similar reactio
18 ic peak current upon incubation in saturated styrene oxide, and an estimate of 1 damaged base in 1000
19 1-mer DNAs containing R and S enantiomers of styrene oxide at N2-guanine were ligated with two additi
20 d linearly with time during incubations with styrene oxide, but only minor changes were detected duri
24 ) = 7.2), styrene epoxidation (pK(a) = 7.7), styrene oxide dissociation (pK(a) = 8.3), and hydroxyfla
25 gion 0.6-1.1 V vs SCE after incubations with styrene oxide, DNA/AQ films gave the best signal-to-back
26 he reaction of simple or activated epoxides (styrene oxide, epichlorohydrin, glycidyl methyl ether) w
28 ds-DNA incubated in solution with saturated styrene oxide gave a linear increase in catalytic peak c
29 1, 2, 3, 4, 5, and 6 bases downstream of the styrene oxide guanine adducts, replication was initiated
31 tion of 3 with excess cis-stilbene oxide and styrene oxide in the absence of reductant to give a 4:1
32 ein monooxygenase that transforms styrene to styrene oxide in the first step of the styrene catabolic
33 he formation of protein adducts derived from styrene oxide in whole blood in 400mg/kg group was obser
34 DNA adducts with methyl methanesulfonate and styrene oxide increased with incubation time with the sa
36 n of a [...GGCGCGCAG...] G reaction site for styrene oxide on an oligonucleotide representing the CYP
37 (regioselective methanolysis ring-opening of styrene oxide), oxidative cyclization catalysis (convers
39 yzes regio- and stereospecific hydrolysis of styrene oxide, serving as an enediyne core epoxide inter
40 rization techniques, salenCo(III)X-catalyzed styrene oxide SO/CO(2) copolymerization and ring-opening
41 n the single-turnover reaction indicate that styrene oxide synthesis is coincident with the formation
42 ed by incubation of DNA at 37 degrees C with styrene oxide, the liver metabolite of styrene, and a su
43 Interestingly, SgcF can also hydrolyze (R)-styrene oxide to afford preferentially the (R)-phenyl vi
44 ransfer from epoxides cis-stilbene oxide and styrene oxide to triphenylphosphine catalyzed by Tp'ReO(
45 5.5:1 mixture of alkene and syn-diolate from styrene oxide under conditions where diolate cyclorevers
47 Bioactivation of styrene to its metabolite styrene oxide was accomplished by incorporating the prot
49 atio of 4.8, suggesting that the reaction of styrene oxide with cysteine residues took place more lik
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