ライフサイエンスコーパス: styrene oxide

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 such as 1-butene oxide, 1-hexene oxide, and styrene oxide.

5 ept for particularly activated cases such as 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.

11 ohols in a one-pot cascade from aldehydes or styrene oxides.

12 e mutant of Gly(262) terminated synthesis on styrene oxide-adducted templates.

13 enyl)styrene oxide and (S)-beta-(N(6)-adenyl)styrene oxide adducts at position X(6) in d(CGGACXAGAAG)

14 The (S)-alpha-(N6-adenyl)styrene oxide adducts at positions X6 in d(CGGACXAGAAG).

15 uctures of the (R)- and (S)-alpha-(N2-guanyl)styrene oxide adducts at X6 in d(GGCAGXTGGTG).d(CACCACCT

16 ational studies of R- and S-alpha-(N6-adenyl)styrene oxide adducts mismatched with deoxycytosine at p

17 resis and HPLC-MS suggested the formation of styrene oxide adducts of DNA bases under similar reactio

18 Conformations of (R)-beta-(N(6)-adenyl)styrene oxide and (S)-beta-(N(6)-adenyl)styrene oxide ad

19 lyzed enantioselective reductive coupling of styrene oxides and aryl iodides is reported.

20 ic peak current upon incubation in saturated styrene oxide, and an estimate of 1 damaged base in 1000

21 coumarin is reported from 4-hydroxycoumarin, styrene oxide, and DMSO in the presence of p-TSA.H(2)O a

22 primary oxygenate product benzaldehyde over styrene oxide at differential styrene conversions (<3%)

23 1-mer DNAs containing R and S enantiomers of styrene oxide at N2-guanine were ligated with two additi

24 d linearly with time during incubations with styrene oxide, but only minor changes were detected duri

25 Styrene oxide-cysteine adduction is predominantly involv

26 hylation- and GC/MS-based approach to detect styrene oxide-derived protein adduction.

27 SgcF efficiently hydrolyzes (S)-styrene oxide, displaying an apparent K(m) of 0.6 +/- 0.

28 ) = 7.2), styrene epoxidation (pK(a) = 7.7), styrene oxide dissociation (pK(a) = 8.3), and hydroxyfla

29 gion 0.6-1.1 V vs SCE after incubations with styrene oxide, DNA/AQ films gave the best signal-to-back

30 he reaction of simple or activated epoxides (styrene oxide, epichlorohydrin, glycidyl methyl ether) w

31 the enzyme in the film generated metabolite styrene oxide from styrene.

32 ds-DNA incubated in solution with saturated styrene oxide gave a linear increase in catalytic peak c

33 1, 2, 3, 4, 5, and 6 bases downstream of the styrene oxide guanine adducts, replication was initiated

34 rformed with 7-methoxy-4-hydroxycoumarin and styrene oxides, having an electron-withdrawing group, th

35 ingle-turnover reactions at 0 degrees C gave styrene oxide in good yields.

36 tion of 3 with excess cis-stilbene oxide and styrene oxide in the absence of reductant to give a 4:1

37 ein monooxygenase that transforms styrene to styrene oxide in the first step of the styrene catabolic

38 he formation of protein adducts derived from styrene oxide in whole blood in 400mg/kg group was obser

39 DNA adducts with methyl methanesulfonate and styrene oxide increased with incubation time with the sa

40 Permethylation of styrene oxide-modified bovine serum albumin released the

41 n of a [...GGCGCGCAG...] G reaction site for styrene oxide on an oligonucleotide representing the CYP

42 (regioselective methanolysis ring-opening of styrene oxide), oxidative cyclization catalysis (convers

43 This styrene oxide reacted with double stranded (ds)-DNA in t

44 r different acid-catalyzed reactions namely, styrene oxide ring opening, vesidryl synthesis, Friedel-

45 AAS catalyzes different reactions (styrene oxide ring-opening, vesidryl synthesis, Friedel-

46 yzes regio- and stereospecific hydrolysis of styrene oxide, serving as an enediyne core epoxide inter

47 rization techniques, salenCo(III)X-catalyzed styrene oxide SO/CO(2) copolymerization and ring-opening

48 n the single-turnover reaction indicate that styrene oxide synthesis is coincident with the formation

49 ed by incubation of DNA at 37 degrees C with styrene oxide, the liver metabolite of styrene, and a su

50 Interestingly, SgcF can also hydrolyze (R)-styrene oxide to afford preferentially the (R)-phenyl vi

51 ransfer from epoxides cis-stilbene oxide and styrene oxide to triphenylphosphine catalyzed by Tp'ReO(

52 5.5:1 mixture of alkene and syn-diolate from styrene oxide under conditions where diolate cyclorevers

53 Damage of DNA by reaction with styrene oxide under the electrode incubation conditions

54 Bioactivation of styrene to its metabolite styrene oxide was accomplished by incorporating the prot

55 Damage of DNA films after reaction with styrene oxide was detected using derivative square wave

56 atio of 4.8, suggesting that the reaction of styrene oxide with cysteine residues took place more lik

57 ntioselective cross-electrophile coupling of styrene oxide with two different aryl iodide substrates.