ライフサイエンスコーパス: crotonaldehyde

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1 o exclusively yield the C4 coupling product, crotonaldehyde.

2 the mutagenic and carcinogenic properties of crotonaldehyde.

3 om cigarette smoke and polluted air, such as crotonaldehyde, acrolein, and oxidizing agents such as h

4 rchain cross-link formation by the analogous crotonaldehyde adduct (2b) was evaluated in a 5'-dC-2b s

5 ially incorporated opposite the acrolein and crotonaldehyde adducts, and dTTP incorporation was prefe

6 Crotonaldehyde adsorbed to Pt(111) as eta(2) surface int

7 alpha,beta-unsaturated aldehydes, acrolein, crotonaldehyde, and prenal, over Pt(111) at Torr pressur

8 ng adducts derived from butadiene, acrolein, crotonaldehyde, and styrene, and examined for effects on

9 g 1,N(2)-deoxyguanosine adducts of acrolein, crotonaldehyde, and trans-4-hydroxynonenal can form cros

10 ine interstrand cross-links arising from the crotonaldehyde- and acetaldehyde-derived R- and S-alpha-

11 a-unsaturated aldehydes such as acrolein and crotonaldehyde are common environmental pollutants prese

12 se (AOR) from P. furiosus using pyruvate and crotonaldehyde as substrates, respectively.

13 ermidine directly reacts with AA to generate crotonaldehyde (CrA), most likely via an enamine aldol c

14 e (dG) with enals, including acrolein (Acr), crotonaldehyde (Cro), pentenal (Pen), heptenal (Hep), an

15 Acrolein- and crotonaldehyde-derived 1,N2-propanodeoxyguanosine (AdG a

16 cyclic adducts, has shown that acrolein- and crotonaldehyde-derived 1,N2-propanodeoxyguanosine adduct

17 Cyclic crotonaldehyde-derived deoxyguanosine (CrA-PdG) adducts

18 The acrolein- and the 6R-crotonaldehyde-derived exocyclic 1,N(2)-dG adducts form

19 The corresponding acrolein- and crotonaldehyde-derived exocyclic 1,N(2)-dG adducts under

20 The cinnamaldehyde- and crotonaldehyde-derived phosphonates 2b and 2c were also

21 sitive to acetaldehyde, but not to acrolein, crotonaldehyde, glyoxal, and methylglyoxal.

22 Methacrolein, methyl vinyl ketone, crotonaldehyde, glyoxal, methyl glyoxal, and benzaldehyd

23 aturated carbonyl compounds like acrolein or crotonaldehyde in acetone-d(6) generates metastable (E)-

24 that acrolein was 2000-fold more potent than crotonaldehyde in blocking DNA binding to an NF-kappaB c

25 ld: 16%) and B (1b, overall yield: 34%) from crotonaldehyde in nine and seven steps, respectively, ha

26 The hydrogenation of crotonaldehyde in the presence of supported platinum nan

27 The repair of acetaldehyde/crotonaldehyde-induced guanine (N2)-guanine (N2) interst

28 Lastly, we found that crotonaldehyde induces the formation of DNA-Top1 complex

29 d aldehydes in cigarette smoke (acrolein and crotonaldehyde) inhibited production of interleukin-2 (I

30 Crotonaldehyde is a representative alpha,beta-unsaturate

31 cy site on the TiO2 surface, the C=O bond of crotonaldehyde is activated, by charge transfer, for hyd

32 arified by carrying out the hydrogenation of crotonaldehyde over both Pt(111) and Pt(100) single crys

33 Crotonaldehyde reacted with Cys-61, but not Arg-307, whe

34 ata to experiments performed with 2-butenal (crotonaldehyde) shows that EpB and 2-butenal decompose t

35 exocyclic 1,N(2)-dG adducts of acrolein and crotonaldehyde, the cross-linking reaction is slow.

36 The 1,4-addition of thioacetic acid and crotonaldehyde to (Z)-3-(acetylsulfanyl)-1-propen-1-ol i

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