ライフサイエンスコーパス: fatty acid hydroperoxide

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1 d to the active ferric form by reaction with fatty acid hydroperoxide.

2 thione peroxidases were equally sensitive to fatty acid hydroperoxides.

3 ion of 4-HNE that should apply also to other fatty acid hydroperoxides.

4 Addition of the fatty acid hydroperoxide 13(S)-hydroperoxyoctadecadienoi

5 able to epoxidize BaP-7,8-diol using various fatty acid hydroperoxides, although at slower rates than

6 Furthermore, fatty acid hydroperoxide and SIN-1 both induced Ohr expr

7 eroxidation process of membrane lipids, MDA, fatty acid hydroperoxides and 7-ketocholesterol.

8 atalyzed oxidation of BaP-7,8-diol, and that fatty acid hydroperoxides and CYP2S1 may play important

9 s a central role in modulating the levels of fatty acid hydroperoxides and peroxynitrite, both of whi

10 Fatty acid hydroperoxides and phospholipids such as lino

11 mitochondrial lipid bilayer are released as fatty acid hydroperoxides and react with the Amplex Red

12 Lipoxygenase-derived fatty acid hydroperoxides are metabolized by CYP74 cytoc

13 es are reactive epoxides biosynthesized from fatty acid hydroperoxides by specialized cytochrome P450

14 Together, these results suggest that fatty acid hydroperoxides can serve as physiological cof

15 also supported both in vitro and in vivo by fatty acid hydroperoxides described in the accompanying

16 Downstream, the LOX products 13-fatty acid hydroperoxides esterified to galactolipids an

17 roxidase cyt c/CL complexes can utilize free fatty acid hydroperoxides (FFA-OOH) at exceptionally hig

18 We also suggest that the release of fatty acid hydroperoxides from denervated muscle mitocho

19 unstable epoxide (an allene oxide) from the fatty acid hydroperoxide generated by the lipoxygenase a

20 Lipoxygenases that form S configuration fatty acid hydroperoxides have been purified or cloned f

21 lcohol synthesis from lipoxygenase products (fatty acid hydroperoxides) in mammalian tissues, there a

22 encode enzymes that catalyze the cleavage of fatty acid hydroperoxides into aldehydes and oxoacids.

23 Allene oxide synthase (AOS) and fatty acid hydroperoxide lyase (HPL) are plant-specific

24 Kinetic analyses with several fatty acid hydroperoxides revealed that 13S-hydroperoxy-

25 tathione peroxidase mimetic and inhibitor of fatty acid hydroperoxides) significantly inhibits the Am

26 ed cytochrome P450s that metabolize a common fatty acid hydroperoxide substrate to different classes

27 laying hydroperoxide isomerase activity with fatty acid hydroperoxides through cycling of the ferrous

28 The conversion of fatty acid hydroperoxides to allene epoxides is catalyze

29 0 or catalase-related hemoproteins transform fatty acid hydroperoxides to allene oxides, highly react

30 plant-specific cytochrome P450s that commit fatty acid hydroperoxides to different branches of oxyli

31 , we demonstrate that CYP2S1 can use various fatty acid hydroperoxides to support epoxidation of BaP-

32 Lipoxygenase (LOX) enzymes form fatty acid hydroperoxides used in membrane remodeling an

33 lase that is specialized for metabolism of a fatty acid hydroperoxide was identified.

34 talase-related hemoprotein reactivity toward fatty acid hydroperoxides, we detected a novel candidate

35 atic branches which can use as substrate the fatty acid hydroperoxides were differentially regulated

36 , the rate constants between Ohr and several fatty acid hydroperoxides were in the 10(7)-10(8) M(-1)s

37 Fatty acid hydroperoxides, which are readily solubilized

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