ライフサイエンスコーパス: octanal

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1 nt aromatic aldehydes and Z-selective with n-octanal.

2 retention times from derivatized methanal to octanal.

3 rofiles for cells that were all sensitive to octanal.

4 r range, while others were activated only by octanal.

5 benzaldehyde, 2-octanone, hexyl acetate and octanal.

6 ls and aldehydes with 1-octen-3-ol, decanal, octanal, 1-hexanol, and nonanal as the compounds with th

7 that the family of C8 compounds (3-octanone, octanal, 1-octen-3-one, 3-octanol and 1-octen-3-ol) is p

8 ect has also been observed for the aliphatic octanal/1-octanol system.

9 dec-2-enal, 3-methylbutanal, ethyl benzoate, octanal, 2-methoxyphenol, 2-methylbutanal and 2-methoxy-

10 r of ageing for all cultivars, and heptanal, octanal and 2-ethyl hexanol as cultivar-specific indicat

11 torage, whereas pentanal, hexanal, heptanal, octanal and 3-undecen-2-one decreased.

12 OR-I7 is activated by low concentrations of octanal and blocked by citral, other receptors were less

13 ficiently as substrates, but does metabolize octanal and decanal efficiently.

14 te, and benzaldehyde; however, retention for octanal and dibutyl disulfide increased.

15 tral, other receptors were less sensitive to octanal and not blocked by citral.

16 Octanal and other aldehydes induce large EOG responses i

17 homologous aldehydes (hexanal, heptanal, and octanal) and ketones (2-hexanone, 2-heptanone, and 2-oct

18 -benzaldehyde, eugenol-benzaldehyde, octanol-octanal, and [+/-]-limonene).

19 rat I7 receptor, prefers heptanal instead of octanal, as a result of a single valine-to-isoleucine su

20 s, we used the response to a common odorant, octanal, as the basis for defining multiple receptor pro

21 interacted non-covalently with PPIs, whereas octanal bound PPIs via covalent and non-covalent forces.

22 titution yielded 9-hydroxynonanoyl-ACP and 1-octanal, corresponding to an obligate "register-shift" o

23 On the basis of nonanal, octanal, decanal and 1-octen-3-ol contents, basmati cult

24 Compounds such as hexanal, heptanal, octanal, decanal, (E)-2-hexenal, (E)-2-decen-1-al, (E,Z)

25 were observed to elute between heptanal and octanal derivatives, while the acrolein derivatives had

26 ns decreased in the order: dibutyl disulfide>octanal>hexyl acetate>2-octanone=benzaldehyde.

27 Dilute mixtures of n-octanal in synthetic air (up to 100 ppm) were photolyzed

28 2-and 3-methyl butanoic acid, hexanoic acid, octanal, indole, phenol, benzaldehyde, dimethyl disulfid

29 ehydes (n-propanal, n-hexanal, n-heptanal, n-octanal, n-nonanal, and 2 methyl 2-propenal), four keton

30 henol, butanal, pentanal, hexanal, heptanal, octanal, nonanal, and decanal-were present at significan

31 trigeminal response were carbonyl compounds octanal, nonanal, benzaldehyde and 2-heptanone suggestin

32 -methyl furfural, mesifurane) and aldehydes (octanal, nonanal, decanal and benzaldeyhde).

33 Hexanal, heptanal, octanal, nonanal, decanal, and 6-methyl-5-hepten-2-one (

34 ith a panel of nine odorants, which included octanal, octanoic acid, octanol and cinnamaldehyde among

35 of experimental and theoretical evidence, n-octanal photolysis predominantly proceeds to form Norris

36 h SsuD, which correlated with an increase in octanal product.

37 Heptanal/1-octen-3-ol and heptanal/octanal ratios were also defined as characterising the a

38 f citral (partial 17 agonist, inhibitor) and octanal, rats recognize 1 or both components over a wide

39 the profiles with that of the one identified octanal receptor, OR-I7, indicated several differences.

40 A lower estimate for the maximal number of octanal receptors is between 33 and 55.

41 red the pharmacological profile of different octanal receptors using Ca(2+) imaging in isolated olfac

42 included the area receiving projections from octanal-responsive sensory neurons expressing the I7 odo

43 ned to recognize mixtures of citronellal and octanal (strong 17 agonists) in many ratios rarely recog

44 This large number of receptors for octanal suggests that, although the peripheral olfactory

45 erpinolene, beta-pinene, alpha-terpineol and octanal were identified as potential markers for ASLT.

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