ライフサイエンスコーパス: decanoic acid

1 -oxo-guanine) as an electron donor generates decanoic acid.

2 98 degrees independently of the presence of decanoic acid.

3 1)) was achieved with the addition of 3.6 mM decanoic acid.

4 ) higher water yield than the currently used decanoic acid.

5 ounds were hexanoic acid, octanoic acid, and decanoic acid.

6 centrations of ethyl decanoate, octanoic and decanoic acids.

7 ntio- and regioselective C5 hydroxylation of decanoic acid 1 to (S)-5-hydroxydecanoic acid 2 is repor

8 ydroxy-dec-2-enoic acid (10-HDA), 10-hydroxy-decanoic acid (10-HDAA), and methyl p-hydroxybenzoate (H

9 Examination of a decanoic acid (10:0) accumulating line revealed a dispro

10 -TAG synthesis upon addition of 2.1 mM (14)C-decanoic acid (10:0) was approximately four times higher

11 in >90% of medium-chain fatty acids, such as decanoic acid (10:0).

12 a K(d) of 1409 +/- 423 nM, but medium-chain (decanoic acid, 10:0) and short-chain (octanoic acid, 8:0

13 oic acid (4-OOA, 10.4 mug bee(-1)) and 4-oxo-decanoic acid (4-ODA, 13.3 mug bee(-1)) at a 0.78 ratio

14 2-O-beta-d-glucoside, and the novel compound decanoic acid-4-O-beta-d-glucoside.

15 GC-MS analysis identified n-decanoic acid (46.21%), beta-myrcene (14.082%), and 2-un

16 hether mTORC1 signaling is also a target for decanoic acid, a key component of the medium-chain trigl

17 explored the possibility that aggregates of decanoic acid, a prebiotic amphiphile, interact with the

18 3,3'-Diindolylmethane and decanoic acid acted as strong positive allosteric modula

19 Decanoic acid acts as a non-competitive antagonist at th

20 l as some but not all related bases, bind to decanoic acid aggregates.

21 s were able to block agonist actions of both decanoic acid and 3,3'-diindolylmethane at GPR84.

22 , but produced a decrease in the contents of decanoic acid and all of the major volatiles excepting a

23 w more rapidly than the wild-type strains on decanoic acid and also grow well on octanoic and hexanoi

24 atanionic coacervate droplets in mixtures of decanoic acid and cetylpyridinium chloride or cetyltrime

25 ant epilepsy that increases plasma levels of decanoic acid and ketones.

26 y these fungicides, while diethyl succinate, decanoic acid, beta-ionone, and citronellol concentratio

27 scherichia coli RRF (ecRRF) with and without decanoic acid bound to a hydrophobic pocket between doma

28 contrast, E. coli fadR strains grow well on decanoic acid but grow only exceedingly slowly on octano

29 the 2nd extracellular loop, in the action of decanoic acid but not of 3,3'-diindolylmethane.

30 Here we show that decanoic acid, but not the ketones beta-hydroxybutryate

31 the bases and ribose inhibit flocculation of decanoic acid by salt.

32 -5-methyl-4-bora-3a,4a-diaza-s-indacene-3-do decanoic acid (C1-BODIPY-C12), have a greatly diminished

33 hydrodynamic size increasing from 3.8 nm for decanoic acid (C10) to 4.4 nm for C18.

34 acid-induced rise in [Ca2+]i in response to decanoic acid (C10), dodecanoic acid (C12) and tetradeca

35 le model system, Dictyostelium, we show that decanoic acid can decrease mTORC1 activity, under condit

36 6:0), octanoic acid/caprylic acid (C8:0), or decanoic acid/capric acid (C10:0) and risk of incident c

37 Here, we show that decanoic acid (DA), a 10-carbon fatty acid and a major c

38 a supramolecular solvent (SUPRAS) made up of decanoic acid (DeA) assemblies was proposed to simplify

39 We then demonstrate that decanoic acid decreases mTORC1 activity in the absence o

40 ically, visible photolysis in a mixture of a decanoic acid ester precursor, hydrogen donor molecules,

41 Recently, decanoic acid has been shown to provide seizure control

42 (d) values for HSA binding of octanoic acid, decanoic acid, hexadecenoic acid, ibuprofen, and warfari

43 ion of HDES (tri-n-octyl phosphine oxide and decanoic acid in an equimolar ratio), tri-(2-ethylhexyl)

44 nhibition of excitatory neurotransmission by decanoic acid in the brain contributes to the anti-convu

45 During ester formation, octanoic and decanoic acids increased initially and then decreased gr

46 Instead, we show that decanoic acid increases expression of energy-related gen

47 ncrease in cellular adenosine levels and the decanoic acid-induced expression of important metabolic

48 y incorporating an aliphatic proton carrier, decanoic acid, into the lipid layer of the HBM.

49 We determine that this effect of decanoic acid is dependent on a ubiquitin regulatory X d

50 ns also show that the presence or absence of decanoic acid leads to changes in ecRRF flexibility.

51 Our data therefore indicate that dietary decanoic acid may provide a new therapeutic approach to

52 d for by increasing concentrations of either decanoic acid or 3,3'-diindolylmethane and was not affec

53 of the state-of-the-art directional solvent (decanoic acid) significantly limits its throughput and e

54 apidly formed by the addition of a colloidal decanoic acid suspension to tetrahydrofuran (THF).

55 re of Rns revealed the presence of a ligand, decanoic acid, that inhibits its activity in a manner si

56 ENT1 activity leads to an enhanced effect of decanoic acid to increase expression of tricarboxylicaci

57 es cell proliferation specifically following decanoic acid treatment.

58 (14)C-Decanoic acid was incorporated equally well in all three

59 10-(Imidazolyl)decanoic acid was the best inhibitor (Kic = 0.9 microM,

60 The binding of 10-(imidazolyl)decanoic acid was too tight for an absolute Kd to be det

61 To search for a mechanism of decanoic acid, we show it has a strong inhibitory effect

62 hat wild-type strains of S. enterica grow on decanoic acid, whereas wild-type E. coli strains cannot.