ライフサイエンスコーパス: diglyceride

1 lly active lipids phosphatidic acid (PA) and diglyceride.

2 wn products inositol 1,4,5-trisphosphate and diglyceride.

3 effect on phosphatidic acid, but not that on diglyceride.

4 his lethal process is potently suppressed by diglyceride.

5 as well as for the lateral segregation of a diglyceride.

6 des and in 2-3-fold accumulation of label in diglycerides.

7 al correlate for IL-1-generated ether-linked diglycerides.

8 Here, we report that the 1-O-alkyl ether diglyceride, 1-O-hexadecyl-2-acetyl-sn-glycerol (HAG), l

9 The main hydrolysis products were 1,2-diglycerides, 2-monoglycerides, glycerol and fatty acids

10 lase, and three out of five putative type II diglyceride acyltransferases (DGATs), the enzymes that c

11 Two ether glucosyl diglyceride analogs were synthesized, and their antiprol

12 ine (ara-C) stimulates the formation of both diglyceride and ceramide in the acute myelogenous leukem

13 g change being observed in the modulation of diglyceride and monoglyceride levels in BAT.

14 of natural ceramides with those of saturated diglycerides and an unsaturated ceramide demonstrates th

15 ers, dimers, oxidized triglyceride monomers, diglycerides and free fatty acids, and induction period

16 tty acids, although small proportions of 1,3-diglycerides and of 1-monoglycerides were also found.

17 centrations of two phosphatidylcholines, two diglycerides and two acyl-carnitines were significantly

18 1,2-Diglycerides and vegetable stanols and/or sterols have b

19 Octanol, 1,2-dioctanoyl-sn-glycerol (a diglyceride), and N-hexanoyl-D-erythrosphingosine (a cer

20 vine cardiolipin, chloroplast monogalactosyl-diglyceride, and dioleoyl phosphatidylethanolamine as a

21 fatty acids and their esters, monoglyceride, diglyceride, and triglyceride.

22 such as phosphatidylcholine, sphingomyelin, diglycerides, and triglycerides were detected and identi

23 cates cytokine receptor-induced ether-linked diglycerides as second messengers that inhibit the bioac

24 pases are differentially activated such that diglyceride breakdown is approximately four times faster

25 gment ions corresponding to loss of the full diglyceride chain as well as the remaining headgroup bou

26 Interestingly, hepatic triglyceride and diglyceride contents were normalized to chow-fed levels

27 Diglyceride DG(18:1/20:0)-sodium adduct and protonated o

28 ding to TG synthesis and steatosis by way of diglyceride (DG) generation.

29 (PEt) instead of phosphatidic acid (PA) and diglyceride (DG).

30 In addition, digalactosyl diglyceride (DGDG) 36:4 was shown to be an effective mar

31 t of sea urchin membrane vesicle PtdIns into diglycerides enriched in long chain, polyunsaturated spe

32 n in 1-monoglycerides and an increase in 1,2-diglycerides, especially in the margarines with higher w

33 aracterized by high levels of triglycerides, diglycerides, fatty acids, ceramides, and oxidized fatty

34 atty acids, together with triacylglycerides, diglycerides, free fatty acids and ergosterol in salmon

35 rolysis, mobilization of intracellular Ca2+, diglyceride generation, and redistribution of protein ki

36 CDP-diglyceride hydrolase (Cdh) catalyzes the same reaction

37 The diglyceride-hydrolyzing lipase was purified from the ext

38 te that production of membrane-destabilizing diglycerides in membranes enriched in PtdIns may facilit

39 and the rate of palmitate incorporation into diglycerides in white muscle was 93% higher in obese rat

40 ut affecting the induced increase in nuclear diglyceride, indicating that the increase in nuclear PLD

41 nterleukin-1 receptor-generated ether-linked diglycerides inhibit immunoprecipitated protein kinase C

42 ramide because, in contrast to the bacterial diglyceride kinase, ceramide is not phosphorylated under

43 Cell-permeable ether-linked diglycerides mimic the effects of interleukin-1 to induc

44 ol, treating human fibroblasts with octanol, diglyceride, or ceramide stimulated the rapid inactivati

45 phosphorylated under conditions specific for diglyceride phosphorylation.

46 dothelin, selectively generates ether-linked diglyceride species (alkyl, acyl- and alkenyl, acylglyce

47 itory profile of these ether-linked glucosyl diglycerides strengthens the hypothesis that such glycol

48 ctive peptides stimulate distinct species of diglycerides that differentially regulate protein kinase

49 The block in diglyceride to triglyceride conversion could not be expl

50 ed defects in FA uptake and in conversion of diglycerides to triglycerides that are similar to those

51 phosphatidic acids but reduced abundance of diglycerides, triglycerides, and phosphatidylglycerol li

52 ated fatty acids beta-sitosterol, sn-1 and 3 diglyceride values.

53 r ones, such as 1- and 2-monoglycerides, 1,2-diglycerides, vegetable stanols and sterols, and sorbic

54 ol (DPG) vesicles (but not with digalactosyl diglyceride vesicles) as demonstrated by flotation in su

55 PLD2 and PAP2b act sequentially to generate diglyceride within this specialized membrane compartment