ライフサイエンスコーパス: gingerol

1 to control (15%+/-0.6 oleoresin, 6.4%+/-0.4 gingerol).

2 rption to simultaneously release ASA and [6]-gingerol.

3 was largely owing to 10-gingerol, but not 6-gingerol.

4 in the fresh ginger extract, followed by 10-gingerol.

5 t LTA(4)H might be a potential target of [6]-gingerol.

6 n vitro relative to the marker compound, [6]-gingerol.

7 dardized by HPLC to contain 17.0 mg/g of [6]-gingerol.

8 enhancement of candied mango by infusion of gingerols.

9 ocyanate (ITC), cinnamaldehyde, allicin, and gingerol].

10 n plcg1(-/-) mutants and show that ginger/10-gingerol (10-G) can rescue the expression of arterial an

11 ingerols infused product (GIP), with 3.67 mg gingerols/100 g and non-infused products (control) were

12 ed higher yield of oleoresin (20%+/-0.5) and gingerol (12.2%+/-0.4) compared to control (15%+/-0.6 ol

13 ract contained high TPC concentration, and 6-gingerol (44.57 mg/gDE), 8-gingerol (8.62 mg/gDE), and 6

14 action with ethanol provided higher yield of gingerol (6.2-6.3%) than the control (5.5%) with compara

15 Apart from 6-gingerol, 6-paradol along with 6- and 8-methyl shogaols

16 ginger (Zingiber officinale Roscoe) viz. [6]-gingerol, [6]-shogaol and zingerone exhibited quorum sen

17 centration, and 6-gingerol (44.57 mg/gDE), 8-gingerol (8.62 mg/gDE), and 6-shogaol (6.92 mg/gDE).

18 [6]-Gingerol, a natural component of ginger, exhibits anti-i

19 Phloretin and [6]-gingerol also decreased the levels of AGEs and CML level

20 pared with other ginger compounds, such as 6-gingerol and 6-shogaol, 6-DHSG showed the most potent an

21 related compounds of the ginger family, [6]-gingerol and [6]-paradol, on EGF-induced cell transforma

22 The [6]-gingerol and [6]-shogaol content of the different produc

23 In addition, [6]-gingerol and EMSCEE tend to increase the LES tone.

24 rase increased the yield of [6]-, [8]-, [10]-gingerols and [6]-shogaol by 64.10, 87.8, 62.78 and 32.0

25 Parameters optimized for maximum recovery of gingerols and [6]-shogaol were ammonium sulphate concent

26 Except for zingerone and 6-gingerol, other gingerols and shogaols at a concentration of 20 muM inhi

27 human health affiliated with its richness in gingerols and shogaols.

28 The pungent bioactive principles of ginger, gingerols and six other gingerol-related compounds were

29 These results suggest that phloretin and [6]-gingerol are potential dietary compounds that can allevi

30 synthesis of a novel prodrug of aspirin, [6]-gingerol aspirinate (GAS).

31 thways such as "stilbenoid, diarylheptanoid, gingerol biosynthesis" were enriched in high weight rabb

32 tory capacity, which was largely owing to 10-gingerol, but not 6-gingerol.

33 zymes to ginger on the oleoresin yield and 6-gingerol content has been investigated.

34 The optimal MA: Glc-based extract with a 6-gingerol content of 1.90+/-0.05 mg/g, an antioxidant act

35 We showed that [6]-gingerol effectively suppressed tumor growth in vivo in

36 ficacy in cancer, the mechanism by which [6]-gingerol exerts its chemopreventive effects remains elus

37 dding vanillin as the crosslinking agent and gingerol extract stabilized silver nanoparticles.

38 Standardized [6]-gingerol extracts were prepared by microwave-assisted ex

39 pothesized that phloretin from apple and [6]-gingerol from ginger inhibit formation of AGEs and suppr

40 was explored for extraction of oleoresin and gingerols from dry powder.

41 [6]-Gingerol, GEE and EMSCEE demonstrated significant and co

42 Presence of pungent gingerols in ginger oleoresin makes it an ideal natural

43 Gingerols infused product (GIP), with 3.67 mg gingerols/

44 systematically optimized at bench-scale for gingerols infusion and subsequent candying treatment in

45 Gingerols infusion retarded the deterioration of all qua

46 6-Gingerol is the major bioactive constituent responsible

47 Except for zingerone and 6-gingerol, other gingerols and shogaols at a concentratio

48 reening, to select the optimal one for GHD 6-gingerol recovery.

49 activities of fresh ginger extract and seven gingerol-related compounds on the neuro-inflammation wer

50 rinciples of ginger, gingerols and six other gingerol-related compounds were determined and identifie

51 (sensory (overall)) > k(total phenolics) > k(gingerols), resulting in multiple cutoff criteria and pr

52 The oleoresin consists of gingerols, shogaols and other non-volatiles as chief bio

53 rification of biologically active molecules (gingerols, shogaols and zingerone) contained in ginger.

54 rious biologically active molecules, such as gingerols, shogaols and zingerone, among others, are the

55 Phloretin or [6]-gingerol supplementation significantly reduced plasma gl

56 supported our prediction by showing that [6]-gingerol suppresses anchorage-independent cancer cell gr

57 also support the anticancer efficacy of [6]-gingerol targeting of LTA(4)H for the prevention of colo

58 , and for example, assigned as [8]- and [10]-gingerol via HPTLC-ESI-HRMS.

59 An isoxazoline derivative of [6]-gingerol was prepared and it exhibited good QSI activity

60 6-Gingerol was the most abundant compound in the fresh gin

61 Phloretin and [6]-gingerol were supplemented at two different doses to C57

62 anced the anti-neuroinflammatory capacity of gingerols yet, conversely, attenuated those of shogaols.