ライフサイエンスコーパス: gingerol

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

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

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

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

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

11 [6]-Gingerol, a natural component of ginger, exhibits anti-i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 6-Gingerol is the major bioactive constituent responsible

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

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

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

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

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

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

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

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

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

39 6-Gingerol was the most abundant compound in the fresh gin

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

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

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