「ANANDAMIDE」の共起表現一覧(1語右で並び替え)
該当件数 : 18件
It goes on to form | anandamide after being cleaved by phospholipases. |
europrotectin D or various endocannabinoids ( | anandamide and its analogs.) |
ounsaturated analogue of the endocannabinoid | anandamide, but unlike anandamide it acts independently |
he human hippocampus are similar to those of | anandamide, but they are 2- to 9-fold higher in periphe |
because of their impaired ability to degrade | anandamide, FAAH KOs also display supersensitivity to e |
gonist (antagonist) and blocks the effect of | anandamide in keratinocytes, leading to pro-allergic ef |
A study published in 1998 shows that | anandamide inhibits human breast cancer cell proliferat |
Later studies confirmed that | anandamide is not found in chocolate and the two compou |
Moreover, | anandamide is thought to be an endogenous ligand for va |
As a result, | anandamide levels in the body and brain are elevated. |
Because of their significantly elevated | anandamide levels, FAAH KOs have an analgesic phenotype |
lso considerably more resistant to FAAH than | anandamide, making it a much more powerful cannabinoid |
(These generate N-palmitoylethanolamine, | anandamide, N-oleoylethanolamine, and N-stearoylethanol |
In an attempt to find | anandamide or anandamide type endocannabinoids, researc |
h CB1 and CB2 receptors, and an inhibitor of | anandamide reuptake. |
s enzyme can cause NAPE-PLD products such as | anandamide to build up to levels 15-fold higher than no |
hanolamides are naturally occurring, such as | anandamide which plays a physiological role as a neurot |
This chemical is a methylated analogue of | anandamide with roughly 4* the potentcy as a CB1 agonis |
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