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1 s and vacuolation of basal epithelial cells (perillyl alcohol).
2 eventive agents, difluoromethylornithine and perillyl alcohol.
3 s been achieved from the monoterpene (S)-(-)-perillyl alcohol.
4 t NF-kappaB pathway as a molecular target of perillyl alcohol activity in different cancer cell types
6 of incubation, an effect that is blocked by perillyl alcohol, an inhibitor of prenyltransferases, bu
7 vasive adenocarcinomas of the colon, whereas perillyl alcohol at 2 g/kg diet inhibited the incidence
9 fibroblasts and adipocytes, the presence of perillyl alcohol blocked the ability of insulin to incre
11 induced by the monoterpene anticancer agent perillyl alcohol correlates to the increased expression
13 ndicate that the colon tumors of animals fed perillyl alcohol exhibited increased apoptosis as compar
15 (AIN-76A) diet or diets containing 1 and 2 g perillyl alcohol/kg diet, representing 40 and 80% MTD le
16 d 80% maximum tolerated dose (MTD) levels of perillyl alcohol on azoxymethane (AOM)-induced colon car
22 mechanisms of action of the anticancer agent perillyl alcohol (POH), presently in Phase II clinical t
29 for the derivatives of carvacrol, thymol and perillyl alcohol were higher (15-30mm) in the case of fi
31 oxy 1-O-glucosides of carvacrol, thymol, and perillyl alcohol were tested against Aspergillus flavus,
32 ckers, the combination of a calcium blocker (perillyl alcohol) with bortezomib suppressed NF-kappaB e
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