2015
DOI: 10.1016/j.canlet.2015.07.005
|View full text |Cite
|
Sign up to set email alerts
|

Diterpenes from rosemary (Rosmarinus officinalis): Defining their potential for anti-cancer activity

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
67
0
1

Year Published

2016
2016
2022
2022

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 113 publications
(69 citation statements)
references
References 71 publications
(82 reference statements)
1
67
0
1
Order By: Relevance
“…Carnosic acid, carnosol and rosmanol (Figure 8) may be the active components contained in rosemary responsible for its anti-cancer activity [217]. …”
Section: Rosemarymentioning
confidence: 99%
“…Carnosic acid, carnosol and rosmanol (Figure 8) may be the active components contained in rosemary responsible for its anti-cancer activity [217]. …”
Section: Rosemarymentioning
confidence: 99%
“…The main polyphenols found in rosemary extract (RE) include the diterpenes carnosic acid (CA) and rosmarinic acid (RA) [11]. Rosemary extract and its polyphenols CA and RA have recently been explored and found to exert potent anticancer effects (reviewed recently in [12,13,14]). To establish a systematic literature review we used the online search engine Pubmed.…”
Section: Introductionmentioning
confidence: 99%
“…For the first compound, MS/MS experiments gave rise to the product ion at m/z 299, which was previously suggested to derive from a neutral loss of CO 2 (Zhang et al, 2012). LC-MS/MS data for metabolite 15 suggested the likely presence of carnosol, a phenolic diterpene having a lactone ring, firstly characterized in 1964 and continuously investigated for its health promoting properties (Bauer et al, 2012;Chun, Kundu, Chae, & Kundu, 2014;Johnson, 2011;Petiwala & Johnson, 2015). In fact, the deprotonated pseudomolecular ion at m/z 329 fragmented to give product ions at m/z 285 (À44 Da), which in turn provided the ions at m/z 269 and 201 (Kontogianni et al, 2013).…”
Section: Phenolic Diterpenesmentioning
confidence: 96%