2018
DOI: 10.1016/j.jff.2018.04.013
|View full text |Cite
|
Sign up to set email alerts
|

Calendula L. species polyphenolic profile and in vitro antifungal activity

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

6
36
0

Year Published

2018
2018
2022
2022

Publication Types

Select...
6
3

Relationship

1
8

Authors

Journals

citations
Cited by 33 publications
(42 citation statements)
references
References 81 publications
6
36
0
Order By: Relevance
“…Overall, 15 hydroxycinnamic acid derivatives were identified in the extracts of S. maritima , S. patens , and P. maritima (Table 1). These derivatives showed UV spectra consistent with what is described in the literature (Table S3) [4,12,13]. Although cinnamic acids naturally occur in the free form, in the analyzed taxa herein discussed, they appeared mainly linked to quinic acid (compounds 1 , 4 , 5 , and 10 ), which is accountable to an important chemical family, the chlorogenic acids.…”
Section: Resultssupporting
confidence: 84%
See 1 more Smart Citation
“…Overall, 15 hydroxycinnamic acid derivatives were identified in the extracts of S. maritima , S. patens , and P. maritima (Table 1). These derivatives showed UV spectra consistent with what is described in the literature (Table S3) [4,12,13]. Although cinnamic acids naturally occur in the free form, in the analyzed taxa herein discussed, they appeared mainly linked to quinic acid (compounds 1 , 4 , 5 , and 10 ), which is accountable to an important chemical family, the chlorogenic acids.…”
Section: Resultssupporting
confidence: 84%
“…The assignment of the different chlorogenic acids (Table 1) was based on the hierarchical keys developed by Clifford and co-workers [14,15]. Consequently, compounds 1 and 4 were, respectively, identified as 3- O - and 5- O -caffeoylquinic acid, due to pseudomolecular ion [M-H] − at m / z 353 (Table 1) and their diagnostic ions at m / z 191 and 179 (Table S3) [4,12,14,16]. As both compounds presented a base peak at m / z 191, the discrimination between the two was made based on the secondary peaks: the isomer 3- O - presented one peak at m / z 135 [caffeic acid-H-CO 2 ] − and the isomer 5- O - at m / z 161 [caffeic acid-H-H 2 O] − (Table S3) [12].…”
Section: Resultsmentioning
confidence: 99%
“…In the case of 4,5- O -dicaffeoylquinic acid (isochlorogenic acid C) 9 ( Figure 1 ; Table 2 Rt = 13.99 min), which was isolated and characterized, the confirmation was also obtained by the injection of the pure compound. In fact, the literature is rich in these acids’ MS data due to their ubiquitous occurrence in plants [ 15 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 ] and consequently, peaks at 4.35, 6.66, 7.12 and 8.55 min with [M − H] − at m / z 353 were identified as 1- O -caffeoylquinic, 4- O -caffeoylquinic, 3- O -caffeoylquinic and 5- O -caffeoylquinic acids, respectively. The 4- O -caffeoylquinic acid is easily distinguished from the others due to its characteristic MS 2 base peak at m / z 173, whereas in the other derivatives the base peak in MS 2 is at m / z 191 ( Table 2 ).…”
Section: Resultsmentioning
confidence: 99%
“…For example, Calendula suffruticosa subsp. algarbensis is particularly active against Aspergillus sp., against yeasts such as Cryptococcus neoformans, and also against some dermatophytes species such as Microsporum canis, Microsporum gypseum, and Trichophyton mentagrophytes (19).…”
Section: Polyphenolsmentioning
confidence: 99%