2016
DOI: 10.1016/j.indcrop.2016.02.048
|View full text |Cite
|
Sign up to set email alerts
|

Chemical composition of medicinal plant Atractylis serratuloides

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 10 publications
(2 citation statements)
references
References 18 publications
0
2
0
Order By: Relevance
“…The molecular formula was determined to be C 30 H 44 O 5 from the pseudomolecular ion peak [M + H] − at m / z 485.3271 (calculated 485.3267) in the HR-ESI-MS. The NMR data of 3 ( Table 3 ) were similar to that of caulophyllogenin [ 13 ], except for the presence of a carbonyl group instead of a methylenoxy in 3. The HMBC spectrum, the correlations between the δ H 3.53 (1H, d, J = 11.5 Hz, H-23a), 3.27 (1H, d, J = 11.5 Hz, H-23b), δ H 0.85 (3H, s, H-24) and the carbonyl group ( δ C 220.0), indicated that this carbonyl group was located at C-3.The ROE correlations of H-16 ( δ H 4.41) with H-26 ( δ H 0.81) suggested H-16 on the same side ( β -oriented), While 16-OH on the other side ( α -oriented).…”
Section: Resultsmentioning
confidence: 72%
“…The molecular formula was determined to be C 30 H 44 O 5 from the pseudomolecular ion peak [M + H] − at m / z 485.3271 (calculated 485.3267) in the HR-ESI-MS. The NMR data of 3 ( Table 3 ) were similar to that of caulophyllogenin [ 13 ], except for the presence of a carbonyl group instead of a methylenoxy in 3. The HMBC spectrum, the correlations between the δ H 3.53 (1H, d, J = 11.5 Hz, H-23a), 3.27 (1H, d, J = 11.5 Hz, H-23b), δ H 0.85 (3H, s, H-24) and the carbonyl group ( δ C 220.0), indicated that this carbonyl group was located at C-3.The ROE correlations of H-16 ( δ H 4.41) with H-26 ( δ H 0.81) suggested H-16 on the same side ( β -oriented), While 16-OH on the other side ( α -oriented).…”
Section: Resultsmentioning
confidence: 72%
“…The Atractylis species are used in folk medicine against urinary retention, intestinal parasites and snakebite poisoning, and for their anti-inflammatory and antipyretic activities (Larrey and Pageaux, 1995, El Rhaffari and Zaid 2002, Daniele et al 2005, Melakhessou et al 2018). In addition, many studies have been reported for Atractylis plants, which allowed the identification of diterpenes, triterpenes, saponins and flavonoids (Sadek et al 1998, Chabani et al 2013, Chabani et al 2016a, Chabani et al 2016b. Atractylis cancellata L., used in folk medicine for the treatment of skin disorders (Bammou et al 2015), is an herbaceous endemic plant; it grows in semi-arid zone of Mediterranean area (Quezel and Santa 1963).…”
Section: Introductionmentioning
confidence: 99%