1966
DOI: 10.1016/s0031-9422(00)82144-5
|View full text |Cite
|
Sign up to set email alerts
|

Steroids and related natural products—xxvii. Salvia apiana

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
17
0

Year Published

1975
1975
2016
2016

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 27 publications
(18 citation statements)
references
References 18 publications
1
17
0
Order By: Relevance
“…The isolated compounds were identified by their NMR and MS spectral analysis as four diterpenes: rosmadial ( I ) (Nakatani & Inatani 1983), carnosol ( II ) (Abreu et al 2008), 16-hydroxycarnosol ( III ) (Luis, Lahlou, Andrés, Sood, et al 1996), sageone ( IV ) (Tada et al 1994); two flavonoids: cirsimaritin ( V ) (Wang et al 2004), salvigenin ( VI ) (Ayatollahii et al 2009); and three triterpenes: oleanolic acid ( VII ) (Pettit et al 1966; Martins et al 2013), uvaol (3β,28-dihydroxy-urs-12-ene) ( VIII ) (Lee et al 2013), ursolic acid ( IX ) (Pettit et al 1966; Silva et al 2008). …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The isolated compounds were identified by their NMR and MS spectral analysis as four diterpenes: rosmadial ( I ) (Nakatani & Inatani 1983), carnosol ( II ) (Abreu et al 2008), 16-hydroxycarnosol ( III ) (Luis, Lahlou, Andrés, Sood, et al 1996), sageone ( IV ) (Tada et al 1994); two flavonoids: cirsimaritin ( V ) (Wang et al 2004), salvigenin ( VI ) (Ayatollahii et al 2009); and three triterpenes: oleanolic acid ( VII ) (Pettit et al 1966; Martins et al 2013), uvaol (3β,28-dihydroxy-urs-12-ene) ( VIII ) (Lee et al 2013), ursolic acid ( IX ) (Pettit et al 1966; Silva et al 2008). …”
Section: Resultsmentioning
confidence: 99%
“…The plant is used for diaphoretic and diuretic effects (Dentali & Hoffmann 1990). Previous to our research, several compounds including flavonoids, mono-, sesqui-, di- and tri terpenes, have been already identified and/or isolated from S. apiana (Pettit et al 1966; González et al 1992; Luis, Lahlou, & Andrés 1996; Luis, Lahlou, Andrés, Sood, et al 1996; Dentali & Hoffmann 1990; Borek et al 2006; Abreu et al 2008; Takeoka et al 2010). However, this plant has not been studied for cannabinoid or opioid receptors activity.…”
Section: Introductionmentioning
confidence: 99%
“…Activity-guided fractionation of the petroleum ether and ethyl acetate extracts from the entire plant of A. unedo using the JB6 cell transformation assay provided one new compound (1) and nine known compounds, namely, -amyrin acetate (2) [12], betulin [13], betulinic acid (5) [14], (À)-catechin (6) [15], 6-hydroxystigmast-4-en-3-one [16], lupeol (3) [17], platanic acid [18], pomolic acid 3-acetate (4) [19], and -sitosterol [20] (figure 1). Of these compounds, only betulinic acid (5) and betulin have been isolated previously from A. unedo [5].…”
Section: Resultsmentioning
confidence: 99%
“…The existing literature for S. apiana discusses the extraction and identification of triterpenes and related constituents found in the roots of this plant. [9][10][11] We respectfully submit this information as the first report of the assay of the essential oil of S. apiana.…”
Section: Gas Chromatography-fidmentioning
confidence: 99%