2019
DOI: 10.5530/pj.2019.11.182
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Chemical Constituents and Anti-Ulcer Activity of Ethylacetate Extract of the Leaves of Sanchezia nobilis Hook.F.

Abstract: Sanchezia nobilis Hook.F. is being paid attention and studied in a lot of different ways. The research of Abu Shuaib Rafshanjani and partners about the evaluation of the safety of Brine shrimp lethality bioassay method on n-hexane and ethylacetate segments, the results showed that both segments were safer than vincristine sulphate. 1 With antimicrobial, antifungal and insecticidal testing by diffusion on agar plates with 15 strains of Gram (+) and Gram (-) bacteria; 6 strains of fungus and insects Tribolium ca… Show more

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Cited by 2 publications
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“…The NMR data of 1 are in accordance with the data reported in the literature for sappanchalcone 15 , 2 for caesalpiniaphenol G 16 , and 3 for quercetin. 17 Compound 1 was obtained as a yellow powder. The belonging to two tri-substituted benzene rings, one methoxyl group at δ H 3.85 (3H, s).…”
Section: Resultsmentioning
confidence: 99%
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“…The NMR data of 1 are in accordance with the data reported in the literature for sappanchalcone 15 , 2 for caesalpiniaphenol G 16 , and 3 for quercetin. 17 Compound 1 was obtained as a yellow powder. The belonging to two tri-substituted benzene rings, one methoxyl group at δ H 3.85 (3H, s).…”
Section: Resultsmentioning
confidence: 99%
“…The 1 H NMR spectrum of 3 displayed five aromatic proton signals, including two meta-coupled proton signals at δ H 6.20 (1H, d, J = 2.0 Hz, H-6) and 6.41 (1H, d, J = 2.0 Hz, H-8) ascribed to the 5,7-dihydroxylated ring A from a flavonoidic skeleton, an ABX system at δ H 7.64 (1H, dd, J = 8.5, 2.0 Hz, H-6ʹ), 7.75 (1H, d, J = 2.0 Hz, H-2ʹ), and 6.90 (1H, d, J = 8.5 Hz, H-5ʹ) ascribed to a 1,3,4-trisubstituted of ring B. The 13 C NMR of 3 showed the presence of 15 aromatic carbon signals.Based on the NMR data and comparison of the data given in the literature, the structure of compound 3 was identified as quercetin 17.…”
mentioning
confidence: 99%