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. 2023 Jun 23;30(8):103716. doi: 10.1016/j.sjbs.2023.103716

Table 1.

Phytochemical screening of C. latifolia extracts using an LC-ESI-MS.

No RT (min) Observed MS (m/z) Molecular ion Compounds Molecular Formula Extracts References
1 3.36 183.06 M + H, +Na Methyl-3-hydroxy-4-methoxybenzoate C9H10O4 HRE, REAE, REE (Seghiri et al., 2006)
2 7.68 301.21 M + H Sugiol C20H28O2 HRE (Chao et al., 2005, Simoneit et al., 2019)
3 12.91 429.37 M + H Stigmastan-3,6-dione C29H48O2 HSE, REAE (Lim et al., 2005)
4 3.61 197.12 M + H Digiprolactone C11H16O3 HLE. LEAE (Lestari et al., 2022)
5 9.94 609.27 M + H Azedarachin C C32H42O10 LEAE (Chao et al., 2005, Priyanto et al., 2023)
6 3.75 489.14 M + H, +Na Curculigoside C22H26O11 REAE, REE (Zhao et al., 2014)
7 3.58 305.102 M + H, +Na Aviprin C16H16O6 REAE (Ishihara et al., 2001)
8 6.14 453.34 M + H Lucialdehyde B C30H44O3 SEAE, REAE (Gao et al., 2010)
9 5.30 181.12 M + H 3-tert-butyl-4-methoxyphenol C11H16O2 HLE (Wiley and Sons., 2023)
10 2.14 125.06 M + H Guaiacol C7H8O2 REE (Dorfner et al., 2003)
11 2.49 317.102 M + H Smilaxin C17H16O6 REE (Woo et al., 1992)
12 2.44 355.102 M + H, +Na 4-O-Caffeoylquinic acid-1 C16H18O9 SEE, LEE (Li et al., 2016)
13 2.93 492.13 M + H, +Na 5,2′,6′-Trihydroxy-7,8-dimethoxy-flavone-2′-O-β-D-glucopyranoside C23H24O12 SEE (Nurul Islam et al., 2013)
14 3.76 288.6 M + H, +Na 5,7,3′,5′-Tetrahydroxyflavanone C15H12O6 SEE (Yang et al., 2016)
15 3.52 303.05 M + H Quercetin C15H10O7 LEE (Chen et al., 2015)