1979
DOI: 10.1021/np50005a014
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Antimicrobial Principles in Mimosa hamata

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Cited by 18 publications
(12 citation statements)
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“…1), gallic acid (1) (Lee, Chiou, Lee, & Kou, 2005), ethyl gallate (2) (Hussain, Modan, Shabbir, & Zaidi, 1979;Zhang, Chen, Pei, & Hua, 2001), 1-O-galloyl-b-D-glucopyranoside (3) (Kashiwada, Nonaka, & Nishioka, 1984), methyl brevifolin carboxylate (4) (Yao & Zuo, 1993), brevifolin (5) (Mahmoud, Sahar, & Irmgard, 1994;Sha, Liu, Wang, & Xu, 2000), corilagin (6) (Mahmoud et al, 1994;Sha et al 2000), ellagic acid (7) (Mahmoud et al, 1994) and 4-O-a-L-rhamnopyranosylellagic acid (8) (Yang et al, 1998), were determined by interpretation of their spectroscopic data (see supplementary data) as well as by comparison with reported data. The structures were further supported by co-TLC with authentic compound samples or hydrolysis followed by co-TLC with authentic compound samples (see supplementary data).…”
Section: Isolation and Structure Determinationmentioning
confidence: 99%
“…1), gallic acid (1) (Lee, Chiou, Lee, & Kou, 2005), ethyl gallate (2) (Hussain, Modan, Shabbir, & Zaidi, 1979;Zhang, Chen, Pei, & Hua, 2001), 1-O-galloyl-b-D-glucopyranoside (3) (Kashiwada, Nonaka, & Nishioka, 1984), methyl brevifolin carboxylate (4) (Yao & Zuo, 1993), brevifolin (5) (Mahmoud, Sahar, & Irmgard, 1994;Sha, Liu, Wang, & Xu, 2000), corilagin (6) (Mahmoud et al, 1994;Sha et al 2000), ellagic acid (7) (Mahmoud et al, 1994) and 4-O-a-L-rhamnopyranosylellagic acid (8) (Yang et al, 1998), were determined by interpretation of their spectroscopic data (see supplementary data) as well as by comparison with reported data. The structures were further supported by co-TLC with authentic compound samples or hydrolysis followed by co-TLC with authentic compound samples (see supplementary data).…”
Section: Isolation and Structure Determinationmentioning
confidence: 99%
“…The isolated compounds (1-3)(l " Fig. 2) were characterized by spectroscopic analysis, including UV, MS, IR, 1 H-NMR, and 13 C-NMR techniques, and comparison of these data with those in the literature [10][11][12][13][14]. The purities of these isolated MG, GA, and PGG (101.1, 95.9 and 86.1 %, respectively) were analyzed by high performance liquid chromatography (HPLC).…”
Section: Extraction and Isolation Of Constituentsmentioning
confidence: 99%
“…The known compounds were identified as myricetin 3-O-a-Lrhamnoside (3) Markham et al, 1978), myricetin 3-O-b-D-glucoside (4) (Agrawal and Bansal, 1989), quercetin 3-O-(3 00 -O-acetyl)-a-L-rhamnoside (5) , quercetin 3-O-a-L-rhamnoside (6) Markham et al, 1978), quercetin 3-O-b-D-glucoside (7) (Markham et al, 1978), (Masuda et al, 1991), kaempferol 3-O-b-D-glucoside (9) (Markham et al, 1978) naringenin (10) (Zhang et al, 2003), (S)-naringenin 5-O-b-D-glucoside (11) (Zhang et al, 2003;Gaffield, 1970), 2 0 ,4 0 ,6 0 ,4-tetrahydroxy- (Zhang et al, 2003), b-sitosterol (13) (Goad, 1991), b-sitosterol palmitate (14) (Nielsen and Kofod, 1963), 24-methylenecholesterol palmitate (15) (Rashkes et al, 1990), 4a-methyl-5a-ergosta-7,24(28)-diene3b,4b-diol (16) (Greca et al, 1991), ethyl gallate (17) (Hussain et al, 1979), gallic acid (18) (Hussain et al, 1979), p-coumaric acid (19) (Ji et al, 2005), and 4-methoxybenzoic acid (20) (Gadgoli and Mishra, 1999) by comparison of their physical and spectroscopic data with literature values (see Supporting Information).…”
Section: Resultsmentioning
confidence: 99%