Research Article

Antibacterial Activity of Chalcone and Dihydrochalcone Compounds from Uvaria chamae Roots against Multidrug-Resistant Bacteria

Table 3

Identified compounds within the antimicrobial fractions.

Retention Time
(min)
λ max
(nm)
Observed m/z
[M-H]-
Identified structures Mass error
(ppm)
Matched Fragments Observed CCS
2)
ChemspiderID

5.14330375.1235“Uvaretin chalcone form”
(2E)-1-[2,4-Dihydroxy-3-(2-hydroxybenzyl)-6methoxyphenyl]-3-phenyl-2-propen-1-one
0.115193.621375497

5.20325375.1237“iso-Uvaretin chalcone form”
(2E)-1-[4,6-Dihydroxy-3-(2-hydroxybenzyl)-2methoxyphenyl]-3-phenyl-2-propen-1-one
- 0.112190.5

5.28-271.0971Uvangoletin- 1.03166.54984098

5.57325361.1082Chamanetin0.711184.310305898

5.76330361.108iso-Chamanetin1.010189.310305892

5.80325377.1393iso-Uvaretin (Chamuvaritin II)0.921191.7133675

5.99339481.1653“Diuvaretin chalcone form”
(2E)-1-[2,4-Dihydroxy-3,5-bis(2-hydroxybenzyl)-6methoxyphenyl]-3-phenyl-2-propen-1-one
- 0.226219.1

6.20330377.1391Uvaretin0.115195.566150

6.40330467.1498Dichamanetin0.114215.29894419

6.70339483.1812Diuvaretin0.221213.62342170

structure deposited in Chemspider and Pubchem.