TY - JOUR
T1 - Chemotaxonomy in the Etlingera Genus from Sulawesi, Indonesia
T2 - Design and molecular docking of antioxidant marker
AU - Hamsidi, Rini
AU - Karmilah,
AU - Daud, Nur Saadah
AU - Malaka, Muhammad Hajrul
AU - Yodha, Agung Wibawa Mahatva
AU - Musdalipah,
AU - Arfan,
AU - Sahidin,
N1 - Publisher Copyright:
© 2024, Society for Indonesian Biodiversity. All rights reserved.
PY - 2024
Y1 - 2024
N2 - Etlingera is one of the important genera in the Zingiberaceae family because of its potential uses. Several studies have been conducted on the Genus Etlingera as nutraceuticals and drugs. Recently new species have been found in the Sulawesi Region, Indonesia, namely E. canarina A.D.Poulsen and E. echinulata A.D.Poulsen. Based on literature review through sciencedirect and springer link, both species unknown for their chemical and pharmacological content, so it is necessary to continue to reveal the deeper potential. The fruits of E. calophrys (K.Schum.) A.D.Poulsen, E. canarina and E. echinulata were extracted with methanol by maceration method. The chemical content of each extract was analyzed using a Liquid Chromatography Mass Spectrometer (LCMS). Antioxidant activity was tested based on the 1,1-Diphenyl-2-Picrylhydrazyl (DPPH) method. The ability as an antioxidant is proven by the molecul ar interactions of marker compounds in inhibiting xanthine oxidase. The secondary metabolites contained in the fruit extracts of E. calophrys, E. canarina and E. echinulata are E-p-Coumatic acid, 1,5-Dimethyl citrate, Trimethyl citrate, Crocetin, Tanshinone IIA, Ethinyl Estradiol, Yakuchinone B, Anisalacetone, Yakuchinone A, Nobilin, α-Estradiol, Momor-cerebroside I, Spinasterone, 12-Hydroxy-methyl abietate, Spinasterol, 2,3-Dihydroxypropyl oleate, 11-Octadecenoate acid methyl ester, Stigmastan-3,6-dione, β-Sitosterol-3-O-β-D-glucopyranoside, Trilaurin, 28-O-Hexahydrophthalate and Fasciculol C. Yakuchinone A and Yakuchinone B are chemotaxonomic marker compounds identified in all species. The antioxidant properties of each extract of 42.27±0.53, 46.59±0.81 and 35.66±0.73 mg/L have been proven by the molecular interactions of the marker compounds in their ability to act as xanthine oxidase inhibitors. The compounds Yakuchinone A and Yakuchinone B are thought to be responsible for the pharmacological activity of the species E. calophrys, E. canarina and E. echinulata. Yakuchinone A and Yakuchinone B are marker compounds because they are distributed in all samples.
AB - Etlingera is one of the important genera in the Zingiberaceae family because of its potential uses. Several studies have been conducted on the Genus Etlingera as nutraceuticals and drugs. Recently new species have been found in the Sulawesi Region, Indonesia, namely E. canarina A.D.Poulsen and E. echinulata A.D.Poulsen. Based on literature review through sciencedirect and springer link, both species unknown for their chemical and pharmacological content, so it is necessary to continue to reveal the deeper potential. The fruits of E. calophrys (K.Schum.) A.D.Poulsen, E. canarina and E. echinulata were extracted with methanol by maceration method. The chemical content of each extract was analyzed using a Liquid Chromatography Mass Spectrometer (LCMS). Antioxidant activity was tested based on the 1,1-Diphenyl-2-Picrylhydrazyl (DPPH) method. The ability as an antioxidant is proven by the molecul ar interactions of marker compounds in inhibiting xanthine oxidase. The secondary metabolites contained in the fruit extracts of E. calophrys, E. canarina and E. echinulata are E-p-Coumatic acid, 1,5-Dimethyl citrate, Trimethyl citrate, Crocetin, Tanshinone IIA, Ethinyl Estradiol, Yakuchinone B, Anisalacetone, Yakuchinone A, Nobilin, α-Estradiol, Momor-cerebroside I, Spinasterone, 12-Hydroxy-methyl abietate, Spinasterol, 2,3-Dihydroxypropyl oleate, 11-Octadecenoate acid methyl ester, Stigmastan-3,6-dione, β-Sitosterol-3-O-β-D-glucopyranoside, Trilaurin, 28-O-Hexahydrophthalate and Fasciculol C. Yakuchinone A and Yakuchinone B are chemotaxonomic marker compounds identified in all species. The antioxidant properties of each extract of 42.27±0.53, 46.59±0.81 and 35.66±0.73 mg/L have been proven by the molecular interactions of the marker compounds in their ability to act as xanthine oxidase inhibitors. The compounds Yakuchinone A and Yakuchinone B are thought to be responsible for the pharmacological activity of the species E. calophrys, E. canarina and E. echinulata. Yakuchinone A and Yakuchinone B are marker compounds because they are distributed in all samples.
KW - Chemotaxonomy
KW - Etlingera calophrys
KW - Etlingera canarina
KW - Etlingera echinulata
KW - Yakuchinone A and Yakuchinone B
UR - http://www.scopus.com/inward/record.url?scp=85185497887&partnerID=8YFLogxK
U2 - 10.13057/biodiv/d250202
DO - 10.13057/biodiv/d250202
M3 - Article
AN - SCOPUS:85185497887
SN - 1412-033X
VL - 25
SP - 449
EP - 457
JO - Biodiversitas
JF - Biodiversitas
IS - 2
ER -