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International Journal of Phytomedicine and Phytotherapy

Table 3 Isolated and identified compounds in Acrostichum aureum

From: Acrostichium aureum Linn: traditional use, phytochemistry and biological activity

S/N

Constituent

Phytochemical Class

Plant

Part

Extracting Solvent

Method of analysis

Reference

i.

Ponasterone

Sterol

WP

Ethanol

GLC, HPLC, NMR, MS

[54, 55]

ii.

Quercetin-3-O-β-D-glucoside

Flavonoid

WP

Methanol

GLC, HPLC, NMR, MS

[12, 54]

iii.

Quercetin-3-O-β-D-glucosyl (6 → 1)-α-L-rhamnoside

Flavonoid

WP

Methanol

HPLC, NMR, MS

[12]

iv.

Quercetin-3-O-α-L-rhamnoside

Flavonoid

WP

Methanol

HPLC,NMR,MS

[12]

v.

Quercetin-3-O-α-L-rhamnosyl-7-O-β-D-glucoside

Flavonoid

WP

Methanol

HPLC, NMR, MS

[12]

vi.

Pterosterone

Sterol

WP

Ethanol

HPLC

[55]

vii.

Kaempferol

Flavonoid

WP

Methanol

HPLC,NMR,MS

[12, 55]

viii.

Quercetin

Flavonoid

WP

Ethanol

HPLC, NMR, MS

[55]

ix.

2-Butanone

Ketone

WP

Ethanol

HPLC

[55]

x.

2 -(methoxycarbonyl)-5-methyl pentyl 2′-methylhexyl phthalate

Phthalate

L

Methanol

RP-HPLC, NMR

HR ESI-MS, FT-IR

[7]

xi.

Patriscabratine

Phenylalanine and derivatives

L

Methanol

HPLC, NMR, MS

[12]

xii.

Tetracosane

Alkane

L

Methanol

HPLC,NMR, MS

[12]

xiii.

(2S,3S)-Pterosin C

Terpenoid

WP

Methanol

HPLC, UV, FT-IR, NMR

[47]

xiv.

(2R)-Pterosin P

Terpenoid

WP

Methanol

HPLC, UV, FT-IR, NM

[47]

xv.

(2S,3S)-Sulphated pterosin C

Terpenoid

WP

Methanol

HPLC, UV, FT-IR, NMR

[47]

xvi.

(2R,3S)-Sulphated pterosin C

Terpenoid

WP

Methanol

HPLC, UV, FT-IR, NMR

[47]

xvii.

Cycloartanol

Sterol

L

Methanol & Dichloromethane

GCMS

[6]

xviii.

24-Methylene cycloartanol

Sterol

L

Methanol & Dichloromethane

GCMS

[6]

xix.

Stigmasterol

Sterol

L

Methanol & Dichloromethane

GCMS

[6]

xx.

γ-Sitosterol

Sterol

L

Methanol & Dichloromethane

GCMS

[6]

xxi.

Campesterol

Sterol

L

Methanol & Dichloromethane

GCMS

[6]

xxii.

β-sitosterol

Sterol

L&R

n-hexane

GCMS

[52]

xxiii.

Taraxerol

Triterpenoid

L&R n-hexane

GCMS

[52]

 

xxiv.

β-amyrin

Triterpenoid

L&R

n-hexane

GCMS

[52]

xxv.

Germanicol

Triterpenoid

L&R

n-hexane

GCMS

[52]

xxvi.

Lupenone

Triterpenoid

L&R

n-hexane

GCMS

[52]

xxvii.

Betulin

Triterpenoid

R

n-hexane

GCMS

[52]

xxviii.

Lupeol

Triterpenoid

L&R

n-hexane

GCMS

[52]

xxix.

α-amyrin

Triterpenoid

L&R

n-hexane

GCMS

[52]

xxx.

Cholesterol

Triterpenoid

L&R

-hexane

GCMS

[52]

xxxi.

Phytol

Triterpenoid

L&R

n-hexane

GCMS

[52]

xxxii.

Squalene

Triterpinoid

L&R

n-hexane

GCMS

[52]

xxxiii.

Nicotinic acid glucoside

Nicotinamide

L

 

Radiolabeling & TLC

[56]

xxxiv.

Glucose

Monosaccarides

G

Hydro-ethanol

GCFID

[57]

xxxv.

Sucrose

Dissacrharides

G

Hydro-ethanol

GCFID

[57]

xxxvi.

myo-inositol

Cyclitol

G

Hydro-ethanol

GCFID

[57]

xxxvii.

D-chiro-inositol

Cyclitol

G

Hydro-ethanol

GCFID

[57]

xxxviii.

D-ononitol

Cyclitol

G

Hydro-ethanol

GCFID

[57]

xxxix.

D-1-O-methyl-muco-inositol

Cyclitol

G

Hydro-ethanol

GCFID

[57]

xl.

D-pinitol

Cyclitol

G

Hydro-ethanol

GCFID

[57]

xli.

4-(3′-O-sulfate-4′-hydroxy phenyl)-2-(R)-butanol

Phenolic sulfate

AP

Methanol

CC, NMR, HR ESI-MS

[4]

xlii.

Dihydrodehydrodiconiferyl alcohol 9-O-sulfate

Phenolic sulfate

AP

Methanol

CC, NMR, HR ESI-MS

[4]

xliii.

4-(3′-O-sulfate-4′-hydroxy phenyl)-2-butanone

Phenolic sulfate

AP

Methanol

CC, NMR, HR ESI-MS

[4]

xliv.

(+)-pinoresinol-4-O-glucoside

Phenol

AP

Methanol

CC, NMR, HR ESI-MS

[4]

xlv.

Dihydrodehydrodiconiferyl alcohol-4-O-glucoside

Phenol

AP

Methanol

CC, NMR, HR ESI-MS

[4]

xlvi.

(+)-isolarisiresinol-9-O-sulfate

Phenolic sulfate

AP

Methanol

CC, NMR, HR ESI-MS

[4]

xlvii.

(+)-pinoresinol-4-O-sulfate

Phenolic sulfate

AP

Methanol

CC, NMR, HR ESI-MS

[4]

xlviii.

Isotachioside

Phenol

AP

Methanol

CC, NMR, HR ESI-MS

[4]

  1. Keys; CC Column chromatography, HPLC High performance liquid chromatography, NMR Nuclear magnetic resonance, MS Mass spectrometry, HR-ESI-MS High resolution electrospray ionization mass spectroscopy, GCFID Gas chromatography-Flame ionization detector, R Roots, L Leaves, AP Area part, WP Whole plant, RP-HPLC Reverse-phase HPLC, FT-IR Fourier-transformed infrared spectroscopy, UV Ultraviolet, TLC Thin layer chromatography, GCMS Gas chromatography-mass spectrometry, G Gametophyte