Stenochlaena palustris, also known as choại in Vietnamese and dilimán or hagnaya in Tagalog, is a type of edible medicinal fern. It is commonly used in folk medicine in India and Malaysia to treat fever, skin diseases, ulcers, and stomachaches. This long-climbing fern has pinnate fronds, thin black scales, and stems that can grow up to 20 meters. Its leaves, which are 30-100 cm long, have been found to have antibacterial properties. The fern also exhibits antifungal, antioxidant, and antiglucosidase activities. In the Philippines, the district of Diliman in Quezon City is named after this fern, and its species name, palustris, means "of the marsh" in Latin, reflecting its common habitat. In Malaysia, the fern is known as "Midin" and is a popular food, often served stir-fried with garlic, dry shrimps, or shrimp paste. In Sabah, it is called "Lembiding" and is commonly cooked with sardines or belacan. In Vietnam, the young fronds, known as đọt choại, are used in soups, salads,

Synonyms Top

Scientific name	Authority	First published in
Chrysodium palustre	Luerss.	Fil. Graeff. : 73 (1871)
Onoclea scandens	Sw.	Syn. Fil. : 112, 309 (1806)
Stenochlaena blumeana	C.Presl	Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 6: 163 (1851)
Stenochlaena fraxinifolia	C.Presl	Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 6: 164 (1851)
Stenochlaena laurifolia	C.Presl	Epimel. Bot. 164. 1851; NPfl. 252 (1849)
Polypodium palustre	Burm.f.	Fl. Ind. : 234 (1768)
Polypodium palustre	(Raddi) Lowe	Ferns 2, t. 45 1858
Stenochlaena hainanensis	Ching & P.S.Chiu	Acta Phytotax. Sin. 9: 364. 1964. (1964)
Lomariopsis palustris	(Burm.f.) Kuhn	Ann. Mus. Bot. Lugduno-Batavi 4: 294. 1869
Acrostichum palustre	C.B.Clarke	Trans. Linn. Soc. London, Bot. 1(8): 577. 1880 [Apr 1880]
Lomaria scandens	Willd.	Sp. Pl., ed. 4 , 5: 293 (1810)
Stenochlaena scandens	(Raddi) J.Sm.	J. Bot. (Hooker) 3: 401 (1841)
Olfersia scandens	C.Presl	Tent. Pterid. 235 (1836)
Pteris scandens	Roxb.	Calcutta J. Nat. Hist. 4: 505 (1844)
Lomariopsis scandens	Mett.	Fil. Hort. Bot. Lips. : 22 (1856)
Lomaria juglandifolia	C.Presl	Reliq. Haenk. 1: 52 (1825)
Lomaria haenkeana	C.Presl	Reliq. Haenk. 1: 53 (1825)
Lomaria scandens	Hook.f. & Baker	Syn. Fil. 182 1868

Common names Top

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Filter by language:

Language	Common/alternative name
bjn	kalakai
Indonesian	lemidi
mad	lambhibing
min	paku limbèh
su	paku hurang
Thai	ลำเท็ง
Tonga	pasivaka
Chinese	光叶藤蕨

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland
  - Western Australia

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
- Southwestern Pacific
  - Fiji
  - Samoa
  - Tonga
  - Wallis-Futuna Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001115653
Tropicos	26610182
INPN	822880
KEW	urn:lsid:ipni.org:names:17223880-1
The Plant List	tro-26610182
Open Tree Of Life	740359
NCBI Taxonomy	32079
IPNI	17223880-1
iNaturalist	346621
GBIF	4079023
EPPO	STKPA
USDA GRIN	403593
Wikipedia	Stenochlaena_palustris

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Dataset of physical properties of histosols topsoils effected by wildfire in Indonesia

Taufik M, Santikaysa IP, Haikal M, Widyastuti MT, Arif C

Data Brief

27-Feb-2024

PMCID:	PMC10964053
doi:	10.1016/j.dib.2024.110257
PMID:	38533113

A comprehensive review on Nepalese wild vegetable food ferns

Bajracharya GB, Bajracharya B

Heliyon

19-Nov-2022

PMCID:	PMC9699988
doi:	10.1016/j.heliyon.2022.e11687
PMID:	36444246

Unveiling Natural and Semisynthetic Acylated Flavonoids: Chemistry and Biological Actions in the Context of Molecular Docking

El-Kersh DM, Abou El-Ezz RF, Fouad M, Farag MA

Molecules

26-Aug-2022

PMCID:	PMC9458193
doi:	10.3390/molecules27175501
PMID:	36080269

Chemistry and Bioactivity of Microsorum scolopendria (Polypodiaceae): Antioxidant Effects on an Epithelial Damage Model

Balada C, Díaz V, Castro M, Echeverría-Bugueño M, Marchant MJ, Guzmán L

Molecules

25-Aug-2022

PMCID:	PMC9457714
doi:	10.3390/molecules27175467
PMID:	36080235

Phylotranscriptomics Illuminates the Placement of Whole Genome Duplications and Gene Retention in Ferns

Pelosi JA, Kim EH, Barbazuk WB, Sessa EB

Front Plant Sci

14-Jul-2022

PMCID:	PMC9330400
doi:	10.3389/fpls.2022.882441
PMID:	35909764

Paleoenvironment reconstruction and peat-forming conditions of Neogene paralic coal sequences from Mukah, Sarawak, Malaysia

Zainal Abidin NS, Mustapha KA, Abdullah WH, Konjing Z

Sci Rep

25-May-2022

PMCID:	PMC9132988
doi:	10.1038/s41598-022-12668-6
PMID:	35614089

Anthocyanins in Chronic Diseases: The Power of Purple

Panchal SK, John OD, Mathai ML, Brown L

Nutrients

23-May-2022

PMCID:	PMC9142943
doi:	10.3390/nu14102161
PMID:	35631301

In vitro α-glucosidase inhibitory activity of Tamarix nilotica shoot extracts and fractions

Daou M, Elnaker NA, Ochsenkühn MA, Amin SA, Yousef AF, Yousef LF

PLoS One

14-Mar-2022

PMCID:	PMC8920278
doi:	10.1371/journal.pone.0264969
PMID:	35286313

A review of Fasciolopsis buski distribution and control in Indonesia

Ridha MR, Indriyati L, Andiarsa D, Wardhana AH

Vet World

26-Oct-2021

PMCID:	PMC8654757
doi:	10.14202/vetworld.2021.2757-2763
PMID:	34903937

Selected physical and chemical properties of soil under different agricultural land-use types in Ile-Ife, Nigeria

Akinde BP, Olakayode AO, Oyedele DJ, Tijani FO

Heliyon

28-Sep-2020

PMCID:	PMC7527570
doi:	10.1016/j.heliyon.2020.e05090
PMID:	33024867

Vascular Epiphytic Medicinal Plants as Sources of Therapeutic Agents: Their Ethnopharmacological Uses, Chemical Composition, and Biological Activities

Nugraha AS, Triatmoko B, Wangchuk P, Keller PA

Biomolecules

24-Jan-2020

PMCID:	PMC7072150
doi:	10.3390/biom10020181
PMID:	31991657

Aligning conservation efforts with resource use around protected areas

Velho N, DeFries RS, Tolonen A, Srinivasan U, Patil A

Ambio

13-Jun-2018

PMCID:	PMC6346598
doi:	10.1007/s13280-018-1064-5
PMID:	29949080

Identification of Potential Anticancer Protein Targets in Cytotoxicity Mediated by Tropical Medicinal Fern Extracts

Tan ST, Ong HC, Chai TT, Wong FC

Pharmacogn Mag

10-Apr-2018

PMCID:	PMC5909320
doi:	10.4103/pm.pm_282_17
PMID:	29720836

A review of the use of pteridophytes for treating human ailments

Baskaran XR, Geo Vigila AV, Zhang SZ, Feng SX, Liao WB

J Zhejiang Univ Sci B

01-Feb-2018

PMCID:	PMC5833325
doi:	10.1631/jzus.B1600344
PMID:	29405039

Large-scale phylogenomic analysis resolves a backbone phylogeny in ferns

Shen H, Jin D, Shu JP, Zhou XL, Lei M, Wei R, Shang H, Wei HJ, Zhang R, Liu L, Gu YF, Zhang XC, Yan YH

Gigascience

24-Nov-2017

PMCID:	PMC5795342
doi:	10.1093/gigascience/gix116
PMID:	29186447

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2S,3S)-2,4,4-trimethyl-3-[(E,3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one	162943036	Click to see CC1C(C(CCC1=O)(C)C)C=CC(C)OC2C(C(C(C(O2)CO)O)O)O	372.50	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
2,4,4-Trimethyl-3-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one	162943035	Click to see CC1C(C(CCC1=O)(C)C)C=CC(C)OC2C(C(C(C(O2)CO)O)O)O	372.50	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(4R,5S)-3,3,5-trimethyl-4-[(Z,2S,5R,13R)-5,9,10-trimethyl-8-oxo-2,13-bis[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]tetradec-9-en-5-yl]cyclohexan-1-one	162978002	Click to see CC1CC(=O)CC(C1C(C)(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)CCC(=O)C(=C(C)CCC(C)OC3C(C(C(C(O3)CO)O)O)O)C)(C)C	746.90	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
(4S,5R)-3,3,5-trimethyl-4-[(Z,2R,5S,13R)-5,9,10-trimethyl-8-oxo-2,13-bis[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]tetradec-9-en-5-yl]cyclohexan-1-one	162978001	Click to see CC1CC(=O)CC(C1C(C)(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)CCC(=O)C(=C(C)CCC(C)OC3C(C(C(C(O3)CO)O)O)O)C)(C)C	746.90	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
3,3,5-Trimethyl-4-[5,9,10-trimethyl-8-oxo-2,13-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]tetradec-9-en-5-yl]cyclohexan-1-one	162978000	Click to see CC1CC(=O)CC(C1C(C)(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)CCC(=O)C(=C(C)CCC(C)OC3C(C(C(C(O3)CO)O)O)O)C)(C)C	746.90	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Lutein	5281243	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CC(CC2(C)C)O)C)C)C	568.90	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids
Longan cerebroside II	132487837	Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	826.20	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids / Simple glycosylceramides / Glycosyl-N-acylsphingosines
2-hydroxy-N-[3-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]tetracosanamide	163068484	Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	826.20	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	154496016	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
3-[[1-(4-Aminobutylamino)-1-oxo-3-phenylpropan-2-yl]carbamoyl]oxirane-2-carboxylic acid	19423296	Click to see C1=CC=C(C=C1)CC(C(=O)NCCCCN)NC(=O)C2C(O2)C(=O)O	349.40	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles / Pyrrolocarbazoles / Indolocarbazoles
(2S,3R,6R)-3-methoxy-2-methyl-29-oxa-1,7,17-triazaoctacyclo[12.12.2.12,6.07,28.08,13.015,19.020,27.021,26]nonacosa-8,10,12,14,19,21,23,25,27-nonaene-4,16-dione	10647233	Click to see CC12C(C(=O)CC(O1)N3C4=CC=CC=C4C5=C6C(=C7C8=CC=CC=C8N2C7=C53)CNC6=O)OC	451.50	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole-3-carboxaldehyde	10256	Click to see C1=CC=C2C(=C1)C(=CN2)C=O	145.16	unknown	https://doi.org/10.1016/S0031-9422(98)00352-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-2-[[(E)-3-[4-[(1R,2R)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]prop-2-enoyl]oxymethyl]-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxyoxan-4-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate	163000409	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)OC(CO)C(C7=CC(=C(C=C7)O)OC)O	966.90	unknown	https://doi.org/10.1021/NP980179F
[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-4-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	10795089	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	740.70	unknown	https://doi.org/10.1021/NP980179F
[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-4-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (Z)-3-(4-hydroxyphenyl)prop-2-enoate	10628812	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	740.70	unknown	https://doi.org/10.1021/NP980179F
[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-4-[3-(4-hydroxyphenyl)prop-2-enoyloxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	162964002	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	740.70	unknown	https://doi.org/10.1021/NP980179F
[(2R,3R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-4-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	163186936	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	740.70	unknown	https://doi.org/10.1021/NP980179F
[(2S,3R,4S,5R,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxan-4-yl] 3-(4-hydroxyphenyl)prop-2-enoate	162987625	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	770.70	unknown	https://doi.org/10.1021/NP980179F
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	57369598	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP980179F
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-4-[3-(4-hydroxyphenyl)prop-2-enoyloxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	73109025	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	740.70	unknown	https://doi.org/10.1021/NP980179F
Kaempferol 3-(3,6-di-p-coumaroylglucoside)	10032927	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	740.70	unknown	https://doi.org/10.1021/NP980179F
kaempferol 3-O-(3"-O-p-coumaroyl, 6"-O-feruloyl)-glucoside	21672200	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	770.70	unknown	https://doi.org/10.1021/NP980179F
Stenopalustroside B	10581033	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O	770.70	unknown	https://doi.org/10.1021/NP980179F
Stenopalustroside E	10724604	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)OC(CO)C(C7=CC(=C(C=C7)O)OC)O	966.90	unknown	https://doi.org/10.1021/NP980179F
Tiliroside	5320686	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP980179F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP980179F
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP980179F
kaempferol 3-O-(3"-O-p-coumaroyl)-glucoside	21672201	Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(OC(C2O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O	594.50	unknown	https://doi.org/10.1021/NP980179F

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Stenochlaena palustris

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