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Lepisorus contortus

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644077e00e2a1124905671
Scientific name Lepisorus contortus
Authority Ching
First published in Bull. Fan Mem. Inst. Biol. 4: 90 (1933)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lepisorus khullarii P.C.Pande & H.C.Pande Ill. Fern Fl. Kumaon Himalaya 1: 67. 2003
Polypodium lineare var. contortum Christ Nuovo Giorn. Bot. Ital., n.s., 4(1): 98, pl. 1, f. 3 1897
Polypodium contortum Christ Bot. Gaz. 51: 347 (1911)
Pleopeltis contorta (Christ) Alston & Bonner Candollea 15: 209. 1956. (1956)
Polypodium lineare f. contortum (Christ) Takeda Notes Roy. Bot. Gard. Edinburgh 8(39): 270 1915
Lepisorus crassirhizoma Ching & Z.Y.Liu Bull. Bot. Res., Harbin 3(4): 3 (1983)
Lepisorus jinfoshanensis Ching Bull. Bot. Res., Harbin 3(4): 4 (1983)
Lepisorus nyalamensis Ching & S.K.Wu Fl. Xizang. 1: 311 (1983)

Common names Top

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Language Common/alternative name
Chinese 一皮草
Chinese 扭瓦韦
Chinese 扭瓦葦

Subspecies (abbr. subsp./ssp.) Top

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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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Myanmar
      • Thailand

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001117826
Tropicos 26612755
KEW urn:lsid:ipni.org:names:17336870-1
The Plant List tro-26612755
Open Tree Of Life 908691
NCBI Taxonomy 699669
IPNI 17336870-1
iNaturalist 976971
GBIF 4025651
EOL 6116082
CMAUP NPO19548

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
Assessing the potential of NS2B/NS3 protease inhibitors biomarker in curbing dengue virus infections: In silico vs. In vitro approach Norshidah H, Leow CH, Ezleen KE, Wahab HA, Vignesh R, Rasul A, Lai NS Front Cell Infect Microbiol 14-Feb-2023
PMCID:PMC9971573
doi:10.3389/fcimb.2023.1061937
PMID:36864886
Antiviral Properties of Polyphenols from Plants Chojnacka K, Skrzypczak D, Izydorczyk G, Mikula K, Szopa D, Witek-Krowiak A Foods 26-Sep-2021
PMCID:PMC8534698
doi:10.3390/foods10102277
PMID:34681326
On the spore ornamentation of the microsoroid ferns (microsoroideae, polypodiaceae) Chen CC, Liu HY, Chen CW, Schneider H, Hyvönen J J Plant Res 29-Nov-2020
PMCID:PMC7817562
doi:10.1007/s10265-020-01238-4
PMID:33251557
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
Structure activity relationship (SAR) and quantitative structure activity relationship (QSAR) studies showed plant flavonoids as potential inhibitors of dengue NS2B-NS3 protease Sarwar MW, Riaz A, Dilshad SM, Al-Qahtani A, Nawaz-Ul-Rehman MS, Mubin M BMC Struct Biol 19-Apr-2018
PMCID:PMC5909242
doi:10.1186/s12900-018-0084-5
PMID:29673347
Phenylethanoid Glycosides: Research Advances in Their Phytochemistry, Pharmacological Activity and Pharmacokinetics Xue Z, Yang B Molecules 29-Jul-2016
PMCID:PMC6273160
doi:10.3390/molecules21080991
PMID:27483229
Medicinal plants of Dagala region in Bhutan: their diversity, distribution, uses and economic potential Wangchuk P, Namgay K, Gayleg K, Dorji Y J Ethnobiol Ethnomed 24-Jun-2016
PMCID:PMC4921017
doi:10.1186/s13002-016-0098-7
PMID:27342801
Exploring the patterns of alpine vegetation of Eastern Bhutan: a case study from the Merak Himalaya Jamtsho K, Sridith K Springerplus 01-Jul-2015
PMCID:PMC4486651
doi:10.1186/s40064-015-1066-8
PMID:26155443
Bioactive compounds from the fern Lepisorus contortus. Yang JH, Kondratyuk TP, Jermihov KC, Marler LE, Qiu X, Choi Y, Cao H, Yu R, Sturdy M, Huang R, Liu Y, Wang LQ, Mesecar AD, van Breemen RB, Pezzuto JM, Fong HH, Chen YG, Zhang HJ J Nat Prod 25-Feb-2011
PMCID:PMC3069126
doi:10.1021/NP100373F
PMID:21261296
Bioactive Compounds from the Fern Lepisorus contortus Yang JH, Kondratyuk TP, Jermihov KC, Marler LE, Qiu X, Choi Y, Cao H, Yu R, Sturdy M, Huang R, Liu Y, Wang LQ, Mesecar AD, van Breemen RB, Pezzuto JM, Fong HH, Chen YG, Zhang HJ J Nat Prod 24-Jan-2011
PMCID:PMC3069126
doi:10.1021/np100373f
PMID:21261296

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives
Atrolactic acid 1303 Click to see CC(C1=CC=CC=C1)(C(=O)O)O 166.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Lignans, neolignans and related compounds
1-(4-Hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]propane-1,3-diol 193323 Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 376.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
threo-Guaiacylglycerol beta-coniferyl ether 14274761 Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 376.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
2-(5a,5b,8,8,11a,13b-Hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl)propan-2-ol 5245211 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)C)C 428.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
Diplopterol 164874 Click to see CC1(CCCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC5C(C)(C)O)C)C)C)C)C 428.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2R,6R,10R)-6,10,14-Trimethylpentadecane-2-ol 11032943 Click to see CC(C)CCCC(C)CCCC(C)CCCC(C)O 270.50 unknown via CMAUP database
(2s,6r,10r)-6,10,14-Trimethylpentadecan-2-ol 14550228 Click to see CC(C)CCCC(C)CCCC(C)CCCC(C)O 270.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
1-(alpha-d-Arabinofuranosyl)uracil 6604651 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
Spongouridine 18323 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2S,3S,4R)-4-methoxy-6-oxo-2-[(E,3S,5R,6S)-3,5,6-triacetyloxyhept-1-enyl]oxan-3-yl] acetate 101267306 Click to see CC(C(CC(C=CC1C(C(CC(=O)O1)OC)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 458.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3S,4R,5R,6S)-2-[2-(3,4-dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 124708093 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)O)O)O 316.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
2-(3,4-dihydroxyphenyl)-ethyl-O-beta-D-glucopyranoside 5316821 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)O)O)O 316.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 13845930 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)O)O)O 316.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3S,4R,5S,6S)-3-[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)oxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163190778 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[(2S,3R,4R,5S,6S)-5-[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,4-dihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163188452 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[(2S,3R,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 124708080 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[(2S,3S,4R,5S,6R)-5-[(2R,3R,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163193765 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=C(C=C3)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)(CO)O 594.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[(2S,3S,4R,5S,6R)-5-[(2S,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-4-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163189334 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[(2S,3S,4R,5S,6S)-5-[(2R,3S,4S)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxan-4-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163195486 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=C(C=C3)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)(CO)O 594.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-2-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-6-(hydroxymethyl)oxan-4-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 75605113 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxan-4-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 75605114 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=C(C=C3)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)(CO)O 594.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 75605035 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=C(C=C3)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)(CO)O 594.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,4-dihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 75605112 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-4-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 74976009 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 78380900 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
beta-(3,4-dihydroxyphenyl)ethyl-3-O-E-caffeoyl-O-[beta-D-apiofuranosyl-(1->2)]-beta-D-glucopyranoside 51042402 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)O)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
beta-(3,4-dihydroxyphenyl)ethyl-6-O-E-caffeoyl-O-[beta-D-apiofuranosyl-(1->2)]-beta-D-glucopyranoside 51042401 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
beta-(4-hydroxyphenyl)ethyl-4-O-E-caffeoyl-O-[beta-D-apiofuranosyl-(1->2)]-beta-D-glucopyranoside 51042201 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=C(C=C3)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)(CO)O 594.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
Calceolarioside B 5273567 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 478.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
Fucatoside A 44254697 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)(CO)O 610.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
Isoquercitin 10813969 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-3-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 15595749 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 478.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
2-(3,4-Dihydroxyphenyl)-5-hydroxy-3-methoxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 78393787 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 624.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
3',4',5,7-tetrahydroxy-3-methoxyflavone-7-O-alpha-L-rhamnopyranosyl-(1->6)-beta-D-glucopyranoside 5495544 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 624.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
4',5,7-trihydroxy-3-methoxyflavone-7-O-alpha-L-arabinofuranosyl(1->6)-beta-D-glucopyranoside 51042404 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC4C(C(C(O4)CO)O)O)O)O)O)C5=CC=C(C=C5)O 594.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
4',5,7-trihydroxy-3-methoxyflavone-7-O-beta-D-glucopyranoside 53317532 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 462.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
4',5,7-trihydroxy-3-methoxyflavone-7-O-rutinoside 53324084 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 608.50 unknown via CMAUP database
5-Hydroxy-2-(4-hydroxyphenyl)-3-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74978410 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 462.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
7-[6-[[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-3-methoxychromen-4-one 75605115 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC4C(C(C(O4)CO)O)O)O)O)O)C5=CC=C(C=C5)O 594.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
Transilin 15595751 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 478.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid 10394 Click to see C1=CC(=CC=C1CCC(=O)O)O 166.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069126/

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