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Microlepia marginata

Microlepia marginata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64404c512f836110980585
Scientific name Microlepia marginata
Authority (Panz.) C.Chr.
First published in Index Filic. 4: 212. 1905 ; & Index Filic. 7: 427. 1906

Description Top

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Synonyms Top

Scientific name Authority First published in
Davallia puberula Wall. Numer. List : n.° 262 (1829)
Davallia pyramidata Wall. Numer. List : n.° 261 (1829)
Davallia roxburghii Wall. Numer. List : n.° 2218 (1830)
Davallia sieboldiana Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 180 (1867)
Davallia scabra D.Don Prodr. Fl. Nepal. 9. 1825 (1825)
Polypodium marginatum Panz. Vollst. Pflanzensyst. 13(1): 199 (1786)
Dicksonia marginalis Sw. J. Bot. (Schrader) 1800(2): 92 (1801)
Davallia marginalis Baker Syn. Fil. : 452 (1868)
Microlepia marginalis Bedd. Ferns Brit. India , Correct.: t. 102 (1870)
Microlepia scabra J.Sm. London J. Bot. 1: 427 (1842)
Microlepia villosa C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 6: 95 (1851)
Nephrodium ciliatum Desv. Mém. Soc. Linn. Paris 6(3): 257 (1827)
Microlepia caudipinnata B.S.Wang Acta Sci. Nat. Univ. Sunyatseni 1961(2): 43 (1961) (1961)
Microlepia marginata var. jinfoshanensis Ching & Z.Y.Liu Bull. Bot. Res., Harbin 3(4): 23 (1983)

Common names Top

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Language Common/alternative name
Japanese フモトシダ
Chinese 华南鳞盖蕨
Chinese 边缘鳞盖蕨
Chinese 邊緣鱗蓋蕨
Chinese 边缘鳞蕨

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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Name Authority First published in
Microlepia marginata f. yakusimensis (H.Itô) Sa.Kurata Enum. Jap. Pterid. 266, 343 1961

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001107360
Tropicos 26600225
KEW urn:lsid:ipni.org:names:17148560-1
The Plant List tro-26600225
Open Tree Of Life 877001
NCBI Taxonomy 749682
IPNI 1113655-2
iNaturalist 371752
GBIF 7265907
EPPO MIEMA
EOL 6092057
CMAUP NPO15880

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
“Diminishing returns” and leaf area-biomass scaling of ferns in subtropical ecosystems Chen S, Li J, Sun J, Zhong Q, Hu D, Cheng D Front Plant Sci 27-Jun-2023
PMCID:PMC10333482
doi:10.3389/fpls.2023.1187704
PMID:37441171
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Biogeochemical niche conservatism relates to plant species diversification and life form evolution in a subtropical montane evergreen broad‐leaved forest Bai K, Zhou X, Lv S, Wei S, Deng L, Tan Y Ecol Evol 03-Dec-2022
PMCID:PMC9719084
doi:10.1002/ece3.9587
PMID:36479033
Untying the Gordian knot of plastid phylogenomic conflict: A case from ferns Wang T, Li TZ, Chen SS, Yang T, Shu JP, Mu YN, Wang KL, Chen JB, Xiang JY, Yan YH Front Plant Sci 24-Nov-2022
PMCID:PMC9730426
doi:10.3389/fpls.2022.918155
PMID:36507421
Plastome phylogenomic analysis reveals evolutionary divergences of Polypodiales suborder Dennstaedtiineae Lu JM, Du XY, Kuo LY, Ebihara A, Perrie LR, Zuo ZY, Shang H, Chang YH, Li DZ BMC Plant Biol 02-Nov-2022
PMCID:PMC9628275
doi:10.1186/s12870-022-03886-1
PMID:36319964
HAG1 and SWI3A/B control of male germ line development in P. patens suggests conservation of epigenetic reproductive control across land plants Genau AC, Li Z, Renzaglia KS, Fernandez Pozo N, Nogué F, Haas FB, Wilhelmsson PK, Ullrich KK, Schreiber M, Meyberg R, Grosche C, Rensing SA Plant Reprod 11-Apr-2021
PMCID:PMC8128824
doi:10.1007/s00497-021-00409-0
PMID:33839924
Chemical and Chemotaxonomical Studes of Ferns. LXXXIII. Constituent Variation of Microlepia Marginata Nobutoshi TANAKA, Kazuo KOBAYASHI, Chie OBATA, Yumi NOSE, Hiroshi WADA, Jiro ENDO, Teruko NAKAMURA, Takao MURAKAMI, Yasuhisa SAIKI Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.113.1_70
Nitrogen Addition Altered the Effect of Belowground C Allocation on Soil Respiration in a Subtropical Forest He T, Wang Q, Wang S, Zhang F PLoS One 23-May-2016
PMCID:PMC4877084
doi:10.1371/journal.pone.0155881
PMID:27213934
The fern-feeder aphids (Hemiptera: Aphididae) from China: a generic account, descriptions of one new genus, one new species, one new subspecies, and keys Su XM, Jiang LY, Qiao GX J Insect Sci 01-Jan-2014
PMCID:PMC4199544
doi:10.1093/jis/14.1.23
PMID:25373170
[Chemical and chemotaxonomical studies of ferns. LXXXV. Constituent variation of Microlepia marginata (2)]. Wada H, Daidouji K, Fuchino H, Endo J, Nakamura T, Tanaka N, Murakami T, Saiki Y Yakugaku Zasshi 01-Jan-1994
doi:10.1248/YAKUSHI1947.114.1_27
PMID:8133456

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
7-(1,2-Dihydroxyethyl)-2-hydroxy-1,1,4a,7-tetramethyl-2,4,4b,5,6,8,10,10a-octahydrophenanthren-3-one 5317421 Click to see CC1(C2CC=C3CC(CCC3C2(CC(=O)C1O)C)(C)C(CO)O)C 336.50 unknown via CMAUP database
7-(1,2-dihydroxyethyl)-3-hydroxy-1,1,4a,4b,7-pentamethyl-6,8,10,10a-tetrahydro-5H-phenanthren-2-one 5317422 Click to see CC1(C2CC=C3CC(CCC3(C2(C=C(C1=O)O)C)C)(C)C(CO)O)C 348.50 unknown via CMAUP database
7-(1,2-Dihydroxyethyl)-3-hydroxy-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydrophenanthren-2-one 5317420 Click to see CC1(C2CC=C3CC(CCC3C2(CC(C1=O)O)C)(C)C(CO)O)C 336.50 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
Fumotoshidin A 192228 Click to see CC1(C2CC=C3CC(CCC3C2(CC(C1=O)O)C)(C)C(CO)O)C 336.50 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(+)-alpha-Funebrene 6552024 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4R,5S,6R)-2-[[(14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methoxy]-6-(hydroxymethyl)-5-methoxyoxane-3,4-diol 11968771 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)COC5C(C(C(C(O5)CO)OC)O)O 498.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
https://doi.org/10.1248/YAKUSHI1947.113.1_70
(2R,3R,4R,5S,6R)-2-[[(1S,4S,5R,9S,10R,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methoxy]-6-(hydroxymethyl)-5-methoxyoxane-3,4-diol 101647902 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)COC5C(C(C(C(O5)CO)OC)O)O 498.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
https://doi.org/10.1248/YAKUSHI1947.113.1_70
(2R,3R,4R,5S,6R)-2-[[(1S,4S,5S,9S,10R,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methoxy]-6-(hydroxymethyl)-5-methoxyoxane-3,4-diol 101647903 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)COC5C(C(C(C(O5)CO)OC)O)O 498.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
https://doi.org/10.1248/YAKUSHI1947.113.1_70
(2R,3R,4R,5S)-2-[[(2R,4aS,4bR,7S,10aS)-7-[(1R)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-2-yl]oxy]-5-(hydroxymethyl)oxolane-3,4-diol 101938072 Click to see CC1(C(CCC2(C1CC=C3C2CCC(C3)(C)C(CO)O)C)OC4C(C(C(O4)CO)O)O)C 454.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
(2S,3R,4S,5R)-2-[[(2S,3S,4aR,4bS,7R,8aS)-7-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-ethenyl-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-3-yl]oxy]oxane-3,4,5-triol 101647899 Click to see CC1(C2CCC3=CC(C(CC3C2(CCC1OC4C(C(C(O4)CO)O)O)C)OC5C(C(C(CO5)O)O)O)(C)C=C)C 568.70 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
https://doi.org/10.1248/YAKUSHI1947.113.1_70
(2S,3R,4S,5R)-2-[[7-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-ethenyl-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-3-yl]oxy]oxane-3,4,5-triol 5319280 Click to see CC1(C2CCC3=CC(C(CC3C2(CCC1OC4C(C(C(O4)CO)O)O)C)OC5C(C(C(CO5)O)O)O)(C)C=C)C 568.70 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
https://doi.org/10.1248/YAKUSHI1947.113.1_70
[(3R,4R,5R,6S)-6-[[(2S,3S,4aR,4bS,7R,8aS)-7-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-ethenyl-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-3-yl]oxy]-4,5-dihydroxyoxan-3-yl] acetate 101647900 Click to see CC(=O)OC1COC(C(C1O)O)OC2CC3C(=CC2(C)C=C)CCC4C3(CCC(C4(C)C)OC5C(C(C(O5)CO)O)O)C 610.70 unknown https://doi.org/10.1248/YAKUSHI1947.113.1_70
https://doi.org/10.1248/YAKUSHI1947.114.1_27
[(3R,4R,5R,6S)-6-[[7-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-ethenyl-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-3-yl]oxy]-4,5-dihydroxyoxan-3-yl] acetate 5319281 Click to see CC(=O)OC1COC(C(C1O)O)OC2CC3C(=CC2(C)C=C)CCC4C3(CCC(C4(C)C)OC5C(C(C(O5)CO)O)O)C 610.70 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
https://doi.org/10.1248/YAKUSHI1947.113.1_70
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(17alpha,23E)-5alpha-Dammara-20,23-diene-3beta,25-diol 9955042 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CC=CC(C)(C)O)C)C)C 442.70 unknown via CMAUP database
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Yamogenin 441900 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
Marinobufagenin 11969465 Click to see CC12CCC(CC1(CCC3C2CCC4(C35C(O5)CC4C6=COC(=O)C=C6)C)O)O 400.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25R)-3beta-[4-O-[4-O-(alpha-L-Rhamnopyranosyl)-alpha-L-rhamnopyranosyl]-beta-D-glucopyranosyloxy]spirosta-5-ene 21603983 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21603986 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1 1015.20 unknown via CMAUP database
Borassoside A 16204068 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Borassoside B 102155844 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
Borassoside C 102155845 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
Borassoside D 16204180 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Borassoside E 16204181 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Borassoside F 16204183 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1 1015.20 unknown via CMAUP database
Collettinside III 10653210 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Disogluside 11827970 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1 576.80 unknown via CMAUP database
Methylprotodioscin 11263254 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown via CMAUP database
Progenin II 44429638 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Prosapogenin A 11061578 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Protodioscin 441891 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Pseudoprotodioscin 21637110 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1031.20 unknown via CMAUP database
Trigonelloside C 441899 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Yamogenin 3-O-neohesperidoside 441901 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Gal(a1-6)a-Man 11724912 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp 5287808 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-methoxy-6-[(1S,2S)-5-methyl-4-oxo-3,6-dioxabicyclo[3.1.0]hexan-2-yl]chromen-2-one 322884 Click to see CC12C(O1)C(OC2=O)C3=C(C=C4C(=C3)C=CC(=O)O4)OC 288.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-7-[(2S,3R,4S,5S,6S)-4-hydroxy-6-(hydroxymethyl)-5-methoxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 162949043 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)OC)O)O)O)O 594.60 unknown https://doi.org/10.1248/YAKUSHI1947.113.1_70
Fumotonaringin 42607924 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)OC)O)O)O)O 594.60 unknown https://doi.org/10.1248/YAKUSHI1947.114.1_27
https://doi.org/10.1248/YAKUSHI1947.113.1_70

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