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Cyperus alopecuroides

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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 UUID643ff4f39ce97334157407
Scientific name Cyperus alopecuroides
Authority Rottb.
First published in Descriptionum et Iconum Rariores et pro maxima parte Novas Plantas 1773

Description Top

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Synonyms Top

Scientific name Authority First published in
Chlorocyperus alopecuroides (Rottb.) Grossh. Fl. Kavkaza 1: 150 (1928)
Cyperus alopecuroides var. digynus Boeckeler Linnaea 36: 322 1870
Cyperus alopecuroides f. latifolius A.Peter ex Kük. Pflanzenr. IV, 20(101): 73 1935
Cyperus alopecuroides f. pallidiflorus (Peter) Kük. Pflanzenr. IV, 20(101): 72 1935
Cyperus bidentatus Poir. Encycl. 7: 250 (1806)
Cyperus compositus R.Br. Prodr. Fl. Nov. Holland. : 217 (1810)
Cyperus exaltatus var. digynus (Boeckeler) F.N.Williams Bull. Herb. Boissier II, 4: 224 1904
Cyperus fastigiatus Forssk. Fl. Aegypt.-Arab. : 14 (1775)
Cyperus glaucus Willd. ex Kunth Enum. Pl. 2: 20 (1837)
Cyperus glomeratus Willd. Sp. Pl., ed. 4 , 1: 277 (1797)
Cyperus poiretii Roem. & Schult. Syst. Veg., ed. 15 bis 2: 223 (1817)
Juncellus alopecuroides C.B.Clarke ex Hook.f. Fl. Brit. India [J. D. Hooker] 6(19): 595. 1893 [Sep 1893] ; et in Th. Dur. & Schinz, Consp. Fl. Afr. 5: 1894 (1895) 543
Juncellus pallidiflorus Peter Abh. Preuss. Akad. Wiss., Phys.-Math. Kl. , n.f., 13(2): 48 (1928)

Common names Top

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Language Common/alternative name
English fostail sedge
English foxtail flatsedge
English matsedge
Arabic سعد ثعلبي
Arabic كرش
Arabic علوب
Arabic سمار
Arabic سمار حلو
Hebrew גומא צפוף
Polish cibora wyczyńcowata

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

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-0000367563
Florida Plant Atlas 1291
USDA Plants CYAL6
Tropicos 9910145
INPN 629512
Flora of Italy 9181
KEW urn:lsid:ipni.org:names:303722-1
The Plant List kew-235580
Open Tree Of Life 3959380
Observations.org 199606
NCBI Taxonomy 1234173
IUCN Red List 164443
IPNI 129650-3
iNaturalist 370148
GBIF 2715045
EPPO CYPAO
EOL 1122179
USDA GRIN 402832
Wikipedia Cyperus_alopecuroides

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
Phytoremediation Perspectives of Seven Aquatic Macrophytes for Removal of Heavy Metals from Polluted Drains in the Nile Delta of Egypt Abdelaal M, Mashaly IA, Srour DS, Dakhil MA, El-Liethy MA, El-Keblawy A, El-Barougy RF, Halmy MW, El-Sherbeny GA Biology (Basel) 20-Jun-2021
PMCID:PMC8235055
doi:10.3390/biology10060560
PMID:34203088
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223
The fodder grass resources for ruminants: A indigenous treasure of local communities of Thal desert Punjab, Pakistan Shaheen H, Qureshi R, Qaseem MF, Bruschi P PLoS One 05-Mar-2020
PMCID:PMC7058357
doi:10.1371/journal.pone.0224061
PMID:32134935
Effects of methylated derivatives of Luteolin isolated from Cyperus alopecuroides in rat H4IIE hepatoma cells*. Michels G, Mohamed GA, Weber N, Chovolou Y, Kampkötter A, Wätjen W, Proksch P Basic Clin Pharmacol Toxicol 01-Feb-2006
doi:10.1111/J.1742-7843.2006.PTO_300.X
PMID:16445590
Phylogenetic Variation in the Silicon Composition of Plants HODSON MJ, WHITE PJ, MEAD A, BROADLEY MR Ann Bot 21-Sep-2005
PMCID:PMC4247092
doi:10.1093/aob/mci255
PMID:16176944
Sesquiterpenes from the essential oil of Cyperus alopecuroides Mesmin Mekem Sonwa, Wilfried A. König, Karl-Heinz Kubeczka, Otakar Motl Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00154-4
A benzoquinone and flavonoids from Cyperus alopecuroides. Nassar MI, Abdel-Razik AF, El-Khrisy Eel-D, Dawidar AA, Bystrom A, Mabry TJ Phytochemistry 01-Jun-2002
doi:10.1016/S0031-9422(02)00060-2
PMID:12031430
Constituents of the essential oil of Cyperus alopecuroides. Sonwa MM, König WA Phytochemistry 01-Feb-2001
doi:10.1016/S0031-9422(00)00374-5
PMID:11249094

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1R,2R,5R,6R,8S)-1,5,9-trimethyltricyclo[6.2.2.02,6]dodec-9-ene 154497378 Click to see CC1CCC2C1CC3CCC2(C=C3C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1R,2R,5R,7Z)-7-ethylidene-1,2,8,8-tetramethylbicyclo[3.2.1]octane 154496428 Click to see CC=C1CC2CCC(C1(C2(C)C)C)C 192.34 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1S,2S,5R,6S,8R)-1,5,9-trimethyltricyclo[6.2.2.02,6]dodec-9-ene 162999184 Click to see CC1CCC2C1CC3CCC2(C=C3C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
7-Ethylidene-1,2,8,8-tetramethylbicyclo[3.2.1]octane 85740510 Click to see CC=C1CC2CCC(C1(C2(C)C)C)C 192.34 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
Cyprotene 91715050 Click to see CC=C1CC2CCC(C1(C2(C)C)C)C 192.34 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
Rotundene 25203405 Click to see CC1CCC2C1CC3CCC2(C=C3C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
https://doi.org/10.1016/S0031-9422(97)00154-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
(1R,3aS,5Z,9E,12aR)-3a,6,10-trimethyl-1-prop-1-en-2-yl-2,3,4,7,8,11,12,12a-octahydro-1H-cyclopenta[11]annulene 162870937 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)C(=C)C)C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1S,3aR,5E,9Z,12aS)-3a,6,10-trimethyl-1-prop-1-en-2-yl-2,3,4,7,8,11,12,12a-octahydro-1H-cyclopenta[11]annulene 162870934 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)C(=C)C)C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1S,3aR,5Z,9E,12aS)-3a,6,10-trimethyl-1-prop-1-en-2-yl-2,3,4,7,8,11,12,12a-octahydro-1H-cyclopenta[11]annulene 162870935 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)C(=C)C)C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
3a,6,10-trimethyl-1-prop-1-en-2-yl-2,3,4,7,8,11,12,12a-octahydro-1H-cyclopenta[11]annulene 74819481 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)C(=C)C)C)C 272.50 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Cyperene 12308843 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1R,2S,6S,7S,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 50919054 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1R,7R,10R)-10,11,11-trimethyltricyclo[5.3.1.01,5]undec-4-ene-4-carbaldehyde 101701628 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C=O 218.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(1S,7R,10S)-4,10,11,11-tetramethyltricyclo[5.3.1.01,5]undeca-2,4-diene 157876041 Click to see CC1CCC2CC3=C(C=CC13C2(C)C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(2R,4aS)-4a,8-Dimethyl-2-(prop-1-en-2-yl)-1,2,3,4,4a,5-hexahydronaphthalene 73015594 Click to see CC1=C2CC(CCC2(CC=C1)C)C(=C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
(3aS,4R,7R)-1,4,9,9-Tetramethyl-5,6,7,8-tetrahydro-4H-3a,7-methanoazulene 74819450 Click to see CC1CCC2CC3=C(C=CC13C2(C)C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
(E)-calamenene 12302242 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
1,4,4a,5,6,7,8,8aalpha-Octahydro-1-methylene-4abeta-methyl-7beta-(1-methylethenyl)naphthalene 12011811 Click to see CC(=C)C1CCC2(CC=CC(=C)C2C1)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
10,11,11-Trimethyltricyclo[5.3.1.01,5]undec-4-ene-4-carbaldehyde 14036824 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C=O 218.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
2,4,11-Eudesmatriene 11571984 Click to see CC1=C2CC(CCC2(CC=C1)C)C(=C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
8a-Methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,8-hexahydronaphthalene 163081583 Click to see CC(=C)C1CCC2(CC=CC(=C)C2C1)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
alpha-Cubebene 442359 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
Cyperene 99856 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
https://doi.org/10.1016/S0031-9422(97)00154-4
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
Patchoula-2,4-diene 42608161 Click to see CC1CCC2CC3=C(C=CC13C2(C)C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
trans-Calamenene 6429022 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(-)-delta-Selinene 12308845 Click to see CC1=C2C=C(CCC2(CCC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
(+)-4,11-Eudesmadien-3-one 273568 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol 14076604 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(2R,4aS,7R)-4a-methyl-1-methylidene-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-2-ol 44576209 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(2R,4aS,7S)-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydro-2H-naphthalen-2-ol 154496427 Click to see CC1=C2CC(CCC2(CCC1O)C)C(=C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(3R,4aR,8aR)-5,8a-dimethyl-3-prop-1-en-2-yl-1,2,3,4,7,8-hexahydronaphthalen-4a-ol 12011812 Click to see CC1=CCCC2(C1(CC(CC2)C(=C)C)O)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
(3R,8aR)-5,8a-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,7,8,8a-hexahydronaphthalene 91733213 Click to see CC1=CCCC2(C1=CC(CC2)C(=C)C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
(3R,8aR)-5,8a-dimethyl-3-prop-1-en-2-yl-2,3,7,8-tetrahydro-1H-naphthalene 101713110 Click to see CC1=CCCC2(C1=CC(CC2)C(=C)C)C 202.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
https://doi.org/10.1016/S0031-9422(97)00154-4
(4aR)-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 5316284 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
5,8a-Dimethyl-3-prop-1-en-2-yl-1,2,3,4,7,8-hexahydronaphthalen-4a-ol 162965390 Click to see CC1=CCCC2(C1(CC(CC2)C(=C)C)O)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
7-epi-alpha-Selinene 10123 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
alfa-Cyperone 12303268 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
alpha-Cyperone 6452086 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
alpha-Selinene 10856614 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
https://doi.org/10.1016/S0031-9422(00)00374-5
Cyperol 14076601 Click to see CC1=C2CC(CCC2(CCC1O)C)C(=C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
delta-Selinene 520383 Click to see CC1=C2C=C(CCC2(CCC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00154-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
5,6,7,10,11,12-Hexahydroxy-5,6,7,8,9,10,11,12-octahydrobenzo[10]annulene-1,4-dione 22297332 Click to see C1CC(C(C(C2=C(C(C(C1O)O)O)C(=O)C=CC2=O)O)O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Alopecuquinone 636698 Click to see C1CC(C(C(C2=C(C(C(C1O)O)O)C(=O)C=CC2=O)O)O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
> Organoheterocyclic compounds / Oxanes
(1aR,3aR,4R,7R,8aS)-1a,4,9,9-Tetramethyloctahydro-3a,7-methanoazuleno[1,8a-b]oxirene 12308850 Click to see CC1CCC2CC34C1(C2(C)C)CCC3(O4)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
https://doi.org/10.1016/S0031-9422(97)00154-4
(1R,4R,6S,8R,11R)-4,11,12,12-tetramethyl-5-oxatetracyclo[6.3.1.01,6.04,6]dodecane 12308851 Click to see CC1CCC2CC34C1(C2(C)C)CCC3(O4)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
https://doi.org/10.1016/S0031-9422(97)00154-4
(1R,4R,6S,8R,11S)-4,11,12,12-tetramethyl-5-oxatetracyclo[6.3.1.01,6.04,6]dodecane 154496526 Click to see CC1CCC2CC34C1(C2(C)C)CCC3(O4)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00374-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1111/J.1742-7843.2006.PTO_300.X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497137 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497665 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
Vicenin-2 3084407 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(02)00060-2
Quercetin 3,4'-dimethyl ether 5380905 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/S0031-9422(02)00060-2

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