Boehmeria nivea - Unknown
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Internal ID UUID64400d532786d207882716
Scientific name Boehmeria nivea
Authority Gaudich.
First published in Bot. Freyc. Voy. 499.

Description Top

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Synonyms Top

Scientific name Authority First published in
Urera lamiifolia Gaudich. Voy. Uranie : 497 (1830)
Urtica utilis hort. ex de Vriese Pl. Ind. Bat. Orient. : 146 (1857)
Urtica tenacissima Roxb. Suppl. Observ. Sunn Hemp Bengal : 41 (1811)
Urtica millettii Hook. & Arn. Bot. Beechey Voy. : 214 (1837)
Urtica nivea L. Sp. Pl. : 985 (1753)
Ramium niveum Kuntze Revis. Gen. Pl. 2: 632 (1891)
Ramium mollicoma Kuntze Revis. Gen. Pl. 2: 633 (1891)
Ramium compactum Kuntze Revis. Gen. Pl. 2: 633 (1891)
Procris nivea Wedd. Prodr. [A. P. de Candolle] 16(1): 206, in syn. 1869 [mid Nov 1869]
Boehmeria nivea f. concolor (Makino) Hatus. Fl. Ryukyus, ed. 2 37, without basionym ref. 1994
Boehmeria nivea subsp. nipononivea (Koidz.) Kitam. Acta Phytotax. Geobot. 20: 208 1962
Boehmeria candicans Hassk. Cat. Pl. Hort. Bot. Bogor. : 79 (1844)
Boehmeria compacta Blume Mus. Bot. 2: 210 (1857)
Boehmeria juncea Bedevian Illustr. Polyglot. Dict. 110 (1936), in syn.
Boehmeria mollicoma Miq. Syst. Verz. Ind. Archip. 2: 100 (1854)
Boehmeria nipononivea Koidz. Acta Phytotax. Geobot. 10: 223 (1941)
Boehmeria nivea var. candicans Wedd.
Boehmeria nivea var. concolor Makino Bot. Mag. (Tokyo) 23: 251 1909
Boehmeria nivea f. nipponivea (Koidz.) Hatus. Fl. Ryukyus 234, ? without basionym ref. 1971
Boehmeria nivea var. nipononivea (Koidz.) W.T.Wang Acta Bot. Yunnan. 3: 320 (1981)
Boehmeria nivea var. tenacissima (Gaudich.) Miq. Fl. Ned. Ind. 1(2): 253 1859
Boehmeria nivea var. viridula (Yamamoto) S.S.Ying Coloured Illustr. Fl. Taiwan 3: 470 (1988):.
Boehmeria tenacissima Gaudich. Bot. Freyc. Voy. 500.
Boehmeria thailandica Yahara Acta Phytotax. Geobot. 32: 4 (1981)
Boehmeria utilis André Rev. Hort. (Paris) 62: 184 (1890)
Boehmeria frutescens var. concolor (Makino) Nakai Bot. Mag. (Tokyo) 41: 514 1927
Boehmeria frutescens var. viridula (Yamam.) Suzuki Short Fl. Formos. 47 1936

Common names Top

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Language Common/alternative name
English ramie
English chinese grass
Spanish boehmeria candicans
Spanish ortiga blanca
Spanish urtica utilis
Spanish urtica tenacissima
Spanish urtica nivea
Spanish urtica lamiifolia
Spanish urera lamiifolia
Spanish ramium niveum
Spanish ramio
Spanish boehmeria utilis
Spanish boehmeria thailandica
Spanish boehmeria tenacissima
Spanish boehmeria nipononivea
Spanish boehmeria juncea
Spanish boehmeria frutescens var. viridula
Spanish boehmeria frutescens var. concolor
Spanish procris nivea
Arabic رامي
Azerbaijani qar bemeriyası
Azerbaijani qar ramisi
azb قار بمریاسی
Belarusian Крапіва кітайская
Belarusian Рамі
Belarusian Кітайская крапіва
Belarusian Рамі белае
Bulgarian рамия
Catalan rami
Czech ramie
German ramie
German rami
Basque rami
Persian رامی
Finnish rami
Finnish kiinanruoho
French ramie
Hebrew סרפד
Hindi रैमी
Croatian ramija
Armenian ռամի
io ramio
Icelandic ramí
Italian ramiè
Japanese カラムシ
Japanese 真麻
Japanese
Japanese
Japanese 苧麻
Japanese 青苧
jv rami
Georgian რამი
Kannada ಕಿತ್ತನಾರು
Korean 모시풀
Lithuanian pluoštinė bemerija
Malay rami
nan toē-á
Norwegian Bokmål kinagress
Dutch ramie
Norwegian Nynorsk kinagras
Polish rami
Polish ramia
Polish szczmiel biały
Portuguese rami
pwn zakilj
Romanian ramie
Russian бомерия белоснежная
Russian ramie
Russian белое рами
Russian бёмерия белоснежная
Russian китайская крапива
Russian рамим
Russian рами белое
su haramay
Swedish ramie
Swedish kinagräs
Swedish rami
tay kagi
tay kgi
Thai ป่านรามี
Turkish rami
trv krig
Vietnamese cây gai
Vietnamese cây lá gai
Vietnamese lá gai
Vietnamese gai
za gobanh
Chinese 苎花
Chinese 竺麻皮
Chinese 伏毛苎麻
Chinese 苎麻
Chinese 苎麻(苧麻)
Chinese 苎麻根
Chinese 苧麻
Chinese 青叶苎麻根
Chinese 青叶苎麻

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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

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Database ID/link to page
World Flora Online wfo-0000567636
UNII 16163IWM0H
Florida Plant Atlas 467
Flora of Alabama 3643
USDA Plants BONI2
Tropicos 33400386
INPN 447647
Flora of Italy 303
KEW urn:lsid:ipni.org:names:55676-3
The Plant List kew-2678359
Missouri Botanical Garden 242351
Open Tree Of Life 594991
Observations.org 135828
NCBI Taxonomy 83906
Nature Serve 2.160157
IPNI 850690-1
iNaturalist 159288
GBIF 2984359
Freebase /m/02w3z9
EPPO BOHNI
EOL 594795
Elurikkus 347921
USDA GRIN 7290
Wikipedia Ramie
CMAUP NPO29449

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_018132145.1 ASM1813214v1 Chromosome Chinese Academy of Agricultural Sciences 2021-04-26 899.8x 257.70 Mb

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
Multiple omics revealed the growth-promoting mechanism of Bacillus velezensis strains on ramie Wang X, Wang Y, Fu Y, Zhai Y, Bai X, Liu T, Li G, Zeng L, Zhu S Front Plant Sci 27-Mar-2024
PMCID:PMC11004232
doi:10.3389/fpls.2024.1367862
PMID:38601307
BnAP2-12 overexpression delays ramie flowering: evidence from AP2/ERF gene expression Zhang X, Peng W, Chen H, Xing H Front Plant Sci 25-Mar-2024
PMCID:PMC10999622
doi:10.3389/fpls.2024.1367837
PMID:38590749
Genome-Wide Analysis of the Xyloglucan Endotransglucosylase/Hydrolase (XTH) Gene Family: Expression Pattern during Magnesium Stress Treatment in the Mulberry Plant (Morus alba L.) Leaves Danso B, Ackah M, Jin X, Ayittey DM, Amoako FK, Zhao W Plants (Basel) 21-Mar-2024
PMCID:PMC10975095
doi:10.3390/plants13060902
PMID:38592929
Characteristics and Quality of Flame-Retarded Ramie Fabrics for the Development of Functional Textiles Wulandari AP, Karlina E, Tanudjaja E, Rohmat A, Kusmoro J, Fadhlillah M, Somantri K, Sahroni R, Fatriasari W Materials (Basel) 20-Mar-2024
PMCID:PMC10972381
doi:10.3390/ma17061416
PMID:38541573
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Exploration of Voids, Acoustic Properties and Vibration Damping Ratio of Cyperus Pangorei Rottb Fiber and Ramie Fiber Reinforced with Epoxy Resin Hybrid Composites Kanniyappan S, Selvaraj SK Polymers (Basel) 18-Mar-2024
PMCID:PMC10976161
doi:10.3390/polym16060832
PMID:38543437
Unlocking the future of precision manufacturing: A comprehensive exploration of 3D printing with fiber-reinforced composites in aerospace, automotive, medical, and consumer industries Tuli NT, Khatun S, Rashid AB Heliyon 05-Mar-2024
PMCID:PMC10943402
doi:10.1016/j.heliyon.2024.e27328
PMID:38495162
Properties of mixture of hemp bast and softwood pulp for filter paper manufacture Yimlamai P, Chitbanyong K, Wanitpinyo K, Puangsin B, Nanta K, Khantayanuwong S, Pisutpiched S, Chaisan T, Fei B, Hiziroglu S Heliyon 01-Feb-2024
PMCID:PMC10850592
doi:10.1016/j.heliyon.2024.e25353
PMID:38333817
Expression of auxin transporter genes in flax (Linum usitatissimum) fibers during gravity response Ibragimova NN, Mokshina NE Vavilovskii Zhurnal Genet Selektsii 01-Feb-2024
PMCID:PMC10917669
doi:10.18699/VJGB-24-05
PMID:38465245
Nitric oxide in plants: an insight on redox activity and responses toward abiotic stress signaling Khator K, Parihar S, Jasik J, Shekhawat GS Plant Signal Behav 08-Jan-2024
PMCID:PMC10793691
doi:10.1080/15592324.2023.2298053
PMID:38190763
Mixed infection of ITPase-encoding potyvirid and secovirid in Mercurialis perennis: evidences for a convergent euphorbia-specific viral counterstrike Mahillon M, Brodard J, Dubuis N, Gugerli P, Blouin AG, Schumpp O Virol J 04-Jan-2024
PMCID:PMC10768138
doi:10.1186/s12985-023-02257-y
PMID:38178191
Integrated Transcriptomics and Metabolomics Analysis Promotes the Understanding of Adventitious Root Formation in Eucommia ulmoides Oliver Du Q, Song K, Wang L, Du L, Du H, Li B, Li H, Yang L, Wang Y, Liu P Plants (Basel) 03-Jan-2024
PMCID:PMC10780705
doi:10.3390/plants13010136
PMID:38202444
Rhamnogalacturonan I with β-(1,4)-Galactan Side Chains as an Ever-Present Component of Tertiary Cell Wall of Plant Fibers Chernova T, Mikshina P, Petrova A, Ibragimova N, Ageeva M, Gorshkova T Int J Mol Sci 08-Dec-2023
PMCID:PMC10743774
doi:10.3390/ijms242417253
PMID:38139081
Comprehensive Analysis of WUSCEL-Related Homeobox Gene Family in Ramie (Boehmeria nivea) Indicates Its Potential Role in Adventitious Root Development Abubakar AS, Wu Y, Chen F, Zhu A, Chen P, Chen K, Qiu X, Huang X, Zhao H, Chen J, Gao G Biology (Basel) 28-Nov-2023
PMCID:PMC10740585
doi:10.3390/biology12121475
PMID:38132301
Molecular Mechanisms Regulating Phenylpropanoid Metabolism in Exogenously-Sprayed Ethylene Forage Ramie Based on Transcriptomic and Metabolomic Analyses Jie H, He P, Zhao L, Ma Y, Jie Y Plants (Basel) 18-Nov-2023
PMCID:PMC10675582
doi:10.3390/plants12223899
PMID:38005796

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 / Anthracenes / Anthraquinones
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(7R,8R,9S)-7,8,9-trihydroxy-12-oxohexadec-10-enoic acid 162846463 Click to see CCCCC(=O)C=CC(C(C(CCCCCC(=O)O)O)O)O 316.39 unknown https://doi.org/10.1080/14786419.2010.488230
(7R,8R,9S)-7,8,9-trihydroxyhexadec-10-enoic acid 163042418 Click to see CCCCCC=CC(C(C(CCCCCC(=O)O)O)O)O 302.41 unknown https://doi.org/10.1080/14786419.2010.488230
(9R,10R,11S)-9,10,11-trihydroxyoctadec-12-enoic acid 162869507 Click to see CCCCCC=CC(C(C(CCCCCCCC(=O)O)O)O)O 330.50 unknown https://doi.org/10.1080/14786419.2010.488230
(E,8R,11S,12S)-8,11,12-trihydroxyoctadec-9-enoic acid 162989953 Click to see CCCCCCC(C(C=CC(CCCCCCC(=O)O)O)O)O 330.50 unknown https://doi.org/10.1080/14786419.2010.488230
(Z,7R,8R,9S)-7,8,9-trihydroxy-12-oxohexadec-10-enoic acid 163193544 Click to see CCCCC(=O)C=CC(C(C(CCCCCC(=O)O)O)O)O 316.39 unknown https://doi.org/10.1080/14786419.2010.488230
(Z,9R,10R,11S)-9,10,11-trihydroxyoctadec-12-enoic acid 96355400 Click to see CCCCCC=CC(C(C(CCCCCCCC(=O)O)O)O)O 330.50 unknown https://doi.org/10.1080/14786419.2010.488230
8,11,12-Trihydroxyoctadec-9-enoic acid 78385598 Click to see CCCCCCC(C(C=CC(CCCCCCC(=O)O)O)O)O 330.50 unknown https://doi.org/10.1080/14786419.2010.488230
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1271/BBB.64.875
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1271/BBB.64.875
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,10R,11R,12aR)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 470602 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 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
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-(3,5-Dihydroxy-phenyl)-2-(4-hydroxy-phenyl)-2,3-dihydro-benzofuran-5-carbaldehyde 636845 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C=O)C4=CC(=CC(=C4)O)O)O 348.30 unknown via CMAUP database
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)vinyl]-2,3-dihydrobenzofuran-2-yl]benzene-1,2-diol 5279244 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown via CMAUP database
Moracin M 185848 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=CC(=CC(=C3)O)O 242.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-O-(6-O-Acetyl-alpha-D-glucopyranosyl)-6-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-beta-D-fructofuranose 11092923 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)O)CO)O)O)O 560.50 unknown via CMAUP database
5-Caffeoylshikimic acid 5281762 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 336.29 unknown via CMAUP database
Caffeic acid methyl ester 689075 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
helonioside A 16745274 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(CO)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O 694.60 unknown via CMAUP database
Helonioside B 21636195 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)CO)O)O)O 736.70 unknown via CMAUP database
Smilaside L 24862701 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O 870.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-2,5-bis[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxolan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 11593148 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC=C(C=C4)O)COC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O 882.80 unknown via CMAUP database
1-O-(4-Hydroxy-trans-cinnamoyl)-2-O-(alpha-D-glucopyranosyl)-6-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-beta-D-fructofuranose 11735009 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 664.60 unknown via CMAUP database
Smilaside C 10919948 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O 840.80 unknown via CMAUP database
Smilaside G 24862591 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 810.70 unknown via CMAUP database
Smilaside H 24862644 Click to see CC(=O)OC1C(C(C(OC1OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)CO)O)O 852.80 unknown via CMAUP database
Smilaside I 24862642 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O 852.80 unknown via CMAUP database
Smilaside J 24850451 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 840.80 unknown via CMAUP database
Smilaside K 24862643 Click to see CC(=O)OC1C(C(C(OC1OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)COC(=O)C=CC5=CC=C(C=C5)O)CO)O)O 882.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin 73160 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
(+)-Epicatechin 182232 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-2alpha-(3-Hydroxy-4-methoxyphenyl)-5-(beta-D-glucopyranosyloxy)-6-methyl-3,4-dihydro-2H-1-benzopyran-3alpha,7-diol 11081337 Click to see CC1=C(C2=C(C=C1O)OC(C(C2)O)C3=CC(=C(C=C3)OC)O)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown via CMAUP database
(2R)-2alpha-(3-Methoxy-4-hydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-6-methyl-3,4-dihydro-2H-1-benzopyran-3alpha,7-diol 10885307 Click to see CC1=C(C2=C(C=C1O)OC(C(C2)O)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 5320854 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
3-[(O-beta-D-Glucopyranosyl-(1->2)-O-beta-D-galactopyranosyl-(1->2)-beta-D-glucopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one 16745399 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)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O 788.70 unknown https://doi.org/10.1080/14786419.2010.488230
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
(E)-2,4,4'-Trihydroxychalcone 5322052 Click to see C1=CC(=CC=C1C(=O)C=CC2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
2,4,4'-Trihydroxychalcone 5057077 Click to see C1=CC(=CC=C1C(=O)C=CC2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown via CMAUP database
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,4S,5S)-2-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 71752015 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown via CMAUP database
Piceid 5281718 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown via CMAUP database

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