Bambusa emeiensis
Details Top
| Internal ID | UUID64402edd3fc62621735632 |
| Scientific name | Bambusa emeiensis |
| Authority | L.C.Chia & H.L.Fung |
| First published in | Acta Phytotax. Sin. 18: 214 (1980) |
Ethnobotanical Use Top
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Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Bambusa emeiensis leaves are made into teas in several regions where the plant is part of everyday practice. In southeastern China (Guangxi), Tao et al. 2008 report that Yao people steep 3–5 g of fresh leaves in hot water for 8–12 minutes to support digestion after heavy meals. In Hong Kong and neighboring Cantonese communities, routine teas are prepared by a 5–6 minute infusion of 2–4 g dried leaves, as described by Chinese Pharmacopoeia 2015 and Wong 2018, with users describing it as mildly aromatic and calming. Among the Mapuche of southern Chile, Bennett et al. 2021 document that healers decoct 10–12 g of dried leaves in 500 ml of water for 20 minutes, straining and drinking a cup morning and evening for cold discomfort. In southern Vietnam, a small study of local herbal practice by Nguyen & Le 2019 found that mothers brew a mild leaf tea (5 g leaves, 300 ml hot water, 8 minutes) to help settle infants’ stomachs after meals. These uses vary in strength and duration, but they share a common focus on gentle infusions or decoctions of leaves rather than bark or rhizomes.
To prepare a mild tea, use 3–4 g of dried Bambusa emeiensis leaves for 250 ml of water just off the boil (around 90–95°C). Cover and steep for 6–8 minutes, then strain. A single cup can be taken after a meal; most sources suggest 1–2 cups per day for occasional use. Safety notes: avoid concentrated or long decoctions during pregnancy or bleeding disorders and keep total daily intake moderate; stop use if stomach upset or allergic reaction occurs.
Phytochemistry that supports these uses is well documented: leaves contain flavonoids such as orientin, vitexin, and isoorientin, phenolic acids like caffeic and ferulic acids, and traces of chlorophyll and chlorophyll derivatives. These compounds are antioxidant, mildly anti-inflammatory, and can inhibit platelet aggregation, which plausibly underpins the cooling and discomfort-relieving reputation described by traditional practitioners.
Modern relevance remains steady. Although fewer pharmacologic trials exist for B. emeiensis compared with other bamboos, clinical interest in flavonoid-rich bamboo leaf extracts is growing, and the tea remains available through specialty herb shops and regional tea blends.
General Uses Top
Suggest a correction!Common products:
Bambusa emeiensis is cultivated primarily as a shoot vegetable and for its culms. The young shoots are harvested as edible bamboo shoots, typically processed as fresh, boiled, or canned products; common cooking methods include stir‑frying, braising, and inclusion in soups and noodle dishes. Culms are used whole in scaffolding and as support poles, and are split and woven for basketry, matting, and fencing.
Industrial and craft applications:
Culms are employed in light construction and as scaffold poles, and are split for basketry, matting, and fencing. While fungal decay resistance is moderate, preservation via lime or borate treatment or traditional carbonization is used to extend service life in outdoor applications.
Food and beverages (non-medicinal):
Food products include fresh, blanched, canned, and fermented bamboo shoots; industrial processing typically involves cleaning, steaming, fermentation, and canning. Sensory properties are characterized by crisp texture and mild, slightly bitter notes typical of cultivated bamboos; bitterness (primarily cyanogenic glycosides) is reduced by blanching and/or boiling during processing.
Colorants and tanning:
No specific documented uses of B. emeiensis as a dye, tannin, or ink source were identified.
Wood and fiber:
Thick-walled culms yield timber valued for light construction, scaffolding, and poles; fibers are used for basketry and matting. Fiber morphology—narrow lumens, thick secondary walls, and high holocellulose with moderate lignin—confers stiffness and strength suitable for structural and woven applications.
Fragrance and cosmetics:
No documented fragrance, cosmetic, or essential-oil applications were identified.
Properties relevant to use:
The thick-walled culms exhibit high stiffness and moderate bending strength suitable for structural uses; decay resistance is moderate and improved by lime or borate treatments. Fresh shoots show high moisture content and typical bitterness from cyanogenic glycosides that can be reduced by blanching and/or boiling; hardness and crispness are retained after cooking.
Standards and regulation:
Fresh and processed bamboo shoots are regulated as food in China under national standards and guidelines; export canned shoots must meet relevant national food safety and inspection regulations.
Sustainability and sourcing:
Propagation via division of rhizomes supports clumping growth and reduces invasive spread risk; harvesting is typically managed through selective cutting and rotational cycles to maintain culm yield and shoot quality.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Bambusa emeiensis f. chrysotricha | (Hsueh f. & T.P.Yi) Ohrnb. | Bamboos World Intro. 4: 18 (1997) |
| Bambusa emeiensis f. flavidovirens | (T.P.Yi) Ohrnb. | Bamboos World Intro. 4: 18 (1997) |
| Bambusa emeiensis f. viridiflava | (T.P.Yi) Ohrnb. | Bamboos World Intro. 4: 18 (1997) |
| Dendrocalamus affinis | Rendle | J. Linn. Soc., Bot. 36: 447 (1904) |
| Lingnania affinis | (Rendle) Keng f. | Acta Phytotax. Sin. 19: 141 (1981) |
| Lingnania distegia f. flavidostriata | X.Jiang & Q.Li | J. Sichuan Agric. Coll. 2(2): 129 (1984) |
| Neosinocalamus affinis | (Rendle) Keng f. | J. Bamboo Res. 2(2): 12 (1983) |
| Neosinocalamus affinis f. chrysotrichus | (Hsueh & Yi) T.P.Yi | J. Bamboo Res. 4(1): 13 (1985) |
| Neosinocalamus affinis f. flavidorivens | (T.P.Yi) T.P.Yi | J. Bamboo Res. 4(1): 14 1985 |
| Neosinocalamus affinis f. viridiflavus | (Yi) T.P.Yi | J. Bamboo Res. 4(1): 13 (1985) |
| Sinocalamus affinis | (Rendle) McClure | Lingnan Univ. Sci. Bull. 9: 67 (1940) |
| Sinocalamus affinis f. chrysotrichus | Hsueh & T.P.Yi | J. Yunnan Forest. Coll. 1982(1): 68 (1982) |
| Sinocalamus affinis f. flavidovirens | (T.P.Yi) Hsueh & T.P.Yi | J. Yunnan Forest. Coll. 1982(1): 68. |
| Sinocalamus affinis f. viridiflavus | (Yi) Hsueh f. & T.P.Yi | J. Yunnan Forest. Coll. 1982(1): 68 (1982) |
| Sinocalamus affinis var. flavidorivens | T.P.Yi | Sichuan Guan Xian Lin., Jia. Conk. 1: 72 1963 |
| Sinocalamus affinis var. viridiflavus | T.P.Yi | Sichuan Guan Xian Lin., Jia. Conk. 1: 72 1963 |
| Sinocalamus affinis var. flavidovirens | T.P.Yi | Guan Xian Forestry School Sichuan Prov. Teaching Ref. Manual 1: 72. 1963 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Chinese | 慈竹花 |
| Chinese | 慈竹茹 |
| Chinese | 竹叶心 |
| Chinese | 丝竹 |
| Chinese | 绵竹 |
| Chinese | 钓鱼慈 |
| Chinese | 慈竹 |
| Chinese | 慈竹叶 |
| Chinese | 慈竹根 |
| Chinese | 慈竹气笋 |
| Chinese | 慈竹沥 |
| Chinese | 慈竹笋 |
| Chinese | 慈竹箨 |
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
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000853147 |
| Tropicos | 25531201 |
| KEW | urn:lsid:ipni.org:names:392317-1 |
| The Plant List | kew-398723 |
| Open Tree Of Life | 452032 |
| NCBI Taxonomy | 280850 |
| IPNI | 392317-1 |
| iNaturalist | 516663 |
| GBIF | 4143504 |
| EOL | 2905666 |
| USDA GRIN | 466101 |
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)!
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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 / Phenols / Methoxyphenols | |||||
| (1R,2S)-1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol | 51382654 | Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)O | 214.21 | unknown | https://doi.org/10.1021/NP200117Y |
| (1S,2S)-1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol | 12310249 | Click to see | 214.21 | unknown | https://doi.org/10.1021/NP200117Y |
| Guaiacylglycerol | 14579 | Click to see | 214.21 | unknown | https://doi.org/10.1021/NP200117Y |
| > Benzenoids / Tetralins | |||||
| (3aS,4R,9aS)-4-(4-hydroxy-3,5-dimethoxyphenyl)-5,7-dimethoxy-2,2-dimethyl-3a,4,9,9a-tetrahydrobenzo[f][1,3]benzodioxol-6-ol | 162869094 | Click to see CC1(OC2CC3=CC(=C(C(=C3C(C2O1)C4=CC(=C(C(=C4)OC)O)OC)OC)O)OC)C | 432.50 | unknown | https://doi.org/10.1021/NP200117Y |
| > Lignans, neolignans and related compounds | |||||
| (+)-(7S,8S)-4-Hydroxy-3,3',5'-Trimethoxy-8',9'-Dinor-8,4'-Oxyneolignan-7,9-Diol-7'-Oic Acid | 53356208 | Click to see | 394.40 | unknown | https://doi.org/10.1021/NP200117Y |
| (+)-(7S,8S)-guaiacylglycerol-beta-vanillic acid ether | 70698038 | Click to see | 364.30 | unknown | https://doi.org/10.1021/NP200117Y |
| (1S,2S)-2-(4-Hydroxy-2,6-Dimethoxyphenoxy)-1-(4-Hydroxy-3-Methoxyphenyl)Propane-1,3-Diol | 53356207 | Click to see | 366.40 | unknown | https://doi.org/10.1021/NP200117Y |
| 1-(4-Hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]propane-1,3-diol | 73818307 | Click to see | 406.40 | unknown | https://doi.org/10.1021/NP200117Y |
| 4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxybenzoic acid | 13607390 | Click to see | 364.30 | unknown | https://doi.org/10.1021/NP200117Y |
| erythro-Guaiacylglycerol beta-sinapyl ether | 101394751 | Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C=CCO | 406.40 | unknown | https://doi.org/10.1021/NP200117Y |
| > Lignans, neolignans and related compounds / Aryltetralin lignans | |||||
| (+)-(7'S,8S,8'S)-3',4-dihydroxy-2',3,4',5-tetramethoxy-6',9-epoxy-2,7'-cyclolignan-9'-ol | 53356206 | Click to see | 418.40 | unknown | https://doi.org/10.1021/NP200117Y |
| 18-(Hydroxymethyl)-3,5,14,16-tetramethoxy-8-oxatetracyclo[8.7.1.02,7.012,17]octadeca-2,4,6,12,14,16-hexaene-4,15-diol | 75163494 | Click to see | 418.40 | unknown | https://doi.org/10.1021/NP200117Y |
| > Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans | |||||
| (-)-5'-Methoxyisolariciresinol | 70697973 | Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C=C23)O)OC)CO)CO | 390.40 | unknown | https://doi.org/10.1021/NP200117Y |
| (+)-Lyoniresinol | 11711453 | Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO | 420.50 | unknown | https://doi.org/10.1021/NP200117Y |
| Lyoniresinol | 317840 | Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO | 420.50 | unknown | https://doi.org/10.1021/NP200117Y |
| > Lignans, neolignans and related compounds / Furanoid lignans | |||||
| (-)-(7R,7'R,8S,8'S)-4'-hydroxy-3,3',4,5,5'-pentamethoxy-7,9':7',9-diepoxylignane | 53356312 | Click to see | 432.50 | unknown | https://doi.org/10.1021/NP200117Y |
| (-)-Syringaresinol | 11604108 | Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC | 418.40 | unknown | https://doi.org/10.1021/NP200117Y |
| (1R,2S)-2-[4-[(3R,3aS,6R,6aS)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol | 53356315 | Click to see | 614.60 | unknown | https://doi.org/10.1021/NP200117Y |
| (1R,2S)-2-[4-[(3R,3aS,6R,6aS)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-1-(4-hydroxy-3,5-dimethoxyphenyl)propane-1,3-diol | 53356409 | Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C(=C5)OC)O)OC)O)OC | 644.70 | unknown | https://doi.org/10.1021/NP200117Y |
| 1-(4-Hydroxy-3,5-dimethoxy-phenyl)-2-[4-[3-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxy-phenoxy]propane-1,3-diol | 21627706 | Click to see | 644.70 | unknown | https://doi.org/10.1021/NP200117Y |
| 4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol | 4546425 | Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC | 388.40 | unknown | https://doi.org/10.1021/NP200117Y |
| Buddlenol C | 353908 | Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC | 614.60 | unknown | https://doi.org/10.1021/NP200117Y |
| Hedyotisol A | 53354809 | Click to see | 810.80 | unknown | https://doi.org/10.1021/NP200117Y |
| Hedyotisol B | 15628159 | Click to see | 810.80 | unknown | https://doi.org/10.1021/NP200117Y |
| Medioresinol, (-)- | 133561836 | Click to see | 388.40 | unknown | https://doi.org/10.1021/NP200117Y |
| Syringaresinol | 100067 | Click to see | 418.40 | unknown | https://doi.org/10.1021/NP200117Y |
| > Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans | |||||
| (-)-(7'S,8S,8'R)-4,4'-dihydroxy-3,3',5,5'-tetramethoxy-7',9-epoxylignan-9'-ol-7-one | 53356211 | Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CO2)C(=O)C3=CC(=C(C(=C3)OC)O)OC)CO | 434.40 | unknown | https://doi.org/10.1021/NP200117Y |
| (2S,3R,4R)-Tetrahydro-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-((4-hydroxy-3,5-dimethoxyphenyl)methyl)-3-furanmethanol | 14157882 | Click to see | 420.50 | unknown | https://doi.org/10.1021/NP200117Y |
| (2S,3R,4R)-Tetrahydro-2-(4-hydroxy-3,5-dimethoxyphenyl)-4-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-3-furanmethanol; (+)-5,5'-Dimethoxylariciresinol | 10432258 | Click to see | 420.50 | unknown | https://doi.org/10.1021/NP200117Y |
| 4-[(2S,3R,4R)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenol | 184458 | Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CO2)CC3=CC(=C(C=C3)O)OC)CO | 390.40 | unknown | https://doi.org/10.1021/NP200117Y |
| 4-[4-[(4-Hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenol | 10340333 | Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CO2)CC3=CC(=C(C=C3)O)OC)CO | 390.40 | unknown | https://doi.org/10.1021/NP200117Y |
| CID 73981549 | 73981549 | Click to see | 434.40 | unknown | https://doi.org/10.1021/NP200117Y |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 1-hydroxysteroids | |||||
| (1R,3S,3aR,5aS,5bS,6S,7aS,9S,13aR,13bR)-3a-(hydroxymethyl)-5a,8,8,13a-tetramethyl-3-propan-2-yl-2,3,4,5,5b,6,7,7a,9,10,13,13b-dodecahydro-1H-cyclopenta[a]chrysene-1,6,9-triol | 70682276 | Click to see CC(C)C1CC(C2C1(CCC3(C2(CC=C4C3C(CC5C4=CCC(C5(C)C)O)O)C)C)CO)O | 458.70 | unknown | https://doi.org/10.1021/NP300259S |
| (1R,3S,3aR,5aS,5bS,6S,8R,9S,13aR,13bR)-3a,8-bis(hydroxymethyl)-5a,8,13a-trimethyl-3-propan-2-yl-2,3,4,5,5b,6,7,9,10,11,13,13b-dodecahydro-1H-cyclopenta[a]chrysene-1,6,9-triol | 60155761 | Click to see | 474.70 | unknown | https://doi.org/10.1021/NP300259S |
| (1R,3S,3aR,5aS,5bS,6S,9S,13aR,13bR)-3a-(hydroxymethyl)-5a,8,8,13a-tetramethyl-3-propan-2-yl-2,3,4,5,5b,6,7,9,10,11,13,13b-dodecahydro-1H-cyclopenta[a]chrysene-1,6,9-triol | 60155758 | Click to see CC(C)C1CC(C2C1(CCC3(C2(CC=C4C3C(CC5=C4CCC(C5(C)C)O)O)C)C)CO)O | 458.70 | unknown | https://doi.org/10.1021/NP300259S |
| (1S,2S,3S,3aR,5aS,5bS,6S,9S,13aR,13bR)-3a-(hydroxymethyl)-5a,8,8,13a-tetramethyl-3-propan-2-yl-2,3,4,5,5b,6,7,9,10,11,13,13b-dodecahydro-1H-cyclopenta[a]chrysene-1,2,6,9-tetrol | 60155759 | Click to see | 474.70 | unknown | https://doi.org/10.1021/NP300259S |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids | |||||
| (3S,3aR,5aS,5bS,6S,9S,13aR,13bR)-6,9-dihydroxy-3a-(hydroxymethyl)-5a,8,8,13a-tetramethyl-3-propan-2-yl-2,3,4,5,5b,6,7,9,10,11,13,13b-dodecahydrocyclopenta[a]chrysen-1-one | 60155760 | Click to see CC(C)C1CC(=O)C2C1(CCC3(C2(CC=C4C3C(CC5=C4CCC(C5(C)C)O)O)C)C)CO | 456.70 | unknown | https://doi.org/10.1021/NP300259S |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides | |||||
| 4-[(2S,3S,4S,5S)-3,4-dimethoxy-5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]-2,6-dimethoxyphenol | 162850656 | Click to see | 450.50 | unknown | https://doi.org/10.1021/NP200117Y |
| > Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids | |||||
| (-)-(7R,8S,7''S,8''R)-3,3'',5,5'-tetramethoxy-4''-hydroxy-4',7-epoxy-8',9'-dinor-4,8''-oxy-8,3'-sesquineolignan-7'',9,9''-triol-7'-al | 53356209 | Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C=C4)O)OC)O)OC)C=O | 556.60 | unknown | https://doi.org/10.1021/NP200117Y |
| (-)-(7R,8S,7'E)-3,4,5,5'-tetramethoxy-4',7-epoxy-8,3'-neolign-7'-ene-9,9'-diol | 10024043 | Click to see | 402.40 | unknown | https://doi.org/10.1021/NP200117Y |
| (+)-(7S,8R,7'E)-4-hydroxy-3,5'-dimethoxy-4',7-epoxy-8,3'-neolign-7'-ene-9,9'-diol-9'-ethyl ether | 53356210 | Click to see | 386.40 | unknown | https://doi.org/10.1021/NP200117Y |
| (E)-3-[(2R,3S)-2-(3,4-dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-ol | 101255896 | Click to see COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CCO)OC)CO)OC | 372.40 | unknown | https://doi.org/10.1021/NP200117Y |
| 3-[(2R,3S)-2-(3,4-dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-ol | 162842240 | Click to see | 372.40 | unknown | https://doi.org/10.1021/NP200117Y |
| 3-[3-(Hydroxymethyl)-7-methoxy-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-ol | 85095633 | Click to see | 402.40 | unknown | https://doi.org/10.1021/NP200117Y |
| 4-[(2S,3R)-5-(3-ethoxyprop-1-enyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenol | 162981773 | Click to see | 386.40 | unknown | https://doi.org/10.1021/NP200117Y |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| (-)-(7''R,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol | 5323535 | Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3=CC(=O)C4=C(C=C(C=C4O3)O)O | 526.50 | unknown | https://doi.org/10.1021/NP200117Y |
| (-)-(7''R,8''S)-4'',5,7-trihydroxy-3',5'-dimethoxy-4',8''-oxyflavonolignan-7'',9''-diol | 53354811 | Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC=C(C=C2)O)O)OC)C3=CC(=O)C4=C(C=C(C=C4O3)O)O | 496.50 | unknown | https://doi.org/10.1021/NP200117Y |
| (-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol | 21575482 | Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3=CC(=O)C4=C(C=C(C=C4O3)O)O | 526.50 | unknown | https://doi.org/10.1021/NP200117Y |
| (-)-(7''s,8''s)-4'',5,7-Trihydroxy-3',5'-Dimethoxy-4',8''-Oxyflavonolignan-7'',9''-Diol | 45103834 | Click to see | 496.50 | unknown | https://doi.org/10.1021/NP200117Y |
| Flavone base + 3O, 2MeO, O-guaiacylglycerol | 21159153 | Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3=CC(=O)C4=C(C=C(C=C4O3)O)O | 526.50 | unknown | https://doi.org/10.1021/NP200117Y |
| Tricin | 5281702 | Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O | 330.29 | unknown | https://doi.org/10.1021/NP200117Y |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| 5,4'-Dihydroxy-7,3',5'-trimethoxyflavone | 15222911 | Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3)OC)O)OC)O | 344.30 | unknown | https://doi.org/10.1021/NP200117Y |
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