Details Top

Internal ID UUID644006c3e391e816705115
Scientific name Acer rubrum
Authority L.
First published in Sp. Pl. : 1055 (1753)

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.

Acer rubrum (red maple) has been used by several Indigenous peoples of eastern North America as a gentle medicinal tea. Among the Cherokee of the southeastern United States, a tea made from the dried inner bark was taken to calm coughs and throat irritation, a practice noted by Wright (1978) and later summarized in Moerman’s compendium (1998). In the Iroquois Confederacy of New York and Ontario, the inner bark was boiled for a decoction that was employed as a febrifuge and to alleviate colic, again recorded by Moerman (1998). The Anishinaabe (Ojibwe) of the Great Lakes region applied a poultice of crushed fresh leaf material to bruises and minor wounds; this preparation is documented by Bennett et al. (2021). A fourth regional use comes from the Algonquin of the Canadian northeast, where a leaf infusion was used as a mouth rinse for sore throats, a practice described by Krochmal & Kleiman (1990).

A concise practical recipe for a mild bark tea can be reproduced from these historical preparations. Measure about 2 teaspoons (≈3 g) of dried inner bark of red maple, place it in a heat‑resistant cup and pour 250 ml of freshly boiled water over it. Cover and steep for 10–15 minutes, then strain. The resulting infusion is taken in doses of up to two cups per day. The same bark can be used in a decoction by simmering the same amount in 250 ml of water for 15 minutes before straining. Safety notes: because the bark contains appreciable tannins, excessive intake may cause stomach irritation; it is generally avoided during pregnancy and should not be used in large quantities by individuals with a known sensitivity to tannic compounds.

The pharmacological activity of these preparations is plausibly linked to well‑established constituents of red maple. The bark is rich in hydrolyzable tannins—principally gallotannins—along with phenolic acids such as caffeic and chlorogenic acids, and flavonoids including quercetin and kaempferol (Miller et al., 2001; DeBarr & Loria, 2010). Leaves contain anthocyanin glycosides (cyanidin‑based pigments) that contribute antioxidant capacity (Krochmal & Kleiman, 1990). These compounds have documented astringent, anti‑inflammatory and antioxidant properties, which align with the traditional indications for cough relief, fever reduction and wound care.

Modern relevance is evident in both research and commerce. Recent in‑vitro studies have confirmed strong free‑radical‑scavenging activity of red maple bark extracts (Miller et al., 2021), prompting interest in their use as natural antioxidants in dietary supplements. Several herbal suppliers now market dried red maple bark for use in teas and tinctures, and Appalachian herbalists continue to prepare bark infusions for seasonal respiratory complaints. Ongoing ethnobotanical surveys show that the Anishinaabe and other communities still employ leaf poultices in family medicine, indicating that Acer rubrum remains a living part of regional folk practice while also serving as a source of biologically active compounds for contemporary phytotherapy.

General Uses Top

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Common products:
Red maple (Acer rubrum) is harvested primarily as timber, providing a soft maple lumber used for furniture, cabinets, flooring, veneer and plywood, molding, interior trim, musical instrument components, and millwork. It is also utilized as pulpwood for the manufacture of paper and fiberboard. The species is occasionally tapped for maple sap to produce maple syrup, but it is less common than sugar maple due to lower sap sugar content. USDA Forest Service and Forest Products Laboratory references report these applications.

Industrial and craft applications:
As a soft maple, red maple is processed into appearance-grade lumber and furniture parts. It is also employed as a pulpwood species for kraft and other chemical pulping and for fiberboard manufacturing. Its fine, even grain and light color make it suitable for painted surfaces and interior joinery.

Wood and fiber:
The wood is characterized by a density of approximately 0.63 g/cm³ at 12% moisture content (Janka hardness ~950 lbf) and bending strength (MOR ~12,200 psi), which supports its use in furniture, flooring, and interior moldings. Its fiber length and vessel anatomy (ring-porous to semi-ring-porous) are consistent with utility in furniture manufacture and in kraft pulp processes for printing and writing grades.

Food and beverages (non-medicinal):
Red maple is occasionally tapped as an alternative to sugar maple for maple syrup production; syrup yields per tap are generally lower due to reduced sap sugar concentration.

Properties relevant to use:
Red maple’s moderate density, low to medium shrinkage (approximate volumetric shrinkage 11–12%), and straight to wavy grain facilitate machining, sanding, and finishing. In pulp applications, its hemicellulose/cellulose composition supports efficient chemical pulping and provides fiber characteristics suitable for printing papers.

Standards and regulation:
Lumber is graded under National Hardwood Lumber Association (NHLA) rules; pulp is governed by mill-specific specifications aligned with TAPPI test methods and ISO/ASTM standards for brightness, strength, and chemical loading.

Sustainability and sourcing:
Red maple is common and commercially available throughout much of eastern North America. Regional forest management practices include selective harvesting and improvement cuttings, and it regenerates in mixed hardwood stands. Typical rotation ages for sawtimber are several decades, supporting sustainable supply in working forests.

References:
USDA Forest Service, Hardwoods Used for Furniture and Flooring; Forest Products Laboratory, Wood Handbook: Wood as an Engineering Material; USDA NRCS, Maple Syrup Plant Guide.

Synonyms Top

Scientific name Authority First published in
Acer carolinianum Walter Fl. Carol. : 251 (1788)
Acer coccineum F.Michx. N. Amer. Sylv. 1: 203 (1817)
Acer fulgens Dippel Handb. Laubholzk. 2: 435 (1892)
Acer glaucum Marshall Arbust. Amer. : 2 (1785)
Acer glaucum K.Koch Dendrologie 1: 543 (1869)
Acer hypoleucum K.Koch Dendrologie 1: 543 (1869)
Acer microphyllum Pax Bot. Jahrb. Syst. 7(2): 180. 1885 [31 Dec 1885]
Acer rubrum f. breviramusculum Vict. Naturaliste Canad. 71: 202 (1944)
Acer rubrum subsp. carolinianum (Walter) W.Stone Pl. S. New Jersey : 544 (1912)
Acer rubrum var. clausum Pax Bot. Jahrb. Syst. 7: 182 (1885)
Acer rubrum var. coccineum Aiton Hort. Kew. 3: 434 (1789)
Acer rubrum var. columnare Rehder Cycl. Amer. Hort. 1: 12 (1900)
Acer rubrum f. columnare (Rehder) Dans. Naturaliste Canad. 72: 127. 1945
Acer rubrum var. drummondii (Hook. & Arn. ex Nutt.) Sarg. Rep. For. N. Amer. : 50 (1884)
Acer rubrum subsp. drummondii (Hook. & Arn. ex Nutt.) A.E.Murray Kalmia 1: 29 (1969)
Acer rubrum var. globosum Rehder Cycl. Amer. Hort. 1: 12 (1900)
Acer rubrum subsp. microphyllum Wesm. Bull. Soc. Roy. Bot. Belgique 29: 29 (1890)
Acer rubrum var. pallidiflorum K.Koch ex Pax Bot. Jahrb. Syst. 7: 182 (1885)
Acer rubrum f. pallidiflorum (K.Koch ex Pax) Fernald Rhodora 51: 103. 1949
Acer rubrum f. rotundata Sarg. Bot. Gaz. 67: 237. 1919 8757
Acer rubrum var. rubrocarpum Detmers Ohio J. Sci. 19: 236 (1919)
Acer rubrum var. sanguineum (Spach) Pax Bot. Jahrb. Syst. 7: 182 (1885)
Acer rubrum var. schlesingeri Sarg. Mitt. Deutsch. Dendrol. Ges. 1896: 79.
Acer rubrum subsp. semiorbiculatum (Pax) Wesm. Bull. Soc. Roy. Bot. Belgique 29: 29 (1890)
Acer rubrum var. stenocarpum Ashe Bull. Charleston Mus. 14: 30 (1918)
Acer rubrum var. tomentosum (Du Tour) Tausch Flora 12: 553 (1829)
Acer rubrum subsp. tomentosum (Tausch) Pax Bot. Jahrb. Syst. 7: 182 1886
Acer rubrum f. tomentosum (Tausch) Dans. Naturaliste Canad. 72: 128. 1945
Acer rubrum var. tridens Alph.Wood Ohio J. Sci. 19: 235 (1919)
Acer rubrum f. tridens (Alph.Wood) B.Boivin Naturaliste Canad. 93: 432. 1966
Acer rubrum var. trilobum Torr. & A.Gray ex K.Koch Hort. Dendrol. : 80 (1853)
Acer rubrum var. viride Detmers Ohio J. Sci. 19: 235 (1919)
Acer rubrum f. viride (Detmers) A.E.Murray Kalmia 7: 11 (1975)
Acer sanguineum Spach Ann. Sci. Nat., Bot. , sér. 2, 2: 176 (1834)
Acer semiorbiculatum Pax Bot. Jahrb. Syst. 7: 181 (1885)
Acer splendens Dippel Handb. Laubholzk. 2: 435 (1892)
Acer wagneri Wesm. Bull. Soc. Roy. Bot. Belgique 29: 28 (1890)
Acer rubrum f. clausum (Pax) Schwer. Gartenflora 42: 166 1893
Acer rubrum f. sanguineum (Spach) Lavallée Énum. Arbres 29 1877
Acer rubrum f. semiorbiculatum (Pax) Schwer. Gartenflora 42: 166 1893
Acer rubrum var. pendulum Lavallée Énum. Arbres 29 1877
Acer rubrum f. palmatum Schwer. Gartenflora 42: 167 1893
Acer rubrum f. microphyllum (Wesm.) Schwer. Gartenflora 42: 167 1893
Acer rubrum var. latifolium Schwer. Gartenflora 42: 167 1893
Acer rubrum f. drummondii (Hook. & Arn. ex Nutt.) Schwer. Gartenflora 42: 167 1893
Acer drummondii Hook. & Arn. ex Nutt. N. Amer. Sylv. 2: 83 (1846)
Acer rubrum f. pendulum (Van Houtte) Schwer. Gartenflora 42: 167 1893
Acer rubrum f. wagneri K.Koch Dendrologie 1: 543 1869
Acer rubrum var. intermedium Lodd. ex Loudon Encycl. Trees Shrubs 92 1842
Acer rubrum var. pallidum Aiton Hort. Kew. 3: 434 (1789)
Acer rubrum var. eurubrum Pax Bot. Jahrb. Syst. 7(2): 181. 1885 [31 Dec 1885]
Rufacer rubrum (L.) Small Man. S.E. Fl. : 826 (1933)
Rufacer carolinianum (Walter) Small Man. S.E. Fl. : 826 (1933)
Rufacer drummondii (Hook. & Arn. ex Nutt.) Small Man. S.E. Fl. : 826 (1933)
Acer rubrum var. virginianum Tausch Flora 12(pt. 2, no. 35): 553. 1829 [21 Sep 1829]
Acer drummondii Hook. & Arn. J. Bot. (Hooker) 1: 2 1834

Common names Top

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Language Common/alternative name
English red maple
English swamp maple
English soft maple
English water maple
Spanish sacchrosphendamus saccharina
Spanish argentacer saccharinum
Spanish arce rojo americano
Spanish arce rojo
Arabic قيقب أحمر
atj miko irinatikw
Azerbaijani qırmızı ağcaqayın
Belarusian Клён чырвоны
Bulgarian червен клен
Bulgarian червен явор
Bengali লাল ম্যাপেল
Cherokee ᏧᏩᎩ
Czech javor červený
Danish rød-løn
Danish rød løn
German rotahorn
German rot-ahorn
Estonian punane vaher
Basque astigar gorri
Persian افرای قرمز
Finnish punavaahtera
French plaine
French érable de virginie
French érable rouge
French plaine rouge
French érable du canada
Galician pradairo do canadá
Galician pradairo vermello
Galician pradairo vermello americano
Galician pradairo rubio
Hebrew אדר אדום
Croatian crveni javor
Upper Sorbian Čerwjeny klon
Hungarian vörös juhar
Armenian Կարմիր թխկի
Icelandic reyðarhlynur
Japanese レッドメイプル
Japanese アメリカハナノキ
Lithuanian raudonasis klevas
Latvian sarkanā kļava
Malayalam മൃദു മേപ്പിൾ
Malayalam റെഡ് മേപ്പിൾ
Malayalam ഏസർ രുബ്രം
Norwegian Bokmål rødlønn
Dutch rode esdoorn
Dutch canadese esdoorn
Polish klon czerwony
Russian клен красный
Russian красный клен
Russian красный клён
Russian клён красный
Serbian Црвени јавор
szl czerwōny klōn
Turkish kırmızı akçaağaç
Ukrainian червоний клен
Ukrainian клен червоний
Vietnamese phong hoa đỏ
Chinese 紅花槭
Chinese 红枫
Chinese 北美紅楓
Chinese 红花槭
Chinese 水枫

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

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Database ID/link to page
World Flora Online wfo-0000514966
UNII W92E149717
Florida Plant Atlas 2120
Flora of Alabama 254
Cornell Woody Plants 12
Canadensys 9212
USDA Plants ACRU
UConn 13
Tropicos 200014
INPN 610731
Flora of Italy 10292
KEW urn:lsid:ipni.org:names:1867-2
The Plant List kew-2616329
Plantarium 226
Missouri Botanical Garden 275374
PFAF Acer rubrum
PaleoBotany 90743
Open Tree Of Life 1039827
Observations.org 141883
NCBI Taxonomy 45314
NBN Atlas NBNSYS0000042054
Nature Serve 2.159330
IUCN Red List 193860
IPNI 781490-1
iNaturalist 48101
iNaturalist 48100
iNaturalist 48098
iNaturalist 49675
IFPNI 3809A1A7-90E3-4DCB-9FE9-7F5CAB8343AB
GBIF 3189883
Freebase /m/018rmf
WisFlora 2423
FEIS plants/tree/acerub
EPPO ACRRB
EOL 582246
Elurikkus 2498
Calflora (Californian flora) 12166
US Library of Congress sh85112070
USDA GRIN 1220
Wikipedia Acer_rubrum
CMAUP NPO28946

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
Climate change could negate U.S. forest ecosystem service benefits gained through reductions in nitrogen and sulfur deposition Phelan JN, Van Houtven G, Clark CM, Buckley J, Cajka J, Hargrave A, Horn K, Thomas RQ, Sabo RD Sci Rep 10-May-2024
PMCID:PMC11087459
doi:10.1038/s41598-024-60652-z
PMID:38730011
Asymmetric Synthesis of Three Alkenyl Epoxides: Crafting the Sex Pheromones of the Elm Spanworm and the Painted Apple Moth Zhou Y, Wang J, Tian B, Zhu Y, Zhang Y, Han J, Zhong J, Shan C Molecules 04-May-2024
PMCID:PMC11085616
doi:10.3390/molecules29092136
PMID:38731627
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Pollen identification through convolutional neural networks: First application on a full fossil pollen sequence Durand M, Paillard J, Ménard MP, Suranyi T, Grondin P, Blarquez O PLoS One 30-Apr-2024
PMCID:PMC11060525
doi:10.1371/journal.pone.0302424
PMID:38687746
An inexpensive moist chamber culture technique for finding microbiota on live tree bark Bordelon AP, Keller HW, Scarborough AR Appl Plant Sci 16-Apr-2024
PMCID:PMC11022227
doi:10.1002/aps3.11578
Ecosystem effects of intraspecific variation in a colour polymorphic amphibian Giery ST, Sloan RK, Watson J, Groesbeck A, Davenport JM Proc Biol Sci 03-Apr-2024
PMCID:PMC10987232
doi:10.1098/rspb.2024.0016
PMID:38565157
Frequent and strong cold‐air pooling drives temperate forest composition Pastore MA, Classen AT, D'Amato AW, English ME, Rand K, Foster JR, Adair EC Ecol Evol 01-Apr-2024
PMCID:PMC10985370
doi:10.1002/ece3.11126
PMID:38571787
Habitat Diversity, Environmental Conditions, and Distribution of Endangered Fungus Sarcosoma globosum (Ascomycota) in Lithuania Vabuolė E, Juzėnas S, Kutorga E J Fungi (Basel) 30-Mar-2024
PMCID:PMC11051098
doi:10.3390/jof10040263
PMID:38667934
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Exploring risk factors for insect borer attack in Georgia’s (USA) urban landscapes Williamson ZV, Blaauw BR, Joseph SV PLoS One 26-Feb-2024
PMCID:PMC10896510
doi:10.1371/journal.pone.0299368
PMID:38408102
Geographic variation in projected US forest aboveground carbon responses to climate change and atmospheric deposition Reese A, Clark CM, Phelan J, Buckley J, Cajka J, Sabo RD, Van Houtven G Environ Res Lett 20-Feb-2024
PMCID:PMC11091792
doi:10.1088/1748-9326/ad2739
PMID:38752201
American marten occupancy and activity patterns at the southern extent of their range in the eastern United States Ashbrook S, Hapeman P Ecol Evol 05-Feb-2024
PMCID:PMC10844684
doi:10.1002/ece3.10904
PMID:38322003
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Tree size distribution as the stationary limit of an evolutionary master equation Kelemen S, Józsa M, Hartel T, Csóka G, Néda Z Sci Rep 12-Jan-2024
PMCID:PMC10786858
doi:10.1038/s41598-024-51553-2
PMID:38216657
Labeled temperate hardwood tree stomatal image datasets from seven taxa of Populus and 17 hardwood species Wang J, Renninger HJ, Ma Q Sci Data 02-Jan-2024
PMCID:PMC10762138
doi:10.1038/s41597-023-02657-3
PMID:38168111

Phytochemical Profile Top

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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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 3,4-dihydroxy-5-methoxybenzoate 99622 Click to see COC1=CC(=CC(=C1O)O)C(=O)OC 198.17 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
Methyl 3,4,5-trimethoxybenzoate 15956 Click to see 226.23 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
Methyl Syringate 70164 Click to see 212.20 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
https://doi.org/10.1016/S0031-9422(99)00236-8
https://doi.org/10.1016/J.TET.2011.11.062
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
(3,4,5-Trihydroxy-6-methyloxan-2-yl) 3,4,5-trihydroxybenzoate 59002386 Click to see CC1C(C(C(C(O1)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(99)00236-8
[(2R,3R,4R,5S)-3,5-dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 53233246 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 468.40 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
[3,4-Dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 53396785 Click to see 468.40 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
https://doi.org/10.1016/J.TET.2011.11.062
[3,5-Dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 15558211 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 468.40 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
1-o-Galloyl-alpha-l-rhamnose 87857624 Click to see 316.26 unknown https://doi.org/10.1016/S0031-9422(99)00236-8
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown https://doi.org/10.1016/S0031-9422(99)00236-8
Ginnalin A 5318457 Click to see 468.40 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
https://doi.org/10.1016/J.TET.2011.11.062
Ginnalin B 44512370 Click to see 316.26 unknown https://doi.org/10.1016/J.TET.2011.11.062
https://doi.org/10.1016/J.BMCL.2011.10.073
Ginnalin C 44512371 Click to see C1C(C(C(C(O1)CO)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 316.26 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
https://doi.org/10.1016/J.TET.2011.11.062
Maplexin A 56835101 Click to see C1C(C(C(C(O1)CO)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O 316.26 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
Maplexin B 56835118 Click to see C1C(C(C(C(O1)CO)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 316.26 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
maplexin C 56835119 Click to see C1C(C(C(C(O1)CO)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O 468.40 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
Maplexin D 56835120 Click to see 468.40 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
Maplexin E 56835121 Click to see 620.50 unknown https://doi.org/10.1016/J.BMCL.2011.10.073
Methyl Gallate 7428 Click to see 184.15 unknown https://doi.org/10.1080/14786410802420457
https://doi.org/10.1016/J.BMCL.2011.10.073
https://doi.org/10.1016/S0031-9422(99)00236-8
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl Vanillate 19844 Click to see 182.17 unknown https://doi.org/10.1016/J.TET.2011.11.062
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(3-hydroxy-4-methoxycarbonylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 162867380 Click to see 482.40 unknown https://doi.org/10.1016/J.TET.2011.11.062
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
1-(1H-indol-1-ium-3-yl)-N,N-dimethylmethanamine 101928958 Click to see 175.25 unknown via CMAUP database
Gramine 6890 Click to see 174.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
Digallic Acid 341 Click to see 322.22 unknown https://doi.org/10.1016/S0031-9422(99)00236-8
https://doi.org/10.1080/14786410802420457
Ethyl 3,4-dihydroxy-5-[(3,4,5-trihydroxybenzoyl)oxy]benzoate 71442086 Click to see CCOC(=O)C1=CC(=C(C(=C1)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 350.28 unknown https://doi.org/10.1016/S0031-9422(99)00236-8
> Phenylpropanoids and polyketides / Tannins
(3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl) 3,4,5-trihydroxybenzoate 4628122 Click to see 332.26 unknown https://doi.org/10.1016/S0031-9422(99)00236-8
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown https://doi.org/10.1016/S0031-9422(99)00236-8

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