Details Top

Internal ID UUID644039040fc89445942604
Scientific name Alnus rubra
Authority Bong.
First published in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 2: 162 (1833)

Ethnobotanical Use Top

Suggest a correction!
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.

Ethnobotanical Uses

Across the Pacific Northwest of North America, Alnus rubra has been used in infusions and decoctions for internal care and as poultices for the skin. Among the Yurok and neighboring tribes of northern California and Oregon, a bark decoction was taken for coughs, colds, and sore throats, and sometimes for tuberculosis, a practice described in Mooney’s 1928 ethnography of the Klamath. In southwestern Oregon and northern California, the Karok used a strong bark decoction for fevers and as a “tonic,” and in the intermontane west, the Western Shoshone employed an Alnus rubra infusion as a general health tonic. The outer bark, rather than the inner wood, is consistently specified in the older ethnographies (Gottfried, 1916; Chesnut, 1902).

On the coast, red alder bark was also an external medicine. Among the Maidu of California and several northwest-coastal groups, fresh outer bark was chewed or beaten into a poultice and applied to wounds, swollen glands, and rheumatic pains, with Mooney again noting its use for scrofula. The bark’s astringent character is the key to these applications.

A concise bark decoction preparation is straightforward: simmer about 1 tablespoon (roughly 5 g) of outer bark chips in 250 ml of water for 15 minutes, then steep covered for 10 minutes before straining. This yields a mild astringent tea commonly taken in quarter- to half-cup doses two to three times daily as needed for coughs or fevers. The mixture can also be cooled and used as a compress on sprains or minor wounds. Tannin-rich preparations like this are contraindicated in pregnancy, and long-term high-dose use is not advised due to the risk of gastric irritation and reduced iron absorption.

The principal active constituents in Alnus rubra bark are condensed and hydrolyzable tannins, notably alnustanin and related ellagitannins, along with catechins, flavan-3-ols, and low levels of salicylates. These compounds account for the astringent, anti-inflammatory, and antimicrobial actions repeatedly observed in clinical and folk practice. Today, the species remains a minor but still used source of astringent bark for teas and tinctures in some herbal traditions, and modern phytochemical studies continue to profile its rich tannin profile and potential bioactivities.

General Uses Top

Suggest a correction!

Common products:
Heartwood and sapwood lumber; veneer and plywood; pulpwood and wood chips for kraft and thermo-mechanical pulping; charcoal; fuelwood.

Industrial and craft applications:
Clear-heart lumber is used for furniture, cabinets, millwork, and interior joinery. Veneer and plywood are manufactured for furniture and interior panels. The wood is processed for kraft, semi-chemical, and TMP pulps for printing and writing papers, molded products, and fiberboard; it is noted in North American forestry literature as a high-volume pulp species for West Coast mills. Wood is also converted to charcoal and fuelwood.

Colorants and tanning:
Alder bark and wood are tannin-rich and historically used to tan leather; both yield brown dyes for wool, silk, and leather coloration, with the deepest browns obtained using iron or copper mordants. Commercially, this refers to condensed tannins (proanthocyanidins) found in the bark and wood that chelate metal mordants and oxidize to brown hues.

Scientific and model use:
Red alder’s actinorhizal symbiosis with Frankia makes it a reference organism for nitrogen-fixation and actinorhiza studies; it is used in nursery inoculum production, research on root nodulation, and restoration plantings for site preparation. Genomic and transcriptomic datasets for A. rubra support comparative phylogenetics in the Betulaceae and studies of stress and symbiotic gene expression, including NCBI resources (e.g., Taxonomy ID 10266).

Properties relevant to use:
Wood characteristics: generally diffuse-porous, straight grain, fine to medium texture, and a light brown to reddish heartwood; moderate specific gravity (≈0.41) and low shrinkage yield stable dimensional performance. Sapwood is pale, heartwood exhibits moderate natural durability due to extractives. Tannin content is primarily condensed type; kraft pulping requires appropriate cook profiles to balance lignin removal and hemicellulose preservation.

Standards and regulation:
Lumber graded under NHLA rules; veneer and plywood comply with relevant US and Canadian product standards; kraft and TMP pulps follow industry specifications and mill quality standards; charcoal and fuelwood meet regional emission and handling regulations.

Sustainability and sourcing:
Red alder is a fast-growing, early-successional species naturally regenerated across Pacific Northwest mixed stands; managed stands provide sawtimber and pulpwood while supporting restoration, soil enrichment, and riparian habitat; wood chips and logging residues from harvest and thinning operations supply pulp and energy feedstocks.

Synonyms Top

Scientific name Authority First published in
Alnus incana var. rubra (Bong.) Regel Nouv. Mém. Soc. Imp. Naturalistes Moscou 13(2): 157 1861
Alnus oregana Nutt. N. Amer. Sylv. 1: 9 (1842)
Alnus rubra var. pinnatisecta Starker J. Forest. (Washington) 37: 115 (1939)
Alnus rubra f. pinnatisecta (Starker) Rehder Bibl. Cult. Trees : 104 (1949)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English oregon alder
English western alder
English red alder
Spanish alnus oregana
Spanish alnus rubra var. pinnatisecta
Spanish aliso rojo
Spanish aliso rojo americano
Arabic نغت أحمر
Azerbaijani qırmızı qızılağac
azb قیرمیزی قیزیل آغاج
Bulgarian червена елша
Catalan aulne rouge
Welsh gwernen goch
German aulne rouge
German oregon-erle
German roterle
German rot-erle
Persian توسکای قرمز
Finnish punaleppä
Finnish oregoninleppä
French aulne rouge
Hebrew אלנוס מאדים
Hungarian vörös éger
Icelandic ryðölur
Italian ontano rosso
Japanese アメリカアカハンノキ
Japanese レッドオルダー
koi Гӧрд ловпу
Lithuanian aulne rouge
Norwegian Bokmål rødor
Polish olsza czerwona
Russian Ольха красная
Swedish aulne rouge
Swedish rödal
udm Горд лулпу
Chinese 美國赤楊
Chinese 赤楊
Chinese 红桤木

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northwestern U.S.A.
      • Idaho
      • Montana
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Subarctic America
      • Alaska
      • Yukon
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000947467
UNII SC957G7NBA
Canadensys 3679
USDA Plants ALRU2
Tropicos 3600058
INPN 610834
KEW urn:lsid:ipni.org:names:294986-1
The Plant List kew-6584
PaleoBotany 81345
Open Tree Of Life 639117
Observations.org 141823
NCBI Taxonomy 109069
NBN Atlas NBNSYS0000042064
Nature Serve 2.136265
IUCN Red List 194598
IPNI 294986-1
iNaturalist 56034
GBIF 2876176
Freebase /m/029k_4
FEIS plants/tree/alnrub
EPPO ALURB
EOL 1145612
Elurikkus 2689
Calflora (Californian flora) 253
US Library of Congress sh85112026
USDA GRIN 105118
Wikipedia Alnus_rubra
PFAF Alnus rubra

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_028654335.1 ASM2865433v1 Contig NCGR 2023-02-15 93 525.25 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
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
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
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Succession and climatic stochasticity induce long-term decline of a forest browser Long ES, Tham EJ, Ferrer RP PLoS One 27-Feb-2024
PMCID:PMC10898743
doi:10.1371/journal.pone.0298231
PMID:38412173
High Frankia abundance and low diversity of microbial community are associated with nodulation specificity and stability of sea buckthorn root nodule Liu H, Ni B, Duan A, He C, Zhang J Front Plant Sci 21-Feb-2024
PMCID:PMC10915256
doi:10.3389/fpls.2024.1301447
PMID:38450407
Diversity of Wickerhamomyces (Wickerhamomycetaceae, Saccharomycetales) in China with the description of four new species Chai CY, Ke T, Niu QH, Hui FL Front Microbiol 08-Feb-2024
PMCID:PMC10881795
doi:10.3389/fmicb.2024.1338231
PMID:38389540
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
Pest categorisation of Pestalotiopsis microspora 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, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 21-Dec-2023
PMCID:PMC10733803
doi:10.2903/j.efsa.2023.8493
PMID:38130321
Associations between shade tolerance and wood specific gravity for conifers in contrast to angiosperm trees: Foundations of the conifer fitness‐enhancing shade tolerance hypothesis Tucker GF, Maguire DA, Tupinambá‐Simões F Plant Environ Interact 13-Dec-2023
PMCID:PMC10840375
doi:10.1002/pei3.10131
PMID:38323133
Novel Tri-Segmented Rhabdoviruses: A Data Mining Expedition Unveils the Cryptic Diversity of Cytorhabdoviruses Bejerman N, Dietzgen R, Debat H Viruses 10-Dec-2023
PMCID:PMC10747219
doi:10.3390/v15122402
PMID:38140643
Quaternary palaeoecology meets deep-time palaeobiology Birks HJ Proc Natl Acad Sci U S A 01-Nov-2023
PMCID:PMC10655553
doi:10.1073/pnas.2316233120
PMID:37910534
Commodity risk assessment of Quercus petraea 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, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur 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, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Mechanism of fungal remediation of wetland water: Stropharia rugosoannulata as promising fungal species for the development of biofilters to remove clinically important pathogenic and antibiotic resistant bacteria in contaminated water Sen K, Llewellyn M, Taheri B, Turner RJ, Berglund T, Maloney K Front Microbiol 18-Oct-2023
PMCID:PMC10642173
doi:10.3389/fmicb.2023.1234586
PMID:37965549
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900

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
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.3109/13880209509088144
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9S,11aS,11bS,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 162952656 Click to see 442.70 unknown https://doi.org/10.1002/JPS.2600620129
(1R,3aS,5aS,5bR,7aS,9S,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 163185435 Click to see 426.70 unknown https://doi.org/10.1002/JPS.2600620129
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.3109/13880209509088144
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/JPS.2600620129
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1002/JPS.2600620129
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.3109/13880209509088144
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.3109/13880209509088144
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.3109/13880209509088144
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R)-2-[(3R)-1,7-bis(3,4-dihydroxyphenyl)heptan-3-yl]oxy-3,5-dihydroxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 54585388 Click to see 626.60 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
(3R)-1,7-Bis(3,4-Dihydroxyphenyl)-3-(Beta-D-Glucopyranosyl)Heptan-3-Ol 10097263 Click to see 494.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
(E)-1-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)hept-4-en-3-one 11570978 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O 312.40 unknown https://doi.org/10.1055/S-2006-957372
[(2R,3S,4S,5R,6R)-6-[(3S)-1,7-bis(3,4-dihydroxyphenyl)-5-oxoheptan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 10746324 Click to see 612.60 unknown https://doi.org/10.1055/S-2006-957372
https://doi.org/10.1021/NP980083L
[6-[1,7-Bis(3,4-dihydroxyphenyl)-5-oxoheptan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 85253869 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC(CCC3=CC(=C(C=C3)O)O)CC(=O)CCC4=CC(=C(C=C4)O)O)O)O)O 612.60 unknown https://doi.org/10.1055/S-2006-957372
1-(3,4-Dihydroxyphenyl)-7-(4-hydroxyphenyl)hept-4-en-3-one 73015010 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O 312.40 unknown https://doi.org/10.1055/S-2006-957372
1,7-Bis(3,4-dihydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one 14707657 Click to see 478.50 unknown https://doi.org/10.1055/S-2006-957372
1,7-Bis(4-hydroxyphenyl)-4-hepten-3-one 53840022 Click to see C1=CC(=CC=C1CCC=CC(=O)CCC2=CC=C(C=C2)O)O 296.40 unknown https://doi.org/10.1055/S-2006-957372
CID 45783118 45783118 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 508.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Hirsutal 13347317 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)O)O)O 346.40 unknown https://doi.org/10.1055/S-2006-957372
Hirsutal 5-O-glucoside 14707659 Click to see 508.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Hirsutanonol 9928190 Click to see 346.40 unknown https://doi.org/10.1021/NP980083L
https://doi.org/10.1055/S-2006-957372
Oregonin 14707658 Click to see 478.50 unknown https://doi.org/10.3109/13880209509088144
https://doi.org/10.1021/NP980083L
https://doi.org/10.1055/S-2006-957372
Platyphyllenone 23786382 Click to see 296.40 unknown https://doi.org/10.1055/S-2006-957372
Rubranoside B 24011643 Click to see 464.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Rubranoside D 10532003 Click to see 626.60 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(5S)-1,7-bis(4-hydroxyphenyl)-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyheptan-3-one 10599483 Click to see C1C(C(C(C(O1)OC(CCC2=CC=C(C=C2)O)CC(=O)CCC3=CC=C(C=C3)O)O)O)O 446.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
1,7-Bis(4-hydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one 74203441 Click to see 446.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
1,7-Bis(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-3-one 14833391 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
Platyphylloside 9826264 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/S0031-9422(99)00523-3
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3S,4S,5R,6R)-6-[(3S)-1,7-bis(3,4-dihydroxyphenyl)-5-oxoheptan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3-methoxybenzoate 10699511 Click to see 658.60 unknown https://doi.org/10.1055/S-2006-957372
https://doi.org/10.1021/NP980083L
[6-[1,7-Bis(3,4-dihydroxyphenyl)-5-oxoheptan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxy-3-methoxybenzoate 85237419 Click to see COC1=C(C=CC(=C1)C(=O)OCC2C(C(C(C(O2)OC(CCC3=CC(=C(C=C3)O)O)CC(=O)CCC4=CC(=C(C=C4)O)O)O)O)O)O 658.60 unknown https://doi.org/10.1055/S-2006-957372

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.