Rhododendron tomentosum - Unknown
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Internal ID UUID644081613e271976813568
Scientific name Rhododendron tomentosum
Authority Harmaja
First published in Ann. Bot. Fenn. 27: 204 (1990)

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Synonyms Top

Scientific name Authority First published in
Ledum tomentosum Stokes Bot. Mat. Med. 2: 502 (-504). 1812
Ledum palustre L. Sp. Pl. : 391 (1753)
Ledum palustriforme A.P.Khokhr. & Mazurenko Sosud. Rast. Sovet. Dal'nego Vostoka 5: 126 (1991)
Ledum decumbens (Aiton) Lodd. ex Steud. Nomencl. Bot. [Steudel], ed. 2. 2: 20. 1840 [dt. 1841; issued in Dec 1840]
Ledum dilatatum Rupr. Beitr. Pflanzenk. Russ. Reiches 4: 57 (1845)
Ledum graveolens Gilib. Fl. Lit. Inch. 2: 199 (1782)
Ledum palustre var. decumbens Aiton Hort. Kew. 2: 65 (1789)
Ledum palustre subsp. decumbens Hultén Kongl. Svenska Vetensk. Acad. Handl. , ser. 3, 8(2): 8 (1930)
Rhododendron subarcticum Harmaja Ann. Bot. Fenn. 27(2): 203. 1990
Ledum palustre var. angustum E.A.Busch Fl. Sib. et Orient. 2: 8 1915
Ledum palustre f. decumbens (Aiton) Y.L.Chou & S.L.Tung in Y.L. Chou, Ligneous Fl. Heilongjiang 463 (1986):.
Ledum maximum (Nakai) A.P.Khokhr. & Mazurenko Sosud. Rast. Sovet. Dal'nego Vostoka 5: 122 (1991)
Ledum palustre var. maximum Nakai
Rhododendron palustre (L.) Kron & Judd Syst. Bot. 15(1): 67. 1990
Rhododendron tomentosum subsp. decumbens (Aiton) (Aiton) Elven & D.F.Murray J. Bot. Res. Inst. Texas 2: 441 (2008)
Ledum palustre f. denudatum (Vict. & J.Rousseau) Boivin Naturaliste Canad. 93: 433 (1966)
Ledum groenlandicum f. denudatum Vict. & J.Rousseau Contr. Inst. Bot. Univ. Montréal 36: 44. 1940
Ledum palustre subsp. longifolium Kitag. Neolin. Fl. Manshur. : 498 (1979)
Ledum palustre var. angustifolium Hook. Fl. Bor.-Amer. 2: 44 (1834)
Ledum palustre var. minus Nakai Trees Shrubs Japan , rev. ed., 1: 19 (1927)
Rhododendron tomentosum subsp. subarcticum G.D.Wallace Madroño 39(1): 77. 1992
Rhododendron subartticum Harmaja Ann. Bot. Fenn. 203. (1990)

Common names Top

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Language Common/alternative name
English northern labrador tea
Azerbaijani bataqlıq ladan kolu
Azerbaijani ledum palustre
ba Һаҙанаҡ
Belarusian Багун балотны
Catalan ledum decumbens
Czech rojovník bahenní
Czech ledum palustre
Welsh te labrador
Danish mosepost
Danish mose-post
Danish rhododendron palustre
Danish ledum palustre
German ledol
German sumpf-porst
German porst
German sumpfporst
Estonian ledum palustre
Estonian sookail
Persian اکلیل کوهی وحشی
Finnish ledum palustre
Finnish suopursu
French ledon des marais
French lédon des marais
French petit thé du labrador
French ledum palustris
Armenian Ճահճախնկենի
Icelandic mýraflóki
Italian ledum palustre
Georgian წყლის იელი
Georgian ledum palustre
Lithuanian gailis
Lithuanian pelkių gailis
Latvian purva vaivariņš
Norwegian Bokmål finnmarkspors
Norwegian Bokmål ledum palustre
Dutch ledum palustre
Norwegian Nynorsk finnmarkspors
Polish bagno zwyczajne
Polish ledum palustre
Russian Багульник болотный
Russian Багуль болотная
Russian lédum palústre
Russian ledum palustre
Yakutian Сугун абаҕата
se guohcarássi
Samogitian gailis
Slovak rojovník močiarny
smn ulâštooŋâs
Swedish skvattram
Swedish getpors
Swedish rhododendron tomentosum harmaja
Turkish ledum palustre
tt Сазлык сазанагы
Ukrainian Багно звичайне
Ukrainian Багно болотяне
Ukrainian ledum palustre
vep ludeghein
Vietnamese ledum palustre
Chinese 杜香
Chinese 宽叶杜香

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.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
sprinkle seed on 10 cm damp sphagnum moss; cover with clear plastic pop bottle cut in half; transplant seedling to acidic mix in shade outdoors when 5 cm high; protect from rodents and give protection in cold frame first winter

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-0001275534
Canadensys 5563
Tropicos 50279929
INPN 934768
KEW urn:lsid:ipni.org:names:961622-1
The Plant List tro-50279929
Plantarium 22241
Open Tree Of Life 945421
NCBI Taxonomy 49170
IPNI 30378322-2
iNaturalist 516757
GBIF 6400569
Freebase /m/0bkz2v
EOL 583648
Elurikkus 578292
USDA GRIN 410675
Wikipedia Rhododendron_tomentosum
CMAUP NPO5517

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
Phytochemical Profiling and Biological Activities of Rhododendron Subsect. Ledum: Discovering the Medicinal Potential of Labrador Tea Species in the Northern Hemisphere Vengrytė M, Raudonė L Plants (Basel) 21-Mar-2024
PMCID:PMC10975282
doi:10.3390/plants13060901
PMID:38592945
Vaccinium uliginosum L. (bog bilberry) and the search for its alleged toxicity: a review Vaneková Z, Holloway P, Rollinger JM Front Toxicol 31-Jan-2024
PMCID:PMC10864615
doi:10.3389/ftox.2024.1358840
PMID:38357417
Soil Microbiome in Conditions of Oil Pollution of Subarctic Ecosystems Melekhina EN, Belykh ES, Kanev VA, Taskaeva AA, Tarabukin DV, Zinovyeva AN, Velegzhaninov IO, Rasova EE, Baturina OA, Kabilov MR, Markarova MY Microorganisms 30-Dec-2023
PMCID:PMC10820038
doi:10.3390/microorganisms12010080
PMID:38257907
Geomagnetic Anomaly in the Growth Response of Peat Moss Sphagnum riparium to Temperature Mironov VL Plants (Basel) 22-Dec-2023
PMCID:PMC10780739
doi:10.3390/plants13010048
PMID:38202356
Therapeutic Potential of Myrtenal and Its Derivatives—A Review Dragomanova S, Andonova V, Volcho K, Salakhutdinov N, Kalfin R, Tancheva L Life (Basel) 20-Oct-2023
PMCID:PMC10608190
doi:10.3390/life13102086
PMID:37895468
Peculiarities of the Variation of Biologically Active Compounds in Fruit of Vaccinium oxycoccos L. Growing in the Čepkeliai State Strict Nature Reserve Šedbarė R, Grigaitė O, Janulis V Molecules 05-Aug-2023
PMCID:PMC10421140
doi:10.3390/molecules28155888
PMID:37570858
From Nature to Lab: A Review of Secondary Metabolite Biosynthetic Pathways, Environmental Influences, and In Vitro Approaches Reshi ZA, Ahmad W, Lukatkin AS, Javed SB Metabolites 28-Jul-2023
PMCID:PMC10456650
doi:10.3390/metabo13080895
PMID:37623839
Plant economic strategies in two contrasting forests Sun K, Sun R, Li Y, Ji H, Jia B, Xu Z BMC Plant Biol 22-Jul-2023
PMCID:PMC10362557
doi:10.1186/s12870-023-04375-9
PMID:37479980
Composition and Biological Activity of the Essential Oils from Wild Horsemint, Yarrow, and Yampah from Subalpine Meadows in Southwestern Montana: Immunomodulatory Activity of Dillapiole Schepetkin IA, Özek G, Özek T, Kirpotina LN, Klein RA, Khlebnikov AI, Quinn MT Plants (Basel) 14-Jul-2023
PMCID:PMC10383985
doi:10.3390/plants12142643
PMID:37514257
Syndromic Surveillance of Health Effects Due to Summer Sun Overexposure: Construction of an Indicator Based on Drug Sales in Pharmacies—Preliminary Study within the PRISME Project Riondel A, Simac L, Catelinois O, Morlan-Salesse C, Bounoure F, Galan B, Mouly D Int J Environ Res Public Health 03-Jul-2023
PMCID:PMC10341648
doi:10.3390/ijerph20136287
PMID:37444134
Oral nicotine pouches with an aftertaste? Part 1: screening and initial toxicological assessment of flavorings and other ingredients Mallock-Ohnesorg N, Rinaldi S, Malke S, Dreiack N, Pieper E, Laux P, Schulz T, Zimmermann R, Luch A Arch Toxicol 30-Jun-2023
PMCID:PMC10404176
doi:10.1007/s00204-023-03538-9
PMID:37389646
Production of secondary metabolites using tissue culture-based biotechnological applications Ozyigit II, Dogan I, Hocaoglu-Ozyigit A, Yalcin B, Erdogan A, Yalcin IE, Cabi E, Kaya Y Front Plant Sci 29-Jun-2023
PMCID:PMC10339834
doi:10.3389/fpls.2023.1132555
PMID:37457343
Plant traits poorly predict winner and loser shrub species in a warming tundra biome García Criado M, Myers-Smith IH, Bjorkman AD, Normand S, Blach-Overgaard A, Thomas HJ, Eskelinen A, Happonen K, Alatalo JM, Anadon-Rosell A, Aubin I, te Beest M, Betway-May KR, Blok D, Buras A, Cerabolini BE, Christie K, Cornelissen JH, Forbes BC, Frei ER, Grogan P, Hermanutz L, Hollister RD, Hudson J, Iturrate-Garcia M, Kaarlejärvi E, Kleyer M, Lamarque LJ, Lembrechts JJ, Lévesque E, Luoto M, Macek P, May JL, Prevéy JS, Schaepman-Strub G, Sheremetiev SN, Siegwart Collier L, Soudzilovskaia NA, Trant A, Venn SE, Virkkala AM Nat Commun 28-Jun-2023
PMCID:PMC10307830
doi:10.1038/s41467-023-39573-4
PMID:37380662
Variations in soil microbial community structure and extracellular enzymatic activities along a forest–wetland ecotone in high‐latitude permafrost regions Fu L, Xie R, Ma D, Zhang M, Liu L Ecol Evol 15-Jun-2023
PMCID:PMC10269122
doi:10.1002/ece3.10205
PMID:37332520
Natural Ingredients of Transdermal Drug Delivery Systems as Permeation Enhancers of Active Substances through the Stratum Corneum Schafer N, Balwierz R, Biernat P, Ochędzan-Siodłak W, Lipok J Mol Pharm 06-Jun-2023
PMCID:PMC10324402
doi:10.1021/acs.molpharmaceut.3c00126
PMID:37279070

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
3,7-Dimethylocta-2,6-dienyl formate 7779 Click to see CC(=CCCC(=CCOC=O)C)C 182.26 unknown via CMAUP database
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(3R,5E)-2,6-dimethylocta-1,5,7-trien-3-ol 92256191 Click to see CC(=C)C(CC=C(C)C=C)O 152.23 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Bornyl acetate 6950274 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
(1R)-5-propan-2-ylbicyclo[3.1.0]hex-2-ene-2-carbaldehyde 92469857 Click to see CC(C)C12CC=C(C1C2)C=O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(1R)-1-Isopropenyl-4-methyl-3-cyclohexene-1beta-ol 16059268 Click to see CC1=CCC(CC1)(C(=C)C)O 152.23 unknown via CMAUP database
3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-, 1-acetate, (1R)- 11469649 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown via CMAUP database
Carvone, (-)- 439570 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
cis-p-Mentha-1(7),8-dien-2-ol 6429040 Click to see CC(=C)C1CCC(=C)C(C1)O 152.23 unknown via CMAUP database
trans-1(7),8-p-Menthadien-2-ol 6428442 Click to see CC(=C)C1CCC(=C)C(C1)O 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Calamenene 11298625 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown via CMAUP database
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
beta-(Z)-Elemenone 22211636 Click to see CC(=C1CC(C(CC1=O)(C)C=C)C(=C)C)C 218.33 unknown via CMAUP database
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Alloaromadendrene 10899740 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
(1aR,4R,4aS,7S,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 42433470 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
(1aR)-1abeta,2,3,4,4a,5,6,7,7aalpha,7bbeta-Decahydro-1,1,4beta,7beta-tetramethyl-1H-cyclopropa[e]azulene-4abeta-ol 100922590 Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O 222.37 unknown via CMAUP database
(1aS,4aS,7R,7aR,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 94249462 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
Palustrol (Ledum) 9794494 Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 7093194 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid 7163172 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5S)-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 1738061 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
3,7-Octadien-2-ol, 2-methyl-6-methylene-, (E)- 5363351 Click to see CC(C)(C=CCC(=C)C=C)O 152.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Alpha-branched alpha,beta-unsaturated ketones
2-Methyl-6-methylene-1,7-octadien-3-one 93231 Click to see CC(=C)C(=O)CCC(=C)C=C 150.22 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1S,5R)-5-propan-2-ylbicyclo[3.1.0]hex-3-en-2-one 21626600 Click to see CC(C)C12CC1C(=O)C=C2 136.19 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans
2,5-Dihydrofuran 15570 Click to see C1C=CCO1 70.09 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
cis-Isoascaridole 6430795 Click to see CC(C)C12CCC(C=C1)(OO2)C 168.23 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
3-(4-Methyl-1,4-pentadienyl)furan 101409012 Click to see CC(=C)CC=CC1=COC=C1 148.20 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
cis-Carvenone oxide 6430794 Click to see CC1CCC2(C(C1=O)O2)C(C)C 168.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin 5273569 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O 208.17 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 O-glycosides
2-[3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]-3,5,7-trihydroxychromen-4-one 100952311 Click to see C1C(C(C(C(O1)OC2=CC(=CC(=C2O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O 450.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
6''-Acetylhyperin 25230434 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 506.40 unknown via CMAUP database
Hyperoside 5281643 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)O)O)O 464.40 unknown via CMAUP database
Quercetin 3-(6''-p-hydroxybenzoylgalactoside) 91666354 Click to see C1=CC(=CC=C1C(=O)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 584.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(6-O-beta-D-Xylopyranosyl-beta-D-glucopyranosyl)oxy]-3',5-dihydroxy-4'-methoxyflavone 6325773 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
8-Demethyleucalyptin 15715157 Click to see CC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)OC)OC 312.30 unknown via CMAUP database
Myricetin 3,7,3',5'-tetramethyl ether 44259713 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)O)OC)O 374.30 unknown via CMAUP database
Pachypodol 5281677 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O 344.30 unknown via CMAUP database

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