Rhododendron ferrugineum - Unknown
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Details Top

Internal ID UUID644072fdde9e4809566016
Scientific name Rhododendron ferrugineum
Authority L.
First published in Sp. Pl. : 392 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Plinthocroma ferrugineum (L.) J.Dulac Fl. Hautes-Pyrénées : 419 (1867)
Azalea ferruginea (L.) Kuntze Revis. Gen. Pl. 2: 386 (1891)
Chamaerhododendron ferrugineum (L.) Bubani Fl. Pyren. 2: 5 (1899)

Common names Top

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Language Common/alternative name
English alpine rose
English snow-rose
English rusty-leaved alpenrose
English alpine-rose
English alpenrose
Spanish laurel rosa
Spanish laurel-rosa
Spanish pentecostera
Spanish rododendro
Spanish rosa de los alpes
Spanish la-rosa
Spanish azalea de montaña
Spanish bujo
Arabic غار وردي
Arabic عصلة
Catalan boix de núria
Catalan boixerica
Catalan barset
Catalan gafet
Catalan ganxet
Catalan talabard
Catalan neret
Catalan gavet
Catalan abarset
Czech pěnišník rezavý
Danish rustbladet alperose
Danish alperose (rhododendron ferrugineum) 'wietings select'
Danish alperose
German rostblättrige alpenrose
German rostrote alpenrose
German rostroter almrausch
Finnish ruostealppiruusu
French laurier-rose des alpes
French rosage
French rose des alpes
frr alpenruus
Swiss German alpenrose
Swiss German rostblettrigi alperose
Croatian alpska ruža
Japanese アルペンローゼ
Georgian ალპური ვარდი
Macedonian алпска роза
Norwegian Bokmål alperose
Dutch roestkleurig alpenroosje
Dutch gewone alpenroos
Dutch alpenroos
Polish różanecznik alpejski
Russian Рододендрон ржавый
Serbo-Croatian alpska ruža
Slovak rododendron hrdzavý
Serbian Алпска ружа
Serbian Горска ружа
Serbian Рододендрон
Serbian Слец
Serbian Црвена алпска ружа
Chinese 阿爾卑斯玫瑰
Chinese 炎のアルペンローゼ
Chinese 阿爾卑斯杜鵑
Chinese 高山玫瑰杜鹃
Chinese 高山玫瑰杜鵑
Chinese 锈色杜鹃

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.
may need chilling, sprinkle seed on 10 cm damp sphagnum moss; cover with clear plastic pop bottle cut in half; transplant seedling to acid mix in shade outdoors when 5 cm high; protect from rodents and give protection in cold frame first winter

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Austria
      • Germany
      • Poland
      • Switzerland
    • Southeastern Europe
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000400806
Tropicos 50094831
INPN 117679
Flora of Italy 3726
KEW urn:lsid:ipni.org:names:332420-1
The Plant List kew-2419736
Open Tree Of Life 702565
Observations.org 125144
NCBI Taxonomy 49622
NBN Atlas NBNSYS0200003010
IUCN Red List 203007
IPNI 332420-1
iNaturalist 130539
GBIF 2883073
Freebase /m/0bv1tr
EPPO RHOFE
EOL 586633
USDA GRIN 5110
Wikipedia Rhododendron_ferrugineum
CMAUP NPO18212

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_025642025.1 ASM2564202v1 Scaffold Iridian Genomes 2022-10-10 80.0x 443.16 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
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
Unveiling Curvularia tuberculata-induced leaf anomalies in Rhododendron ferrugineum: implications in cultural-ecological conservation and harnessing microbial intervention in socio-economic advancement Dhar J, Hazra A, Patra R, Kumar V, Subramaniyan V, Kumarasamy V, Mitra AK, Sayed AA, Aleya L, El-Demerdash FM, Almutairi MH, Akash S, Abdel-Daim MM, Kant A, Dhara B Front Microbiol 11-Jan-2024
PMCID:PMC10808759
doi:10.3389/fmicb.2023.1280120
PMID:38274748
Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy Sulaiman N, Zocchi DM, Borrello MT, Mattalia G, Antoniazzi L, Berlinghof SE, Bewick A, Häfliger I, Schembs M, Torri L, Pieroni A Plants (Basel) 22-Dec-2023
PMCID:PMC10780445
doi:10.3390/plants13010043
PMID:38202351
The foraging ecology of yellow-billed and red- billed choughs changed between two climatically different years Rolando A, Basso C, Brunelli N, Bocca M, Laini A Sci Rep 27-Nov-2023
PMCID:PMC10684611
doi:10.1038/s41598-023-46336-0
PMID:38016972
Male reproductive success is not strongly affected by phenological changes in mate availability in monoecious Sagittaria latifolia Kwok A, Stephens S, Dorken M R Soc Open Sci 27-Sep-2023
PMCID:PMC10523072
doi:10.1098/rsos.231117
PMID:37771970
Influences of Maternal Weight and Geographic Factors on Offspring Traits of the Edible Dormouse in the NE of the Iberian Peninsula Míguez S, Torre I, Arrizabalaga A, Freixas L Life (Basel) 21-May-2023
PMCID:PMC10221900
doi:10.3390/life13051223
PMID:37240868
A Comparison of Small Rodent Assemblages after a 20 Year Interval in the Alps Ferrari G, Scaravelli D, Mustoni A, Armanini M, Zibordi F, Devineau O, Cagnacci F, Grasso DA, Ossi F Animals (Basel) 19-Apr-2023
PMCID:PMC10135415
doi:10.3390/ani13081407
PMID:37106970
Nitrogen translocation by Highland cattle grazing in Alnus viridis-encroached pastures Svensk M, Pittarello M, Mariotte P, Nota G, Schneider MK, Frund D, Dubois S, Allan E, Probo M Nutr Cycl Agroecosyst 10-Apr-2023
PMCID:PMC10129924
doi:10.1007/s10705-023-10282-0
PMID:37124631
Erratum: Vessels in a Rhododendron ferrugineum (L.) population do not trace temperature anymore at the alpine shrubline N/A Front Plant Sci 06-Mar-2023
PMCID:PMC10025565
doi:10.3389/fpls.2023.1170080
PMID:36950363
Deep Learning Approach for Predicting the Therapeutic Usages of Unani Formulas towards Finding Essential Compounds Wijaya SH, Nasution AK, Batubara I, Gao P, Huang M, Ono N, Kanaya S, Altaf-Ul-Amin M Life (Basel) 03-Feb-2023
PMCID:PMC9959740
doi:10.3390/life13020439
PMID:36836796
Vessels in a Rhododendron ferrugineum (L.) population do not trace temperature anymore at the alpine shrubline Piccinelli S, Francon L, Corona C, Stoffel M, Slamova L, Cannone N Front Plant Sci 12-Jan-2023
PMCID:PMC9879627
doi:10.3389/fpls.2022.1023384
PMID:36714740
Multimodal pathogen transmission as a limiting factor in host distribution Uricchio LH, Bruns EL, Hood M, Boots M, Antonovics J Ecology 08-Jan-2023
PMCID:PMC9992245
doi:10.1002/ecy.3956
PMID:36511901
New insights on patterns of genetic admixture and phylogeographic history in Iberian high mountain populations of midwife toads Lucati F, Miró A, Bosch J, Caner J, Jowers MJ, Rivera X, Donaire-Barroso D, Rebelo R, Ventura M PLoS One 01-Dec-2022
PMCID:PMC9714896
doi:10.1371/journal.pone.0277298
PMID:36454960
Tackling the Future Pandemics: Broad-Spectrum Antiviral Agents (BSAAs) Based on A-Type Proanthocyanidins Maffei ME, Salata C, Gribaudo G Molecules 30-Nov-2022
PMCID:PMC9736452
doi:10.3390/molecules27238353
PMID:36500445
Physiological mechanisms underlying extreme longevity in mountain pine trees Pasques O, Munné-Bosch S Plant Physiol 28-Nov-2022
PMCID:PMC9922391
doi:10.1093/plphys/kiac540
PMID:36440969

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 / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1021/NP100778K
Sodium Benzoate 517055 Click to see C1=CC=C(C=C1)C(=O)[O-].[Na+] 144.10 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
2-Hydroxy-3-methoxybenzoic acid 70140 Click to see COC1=CC=CC(=C1O)C(=O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown https://doi.org/10.1021/NP100778K
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic acid 19 Click to see C1=CC(=C(C(=C1)O)O)C(=O)O 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methyl 2,4-dihydroxy-6-methylbenzoate 76658 Click to see CC1=CC(=CC(=C1C(=O)OC)O)O 182.17 unknown https://doi.org/10.1021/NP100778K
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron;phenoxide 20488062 Click to see [H+].C1=CC=C(C=C1)[O-] 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown via CMAUP database
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
8,11,13-Abietatriene-3beta-ol 13996029 Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C 286.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Dihydrosolidagenone 101717490 Click to see CC1CC(=O)C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C 318.40 unknown via CMAUP database
Rotundifuran 9841926 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown via CMAUP database
Vitetrifolin B 15543011 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown via CMAUP database
Vitetrifolin C 15543012 Click to see CC1C(C=C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 360.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)81225-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81225-X
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)81225-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate 93317 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
gamma-Tocopherol 92729 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5aS,6S,9R,9aR)-9-(6-hydroxy-6-methylhepta-1,4-dien-2-yl)-3,6-dimethyl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-1,6-diol 162871017 Click to see CC1=CC(=C2C3C(CCC(C3OC2=C1)(C)O)C(=C)CC=CC(C)(C)O)O 358.50 unknown https://doi.org/10.1021/NP100778K
(5aS,6S,9R,9aR)-9-[(5R)-5-hydroxy-6-methylhepta-1,6-dien-2-yl]-3,6-dimethyl-7,8,9,9a-tetrahydro-5aH-dibenzofuran-1,6-diol 163014233 Click to see CC1=CC(=C2C3C(CCC(C3OC2=C1)(C)O)C(=C)CCC(C(=C)C)O)O 358.50 unknown https://doi.org/10.1021/NP100778K
ferruginene A, (rel)- 52951886 Click to see CC1=CC(=C2C3C(CCC(C3OC2=C1)(C)O)C(=C)CCC(C(=C)C)O)O 358.50 unknown https://doi.org/10.1021/NP100778K
ferruginene B, (rel)- 52951887 Click to see CC1=CC(=C2C3C(CCC(C3OC2=C1)(C)O)C(=C)CC=CC(C)(C)O)O 358.50 unknown https://doi.org/10.1021/NP100778K
Ferruginene C 52951888 Click to see CC1=CC(C(CC1)C(=C)CCC(C(=C)C)O)C2=C(C=C(C=C2O)C)O 342.50 unknown https://doi.org/10.1021/NP100778K
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1R,4aS,5R,7aR)-5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate 51346123 Click to see C1=COC(C2C1C(C=C2COC(=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 466.40 unknown via CMAUP database
6'-O-p-Hydroxybenzoylmussaenosidic acid 23955877 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C4=CC=C(C=C4)O)O)O)O)O 496.50 unknown via CMAUP database
Mussaenosidic acid 21633105 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown via CMAUP database
Negundoside 9935561 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O 496.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(5S,6R,8R,9R,10S)-6-Acetoxy-9,15-dihydroxylabda-13-ene-16-oic acid 16,15-lactone 10022565 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
(8alpha)-9,16-Dihydroxylabda-13-ene-15-oic acid gamma-lactone 102105798 Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C 320.50 unknown via CMAUP database
Previtexilactone 21636179 Click to see CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
Vitexilactone 21636178 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,10R,11R,12aR,14bS)-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 5316084 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 https://doi.org/10.1021/NP100778K
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 293273 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1021/NP100778K
23-Hydroxyursolic Acid 14136881 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1021/NP100778K
3-Epiursolic acid 7163177 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
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1007/BF00569023
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1007/BF00569023
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Corosolic acid 6918774 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 https://doi.org/10.1021/NP100778K
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1007/BF00569023
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1021/NP100778K
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1007/BF00569023
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1021/NP100778K
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP100778K
Uvaol 92802 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1021/NP100778K
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(1R,2R,4aalpha,5'E)-2alpha,5,5,8abeta-Tetramethyl-4beta-acetoxy-4',5'-dihydrospiro[decalin-1,2'(3'H)-furan]-5'-ylidene]acetic acid 101357917 Click to see CC1CC(C2C(CCCC2(C13CCC(=CC(=O)O)O3)C)(C)C)OC(=O)C 364.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[2,6-Dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 74155556 Click to see CC(=O)C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(97)00475-5
Phloracetophenone 4'-O-glucoside 23928130 Click to see CC(=O)C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(97)00475-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2',4',6'-Trihydroxyacetophenone 68073 Click to see CC(=O)C1=C(C=C(C=C1O)O)O 168.15 unknown https://doi.org/10.1016/S0031-9422(97)00475-5
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Isoambreinolide 15559824 Click to see CC1CCC2C(CCCC2(C13CCC(=O)O3)C)(C)C 264.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1 11208535 Click to see CC1CCC2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C 290.40 unknown via CMAUP database
Vitex norditerpenoid 2 11462191 Click to see CC1CC(C2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C)OC(=O)C 348.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1021/NP100778K
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Farrerol 442396 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O 300.30 unknown https://doi.org/10.1021/NP100778K
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 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 / Flavonoid-3-O-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 162887296 Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(98)00080-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51521831 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 https://doi.org/10.1016/S0031-9422(98)00080-6
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 https://doi.org/10.1016/S0031-9422(98)00080-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6,3',4'-tetramethoxyflavone 5379563 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)OC 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown via CMAUP database

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