PlantaeDB Logo
Login Sign-up

Phlomis aurea

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

Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fe700cd05e196068727
Scientific name Phlomis aurea
Authority Decne.
First published in Ann. Sci. Nat., Bot. , sér. 2, 2: 251 (1834)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Phlomis flavescens Mill. Gard. Dict. ed. 8 : n.º 10 (1768)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English sinai jerusalem sage
Arabic أذينة ذهبية

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000269191
USDA Plants PHAU12
Tropicos 100241443
KEW urn:lsid:ipni.org:names:453802-1
The Plant List kew-152131
Open Tree Of Life 398653
NCBI Taxonomy 997702
IUCN Red List 84119983
IPNI 453802-1
iNaturalist 880470
GBIF 3888595

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
Antimicrobial Potential of Different Isolates of Chaetomium globosum Combined with Liquid Chromatography Tandem Mass Spectrometry Chemical Profiling Goda MS, El-Kattan N, Abdel-Azeem MA, Allam KA, Badr JM, Nassar NA, Almalki AJ, Alharbi M, Elhady SS, Eltamany EE Biomolecules 21-Nov-2023
PMCID:PMC10742071
doi:10.3390/biom13121683
PMID:38136556
Unleashing Nature’s potential: a computational approach to discovering novel VEGFR-2 inhibitors from African natural compound using virtual screening, ADMET analysis, molecular dynamics, and MMPBSA calculations Baammi S, El Allali A, Daoud R Front Mol Biosci 20-Sep-2023
PMCID:PMC10548200
doi:10.3389/fmolb.2023.1227643
PMID:37800126
Sheep tail fat inhibits the proliferation of non-small-cell lung cancer cells in vitro and in vivo Xu C, Zhang L, He H, Liu X, Pei X, Ma T, Ma B, Lin W, Zhang B Front Pharmacol 11-Aug-2022
PMCID:PMC9403308
doi:10.3389/fphar.2022.917513
PMID:36034869
Plant Oxidative Stress: Biology, Physiology and Mitigation Hasanuzzaman M, Fujita M Plants (Basel) 28-Apr-2022
PMCID:PMC9104056
doi:10.3390/plants11091185
PMID:35567186
In Vitro Propagation, Genetic Assessment, and Medium-Term Conservation of the Coastal Endangered Species Tetraclinis articulata (Vahl) Masters (Cupressaceae) from Adult Trees Juan-Vicedo J, Serrano-Martínez F, Cano-Castillo M, Casas JL Plants (Basel) 11-Jan-2022
PMCID:PMC8778163
doi:10.3390/plants11020187
PMID:35050075
In silico study of potential anti-SARS cell entry phytoligands from Phlomis aurea: a promising avenue for prophylaxis Khattab AR, Teleb M, Kamel MS Future Virol 28-Oct-2021
PMCID:PMC8559586
doi:10.2217/fvl-2021-0031
PMID:34745316
Phylogenetic relationships and DNA barcoding of nine endangered medicinal plant species endemic to Saint Katherine protectorate Hashim AM, Alatawi A, Altaf FM, Qari SH, Elhady ME, Osman GH, Abouseadaa HH Saudi J Biol Sci 01-Jan-2021
PMCID:PMC7938155
doi:10.1016/j.sjbs.2020.12.043
PMID:33732078
Oxidative Stress Responses of Some Endemic Plants to High Altitudes by Intensifying Antioxidants and Secondary Metabolites Content Hashim AM, Alharbi BM, Abdulmajeed AM, Elkelish A, Hozzein WN, Hassan HM Plants (Basel) 09-Jul-2020
PMCID:PMC7412441
doi:10.3390/plants9070869
PMID:32659963
Anti-rheumatoid Activity of Secondary Metabolites Produced by Endophytic Chaetomium globosum Abdel-Azeem AM, Zaki SM, Khalil WF, Makhlouf NA, Farghaly LM Front Microbiol 20-Sep-2016
PMCID:PMC5029229
doi:10.3389/fmicb.2016.01477
PMID:27703452
Iridoids from Phlomis aurea Decne Growing in Egypt E. A. Aboutabl, M. R. Meselhy, M. S. Afifi Wiley 29-Jun-2005
doi:10.1002/CHIN.200301194
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Flavonoids of Phlomis aurea and P. floccosa Sabry I. El-Negoumy, Mohamed F. Abdalla, Nabiel A.M. Saleh Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)88052-9
Iridoid and megastigmane glycosides from Phlomis aurea. Kamel MS, Mohamed KM, Hassanean HA, Ohtani K, Kasai R, Yamasaki K Phytochemistry 01-Oct-2000
doi:10.1016/S0031-9422(00)00331-9
PMID:11117884

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
> Benzenoids / Benzene and substituted derivatives / Anilides / Aromatic anilides / Benzanilides
2-[[3-[(3,4-difluorophenyl)sulfonylamino]benzoyl]amino]-N-(4-fluorophenyl)benzamide 2421196 Click to see C1=CC=C(C(=C1)C(=O)NC2=CC=C(C=C2)F)NC(=O)C3=CC(=CC=C3)NS(=O)(=O)C4=CC(=C(C=C4)F)F 525.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73636 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107782 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Acanthoside D 226371 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,2R)-4-[(1R,4S,6S)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-yl]oxyoxane-3,4,5-triol 162915721 Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O 388.50 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
2-(Hydroxymethyl)-6-[4-(4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)but-3-en-2-yloxy]oxane-3,4,5-triol 75995908 Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O 388.50 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Phlomuroside 637144 Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O 388.50 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-[4-Hydroxy-7-(3-methylbut-2-enyl)-1,3-dihydro-2-benzofuran-1-yl]octane-2,3-diol 162851137 Click to see CCCCCC(C(CC1C2=C(C=CC(=C2CO1)O)CC=C(C)C)O)O 348.50 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epiloganin 10548420 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1002/CHIN.200301194
https://doi.org/10.1016/S0031-9422(00)00331-9
Auroside 45027862 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1002/CHIN.200301194
https://doi.org/10.1016/S0031-9422(00)00331-9
Ipolamiide 442425 Click to see CC1(CCC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Lamiide 443327 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 422.40 unknown https://doi.org/10.1002/CHIN.200301194
https://doi.org/10.1016/S0031-9422(00)00331-9
methyl (1S,4aR,6S,7R,7aS)-4a,6,7-trihydroxy-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 163063657 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
methyl (1S,4aR,6S,7S,7aR)-4a,6-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 21607798 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
methyl (1S,4aS,6S,7S,7aR)-6-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 35755834 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Methyl (4aR,6S,7S)-1-(beta-D-glucopyranosyloxy)-4a,6-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 121232918 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
methyl 4a,6-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 73800781 Click to see CC1C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Methyl 4a,6,7-trihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 4204894 Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Methyl 4a,7-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 3515874 Click to see CC1(CCC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Methyl 6-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 601562 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-(2-phenylethoxy)oxan-3-yl]oxyoxane-3,4,5-triol 14704527 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=CC=C3)CO)O)O)O)O)O 416.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
2-[4,5-Dihydroxy-6-(hydroxymethyl)-2-phenylmethoxyoxan-3-yl]oxyoxane-3,4,5-triol 74378451 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCC3=CC=CC=C3)CO)O)O)O)O)O 402.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Benzyl 2-O-beta-D-xylopyranosyl-beta-D-glucopyranoside 10763616 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCC3=CC=CC=C3)CO)O)O)O)O)O 402.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
methyl (1S,3R,6S,7S,7aR)-6-hydroxy-3-methoxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101085900 Click to see CC1C(CC2=C(C(OC(C12)OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)OC)O 420.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
methyl (1S,3S,6S,7S,7aR)-6-hydroxy-3-methoxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101085901 Click to see CC1C(CC2=C(C(OC(C12)OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)OC)O 420.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Methyl 6-hydroxy-3-methoxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162850731 Click to see CC1C(CC2=C(C(OC(C12)OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)OC)O 420.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
NCGC00384762-01_C19H28O10_beta-D-Glucopyranoside, 2-phenylethyl 2-O-beta-D-xylopyranosyl- 24121293 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=CC=C3)CO)O)O)O)O)O 416.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Xyl(b1-2)L-Glc(b)-O-Bn 163186828 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCC3=CC=CC=C3)CO)O)O)O)O)O 402.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Xyl(b1-2)L-Glc(b)-O-EtPh 163187636 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=CC=C3)CO)O)O)O)O)O 416.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Forsythoside B 23928102 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1002/CHIN.200301194
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Acteoside;Kusaginin;TJC160 354009 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(86)88052-9
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(86)88052-9
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/0031-9422(86)88052-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Lucenin 2 44257937 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 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/10.1002/CHIN.200301194
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[3,4,5-Trihydroxy-6-[[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162986376 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1016/0031-9422(86)88052-9
[3,4,5-Trihydroxy-6-[[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 334350 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C5=CC=C(C=C5)O 580.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162916367 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-7-[[6-O-[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]-beta-D-glucopyranosyl]oxy]-, (2S)- 21630092 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C5=CC=C(C=C5)O 580.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
4H-1-Benzopyran-4-one,2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-7-((6-O-((2E)-3-(4-hydroxyphenyl)-1-oxo-2-propenyl)-beta-D-glucopyranosyl)oxy)- 6451088 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C5=CC=C(C=C5)O 580.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,5S)-3,4,5-trihydroxy-6-[[(2R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 133612286 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(86)88052-9
7-(beta-D-Galactopyranosyloxy)-5-hydroxy-2-(4-Methoxyphenyl)- 5291487 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(86)88052-9
Chrysoeriol-7-O-beta-D-glucoside 13871877 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Hispidulin 7-glucoside 44258433 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(86)88052-9
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9
https://doi.org/10.1016/0031-9422(86)88052-9
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1016/0031-9422(86)88052-9
Thermopsoside 11294177 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(86)88052-9
https://doi.org/10.1016/S0031-9422(00)00331-9
Tilianin 5321954 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(00)00331-9

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.