Lithospermum officinale - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Lithospermum officinale - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643ff451871af925966354
Scientific name Lithospermum officinale
Authority L.
First published in Sp. Pl. : 132 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lithospermum majus Gilib. Fl. Lit. Inch. 1: 21 (1782)
Lithospermum ochroleucum Stokes Bot. Mat. Med. 1: 270 (1812)
Margarospermum officinale Decne. Voy. Inde 4: 122 (1843)
Lithospermum officinale var. stewartii Kazmi J. Arnold Arbor. 52: 358 (1971)

Common names Top

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Language Common/alternative name
English european stoneseed
English common gromwell
Arabic حجرية البذر المخزنية
Azerbaijani dərman səfərotu
Belarusian верабейнік лекавы
Bulgarian просо птиче
Catalan mill del sol
Czech kamejka lékařská
Welsh maenhad
Danish lægestenfrø
Danish læge-stenfrø
German gebräuchlicher steinsame
German echter steinsame
Estonian suur rusujuur
Persian سنگدانه
Finnish rohtorusojuuri
French grémil officinal
Irish gormail
Hungarian kőmagvú gyöngyköles
Armenian Կաքավկրկուտ դեղատու
Georgian კაკბის საკენკელა
Lithuanian vaistinis kietagrūdis
Norwegian Bokmål legesteinfrø
Dutch glad parelzaad
Norwegian Nynorsk lækjesteinfrø
Polish nawrot lekarski
Russian деребянка
Russian Воробейник лекарственный
Slovak kamienka lekárska
Swedish stenfrö
Chinese 小花紫草
Chinese 白果紫草
Chinese 珍珠透骨草

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.
Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • Inner Mongolia
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Siberia
      • Altay
      • Buryatiya
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
    • Western Asia
      • Afghanistan
      • Iran
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
    • Western Canada
      • Manitoba
  • Southern America
    • Southern South America
      • Argentina South
    • Western South America
      • Colombia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000361802
UNII 2C36AK404P
Canadensys 3787
USDA Plants LIOF
Tropicos 4000135
INPN 106396
Flora of Italy 4254
KEW urn:lsid:ipni.org:names:118163-1
The Plant List kew-2343333
Open Tree Of Life 382392
Observations.org 6995
NCBI Taxonomy 475907
NBN Atlas NBNSYS0000004016
Nature Serve 2.140416
IPNI 118163-1
iNaturalist 204348
GBIF 2926086
Freebase /m/0d7m18
WisFlora 4098
EPPO LITOF
EOL 581953
Elurikkus 5514
US Library of Congress sh2003007698
USDA GRIN 22416
Wikipedia Lithospermum_officinale
CMAUP NPO8642
Plantarium 23078

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
Pharmacological Significance of Boraginaceae with Special Insights into Shikonin and Its Potential in the Food Industry Gautam S, Lapčík L, Lapčíková B Foods 27-Apr-2024
PMCID:PMC11082953
doi:10.3390/foods13091350
PMID:38731721
Exploring the Pharmacological Potential of Lithospermum officinale L.: A Review of Phytochemicals and Ethnomedicinal Uses Barkizatova G, Turgumbayeva A, Zhakipbekov K, Bekesheva K, Arystanov Z, Arystanova T, Kayupova F, Zhumalina K, Toxanbayeva Z, Ibragimova A, Blinova O, Utegenova G, Iztileu N, Shynykul Z Molecules 19-Apr-2024
PMCID:PMC11055044
doi:10.3390/molecules29081856
PMID:38675676
Endophytes: a uniquely tailored source of potential antibiotic adjuvants Moussa AY Arch Microbiol 06-Apr-2024
PMCID:PMC10998792
doi:10.1007/s00203-024-03891-y
PMID:38581477
Investigation the biological activities and the metabolite profiles of endophytic fungi isolated from Gundelia tournefortii L. Ebadi M, Ahmadi F, Tahmouresi H, Pazhang M, Mollaei S Sci Rep 25-Mar-2024
PMCID:PMC10963752
doi:10.1038/s41598-024-57222-8
PMID:38528041
Biological Activity of Fermented Plant Extracts for Potential Dermal Applications Herman A, Herman AP Pharmaceutics 14-Dec-2023
PMCID:PMC10748213
doi:10.3390/pharmaceutics15122775
PMID:38140115
Recent Advances in the Detection of Food Toxins Using Mass Spectrometry Ahuja V, Singh A, Paul D, Dasgupta D, Urajová P, Ghosh S, Singh R, Sahoo G, Ewe D, Saurav K Chem Res Toxicol 07-Dec-2023
PMCID:PMC10731662
doi:10.1021/acs.chemrestox.3c00241
PMID:38059476
Microbial fortification of pharmacological metabolites in medicinal plants Wu X, Yang Y, Zhang H Comput Struct Biotechnol J 13-Oct-2023
PMCID:PMC10589376
doi:10.1016/j.csbj.2023.10.024
PMID:37867972
Diversity, Antimicrobial, Antioxidant, and Anticancer Activity of Culturable Fungal Endophyte Communities in Cordia dichotoma Sharma M, Bharti S, Goswami A, Mallubhotla S Molecules 04-Oct-2023
PMCID:PMC10574381
doi:10.3390/molecules28196926
PMID:37836769
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
Ethnobotany for food security and ecological transition: wild food plant gathering and consumption among four cultural groups in Kurram District, NW Pakistan Hussain ST, Muhammad S, Khan S, Hussain W, Pieroni A J Ethnobiol Ethnomed 01-Sep-2023
PMCID:PMC10472554
doi:10.1186/s13002-023-00607-2
PMID:37658453
Arbuscular mycorrhizal fungi impact the production of alkannin/shikonin and their derivatives in Alkanna tinctoria Tausch. grown in semi-hydroponic and pot cultivation systems Zhao Y, Cartabia A, Garcés-Ruiz M, Herent MF, Quetin-Leclercq J, Ortiz S, Declerck S, Lalaymia I Front Microbiol 10-Aug-2023
PMCID:PMC10447974
doi:10.3389/fmicb.2023.1216029
PMID:37637105
Natural Plant-Derived Compounds in Food and Cosmetics: A Paradigm of Shikonin and Its Derivatives Malik S, Brudzyńska P, Khan MR, Sytar O, Makhzoum A, Sionkowska A Materials (Basel) 14-Jun-2023
PMCID:PMC10304009
doi:10.3390/ma16124377
PMID:37374560
Editorial: Plant chemoecology: Integrating micro- and macrolevel approaches in regulating secondary metabolism Guo J, Deng J, Liu J Front Plant Sci 20-Jan-2023
PMCID:PMC9897056
doi:10.3389/fpls.2022.1119152
PMID:36743584
The endophytic Fusarium strains: a treasure trove of natural products Ahmed AM, Mahmoud BK, Millán-Aguiñaga N, Abdelmohsen UR, Fouad MA RSC Adv 09-Jan-2023
PMCID:PMC9827111
doi:10.1039/d2ra04126j
PMID:36686899
Dynamics of alkannin/shikonin biosynthesis in response to jasmonate and salicylic acid in Lithospermum officinale Ahmad M, Varela Alonso A, Koletti AE, Rodić N, Reichelt M, Rödel P, Assimopoulou AN, Paun O, Declerck S, Schneider C, Molin EM Sci Rep 12-Oct-2022
PMCID:PMC9554848
doi:10.1038/s41598-022-21322-0
PMID:36224205

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
> Alkaloids and derivatives
[7-(3-hydroxy-3-methylbutanoyl)oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-(1-acetyloxyethyl)-2,3-dihydroxy-3-methylbutanoate 162948400 Click to see CC(C(C(=O)OCC1=CCN2C1C(CC2)OC(=O)CC(C)(C)O)(C(C)(C)O)O)OC(=O)C 457.50 unknown https://doi.org/10.1016/0031-9422(94)85040-2
[7-(3-hydroxy-3-methylbutanoyl)oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 163001098 Click to see CC(C(C(=O)OCC1=CCN2C1C(CC2)OC(=O)CC(C)(C)O)(C(C)(C)O)O)O 415.50 unknown https://doi.org/10.1016/0031-9422(94)85040-2
Acetyllythosenine 101674027 Click to see CC(C(C(=O)OCC1=CCN2C1C(CC2)OC(=O)CC(C)(C)O)(C(C)(C)O)O)OC(=O)C 457.50 unknown https://doi.org/10.1016/0031-9422(94)85040-2
Lithosenine 101674026 Click to see CC(C(C(=O)OCC1=CCN2C1C(CC2)OC(=O)CC(C)(C)O)(C(C)(C)O)O)O 415.50 unknown https://doi.org/10.1016/0031-9422(94)85040-2
> Alkaloids and derivatives / Aporphines
N-acetylanonaine 6453733 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 307.30 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Arnottianamide 3085181 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O 381.40 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
[(E)-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-hydroxy-4-methylpent-2-enyl] 2-methylbutanoate 5319056 Click to see CCC(C)C(=O)OC(C=CC(C)(C)O)C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 388.40 unknown via CMAUP database
[3,5,5,5-Tetradeuterio-1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-4-(trideuteriomethyl)pent-3-enyl] acetate 131674214 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)OC(=O)C)C 337.40 unknown https://doi.org/10.1142/S0192415X08005631
2-Methylprop-1-enyl 2-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-5-methylhex-4-enoate 5320198 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)C(=O)OC=C(C)C)C 370.40 unknown via CMAUP database
C.I. Natural Red 20 5208 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O)C 288.29 unknown https://doi.org/10.1007/BF00564952
https://doi.org/10.1007/BF00566995
Shikonin 479503 Click to see CC(=CCC(C1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)O)C 288.29 unknown https://doi.org/10.1007/BF00564952
https://doi.org/10.1007/BF00566995
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8E,10E,12E)-N-(2-hydroxy-2-methylpropyl)tetradeca-2,4,8,10,12-pentaenamide 14135316 Click to see CC=CC=CC=CCCC=CC=CC(=O)NCC(C)(C)O 289.40 unknown via CMAUP database
(2E,4E,8Z,11E)-N-(2-hydroxy-2-methylpropyl)tetradeca-2,4,8,11-tetraenamide 14135320 Click to see CCC=CCC=CCCC=CC=CC(=O)NCC(C)(C)O 291.40 unknown via CMAUP database
(2E,4E,8Z,11Z)-N-(2-hydroxy-2-methylpropyl)tetradeca-2,4,8,11-tetraenamide 14135319 Click to see CCC=CCC=CCCC=CC=CC(=O)NCC(C)(C)O 291.40 unknown via CMAUP database
(2E,6R,7E,9E)-6-hydroxy-N-(2-hydroxy-2-methylpropyl)-11-oxododeca-2,7,9-trienamide 101357058 Click to see CC(=O)C=CC=CC(CCC=CC(=O)NCC(C)(C)O)O 295.37 unknown via CMAUP database
(2E,6Z,8E,10Z)-N-(2-hydroxy-2-methylpropyl)dodeca-2,6,8,10-tetraenamide 46870578 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-alpha-sanshool 10084135 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-Beta-Sanshool 10220912 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-gamma-Sanshool 14135317 Click to see CC=CC=CC=CCCC=CC=CC(=O)NCC(C)(C)O 289.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown via CMAUP database
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Terpinen-4-ol 5325830 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(4,16-Dihydroxy-2,6,14,17-tetramethyl-3,11-dioxo-10-oxatetracyclo[7.7.1.02,7.013,17]heptadecan-15-yl) acetate 5321291 Click to see CC1CC(C(=O)C2(C1CC3C4(C2C(C(C(C4CC(=O)O3)C)OC(=O)C)O)C)C)O 408.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2Z)-2-[4,5-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 6079060 Click to see C1=CC(=CC#N)C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1016/S0031-9422(00)89236-5
Lithospermoside 10065132 Click to see C1=CC(=CC#N)C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1016/S0031-9422(00)89236-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(R-(E))-5-Isopropyl-8-methylnona-6,8-dien-2-one 16058296 Click to see CC(C)C(CCC(=O)C)C=CC(=C)C 194.31 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Nitidine 4501 Click to see C[N+]1=CC2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC 348.40 unknown via CMAUP database
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
Schinifoline 133504 Click to see CCCCCCCC1=CC(=O)C2=CC=CC=C2N1C 257.37 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Zanthobungeanine 5315422 Click to see CC1(C=CC2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)C 271.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Lithospermic acid 6441498 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)O)O)O 538.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,6-Trihydroxy-7,4'-dimethoxyflavone 5322058 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)O)O)O 330.29 unknown via CMAUP database
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 / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 5317847 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 94858662 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown via CMAUP database
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 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
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)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)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,7-Bis(beta-D-glucopyranosyloxy)-3',5-dihydroxy-4'-methoxyflavone 102574483 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 640.50 unknown via CMAUP database
Isorhamnetin 7-glucoside 6455477 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown via CMAUP database

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